WO2019185612A1 - Method of reducing soil water repellency - Google Patents

Method of reducing soil water repellency Download PDF

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Publication number
WO2019185612A1
WO2019185612A1 PCT/EP2019/057548 EP2019057548W WO2019185612A1 WO 2019185612 A1 WO2019185612 A1 WO 2019185612A1 EP 2019057548 W EP2019057548 W EP 2019057548W WO 2019185612 A1 WO2019185612 A1 WO 2019185612A1
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WO
WIPO (PCT)
Prior art keywords
seq
soil
lipase
polypeptide
acid sequence
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PCT/EP2019/057548
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French (fr)
Inventor
Alexander Wissemeier
Uwe Thiel
Kai-Uwe Baldenius
Oliver Spangenberg
David Edward Mainwaring
Pandiyan Murugaraj
Wolfgang Weigelt
Sonja KUEBELBECK
Grit BAIER
Original Assignee
Basf Se
Grains Research And Development Corporation (Grdc)
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Application filed by Basf Se, Grains Research And Development Corporation (Grdc) filed Critical Basf Se
Publication of WO2019185612A1 publication Critical patent/WO2019185612A1/en

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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/16—Hydrolases (3) acting on ester bonds (3.1)
    • C12N9/18—Carboxylic ester hydrolases (3.1.1)
    • C12N9/20—Triglyceride splitting, e.g. by means of lipase
    • C—CHEMISTRY; METALLURGY
    • C05—FERTILISERS; MANUFACTURE THEREOF
    • C05F—ORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C, e.g. FERTILISERS FROM WASTE OR REFUSE
    • C05F11/00—Other organic fertilisers
    • C05F11/10—Fertilisers containing plant vitamins or hormones
    • C—CHEMISTRY; METALLURGY
    • C05—FERTILISERS; MANUFACTURE THEREOF
    • C05G—MIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
    • C05G3/00—Mixtures of one or more fertilisers with additives not having a specially fertilising activity
    • C05G3/70—Mixtures of one or more fertilisers with additives not having a specially fertilising activity for affecting wettability, e.g. drying agents
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K17/00—Soil-conditioning materials or soil-stabilising materials
    • C09K17/40—Soil-conditioning materials or soil-stabilising materials containing mixtures of inorganic and organic compounds

Definitions

  • the present invention relates to a method of reducing soil water repellency and/or for increasing water holding capacity using a lipase.
  • Soil water repellency is a condition where soil does not spontaneously wet when a drop of water is applied to the soil surface, i.e. the soil is too hydrophobic (Muller and Deuer (2011 ) Agric., Ecosystems and Environ. 144: 208-221). Hydrophobic soils occur in many countries on various lands, such as agricultural, pasture, coastal dune sands, forest, shrub lands, parks, turfgrass soils, no-till agriculture, and soils irrigated with treated wastewater. A substantial inter- est in soil water repellency soils has grown in recent times (WO 2013/181240; Dekker et al. (2005) Aust. J. of Soil Res. 43: 403-441 ).
  • Soil water repellency can cause undesirable consequences such as environmental deterioration and considerable losses in crop production. Soil water repellency becomes especially problem- atic on water relationships and can cause associated environmental issues, such as, but not limited to, reduction in soil water intake, uneven wetting patterns, reduced irrigation efficiency and effective precipitation, increased preferential flow that can have adverse effects on aquifer contamination, greater runoff and erosion, limited seed and vegetative establishment, and re-umbled plant growth and quality (Doerr et al. (2000). Earth-Sci. Reviews 51 : 33-65; Muller and Deuer (201 1 )).
  • soil water repellency across large areas of crop-producing fields leads to reduction or complete loss of already planted crops as well as reduction in soil quality and wa- tering problems for the next set of seeds.
  • soil water repellency is a reoccurring problem called“localized dry spot” (LDS).
  • LDS soil water repellency appears as irregular dry areas from a few centimeters to several meters diameter with the repellency usually extending from the surface of the soils into 5-10 cm depth.
  • the primary cause of soil water repellency is the formation of a coating of hydrophobic, organic material on soil particles.
  • This hydrophobic organic material can include surface waxes, fatty ac- ids, and other organics such as lignin, a phenolic polymer. These materials originate from plant leaves and other decomposing organic matter, plant root exudates, fungal hyphae/exudates, and volatized organic materials condensing on soil particles following forest or grassland fires (Atanassova and Doerr (2010) Europ. J. of Soil Sci. 61 : 298-313). Sandy soils are especially susceptible to soil water repellency due to a lower particle surface area.
  • the present inventors have surprisingly found that the application of a lipase to soil leads to a reduced soil water repellency and an increased water holding capacity of non-wetting soils. Ad- ditionally, the application of a lipase also increases the water availability in wetting soils.
  • the present invention relates to the use of an isolated polypeptide having lipase ac- tivity for increasing the water availability in soil.
  • the soil water repellency of non-wetting soil is reduced and/or the water holding capacity of non-wetting soils is increased.
  • the water holding capacity of wetting soil is increased and/or the evapo- ration from wetting soil is decreased.
  • the isolated polypeptide having lipase activity may be selected from the group consisting of:
  • polypeptide having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28,
  • SEQ ID NO: 30 SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56, SEQ ID NO: 58, SEQ ID NO: 60, SEQ ID NO: 62,
  • SEQ ID NO: 98 SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, SEQ ID NO: 1 10, SEQ ID NO: 112, SEQ ID NO: 1 14, SEQ ID NO: 116, SEQ ID NO: 1 18, SEQ ID NO: 120, SEQ ID NO: 122, SEQ ID NO: 124, SEQ ID NO: 126, SEQ ID NO: 128, SEQ ID NO: 130, SEQ ID NO: 132, SEQ ID NO: 134, SEQ ID NO: 136, SEQ ID NO: 138, SEQ ID NO: 140, SEQ ID NO: 142, SEQ ID NO: 143, SEQ ID NO: 146, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 152, SEQ ID NO: 154, SEQ ID NO: 156, SEQ ID NO: 158, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID
  • SEQ ID NO: 51 SEQ ID NO: 53, SEQ ID NO: 55, SEQ ID NO: 57, SEQ ID NO: 59, SEQ ID NO: 61 , SEQ ID NO: 63, SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 71 , SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 77, SEQ ID NO: 79, SEQ ID NO: 81 , SEQ ID NO: 83,
  • polypeptide having lipase activity is selected from the group consisting of
  • polypeptide having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100, SEQ ID NO: 1 14, SEQ ID NO: 142, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 156, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 182, SEQ ID NO: 186, SEQ ID NO: 194, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 214, SEQ ID NO: 218, SEQ ID NO: 224, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 244, SEQ ID NO: 26
  • polypeptide having lipase activity is selected from the group consisting of:
  • polypeptide having the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 90, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100 or SEQ ID NO: 114 or an enzymatically active frag- ment thereof having lipase activity;
  • polypeptide having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 90, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100 or SEQ ID NO: 114 or an enzymatically active fragment thereof having lipase activity;
  • a polypeptide encoded by a nucleic acid sequence which hybridizes to the complement of the nucleic acid sequence according to SEQ ID NO: 955, SEQ ID NO: 89, SEQ ID NO: 3, SEQ ID NO: 15, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 75, SEQ ID NO: 99 or SEQ ID NO: 113 under stringent conditions.
  • the polypeptide having lipase activity is selected from the group consist- ing of: (i) a polypeptide having the amino acid sequence according to SEQ ID NO: 956 or SEQ ID NO: 90 or an enzymatically active fragment thereof having lipase activity;
  • the polypeptide having lipase activity may be used in combination with at least one soil addi- tive, preferably selected from the group of surfactants, fertilizers, nitrification inhibitors and/or pesticides, preferably fungicides.
  • the polypeptide having lipase activity is applied in a concentration of be- tween 0.01 kg to 600 kg of polypeptide per hectare, preferably of between 0.16 kg to 100 kg per hectare, more preferably of between 0.6 kg to 20 kg per hectare, most preferably of between 1 kg to 5 kg per hectare.
  • the soil may be selected from agricultural land, pasture, coastal dune sands, forest, shrub lands, parks, turfgrass soils, no-till agriculture, and soils irrigated with treated wastewater.
  • the present invention also relates to a method for increasing the water availability in soil corn- prising treating an area of groundcover with an isolated polypeptide having lipase activity.
  • the soil water repellency of non-wetting soil is reduced and/or the water holding capacity of non-wetting soil is increased.
  • the water holding capacity of wetting soil is increased and/or the evapo- ration from wetting soil is decreased.
  • the polypeptide having lipase activity may be as defined in any one of claims 4 to 6.
  • polypeptide having lipase activity may be selected from the group consisting of:
  • polypeptide having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956 or an enzymatically active fragment thereof having lipase activity;
  • polypeptide encoded by a nucleic acid sequence which hybridizes to the complement of the nucleic acid sequence according to SEQ ID NO: 955 under stringent conditions.
  • the polypeptide or an enzymatically active fragment thereof having lipase activity is used in combination with at least one soil additive, preferably selected from the group of surfactants, fertilizers, nitrification inhibitors and/or pesticides, preferably fungicides.
  • the polypeptide or an enzymatically active fragment thereof having lipase activity may be ap- plied in a concentration of between 0.01 kg to 600 kg of polypeptide per hectare, preferably of between 0.16 kg to 100 kg per hectare, more preferably of between 0.6 kg to 20 kg per hectare, most preferably of between 1 kg to 5 kg per hectare.
  • the present invention also relates to the use of an isolated polypeptide having lipase activity for promoting plant growth.
  • the polypeptide having lipase activity may be as defined in any one of claims 4 to 6.
  • polypeptide having lipase activity may be selected from the group consisting of:
  • polypeptide having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956 or an enzymatically active fragment thereof having lipase activity;
  • FIG. 1 shows the experimental setup for determining soil parameters.
  • Figure 1 A is a schematic drawing of the columns prepared for assessing water droplet penetra- tion time (WDPT), water infiltration time, and water holding capacity of soil samples.
  • WDPT water droplet penetra- tion time
  • FIG. 1 B is a schematic drawing of the experimental set-up for assessing WDPT, water infiltra tion time, and water holding capacity of soil samples.
  • FIG. 2 contains bar graphs illustrating WDPT (FIG. 2A) and water infiltration time (FIG. 2B) of three different soils treated with either a water control (white bars) or a 0.06% (w/v) lipase solu- tion (black bars). Limburgerhof wetting soil serves as a control; the two non-wetting soils (Peter Black and South Stirling) are from Western Australia.
  • FIG. 3 contains line graphs illustrating WDPT (FIG. 3A) of the non-wetting soil South Stirling as well as water infiltration time (FIG. 3B) and water holding capacity (FIG. 3C) of two different non-wetting soils from Western Australia (diamonds: Peter Black; inverted triangles: South Stir- ling) treated with different lipase concentrations.
  • FIG. 4 contains bar graphs illustrating percolated (leached) water (FIG. 4A), evaporation (FIG. 4B), and plant shoot fresh and dry weight (FIG 4C) of the wetting soil Limburgerhof treated with 0.06% (w/v) lipase solution (black bars) or only water (white bars).
  • FIG.5 shows the dynamic water contact angles for the non-wetting soil South Stirling soil after treatment with chitinase, laccase or lipase plus two controls (water treated and untreated soil).
  • FIG. 6 shows the experimental setup for determining soil parameters depending on the soil depth (FIG. 6A), the initial infiltration (FIG. 6B), water droplet penetration time (WDPT; FIG. 6C), the infiltration after drying (FIG. 6D) and the water holding capacity (FIG. 6E) of putting green treated with 0.04% (w/v) lipase solution (black squares), 0.42% (w/v) the wetting agent KICK (grey circles) or only water (white squares).
  • FIG. 7 shows the experimental setup to simulate long term effects by adding water to the soil columns (FIG. 7A), the water infiltration time at three different timepoints (FIG. 7B) and the wa- ter holding capacity at three different timepoints (FIG. 7C) of putting green treated with 0.04% (w/v) lipase solution (black bars), 0.42% (w/v) the wetting agent KICK (grey bars) or only water (white bars).
  • FIG. 8 shows the growth of turf grass in putting green treated with 0.03% (w/v) lipase solution (black bar) or only water (white bar).
  • steps of a method or use or assay there is no time or time interval coherence between the steps, i.e. the steps may be carried out simultaneously or there may be time intervals of sec- onds, minutes, hours, days, weeks, months or even years between such steps, unless other- wise indicated in the application as set forth herein above or below.
  • the present invention is based on the finding that the application of a li- pase to soil increases the water availability in soil.
  • water availability refers to the amount of water which is present in a given volume of soil. This amount of water can be taken up by plants and used for growing. Hence, by improving the water availability in soil the soil is more suitable for growing plants.
  • the water availability in soil is increased by at least 3% or 5%, preferably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15%.
  • the amount of water which can be taken up by plants treated in accordance with the present invention is increased by at least 3% or 5%, pref- erably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15% compared to a soil which has not been treated in accordance with the present invention.
  • the application of a lipase reduces soil water repellency and/or increases the water holding capacity of non-wetting soil.
  • soil water repellency is a condition where soil does not spontaneously wet when a drop of water is applied to the surface. It reduces the affinity of soils to water such that they resist wetting for variable periods. It may be present in a large area and therefore affect agriculture. Such large areas of water-repellent soil predominantly occur in Australia as well as in North and South America.
  • soil water repellency may present as "localized dry spots” which are irregular dry areas from a few centimeters to several meters diameter and mainly occur on sandy turfgrass soils and grasslands.
  • soil water repellency may present as "fairy rings" which are caused by fungi, in particular by basidiomycetes and which have a round shape. The fairy rings can range from a few centimeters to 20 meters in diameter, particularly from 0.5 m to 5m in diameter.
  • the organic matter contributing to hydrophobic organic coatings in soils with soil water repel- lency arises from sources such as, but not limited to: a) plant vegetation and root exudates with certain plant species especially prone to causing SWR, such as pine, gum, and oak trees and grasses; b) decomposition products from soil microbial activity, soil microorganism biomass such as fungal hyphae, and root exudates; c) applied organic amendments; d) ashed or volatized organic materials condensing on soil particles following forest or grassland fires; and e) organic matter in treated waste water used for irrigation. Regardless of soil type or organic matter source, soil drying increases repellency with air-drying greatly enhancing SWR severity.
  • the typical types of organic compounds suggested to be involved in soil water repellency in- clude: a) high molecular weight, polar fatty acids and their esters (alkanes that are derived from plant and cuticular waxes); b) other alkanes (paraffin-like compounds), microbial derived waxes, alkanols, phytanols, phytanes; c) amphiphilic (partially hydrophobic) lipids, stigmasterols and plant derived sterols that have polar (hydrophilic) and non-polar (hydrophobic) groups; d) other polar molecules such as sugars, gylocsides, aromatic acids, and low molecular weight organic acids; e) humic and fulvic acids from soil microbial activity or possibly added as amendments; and f) hydrophobins, cysteine rich proteins expressed only by filamentous fungi.
  • the soil water repellency can be measured and classified by a variety of methods.
  • the water droplet penetration time (WDPT) test is based on the time taken for a drop of water to infiltrate into an air- or oven-dried soil sample (Dekker et al. (1998) Soil Sci. 163: 780-796). A description of this method is provided in the examples section herein.
  • the molarity of ethanol droplet (MED) or ethanol test uses a series of aqueous ethanol solutions prepared in concentrations ranging between 0% and 36%.
  • the degree of soil water repellency is then defined as the ethanol percentage or molarity of the least concentrated ethanol solution that is absorbed by the soil in a mean time of ⁇ 10 s (DeBano et al. (2000) J. Hydrol. 231 :4-32).
  • sorptivity of wa- ter which is influenced by repellency is compared to the sorptivity of ethanol which is not influ enced by repellency (Tillman et al. (1999) Austr. J. Soil Res. 27: 637-644).
  • the contact angle between water and soil may be measured e.g. by the capillary rise method (Woche et al. (2005) Eur. J. Soil Sci. 56: 239-251 ).
  • the soil water repellency of non-wetting soils is reduced by at least 10% or 20%, preferably by at least 30% or 40%, more preferably by at least 50% or 60% and most preferably by at least 70% or 75%. If the soil water repellency is meas- ured using the WDPT test, the time taken for a drop to infiltrate the soil is reduced by at least 10% or 20%, preferably by at least 30% or 40%, more preferably by at least 50% or 60% and most preferably by at least 70% or 75%.
  • water holding capacity refers to the amount of water that a given amount of soil can hold. This has an impact on the water supply of any crops planted on the soil, but also on the retention of nutrients and pesticides by the soil.
  • the water holding capacity can be determined by applying a defined amount of water onto a defined amount of soil and after a certain period of time such as two hours weighing the soil. The difference between the weight of the soil after applying the water and before applying the water is the amount of water which is held by the soil.
  • the water holding capacity can be determined by placing a water saturated soil sample on a porous ceramic plate which is then placed in closed chambers and a known amount of pressure is applied to the chamber which forces water out of the soil sample and into the porous plate and out of the chamber.
  • the water holding capacity can also be determined by measuring the amount of water leached through the soil after a defined amount of soil has been watered with an amount of water which exceeds the water holding capacity. A lower amount of water which has leached from the soil indicates an increased water holding capacity.
  • the water holding capacity of non-wetting soil is increased by at least 3% or 5%, preferably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15%.
  • the amount of water which is present in the soil after a certain period of time after application is increased by at least 3% or 5%, pref- erably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15% compared to a soil which has not been treated in accordance with the present invention.
  • the soil water repellency of non-wet- ting soil is reduced and the water holding capacity of non-wetting soil is increased.
  • the soil wa- ter repellency of non-wetting soil is reduced by at least 10% and the water holding capacity of non-wetting soil is increased by at least 3%, preferably the soil water repellency of non-wetting soil is reduced by at least 30% and the water holding capacity of non-wetting soil is increased by at least 8%, more preferably the soil water repellency of non-wetting soil is reduced by at least 50% and the water holding capacity of non-wetting soil is increased by at least 12% and most preferably the soil water repellency of non-wetting soil is reduced by at least 70% and the water holding capacity of non-wetting soil is increased by at least 15%.
  • evaporation refers to the process of losing water over a surface, particularly a soil surface.
  • the evaporation can be determined by adding water to a soil sample and leaving the soil sample for a period of several days, for example eight days, without watering. After this pe- riod the soil sample is weighed and the difference in weight at the timepoint after adding the wa- ter and the weight after the period of leaving the soil is determined. This difference is defined as evaporation.
  • the water holding capacity of wetting soil is in- creased by at least 5% or 8%, preferably by at least 10% or 12%, more preferably by at least 15% or 18% and most preferably by at least 20%.
  • the evaporation from wetting soil is reduced by at least 1 %, preferably by at least 2%, more preferably by at least 3% and most preferably by at least 4%.
  • the water holding capacity of wetting soil is in- creased by at least 5% or 8% and the evaporation from wetting soil is reduced by at least 1 %, preferably the water holding capacity of wetting soil is increased by at least 10% or 12% and the evaporation from wetting soil is reduced by at least 2%, more preferably the water holding ca- pacity of wetting soil is increased by at least 15% or 18% and the evaporation from wetting soil is reduced by at least 3% and most preferably the water holding capacity of wetting soil is in- creased by at least 20% and the evaporation from wetting soil is reduced by at least 4% corn- pared to a soil which has not been treated in accordance with the present invention.
  • soil refers to material forming the surface of the earth and including a mixture of or- ganic material and minerals. Soil includes materials such as mud, sand, silt, and clay. It may it- self form the surface of the earth in areas, and in other areas it may underlie other types of groundcover, such as grass and other plants and vegetation, gravel, pebbles, and the like. Pref- erably, the soil is sandy soil characterized by a low particle-surface area.
  • the soil may be agricultural land, pasture, coastal dune sands, forest, shrub lands, parks, turfgrass soils, potting mixes or soils irrigated with treated wastewater.
  • the soil is agricultural land which means that it is used for planting crops.
  • the agricultural land has not been treated by tillage (so-called no-till agriculture).
  • the agricultural land may comprise huge areas of non-wetting soil of several square kilometers as contrasted to localized dry spots which have a size of at most several meters.
  • the total area of agricultural land having water repellent soil is about 5 million hectares.
  • the soil is not a turfgrass soil.
  • Turfgrass refers to any vegetative ground covering such as, but not limited to, various species of grasses used for lawns, fields, golf course grounds, and the like.
  • the soil is turfgrass soil, for example turfgrass soil from a golf course.
  • the turfgrass soil may have one or more localized dry spots (LDS). LDS are irregular dry areas from a few centimeters to several meters diameter with the repellency usually extending from the surface into a depth of 5 to 10 cm.
  • the turfgrass soil may have one or more "fairy rings" which are caused by fungi, in particular by basidiomycetes and which have a round shape.
  • the fairy rings can range from a few centimeters to 20 meters in diameter, particularly from 0.5 m to 5 m in diameter.
  • the turfgrass soil has at least one localized dry spot and at least one fairy ring.
  • the soil is non-wetting soil.
  • non-wetting soil refers to a soil which does not spontaneously wet when a drop of water is applied to its surface.
  • the non-wetting soil can be characterized by the water droplet penetration time test as explained above.
  • the non- wetting soil has a water droplet penetration time of at least 5 seconds, preferably of at least 20 or at least 100 seconds, more preferably of at least 300 or 500 seconds, even more preferably of at least 700 or 1000 seconds and most preferably at least 1 ,200 seconds.
  • the non-wetting soil can also be defined by the MED test discussed above.
  • the non- wetting soil requires a molarity of ethanol of at least 0.2, preferably of at least 0.5, more prefera- bly of at least 1.0 and most preferably of at least 2.0 to absorb the solution into the soil.
  • the non-wetting soil can also be defined by the contact angle between wa- ter and soil as determined for example by the capillary rise method.
  • the non-wetting soil is de- fined by a contact angle of greater than 90°.
  • the soil is wetting soil.
  • the term "wetting soil” refers to a soil which sponta- neously wets when a drop of water is applied to its surface.
  • the wetting soil can be character- ized by the water droplet penetration time test as explained above.
  • the wetting soil has a water droplet penetration time of less than 5 seconds.
  • the wetting soil can also be defined by the contact angle between water and soil as determined for example by the capillary rise method.
  • the wetting soil is defined by a contact angle of less than 90°.
  • the wetting soil can also be defined by the MED test discussed above.
  • the non-wetting soil requires a molarity of ethanol of 0 to absorb the solution into the soil.
  • isolated polypeptide refers to a polypeptide that has been separated from its biologi cal source such as a bacterium or fungus producing the polypeptide, for example by centrifuga- tion or filtration. After separating the polypeptide from the biological source it may be purified to remove other components from the biological source or medium components. Hence, the term “isolated polypeptide” includes both purified polypeptides and polypeptides which are present in a cell culture supernatant or the like.
  • the isolated polypeptide used according to the present invention has lipase activity.
  • Lipases (E.C. 3.1.1.3) are hydrolytic enzymes that are known to cleave ester bonds in lipids. Lipases in- clude phospholipases, triacylglycerol lipases, and galactolipases.
  • the enzyme used in the method of the present invention is preferably a triacylglycerol lipase which cleaves the ester bond between glycerol and fatty acids, resulting in the release of fatty acids from the glycerol.
  • the lipase used in the context of the present invention is selected from the group consisting of: (i) a lipase having the amino acid sequence according to according to any one of SEQ ID NOs: SEQ ID NO: 956, SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56, SEQ ID NO: 58, SEQ ID NO: 60
  • SEQ ID NO: 955 SEQ ID NO: 1 , SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 1 1 , SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 19, SEQ ID NO: 21 , SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 27, SEQ ID NO: 29, SEQ ID NO: 31 , SEQ ID NO: 33, SEQ ID NO: 35, SEQ ID NO: 37, SEQ ID NO: 39, SEQ ID NO: 41 , SEQ ID NO: 43, SEQ ID NO: 45, SEQ ID NO: 47, SEQ ID NO: 49, SEQ ID NO: 51 , SEQ ID NO: 53, SEQ ID NO: 55, SEQ ID NO: 57, SEQ ID NO: 59, SEQ ID NO: 61 , SEQ ID NO: 63, SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69,
  • a lipase having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56, SEQ ID NO: 58, SEQ ID NO: 60, SEQ ID NO: 62, SEQ ID NO: 64, SEQ ID NO: 66,
  • SEQ ID NO: 63 SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 71 , SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 77, SEQ ID NO: 79, SEQ ID NO: 81 , SEQ ID NO: 83, SEQ ID NO: 85, SEQ ID NO: 87, SEQ ID NO: 89, SEQ ID NO: 91 , SEQ ID NO: 93, SEQ ID NO: 95,
  • the lipase is not an Aspergillus niger ⁇ ase.
  • the lipase used in the context of the present invention is selected from the group consisting of:
  • SEQ ID NO: 15 SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 75, SEQ ID NO: 99, SEQ ID NO: 113, SEQ ID NO: 141 , SEQ ID NO: 147, SEQ ID NO:
  • SEQ ID NO: 155 SEQ ID NO: 159, SEQ ID NO: 161 , SEQ ID NO: 163, SEQ ID NO: 169, SEQ ID NO: 171 , SEQ ID NO: 181 , SEQ ID NO: 185, SEQ ID NO: 193, SEQ ID NO: 203, SEQ ID NO: 205, SEQ ID NO: 213, SEQ ID NO: 217, SEQ ID NO: 223, SEQ ID NO: 227, SEQ ID NO: 229, SEQ ID NO: 243, SEQ ID NO: 261 , SEQ ID NO: 267, SEQ ID NO: 269, SEQ ID NO: 281 , SEQ ID NO: 291 , SEQ ID NO: 297, SEQ ID NO: 299, SEQ ID NO: 305, SEQ ID NO: 319, SEQ ID NO: 339, SEQ ID NO: 367, SEQ ID NO: 393, SEQ ID NO: 421 , SEQ ID NO: 423, SEQ ID NO:
  • a lipase having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100, SEQ ID NO: 1 14, SEQ ID NO: 142, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 156, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 182, SEQ ID NO: 186, SEQ ID NO: 194, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 214, SEQ ID NO: 218, SEQ ID NO: 224, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 244, SEQ ID NO:
  • the lipase used in the context of the present invention is selected from the group consisting of:
  • a lipase having the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 90, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100 or SEQ ID NO: 114 or an enzymatically active fragment thereof having lipase activity;
  • the lipase used in the context of the present invention is selected from the group consisting of:
  • a lipase having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956 or SEQ ID NO: 90 or an enzymatically active frag- ment thereof having lipase activity;
  • the lipase used in the context of the present invention is selected from the group consisting of:
  • a lipase having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956 or an enzymatically active fragment thereof having lipase activity;
  • an "enzymatically active fragment" of a lipase is understood to refer to a smaller part of the li- pase which consists of a contiguous amino acid sequence found in the amino acid sequence of the lipase and which has lipase activity.
  • the skilled person knows that for a fragment to be en- zymatically active the fragment has to comprise at least the amino acids present in the catalytic centre of the lipase. These amino acids are either known for a given lipase or can easily be identified by the skilled person, for example by homology screening or mutagenesis. For exam- pie, an enzymatically active fragment of the lipase according to SEQ ID No.
  • a "fragment" of a nucleic acid sequence encoding an enzymatically active fragment of a lipase is understood to refer to a smaller part of the nucleic acid sequence which consists of a contigu- ous nucleic acid sequence found in the nucleic acid sequence of the lipase and which encodes a protein having lipase activity.
  • the fragment of an enzyme to be enzymatically active has to comprise at least the amino acids present in the cata- lytic centre of the lipase. These amino acids are either known for a given lipase or can easily be identified by the skilled person, for example by homology screening or mutagenesis.
  • the fragment of the nucleic acid sequence according to SEQ ID No. 955 encodes at least amino acid residues 87 to 285 of SEQ ID No. 956, more preferably it encodes at least amino acid residues 61 to 291 of SEQ ID No. 956, even more preferably it encodes at least amino acid residues 41 to 301 of SEQ ID No. 956 and most preferably it encodes at least amino acid resi- dues 11 to 311 of SEQ ID No. 956.
  • a lipase having an amino acid sequence with at least 70, 75 or 80 % sequence identity, preferably with at least 81 , 82, 83, 84, 85 or 86% sequence identity, more preferably with at least 87, 88, 89 or 90% sequence identity even more preferably with at least
  • SEQ ID NO: 92 SEQ ID NO: 94, SEQ ID NO: 96, SEQ ID NO: 98, SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, SEQ ID NO: 1 10, SEQ ID NO: 112, SEQ ID NO: 1 14, SEQ ID NO: 116, SEQ ID NO: 118, SEQ ID NO: 120, SEQ ID NO: 122, SEQ ID NO: 124, SEQ ID NO: 126, SEQ ID NO: 128, SEQ ID NO: 130, SEQ ID NO: 132, SEQ ID NO: 134, SEQ ID NO: 136, SEQ ID NO: 138, SEQ ID NO: 140, SEQ ID NO: 142, SEQ ID NO: 143, SEQ ID NO: 146, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 152, SEQ ID NO: 154, SEQ ID NO: 156,
  • the lipases having the aforementioned sequence identity to the sequence according to SEQ ID No. 956 preferably comprise the amino acid serine on position 87 of SEQ ID No. 956, the amino acid aspartate on position 241 of SEQ ID No. 956 and the amino acid histidine on position 285 of SEQ ID No. 956.
  • a lipase with at least 70% sequence identity to the amino acid sequence ac- cording to SEQ ID NO: 956 is used which reduces the soil water repellency of non-wetting soils by at least 10% or 20%, preferably by at least 30% or 40%, more preferably by at least 50% or 60% and most preferably by at least 70% or 75%.
  • a lipase with at least 80% sequence identity to the amino acid sequence according to SEQ ID NO: 956 is used which re- Jerusalem the soil water repellency of non-wetting soils by at least 10% or 20%, preferably by at least 30% or 40%, more preferably by at least 50% or 60% and most preferably by at least 70% or 75%.
  • a lipase with at least 90% sequence identity to the amino acid se- quence according to SEQ ID NO: 956 is used which reduces the soil water repellency of non- wetting soils by at least 10% or 20%, preferably by at least 30% or 40%, more preferably by at least 50% or 60% and most preferably by at least 70% or 75%.
  • a lipase with at least 95% sequence identity to the amino acid sequence according to SEQ ID NO: 956 is used which reduces the soil water repellency of non-wetting soils by at least 10% or 20%, pref- erably by at least 30% or 40%, more preferably by at least 50% or 60% and most preferably by at least 70% or 75%.
  • a lipase with at least 70% sequence identity to the amino acid sequence ac- cording to SEQ ID NO: 956 is used which increases the water holding capacity of non-wetting soils by at least 3% or 5%, preferably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15%.
  • a lipase with at least 80% sequence identity to the amino acid sequence according to SEQ ID NO: 956 is used which increases the water holding capacity of non-wetting soils by at least 3% or 5%, preferably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15%.
  • a lipase with at least 90% sequence identity to the amino acid sequence according to SEQ ID NO: 956 is used which increases the water holding capacity of non-wetting soils by at least 3% or 5%, preferably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15%.
  • a lipase with at least 95% sequence identity to the amino acid sequence according to SEQ ID NO: 956 is used which increases the water holding capac- ity of non-wetting soils by at least 3% or 5%, preferably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15%.
  • Sequence Identity means a com- parison of a first amino acid sequence to a second amino acid sequence, or a comparison of a first nucleic acid sequence to a second nucleic acid sequence and is calculated as a percentage based on the comparison. The result of this calculation can be described as“percent identical” or “percent ID.”
  • a sequence alignment can be used to calculate the sequence identity by one of two different approaches.
  • first approach both, mismatches at a single position and gaps at a single position are counted as non-identical positions in final sequence identity calculation.
  • second approach mismatches at a single position are counted as non-identical positions in final sequence identity calculation; however, gaps at a single position are not counted (ignored) as non-identical positions in final sequence identity calculation.
  • gaps at a single position are not counted (ignored) as non-identical positions in final sequence identity calculation.
  • ap- proach gaps are ignored in final sequence identity calculation.
  • sequence identity is determined by a program, which pro- Jerusalem an alignment, and calculates identity counting both mismatches at a single position and gaps at a single position as non-identical positions in final sequence identity calculation.
  • EMBOS Needle
  • Needleman and Wun- sch Needleman and Wunsch (1970) J. Mol. Biol.
  • sequence identity can be calculated from a pairwise alignment showing only a local region of the first sequence or the second sequence (“Local Iden- tity”).
  • program Blast NCBI
  • % sequence identity (# of identical residues / length of alignment) x 100)].
  • a sequence alignment is calculated with mismatches at a single po- sition being counted as non-identical positions in final sequence identity calculation; however, gaps at a single position are not counted (i.e. they are ignored) as non-identical positions in final sequence identity calculation.
  • the sequence alignment is generated by using the algorithm of Needleman and Wunsch (J. Mol. Biol. (1979) 48, p. 443-453).
  • nucleic acid sequence hybridizing under stringent conditions with a complementary se- quence of a nucleic acid sequence according to SEQ ID No. 2 or an enzymatically active frag- ment thereof encodes a protein having lipase activity.
  • hybridizing under stringent conditions denotes in the context of the present invention that the hybridization is implemented in vitro under conditions which are stringent enough to en- sure a specific hybridization.
  • Stringent in vitro hybridization conditions are known to those skilled in the art and may be taken from the literature (e.g. Sambrook and Russell (2001 ) Molec ular Cloning: A Laboratory Manual, 3rd edition, Cold Spring Harbour Laboratory Press, Cold Spring Harbour, NY).
  • specific hybridization refers to the circumstance that a mole- cule, under stringent conditions, preferably binds to a certain nucleic acid sequence, i.e. the tar- get sequence, if the same is part of a complex mixture of, e.g. DNA or RNA molecules, but does not, or at least very rarely, bind to other sequences.
  • Stringent conditions depend on the circumstances. Longer sequences hybridize specifically at higher temperatures. In general, stringent conditions are chosen such that the hybridization temperature is about 5°C below the melting point (T m ) of the specific sequence at a defined ionic strength and at a defined pH value. T m is the temperature (at a defined pH value, a defined ionic strength and a defined nucleic acid concentration), at which 50% of the molecules comple- mentary to the target sequence hybridize to the target sequence in the state of equilibrium.
  • stringent conditions are conditions, where the salt concentration has a sodium ion con- centration (or concentration of a different salt) of at least about 0.01 to 1 .0 M at a pH value be- tween 7.0 and 8.3, and the temperature is at least 30°C for small molecules (i.e. 10 to 50 nucle- otides, for example).
  • stringent conditions may include the addition of substances, such as, e. g., formamide, which destabilise the hybrids.
  • substances such as, e. g., formamide, which destabilise the hybrids.
  • said stringent conditions are chosen such that sequences which are about 65%, preferably at least about 70%, and especially preferably at least about 75% or higher homologous to each other, normally remain hybridized to each other.
  • a preferred but non-limiting example of stringent hybridization conditions is hybridizations in 6 x sodium chloride/sodium citrate (SSC) at about 45°C, followed by one or more washing steps in 0.2 x SSC, 0.1 % SDS at 50 to 65°C.
  • the temperature depends on the type of the nucleic acid and is between 42°C and 58°C in an aqueous buffer having a concentration of 0.1 to 5 x SSC (pH value 7.2).
  • the tem- perature is about 42°C under standard conditions.
  • the hybridisation conditions for DNA:DNA hybrids are, for example, 0.1 x SSC and 20°C to 45°C, preferably 30°C to 45°C.
  • the hybridisation conditions for DNA:RNA hybrids are, for example, 0.1 x SSC and 30°C to 55°C, preferably between 45°C and 55°C.
  • the above-mentioned hybridization temperatures are determined, for example, for a nucleic acid which is 100 base pairs long and has a G/C con- tent of 50% in the absence of formamide.
  • Typical hybridization and washing buffers for example have the following composition:
  • Hybridization solution pre-hybridization solution
  • Pre-hybridization at least 2 h at 50 - 55 °C
  • Hybridization over night at 55 - 60 °C
  • proteins encoded by the nucleic acid sequence hybridizing under stringent conditions to the complement of the sequence according to SEQ ID No. 955 preferably comprise the amino acid serine on position 87 of SEQ ID No. 956, the amino acid aspartate on position 241 of SEQ ID No. 1 and the amino acid histidine on position 285 of SEQ ID No. 956.
  • variants have lipase activity, i.e. the ability to cleave a suitable lipid substrate.
  • the variants of the lipase have essentially the same lipase activity as the wild-type lipase char- acterized by any of the specific sequences disclosed herein, i.e. the activity of the variants is at least 50% or 60%, preferably at least 70% or 80%, more preferably 85% or 90% and most pref- erably at least 95% or 98% of the activity of the wild-type lipase characterized by the corre- sponding sequences according to any one of the specific sequences disclosed herein.
  • the activity of the variants can be compared with the activity of the corresponding wild-type li- pase by incubating the variant and the wild-type lipase with a suitable substrate under suitable conditions and detecting the amount of the cleavage products of the variant and the wild-type lipase.
  • a suitable substrate for the lipase according to SEQ ID NO. 956 is osra-nitrophenyl pal- mitate ( >NPP) (Winkler and Stuckmann (1979) J. Bacteriol. 138: 663-670).
  • an ol- ive oil emulsion may be used (Frenken et al. (1992) Appl. Environm. Microbiol. 58(12): 3787- 3791 ).
  • the lipase or an enzymatically active variant thereof as described herein is preferably recombi- nantly produced using a bacteria, fungi, or yeast expression system.“Expression system” also means a host microorganism, expression hosts, host cell, production organism, or production strain and each of these terms can be used interchangeably for this disclosure.
  • expression systems include but are not limited to: Aspergillus niger, Aspergillus oryzae, Han- senula polymorpha, Thermomyces lanuginosus, Fusarium oxysporum, Fusarium heterosporum, Escherichia coH, Bacillus, preferably Bacillus subti/is, or Bacillus Hcheniformis, Pseudomonas, preferably Pseudomonas fluorescens, Pichia pastoris (also known as Komagataella phaffii), My- celiopthora thermophile ( C1 ' ), Schizosaccharomyces pombe, Trichoderma, preferably Tricho- derma reesei and Saccharomyces, preferably Saccharomyces cerevisiae.
  • the lipase or an enzymatically active variant thereof as described herein is produced using one of the expression systems listed above.
  • Suitable vectors for expressing the lipase and cultivation con- ditions for producing the lipase are known to the skilled person.
  • the lipase or an enzymatically active variant thereof as described herein may be isolated from the host microorganism by well-known methods including centrifugation and filtration which re- move most of the host cell components. If a higher degree of purity is desired, the lipase may be subjected to further purification steps such as anion or cation exchange chromatography, hy- drophobic interaction chromatography, mixed mode chromatography or hydroxyapatite chroma- tography.
  • the isolated lipase may be used directly or it may be subjected to a drying step such as a spray-drying step. If the isolated lipase is dried, e.g. spray-dried or lyophilized, it has to be dissolved in a suitable solvent, before it is applied to the soil.
  • the lipase or an enzymatically active variant thereof as described above may be used in combi- nation with another enzyme which may be useful in reducing soil water repellency or enhancing water holding capacity.
  • This other enzyme may be selected from the group consisting of amyl- ases, cellulases, chitinases, esterases, beta-glucosidases, laccases, pectinases, proteases and xylanases.
  • the lipase or a variant thereof is used in combination with a chitinase, a laccase, a pectinase and/or a protease.
  • the chitinase may be from Streptomyces griseus.
  • the laccase may be from Pycnoporus sp. SYBC-L3.
  • the pectinase may be from Aspergillus niger and the protease may be from Aspergillus oryzae
  • the lipase may be used in a composition with at least one auxiliary.
  • the at least one auxiliary may be a liquid carrier which may be selected from the group of water and organic solvents.
  • the at least one auxiliary may be a solid carrier selected from the group of phytogels, hydro- gels, mineral earths, meal, cellulose powder, fumed silica or precipitated silica, polysaccharides, or compost.
  • the lipase may be used in combination with at least one soil additive.
  • the soil additive may be selected from the group consisting of surfactants, fertilizers, nitrification inhibitors and/or pesti- cides.
  • surfactant (synonymously used herein with“surface active agent” and “wetting agent”) means an organic chemical that, when added to a liquid, changes the properties of that liquid at an in- terface. According to its ionic charge, a surfactant is called non-ionic, anionic, cationic, or am- photeric. Other examples of surfactants include block polymers and polyelectrolytes. Non-limiting examples of surfactants are disclosed McCutcheon's 2016 Detergents and Emulsi fiers, and McCutcheon's 2016 Functional Materials, both North American and International Edi- tion, MC Publishing Co, 2016 edition. Further useful examples are disclosed in earlier editions of the same publications which are known to those skilled in the art.
  • Non-ionic surfactant means a surfactant that contains neither positively nor negatively charged (i.e. ionic) functional groups. In contrast to anionic and cationic surfactants, non-ionic surfac- tants do not ionize in solution. Mixtures of two or more different non-ionic surfactants may also be used. Examples provided below for surfactants of any kind are to be understood to be non- limiting.
  • Non-ionic surfactants may be compounds of the general formulae (la) and (lb):
  • R 1 is selected from C1-C23 alkyl and C2-C23 alkenyl, wherein alkyl and/or alkenyl are linear or branched; examples are n-C7Hi 5 , n-CgH-ig, n-CnH23, n-Ci3H27, n-C-isHs-i, n-C F s, i-CgH-ig, i- C12H25.
  • R 2 is selected from H, C1-C20 alkyl and C2-C20 alkenyl, wherein alkyl and/or alkenyl are linear or branched.
  • R 3 and R 4 each independently selected from C1-C16 alkyl, wherein alkyl is linear or branched; examples are methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, sec-pentyl, neopentyl, 1 ,2-dimethylpropyl, isoamyl, n-hexyl, isohexyl, sec-hexyl, n- heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl, isodecyl.
  • R 5 is selected from H and C1-C18 alkyl, wherein alkyl is linear or branched.
  • m is in the range of zero to 200, preferably 1 -80, more preferably 3-20; n and o, each inde- pendently in the range of zero to 100; n preferably is in the range of 1 to 10, more preferably 1 to 6; o preferably is in the range of 1 to 50, more preferably 4 to 25.
  • the sum of m, n and o is at least one, preferably the sum of m, n and o is in the range of 5 to 100, more preferably in the range of from 9 to 50.
  • non-ionic surfactants of the general formula (I) may be of any structure, is it block or ran- dom structure, and is not limited to the displayed sequence of formula (I).
  • Non-ionic surfactants may further be compounds of the general formula (II), which might be called alkyl-polyglycosides (APG):
  • R 1 is selected from C 1 -C 17 alkyl and C 2 -C 17 alkenyl, wherein alkyl and/or alkenyl are linear or branched; examples are n-C7Hi 5 , n-CgH-ig, n-CnH23, n-Ci3H27, n-CisH3i, n-C ⁇ Hss, i-CgH-ig, i- C12H25.
  • R 2 is selected from H, C1-C17 alkyl and C2-C17 alkenyl, wherein alkyl and/or alkenyl are linear or branched.
  • G 1 is selected from monosaccharides with 4 to 6 carbon atoms, such as glucose and xylose.
  • the integer w of the general formula (II) is in the range of from 1.1 to 4, w being an average number.
  • Non-ionic surfactants may further be compounds of general formula (III):
  • AO is selected from ethylene oxide (EO), propylene oxide (PO), butylene oxide (BO), and mix- tures thereof.
  • R 6 is selected from C 5 -C 17 alkyl and C 5 -C 17 alkenyl, wherein alkyl and/or alkenyl are linear or branched.
  • R 7 is selected from H, Ci-Cie-alkyl, wherein alkyl is linear or branched.
  • Non-ionic surfactants may further be selected from sorbitan esters and/or ethoxylated or propoxylated sorbitan esters.
  • Non-limiting examples are products sold under the trade names
  • Non-ionic surfactants may further be selected from alkoxylated mono- or di-alkylamines, fatty acid monoethanolamides (FAMA), fatty acid diethanolamides (FADA), ethoxylated fatty acid monoethanolamides (EFAM), propoxylated fatty acid monoethanolamides (PFAM), polyhydroxy alkyl fatty acid amides, or N-acyl N-alkyl derivatives of glucosamine (glucamides, GA, or fatty acid glucamide, FAGA), and combinations thereof.
  • FAMA fatty acid monoethanolamides
  • FADA fatty acid diethanolamides
  • EFAM ethoxylated fatty acid monoethanolamides
  • PFAM propoxylated fatty acid monoethanolamides
  • polyhydroxy alkyl fatty acid amides or N-acyl N-alkyl derivatives of glucosamine (glucamides, GA, or fatty acid glucamide, FAGA), and combinations thereof.
  • Amphoteric surfactants are those, depending on pH, which can be either cationic, zwitterionic or anionic. Mixtures of two or more different amphoteric surfactants may also be used.
  • Surfactants may be compounds comprising amphoteric structures of general formula (IV), which might be called modified amino acids (proteinogenic as well as non-proteinogenic):
  • R 8 is selected from H, C 1 -C 4 alkyl, C 2 -C 4 alkenyl, wherein alkyl and/or are linear or branched.
  • R 9 is selected from C1-C22- alkyl, C2-C22- alkenyl, C10-C22 alkylcarbonyl, and C10-C22 alkenylcar- bonyl.
  • R 10 is selected from H, methyl, -(CH 2 ) 3 NHC(NH)NH 2 , -CH 2 C(0)NH 2 , -CH 2 C(0)0H, - (CH 2 ) 2 C(0)NH 2 , -(CH 2 ) 2 C(0)0H, (imidazole-4-yl)-methyl, -CH(CH 3 )C 2 H 5 , -CH 2 CH(CH 3 ) 2 , - (CH 2 ) 4 NH 2 , benzyl, hydroxymethyl, -CH(OH)CH 3 , (indole-3-yl)-methyl, (4-hydroxy-phenyl)-me- thyl, isopropyl, -(CH 2 ) 2 SCH 3 , and -CH 2 SH.
  • R x is selected from H and Ci-C 4 -alkyl.
  • Surfactants may further be compounds comprising amphoteric structures of general formulae (Va), (Vb), or (Vc), which might be called betaines and/or sulfobetaines:
  • R 11 is selected from linear or branched C 7 -C 22 alkyl and linear or branched C 7 -C 22 alkenyl.
  • R 12 are each independently selected from linear C 1 -C 4 alkyl.
  • R 13 is selected from C 1 -C 5 alkyl and hydroxy C 1 -C 5 alkyl; for example 2-hydroxypropyl.
  • A- is selected from carboxylate and sulfonate.
  • Surfactants may further be compounds comprising amphoteric structures of general formula (VI), which might be called alkyl-amphocarboxylates:
  • R 11 is selected from C 7 -C 22 alkyl and C 7 -C 22 alkenyl, wherein alkyl and/or alkenyl are linear or branched, preferably linear.
  • R 14 is selected from -CH 2 C(0)0-M + , -CH 2 CH 2 C(0)0-M + and -CH 2 CH(0H)CH 2 S0 3 -M + .
  • R 15 is selected from H and -CH 2 C(0)O
  • the integer r in general formula (VI) is in the range of 2 to 6.
  • Non-limiting examples of further suitable alkyl-amphocarboxylates include sodium cocoampho- acetate, sodium lauroamphoacetate, sodium capryloamphoacetate, disodium cocoamphodiace- tate, disodium lauroamphodiacetate, disodium caprylamphodiacetate, disodium capryloam- phodiacetate, disodium cocoamphodipropionate, disodium lauroamphodipropionate, disodium caprylamphodipropionate, and disodium capryloamphodipropionate.
  • Surfactants may further be compounds comprising amphoteric structures of general formula (VII), which might be called amine oxides (AO):
  • R 16 is selected from Cs-C-is linear or branched alkyl, hydroxy Cs-C-is alkyl, acylamidopropoyl and C8-C18 alkyl phenyl group; wherein alkyl and/or alkenyl are linear or branched.
  • R 17 is selected from C 2 -C 3 alkylene, hydroxy C 2 -C 3 alkylene, and mixtures thereof.
  • each residue can be independently selected from Ci-C 3 alkyl and hydroxy Ci-C 3 ;
  • R 15 groups can be attached to each other, e.g., through an oxygen or nitrogen atom, to form a ring structure.
  • integer x in general formula (VII) is in the range of 0 to 5, preferably from 0 to 3, most pref- erably 0.
  • Non-limiting examples of further suitable amine oxides include C10-C18 alkyl dimethyl amine ox- ides and C8-C18 alkoxy ethyl dihydroxyethyl amine oxides.
  • Examples of such materials include dimethyloctyl amine oxide, diethyldecyl amine oxide, bis-(2-hydroxyethyl)dodecyl amine oxide, dimethyldodecylamine oxide, dipropyltetradecyl amine oxide, methylethylhexadecyl amine ox ide, dodecylamidopropyl dimethyl amine oxide, cetyl dimethyl amine oxide, stearyl dimethyl amine oxide, tallow dimethyl amine oxide and dimethyl-2-hydroxyoctadecyl amine oxide.
  • a fur- ther example of a suitable amine oxide is cocamidylpropyl dimethylaminoxide, sometimes also called cocamidopropylamine
  • Anionic surfactant means a surfactant with a negatively charged ionic group.
  • Anionic surfactants include, but are not limited to, surface-active compounds that contain a hydrophobic group and at least one water-solubilizing anionic group, usually selected from sulfates, sulfonate, and car- boxylates to form a water-soluble compound. Mixtures of two or more different anionic surfac- tants may also be used. Mixtures of non-ionic and/or amphoteric and/or anionic surfactants may also be used.
  • Anionic surfactants may be compounds of general formula (VIII), which might be called (fatty) alcohol/alkyl (ethoxy/ether) sulfates [(F)A(E)S] when A- is S0 3 -, (fatty) alcohol/alkyl (eth- oxy/ether) carboxylate [(F)A(E)C] when A- is -RCOO:
  • R 1 is selected from Ci-C23-alkyl (such as 1 -, 2-, 3-, 4- Ci-C23-alkyl) and C2-C23-alkenyl, wherein alkyl and/or alkenyl are linear or branched, and wherein 2-, 3-, or 4-alkyl; examples are n-CzHis, n-CgH-ig, n-CnH23, n-Ci3H27, n-CisH3i, n-C- ⁇ Ftas, i-CgH-ig, i-Ci2H25.
  • Ci-C23-alkyl such as 1 -, 2-, 3-, 4- Ci-C23-alkyl
  • C2-C23-alkenyl wherein alkyl and/or alkenyl are linear or branched, and wherein 2-, 3-, or 4-alkyl
  • examples are n-CzHis, n-CgH-ig, n-CnH23,
  • R 2 is selected from H, Ci-C2o-alkyl and C2-C2o-alkenyl, wherein alkyl and/or alkenyl are linear or branched.
  • R 3 and R 4 each independently selected from Ci-Ci 6 -alkyl, wherein alkyl is linear or branched; examples are methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, sec-pentyl, neopentyl, 1 ,2-dimethylpropyl, isoamyl, n-hexyl, isohexyl, sec-hexyl, n- heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl, isodecyl.
  • A- is selected from -RCOO, -SO 3 and RSO 3 , wherein R is selected from linear or branched C 1 - Ce-alkyl, and C 1 -C 4 hydroxyalkyl, wherein alkyl is.
  • M + is selected from H and salt forming cations.
  • Salt forming cations may be monovalent or multi- valent; hence M + equals 1/v M v+ . Examples include but are not limited to sodium, potassium, magnesium, calcium, ammonium, and the ammonium salt of mono-, di, and triethanolamine.
  • m is in the range of zero to 200, preferably 1 -80, more preferably 3-20; n and o, each inde- pendently in the range of zero to 100; n preferably is in the range of 1 to 10, more preferably 1 to 6; o preferably is in the range of 1 to 50, more preferably 4 to 25.
  • the sum of m, n and o is at least one, preferably the sum of m, n and o is in the range of 5 to 100, more preferably in the range of from 9 to 50.
  • Anionic surfactants of the general formula (VIII) may be of any structure, block copolymers or random copolymers.
  • anionic surfactants include salts (M + ) of C12-C18 sulfo fatty acid alkyl esters (such as C12-C18 sulfo fatty acid methyl esters), Cio-C-i 8 -alkylarylsulfonic acids (such as n-C-io- Cis-alkylbenzene sulfonic acids) and C10-C18 alkyl alkoxy carboxylates.
  • M + in all cases is selected from salt forming cations.
  • Salt forming cations may be monovalent or multivalent; hence M + equals 1/v M v+ . Examples include but are not limited to sodium, potas- sium, magnesium, calcium, ammonium, and the ammonium salt of mono-, di, and triethanola- mine.
  • Non-limiting examples of further suitable anionic surfactants include branched alkylbenzenesul- fonates (BABS), phenylalkanesulfonates, alpha-olefinsulfonates (AOS), olefin sulfonates, al- kene sulfonates, alkane-2, 3-diylbis(sulfates), hydroxyalkanesulfonates and disulfonates, sec- ondary alkanesulfonates (SAS), paraffin sulfonates (PS), sulfonated fatty acid glycerol esters, alkyl- or alkenylsuccinic acid, fatty acid derivatives of amino acids, diesters and monoesters of sulfo-succinic acid.
  • BABS branched alkylbenzenesul- fonates
  • AOS alpha-olefinsulfonates
  • olefin sulfonates
  • Anionic surfactants may be compounds of general formula (IX), which might be called N-acyl amino acid surfactants:
  • R 19 is selected from linear or branched C6-C22-alkyl and linear or branched C6-C22-alkenyl such as oleyl.
  • R 20 is selected from H and Ci-C 4 -alkyl.
  • R 21 is selected from H, methyl, -(CH 2 ) 3 NHC(NH)NH2, -CH 2 C(0)NH 2 , -CH 2 C(0)0H, - (CH 2 ) 2 C(0)NH 2 , -(CH 2 ) 2 C(0)0H, (imidazole-4-yl)-methyl, -CH(CH 3 )C 2 H 5 , -CH 2 CH(CH 3 ) 2 , - (CH 2 ) 4 NH 2 , benzyl, hydroxymethyl, -CH(OH)CH 3 , (indole-3-yl)-methyl, (4-hydroxy-phenyl)-me- thyl, isopropyl, -(CH2)2SCH 3 , and -CH2SH.
  • R 22 is selected from -COOX and -CH 2 S0 3 X, wherein X is selected from Li + , Na + and K + .
  • Non-limiting examples of suitable N-acyl amino acid surfactants are the mono- and di-carbox- ylate salts (e.g., sodium, potassium, ammonium and ammonium salt of mono-, di, and triethano- lamine) of N-acylated glutamic acid, for example, sodium cocoyl glutamate, sodium lauroyl glu tamate, sodium myristoyl glutamate, sodium palmitoyl glutamate, sodium stearoyl glutamate, disodium cocoyl glutamate, disodium stearoyl glutamate, potassium cocoyl glutamate, potas- sium lauroyl glutamate, and potassium myristoyl glutamate; the carboxylate salts (e.g., sodium, potassium, ammonium and ammonium salt of mono-, di, and triethanolamine) of N-acylated ala- nine, for example, sodium cocoyl alaninate, and triethanolamine lauroyl alaninate; the carbox
  • Anionic surfactants may further be selected from the group of soaps.
  • Suitable are salts (M + ) of saturated and unsaturated C12-C18 fatty acids, such as lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, oleic acid, (hydrated) erucic acid.
  • M + is selected from salt forming cat- ions. Salt forming cations may be monovalent or multivalent; hence M + equals 1/v M v+ .
  • Exam- pies include but are not limited to sodium, potassium, magnesium, calcium, ammonium, and the ammonium salt of mono-, di, and triethanolamine.
  • suitable soaps include soap mixtures derived from natural fatty acids such as tallow, coconut oil, palm kernel oil, laurel oil, olive oil, or canola oil.
  • Such soap mixtures comprise soaps of lauric acid and/or myristic acid and/or palmitic acid and/or stearic acid and/or oleic acid and/or linoleic acid in different amounts, depending on the natural fatty ac- ids from which the soaps are derived.
  • anionic surfactants include salts (M + ) of sulfates, sul- fonates or carboxylates derived from natural fatty acids such as tallow, coconut oil, palm kernel oil, laurel oil, olive oil, or canola oil.
  • Such anionic surfactants comprise sulfates, sulfonates or carboxylates of lauric acid and/or myristic acid and/or palmitic acid and/or stearic acid and/or oleic acid and/or linoleic acid in different amounts, depending on the natural fatty acids from which the soaps are derived.
  • Cationic surfactant means a surfactant with a positively charged ionic group.
  • these cationic moieties are nitrogen containing groups such as quaternary ammonium or protonated amino groups.
  • the cationic protonated amines can be primary, secondary, or tertiary amines.
  • Cationic surfactants may be compounds of the general formula (X) which might be called qua- ternary ammonium compounds (quats):
  • R 23 is selected from H, C1-C4 alkyl (such as methyl) and C2-C4 alkenyl, wherein alkyl and/or alkenyl is linear or branched.
  • R 24 is selected from C 1 -C 4 alkyl (such as methyl), C 2 -C 4 alkenyl and C 1 -C 4 hydroxyalkyl (such as hydroxyethyl), wherein alkyl and/or alkenyl is linear or branched.
  • R 25 is selected from C1-C22 alkyl (such as methyl, C18 alkyl), C2-C4 alkenyl, C12-C22 alkylcarbon- yloxymethyl and C12-C22 alkylcarbonyloxyethyl (such as C16-C18 alkylcarbonyloxyethyl), wherein alkyl and/or alkenyl is linear or branched.
  • R 26 is selected from C12-C18 alkyl, C2-C4 alkenyl, C12-C22 alkylcarbonyloxymethyl, C12-C22 alkyl- carbonyloxyethyl and 3-(Ci2-C22 alkylcarbonyloxy)-2(Ci2-C22 alkylcarbonyloxy)-propyl.
  • X is selected from halogenid, such as Ch or Br.
  • Non-limiting examples of further cationic surfactants include, amines such as primary, second- ary and tertiary monoamines with C18 alkyl or alkenyl chains, ethoxylated alkylamines, alkox- ylates of ethylenediamine, imidazoles (such as 1-(2-hydroxyethyl)-2-imidazoline, 2-alkyl-1-(2- hydroxyethyl)-2-imidazoline, and the like), quaternary ammonium salts like alkylquaternary am- monium chloride surfactants such as n-alkyl(Ci2-Ci8)dimethylbenzyl ammonium chloride, n- tetradecyldimethylbenzylammonium chloride monohydrate, and a naphthylene-substituted qua- ternary ammonium chloride such as dimethyl-1 -naphthylmethylammonium chloride.
  • amines such as primary
  • Particularly suitable cationic surfactants that may be:
  • ester quats in particular quaternary esterified mono-, di- and trialkanolamines which are esterified with C8-C22-carboxylic acids;
  • imidazoline quats in particular 1-alkylimidazolinium salts of formulae XI or XII
  • R 27 is selected from Ci-C25-alkyl and C2-C25-alkenyl
  • R 28 is selected from Ci-C 4 -alkyl and hydroxy-Ci-C4-alkyl
  • R 29 is selected from Ci-C4-alkyl, hydroxy-Ci -C h alky I and a R * -(CO)-R 30 -(CH 2 )r radical, wherein R * is selected from Ci-C2i-alkyl and C2-C2i-alkenyl; R 30 is selected from-O- and -NH-; j is 2 or 3.
  • Suitable block polymers are block polymers of the A-B or A-B-A type comprising blocks of poly- ethylene oxide and polypropylene oxide or higher alkylene oxide or of the A-B-C type compris- ing alkanol, polyethylene oxide and polypropylene oxide or higher alkylene oxide.
  • the surfactant is an ethylene oxide-propylene oxide block copolymer (EO/PO) or a blend of alkyl polyglycoside and ethylene oxide-propylene oxide block copolymer (APG-EO/PO).
  • EO/PO ethylene oxide-propylene oxide block copolymer
  • APG-EO/PO ethylene oxide-propylene oxide block copolymer
  • Such surfac- tants are marketed as ACA 1853 (EO/PO) and ACA 1848 (APG-EO/PO), respectively.
  • Suitable polyelectrolytes are polyacids or polybases.
  • polyacids are alkali salts of polyacrylic acid or polyacid comb polymers.
  • polybases are polyvinylamines or poly- ethyleneamines.
  • surfactants are commercially available for reducing soil water repellency. These in- clude, but are not limited to, Kick ® (available from Compo), Clearing (available from Collier Turf Care), Primer ® 604 (available from Plant Products) and Aqueduct ® , Revolution ® , ACA 1853 and ACA 1848 (all available from Aquatrols).
  • the surfactant comprises a block polymer (P) comprising at least one polyethyleneoxide moiety and at least one polypropyleneoxide moiety, an alcohol alkoxylate (E) and/or an alcohol ethoxylate (L) of the general formula (XIII)
  • R 3 -0-(C 2 H 4 0)s-H (XIII) wherein R 3 is linear or branched Cs to C 20 alkyl, and
  • s has a value of from 1 to 40.
  • the block polymer (P) is preferably a triblock polymer comprising one polyethyleneoxide moiety and two polypropyleneoxide moieties, or two polyethyleneoxide moieties and one polypropylene- oxide moiety.
  • the block polymer (P) is a pentablock polymer comprising two polyethyleneoxide moieties and three polypropyleneoxide moieties, or three polyethyleneoxide moieties and two polypropyleneoxide moieties.
  • the block polymer (P) comprises
  • the block polymer (P) is or comprises a polyethyleneox- ide polypropyleneoxide polyethyleneoxide (EO-PO-EO) triblock polymer.
  • the polypropyleneox- ide moiety in the EO-PO-EO triblock polymer may have a molar mass of 250 to 5000 g/mol, preferably from 400 to 3000 g/mol, and in particular from 600 to 1500 g/mol.
  • the EO-PO-EO triblock polymer may contain 3 to 90 mol%, preferably 25 to 85 mol%, and in particular 50 to 80 mol% of the polypropyleneoxide moiety.
  • the block polymer (P) is or comprises a polyethyleneox- ide polypropyleneoxide polyethyleneoxide polypropyleneoxide polyethyleneoxide (EO-PO-EO- PO-EO) pentablock polymer.
  • the polypropyleneoxide moiety in the EO-PO-EO-PO-EO pen- tablock polymer may have a molar mass of 500 to 5000 g/mol, preferably from 750 to 3500 g/mol, and in particular from 1000 to 2500 g/mol.
  • the EO-PO-EO triblock polymer may contain 3 to 90 mol%, preferably 25 to 80 mol%, and in particular 50 to 70 mol% of the polypropylene- oxide moiety.
  • the alcohol alkoxylate (E) is selected in particular among alcohol alkoxylates of the formula (XIV)
  • R is branched C5-C 3 o-alkyl; m, n, p independently of one another are an integer from 2 to 16, preferably 2, 3, 4 or 5;
  • x+y+z have a value of 1 to 100.
  • m is 2
  • x is from 5.0 to 5.5
  • n 3
  • y is from 4.5 to 5.0
  • p 2
  • z is from 2 to 2.5.
  • Preferred substances are EO/PO block alcohol alkoxylates in which the EO:PO ratio is 1 : 1 to 4:1 , in particular 1.3:1 to 3:1.
  • the degree of ethoxylation is, as a rule, 1 to 20, preferably 2 to 15, in particular 4 to 10
  • the degree of propoxylation is, as a rule, 1 to 20, preferably 1 to 8, in particular 2 to 6.
  • the total degree of alkoxylation, i.e. the total of EO and PO units, is, as a rule, 2 to 40, preferably 3.to 25, in particular 6 to 15.
  • these alcohol alkoxylates take the form of the EO type, with the EO block being bonded terminally, however.
  • Preferred PO/EO block alcohol alkoxylates are those in which the PO:EO ratio is 1 :10 to 3:1 , in particular 1 :6 to 1.5:1.
  • the degree of ethoxylation is, as a rule, 1 to 20, preferably 2 to 15, in particular 4 to 10
  • the degree of propoxylation is, as a rule, 0.5 to 10, preferably 0.5 to 8, in particular 1 to 6.
  • the total degree of alkoxylation i.e. the total of EO and PO units given as an average number, is, as a rule, 1.5 to 30, preferably 2.5 to 21 , in particular 5 to 16.
  • the alcohol alkoxylates (E) are based on primary, alpha-branched alcohols of the general formula (XV) in which
  • R 1 , R 2 independently of one another are hydrogen or Ci-C26-alkyl.
  • R 1 and R 2 independently of one another are Ci-C 6 -alkyl, in particular C2-C 4 -alkyl, for example C3-alkyl.
  • Such alcohols are also referred to as Guerbet alcohols. They can be obtained for example by dimerization of corresponding primary alcohols (for example R 1 ⁇ 2 CH2CH20H) at elevated tem- perature, for example 180 to 300°C, in the presence of an alkaline condensing agent such as potassium hydroxide.
  • corresponding primary alcohols for example R 1 ⁇ 2 CH2CH20H
  • an alkaline condensing agent such as potassium hydroxide
  • Alkoxylates which are employed for the purposes of this preferred embodiment, which is based on Guebert alcohols, are mainly alkoxylates of the EO type. Particularly preferred are ethox- ylates with a degree of ethoxylation of 1 to 50, preferably 2 to 20, in particular approximately 3 to 10. The correspondingly ethoxylated 2-propylheptanols may be mentioned especially among these.
  • the alcohol alkoxylates to be used are based on C13-oxo alcohols.
  • C13-oxo alcohol refers to an alcohol mixture whose main component is formed by at least one branched C13-alcohol (isotridecanol).
  • C13-alcohols include, in par- ticular, tetramethylnonanols, for example 2,4,6,8-tetramethyM -nonanol or 3,4,6,8-tetramethyM - nonanol and furthermore ethyldimethylnonanols such as 5-ethyl-4,7-dimethyl-1 -nonanol.
  • Suitable C13-alcohol mixtures can generally be obtained by hydrogenation of hydroformylated trimeric butane, as described in US2005/0170968. In particular, it is possible to proceed as fol- lows:
  • the C12-olefin fraction is hydroformylated by reacton with carbon monoxide and hydrogen in the presence of a suitable catalyst
  • Advantageous C13-alcohol mixtures are essentially free from halogens, i.e. they contain less than 3 ppm by weight, in particular less than 1 ppm by weight, of halogen, in particular chlorine.
  • the alcohol alkoxylates (E) may have an average molecular weight of preferably at least 200 g/mol, more preferably at least 300 g/mol, most preferably at least 400 g/mol, particularly prefer- ably at least 500 g/mol, particularly more preferably at least 600 g/mol, particularly most prefera- bly at least 650 g/mol.
  • the alcohol alkoxylates (E) may have an average molecular weight of preferably up to 10000 g/mol, more preferably up to 5000 g/mol, most preferably up to 3000 g/mol, particularly preferably up to 2000 g/mol, particularly more preferably up to 1500 g/mol, particularly most preferably up to 1200 g/mol, particularly up to 1000 g/mol, for example up to 850 g/mol.
  • the alcohol alkoxylates (E) may have an average molecular weight of from 300 to 2000 g/mol, preferably from 400 to 1000 g/mol, and particularly from 650 to 850 g/mol.
  • R 3 -0-(C 2 H 4 0)s-H (XIII) wherein R 3 is linear or branched Cs to C20 alkyl, and
  • s has a value of from 1 to 40
  • R 3 is preferably branched C10 to C15 alkyl, more preferably branched C12 to C14 alkyl, most preferably isotridecyl.
  • s has a value of from 1 to 40, preferably 2 to 30, more preferably 3 to 20, most preferably 4 to 15, particularly preferably 5 to 10, particularly preferably 7 to 9, for example 8.
  • Suitable C13-alcohol mixtures for example isotridecanol mixtures, as precursor for alcohol eth- oxylate (L), can generally be obtained by hydrogenation of hydroformylated trimeric butene. In particular, it is possible to proceed as follows:
  • the C12-olefin fraction is hydroformylated by reacton with carbon monoxide and hydrogen in the presence of a suitable catalyst
  • C13-alcohol mixtures for example isotridecanol mixtures, as precursor for alcohol ethoxylate (L)
  • the degree of branching is defined as the number of methyl groups in one molecule of the alcohol minus 1.
  • the mean degree of branching is the statistical mean of the degrees of branching of the molecules of a sample. The mean number of methyl groups in the molecules of a sample can be determined readily by 'H-NMR spectroscopy.
  • the alcohol ethoxylate (L) may have an average molecular weight of preferably at least 200 g/mol, more preferably at least 300 g/mol, most preferably at least 350 g/mol, particularly prefer- ably at least 400 g/mol, particularly more preferably at least 450 g/mol, particularly most prefera- bly at least 500 g/mol.
  • the alcohol alkoxylates (E) may have an average molecular weight of preferably up to 2000 g/mol, more preferably up to 1500 g/mol, most preferably up to 1000 g/mol, particularly preferably up to 800 g/mol, particularly more preferably up to 700 g/mol, par- ticularly most preferably up to 650 g/mol, particularly up to 600 g/mol.
  • the alcohol ethoxylate (L) may have an average molecular weight of from 200 to 2000 g/mol, preferably from 400 to 1000 g/mol, and particularly from 500 to 600 g/mol.
  • the surfactant is a composition (A) comprising a block polymer (P) comprising at least one polyethyleneoxide moiety and at least one polypropyleneoxide moiety, and an alcohol alkoxylate (E) as discussed above.
  • the block polymer (P) is contained in an amount of from 4 wt.-% to 96 wt.-%, more preferably from 8 wt.-% to 92 wt.-%, most preferably from 12 wt.-% to 88 wt.-%, particularly preferably from 16 w.-% to 84 wt.-%, particularly more preferably from 20 wt.-% to 80 wt.-%, particularly even more preferably from 24 wt.-% to 76 wt.-%, particularly most prefera- bly from 28 wt.-% to 72 wt.-%, for example preferably from 32 wt.-% to 68 wt.-%, for example more preferably from 36 wt.-% to 64 wt.-%, for example even more preferably from 40 wt.-% to 60 wt.-%, for example most preferably from 44 wt.-% to 56 wt.-
  • the alcohol alkoxylate (E) is contained in an amount of from 4 wt.-% to 96 wt.-%, more preferably from 8 wt.-% to 92 wt.-%, most preferably from 12 wt.-% to 88 wt- %, particularly preferably from 16 w.-% to 84 wt.-%, particularly more preferably from 20 wt.-% to 80 wt.-%, particularly even more preferably from 24 wt.-% to 76 wt.-%, particularly most pref- erably from 28 wt.-% to 72 wt.-%, for example preferably from 32 wt.-% to 68 wt.-%, for example more preferably from 36 wt.-% to 64 wt.-%, for example even more preferably from 40 wt.-% to 60 wt.-%, for example most preferably from 44 wt.-% to 56 wt
  • the surfactant is a composition (B) comprising an alcohol eth- oxylate (L) of the general formula (XIII)
  • R 3 is linear or branched Cs to C20 alkyl
  • s has a value of from 1 to 40
  • the alcohol ethoxylate (L) is contained in an amount of from 4 wt.-% to 96 wt.-%, more preferably from 8 wt.-% to 92 wt.-%, most preferably from 12 wt.-% to 88 wt- %, particularly preferably from 16 w.-% to 84 wt.-%, particularly more preferably from 20 wt.-% to 80 wt.-%, particularly even more preferably from 24 wt.-% to 76 wt.-%, particularly most pref- erably from 28 wt.-% to 72 wt.-%, for example preferably from 32 wt.-% to 68 wt.-%, for example more preferably from 36 wt.-% to 64 wt.-%, for example even more preferably from 40 wt.-% to 60 wt.-%, for example most preferably from 44 wt.-% to 56 w
  • the surfactant comprises sodium-di-ethyl-hexyl-sulfosucccinate and an iso C13-alcohol ethoxylate.
  • the surfactant comprises a mixture of ethylenoxide-propyleneoxide block copolymer, 2-propylheptanol and a triblock polymer of ethylenoxide-propyleneoxide-eth- ylenoxide.
  • the surfactant comprises a mixture of equal volumes of (a) ethylenoxide- propyleneoxide block copolymer; and (b) 2-propylheptanol and a triblock polymer of ethylenox- ide-propyleneoxide-ethylenoxide.
  • solvents or liquid carriers, solid carriers, surfactants, adjuvants, dispersants, emulsifiers, wetters, adjuvants, solubilizers, penetration enhancers, protective col- loids, adhesion agents, thickeners, humectants, compatibilizers, bactericides, anti-freezing agents, anti-foaming agents, colorants, tackifiers, binders, preservatives, antioxidants, and odorants may be used in addition to the lipase.
  • Suitable solvents and liquid carriers are water and organic solvents, such as mineral oil frac- tions of medium to high boiling point, e.g. kerosene, diesel oil; oils of vegetable or animal origin; aliphatic, cyclic and aromatic hydrocarbons, e. g. toluene, paraffin, tetrahydronaphthalene, alkyl- ated naphthalenes; alcohols, e.g. ethanol, propanol, butanol, cyclohexanol; glycols; DMSO; ke- tones, e.g. cyclohexanone; esters, e.g.
  • mineral oil frac- tions of medium to high boiling point e.g. kerosene, diesel oil
  • oils of vegetable or animal origin oils of vegetable or animal origin
  • aliphatic, cyclic and aromatic hydrocarbons e. g. toluene, paraffin, tetrahydronaphthalene, al
  • lactates carbonates, fatty acid esters, gammabutyrolac- tone; fatty acids; phosphonates; amines; amides, e.g. N-methylpyrrolidone, fatty acid dimethyla- mides; and mixtures thereof.
  • the solvent is water.
  • Suitable solid carriers or fillers are mineral earths, e.g. silicates, silica gels, talc, kaolins, lime- stone, lime, chalk, clays, dolomite, diatomaceous earth, bentonite, calcium sulfate, magnesium sulfate, magnesium oxide; polysaccharides, e.g. cellulose, starch; fertilizers, e.g. ammonium sulfate, ammonium phosphate, ammonium nitrate, urea; products of vegetable origin, e.g. ce- real meal, tree bark meal, wood meal, nutshell meal, and mixtures thereof.
  • mineral earths e.g. silicates, silica gels, talc, kaolins, lime- stone, lime, chalk, clays, dolomite, diatomaceous earth, bentonite, calcium sulfate, magnesium sulfate, magnesium oxide
  • polysaccharides e.g. cellulose, starch
  • Suitable thickeners are polysaccharides (e.g. starch, xanthan gum, carboxymethylcellulose), anorganic clays (organically modified or unmodified), polycarboxylates, superabsorbent poly- mers and silicates.
  • Suitable bactericides are bronopol and isothiazolinone derivatives such as alkylisothiazolinones and benzisothiazolinones.
  • Suitable anti-freezing agents are ethylene glycol, propylene glycol, urea and glycerin.
  • Suitable anti-foaming agents are silicones, long chain alcohols, and salts of fatty acids.
  • Suitable colorants e.g. in red, blue, or green
  • pigments of low water solubility and water- soluble dyes are examples.
  • inorganic colorants such as iron oxide, titan oxide, iron hexacyanoferrate,
  • metal-complex dyes such as chromium-complex dyes, for example Orasol Yellow 141 ,
  • organic colorants such as alizarin-, azo- and phthalocyanine colorants.
  • Preferred colorants are metal-complex dyes, more preferably chromium-complex dyes
  • Suitable tackifiers or binders are polyvinylpyrrolidones, polyvinylacetates, polyvinyl alcohols, polyacrylates, biological or synthetic waxes, and cellulose ethers.
  • Suitable preservatives include e.g. sodium benzoate, benzoic acid, sorbic acid, and derivatives thereof.
  • Suitable antioxidants include sulfites, ascorbic acid, tocopherol, tocopherol acetate, tocotrienol, melatonin, carotene, beta-carotene, ubiquinol, and derivatives thereof. Tocophercol acetate is preferred as antioxidant.
  • compounds which stabilize the lipase enzyme may be used, such as buffers, chela- tors, anti-oxidants, non-ionic surfactants, sugars, proteins (e.g. BSA) and heavy metal and phe- nol scavengers.
  • fertilizers and/or nitrification inhibitors and/or urease inhibitors may be used in addition to the lipase or a variant thereof as defined herein.
  • fertilizer includes any chemical compound that improves the levels of available plant nutrients and/or the chemical and physical properties of soil, thereby directly or indirectly promoting plant growth, yield, and quality. Fertilizers are typically applied either through the soil (for uptake by plant roots) or by foliar feeding (for uptake through leaves).
  • the term “fertilizer” can be subdivided into two major categories: a) organic fertilizers (composed of decayed plant/animal matter) and b) inorganic fertilizers (composed of chemicals and minerals).
  • Inorganic fertilizers are usually manufactured through chemical processes (such as the Haber- Bosch process), also using naturally occurring deposits, while chemically altering them (e.g. concentrated triple superphosphate). Naturally occurring water soluble inorganic fertilizers in- clude Chilean sodium nitrate.
  • the fertilizer is preferably a urea-containing fertilizer, and/or P-containing fertilizer, and/or a K fertilizer (potassium-containing fertilizer), and/or a N fertilizer (nitrogen-containing fertilizer), and/or a NK fertilizer (nitrogen-potassium fertilizer), and/or a NPK (nitrogen-phosphorous-potas- sium fertilizer), and/or a single or dual element fertilizer containing S, Ca, Mg, Fe, Mn, Cu, Zn, Mo, B, Ni, Cl, or a combination thereof.
  • a“urea-containing fertilizer” is defined as a fertilizer comprising at least one component selected from the group consisting of urea, urea ammonium nitrate (UAN), and sus- pensions of isobutylidene diurea (IBDU), crotonylidene diurea (CDU) and urea formaldehyde (UF), urea-acetaldehyde, and ureaglyoxal condensates.
  • IBDU isobutylidene diurea
  • CDU crotonylidene diurea
  • UF formaldehyde
  • urea-acetaldehyde ureaglyoxal condensates.
  • the urea-containing fertilizer is urea or urea ammo- nium nitrate (UAN).
  • the urea In customary commercial fertilizer quality, the urea has a purity of at least 90%, and may for ex- ample be in crystalline, granulated, compacted, prilled or ground form.
  • the urea-containing fertilizer may be used together with a urease inhibitor.
  • Urease is an en- zyme which hydrolyzes urea to ammonia and carbon dioxide.
  • high urease activity during treatment with urea-containing fertilizers causes significant environmental and economic problems due to the release of ammonia which may be toxic to the plants and which deprives the plants of urea. Accordingly, it is desirable to inhibit the action of urease.
  • Inhibitors of urease activity may comprise (i) substrate structural analogs of urea as e.g. hydroxyurea or hydroxamic acid or (ii) inhibitors which affect the mechanism of the urease reaction.
  • the later may be di- vided in the four groups of (i) phosphorodiamidates or phosphorotriamidiates as e.g. N-(n-bu- tyl)thiophosphoric triamide, (ii) thiols as e.g. cysteamine, (iii) hydroxamic acids and its deriva- tives as e.g. acetohydroxamic acid, and (iv) ligands and chelators of the nickel ion in the active center of ureases as e.g. fluoride ions.
  • Urease inhibitors are also discussed in Upadhyay (2012) Ind. J. Biotechnol. 1 1 : 381-388 and in "Improving Efficiency of Urea Fertlizers by Inhibition of Soil Urease Activity" by Kiss and Simihaian (2002), Springer Netherlands, ISBN 978-1-4020- 0493-3.
  • the“P-containing fertilizer” is any fertilizer providing any form of the chemical element phosphorus (P) or containing any chemical compounds incorporating the chemical ele- ment phosphorus (P), including but not limited to phosphate-containing fertilizers or fertilizers containing P.
  • the P-containing fertilizer is selected from the group consisting of a NPK fertilizer, a NP fertilizer, a PK fertilizer, or a P fertilizer.
  • the P-containing fertilizer is a NPK fertilizer.
  • combinations of these fertilizers may be used as ad- ditional P-containing fertilizer.
  • P fertilizers, K fertilizers, and N fertilizers are straight fertilizers, i.e. fertilizers that contain only one of the nutritive elements P, K, and N. It is to be understood, however, that these fertilizers may additionally comprise at least one additional nutritive element selected from S, Ca, Mg, Fe, Mn, Cu, Zn, Mo, B, Ni, and Cl.
  • NPK fertilizers, NP fertilizers, and PK fertilizers are multinutrient fertilizers, i.e. fertilizers that comprise combinations of the nutritive elements P, K, and N as indicated by the terms“NPK”, “NP”, and“PK”. It is to be understood, however, that these fertilizers may additionally comprise at least one additional nutritive element selected from S, Ca, Mg, Fe, Mn, Cu, Zn, Mo, B, Ni and Cl.
  • the NPK fertilizers, NP fertilizers, and PK fertilizers may be provided as complex fertilizers or bulk-blend or blended fertilizers.
  • complex fertilizer refers to a compound fertilizer formed by mixing ingredients that react chemically. In bulk-blend or blended fertilizers, two or more granular fertilizers of similar size are mixed to form a compound fertilizer.
  • Dual element fertilizers are preferably dual element fertilizers with Ca, Mg, Fe, Mn, Zn or Ni which may be applied as soluble salts of chloride, sulfate, nitrate or in chelated form (e.g.
  • Single or dual element fertilizers of Mo are available as salts of molybdate, B as boric acid or borates.
  • Ammonium (NH 4 + ) compounds present in nitrogen-containing fertilizers are converted by soil microorganisms to nitrates (NO 3 ) in a relatively short time in a process known as nitrification.
  • the nitrification process typically leads to nitrogen leakage and environmental pollution.
  • approximately 50% of the applied nitrogen fertilizers are lost during the year following fertilizer addition (see Nelson and Huber; Nitrification inhibitors for corn pro- duction (2001 ), National Corn Handbook, Iowa State University).
  • nitrification inhibitors mostly together with fertilizers, can be used.
  • Suitable nitrification inhibitors include linoleic acid, alpha-linolenic acid, methyl p-coumarate, methyl feru- late, methyl 3-(4-hydroxyphenyl) propionate (MHPP), Karanjin, brachialacton, p-benzoquinone sorgoleone, 2-chloro-6-(trichloromethyl)-pyridine (nitrapyrin or N-serve), dicyandiamide (DCD, DIDIN), 3,4-dimethyl pyrazole phosphate (DMPP, ENTEC), 4-amino-1 ,2,4-triazole hydrochloride (ATC), 1 -amido-2 -thiourea (ASU), 2-amino-4-chloro-6-methylpyrimidine (AM), 2-mercapto-ben- zothiazole (MBT), 5-ethoxy-3-trich
  • Pesticides are substances which aim to control pests and include herbicides, insecticides, ne- maticides, mollluscicides, piscicides, avicdes, rodenticides, bactericides, insect repellents, ani- mal repellents, antimicrobials and fungicides.
  • the water-repellent soil is a fairy ring caused by basidiomycetes
  • a fungicide is used in combination with the lipase.
  • the fungizide is a fungizide which can be ap- plied through the soil.
  • the present invention also relates to the use of (a) an isolated polypeptide having lipase activity; and (b) at least one fungicide for the treatment of at least one fairy ring.
  • the present invention also relates to a method for treating at least one fairy ring comprising ap- plying (a) an isolated polypeptide having lipase activity; (b) at least one fungicide to an area of groundcover.
  • the lipase is one of the specific lipases disclosed herein and more preferably it is the lipase according to SEQ ID No. 956 or an enzymatically active variant thereof.
  • Suitable fungicides include strobilurins, carboximides, oxidizing agents, polyoxins and sterol de- methylation inhibitors. Specific examples include, but are not limited to, Azoxystrobin, Triflox- istrobin, Picoxystrobin, Pyraclostrobin, Sedaxane, Penthiopyrad, Penflufe, Fluopyram, Fluxapy- roxad, Boscalid, Oxathiapiprolin, Metalaxyl, Metalaxyl-M, Ethaboxam, DMM, Cyproconazole, Difenoconazole, Prothioconazole, Flutriafol, Thiabendazole, Ipconazole, Tebuconazole, Triad- imenol, Prochloraz, Fluquinconazole, TTZ, Fludioxinil, Carboxin, Silthiofarm, Ziram, Thiram, Carbendazim, TPM, Valifenalate, Oxa
  • fungicides which are marketed for the treatment of fairy rings and which may be used in combination with the lipase include azoxystrobin (marketed under the name Heritage ® ), flutolanil (marketed under the name Prostar ® ), hydrogen dioxide (marketed under the name Zerotol ® ), polyoxin D (marketed under the name Endorse ® ), triadimefon (marketed un- der the name Bayleton ® FLO), pyraclostrobin (marketed under the name Insignia ® ), a mixture of pyraclostrobin and triticonazole (marketed under the name Pillar ® G Intrinsic), a mixture of azoxystrobin and propiconazole (marketed under the name Headway ® ) and a mixture of triad- imefon and trifloxystrobin (marketed under the name Tartan ® Stressgard ® ).
  • azoxystrobin marketed under the name Heritage ®
  • flutolanil marketed under the name Prostar ®
  • Insecticides which may be used in combination with the lipase include, but are not limited to, Fipronil, BAS 450, IL-39, Clothianidin, Thiamethoxam, Acetamiprid, Dinotefuran, Imidacloprid, Thiacloprid, Sulfoxaflor, Methiocarb, Tefluthrin, Bifenthrin, Cypermethrin, Alphacypermethrin, Spinosad, Cyazypyr, Rynaxapyr, Thiodicarb, Triflumezopyrim (Mesoionic), Acephate, Chlorpyri- phos, Flupyradifurone, Tetraniliprole, IL-101 , S-1587, Oxazosulfyl, Cyclaniliprole and Fluxamet- amide.
  • an insecticide selected from the group consisting of Fipronil, BAS 450, IL-39, Clothianidin, Thiamethoxam, Imidacloprid, Thiacloprid, Sulfoxaflor, Tefluthrin, Spinosad, Cyazypyr, Rynaxapyr, Triflumezopyrim (Mesoionic), Acephate and Chlorpyriphos is used in combination with the lipase.
  • an insecticide selected from the group consisting of Fipronil, BAS 450, IL-39, Clothianidin, Thiamethoxam, Imidacloprid, Thiacloprid, Sulfoxaflor, Tefluthrin, Spinosad, Cyazypyr, Rynaxapyr, Triflumezopyrim (Mesoionic), Acephate and Chlorpyriphos is used in combination with the lipase.
  • Nematicides which may be used in combination with the lipase include, but are not limited to, Thiodicarb, Abamectin, Tioxazafen, Bacillus firmus and Pasteuria nishizawae.
  • the polypeptide having lipase activity may be applied to the groundcover in a concentration of between 0.001 kg to 60 kg of polypeptide per hectare, preferably of between 0.016 kg to 10 kg per hectare, more preferably of between 0.06 kg to 2 kg per hectare, most preferably of be- tween 0.1 kg to 0.5 kg per hectare.
  • the polypeptide having lipase activity may be applied to the groundcover in a concentration of between 0.01 kg to 600 kg of polypeptide per hectare, preferably of between 0.16 kg to 100 kg per hectare, more preferably of between 0.6 kg to 20 kg per hectare, most preferably of be- tween 1 kg to 5 kg per hectare.
  • the lipase is dissolved in water in a concentration of 0.001 % to 5% or 3% w/v, preferably of 0.002% to 2% or 1 % w/v, more preferably of 0.003% to 0.08 or 0.06% w/v, even more preferably of 0.004% to 0.04% or 0.03% w/v and most preferably of 0.005% to 0.01 %.
  • concentration of the lipase is 0.006% w/v.
  • the lipase is dissolved in water in a concentration of 0.01 % to 50% or 30% w/v, preferably of 0.02% to 20% or 10% w/v, more preferably of 0.03% to 0.8 or 0.6% w/v, even more preferably of 0.04% to 0.4% or 0.3% w/v and most preferably of 0.05% to 0.1 %.
  • concentration of the lipase is 0.06% w/v.
  • the lipase is dissolved in water in a concentration of 0.001 % to 0.01 % w/v, preferably of 0.002% to 0.008% w/v, more preferably of 0.003% to 0.007% and most preferably of 0.006% (w/v).
  • the lipase is dissolved in water in a concentration of 0.1 % to 5% w/v, preferably of 0.5% to 3% w/v, more preferably of 0.8% to 2% and most preferably of 1 % (w/v).
  • the li- pase is dissolved in a great volume of water for application to a great area of soil.
  • small vol- ume applications the lipase is dissolved in a small volume of water for application to a small area.
  • the lipase is dissolved in water in a concentration of 0.01 % to 0.1 % w/v, preferably of 0.02% to 0.08% w/v, more preferably of 0.03% to 0.07% and most preferably of 0.06% (w/v).
  • the lipase is dissolved in water in a concentration of 1 % to 50% w/v, preferably of 5% to 30% w/v, more preferably of 8% to 20% and most preferably of 10% (w/v).
  • the lipase is dissolved in a great volume of water for application to a great area of soil.
  • the lipase is dissolved in a small volume of water for application to a small area.
  • the lipase may be supplied as a concentrated suspension and diluted to the concentrations in- dicated above before the application to soil.
  • the lipase may also be supplied in powder form and either dissolved before the application to soil or applied to the soil in powder form. If the li- pase is applied to the soil in powder form, it is washed into the soil by rain or irrigation water with a volume of 0.5 L to 15 L, preferably with a volume of 1 L to 10 L per square meter, more preferably with a volume of 4 to 8 L per square meter shortly after application.
  • the lipase is applied to an area of groundcover.
  • groundcover includes, but is not limited to, soil, natural soil, potting soil, sand, silt, clay, turfgrasses and other plants and forms of vegetation used to cover and pro- tect the soil, as well as composites of organic materials that form within or as part of such groundcovers, such as thatch and mat layers, and also includes potting mixes.
  • groundcover is soil, more preferably, groundcover is water-repellent or non-wetting soil.
  • groundcover is potting mix. Potting mix, which is also re- ferred to potting soil, is typically a soilless blend of ingredients that is used to grow plants, pref- erably, the potting mix comprises a combination of peat moss, vermiculite, coir fiber, perlite, pine bark, sand, compost, and further ingredients. The potting mix may also comprise native soil.
  • applying includes any activity by which the lipase come into contact with the area of groundcover.
  • the lipase can be dissolved in water and applied as a solution.
  • a granulate can be prepared from the lipase and the granulate is then applied to the groundcover in solid form which is dissolved when water is applied to the soil.
  • the lipase is applied in irrigation water. In one embodiment the lipase is ap- plied extensively and non-directional to turfgrass soil. In one embodiment the lipase is applied extensively and non-directional to turfgrass soil in irrigation water. In one embodiment the lipase is applied directional to turfgrass soil using a watering can.
  • the lipase is applied to turfgrass soil as part of a topdressing which corn- prises particles to which the lipase is coupled.
  • Topdressing refers to a material applied to the top of a ground covering, usually in order to obtain a desirable effect on the groundcover, and includes sand or other particulate material.
  • the application of the lipase serves to prepare a non-wetting soil for the seeding of crops.
  • the lipase is applied selectively to those locations of the non-wetting soil where the seeds will be placed, e.g. the seeding row, so that they can prepare the soil for seed uptake.
  • the lipase is applied non-selectively to the en- tire application site (so-called blanket application).
  • lipases and in particular the lipase according to SEQ ID NO: 956 can be used for promoting plant growth.
  • the term "promoting plant growth” means that upon applica- tion of a lipase to the plant, the dry weight of the plant increases within a period of 10 to 20 days, preferably of 12 to 18 days and most preferably a period of 14 days by at least 5%, prefer- ably by at least 10%, 15% or 20%, more preferably by at least 25%, 30% or 35% even more preferably by at least 40% or 45% and most preferably by at least 50%.
  • the term "promoting plant growth” means that upon application of a lipase to the plant, the dry weight of the plant increases within a period of 10 to 20 days, preferably within a period of 12 to 18 days and most preferably within a period of 14 days by 5% to 70%, preferably by 10% to 65%, more preferably by 20% to 60% and most preferably by 40 to 50%.
  • plant is intended to comprise any plant including dicotyledonous and monocotyle- donous plants.
  • the plant is a monocotyledonous plant and more preferably it is turf grass.
  • Soil was sampled freshly.
  • Harvested soils were a wetting soil from Limburgerhof, serving as a control, and two non-wetting soils from Western Australia: Peter Black and South Stirling.
  • the harvested soil samples were dried and subsequently sieved through a 500 pm sieve.
  • Approxi- mately 3 g dry sample soil, 4 g dry silica sand, and 10 mg cotton wool were placed into a 5 mL syringe as column filling, with the cotton wool forming the bottom layer on the narrow end of the syringe, the silica sand forming the middle layer, and the soil sample forming the topmost layer on the wide end of the syringe (see Figure 1 A). Columns prepared in this way were weighed to determine the dry weight.
  • lipase solution was prepared by dissolving powdered, lyophilized lipase ac- cording to SEQ ID No. 956 (also designated as “Lipase BP” or “Lipase BP 2015”) in pure dis- tilled water (DW).
  • the prepared columns were then treated with either 1 mL lipase solution (0.06%) or with 1 mL distilled water (DW) as a control, applied to the top of the sample soil layer.
  • the columns were left to incubate for 24 hours at room temperature (RT) followed by rins- ing with 2 mL DW and drying at 45°C for 48 hours.
  • the water droplet penetration time was measured by adding 20 pL of DW to the dried columns and recording the time needed for the entirety of the 20 pL volume to penetrate into the sample soil layer. Thereafter, water infiltration time was measured next by adding 2 mL DW to the top of the sample soil layer and recording the time needed for the entirety of the 2 mL vol- ume to infiltrate into the column. Finally, 2 hours after measuring infiltration time, the columns were weighed again ( Figure 1 B). Any increase in weight over the initially measured dry weight was due to water retention in the column layers and could be correlated to the water volume re- tained, thereby providing the water holding capacity.
  • lipase treatment of non-wetting soils overcomes soil water repellency (reduced WDPT and water infiltration time), i.e. lipase treatment improves water availability to the soil.
  • Example 2 In order to assess concentration dependency of the effect of lipase treatment on the non-wetting soils, the same experimental set up described in Example 1 was used for South Stirling or Peter Black soil, and the concentration of the lipase according to SEQ ID No. 956 (also called “Lipase BP” or “Lipase BP 2015”) was varied from 0.02% - 0.06% w/v in the applied lipase solution.
  • WDPT was markedly reduced by lipase treatment at concentrations as low as 0.02% w/v (see Figure 3A).
  • water infiltration time was reduced upon treatment with as little as 0.02% lipase, although higher lipase concentrations led to a greater effect, especially in South Stirling soil (see Figure 3B).
  • the water holding capacity of both soils increased linearly with increasing concentration of lipase (see Figure 3C).
  • Plastic pots (upper diameter 13 cm) were filled with exactly 1000 g of previously dried soil Lim- burgerhof and placed in a growth chamber with 16 h light and 8 h dark period at 20 °C ( ⁇ 2 °C).
  • the main characteristics of soil Limburgerhof are pH(CaCl2) 6.8, with a mineral content of 73% sand, 24% silt, and 3 % clay, classified according to FAO as sandy loam.
  • the two treatments were tap water (120 mL/per pot) or 120 mL tap water with 0.06% (w/v) of the lipase according to SEQ ID No. 956.
  • the amount of 120 mL wa- ter was divided into 6 x 20 mL doses .
  • Per treatment n 7 pots were used and the 14 pots were randomly placed central in the growth chamber. The pots were covered and allowed to stand for 24 h. Then each pot received in total 130 mL of deionized water split up over an hour into 7 pro- portions simulating rain, which exceeded the water holding capacity of the pots.
  • the amount of water leached was collected in saucers and weighed (see Figure 4A). The lower amount of wa- ter leached from the pots treated with lipase indicates an increased water holding capacity due to the treatment with the lipase.
  • each pot could dry further for another 4 days and at day 13 after the lipase treatment each pot was watered to exactly 55% of its maximum water holding capacity and seeded with 15 wheat seeds per pot. Up to day 19 each pot was watered daily up to 55% of its WHC. Then, at day 19 each pot received uniformly 80 mL of water Thereafter, the plants were singled out to uniformly 10 emerged plants per pot and each pot was individually watered to 55% WHC.
  • Enzyme treatment of the South Stirling soil used the following quantities of enzyme: Lipase, 0.0015 g/g soil, Laccase, 8U/g soil, and Chitinase, 0.11 1 U/g soil.
  • Enzyme pre-treatment was carried out by adding 10 ml aqueous enzyme solution to 10 grams of soil particles (sieved to ⁇ 2 mm) in a 50 ml capacity polypropylene container which was then placed in a roller mixer for 24 hr incubation time. Soil particles were then separated by centrifuging followed by thorough washing with doubly distilled water to remove excess enzyme. Finally the soil particles were dried at 80 ° C.
  • a flat adhesive surface was prepared by covering a microscope glass slide with a double sided adhesive polyimide tape.
  • Enzyme modified soil particles prepared according to the method above were uniformly distributed over a 2 cm by 1 cm adhesive area and a uniform load of 250 g was applied over this particulate surface for 30 s after which, the slide was carefully tapped to remove any excess particles. This yielded a compactly packed monolayer of particles, repre- senting a soil surface containing hierarchical roughness where the particle surface nanoscale topology was superimposed onto the microscale packing roughness, analogous to a wetting front within a particulate bed (Truong et al. (2014) Journal of Colloid and Interface Science 460: 61-70).
  • the sessile drop method was used for measuring static water contact angles under ambient conditions (20 °C, 40 % RH) using a Contact Angle Goniometer equipped with a nanodispenser (model FTA1000c, First Ten Angstroms, Inc., Portsmouth, VA, USA).
  • the droplet volume used was 1.0 pL and 10 replicate the contact angles were evaluated by recording 50 images over 2 s with a Pelcomodel PCHM 575-4 camera and measuring contact angles after the droplet had rested on the surface for a period of 2 s (Truong et al. (2014) Journal of Colloid and Interface Science 460: 61-70).
  • Dynamic spreading of the water droplets on enzyme modified soil surfaces was recorded in the first 60 seconds of contact using a Prosilica Model Navitar 444037 camera at a speed of 2 frames per second.
  • the contact angle was determined by image analysis using the FTA Win- dows Mode 32 software.
  • Fig. 5 shows the dynamic water contact angles for South Stirling soil which was originally se- verely hydrophobic (MED 4.0) after treatment with the three enzymes plus the two controls (wa- ter treated and untreated soil).
  • MED 4.0 se- verely hydrophobic
  • Table 1 Water contact angles for enzyme modified soil particulate surfaces and their compari- son with untreated and water treated counterparts.
  • the experimental set up ( Figure 6A) was the same as in Example 1 with the difference that the columns were filled with 6.000 g turf soil and the Water Droplet Penetration Time (WDPT) test was performed with 15 pL demineralized water and that the final weighing was done 24 h after soil saturation with water. There were 5 replications per treatment.
  • the lipase according to SEQ ID No. 956 was applied at a concentration of 0.04% (w/v) dissolved in water and the wetting agent KICK was applied at a concentration of 0.42 % (w/v).
  • Figures 6B and 6D show that both the lipase and the wetting agent decreased the water infiltra tion time at a soil depth of 0 to 4 cm compared to water.
  • Figure 6C shows that the application of both lipase and wetting agent decreased the water droplet penetration time (WDPT) at a soil depth of 0 to 6 cm compared to water.
  • Figure 6E shows that both lipase and wetting agent in- crease the water holding capacity of soil at a soil depth of 0 to 6 cm compared to water.
  • WDPT water droplet penetration time
  • Figure 8 shows that treatment with lipase increases the dry weight of the putting green by about 50% compared to the water control.

Abstract

The present invention relates to a method of increasing water availability in soil using a lipase.

Description

METHOD OF REDUCING SOIL WATER REPELLENCY
FIELD OF THE INVENTION
The present invention relates to a method of reducing soil water repellency and/or for increasing water holding capacity using a lipase.
BACKGROUND OF THE INVENTION
Soil water repellency (SWR) is a condition where soil does not spontaneously wet when a drop of water is applied to the soil surface, i.e. the soil is too hydrophobic (Muller and Deuer (2011 ) Agric., Ecosystems and Environ. 144: 208-221). Hydrophobic soils occur in many countries on various lands, such as agricultural, pasture, coastal dune sands, forest, shrub lands, parks, turfgrass soils, no-till agriculture, and soils irrigated with treated wastewater. A substantial inter- est in soil water repellency soils has grown in recent times (WO 2013/181240; Dekker et al. (2005) Aust. J. of Soil Res. 43: 403-441 ).
Soil water repellency can cause undesirable consequences such as environmental deterioration and considerable losses in crop production. Soil water repellency becomes especially problem- atic on water relationships and can cause associated environmental issues, such as, but not limited to, reduction in soil water intake, uneven wetting patterns, reduced irrigation efficiency and effective precipitation, increased preferential flow that can have adverse effects on aquifer contamination, greater runoff and erosion, limited seed and vegetative establishment, and re- duced plant growth and quality (Doerr et al. (2000). Earth-Sci. Reviews 51 : 33-65; Muller and Deuer (201 1 )).
In agricultural settings, soil water repellency across large areas of crop-producing fields leads to reduction or complete loss of already planted crops as well as reduction in soil quality and wa- tering problems for the next set of seeds. On sandy turfgrass soils and grasslands, on the other hand, soil water repellency is a reoccurring problem called“localized dry spot” (LDS). In LDS, soil water repellency appears as irregular dry areas from a few centimeters to several meters diameter with the repellency usually extending from the surface of the soils into 5-10 cm depth. A second soil water repellency situation on turfgrass sites that can appear on all soil types oc- curs within the dry area of basidiomycete induced“fairy-ring” (Barton and Colmer (2011 ) Agric. Water Management 99:1-7).
The primary cause of soil water repellency is the formation of a coating of hydrophobic, organic material on soil particles. This hydrophobic organic material can include surface waxes, fatty ac- ids, and other organics such as lignin, a phenolic polymer. These materials originate from plant leaves and other decomposing organic matter, plant root exudates, fungal hyphae/exudates, and volatized organic materials condensing on soil particles following forest or grassland fires (Atanassova and Doerr (2010) Europ. J. of Soil Sci. 61 : 298-313). Sandy soils are especially susceptible to soil water repellency due to a lower particle surface area. Once sands become coated by organics and upon drying to a critical moisture level, they exhibit a hydrophobic na- ture and, thereafter, resist rewetting. The conventional remediation practice involves the use of wetting agents (surfactants). It is known in the art that single surfactants can improve soil water infiltration (SWI) and reduce soil water repellency (see, e.g., PCT/EP2018/052676). When used on specific soils, the effect of single surfactants on improving SWI and reducing soil water repellency can be very limited (Da- vies et al. (2012) Crop Updates 2012, p.358-p.362). Further, this approach is indirect, costly, and only produces short-term alleviation of the problem, requiring repeated applications of the surfactants to maintain effectiveness (Muller and Deuer (201 1 ); Moore et al. (2010) J. Hydrol. Hydrochem. 58(3): 142-148).
Biological methods involving microorganisms capable of degrading wax in soil have been de- scribed (Roper (2006) Biologia 61/Suppl. 19: S358-S362), but to see a significant effect, a great amount of microorganisms was necessary which is no longer economic. In another approach, enzymes such as laccase, pectinase, chitinase, and protease (WO 2013/181240 A2; Zeng (2014) HortScience 49(5): 662-666) have been applied to turfgrass and showed a reduction in soil water repellency, while other enzymes such as esterases and lipases did not show this ef- fect.
Hence, there is still a need for an efficient method for managing the water availability in soils, in particular in non-wetting soils.
SUMMARY OF THE INVENTION
The present inventors have surprisingly found that the application of a lipase to soil leads to a reduced soil water repellency and an increased water holding capacity of non-wetting soils. Ad- ditionally, the application of a lipase also increases the water availability in wetting soils.
Accordingly, the present invention relates to the use of an isolated polypeptide having lipase ac- tivity for increasing the water availability in soil.
In one embodiment the soil water repellency of non-wetting soil is reduced and/or the water holding capacity of non-wetting soils is increased.
In another embodiment the water holding capacity of wetting soil is increased and/or the evapo- ration from wetting soil is decreased.
The isolated polypeptide having lipase activity may be selected from the group consisting of:
(i) a polypeptide having the amino acid sequence according to according to any one of SEQ ID NOs: SEQ ID NO: 956, SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56, SEQ ID NO: 58, SEQ ID NO: 60, SEQ ID NO: 62, SEQ ID NO: 64, SEQ ID NO: 66, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 72, SEQ ID NO: 74, SEQ ID NO: 76, SEQ ID NO: 78, SEQ ID NO: 80, SEQ ID NO: 82, SEQ ID NO: 84, SEQ ID NO: 86, SEQ ID NO: 88, SEQ ID NO: 90, SEQ ID NO: 92, SEQ ID NO: 94, SEQ ID NO: 96, SEQ ID NO: 98, SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, SEQ ID NO: 110, SEQ ID NO: 1 12, SEQ ID NO: 114, SEQ ID NO: 116, SEQ ID NO: 1 18, SEQ ID NO: 120, SEQ ID NO: 122, SEQ ID NO: 124, SEQ ID NO: 126, SEQ ID NO: 128, SEQ ID NO: 130, SEQ ID NO: 132, SEQ ID NO: 134, SEQ ID NO: 136, SEQ ID NO: 138, SEQ ID NO: 140, SEQ ID NO: 142, SEQ ID NO: 143, SEQ ID NO: 146, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 152, SEQ ID NO: 154, SEQ ID NO: 156, SEQ ID NO: 158, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 166, SEQ ID NO: 168, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 174, SEQ ID NO: 176, SEQ ID NO: 178, SEQ ID NO: 180, SEQ ID NO: 182, SEQ ID NO: 184, SEQ ID NO: 186, SEQ ID NO: 188, SEQ ID NO: 190, SEQ ID NO: 192, SEQ ID NO: 194, SEQ ID NO: 196, SEQ ID NO: 198, SEQ ID NO: 200, SEQ ID NO: 202, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 208, SEQ ID NO: 210, SEQ ID NO: 212, SEQ ID NO: 214, SEQ ID NO: 216, SEQ ID NO: 218, SEQ ID NO: 220, SEQ ID NO: 222, SEQ ID NO: 224, SEQ ID NO: 226, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 232, SEQ ID NO: 234, SEQ ID NO: 236, SEQ ID NO: 238, SEQ ID NO: 240, SEQ ID NO: 242, SEQ ID NO: 244, SEQ ID NO: 246, SEQ ID NO: 248, SEQ ID NO: 250, SEQ ID NO: 252, SEQ ID NO: 254, SEQ ID NO: 256, SEQ ID NO: 258, SEQ ID NO: 260, SEQ ID NO: 262, SEQ ID NO: 264, SEQ ID NO: 266, SEQ ID NO: 268, SEQ ID NO: 270, SEQ ID NO: 272, SEQ ID NO: 274, SEQ ID NO: 276, SEQ ID NO: 278, SEQ ID NO: 280, SEQ ID NO: 282, SEQ ID NO: 284, SEQ ID NO: 286, SEQ ID NO: 288, SEQ ID NO: 290, SEQ ID NO: 292, SEQ ID NO: 294, SEQ ID NO: 296, SEQ ID NO: 298, SEQ ID NO: 300, SEQ ID NO: 302, SEQ ID NO: 304, SEQ ID NO: 306, SEQ ID NO: 308, SEQ ID NO: 310, SEQ ID NO: 312, SEQ ID NO: 314, SEQ ID NO: 316, SEQ ID NO: 318, SEQ ID NO: 320, SEQ ID NO: 322, SEQ ID NO: 324, SEQ ID NO: 326, SEQ ID NO: 328, SEQ ID NO: 330, SEQ ID NO: 332, SEQ ID NO: 334, SEQ ID NO: 336, SEQ ID NO: 338, SEQ ID NO: 340, SEQ ID NO: 342, SEQ ID NO: 344, SEQ ID NO: 346, SEQ ID NO: 348, SEQ ID NO: 350, SEQ ID NO: 352, SEQ ID NO: 354, SEQ ID NO: 356, SEQ ID NO: 358, SEQ ID NO: 360, SEQ ID NO: 362, SEQ ID NO: 364, SEQ ID NO: 366, SEQ ID NO: 368, SEQ ID NO: 370, SEQ ID NO: 372, SEQ ID NO: 374, SEQ ID NO: 376, SEQ ID NO: 378, SEQ ID NO: 380, SEQ ID NO: 382, SEQ ID NO: 384, SEQ ID NO: 386, SEQ ID NO: 388, SEQ ID NO: 390, SEQ ID NO: 392, SEQ ID NO: 394, SEQ ID NO: 396, SEQ ID NO: 398, SEQ ID NO: 400, SEQ ID NO: 402, SEQ ID NO: 404, SEQ ID NO: 406, SEQ ID NO: 408, SEQ ID NO: 410, SEQ ID NO: 412, SEQ ID NO: 414, SEQ ID NO: 416, SEQ ID NO: 418, SEQ ID NO: 420, SEQ ID NO: 422, SEQ ID NO: 424, SEQ ID NO: 426, SEQ ID NO: 428, SEQ ID NO: 430, SEQ ID NO: 432, SEQ ID NO: 434, SEQ ID NO: 436, SEQ ID NO: 438, SEQ ID NO: 440, SEQ ID NO: 442, SEQ ID NO: 444, SEQ ID NO: 446, SEQ ID NO: 448, SEQ ID NO: 450, SEQ ID NO: 452, SEQ ID NO: 454, SEQ ID NO: 456, SEQ ID NO: 458, SEQ ID NO: 460, SEQ ID NO: 462, SEQ ID NO: 464, SEQ ID NO: 466, SEQ ID NO: 468, SEQ ID NO: 470, SEQ ID NO: 472, SEQ ID NO: 474, SEQ ID NO: 476, SEQ ID NO: 478, SEQ ID NO: 480, SEQ ID NO: 482, SEQ ID NO: 484, SEQ ID NO: 486, SEQ ID NO: 488, SEQ ID NO: 490, SEQ ID NO: 492, SEQ ID NO: 494, SEQ ID NO: 496, SEQ ID NO: 498, SEQ ID NO: 500, SEQ ID NO: 502, SEQ ID NO: 504, SEQ ID NO: 506, SEQ ID NO: 508, SEQ ID NO: 510, SEQ ID NO: 512, SEQ ID NO: 514, SEQ ID NO: 516, SEQ ID NO: 518, SEQ ID NO: 520, SEQ ID NO: 522, SEQ ID NO: 524, SEQ ID NO: 526, SEQ ID NO: 528, SEQ ID NO: 530, SEQ ID NO: 532, SEQ ID NO: 534, SEQ ID NO: 536, SEQ ID NO: 538, SEQ ID NO: 540, SEQ ID NO: 542, SEQ ID NO: 544, SEQ ID NO: 546, SEQ ID NO: 548, SEQ ID NO: 550, SEQ ID NO: 552, SEQ ID NO: 554, SEQ ID NO: 556, SEQ ID NO: 558, SEQ ID NO: 560, SEQ ID NO: 562, SEQ ID NO: 564, SEQ ID NO: 566, SEQ ID NO: 568, SEQ ID NO: 570, SEQ ID NO: 572, SEQ ID NO: 574, SEQ ID NO: 576, SEQ ID NO: 578, SEQ ID NO: 580, SEQ ID NO: 582, SEQ ID NO: 584, SEQ ID NO: 586, SEQ ID NO: 588, SEQ ID NO: 590, SEQ ID NO: 592, SEQ ID NO: 594, SEQ ID NO: 596, SEQ ID NO: 598, SEQ ID NO: 600, SEQ ID NO: 602, SEQ ID NO: 604, SEQ ID NO: 606, SEQ ID NO: 608, SEQ ID NO: 610, SEQ ID NO: 612, SEQ ID NO: 614, SEQ ID NO: 616, SEQ ID NO: 618, SEQ ID NO: 620, SEQ ID NO: 622, SEQ ID NO: 624, SEQ ID NO: 626, SEQ ID NO: 628, SEQ ID NO: 630, SEQ ID NO: 632, SEQ ID NO: 634, SEQ ID NO: 636, SEQ ID NO: 638, SEQ ID NO: 640, SEQ ID NO: 642, SEQ ID NO: 644, SEQ ID NO: 646, SEQ ID NO: 648, SEQ ID NO: 650, SEQ ID NO: 652, SEQ ID NO: 654, SEQ ID NO: 656, SEQ ID NO: 658, SEQ ID NO: 660, SEQ ID NO: 662, SEQ ID NO: 664, SEQ ID NO: 666, SEQ ID NO: 668, SEQ ID NO: 670, SEQ ID NO: 672, SEQ ID NO: 674, SEQ ID NO: 676, SEQ ID NO: 678, SEQ ID NO: 680, SEQ ID NO: 682, SEQ ID NO: 684, SEQ ID NO: 686, SEQ ID NO: 688, SEQ ID NO: 690, SEQ ID NO: 692, SEQ ID NO: 694, SEQ ID NO: 696, SEQ ID NO: 698, SEQ ID NO: 700, SEQ ID NO: 702, SEQ ID NO: 704, SEQ ID NO: 706, SEQ ID NO: 708, SEQ ID NO: 710, SEQ ID NO: 712, SEQ ID NO: 714, SEQ ID NO: 716, SEQ ID NO: 718, SEQ ID NO: 720, SEQ ID NO: 722, SEQ ID NO: 724, SEQ ID NO: 726, SEQ ID NO: 728, SEQ ID NO: 730, SEQ ID NO: 732, SEQ ID NO: 734, SEQ ID NO: 736, SEQ ID NO: 738, SEQ ID NO: 740, SEQ ID NO: 742, SEQ ID NO: 744, SEQ ID NO: 746, SEQ ID NO: 748, SEQ ID NO: 750, SEQ ID NO: 752, SEQ ID NO: 754, SEQ ID NO: 756, SEQ ID NO: 758, SEQ ID NO: 760, SEQ ID NO: 762, SEQ ID NO: 764, SEQ ID NO: 766, SEQ ID NO: 768, SEQ ID NO: 770, SEQ ID NO: 772, SEQ ID NO: 774, SEQ ID NO: 776, SEQ ID NO: 778, SEQ ID NO: 780, SEQ ID NO: 782, SEQ ID NO: 784, SEQ ID NO: 786, SEQ ID NO: 788, SEQ ID NO: 790, SEQ ID NO: 792, SEQ ID NO: 794, SEQ ID NO : 796, SEQ ID NO: 798, SEQ ID NO: 800, SEQ ID NO: 802, SEQ ID NO: 804, SEQ ID NO: 806, SEQ ID NO: 808, SEQ ID NO: 810, SEQ ID NO: 812, SEQ ID NO: 814, SEQ ID NO: 816, SEQ ID NO: 818, SEQ ID NO: 820, SEQ ID NO: 822, SEQ ID NO: 824, SEQ ID NO: 826, SEQ ID NO: 828, SEQ ID NO: 830, SEQ ID NO: 832, SEQ ID NO: 834, SEQ ID NO: 836, SEQ ID NO: 838, SEQ ID NO: 840, SEQ ID NO: 842, SEQ ID NO: 844, SEQ ID NO: 846, SEQ ID NO: 848, SEQ ID NO: 850, SEQ ID NO: 852, SEQ ID NO: 854, SEQ ID NO: 856, SEQ ID NO: 858, SEQ ID NO: 860, SEQ ID NO: 862, SEQ ID NO: 864, SEQ ID NO: 866, SEQ ID NO: 868, SEQ ID NO: 870, SEQ ID NO: 872, SEQ ID NO: 874, SEQ ID NO: 876, SEQ ID NO: 878, SEQ ID NO: 880, SEQ ID NO: 882, SEQ ID NO: 884, SEQ ID NO: 886, SEQ ID NO: 888, SEQ ID NO: 890, SEQ ID NO: 892, SEQ ID NO: 894, SEQ ID NO: 896, SEQ ID NO: 898, SEQ ID NO: 900, SEQ ID NO: 902, SEQ ID NO: 904, SEQ ID NO: 906, SEQ ID NO: 908, SEQ ID NO: 910, SEQ ID NO: 912, SEQ ID NO: 914, SEQ ID NO: 916, SEQ ID NO: 918, SEQ ID NO: 920, SEQ ID NO: 922, SEQ ID NO: 924, SEQ ID NO: 926, SEQ ID NO: 928, SEQ ID NO: 930, SEQ ID NO: 932, SEQ ID NO: 934, SEQ ID NO: 936, SEQ ID NO: 938, SEQ ID NO: 940, SEQ ID NO: 942, SEQ ID NO: 944, SEQ ID NO: 946, SEQ ID NO: 948, SEQ ID NO: 950, SEQ ID NO: 952 or SEQ ID NO: 954 or an enzymatically active fragment thereof having lipase activity;
(ii) a polypeptide encoded by the nucleic acid sequence according to any one of SEQ ID Nos. SEQ ID NO: 955, SEQ ID NO: 1 , SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 1 1 , SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 19, SEQ ID NO: 21 , SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 27, SEQ ID NO: 29, SEQ ID NO: 31 , SEQ ID NO: 33, SEQ ID NO: 35, SEQ ID NO: 37, SEQ ID NO: 39, SEQ ID NO: 41 , SEQ ID NO: 43, SEQ ID NO: 45, SEQ ID NO: 47, SEQ ID NO: 49, SEQ ID NO: 51 , SEQ ID NO: 53, SEQ ID NO: 55, SEQ ID NO: 57, SEQ ID NO: 59, SEQ ID NO: 61 , SEQ ID NO: 63, SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 71 , SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 77, SEQ ID NO: 79, SEQ ID NO: 81 , SEQ ID NO: 83, SEQ ID NO: 85, SEQ ID NO: 87, SEQ ID NO: 89, SEQ ID NO: 91 , SEQ ID NO: 93, SEQ ID NO: 95, SEQ ID NO: 97, SEQ ID NO: 99, SEQ ID NO: 101 , SEQ ID NO: 103, SEQ ID NO: 105, SEQ ID NO: 107, SEQ ID NO: 109, SEQ ID NO: 1 1 1 , SEQ ID NO: 1 13, SEQ ID NO: 1 15, SEQ ID NO: 1 17, SEQ ID NO: 1 19, SEQ ID NO: 121 , SEQ ID NO: 123, SEQ ID NO: 125, SEQ ID NO: 127, SEQ ID NO: 129, SEQ ID NO: 131 , SEQ ID NO: 133, SEQ ID NO: 135, SEQ ID NO: 137, SEQ ID NO: 139, SEQ ID NO: 141 , SEQ ID NO: 143, SEQ ID NO: 145, SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 151 , SEQ ID NO: 153, SEQ ID NO: 155, SEQ ID NO: 157, SEQ ID NO: 159, SEQ ID NO: 161 , SEQ ID NO: 163, SEQ ID NO: 165, SEQ ID NO: 167, SEQ ID NO: 169, SEQ ID NO: 171 , SEQ ID NO: 173, SEQ ID NO: 175, SEQ ID NO: 177, SEQ ID NO: 179, SEQ ID NO: 181 , SEQ ID NO: 183, SEQ ID NO: 185, SEQ ID NO: 187, SEQ ID NO: 189, SEQ ID NO: 191 , SEQ ID NO: 193, SEQ ID NO: 195, SEQ ID NO: 197, SEQ ID NO: 199, SEQ ID NO: 201 , SEQ ID NO: 203, SEQ ID NO: 205, SEQ ID NO: 207, SEQ ID NO: 209, SEQ ID NO: 21 1 , SEQ ID NO: 213, SEQ ID NO: 215, SEQ ID NO: 217, SEQ ID NO: 219, SEQ ID NO: 221 , SEQ ID NO: 223, SEQ ID NO: 225, SEQ ID NO: 227, SEQ ID NO: 229, SEQ ID NO: 231 , SEQ ID NO: 233, SEQ ID NO: 235, SEQ ID NO: 237, SEQ ID NO: 239, SEQ ID NO: 241 , SEQ ID NO: 243, SEQ ID NO: 245, SEQ ID NO: 247, SEQ ID NO: 249, SEQ ID NO: 251 , SEQ ID NO: 253, SEQ ID NO: 255, SEQ ID NO: 257, SEQ ID NO: 259, SEQ ID NO: 261 , SEQ ID NO: 263, SEQ ID NO: 265, SEQ ID NO: 267, SEQ ID NO: 269, SEQ ID NO: 271 , SEQ ID NO: 273, SEQ ID NO: 275, SEQ ID NO: 277, SEQ ID NO: 279, SEQ ID NO: 281 , SEQ ID NO: 283, SEQ ID NO: 285, SEQ ID NO: 287, SEQ ID NO: 289, SEQ ID NO: 291 , SEQ ID NO: 293, SEQ ID NO: 295, SEQ ID NO: 297, SEQ ID NO: 299, SEQ ID NO: 301 , SEQ ID NO: 303, SEQ ID NO: 305, SEQ ID NO: 307, SEQ ID NO: 309, SEQ ID NO: 31 1 , SEQ ID NO: 313, SEQ ID NO: 315, SEQ ID NO: 317, SEQ ID NO: 319, SEQ ID NO: 321 , SEQ ID NO: 323, SEQ ID NO: 325, SEQ ID NO: 327, SEQ ID NO: 329, SEQ ID NO: 331 , SEQ ID NO: 333, SEQ ID NO: 335, SEQ ID NO: 337, SEQ ID NO: 339, SEQ ID NO: 341 , SEQ ID NO: 343, SEQ ID NO: 345, SEQ ID NO: 347, SEQ ID NO: 349, SEQ ID NO: 351 , SEQ ID NO: 353, SEQ ID NO: 355, SEQ ID NO: 357, SEQ ID NO: 359, SEQ ID NO: 361 , SEQ ID NO: 363, SEQ ID NO: 365, SEQ ID NO: 367, SEQ ID NO: 369, SEQ ID NO: 371 , SEQ ID NO: 373, SEQ ID NO: 375, SEQ ID NO: 377, SEQ ID NO: 379, SEQ ID NO: 381 , SEQ ID NO: 383, SEQ ID NO: 385, SEQ ID NO: 387, SEQ ID NO: 389, SEQ ID NO: 391 , SEQ ID NO: 393, SEQ ID NO: 395, SEQ ID NO: 397, SEQ ID NO: 399, SEQ ID NO: 401 , SEQ ID NO: 403, SEQ ID NO: 405, SEQ ID NO: 407, SEQ ID NO: 409, SEQ ID NO: 41 1 , SEQ ID NO: 413, SEQ ID NO: 415, SEQ ID NO: 417, SEQ ID NO: 419, SEQ ID NO: 421 , SEQ ID NO: 423, SEQ ID NO: 425, SEQ ID NO: 427, SEQ ID NO: 429, SEQ ID NO: 431 , SEQ ID NO: 433, SEQ ID NO: 435, SEQ ID NO: 437, SEQ ID NO: 439, SEQ ID NO: 441 , SEQ ID NO: 443, SEQ ID NO: 445, SEQ ID NO: 447, SEQ ID NO: 449, SEQ ID NO: 451 , SEQ ID NO: 453, SEQ ID NO: 455, SEQ ID NO: 457, SEQ ID NO: 459, SEQ ID NO: 461 , SEQ ID NO: 463, SEQ ID NO: 465, SEQ ID NO: 467, SEQ ID NO: 469, SEQ ID NO: 471 , SEQ ID NO: 473, SEQ ID NO: 475, SEQ ID NO: 477, SEQ ID. NO: 479, SEQ ID NO: 481 , SEQ ID NO: 483, SEQ ID NO: 485, SEQ ID NO: 487, SEQ ID NO: 489, SEQ ID NO: 491 , SEQ ID NO: 493, SEQ ID NO: 495, SEQ ID NO: 497, SEQ ID NO: 499, SEQ ID NO: 501 , SEQ ID NO: 503, SEQ ID NO: 505, SEQ ID NO: 507, SEQ ID NO: 509, SEQ ID NO: 51 1 , SEQ ID NO: 513, SEQ ID NO: 515, SEQ ID NO: 517, SEQ ID NO: 519, SEQ ID NO: 521 , SEQ ID NO: 523, SEQ ID NO: 525, SEQ ID NO: 527, SEQ ID NO: 529, SEQ ID NO: 531 , SEQ ID NO: 533, SEQ ID NO: 535, SEQ ID NO: 537, SEQ ID NO: 539, SEQ ID NO: 541 , SEQ ID NO: 543, SEQ ID NO: 545, SEQ ID NO: 547, SEQ ID NO: 549, SEQ ID NO: 551 , SEQ ID NO: 553, SEQ ID NO: 555, SEQ ID NO: 557, SEQ ID NO: 559, SEQ ID NO: 561 , SEQ ID NO: 563, SEQ ID NO: 565, SEQ ID NO: 567, SEQ ID NO: 569, SEQ ID NO: 571 , SEQ ID NO: 573, SEQ ID NO: 575, SEQ ID NO: 577, SEQ ID NO: 579, SEQ ID NO: 581 , SEQ ID NO: 583, SEQ ID NO: 585, SEQ ID NO: 587, SEQ ID NO: 589, SEQ ID NO: 591 , SEQ ID NO: 593, SEQ ID NO: 595, SEQ ID NO: 597, SEQ ID NO: 599, SEQ ID NO: 601 , SEQ ID NO: 603, SEQ ID NO: 605, SEQ ID NO: 607, SEQ ID NO: 609, SEQ ID NO: 61 1 , SEQ ID NO: 613, SEQ ID NO: 615, SEQ ID NO: 617, SEQ ID NO: 619, SEQ ID NO: 621 , SEQ ID NO: 623, SEQ ID NO: 625, SEQ ID NO: 627, SEQ ID NO: 629, SEQ ID NO: 631 , SEQ ID NO: 633, SEQ ID NO: 635, SEQ ID NO: 637, SEQ ID NO: 639, SEQ ID NO: 641 , SEQ ID NO: 643, SEQ ID NO: 645, SEQ ID NO: 647, SEQ ID NO: 649, SEQ ID NO: 651 , SEQ ID NO: 653, SEQ ID NO: 655, SEQ ID NO: 657, SEQ ID NO: 659, SEQ ID NO: 661 , SEQ ID NO: 663, SEQ ID NO: 665, SEQ ID NO: 667, SEQ ID NO: 669, SEQ ID NO: 671 , SEQ ID NO: 673, SEQ ID NO: 675, SEQ ID NO: 677, SEQ ID NO: 679, SEQ ID NO: 681 , SEQ ID NO: 683, SEQ ID NO: 685, SEQ ID NO: 687, SEQ ID NO: 689, SEQ ID NO: 691 , SEQ ID NO: 693, SEQ ID NO: 695, SEQ ID NO: 697, SEQ ID NO: 699, SEQ ID NO: 701 , SEQ ID NO: 703, SEQ ID NO: 705, SEQ ID NO: 707, SEQ ID NO: 709, SEQ ID NO: 71 1 , SEQ ID NO: 713, SEQ ID NO: 715, SEQ ID NO: 717, SEQ ID NO: 719, SEQ ID NO: 721 , SEQ ID NO: 723, SEQ ID NO: 725, SEQ ID NO: 727, SEQ ID NO: 729, SEQ ID NO: 731 , SEQ ID NO: 733, SEQ ID NO: 735, SEQ ID NO: 737, SEQ ID NO: 739, SEQ ID NO: 741 , SEQ ID NO: 743, SEQ ID NO: 745, SEQ ID NO: 747, SEQ ID NO : 749, SEQ ID NO: 751 , SEQ ID NO : 753, SEQ ID NO : 755, SEQ ID NO: 757, SEQ ID NO: 759, SEQ ID NO: 761 , SEQ ID NO: 763, SEQ ID NO: 765, SEQ ID NO : 767, SEQ ID NO : 769, SEQ ID NO : 771 , SEQ ID NO: 773, SEQ ID NO: 775, SEQ ID NO: 777, SEQ ID NO: 779, SEQ ID NO: 781 , SEQ ID NO: 783, SEQ ID NO: 785, SEQ ID NO: 787, SEQ ID NO: 789, SEQ ID NO: 791 , SEQ ID NO: 793, SEQ ID NO: 795, SEQ ID NO: 797, SEQ ID NO: 799, SEQ ID NO: 801 , SEQ ID NO: 803, SEQ ID NO: 805, SEQ ID NO: 807, SEQ ID NO: 809, SEQ ID NO: 81 1 , SEQ ID NO: 813, SEQ ID NO: 815, SEQ ID NO: 817, SEQ ID NO: 819, SEQ ID NO: 821 , SEQ ID NO: 823, SEQ ID NO: 825, SEQ ID NO: 827, SEQ ID NO: 829, SEQ ID NO: 831 , SEQ ID NO: 833, SEQ ID NO: 835, SEQ ID NO: 837, SEQ ID NO: 839, SEQ ID NO: 841 , SEQ ID NO: 843, SEQ ID NO: 845, SEQ ID NO: 847, SEQ ID NO: 849, SEQ ID NO: 851 , SEQ ID NO: 853, SEQ ID NO: 855, SEQ ID NO: 857, SEQ ID NO: 859, SEQ ID NO: 861 , SEQ ID NO: 863, SEQ ID NO: 865, SEQ ID NO: 867, SEQ ID NO: 869, SEQ ID NO: 871 , SEQ ID NO: 873, SEQ ID NO: 875, SEQ ID NO: 877, SEQ ID NO: 879, SEQ ID NO: 881 , SEQ ID NO: 883, SEQ ID NO: 885, SEQ ID NO: 887, SEQ ID NO: 889, SEQ ID NO: 891 , SEQ ID NO: 893, SEQ ID NO: 895, SEQ ID NO: 897, SEQ ID NO: 899, SEQ ID NO: 901 , SEQ ID NO: 903, SEQ ID NO: 905, SEQ ID NO: 907, SEQ ID NO: 909, SEQ ID NO: 91 1 , SEQ ID NO: 913, SEQ ID NO: 915, SEQ ID NO: 917, SEQ ID NO: 919, SEQ ID NO: 921 , SEQ ID NO: 923, SEQ ID NO: 925, SEQ ID NO: 927, SEQ ID NO: 929, SEQ ID NO: 931 , SEQ ID NO: 933, SEQ ID NO: 935, SEQ ID NO: 937, SEQ ID NO: 939, SEQ ID NO: 941 , SEQ ID NO: 943, SEQ ID NO: 945, SEQ ID NO: 947, SEQ ID NO: 949, SEQ ID NO: 951 or SEQ ID NO: 953 or an enzymatically active fragment thereof having lipase activity;
(iii) a polypeptide having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28,
SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56, SEQ ID NO: 58, SEQ ID NO: 60, SEQ ID NO: 62,
SEQ ID NO: 64, SEQ ID NO: 66, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 72, SEQ ID NO: 74, SEQ ID NO: 76, SEQ ID NO: 78, SEQ ID NO: 80, SEQ ID NO: 82, SEQ ID NO: 84, SEQ ID NO: 86, SEQ ID NO: 88, SEQ ID NO: 90, SEQ ID NO: 92, SEQ ID NO: 94, SEQ ID NO: 96,
SEQ ID NO: 98, SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, SEQ ID NO: 1 10, SEQ ID NO: 112, SEQ ID NO: 1 14, SEQ ID NO: 116, SEQ ID NO: 1 18, SEQ ID NO: 120, SEQ ID NO: 122, SEQ ID NO: 124, SEQ ID NO: 126, SEQ ID NO: 128, SEQ ID NO: 130, SEQ ID NO: 132, SEQ ID NO: 134, SEQ ID NO: 136, SEQ ID NO: 138, SEQ ID NO: 140, SEQ ID NO: 142, SEQ ID NO: 143, SEQ ID NO: 146, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 152, SEQ ID NO: 154, SEQ ID NO: 156, SEQ ID NO: 158, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 166, SEQ ID NO: 168, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 174, SEQ ID NO: 176, SEQ ID NO: 178, SEQ ID NO: 180, SEQ ID NO: 182, SEQ ID NO: 184, SEQ ID NO: 186, SEQ ID NO: 188, SEQ ID NO: 190, SEQ ID NO: 192, SEQ ID NO: 194, SEQ ID NO: 196, SEQ ID NO: 198, SEQ ID NO: 200, SEQ ID NO: 202, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 208, SEQ ID NO: 210, SEQ ID NO: 212, SEQ ID NO: 214, SEQ ID NO: 216, SEQ ID NO: 218, SEQ ID NO: 220, SEQ ID NO: 222, SEQ ID NO: 224, SEQ ID NO: 226, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 232, SEQ ID NO: 234, SEQ ID NO: 236, SEQ ID NO: 238, SEQ ID NO: 240, SEQ ID NO: 242, SEQ ID NO: 244, SEQ ID NO: 246, SEQ ID NO: 248, SEQ ID NO: 250, SEQ ID NO: 252, SEQ ID NO: 254, SEQ ID NO: 256, SEQ ID NO: 258, SEQ ID NO: 260, SEQ ID NO: 262, SEQ ID NO: 264, SEQ ID NO: 266, SEQ ID NO: 268, SEQ ID NO: 270, SEQ ID NO: 272, SEQ ID NO: 274, SEQ ID NO: 276, SEQ ID NO: 278, SEQ ID NO: 280, SEQ ID NO: 282, SEQ ID NO: 284, SEQ ID NO: 286, SEQ ID NO: 288, SEQ ID NO: 290, SEQ ID NO: 292, SEQ ID NO: 294, SEQ ID NO: 296, SEQ ID NO: 298, SEQ ID NO: 300, SEQ ID NO: 302, SEQ ID NO: 304, SEQ ID NO: 306, SEQ ID NO: 308, SEQ ID NO: 310, SEQ ID NO: 312, SEQ ID NO: 314, SEQ ID NO: 316, SEQ ID NO: 318, SEQ ID NO: 320, SEQ ID NO: 322, SEQ ID NO: 324, SEQ ID NO: 326, SEQ ID NO: 328, SEQ ID NO: 330, SEQ ID NO: 332, SEQ ID NO: 334, SEQ ID NO: 336, SEQ ID NO: 338, SEQ ID NO: 340, SEQ ID NO: 342, SEQ ID NO: 344, SEQ ID NO: 346, SEQ ID NO: 348, SEQ ID NO: 350, SEQ ID NO: 352, SEQ ID NO: 354, SEQ ID NO: 356, SEQ ID NO: 358, SEQ ID NO: 360, SEQ ID NO: 362, SEQ ID NO: 364, SEQ ID NO: 366, SEQ ID NO: 368, SEQ ID NO: 370, SEQ ID NO: 372, SEQ ID NO: 374, SEQ ID NO: 376, SEQ ID NO: 378, SEQ ID NO: 380, SEQ ID NO: 382, SEQ ID NO: 384, SEQ ID NO: 386, SEQ ID NO: 388, SEQ ID NO: 390, SEQ ID NO: 392, SEQ ID NO: 394, SEQ ID NO: 396, SEQ ID NO: 398, SEQ ID NO: 400, SEQ ID NO: 402, SEQ ID NO: 404, SEQ ID NO: 406, SEQ ID NO: 408, SEQ ID NO: 410, SEQ ID NO: 412, SEQ ID NO: 414, SEQ ID NO: 416, SEQ ID NO: 418, SEQ ID NO: 420, SEQ ID NO: 422, SEQ ID NO: 424, SEQ ID NO: 426, SEQ ID NO: 428, SEQ ID NO: 430, SEQ ID NO: 432, SEQ ID NO: 434, SEQ ID NO: 436, SEQ ID NO: 438, SEQ ID NO: 440, SEQ ID NO: 442, SEQ ID NO: 444, SEQ ID NO: 446, SEQ ID NO: 448, SEQ ID NO: 450, SEQ ID NO: 452, SEQ ID NO: 454, SEQ ID NO: 456, SEQ ID NO: 458, SEQ ID NO: 460, SEQ ID NO: 462, SEQ ID NO: 464, SEQ ID NO: 466, SEQ ID NO: 468, SEQ ID NO: 470, SEQ ID NO: 472, SEQ ID NO: 474, SEQ ID NO: 476, SEQ ID NO: 478, SEQ ID NO: 480, SEQ ID NO: 482, SEQ ID NO: 484, SEQ ID NO: 486, SEQ ID NO: 488, SEQ ID NO: 490, SEQ ID NO: 492, SEQ ID NO: 494, SEQ ID NO: 496, SEQ ID NO: 498, SEQ ID NO: 500, SEQ ID NO: 502, SEQ ID NO: 504, SEQ ID NO: 506, SEQ ID NO: 508, SEQ ID NO: 510, SEQ ID NO: 512, SEQ ID NO: 514, SEQ ID NO: 516, SEQ ID NO: 518, SEQ ID NO: 520, SEQ ID NO: 522, SEQ ID NO: 524, SEQ ID NO: 526, SEQ ID NO: 528, SEQ ID NO: 530, SEQ ID NO: 532, SEQ ID NO: 534, SEQ ID NO: 536, SEQ ID NO: 538, SEQ ID NO: 540, SEQ ID NO: 542, SEQ ID NO: 544, SEQ ID NO: 546, SEQ ID NO: 548, SEQ ID NO: 550, SEQ ID NO: 552, SEQ ID NO: 554, SEQ ID NO: 556, SEQ ID NO: 558, SEQ ID NO: 560, SEQ ID NO: 562, SEQ ID NO: 564, SEQ ID NO: 566, SEQ ID NO: 568, SEQ ID NO: 570, SEQ ID NO: 572, SEQ ID NO: 574, SEQ ID NO: 576, SEQ ID NO: 578, SEQ ID NO: 580, SEQ ID NO: 582, SEQ ID NO: 584, SEQ ID NO: 586, SEQ ID NO: 588, SEQ ID NO: 590, SEQ ID NO: 592, SEQ ID NO: 594, SEQ ID NO: 596, SEQ ID NO: 598, SEQ ID NO: 600, SEQ ID NO: 602, SEQ ID NO: 604, SEQ ID NO: 606, SEQ ID NO: 608, SEQ ID NO: 610, SEQ ID NO: 612, SEQ ID NO: 614, SEQ ID NO: 616, SEQ ID NO: 618, SEQ ID NO: 620, SEQ ID NO: 622, SEQ ID NO: 624, SEQ ID NO: 626, SEQ ID NO: 628, SEQ ID NO: 630, SEQ ID NO: 632, SEQ ID NO: 634, SEQ ID NO: 636, SEQ ID NO: 638, SEQ ID NO: 640, SEQ ID NO: 642, SEQ ID NO: 644, SEQ ID NO: 646, SEQ ID NO: 648, SEQ ID NO: 650, SEQ ID NO: 652, SEQ ID NO: 654, SEQ ID NO: 656, SEQ ID NO: 658, SEQ ID NO: 660, SEQ ID NO: 662, SEQ ID NO: 664, SEQ ID NO: 666, SEQ ID NO: 668, SEQ ID NO: 670, SEQ ID NO: 672, SEQ ID NO: 674, SEQ ID NO: 676, SEQ ID NO: 678, SEQ ID NO: 680, SEQ ID NO: 682, SEQ ID NO: 684, SEQ ID NO: 686, SEQ ID NO: 688, SEQ ID NO: 690, SEQ ID NO: 692, SEQ ID NO: 694, SEQ ID NO: 696, SEQ ID NO: 698, SEQ ID NO: 700, SEQ ID NO: 702, SEQ ID NO: 704, SEQ ID NO: 706, SEQ ID NO: 708, SEQ ID NO: 710, SEQ ID NO: 712, SEQ ID NO: 714, SEQ ID NO: 716, SEQ ID NO: 718, SEQ ID NO: 720, SEQ ID NO: 722, SEQ ID NO: 724, SEQ ID NO: 726, SEQ ID NO: 728, SEQ ID NO: 730, SEQ ID NO: 732, SEQ ID NO: 734, SEQ ID NO: 736, SEQ ID NO: 738, SEQ ID NO: 740, SEQ ID NO: 742, SEQ ID NO: 744, SEQ ID NO: 746, SEQ ID NO: 748, SEQ ID NO: 750, SEQ ID NO: 752, SEQ ID NO: 754, SEQ ID NO: 756, SEQ ID NO: 758, SEQ ID NO: 760, SEQ ID NO: 762, SEQ ID NO: 764, SEQ ID NO: 766, SEQ ID NO: 768, SEQ ID NO: 770, SEQ ID NO: 772, SEQ ID NO: 774, SEQ ID NO: 776, SEQ ID NO: 778, SEQ ID NO: 780, SEQ ID NO: 782, SEQ ID NO: 784, SEQ ID NO: 786, SEQ ID NO: 788, SEQ ID NO: 790, SEQ ID NO: 792, SEQ ID NO: 794, SEQ ID NO : 796, SEQ ID NO: 798, SEQ ID NO: 800, SEQ ID NO: 802, SEQ ID NO: 804, SEQ ID NO: 806, SEQ ID NO: 808, SEQ ID NO: 810, SEQ ID NO: 812, SEQ ID NO: 814, SEQ ID NO: 816, SEQ ID NO: 818, SEQ ID NO: 820, SEQ ID NO: 822, SEQ ID NO: 824, SEQ ID NO: 826, SEQ ID NO: 828, SEQ ID NO: 830, SEQ ID NO: 832, SEQ ID NO: 834, SEQ ID NO: 836, SEQ ID NO: 838, SEQ ID NO: 840, SEQ ID NO: 842, SEQ ID NO: 844, SEQ ID NO: 846, SEQ ID NO: 848, SEQ ID NO: 850, SEQ ID NO: 852, SEQ ID NO: 854, SEQ ID NO: 856, SEQ ID NO: 858, SEQ ID NO: 860, SEQ ID NO: 862, SEQ ID NO: 864, SEQ ID NO: 866, SEQ ID NO: 868, SEQ ID NO: 870, SEQ ID NO: 872, SEQ ID NO: 874, SEQ ID NO: 876, SEQ ID NO: 878, SEQ ID NO: 880, SEQ ID NO: 882, SEQ ID NO: 884, SEQ ID NO: 886, SEQ ID NO: 888, SEQ ID NO: 890, SEQ ID NO: 892, SEQ ID NO: 894, SEQ ID NO: 896, SEQ ID NO: 898, SEQ ID NO: 900, SEQ ID NO: 902, SEQ ID NO: 904, SEQ ID NO: 906, SEQ ID NO: 908, SEQ ID NO: 910, SEQ ID NO: 912, SEQ ID NO: 914, SEQ ID NO: 916, SEQ ID NO: 918, SEQ ID NO: 920, SEQ ID NO: 922, SEQ ID NO: 924, SEQ ID NO: 926, SEQ ID NO: 928, SEQ ID NO: 930, SEQ ID NO: 932, SEQ ID NO: 934, SEQ ID NO: 936, SEQ ID NO: 938, SEQ ID NO: 940, SEQ ID NO: 942, SEQ ID NO: 944, SEQ ID NO: 946, SEQ ID NO: 948, SEQ ID NO: 950, SEQ ID NO: 952 or SEQ ID NO: 954 or an enzymatically active fragment thereof having lipase activity; and
(iv) a polypeptide encoded by a nucleic acid sequence which hybridizes to the complement of the nucleic acid sequence according to any of SEQ ID NO: 955, SEQ ID NO: 1 , SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 1 1 , SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 19, SEQ ID NO: 21 , SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 27, SEQ ID NO: 29, SEQ ID NO: 31 , SEQ ID NO: 33, SEQ ID NO: 35, SEQ ID NO: 37, SEQ ID NO: 39, SEQ ID NO: 41 , SEQ ID NO: 43, SEQ ID NO: 45, SEQ ID NO: 47, SEQ ID NO: 49,
SEQ ID NO: 51 , SEQ ID NO: 53, SEQ ID NO: 55, SEQ ID NO: 57, SEQ ID NO: 59, SEQ ID NO: 61 , SEQ ID NO: 63, SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 71 , SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 77, SEQ ID NO: 79, SEQ ID NO: 81 , SEQ ID NO: 83,
SEQ ID NO: 85, SEQ ID NO: 87, SEQ ID NO: 89, SEQ ID NO: 91 , SEQ ID NO: 93, SEQ ID NO: 95, SEQ ID NO: 97, SEQ ID NO: 99, SEQ ID NO: 101 , SEQ ID NO: 103, SEQ ID NO: 105, SEQ ID NO: 107, SEQ ID NO: 109, SEQ ID NO: 11 1 , SEQ ID NO: 1 13, SEQ ID NO: 115, SEQ ID NO: 1 17, SEQ ID NO: 119, SEQ ID NO: 121 , SEQ ID NO: 123, SEQ ID NO: 125, SEQ ID NO: 127, SEQ ID NO: 129, SEQ ID NO: 131 , SEQ ID NO: 133, SEQ ID NO: 135, SEQ ID NO: 137, SEQ ID NO: 139, SEQ ID NO: 141 , SEQ ID NO: 143, SEQ ID NO: 145, SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 151 , SEQ ID NO: 153, SEQ ID NO: 155, SEQ ID NO: 157, SEQ ID NO: 159, SEQ ID NO: 161 , SEQ ID NO: 163, SEQ ID NO: 165, SEQ ID NO: 167, SEQ ID NO: 169, SEQ ID NO: 171 , SEQ ID NO: 173, SEQ ID NO: 175, SEQ ID NO: 177, SEQ ID NO: 179, SEQ ID NO: 181 , SEQ ID NO: 183, SEQ ID NO: 185, SEQ ID NO: 187, SEQ ID NO: 189, SEQ ID NO: 191 , SEQ ID NO: 193, SEQ ID NO: 195, SEQ ID NO: 197, SEQ ID NO: 199, SEQ ID NO: 201 , SEQ ID NO: 203, SEQ ID NO: 205, SEQ ID NO: 207, SEQ ID NO: 209, SEQ ID NO: 211 , SEQ ID NO: 213, SEQ ID NO: 215, SEQ ID NO: 217, SEQ ID NO: 219, SEQ ID NO: 221 , SEQ ID NO: 223, SEQ ID NO: 225, SEQ ID NO: 227, SEQ ID NO: 229, SEQ ID NO: 231 , SEQ ID NO: 233, SEQ ID NO: 235, SEQ ID NO: 237, SEQ ID NO: 239, SEQ ID NO: 241 , SEQ ID NO: 243, SEQ ID NO: 245, SEQ ID NO: 247, SEQ ID NO: 249, SEQ ID NO: 251 , SEQ ID NO: 253, SEQ ID NO: 255, SEQ ID NO: 257, SEQ ID NO: 259, SEQ ID NO: 261 , SEQ ID NO: 263, SEQ ID NO: 265, SEQ ID NO: 267, SEQ ID NO: 269, SEQ ID NO: 271 , SEQ ID NO: 273, SEQ ID NO: 275, SEQ ID NO: 277, SEQ ID NO: 279, SEQ ID NO: 281 , SEQ ID NO: 283, SEQ ID NO: 285, SEQ ID NO: 287, SEQ ID NO: 289, SEQ ID NO: 291 , SEQ ID NO: 293, SEQ ID NO: 295, SEQ ID NO: 297, SEQ ID NO: 299, SEQ ID NO: 301 , SEQ ID NO: 303, SEQ ID NO: 305, SEQ ID NO: 307, SEQ ID NO: 309, SEQ ID NO: 311 , SEQ ID NO: 313, SEQ ID NO: 315, SEQ ID NO: 317, SEQ ID NO: 319, SEQ ID NO: 321 , SEQ ID NO: 323, SEQ ID NO: 325, SEQ ID NO: 327, SEQ ID NO: 329, SEQ ID NO: 331 , SEQ ID NO: 333, SEQ ID NO: 335, SEQ ID NO: 337, SEQ ID NO: 339, SEQ ID NO: 341 , SEQ ID NO: 343, SEQ ID NO: 345, SEQ ID NO: 347, SEQ ID NO: 349, SEQ ID NO: 351 , SEQ ID NO: 353, SEQ ID NO: 355, SEQ ID NO: 357, SEQ ID NO: 359, SEQ ID NO: 361 , SEQ ID NO: 363, SEQ ID NO: 365, SEQ ID NO: 367, SEQ ID NO: 369, SEQ ID NO: 371 , SEQ ID NO: 373, SEQ ID NO: 375, SEQ ID NO: 377, SEQ ID NO: 379, SEQ ID NO: 381 , SEQ ID NO: 383, SEQ ID NO: 385, SEQ ID NO: 387, SEQ ID NO: 389, SEQ ID NO: 391 , SEQ ID NO: 393, SEQ ID NO: 395, SEQ ID NO: 397, SEQ ID NO: 399, SEQ ID NO: 401 , SEQ ID NO: 403, SEQ ID NO: 405, SEQ ID NO: 407, SEQ ID NO: 409, SEQ ID NO: 41 1 , SEQ ID NO: 413, SEQ ID NO: 415, SEQ ID NO: 417, SEQ ID NO: 419, SEQ ID NO: 421 , SEQ ID NO: 423, SEQ ID NO: 425, SEQ ID NO: 427, SEQ ID NO: 429, SEQ ID NO: 431 , SEQ ID NO: 433, SEQ ID NO: 435, SEQ ID NO: 437, SEQ ID NO: 439, SEQ ID NO: 441 , SEQ ID NO: 443, SEQ ID NO: 445, SEQ ID NO: 447, SEQ ID NO: 449, SEQ ID NO: 451 , SEQ ID NO: 453, SEQ ID NO: 455, SEQ ID NO: 457, SEQ ID NO: 459, SEQ ID NO: 461 , SEQ ID NO: 463, SEQ ID NO: 465, SEQ ID NO: 467, SEQ ID NO: 469, SEQ ID NO: 471 , SEQ ID NO: 473, SEQ ID NO: 475, SEQ ID NO: 477, SEQ ID. NO: 479, SEQ ID NO: 481 , SEQ ID NO: 483, SEQ ID NO: 485, SEQ ID NO: 487, SEQ ID NO: 489, SEQ ID NO: 491 , SEQ ID NO: 493, SEQ ID NO: 495, SEQ ID NO: 497, SEQ ID NO: 499, SEQ ID NO: 501 , SEQ ID NO: 503, SEQ ID NO: 505, SEQ ID NO: 507, SEQ ID NO: 509, SEQ ID NO: 51 1 , SEQ ID NO: 513, SEQ ID NO: 515, SEQ ID NO: 517, SEQ ID NO: 519, SEQ ID NO: 521 , SEQ ID NO: 523, SEQ ID NO: 525, SEQ ID NO: 527, SEQ ID NO: 529, SEQ ID NO: 531 , SEQ ID NO: 533, SEQ ID NO: 535, SEQ ID NO: 537, SEQ ID NO: 539, SEQ ID NO: 541 , SEQ ID NO: 543, SEQ ID NO: 545, SEQ ID NO: 547, SEQ ID NO: 549, SEQ ID NO: 551 , SEQ ID NO: 553, SEQ ID NO: 555, SEQ ID NO: 557, SEQ ID NO: 559, SEQ ID NO: 561 , SEQ ID NO: 563, SEQ ID NO: 565, SEQ ID NO: 567, SEQ ID NO: 569, SEQ ID NO: 571 , SEQ ID NO: 573, SEQ ID NO: 575, SEQ ID NO: 577, SEQ ID NO: 579, SEQ ID NO: 581 , SEQ ID NO: 583, SEQ ID NO: 585, SEQ ID NO: 587, SEQ ID NO: 589, SEQ ID NO: 591 , SEQ ID NO: 593, SEQ ID NO: 595, SEQ ID NO: 597, SEQ ID NO: 599, SEQ ID NO: 601 , SEQ ID NO: 603, SEQ ID NO: 605, SEQ ID NO: 607, SEQ ID NO: 609, SEQ ID NO: 61 1 , SEQ ID NO: 613, SEQ ID NO: 615, SEQ ID NO: 617, SEQ ID NO: 619, SEQ ID NO: 621 , SEQ ID NO: 623, SEQ ID NO: 625, SEQ ID NO: 627, SEQ ID NO: 629, SEQ ID NO: 631 , SEQ ID NO: 633, SEQ ID NO: 635, SEQ ID NO: 637, SEQ ID NO: 639, SEQ ID NO: 641 , SEQ ID NO: 643, SEQ ID NO: 645, SEQ ID NO: 647, SEQ ID NO: 649, SEQ ID NO: 651 , SEQ ID NO: 653, SEQ ID NO: 655, SEQ ID NO: 657, SEQ ID NO: 659, SEQ ID NO: 661 , SEQ ID NO: 663, SEQ ID NO: 665, SEQ ID NO: 667, SEQ ID NO: 669, SEQ ID NO: 671 , SEQ ID NO: 673, SEQ ID NO: 675, SEQ ID NO: 677, SEQ ID NO: 679, SEQ ID NO: 681 , SEQ ID NO: 683, SEQ ID NO: 685, SEQ ID NO: 687, SEQ ID NO: 689, SEQ ID NO: 691 , SEQ ID NO: 693, SEQ ID NO: 695, SEQ ID NO: 697, SEQ ID NO: 699, SEQ ID NO: 701 , SEQ ID NO: 703, SEQ ID NO: 705, SEQ ID NO: 707, SEQ ID NO: 709, SEQ ID NO: 71 1 , SEQ ID NO: 713, SEQ ID NO: 715, SEQ ID NO: 717, SEQ ID NO: 719, SEQ ID NO: 721 , SEQ ID NO: 723, SEQ ID NO: 725, SEQ ID NO: 727, SEQ ID NO: 729, SEQ ID NO: 731 , SEQ ID NO: 733, SEQ ID NO: 735, SEQ ID NO: 737, SEQ ID NO: 739, SEQ ID NO: 741 , SEQ ID NO: 743, SEQ ID NO: 745, SEQ ID NO: 747, SEQ ID NO: 749, SEQ ID NO: 751 , SEQ ID NO: 753, SEQ ID NO: 755, SEQ ID NO: 757, SEQ ID NO: 759, SEQ ID NO: 761 , SEQ ID NO: 763, SEQ ID NO: 765, SEQ ID NO : 767, SEQ ID NO : 769, SEQ ID NO : 771 , SEQ ID NO: 773, SEQ ID NO: 775, SEQ ID NO: 777, SEQ ID NO: 779, SEQ ID NO: 781 , SEQ ID NO: 783, SEQ ID NO: 785, SEQ ID NO: 787, SEQ ID NO: 789, SEQ ID NO: 791 , SEQ ID NO: 793, SEQ ID NO: 795, SEQ ID NO: 797, SEQ ID NO: 799, SEQ ID NO: 801 , SEQ ID NO: 803, SEQ ID NO: 805, SEQ ID NO: 807, SEQ ID NO: 809, SEQ ID NO: 81 1 , SEQ ID NO: 813, SEQ ID NO: 815, SEQ ID NO: 817, SEQ ID NO: 819, SEQ ID NO: 821 , SEQ ID NO: 823, SEQ ID NO: 825, SEQ ID NO: 827, SEQ ID NO: 829, SEQ ID NO: 831 , SEQ ID NO: 833, SEQ ID NO: 835, SEQ ID NO: 837, SEQ ID NO: 839, SEQ ID NO: 841 , SEQ ID NO: 843, SEQ ID NO: 845, SEQ ID NO: 847, SEQ ID NO: 849, SEQ ID NO: 851 , SEQ ID NO: 853, SEQ ID NO: 855, SEQ ID NO: 857, SEQ ID NO: 859, SEQ ID NO: 861 , SEQ ID NO: 863, SEQ ID NO: 865, SEQ ID NO: 867, SEQ ID NO: 869, SEQ ID NO: 871 , SEQ ID NO: 873, SEQ ID NO: 875, SEQ ID NO: 877, SEQ ID NO: 879, SEQ ID NO: 881 , SEQ ID NO: 883, SEQ ID NO: 885, SEQ ID NO: 887, SEQ ID NO: 889, SEQ ID NO: 891 , SEQ ID NO: 893, SEQ ID NO: 895, SEQ ID NO: 897, SEQ ID NO: 899, SEQ ID NO: 901 , SEQ ID NO: 903, SEQ ID NO: 905, SEQ ID NO: 907, SEQ ID NO: 909, SEQ ID NO: 911 , SEQ ID NO: 913, SEQ ID NO: 915, SEQ ID NO: 917, SEQ ID NO: 919, SEQ ID NO: 921 , SEQ ID NO: 923, SEQ ID NO: 925, SEQ ID NO: 927, SEQ ID NO: 929, SEQ ID NO: 931 , SEQ ID NO: 933, SEQ ID NO: 935, SEQ ID NO: 937, SEQ ID NO: 939, SEQ ID NO: 941 , SEQ ID NO: 943, SEQ ID NO: 945, SEQ ID NO: 947, SEQ ID NO: 949, SEQ ID NO: 951 or SEQ ID NO: 953 under stringent conditions.
Preferably, the polypeptide having lipase activity is selected from the group consisting of
(i) a polypeptide having the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100, SEQ ID NO: 1 14, SEQ ID NO: 142, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 156, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 182, SEQ ID NO: 186, SEQ ID NO: 194, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 214, SEQ ID NO: 218, SEQ ID NO: 224, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 244, SEQ ID NO: 262, SEQ ID NO: 268, SEQ ID NO: 270, SEQ ID NO: 282, SEQ ID NO: 292, SEQ ID NO: 298, SEQ ID NO: 300, SEQ ID NO: 306, SEQ ID NO: 320, SEQ ID NO: 340, SEQ ID NO: 368, SEQ ID NO: 394, SEQ ID NO: 422, SEQ ID NO: 424, SEQ ID NO: 426, SEQ ID NO: 428, SEQ ID NO: 440, SEQ ID NO: 454, SEQ ID NO: 456, SEQ ID NO: 460, SEQ ID NO: 464, SEQ ID NO: 466, SEQ ID NO: 478, SEQ ID NO: 480, SEQ ID NO : 482, SEQ ID NO: 488, SEQ ID NO: 490, SEQ ID NO: 492, SEQ ID NO: 500, SEQ ID NO: 504, SEQ ID NO: 508, SEQ ID NO: 510, SEQ ID NO: 520, SEQ ID NO: 522, SEQ ID NO: 552, SEQ ID NO: 556, SEQ ID NO: 558, SEQ ID NO: 564, SEQ ID NO: 572, SEQ ID NO: 578, SEQ ID NO: 588, SEQ ID NO : 590, SEQ ID NO : 592, SEQ ID NO : 594, SEQ ID NO : 596, SEQ ID NO: 600, SEQ ID NO: 606, SEQ ID NO: 630, SEQ ID NO: 638, SEQ ID NO: 642, SEQ ID NO: 650, SEQ ID NO: 660, SEQ ID NO: 662, SEQ ID NO: 682, SEQ ID NO: 690, SEQ ID NO: 708, SEQ ID NO: 710, SEQ ID NO: 712, SEQ ID NO: 728, SEQ ID NO: 730, SEQ ID NO: 732, SEQ ID NO: 734, SEQ ID NO: 736, SEQ ID NO: 740, SEQ ID NO: 742, SEQ ID NO: 748, SEQ ID NO: 760, SEQ ID NO: 770, SEQ ID NO: 780, ID NO: 784, SEQ ID NO: 788, SEQ ID NO: 790, SEQ ID NO: 810, SEQ ID NO: 812, SEQ ID NO: 828, SEQ ID NO: 842, SEQ ID NO: 856, SEQ ID NO: 862, SEQ ID NO: 876, SEQ ID NO: 892, SEQ ID NO: 910, SEQ ID NO: 912, SEQ ID NO: 914, SEQ ID NO: 930, SEQ ID NO: 934, SEQ ID NO: 940 or SEQ ID NO: 952, or an enzymati- cally active fragment thereof having lipase activity;
(ii) a polypeptide encoded by the nucleic acid sequence according to SEQ ID NO: 955, SEQ ID NO: 3, SEQ ID NO: 15, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 75, SEQ ID NO: 99, SEQ ID NO: 113, SEQ ID NO: 141 , SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 155, SEQ ID NO: 159, SEQ ID NO: 161 , SEQ ID NO: 163, SEQ ID NO: 169, SEQ ID NO: 171 , SEQ ID NO: 181 , SEQ ID NO: 185, SEQ ID NO: 193, SEQ ID NO: 203, SEQ ID NO: 205, SEQ ID NO: 213, SEQ ID NO: 217, SEQ ID NO: 223, SEQ ID NO: 227, SEQ ID NO: 229, SEQ ID NO: 243, SEQ ID NO: 261 , SEQ ID NO: 267, SEQ ID NO: 269, SEQ ID NO: 281 , SEQ ID NO: 291 , SEQ ID NO: 297, SEQ ID NO: 299, SEQ ID NO: 305, SEQ ID NO: 319, SEQ ID NO: 339, SEQ ID NO: 367, SEQ ID NO: 393, SEQ ID NO: 421 , SEQ ID NO: 423, SEQ ID NO: 425, SEQ ID NO: 427, SEQ ID NO: 439, SEQ ID NO: 453, SEQ ID NO: 455, SEQ ID NO: 459, SEQ ID NO: 463, SEQ ID NO: 465, SEQ ID NO: 477, SEQ ID NO: 479, SEQ ID NO : 481 , SEQ ID NO: 487, SEQ ID NO: 489, SEQ ID NO: 491 , SEQ ID NO: 499, SEQ ID NO: 503, SEQ ID NO: 507, SEQ ID NO: 509, SEQ ID NO: 519, SEQ ID NO: 521 , SEQ ID NO: 551 , SEQ ID NO: 555, SEQ ID NO: 557, SEQ ID NO: 563, SEQ ID NO: 571 , SEQ ID NO: 577, SEQ ID NO: 587, SEQ ID NO: 589, SEQ ID NO: 591 , SEQ ID NO: 593, SEQ ID NO: 595, SEQ ID NO: 599, SEQ ID NO: 605, SEQ ID NO: 629, SEQ ID NO: 637, SEQ ID NO: 641 , SEQ ID NO: 649, SEQ ID NO: 659, SEQ ID NO: 661 , SEQ ID NO: 681 , SEQ ID NO: 689, SEQ ID NO: 707, SEQ ID NO: 709, SEQ ID NO: 711 , SEQ ID NO: 727, SEQ ID NO: 729, SEQ ID NO: 731 , SEQ ID NO: 733, SEQ ID NO: 735, SEQ ID NO: 739, SEQ ID NO: 741 , SEQ ID NO: 747, SEQ ID NO: 759, SEQ ID NO: 769, SEQ ID NO: 779, ID NO: 783, SEQ ID NO: 787, SEQ ID NO: 789, SEQ ID NO: 809, SEQ ID NO: 811 , SEQ ID NO: 827, SEQ ID NO: 841 , SEQ ID NO: 855, SEQ ID NO: 861 , SEQ ID NO: 875, SEQ ID NO: 891 , SEQ ID NO: 909, SEQ ID NO: 91 1 , SEQ ID NO: 913, SEQ ID NO: 929, SEQ ID NO: 933, SEQ ID NO: 939 or SEQ ID NO: 951 or an enzymati- cally active fragment thereof having lipase activity;
(iii) a polypeptide having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100, SEQ ID NO: 1 14, SEQ ID NO: 142, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 156, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 182, SEQ ID NO: 186, SEQ ID NO: 194, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 214, SEQ ID NO: 218, SEQ ID NO: 224, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 244, SEQ ID NO: 262, SEQ ID NO: 268, SEQ ID NO: 270, SEQ ID NO: 282, SEQ ID NO: 292, SEQ ID NO: 298, SEQ ID NO: 300, SEQ ID NO: 306, SEQ ID NO: 320, SEQ ID NO: 340, SEQ ID NO: 368, SEQ ID NO: 394, SEQ ID NO: 422, SEQ ID NO: 424, SEQ ID NO: 426, SEQ ID NO: 428, SEQ ID NO: 440, SEQ ID NO: 454, SEQ ID NO: 456, SEQ ID NO: 460, SEQ ID NO: 464, SEQ ID NO: 466, SEQ ID NO: 478, SEQ ID NO: 480, SEQ ID NO : 482, SEQ ID NO: 488, SEQ ID NO: 490, SEQ ID NO: 492, SEQ ID NO: 500, SEQ ID NO: 504, SEQ ID NO: 508, SEQ ID NO: 510, SEQ ID NO: 520, SEQ ID NO: 522, SEQ ID NO: 552, SEQ ID NO: 556, SEQ ID NO: 558, SEQ ID NO: 564, SEQ ID NO: 572, SEQ ID NO: 578, SEQ ID NO: 588, SEQ ID NO : 590, SEQ ID NO : 592, SEQ ID NO : 594, SEQ ID NO : 596, SEQ ID NO: 600, SEQ ID NO: 606,
SEQ ID NO: 630, SEQ ID NO: 638, SEQ ID NO: 642, SEQ ID NO: 650, SEQ ID NO: 660, SEQ ID NO: 662, SEQ ID NO: 682, SEQ ID NO: 690, SEQ ID NO: 708, SEQ ID NO: 710, SEQ ID NO: 712, SEQ ID NO: 728, SEQ ID NO: 730, SEQ ID NO: 732, SEQ ID NO: 734, SEQ ID NO: 736, SEQ ID NO: 740, SEQ ID NO: 742, SEQ ID NO: 748, SEQ ID NO: 760, SEQ ID NO: 770, SEQ ID NO: 780, ID NO: 784, SEQ ID NO: 788, SEQ ID NO: 790, SEQ ID NO: 810, SEQ ID NO: 812, SEQ ID NO: 828, SEQ ID NO: 842, SEQ ID NO: 856, SEQ ID NO: 862, SEQ ID NO: 876, SEQ ID NO: 892, SEQ ID NO: 910, SEQ ID NO: 912, SEQ ID NO: 914, SEQ ID NO: 930, SEQ ID NO: 934, SEQ ID NO: 940 or SEQ ID NO: 952 or an enzymatically active fragment thereof having lipase activity; and
(iv) a polypeptide encoded by a nucleic acid sequence which hybridizes to the complement of the nucleic acid sequence according to any of SEQ ID NO: 955, SEQ ID NO: 3, SEQ ID NO: 15, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 75, SEQ ID NO: 99, SEQ ID NO: 113, SEQ ID NO: 141 , SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 155, SEQ ID NO: 159, SEQ ID NO: 161 , SEQ ID NO: 163, SEQ ID NO: 169, SEQ ID NO: 171 , SEQ ID NO: 181 , SEQ ID NO: 185, SEQ ID NO: 193, SEQ ID NO: 203, SEQ ID NO: 205, SEQ ID NO: 213, SEQ ID NO: 217, SEQ ID NO: 223, SEQ ID NO: 227, SEQ ID NO: 229, SEQ ID NO: 243, SEQ ID NO: 261 , SEQ ID NO: 267, SEQ ID NO: 269, SEQ ID NO: 281 , SEQ ID NO: 291 , SEQ ID NO: 297, SEQ ID NO: 299, SEQ ID NO: 305, SEQ ID NO: 319, SEQ ID NO: 339, SEQ ID NO: 367, SEQ ID NO: 393, SEQ ID NO: 421 , SEQ ID NO: 423, SEQ ID NO: 425, SEQ ID NO: 427, SEQ ID NO: 439, SEQ ID NO: 453, SEQ ID NO: 455, SEQ ID NO: 459, SEQ ID NO: 463, SEQ ID NO: 465, SEQ ID NO: 477, SEQ ID NO: 479, SEQ ID NO : 481 , SEQ ID NO: 487, SEQ ID NO: 489, SEQ ID NO: 491 , SEQ ID NO: 499, SEQ ID NO: 503, SEQ ID NO: 507, SEQ ID NO: 509, SEQ ID NO: 519, SEQ ID NO: 521 , SEQ ID NO: 551 , SEQ ID NO: 555, SEQ ID NO: 557, SEQ ID NO: 563, SEQ ID NO: 571 , SEQ ID NO: 577, SEQ ID NO: 587, SEQ ID NO: 589, SEQ ID NO: 591 , SEQ ID NO: 593, SEQ ID NO: 595, SEQ ID NO: 599, SEQ ID NO: 605, SEQ ID NO: 629, SEQ ID NO: 637, SEQ ID NO: 641 , SEQ ID NO: 649, SEQ ID NO: 659, SEQ ID NO: 661 , SEQ ID NO: 681 , SEQ ID NO: 689, SEQ ID NO: 707, SEQ ID NO: 709, SEQ ID NO: 711 , SEQ ID NO: 727, SEQ ID NO: 729, SEQ ID NO: 731 , SEQ ID NO: 733, SEQ ID NO: 735, SEQ ID NO: 739, SEQ ID NO: 741 , SEQ ID NO: 747, SEQ ID NO: 759, SEQ ID NO: 769, SEQ ID NO: 779, ID NO: 783, SEQ ID NO: 787, SEQ ID NO: 789, SEQ ID NO: 809, SEQ ID NO: 811 , SEQ ID NO: 827, SEQ ID NO: 841 , SEQ ID NO: 855, SEQ ID NO: 861 , SEQ ID NO: 875, SEQ ID NO: 891 , SEQ ID NO: 909, SEQ ID NO: 91 1 , SEQ ID NO: 913, SEQ ID NO: 929, SEQ ID NO: 933, SEQ ID NO: 939 or SEQ ID NO: 951 under stringent conditions.
More preferably, the polypeptide having lipase activity is selected from the group consisting of:
(i) a polypeptide having the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 90, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100 or SEQ ID NO: 114 or an enzymatically active frag- ment thereof having lipase activity;
(ii) a polypeptide encoded by the nucleic acid sequence according to SEQ ID NO: 955, SEQ ID NO: 89, SEQ ID NO: 3, SEQ ID NO: 15, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 75, SEQ ID NO: 99 or SEQ ID NO: 113 or an enzymatically active frag- ment thereof having lipase activity;
(iii) a polypeptide having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 90, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100 or SEQ ID NO: 114 or an enzymatically active fragment thereof having lipase activity; and
(iv) a polypeptide encoded by a nucleic acid sequence which hybridizes to the complement of the nucleic acid sequence according to SEQ ID NO: 955, SEQ ID NO: 89, SEQ ID NO: 3, SEQ ID NO: 15, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 75, SEQ ID NO: 99 or SEQ ID NO: 113 under stringent conditions.
Even more preferably, the polypeptide having lipase activity is selected from the group consist- ing of: (i) a polypeptide having the amino acid sequence according to SEQ ID NO: 956 or SEQ ID NO: 90 or an enzymatically active fragment thereof having lipase activity;
(ii) a polypeptide encoded by the nucleic acid sequence according to SEQ ID NO: 955 or SEQ ID NO: 89 or an enzymatically active fragment thereof having lipase activity;
(iii) a polypeptide having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956 or SEQ ID NO: 90 or an enzymatically ac- tive fragment thereof having lipase activity; and
(iv) a polypeptide encoded by a nucleic acid sequence which hybridizes to the complement of the nucleic acid sequence according to SEQ ID NO: 955 or SEQ ID NO: 89 under stringent con- ditions.
The polypeptide having lipase activity may be used in combination with at least one soil addi- tive, preferably selected from the group of surfactants, fertilizers, nitrification inhibitors and/or pesticides, preferably fungicides.
In one embodiment the polypeptide having lipase activity is applied in a concentration of be- tween 0.01 kg to 600 kg of polypeptide per hectare, preferably of between 0.16 kg to 100 kg per hectare, more preferably of between 0.6 kg to 20 kg per hectare, most preferably of between 1 kg to 5 kg per hectare.
The soil may be selected from agricultural land, pasture, coastal dune sands, forest, shrub lands, parks, turfgrass soils, no-till agriculture, and soils irrigated with treated wastewater.
The present invention also relates to a method for increasing the water availability in soil corn- prising treating an area of groundcover with an isolated polypeptide having lipase activity.
In one embodiment the soil water repellency of non-wetting soil is reduced and/or the water holding capacity of non-wetting soil is increased.
In another embodiment the water holding capacity of wetting soil is increased and/or the evapo- ration from wetting soil is decreased.
The polypeptide having lipase activity may be as defined in any one of claims 4 to 6.
In particular, the polypeptide having lipase activity may be selected from the group consisting of:
(i) a polypeptide having the amino acid sequence according to SEQ ID NO: 956 or an enzymati- cally active fragment thereof having lipase activity;
(ii) a polypeptide encoded by the nucleic acid sequence according to SEQ ID NO: 955 or an en- zymatically active fragment thereof having lipase activity;
(iii) a polypeptide having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956 or an enzymatically active fragment thereof having lipase activity; and
(iv) a polypeptide encoded by a nucleic acid sequence which hybridizes to the complement of the nucleic acid sequence according to SEQ ID NO: 955 under stringent conditions. In one embodiment the polypeptide or an enzymatically active fragment thereof having lipase activity is used in combination with at least one soil additive, preferably selected from the group of surfactants, fertilizers, nitrification inhibitors and/or pesticides, preferably fungicides.
The polypeptide or an enzymatically active fragment thereof having lipase activity may be ap- plied in a concentration of between 0.01 kg to 600 kg of polypeptide per hectare, preferably of between 0.16 kg to 100 kg per hectare, more preferably of between 0.6 kg to 20 kg per hectare, most preferably of between 1 kg to 5 kg per hectare.
The present invention also relates to the use of an isolated polypeptide having lipase activity for promoting plant growth.
The polypeptide having lipase activity may be as defined in any one of claims 4 to 6.
In particular, the polypeptide having lipase activity may be selected from the group consisting of:
(i) a polypeptide having the amino acid sequence according to SEQ ID NO: 956 or an enzymati- cally active fragment thereof having lipase activity;
(ii) a polypeptide encoded by the nucleic acid sequence according to SEQ ID NO: 955 or an en- zymatically active fragment thereof having lipase activity;
(iii) a polypeptide having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956 or an enzymatically active fragment thereof having lipase activity; and
(iv) a polypeptide encoded by a nucleic acid sequence which hybridizes to the complement of the nucleic acid sequence according to SEQ ID NO: 955 under stringent conditions.
BRIEF DESCRIPTION OF THE DRAWINGS
The disclosure can be better understood with reference to the following drawings,
which are described in the description and examples below.
FIG. 1 shows the experimental setup for determining soil parameters.
Figure 1 A is a schematic drawing of the columns prepared for assessing water droplet penetra- tion time (WDPT), water infiltration time, and water holding capacity of soil samples.
FIG. 1 B is a schematic drawing of the experimental set-up for assessing WDPT, water infiltra tion time, and water holding capacity of soil samples.
FIG. 2 contains bar graphs illustrating WDPT (FIG. 2A) and water infiltration time (FIG. 2B) of three different soils treated with either a water control (white bars) or a 0.06% (w/v) lipase solu- tion (black bars). Limburgerhof wetting soil serves as a control; the two non-wetting soils (Peter Black and South Stirling) are from Western Australia. FIG. 3 contains line graphs illustrating WDPT (FIG. 3A) of the non-wetting soil South Stirling as well as water infiltration time (FIG. 3B) and water holding capacity (FIG. 3C) of two different non-wetting soils from Western Australia (diamonds: Peter Black; inverted triangles: South Stir- ling) treated with different lipase concentrations.
FIG. 4 contains bar graphs illustrating percolated (leached) water (FIG. 4A), evaporation (FIG. 4B), and plant shoot fresh and dry weight (FIG 4C) of the wetting soil Limburgerhof treated with 0.06% (w/v) lipase solution (black bars) or only water (white bars).
FIG.5 shows the dynamic water contact angles for the non-wetting soil South Stirling soil after treatment with chitinase, laccase or lipase plus two controls (water treated and untreated soil).
FIG. 6 shows the experimental setup for determining soil parameters depending on the soil depth (FIG. 6A), the initial infiltration (FIG. 6B), water droplet penetration time (WDPT; FIG. 6C), the infiltration after drying (FIG. 6D) and the water holding capacity (FIG. 6E) of putting green treated with 0.04% (w/v) lipase solution (black squares), 0.42% (w/v) the wetting agent KICK (grey circles) or only water (white squares).
FIG. 7 shows the experimental setup to simulate long term effects by adding water to the soil columns (FIG. 7A), the water infiltration time at three different timepoints (FIG. 7B) and the wa- ter holding capacity at three different timepoints (FIG. 7C) of putting green treated with 0.04% (w/v) lipase solution (black bars), 0.42% (w/v) the wetting agent KICK (grey bars) or only water (white bars).
FIG. 8 shows the growth of turf grass in putting green treated with 0.03% (w/v) lipase solution (black bar) or only water (white bar).
DETAILED DESCRIPTION OF THE INVENTION
Although the present invention will be described with respect to particular embodiments, this de- scription is not to be construed in a limiting sense.
Before describing in detail exemplary embodiments of the present invention, definitions im- portant for understanding the present invention are given. Unless stated otherwise or apparent from the nature of the definition, the definitions apply to all methods and uses described herein.
As used in this specification and in the appended claims, the singular forms of "a" and "an" also include the respective plurals unless the context clearly dictates otherwise. In the context of the present invention, the terms "about" and "approximately" denote an interval of accuracy that a person skilled in the art will understand to still ensure the technical effect of the feature in ques- tion. The term typically indicates a deviation from the indicated numerical value of ±20 %, pref- erably ±15 %, more preferably ±10 %, and even more preferably ±5 %. It is to be understood that the term "comprising" is not limiting. For the purposes of the present invention the term "consisting of is considered to be a preferred embodiment of the term "corn- prising". If hereinafter a group is defined to comprise at least a certain number of embodiments, this is meant to also encompass a group which preferably consists of these embodiments only.
Furthermore, the terms "first", "second", "third" or "(a)", "(b)", "(c)", "(d)" etc. and the like in the description and in the claims, are used for distinguishing between similar elements and not nec- essarily for describing a sequential or chronological order. It is to be understood that the terms so used are interchangeable under appropriate circumstances and that the embodiments of the invention described herein are capable of operation in other sequences than described or illus trated herein. In case the terms "first", "second", "third" or "(a)", "(b)", "(c)", "(d)", "i", "ii" etc. re- late to steps of a method or use or assay there is no time or time interval coherence between the steps, i.e. the steps may be carried out simultaneously or there may be time intervals of sec- onds, minutes, hours, days, weeks, months or even years between such steps, unless other- wise indicated in the application as set forth herein above or below.
It is to be understood that this invention is not limited to the particular methodology, protocols, reagents etc. described herein as these may vary. It is also to be understood that the terminol- ogy used herein is for the purpose of describing particular embodiments only, and is not in- tended to limit the scope of the present invention that will be limited only by the appended claims. Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art.
As discussed above, the present invention is based on the finding that the application of a li- pase to soil increases the water availability in soil.
The term "water availability" refers to the amount of water which is present in a given volume of soil. This amount of water can be taken up by plants and used for growing. Hence, by improving the water availability in soil the soil is more suitable for growing plants.
By the use and method of the present invention the water availability in soil is increased by at least 3% or 5%, preferably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15%. This means that the amount of water which can be taken up by plants treated in accordance with the present invention is increased by at least 3% or 5%, pref- erably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15% compared to a soil which has not been treated in accordance with the present invention.
In one embodiment, the application of a lipase reduces soil water repellency and/or increases the water holding capacity of non-wetting soil.
The term "soil water repellency" (SWR) is a condition where soil does not spontaneously wet when a drop of water is applied to the surface. It reduces the affinity of soils to water such that they resist wetting for variable periods. It may be present in a large area and therefore affect agriculture. Such large areas of water-repellent soil predominantly occur in Australia as well as in North and South America. Alternatively, soil water repellency may present as "localized dry spots" which are irregular dry areas from a few centimeters to several meters diameter and mainly occur on sandy turfgrass soils and grasslands. Also alternatively, soil water repellency may present as "fairy rings" which are caused by fungi, in particular by basidiomycetes and which have a round shape. The fairy rings can range from a few centimeters to 20 meters in diameter, particularly from 0.5 m to 5m in diameter.
The organic matter contributing to hydrophobic organic coatings in soils with soil water repel- lency arises from sources such as, but not limited to: a) plant vegetation and root exudates with certain plant species especially prone to causing SWR, such as pine, gum, and oak trees and grasses; b) decomposition products from soil microbial activity, soil microorganism biomass such as fungal hyphae, and root exudates; c) applied organic amendments; d) ashed or volatized organic materials condensing on soil particles following forest or grassland fires; and e) organic matter in treated waste water used for irrigation. Regardless of soil type or organic matter source, soil drying increases repellency with air-drying greatly enhancing SWR severity.
The typical types of organic compounds suggested to be involved in soil water repellency in- clude: a) high molecular weight, polar fatty acids and their esters (alkanes that are derived from plant and cuticular waxes); b) other alkanes (paraffin-like compounds), microbial derived waxes, alkanols, phytanols, phytanes; c) amphiphilic (partially hydrophobic) lipids, stigmasterols and plant derived sterols that have polar (hydrophilic) and non-polar (hydrophobic) groups; d) other polar molecules such as sugars, gylocsides, aromatic acids, and low molecular weight organic acids; e) humic and fulvic acids from soil microbial activity or possibly added as amendments; and f) hydrophobins, cysteine rich proteins expressed only by filamentous fungi.
The soil water repellency can be measured and classified by a variety of methods. The water droplet penetration time (WDPT) test is based on the time taken for a drop of water to infiltrate into an air- or oven-dried soil sample (Dekker et al. (1998) Soil Sci. 163: 780-796). A description of this method is provided in the examples section herein. The molarity of ethanol droplet (MED) or ethanol test uses a series of aqueous ethanol solutions prepared in concentrations ranging between 0% and 36%. Drops of the various solutions are placed on the surface of soil samples, and the degree of soil water repellency is then defined as the ethanol percentage or molarity of the least concentrated ethanol solution that is absorbed by the soil in a mean time of <10 s (DeBano et al. (2000) J. Hydrol. 231 :4-32). In the intrinsic sorptivity method the sorptivity of wa- ter which is influenced by repellency is compared to the sorptivity of ethanol which is not influ enced by repellency (Tillman et al. (1999) Austr. J. Soil Res. 27: 637-644). Further, the contact angle between water and soil may be measured e.g. by the capillary rise method (Woche et al. (2005) Eur. J. Soil Sci. 56: 239-251 ).
By the use and method of the present invention the soil water repellency of non-wetting soils is reduced by at least 10% or 20%, preferably by at least 30% or 40%, more preferably by at least 50% or 60% and most preferably by at least 70% or 75%. If the soil water repellency is meas- ured using the WDPT test, the time taken for a drop to infiltrate the soil is reduced by at least 10% or 20%, preferably by at least 30% or 40%, more preferably by at least 50% or 60% and most preferably by at least 70% or 75%.
The term "water holding capacity" refers to the amount of water that a given amount of soil can hold. This has an impact on the water supply of any crops planted on the soil, but also on the retention of nutrients and pesticides by the soil. The water holding capacity can be determined by applying a defined amount of water onto a defined amount of soil and after a certain period of time such as two hours weighing the soil. The difference between the weight of the soil after applying the water and before applying the water is the amount of water which is held by the soil. Alternatively, the water holding capacity can be determined by placing a water saturated soil sample on a porous ceramic plate which is then placed in closed chambers and a known amount of pressure is applied to the chamber which forces water out of the soil sample and into the porous plate and out of the chamber. The water holding capacity can also be determined by measuring the amount of water leached through the soil after a defined amount of soil has been watered with an amount of water which exceeds the water holding capacity. A lower amount of water which has leached from the soil indicates an increased water holding capacity.
By the use and method of the present invention the water holding capacity of non-wetting soil is increased by at least 3% or 5%, preferably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15%. This means that the amount of water which is present in the soil after a certain period of time after application is increased by at least 3% or 5%, pref- erably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15% compared to a soil which has not been treated in accordance with the present invention.
Preferably, by the use and method of the present invention the soil water repellency of non-wet- ting soil is reduced and the water holding capacity of non-wetting soil is increased. The soil wa- ter repellency of non-wetting soil is reduced by at least 10% and the water holding capacity of non-wetting soil is increased by at least 3%, preferably the soil water repellency of non-wetting soil is reduced by at least 30% and the water holding capacity of non-wetting soil is increased by at least 8%, more preferably the soil water repellency of non-wetting soil is reduced by at least 50% and the water holding capacity of non-wetting soil is increased by at least 12% and most preferably the soil water repellency of non-wetting soil is reduced by at least 70% and the water holding capacity of non-wetting soil is increased by at least 15%.
The term "evaporation" refers to the process of losing water over a surface, particularly a soil surface. The evaporation can be determined by adding water to a soil sample and leaving the soil sample for a period of several days, for example eight days, without watering. After this pe- riod the soil sample is weighed and the difference in weight at the timepoint after adding the wa- ter and the weight after the period of leaving the soil is determined. This difference is defined as evaporation.
By the use and method of the present invention the water holding capacity of wetting soil is in- creased by at least 5% or 8%, preferably by at least 10% or 12%, more preferably by at least 15% or 18% and most preferably by at least 20%. This means that the amount of water which percolates through a water-saturated soil is decreased by at least 5% or 8%, preferably by at least 10% or 12%, more preferably by at least 15% or 18% and most preferably by at least 20% compared to a soil which has not been treated in accordance with the present invention.
By the use and method of the present invention the evaporation from wetting soil is reduced by at least 1 %, preferably by at least 2%, more preferably by at least 3% and most preferably by at least 4%. This means that after adding water to a pot containing wetting soil and leaving the pot without watering for a period of five to ten days, preferably of eight days, the loss of weight is reduced by at least 1 %, preferably by at least 2%, more preferably by at least 3% and most preferably by at least 4% compared to a soil which has not been treated in accordance with the present invention.
By the use and method of the present invention the water holding capacity of wetting soil is in- creased by at least 5% or 8% and the evaporation from wetting soil is reduced by at least 1 %, preferably the water holding capacity of wetting soil is increased by at least 10% or 12% and the evaporation from wetting soil is reduced by at least 2%, more preferably the water holding ca- pacity of wetting soil is increased by at least 15% or 18% and the evaporation from wetting soil is reduced by at least 3% and most preferably the water holding capacity of wetting soil is in- creased by at least 20% and the evaporation from wetting soil is reduced by at least 4% corn- pared to a soil which has not been treated in accordance with the present invention.
The term "soil" refers to material forming the surface of the earth and including a mixture of or- ganic material and minerals. Soil includes materials such as mud, sand, silt, and clay. It may it- self form the surface of the earth in areas, and in other areas it may underlie other types of groundcover, such as grass and other plants and vegetation, gravel, pebbles, and the like. Pref- erably, the soil is sandy soil characterized by a low particle-surface area.
The soil may be agricultural land, pasture, coastal dune sands, forest, shrub lands, parks, turfgrass soils, potting mixes or soils irrigated with treated wastewater.
In one embodiment, the soil is agricultural land which means that it is used for planting crops. Preferably, the agricultural land has not been treated by tillage (so-called no-till agriculture).
This means that the soil has not been disturbed by tillage. The agricultural land may comprise huge areas of non-wetting soil of several square kilometers as contrasted to localized dry spots which have a size of at most several meters. In Western Australia the total area of agricultural land having water repellent soil is about 5 million hectares.
In one embodiment the soil is not a turfgrass soil.
The term "turfgrass" refers to any vegetative ground covering such as, but not limited to, various species of grasses used for lawns, fields, golf course grounds, and the like.
In another embodiment the soil is turfgrass soil, for example turfgrass soil from a golf course. The turfgrass soil may have one or more localized dry spots (LDS). LDS are irregular dry areas from a few centimeters to several meters diameter with the repellency usually extending from the surface into a depth of 5 to 10 cm. Additionally or alternatively, the turfgrass soil may have one or more "fairy rings" which are caused by fungi, in particular by basidiomycetes and which have a round shape. The fairy rings can range from a few centimeters to 20 meters in diameter, particularly from 0.5 m to 5 m in diameter. In one embodiment the turfgrass soil has at least one localized dry spot and at least one fairy ring.
In one embodiment, the soil is non-wetting soil. The term "non-wetting soil" refers to a soil which does not spontaneously wet when a drop of water is applied to its surface. The non-wetting soil can be characterized by the water droplet penetration time test as explained above. The non- wetting soil has a water droplet penetration time of at least 5 seconds, preferably of at least 20 or at least 100 seconds, more preferably of at least 300 or 500 seconds, even more preferably of at least 700 or 1000 seconds and most preferably at least 1 ,200 seconds. Alternatively or ad- ditionally, the non-wetting soil can also be defined by the MED test discussed above. The non- wetting soil requires a molarity of ethanol of at least 0.2, preferably of at least 0.5, more prefera- bly of at least 1.0 and most preferably of at least 2.0 to absorb the solution into the soil. Alterna- tively or additionally, the non-wetting soil can also be defined by the contact angle between wa- ter and soil as determined for example by the capillary rise method. The non-wetting soil is de- fined by a contact angle of greater than 90°.
In one embodiment, the soil is wetting soil. The term "wetting soil" refers to a soil which sponta- neously wets when a drop of water is applied to its surface. The wetting soil can be character- ized by the water droplet penetration time test as explained above. The wetting soil has a water droplet penetration time of less than 5 seconds. Alternatively or additionally, the wetting soil can also be defined by the contact angle between water and soil as determined for example by the capillary rise method. The wetting soil is defined by a contact angle of less than 90°. Alterna- tively or additionally, the wetting soil can also be defined by the MED test discussed above. The non-wetting soil requires a molarity of ethanol of 0 to absorb the solution into the soil.
The term "isolated polypeptide" refers to a polypeptide that has been separated from its biologi cal source such as a bacterium or fungus producing the polypeptide, for example by centrifuga- tion or filtration. After separating the polypeptide from the biological source it may be purified to remove other components from the biological source or medium components. Hence, the term "isolated polypeptide" includes both purified polypeptides and polypeptides which are present in a cell culture supernatant or the like.
The isolated polypeptide used according to the present invention has lipase activity. Lipases (E.C. 3.1.1.3) are hydrolytic enzymes that are known to cleave ester bonds in lipids. Lipases in- clude phospholipases, triacylglycerol lipases, and galactolipases. The enzyme used in the method of the present invention is preferably a triacylglycerol lipase which cleaves the ester bond between glycerol and fatty acids, resulting in the release of fatty acids from the glycerol.
Preferably, the lipase used in the context of the present invention is selected from the group consisting of: (i) a lipase having the amino acid sequence according to according to any one of SEQ ID NOs: SEQ ID NO: 956, SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56, SEQ ID NO: 58, SEQ ID NO: 60, SEQ ID NO: 62, SEQ ID NO: 64, SEQ ID NO: 66, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 72, SEQ ID NO: 74, SEQ ID NO: 76, SEQ ID NO: 78, SEQ ID NO: 80, SEQ ID NO: 82, SEQ ID NO: 84, SEQ ID NO: 86, SEQ ID NO: 88, SEQ ID NO: 90, SEQ ID NO: 92, SEQ ID NO: 94, SEQ ID NO: 96, SEQ ID NO: 98, SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, SEQ ID NO: 110, SEQ ID NO: 1 12, SEQ ID NO: 114, SEQ ID NO: 116, SEQ ID NO: 1 18, SEQ ID NO: 120, SEQ ID NO: 122, SEQ ID NO: 124, SEQ ID NO: 126, SEQ ID NO: 128, SEQ ID NO: 130, SEQ ID NO: 132, SEQ ID NO: 134, SEQ ID NO: 136, SEQ ID NO: 138, SEQ ID NO: 140, SEQ ID NO: 142, SEQ ID NO: 143, SEQ ID NO: 146, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 152, SEQ ID NO: 154, SEQ ID NO: 156, SEQ ID NO: 158, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 166, SEQ ID NO: 168, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 174, SEQ ID NO: 176, SEQ ID NO: 178, SEQ ID NO: 180, SEQ ID NO: 182, SEQ ID NO: 184, SEQ ID NO: 186, SEQ ID NO: 188, SEQ ID NO: 190, SEQ ID NO: 192, SEQ ID NO: 194, SEQ ID NO: 196, SEQ ID NO: 198, SEQ ID NO: 200, SEQ ID NO: 202, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 208, SEQ ID NO: 210, SEQ ID NO: 212, SEQ ID NO: 214, SEQ ID NO: 216, SEQ ID NO: 218, SEQ ID NO: 220, SEQ ID NO: 222, SEQ ID NO: 224, SEQ ID NO: 226, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 232, SEQ ID NO: 234, SEQ ID NO: 236, SEQ ID NO: 238, SEQ ID NO: 240, SEQ ID NO: 242, SEQ ID NO: 244, SEQ ID NO: 246, SEQ ID NO: 248, SEQ ID NO: 250, SEQ ID NO: 252, SEQ ID NO: 254, SEQ ID NO: 256, SEQ ID NO: 258, SEQ ID NO: 260, SEQ ID NO: 262, SEQ ID NO: 264, SEQ ID NO: 266, SEQ ID NO: 268, SEQ ID NO: 270, SEQ ID NO: 272, SEQ ID NO: 274, SEQ ID NO: 276, SEQ ID NO: 278, SEQ ID NO: 280, SEQ ID NO: 282, SEQ ID NO: 284, SEQ ID NO: 286, SEQ ID NO: 288, SEQ ID NO: 290, SEQ ID NO: 292, SEQ ID NO: 294, SEQ ID NO: 296, SEQ ID NO: 298, SEQ ID NO: 300, SEQ ID NO: 302, SEQ ID NO: 304, SEQ ID NO: 306, SEQ ID NO: 308, SEQ ID NO: 310, SEQ ID NO: 312, SEQ ID NO: 314, SEQ ID NO: 316, SEQ ID NO: 318, SEQ ID NO: 320, SEQ ID NO: 322, SEQ ID NO: 324, SEQ ID NO: 326, SEQ ID NO: 328, SEQ ID NO: 330, SEQ ID NO: 332, SEQ ID NO: 334, SEQ ID NO: 336, SEQ ID NO: 338, SEQ ID NO: 340, SEQ ID NO: 342, SEQ ID NO: 344, SEQ ID NO: 346, SEQ ID NO: 348, SEQ ID NO: 350, SEQ ID NO: 352, SEQ ID NO: 354, SEQ ID NO: 356, SEQ ID NO: 358, SEQ ID NO: 360, SEQ ID NO: 362, SEQ ID NO: 364, SEQ ID NO: 366, SEQ ID NO: 368, SEQ ID NO: 370, SEQ ID NO: 372, SEQ ID NO: 374, SEQ ID NO: 376, SEQ ID NO: 378, SEQ ID NO: 380, SEQ ID NO: 382, SEQ ID NO: 384, SEQ ID NO: 386, SEQ ID NO: 388, SEQ ID NO: 390, SEQ ID NO: 392, SEQ ID NO: 394, SEQ ID NO: 396, SEQ ID NO: 398, SEQ ID NO: 400, SEQ ID NO: 402, SEQ ID NO: 404, SEQ ID NO: 406, SEQ ID NO: 408, SEQ ID NO: 410, SEQ ID NO: 412, SEQ ID NO: 414, SEQ ID NO: 416, SEQ ID NO: 418, SEQ ID NO: 420, SEQ ID NO: 422, SEQ ID NO: 424, SEQ ID NO: 426, SEQ ID NO: 428, SEQ ID NO: 430, SEQ ID NO: 432, SEQ ID NO: 434, SEQ ID NO: 436, SEQ ID NO: 438, SEQ ID NO: 440, SEQ ID NO: 442, SEQ ID NO: 444, SEQ ID NO: 446, SEQ ID NO: 448, SEQ ID NO: 450, SEQ ID NO: 452, SEQ ID NO: 454, SEQ ID NO: 456, SEQ ID NO: 458, SEQ ID NO: 460, SEQ ID NO: 462, SEQ ID NO: 464, SEQ ID NO: 466, SEQ ID NO: 468, SEQ ID NO: 470, SEQ ID NO: 472, SEQ ID NO: 474, SEQ ID NO: 476, SEQ ID NO: 478, SEQ ID NO: 480, SEQ ID NO: 482, SEQ ID NO: 484, SEQ ID NO: 486, SEQ ID NO: 488, SEQ ID NO: 490, SEQ ID NO: 492, SEQ ID NO: 494, SEQ ID NO: 496, SEQ ID NO: 498, SEQ ID NO: 500, SEQ ID NO: 502, SEQ ID NO: 504, SEQ ID NO: 506, SEQ ID NO: 508, SEQ ID NO: 510, SEQ ID NO: 512, SEQ ID NO: 514, SEQ ID NO: 516, SEQ ID NO: 518, SEQ ID NO: 520, SEQ ID NO: 522, SEQ ID NO: 524, SEQ ID NO: 526, SEQ ID NO: 528, SEQ ID NO: 530, SEQ ID NO: 532, SEQ ID NO: 534, SEQ ID NO: 536, SEQ ID NO: 538, SEQ ID NO: 540, SEQ ID NO: 542, SEQ ID NO: 544, SEQ ID NO: 546, SEQ ID NO: 548, SEQ ID NO: 550, SEQ ID NO: 552, SEQ ID NO: 554, SEQ ID NO: 556, SEQ ID NO: 558, SEQ ID NO: 560, SEQ ID NO: 562, SEQ ID NO: 564, SEQ ID NO: 566, SEQ ID NO: 568, SEQ ID NO: 570, SEQ ID NO: 572, SEQ ID NO: 574, SEQ ID NO: 576, SEQ ID NO: 578, SEQ ID NO: 580, SEQ ID NO: 582, SEQ ID NO: 584, SEQ ID NO: 586, SEQ ID NO: 588, SEQ ID NO: 590, SEQ ID NO: 592, SEQ ID NO: 594, SEQ ID NO: 596, SEQ ID NO: 598, SEQ ID NO: 600, SEQ ID NO: 602, SEQ ID NO: 604, SEQ ID NO: 606, SEQ ID NO: 608, SEQ ID NO: 610, SEQ ID NO: 612, SEQ ID NO: 614, SEQ ID NO: 616, SEQ ID NO: 618, SEQ ID NO: 620, SEQ ID NO: 622, SEQ ID NO: 624, SEQ ID NO: 626, SEQ ID NO: 628, SEQ ID NO: 630, SEQ ID NO: 632, SEQ ID NO: 634, SEQ ID NO: 636, SEQ ID NO: 638, SEQ ID NO: 640, SEQ ID NO: 642, SEQ ID NO: 644, SEQ ID NO: 646, SEQ ID NO: 648, SEQ ID NO: 650, SEQ ID NO: 652, SEQ ID NO: 654, SEQ ID NO: 656, SEQ ID NO: 658, SEQ ID NO: 660, SEQ ID NO: 662, SEQ ID NO: 664, SEQ ID NO: 666, SEQ ID NO: 668, SEQ ID NO: 670, SEQ ID NO: 672, SEQ ID NO: 674, SEQ ID NO: 676, SEQ ID NO: 678, SEQ ID NO: 680, SEQ ID NO: 682, SEQ ID NO: 684, SEQ ID NO: 686, SEQ ID NO: 688, SEQ ID NO: 690, SEQ ID NO: 692, SEQ ID NO: 694, SEQ ID NO: 696, SEQ ID NO: 698, SEQ ID NO: 700, SEQ ID NO: 702, SEQ ID NO: 704, SEQ ID NO: 706, SEQ ID NO: 708, SEQ ID NO: 710, SEQ ID NO: 712, SEQ ID NO: 714, SEQ ID NO: 716, SEQ ID NO: 718, SEQ ID NO: 720, SEQ ID NO: 722, SEQ ID NO: 724, SEQ ID NO: 726, SEQ ID NO: 728, SEQ ID NO: 730, SEQ ID NO: 732, SEQ ID NO: 734, SEQ ID NO: 736, SEQ ID NO: 738, SEQ ID NO: 740, SEQ ID NO: 742, SEQ ID NO: 744, SEQ ID NO: 746, SEQ ID NO: 748, SEQ ID NO: 750, SEQ ID NO: 752, SEQ ID NO: 754, SEQ ID NO: 756, SEQ ID NO: 758, SEQ ID NO: 760, SEQ ID NO: 762, SEQ ID NO: 764, SEQ ID NO: 766, SEQ ID NO: 768, SEQ ID NO: 770, SEQ ID NO: 772, SEQ ID NO: 774, SEQ ID NO: 776, SEQ ID NO: 778, SEQ ID NO: 780, SEQ ID NO: 782, SEQ ID NO: 784, SEQ ID NO: 786, SEQ ID NO: 788, SEQ ID NO: 790, SEQ ID NO: 792, SEQ ID NO: 794, SEQ ID NO : 796, SEQ ID NO: 798, SEQ ID NO: 800, SEQ ID NO: 802, SEQ ID NO: 804, SEQ ID NO: 806, SEQ ID NO: 808, SEQ ID NO: 810, SEQ ID NO: 812, SEQ ID NO: 814, SEQ ID NO: 816, SEQ ID NO: 818, SEQ ID NO: 820, SEQ ID NO: 822, SEQ ID NO: 824, SEQ ID NO: 826, SEQ ID NO: 828, SEQ ID NO: 830, SEQ ID NO: 832, SEQ ID NO: 834, SEQ ID NO: 836, SEQ ID NO: 838, SEQ ID NO: 840, SEQ ID NO: 842, SEQ ID NO: 844, SEQ ID NO: 846, SEQ ID NO: 848, SEQ ID NO: 850, SEQ ID NO: 852, SEQ ID NO: 854, SEQ ID NO: 856, SEQ ID NO: 858, SEQ ID NO: 860, SEQ ID NO: 862, SEQ ID NO: 864, SEQ ID NO: 866, SEQ ID NO: 868, SEQ ID NO: 870, SEQ ID NO: 872, SEQ ID NO: 874, SEQ ID NO: 876, SEQ ID NO: 878, SEQ ID NO: 880, SEQ ID NO: 882, SEQ ID NO: 884, SEQ ID NO: 886, SEQ ID NO: 888, SEQ ID NO: 890, SEQ ID NO: 892, SEQ ID NO: 894, SEQ ID NO: 896, SEQ ID NO: 898, SEQ ID NO: 900, SEQ ID NO: 902, SEQ ID NO: 904, SEQ ID NO: 906, SEQ ID NO: 908, SEQ ID NO: 910, SEQ ID NO: 912, SEQ ID NO: 914, SEQ ID NO: 916, SEQ ID NO: 918, SEQ ID NO: 920, SEQ ID NO: 922, SEQ ID NO: 924, SEQ ID NO: 926, SEQ ID NO: 928, SEQ ID NO: 930, SEQ ID NO: 932, SEQ ID NO: 934, SEQ ID NO: 936, SEQ ID NO: 938, SEQ ID NO: 940, SEQ ID NO: 942, SEQ ID NO: 944, SEQ ID NO: 946, SEQ ID NO: 948, SEQ ID NO: 950, SEQ ID NO: 952 or SEQ ID NO: 954 or an enzymatically active fragment thereof having lipase activity; (ii) a lipase encoded by the nucleic acid sequence according to any one of SEQ ID Nos. SEQ ID NO: 955, SEQ ID NO: 1 , SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 1 1 , SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 19, SEQ ID NO: 21 , SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 27, SEQ ID NO: 29, SEQ ID NO: 31 , SEQ ID NO: 33, SEQ ID NO: 35, SEQ ID NO: 37, SEQ ID NO: 39, SEQ ID NO: 41 , SEQ ID NO: 43, SEQ ID NO: 45, SEQ ID NO: 47, SEQ ID NO: 49, SEQ ID NO: 51 , SEQ ID NO: 53, SEQ ID NO: 55, SEQ ID NO: 57, SEQ ID NO: 59, SEQ ID NO: 61 , SEQ ID NO: 63, SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 71 , SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 77, SEQ ID NO: 79, SEQ ID NO: 81 , SEQ ID NO: 83, SEQ ID NO: 85, SEQ ID NO: 87, SEQ ID NO: 89, SEQ ID NO: 91 , SEQ ID NO: 93, SEQ ID NO: 95, SEQ ID NO: 97, SEQ ID NO: 99, SEQ ID NO: 101 , SEQ ID NO: 103, SEQ ID NO: 105, SEQ ID NO: 107, SEQ ID NO: 109, SEQ ID NO: 1 1 1 , SEQ ID NO: 1 13, SEQ ID NO: 1 15, SEQ ID NO: 1 17, SEQ ID NO: 1 19, SEQ ID NO: 121 , SEQ ID NO: 123, SEQ ID NO: 125, SEQ ID NO: 127, SEQ ID NO: 129, SEQ ID NO: 131 , SEQ ID NO: 133, SEQ ID NO: 135, SEQ ID NO: 137, SEQ ID NO: 139, SEQ ID NO: 141 , SEQ ID NO: 143, SEQ ID NO: 145, SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 151 , SEQ ID NO: 153, SEQ ID NO: 155, SEQ ID NO: 157, SEQ ID NO: 159, SEQ ID NO: 161 , SEQ ID NO: 163, SEQ ID NO: 165, SEQ ID NO: 167, SEQ ID NO: 169, SEQ ID NO: 171 , SEQ ID NO: 173, SEQ ID NO: 175, SEQ ID NO: 177, SEQ ID NO: 179, SEQ ID NO: 181 , SEQ ID NO: 183, SEQ ID NO: 185, SEQ ID NO: 187, SEQ ID NO: 189, SEQ ID NO: 191 , SEQ ID NO: 193, SEQ ID NO: 195, SEQ ID NO: 197, SEQ ID NO: 199, SEQ ID NO: 201 , SEQ ID NO: 203, SEQ ID NO: 205, SEQ ID NO: 207, SEQ ID NO: 209, SEQ ID NO: 21 1 , SEQ ID NO: 213, SEQ ID NO: 215, SEQ ID NO: 217, SEQ ID NO: 219, SEQ ID NO: 221 , SEQ ID NO: 223, SEQ ID NO: 225, SEQ ID NO: 227, SEQ ID NO: 229, SEQ ID NO: 231 , SEQ ID NO: 233, SEQ ID NO: 235, SEQ ID NO: 237, SEQ ID NO: 239, SEQ ID NO: 241 , SEQ ID NO: 243, SEQ ID NO: 245, SEQ ID NO: 247, SEQ ID NO: 249, SEQ ID NO: 251 , SEQ ID NO: 253, SEQ ID NO: 255, SEQ ID NO: 257, SEQ ID NO: 259, SEQ ID NO: 261 , SEQ ID NO: 263, SEQ ID NO: 265, SEQ ID NO: 267, SEQ ID NO: 269, SEQ ID NO: 271 , SEQ ID NO: 273, SEQ ID NO: 275, SEQ ID NO: 277, SEQ ID NO: 279, SEQ ID NO: 281 , SEQ ID NO: 283, SEQ ID NO: 285, SEQ ID NO: 287, SEQ ID NO: 289, SEQ ID NO: 291 , SEQ ID NO: 293, SEQ ID NO: 295, SEQ ID NO: 297, SEQ ID NO: 299, SEQ ID NO: 301 , SEQ ID NO: 303, SEQ ID NO: 305, SEQ ID NO: 307, SEQ ID NO: 309, SEQ ID NO: 31 1 , SEQ ID NO: 313, SEQ ID NO: 315, SEQ ID NO: 317, SEQ ID NO: 319, SEQ ID NO: 321 , SEQ ID NO: 323, SEQ ID NO: 325, SEQ ID NO: 327, SEQ ID NO: 329, SEQ ID NO: 331 , SEQ ID NO: 333, SEQ ID NO: 335, SEQ ID NO: 337, SEQ ID NO: 339, SEQ ID NO: 341 , SEQ ID NO: 343, SEQ ID NO: 345, SEQ ID NO: 347, SEQ ID NO: 349, SEQ ID NO: 351 , SEQ ID NO: 353, SEQ ID NO: 355, SEQ ID NO: 357, SEQ ID NO: 359, SEQ ID NO: 361 , SEQ ID NO: 363, SEQ ID NO: 365, SEQ ID NO: 367, SEQ ID NO: 369, SEQ ID NO: 371 , SEQ ID NO: 373, SEQ ID NO: 375, SEQ ID NO: 377, SEQ ID NO: 379, SEQ ID NO: 381 , SEQ ID NO: 383, SEQ ID NO: 385, SEQ ID NO: 387, SEQ ID NO: 389, SEQ ID NO: 391 , SEQ ID NO: 393, SEQ ID NO: 395, SEQ ID NO: 397, SEQ ID NO: 399, SEQ ID NO: 401 , SEQ ID NO: 403, SEQ ID NO: 405, SEQ ID NO: 407, SEQ ID NO: 409, SEQ ID NO: 41 1 , SEQ ID NO: 413, SEQ ID NO: 415, SEQ ID NO: 417, SEQ ID NO: 419, SEQ ID NO: 421 , SEQ ID NO: 423, SEQ ID NO: 425, SEQ ID NO: 427, SEQ ID NO: 429, SEQ ID NO: 431 , SEQ ID NO: 433, SEQ ID NO: 435, SEQ ID NO: 437, SEQ ID NO: 439, SEQ ID NO: 441 , SEQ ID NO: 443, SEQ ID NO: 445, SEQ ID NO: 447, SEQ ID NO: 449, SEQ ID NO: 451 , SEQ ID NO: 453, SEQ ID NO: 455, SEQ ID NO: 457, SEQ ID NO: 459, SEQ ID NO: 461 , SEQ ID NO: 463, SEQ ID NO: 465, SEQ ID NO: 467, SEQ ID NO: 469, SEQ ID NO: 471 , SEQ ID NO: 473, SEQ ID NO: 475, SEQ ID NO: 477, SEQ ID. NO: 479, SEQ ID NO: 481 , SEQ ID NO: 483, SEQ ID NO: 485, SEQ ID NO: 487, SEQ ID NO: 489, SEQ ID NO: 491 , SEQ ID NO: 493, SEQ ID NO: 495, SEQ ID NO: 497, SEQ ID NO: 499, SEQ ID NO: 501 , SEQ ID NO: 503, SEQ ID NO: 505, SEQ ID NO: 507, SEQ ID NO: 509, SEQ ID NO: 51 1 , SEQ ID NO: 513, SEQ ID NO: 515, SEQ ID NO: 517, SEQ ID NO: 519, SEQ ID NO: 521 , SEQ ID NO: 523, SEQ ID NO: 525, SEQ ID NO: 527, SEQ ID NO: 529, SEQ ID NO: 531 , SEQ ID NO: 533, SEQ ID NO: 535, SEQ ID NO: 537, SEQ ID NO: 539, SEQ ID NO: 541 , SEQ ID NO: 543, SEQ ID NO: 545, SEQ ID NO: 547, SEQ ID NO: 549, SEQ ID NO: 551 , SEQ ID NO: 553, SEQ ID NO: 555, SEQ ID NO: 557, SEQ ID NO: 559, SEQ ID NO: 561 , SEQ ID NO: 563, SEQ ID NO: 565, SEQ ID NO: 567, SEQ ID NO: 569, SEQ ID NO: 571 , SEQ ID NO: 573, SEQ ID NO: 575, SEQ ID NO: 577, SEQ ID NO: 579, SEQ ID NO: 581 , SEQ ID NO: 583, SEQ ID NO: 585, SEQ ID NO: 587, SEQ ID NO: 589, SEQ ID NO: 591 , SEQ ID NO: 593, SEQ ID NO: 595, SEQ ID NO: 597, SEQ ID NO: 599, SEQ ID NO: 601 , SEQ ID NO: 603, SEQ ID NO: 605, SEQ ID NO: 607, SEQ ID NO: 609, SEQ ID NO: 61 1 , SEQ ID NO: 613, SEQ ID NO: 615, SEQ ID NO: 617, SEQ ID NO: 619, SEQ ID NO: 621 , SEQ ID NO: 623, SEQ ID NO: 625, SEQ ID NO: 627, SEQ ID NO: 629, SEQ ID NO: 631 , SEQ ID NO: 633, SEQ ID NO: 635, SEQ ID NO: 637, SEQ ID NO: 639, SEQ ID NO: 641 , SEQ ID NO: 643, SEQ ID NO: 645, SEQ ID NO: 647, SEQ ID NO: 649, SEQ ID NO: 651 , SEQ ID NO: 653, SEQ ID NO: 655, SEQ ID NO: 657, SEQ ID NO: 659, SEQ ID NO: 661 , SEQ ID NO: 663, SEQ ID NO: 665, SEQ ID NO: 667, SEQ ID NO: 669, SEQ ID NO: 671 , SEQ ID NO: 673, SEQ ID NO: 675, SEQ ID NO: 677, SEQ ID NO: 679, SEQ ID NO: 681 , SEQ ID NO: 683, SEQ ID NO: 685, SEQ ID NO: 687, SEQ ID NO: 689, SEQ ID NO: 691 , SEQ ID NO: 693, SEQ ID NO: 695, SEQ ID NO: 697, SEQ ID NO: 699, SEQ ID NO: 701 , SEQ ID NO: 703, SEQ ID NO: 705, SEQ ID NO: 707, SEQ ID NO: 709, SEQ ID NO: 71 1 , SEQ ID NO: 713, SEQ ID NO: 715, SEQ ID NO: 717, SEQ ID NO: 719, SEQ ID NO: 721 , SEQ ID NO: 723, SEQ ID NO: 725, SEQ ID NO: 727, SEQ ID NO: 729, SEQ ID NO: 731 , SEQ ID NO: 733, SEQ ID NO: 735, SEQ ID NO: 737, SEQ ID NO: 739, SEQ ID NO: 741 , SEQ ID NO: 743, SEQ ID NO: 745, SEQ ID NO: 747, SEQ ID NO : 749, SEQ ID NO: 751 , SEQ ID NO : 753, SEQ ID NO : 755, SEQ ID NO: 757, SEQ ID NO: 759, SEQ ID NO: 761 , SEQ ID NO: 763, SEQ ID NO: 765, SEQ ID NO : 767, SEQ ID NO : 769, SEQ ID NO : 771 , SEQ ID NO: 773, SEQ ID NO: 775, SEQ ID NO: 777, SEQ ID NO: 779, SEQ ID NO: 781 , SEQ ID NO: 783, SEQ ID NO: 785, SEQ ID NO: 787, SEQ ID NO: 789, SEQ ID NO: 791 , SEQ ID NO: 793, SEQ ID NO: 795, SEQ ID NO: 797, SEQ ID NO: 799, SEQ ID NO: 801 , SEQ ID NO: 803, SEQ ID NO: 805, SEQ ID NO: 807, SEQ ID NO: 809, SEQ ID NO: 81 1 , SEQ ID NO: 813, SEQ ID NO: 815, SEQ ID NO: 817, SEQ ID NO: 819, SEQ ID NO: 821 , SEQ ID NO: 823, SEQ ID NO: 825, SEQ ID NO: 827, SEQ ID NO: 829, SEQ ID NO: 831 , SEQ ID NO: 833, SEQ ID NO: 835, SEQ ID NO: 837, SEQ ID NO: 839, SEQ ID NO: 841 , SEQ ID NO: 843, SEQ ID NO: 845, SEQ ID NO: 847, SEQ ID NO: 849, SEQ ID NO: 851 , SEQ ID NO: 853, SEQ ID NO: 855, SEQ ID NO: 857, SEQ ID NO: 859, SEQ ID NO: 861 , SEQ ID NO: 863, SEQ ID NO: 865, SEQ ID NO: 867, SEQ ID NO: 869, SEQ ID NO: 871 , SEQ ID NO: 873, SEQ ID NO: 875, SEQ ID NO: 877, SEQ ID NO: 879, SEQ ID NO: 881 , SEQ ID NO: 883, SEQ ID NO: 885, SEQ ID NO: 887, SEQ ID NO: 889, SEQ ID NO: 891 , SEQ ID NO: 893, SEQ ID NO: 895, SEQ ID NO: 897, SEQ ID NO: 899, SEQ ID NO: 901 , SEQ ID NO: 903, SEQ ID NO: 905, SEQ ID NO: 907, SEQ ID NO: 909, SEQ ID NO: 911 , SEQ ID NO: 913, SEQ ID NO: 915, SEQ ID NO: 917, SEQ ID NO: 919, SEQ ID NO: 921 , SEQ ID NO: 923, SEQ ID NO: 925, SEQ ID NO: 927, SEQ ID NO: 929, SEQ ID NO: 931 , SEQ ID NO: 933, SEQ ID NO: 935, SEQ ID NO: 937, SEQ ID NO: 939, SEQ ID NO: 941 , SEQ ID NO: 943, SEQ ID NO: 945, SEQ ID NO: 947, SEQ ID NO: 949, SEQ ID NO: 951 or SEQ ID NO: 953 or an enzymatically active fragment thereof having lipase activity;
(iii) a lipase having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56, SEQ ID NO: 58, SEQ ID NO: 60, SEQ ID NO: 62, SEQ ID NO: 64, SEQ ID NO: 66, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 72, SEQ ID NO: 74, SEQ ID NO: 76, SEQ ID NO: 78, SEQ ID NO: 80, SEQ ID NO: 82, SEQ ID NO: 84, SEQ ID NO: 86, SEQ ID NO: 88, SEQ ID NO: 90, SEQ ID NO: 92, SEQ ID NO: 94, SEQ ID NO: 96, SEQ ID NO: 98, SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, SEQ ID NO: 1 10, SEQ ID NO: 112, SEQ ID NO: 1 14, SEQ ID NO: 116, SEQ ID NO: 118, SEQ ID NO: 120, SEQ ID NO: 122, SEQ ID NO: 124, SEQ ID NO: 126, SEQ ID NO: 128, SEQ ID NO: 130, SEQ ID NO: 132, SEQ ID NO: 134, SEQ ID NO: 136, SEQ ID NO: 138, SEQ ID NO: 140, SEQ ID NO: 142, SEQ ID NO: 143, SEQ ID NO: 146, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 152, SEQ ID NO: 154, SEQ ID NO: 156, SEQ ID NO: 158, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 166, SEQ ID NO: 168, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 174, SEQ ID NO: 176, SEQ ID NO: 178, SEQ ID NO: 180, SEQ ID NO: 182, SEQ ID NO: 184, SEQ ID NO: 186, SEQ ID NO: 188, SEQ ID NO: 190, SEQ ID NO: 192, SEQ ID NO: 194, SEQ ID NO: 196, SEQ ID NO: 198, SEQ ID NO: 200, SEQ ID NO: 202, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 208, SEQ ID NO: 210, SEQ ID NO: 212, SEQ ID NO: 214, SEQ ID NO: 216, SEQ ID NO: 218, SEQ ID NO: 220, SEQ ID NO: 222, SEQ ID NO: 224, SEQ ID NO: 226, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 232, SEQ ID NO: 234, SEQ ID NO: 236, SEQ ID NO: 238, SEQ ID NO: 240, SEQ ID NO: 242, SEQ ID NO: 244, SEQ ID NO: 246, SEQ ID NO: 248, SEQ ID NO: 250, SEQ ID NO: 252, SEQ ID NO: 254, SEQ ID NO: 256, SEQ ID NO: 258, SEQ ID NO: 260, SEQ ID NO: 262, SEQ ID NO: 264, SEQ ID NO: 266, SEQ ID NO: 268, SEQ ID NO: 270, SEQ ID NO: 272, SEQ ID NO: 274, SEQ ID NO: 276, SEQ ID NO: 278, SEQ ID NO: 280, SEQ ID NO: 282, SEQ ID NO: 284, SEQ ID NO: 286, SEQ ID NO: 288, SEQ ID NO: 290, SEQ ID NO: 292, SEQ ID NO: 294, SEQ ID NO: 296, SEQ ID NO: 298, SEQ ID NO: 300, SEQ ID NO: 302, SEQ ID NO: 304, SEQ ID NO: 306, SEQ ID NO: 308, SEQ ID NO: 310, SEQ ID NO: 312, SEQ ID NO: 314, SEQ ID NO: 316, SEQ ID NO: 318, SEQ ID NO: 320, SEQ ID NO: 322, SEQ ID NO: 324, SEQ ID NO: 326, SEQ ID NO: 328, SEQ ID NO: 330, SEQ ID NO: 332, SEQ ID NO: 334, SEQ ID NO: 336, SEQ ID NO: 338, SEQ ID NO: 340, SEQ ID NO: 342, SEQ ID NO: 344, SEQ ID NO: 346, SEQ ID NO: 348, SEQ ID NO: 350, SEQ ID NO: 352, SEQ ID NO: 354, SEQ ID NO: 356, SEQ ID NO: 358, SEQ ID NO: 360, SEQ ID NO: 362, SEQ ID NO: 364, SEQ ID NO: 366, SEQ ID NO: 368, SEQ ID NO: 370, SEQ ID NO: 372, SEQ ID NO: 374, SEQ ID NO: 376, SEQ ID NO: 378, SEQ ID NO: 380, SEQ ID NO: 382, SEQ ID NO: 384, SEQ ID NO: 386, SEQ ID NO: 388, SEQ ID NO: 390, SEQ ID NO: 392, SEQ ID NO: 394, SEQ ID NO: 396, SEQ ID NO: 398, SEQ ID NO: 400, SEQ ID NO: 402, SEQ ID NO: 404, SEQ ID NO: 406, SEQ ID NO: 408, SEQ ID NO: 410, SEQ ID NO: 412, SEQ ID NO: 414, SEQ ID NO: 416, SEQ ID NO: 418, SEQ ID NO: 420, SEQ ID NO: 422, SEQ ID NO: 424, SEQ ID NO: 426, SEQ ID NO: 428, SEQ ID NO: 430, SEQ ID NO: 432, SEQ ID NO: 434, SEQ ID NO: 436, SEQ ID NO: 438, SEQ ID NO: 440, SEQ ID NO: 442, SEQ ID NO: 444, SEQ ID NO: 446, SEQ ID NO: 448, SEQ ID NO: 450, SEQ ID NO: 452, SEQ ID NO: 454, SEQ ID NO: 456, SEQ ID NO: 458, SEQ ID NO: 460, SEQ ID NO: 462, SEQ ID NO: 464, SEQ ID NO: 466, SEQ ID NO: 468, SEQ ID NO: 470, SEQ ID NO: 472, SEQ ID NO: 474, SEQ ID NO: 476, SEQ ID NO: 478, SEQ ID NO: 480, SEQ ID NO: 482, SEQ ID NO: 484, SEQ ID NO: 486, SEQ ID NO: 488, SEQ ID NO: 490, SEQ ID NO: 492, SEQ ID NO: 494, SEQ ID NO: 496, SEQ ID NO: 498, SEQ ID NO: 500, SEQ ID NO: 502, SEQ ID NO: 504, SEQ ID NO: 506, SEQ ID NO: 508, SEQ ID NO: 510, SEQ ID NO: 512, SEQ ID NO: 514, SEQ ID NO: 516, SEQ ID NO: 518, SEQ ID NO: 520, SEQ ID NO: 522, SEQ ID NO: 524, SEQ ID NO: 526, SEQ ID NO: 528, SEQ ID NO: 530, SEQ ID NO: 532, SEQ ID NO: 534, SEQ ID NO: 536, SEQ ID NO: 538, SEQ ID NO: 540, SEQ ID NO: 542, SEQ ID NO: 544, SEQ ID NO: 546, SEQ ID NO: 548, SEQ ID NO: 550, SEQ ID NO: 552, SEQ ID NO: 554, SEQ ID NO: 556, SEQ ID NO: 558, SEQ ID NO: 560, SEQ ID NO: 562, SEQ ID NO: 564, SEQ ID NO: 566, SEQ ID NO: 568, SEQ ID NO: 570, SEQ ID NO: 572, SEQ ID NO: 574, SEQ ID NO: 576, SEQ ID NO: 578, SEQ ID NO: 580, SEQ ID NO: 582, SEQ ID NO: 584, SEQ ID NO: 586, SEQ ID NO: 588, SEQ ID NO: 590, SEQ ID NO: 592, SEQ ID NO: 594, SEQ ID NO: 596, SEQ ID NO: 598, SEQ ID NO: 600, SEQ ID NO: 602, SEQ ID NO: 604, SEQ ID NO: 606, SEQ ID NO: 608, SEQ ID NO: 610, SEQ ID NO: 612, SEQ ID NO: 614, SEQ ID NO: 616, SEQ ID NO: 618, SEQ ID NO: 620, SEQ ID NO: 622, SEQ ID NO: 624, SEQ ID NO: 626, SEQ ID NO: 628, SEQ ID NO: 630, SEQ ID NO: 632, SEQ ID NO: 634, SEQ ID NO: 636, SEQ ID NO: 638, SEQ ID NO: 640, SEQ ID NO: 642, SEQ ID NO: 644, SEQ ID NO: 646, SEQ ID NO: 648, SEQ ID NO: 650, SEQ ID NO: 652, SEQ ID NO: 654, SEQ ID NO: 656, SEQ ID NO: 658, SEQ ID NO: 660, SEQ ID NO: 662, SEQ ID NO: 664, SEQ ID NO: 666, SEQ ID NO: 668, SEQ ID NO: 670, SEQ ID NO: 672, SEQ ID NO: 674, SEQ ID NO: 676, SEQ ID NO: 678, SEQ ID NO: 680, SEQ ID NO: 682, SEQ ID NO: 684, SEQ ID NO: 686, SEQ ID NO: 688, SEQ ID NO: 690, SEQ ID NO: 692, SEQ ID NO: 694, SEQ ID NO: 696, SEQ ID NO: 698, SEQ ID NO: 700, SEQ ID NO: 702, SEQ ID NO: 704, SEQ ID NO: 706, SEQ ID NO: 708, SEQ ID NO: 710, SEQ ID NO: 712, SEQ ID NO: 714, SEQ ID NO: 716, SEQ ID NO: 718, SEQ ID NO: 720, SEQ ID NO: 722, SEQ ID NO: 724, SEQ ID NO: 726, SEQ ID NO: 728, SEQ ID NO: 730, SEQ ID NO: 732, SEQ ID NO: 734, SEQ ID NO: 736, SEQ ID NO: 738, SEQ ID NO: 740, SEQ ID NO: 742, SEQ ID NO: 744, SEQ ID NO: 746, SEQ ID NO: 748, SEQ ID NO: 750, SEQ ID NO: 752, SEQ ID NO: 754, SEQ ID NO: 756, SEQ ID NO: 758, SEQ ID NO: 760, SEQ ID NO: 762, SEQ ID NO: 764, SEQ ID NO: 766, SEQ ID NO: 768, SEQ ID NO: 770, SEQ ID NO: 772, SEQ ID NO: 774, SEQ ID NO: 776, SEQ ID NO: 778, SEQ ID NO: 780, SEQ ID NO: 782, SEQ ID NO: 784, SEQ ID NO: 786, SEQ ID NO: 788, SEQ ID NO: 790, SEQ ID NO: 792, SEQ ID NO: 794, SEQ ID NO : 796, SEQ ID NO: 798, SEQ ID NO: 800, SEQ ID NO: 802, SEQ ID NO: 804, SEQ ID NO: 806, SEQ ID NO: 808, SEQ ID NO: 810, SEQ ID NO: 812, SEQ ID NO: 814, SEQ ID NO: 816, SEQ ID NO: 818, SEQ ID NO: 820, SEQ ID NO: 822, SEQ ID NO: 824, SEQ ID NO: 826, SEQ ID NO: 828, SEQ ID NO: 830, SEQ ID NO: 832, SEQ ID NO: 834, SEQ ID NO: 836, SEQ ID NO: 838, SEQ ID NO: 840, SEQ ID NO: 842, SEQ ID NO: 844, SEQ ID NO: 846, SEQ ID NO: 848, SEQ ID NO: 850, SEQ ID NO: 852, SEQ ID NO: 854, SEQ ID NO: 856, SEQ ID NO: 858, SEQ ID NO: 860, SEQ ID NO: 862, SEQ ID NO: 864, SEQ ID NO: 866, SEQ ID NO: 868, SEQ ID NO: 870, SEQ ID NO: 872, SEQ ID NO: 874, SEQ ID NO: 876, SEQ ID NO: 878, SEQ ID NO: 880, SEQ ID NO: 882, SEQ ID NO: 884, SEQ ID NO: 886, SEQ ID NO: 888, SEQ ID NO: 890, SEQ ID NO: 892, SEQ ID NO: 894, SEQ ID NO: 896, SEQ ID NO: 898, SEQ ID NO: 900, SEQ ID NO: 902, SEQ ID NO: 904, SEQ ID NO: 906, SEQ ID NO: 908, SEQ ID NO: 910, SEQ ID NO: 912, SEQ ID NO: 914, SEQ ID NO: 916, SEQ ID NO: 918, SEQ ID NO: 920, SEQ ID NO: 922, SEQ ID NO: 924, SEQ ID NO: 926, SEQ ID NO: 928, SEQ ID NO: 930, SEQ ID NO: 932, SEQ ID NO: 934, SEQ ID NO: 936, SEQ ID NO: 938, SEQ ID NO: 940, SEQ ID NO: 942, SEQ ID NO: 944, SEQ ID NO: 946, SEQ ID NO: 948, SEQ ID NO: 950, SEQ ID NO: 952 or SEQ ID NO: 954 or an enzymatically active fragment thereof having lipase activity; and
(iv) a lipase encoded by a nucleic acid sequence which hybridizes to the complement of the nu- cleic acid sequence according to any of SEQ ID NO: 955, SEQ ID NO: 1 , SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11 , SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 19, SEQ ID NO: 21 , SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 27, SEQ ID NO: 29, SEQ ID NO: 31 , SEQ ID NO: 33, SEQ ID NO: 35, SEQ ID NO: 37, SEQ ID NO: 39, SEQ ID NO: 41 , SEQ ID NO: 43, SEQ ID NO: 45, SEQ ID NO: 47, SEQ ID NO: 49, SEQ ID NO: 51 , SEQ ID NO: 53, SEQ ID NO: 55, SEQ ID NO: 57, SEQ ID NO: 59, SEQ ID NO: 61 ,
SEQ ID NO: 63, SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 71 , SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 77, SEQ ID NO: 79, SEQ ID NO: 81 , SEQ ID NO: 83, SEQ ID NO: 85, SEQ ID NO: 87, SEQ ID NO: 89, SEQ ID NO: 91 , SEQ ID NO: 93, SEQ ID NO: 95,
SEQ ID NO: 97, SEQ ID NO: 99, SEQ ID NO: 101 , SEQ ID NO: 103, SEQ ID NO: 105, SEQ ID NO: 107, SEQ ID NO: 109, SEQ ID NO: 1 11 , SEQ ID NO: 113, SEQ ID NO: 115, SEQ ID NO: 1 17, SEQ ID NO: 1 19, SEQ ID NO: 121 , SEQ ID NO: 123, SEQ ID NO: 125, SEQ ID NO: 127, SEQ ID NO: 129, SEQ ID NO: 131 , SEQ ID NO: 133, SEQ ID NO: 135, SEQ ID NO: 137, SEQ ID NO: 139, SEQ ID NO: 141 , SEQ ID NO: 143, SEQ ID NO: 145, SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 151 , SEQ ID NO: 153, SEQ ID NO: 155, SEQ ID NO: 157, SEQ ID NO: 159, SEQ ID NO: 161 , SEQ ID NO: 163, SEQ ID NO: 165, SEQ ID NO: 167, SEQ ID NO: 169, SEQ ID NO: 171 , SEQ ID NO: 173, SEQ ID NO: 175, SEQ ID NO: 177, SEQ ID NO: 179, SEQ ID NO: 181 , SEQ ID NO: 183, SEQ ID NO: 185, SEQ ID NO: 187, SEQ ID NO: 189, SEQ ID NO: 191 , SEQ ID NO: 193, SEQ ID NO: 195, SEQ ID NO: 197, SEQ ID NO: 199, SEQ ID NO: 201 , SEQ ID NO: 203, SEQ ID NO: 205, SEQ ID NO: 207, SEQ ID NO: 209, SEQ ID NO: 21 1 , SEQ ID NO: 213, SEQ ID NO: 215, SEQ ID NO: 217, SEQ ID NO: 219, SEQ ID NO: 221 , SEQ ID NO: 223, SEQ ID NO: 225, SEQ ID NO: 227, SEQ ID NO: 229, SEQ ID NO: 231 , SEQ ID NO: 233, SEQ ID NO: 235, SEQ ID NO: 237, SEQ ID NO: 239, SEQ ID NO: 241 , SEQ ID NO: 243, SEQ ID NO: 245, SEQ ID NO: 247, SEQ ID NO: 249, SEQ ID NO: 251 , SEQ ID NO: 253, SEQ ID NO: 255, SEQ ID NO: 257, SEQ ID NO: 259, SEQ ID NO: 261 , SEQ ID NO: 263, SEQ ID NO: 265, SEQ ID NO: 267, SEQ ID NO: 269, SEQ ID NO: 271 , SEQ ID NO: 273, SEQ ID NO: 275, SEQ ID NO: 277, SEQ ID NO: 279, SEQ ID NO: 281 , SEQ ID NO: 283, SEQ ID NO: 285, SEQ ID NO: 287, SEQ ID NO: 289, SEQ ID NO: 291 , SEQ ID NO: 293, SEQ ID NO: 295, SEQ ID NO: 297, SEQ ID NO: 299, SEQ ID NO: 301 , SEQ ID NO: 303, SEQ ID NO: 305, SEQ ID NO: 307, SEQ ID NO: 309, SEQ ID NO: 31 1 , SEQ ID NO: 313, SEQ ID NO: 315, SEQ ID NO: 317, SEQ ID NO: 319, SEQ ID NO: 321 , SEQ ID NO: 323, SEQ ID NO: 325, SEQ ID NO: 327, SEQ ID NO: 329, SEQ ID NO: 331 , SEQ ID NO: 333, SEQ ID NO: 335, SEQ ID NO: 337, SEQ ID NO: 339, SEQ ID NO: 341 , SEQ ID NO: 343, SEQ ID NO: 345, SEQ ID NO: 347, SEQ ID NO: 349, SEQ ID NO: 351 , SEQ ID NO: 353, SEQ ID NO: 355, SEQ ID NO: 357, SEQ ID NO: 359, SEQ ID NO: 361 , SEQ ID NO: 363, SEQ ID NO: 365, SEQ ID NO: 367, SEQ ID NO: 369, SEQ ID NO: 371 , SEQ ID NO: 373, SEQ ID NO: 375, SEQ ID NO: 377, SEQ ID NO: 379, SEQ ID NO: 381 , SEQ ID NO: 383, SEQ ID NO: 385, SEQ ID NO: 387, SEQ ID NO: 389, SEQ ID NO: 391 , SEQ ID NO: 393, SEQ ID NO: 395, SEQ ID NO: 397, SEQ ID NO: 399, SEQ ID NO: 401 , SEQ ID NO: 403, SEQ ID NO: 405, SEQ ID NO: 407, SEQ ID NO: 409, SEQ ID NO: 41 1 , SEQ ID NO: 413, SEQ ID NO: 415, SEQ ID NO: 417, SEQ ID NO: 419, SEQ ID NO: 421 , SEQ ID NO: 423, SEQ ID NO: 425, SEQ ID NO: 427, SEQ ID NO: 429, SEQ ID NO: 431 , SEQ ID NO: 433, SEQ ID NO: 435, SEQ ID NO: 437, SEQ ID NO: 439, SEQ ID NO: 441 , SEQ ID NO: 443, SEQ ID NO: 445, SEQ ID NO: 447, SEQ ID NO: 449, SEQ ID NO: 451 , SEQ ID NO: 453, SEQ ID NO: 455, SEQ ID NO: 457, SEQ ID NO: 459, SEQ ID NO: 461 , SEQ ID NO: 463, SEQ ID NO: 465, SEQ ID NO: 467, SEQ ID NO: 469, SEQ ID NO: 471 , SEQ ID NO: 473, SEQ ID NO: 475, SEQ ID NO: 477, SEQ ID. NO: 479, SEQ ID NO: 481 , SEQ ID NO: 483, SEQ ID NO: 485, SEQ ID NO: 487, SEQ ID NO: 489, SEQ ID NO: 491 , SEQ ID NO: 493, SEQ ID NO: 495, SEQ ID NO: 497, SEQ ID NO: 499, SEQ ID NO: 501 , SEQ ID NO: 503, SEQ ID NO: 505, SEQ ID NO: 507, SEQ ID NO: 509, SEQ ID NO: 51 1 , SEQ ID NO: 513, SEQ ID NO: 515, SEQ ID NO: 517, SEQ ID NO: 519, SEQ ID NO: 521 , SEQ ID NO: 523, SEQ ID NO: 525, SEQ ID NO: 527, SEQ ID NO: 529, SEQ ID NO: 531 , SEQ ID NO: 533, SEQ ID NO: 535, SEQ ID NO: 537, SEQ ID NO: 539, SEQ ID NO: 541 , SEQ ID NO: 543, SEQ ID NO: 545, SEQ ID NO: 547, SEQ ID NO: 549, SEQ ID NO: 551 , SEQ ID NO: 553, SEQ ID NO: 555, SEQ ID NO: 557, SEQ ID NO: 559, SEQ ID NO: 561 , SEQ ID NO: 563, SEQ ID NO: 565, SEQ ID NO: 567, SEQ ID NO: 569, SEQ ID NO: 571 , SEQ ID NO: 573, SEQ ID NO: 575, SEQ ID NO: 577, SEQ ID NO: 579, SEQ ID NO: 581 , SEQ ID NO: 583, SEQ ID NO: 585, SEQ ID NO: 587, SEQ ID NO: 589, SEQ ID NO: 591 , SEQ ID NO: 593, SEQ ID NO: 595, SEQ ID NO: 597, SEQ ID NO: 599, SEQ ID NO: 601 , SEQ ID NO: 603, SEQ ID NO: 605, SEQ ID NO: 607, SEQ ID NO: 609, SEQ ID NO: 61 1 , SEQ ID NO: 613, SEQ ID NO: 615, SEQ ID NO: 617, SEQ ID NO: 619, SEQ ID NO: 621 , SEQ ID NO: 623, SEQ ID NO: 625, SEQ ID NO: 627, SEQ ID NO: 629, SEQ ID NO: 631 , SEQ ID NO: 633, SEQ ID NO: 635, SEQ ID NO: 637, SEQ ID NO: 639, SEQ ID NO: 641 , SEQ ID NO: 643, SEQ ID NO: 645, SEQ ID NO: 647, SEQ ID NO: 649, SEQ ID NO: 651 , SEQ ID NO: 653, SEQ ID NO: 655, SEQ ID NO: 657, SEQ ID NO: 659, SEQ ID NO: 661 , SEQ ID NO: 663, SEQ ID NO: 665, SEQ ID NO: 667, SEQ ID NO: 669, SEQ ID NO: 671 , SEQ ID NO: 673, SEQ ID NO: 675, SEQ ID NO: 677, SEQ ID NO: 679, SEQ ID NO: 681 , SEQ ID NO: 683, SEQ ID NO: 685, SEQ ID NO: 687, SEQ ID NO: 689, SEQ ID NO: 691 , SEQ ID NO: 693, SEQ ID NO: 695, SEQ ID NO: 697, SEQ ID NO: 699, SEQ ID NO: 701 , SEQ ID NO: 703, SEQ ID NO: 705, SEQ ID NO: 707, SEQ ID NO: 709, SEQ ID NO: 71 1 , SEQ ID NO: 713, SEQ ID NO: 715, SEQ ID NO: 717, SEQ ID NO: 719, SEQ ID NO: 721 , SEQ ID NO: 723, SEQ ID NO: 725, SEQ ID NO: 727, SEQ ID NO: 729, SEQ ID NO: 731 , SEQ ID NO: 733, SEQ ID NO: 735, SEQ ID NO: 737, SEQ ID NO: 739, SEQ ID NO: 741 , SEQ ID NO: 743, SEQ ID NO: 745, SEQ ID NO: 747, SEQ ID NO: 749, SEQ ID NO: 751 , SEQ ID NO: 753, SEQ ID NO: 755, SEQ ID NO: 757, SEQ ID NO: 759, SEQ ID NO: 761 , SEQ ID NO: 763, SEQ ID NO: 765, SEQ ID NO : 767, SEQ ID NO : 769, SEQ ID NO : 771 , SEQ ID NO: 773, SEQ ID NO: 775, SEQ ID NO: 777, SEQ ID NO: 779, SEQ ID NO: 781 , SEQ ID NO: 783, SEQ ID NO: 785, SEQ ID NO: 787, SEQ ID NO: 789, SEQ ID NO: 791 , SEQ ID NO: 793, SEQ ID NO: 795, SEQ ID NO: 797, SEQ ID NO: 799, SEQ ID NO: 801 , SEQ ID NO: 803, SEQ ID NO: 805, SEQ ID NO: 807, SEQ ID NO: 809, SEQ ID NO: 811 , SEQ ID NO: 813, SEQ ID NO: 815, SEQ ID NO: 817, SEQ ID NO: 819, SEQ ID NO: 821 , SEQ ID NO: 823, SEQ ID NO: 825, SEQ ID NO: 827, SEQ ID NO: 829, SEQ ID NO: 831 , SEQ ID NO: 833, SEQ ID NO: 835, SEQ ID NO: 837, SEQ ID NO: 839, SEQ ID NO: 841 , SEQ ID NO: 843, SEQ ID NO: 845, SEQ ID NO: 847, SEQ ID NO: 849, SEQ ID NO: 851 , SEQ ID NO: 853, SEQ ID NO: 855, SEQ ID NO: 857, SEQ ID NO: 859, SEQ ID NO: 861 , SEQ ID NO: 863, SEQ ID NO: 865, SEQ ID NO: 867, SEQ ID NO: 869, SEQ ID NO: 871 , SEQ ID NO: 873, SEQ ID NO: 875, SEQ ID NO: 877, SEQ ID NO: 879, SEQ ID NO: 881 , SEQ ID NO: 883, SEQ ID NO: 885, SEQ ID NO: 887, SEQ ID NO: 889, SEQ ID NO: 891 , SEQ ID NO: 893, SEQ ID NO: 895, SEQ ID NO: 897, SEQ ID NO: 899, SEQ ID NO: 901 , SEQ ID NO: 903, SEQ ID NO: 905, SEQ ID NO: 907, SEQ ID NO: 909, SEQ ID NO: 911 , SEQ ID NO: 913, SEQ ID NO: 915, SEQ ID NO: 917, SEQ ID NO: 919, SEQ ID NO: 921 , SEQ ID NO: 923, SEQ ID NO: 925, SEQ ID NO: 927, SEQ ID NO: 929, SEQ ID NO: 931 , SEQ ID NO: 933, SEQ ID NO: 935, SEQ ID NO: 937, SEQ ID NO: 939, SEQ ID NO: 941 , SEQ ID NO: 943, SEQ ID NO: 945, SEQ ID NO: 947, SEQ ID NO: 949, SEQ ID NO: 951 or SEQ ID NO: 953 under stringent conditions.
Also preferably, the lipase is not an Aspergillus niger\\ ase.
More preferably, the lipase used in the context of the present invention is selected from the group consisting of:
(i) a lipase having the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100, SEQ ID NO: 114, SEQ ID NO: 142, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 156, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 182, SEQ ID NO: 186, SEQ ID NO: 194, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 214, SEQ ID NO: 218, SEQ ID NO: 224, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 244, SEQ ID NO: 262, SEQ ID NO: 268, SEQ ID NO: 270, SEQ ID NO: 282, SEQ ID NO: 292, SEQ ID NO: 298, SEQ ID NO: 300, SEQ ID NO: 306, SEQ ID NO: 320, SEQ ID NO: 340, SEQ ID NO: 368, SEQ ID NO: 394, SEQ ID NO: 422, SEQ ID NO: 424, SEQ ID NO: 426, SEQ ID NO: 428, SEQ ID NO: 440, SEQ ID NO: 454, SEQ ID NO: 456, SEQ ID NO: 460, SEQ ID NO: 464, SEQ ID NO: 466, SEQ ID NO: 478, SEQ ID NO: 480, SEQ ID NO : 482, SEQ ID NO: 488, SEQ ID NO: 490, SEQ ID NO: 492, SEQ ID NO: 500, SEQ ID NO: 504, SEQ ID NO: 508, SEQ ID NO: 510, SEQ ID NO: 520, SEQ ID NO: 522, SEQ ID NO: 552, SEQ ID NO: 556, SEQ ID NO: 558, SEQ ID NO: 564, SEQ ID NO: 572, SEQ ID NO: 578, SEQ ID NO: 588, SEQ ID NO : 590, SEQ ID NO : 592, SEQ ID NO : 594, SEQ ID NO : 596, SEQ ID NO: 600, SEQ ID NO: 606, SEQ ID NO: 630, SEQ ID NO: 638, SEQ ID NO: 642, SEQ ID NO: 650, SEQ ID NO: 660, SEQ ID NO: 662, SEQ ID NO: 682, SEQ ID NO: 690, SEQ ID NO: 708, SEQ ID NO: 710, SEQ ID NO: 712, SEQ ID NO: 728, SEQ ID NO: 730, SEQ ID NO: 732, SEQ ID NO: 734, SEQ ID NO: 736, SEQ ID NO: 740, SEQ ID NO: 742, SEQ ID NO: 748, SEQ ID NO: 760, SEQ ID NO: 770, SEQ ID NO: 780, ID NO: 784, SEQ ID NO: 788, SEQ ID NO: 790, SEQ ID NO: 810, SEQ ID NO: 812, SEQ ID NO: 828, SEQ ID NO: 842, SEQ ID NO: 856, SEQ ID NO: 862, SEQ ID NO: 876, SEQ ID NO: 892, SEQ ID NO: 910, SEQ ID NO: 912, SEQ ID NO: 914, SEQ ID NO: 930, SEQ ID NO: 934, SEQ ID NO: 940 or SEQ ID NO: 952, or an enzymatically active fragment thereof having lipase activity;
(ii) a lipase encoded by the nucleic acid sequence according to SEQ ID NO: 955, SEQ ID NO:
3, SEQ ID NO: 15, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 75, SEQ ID NO: 99, SEQ ID NO: 113, SEQ ID NO: 141 , SEQ ID NO: 147, SEQ ID NO:
149, SEQ ID NO: 155, SEQ ID NO: 159, SEQ ID NO: 161 , SEQ ID NO: 163, SEQ ID NO: 169, SEQ ID NO: 171 , SEQ ID NO: 181 , SEQ ID NO: 185, SEQ ID NO: 193, SEQ ID NO: 203, SEQ ID NO: 205, SEQ ID NO: 213, SEQ ID NO: 217, SEQ ID NO: 223, SEQ ID NO: 227, SEQ ID NO: 229, SEQ ID NO: 243, SEQ ID NO: 261 , SEQ ID NO: 267, SEQ ID NO: 269, SEQ ID NO: 281 , SEQ ID NO: 291 , SEQ ID NO: 297, SEQ ID NO: 299, SEQ ID NO: 305, SEQ ID NO: 319, SEQ ID NO: 339, SEQ ID NO: 367, SEQ ID NO: 393, SEQ ID NO: 421 , SEQ ID NO: 423, SEQ ID NO: 425, SEQ ID NO: 427, SEQ ID NO: 439, SEQ ID NO: 453, SEQ ID NO: 455, SEQ ID NO: 459, SEQ ID NO: 463, SEQ ID NO: 465, SEQ ID NO: 477, SEQ ID NO: 479, SEQ ID NO : 481 , SEQ ID NO: 487, SEQ ID NO: 489, SEQ ID NO: 491 , SEQ ID NO: 499, SEQ ID NO: 503, SEQ ID NO: 507, SEQ ID NO: 509, SEQ ID NO: 519, SEQ ID NO: 521 , SEQ ID NO: 551 , SEQ ID NO: 555, SEQ ID NO: 557, SEQ ID NO: 563, SEQ ID NO: 571 , SEQ ID NO: 577, SEQ ID NO: 587, SEQ ID NO: 589, SEQ ID NO: 591 , SEQ ID NO: 593, SEQ ID NO: 595, SEQ ID NO: 599, SEQ ID NO: 605, SEQ ID NO: 629, SEQ ID NO: 637, SEQ ID NO: 641 , SEQ ID NO: 649, SEQ ID NO: 659, SEQ ID NO: 661 , SEQ ID NO: 681 , SEQ ID NO: 689, SEQ ID NO: 707, SEQ ID NO: 709, SEQ ID NO: 711 , SEQ ID NO: 727, SEQ ID NO: 729, SEQ ID NO: 731 , SEQ ID NO: 733, SEQ ID NO: 735, SEQ ID NO: 739, SEQ ID NO: 741 , SEQ ID NO: 747, SEQ ID NO: 759, SEQ ID NO: 769, SEQ ID NO: 779, ID NO: 783, SEQ ID NO: 787, SEQ ID NO: 789, SEQ ID NO: 809, SEQ ID NO: 811 , SEQ ID NO: 827, SEQ ID NO: 841 , SEQ ID NO: 855, SEQ ID NO: 861 , SEQ ID NO: 875, SEQ ID NO: 891 , SEQ ID NO: 909, SEQ ID NO: 91 1 , SEQ ID NO: 913, SEQ ID NO: 929, SEQ ID NO: 933, SEQ ID NO: 939 or SEQ ID NO: 951 or an enzymati- cally active fragment thereof having lipase activity;
(iii) a lipase having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100, SEQ ID NO: 1 14, SEQ ID NO: 142, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 156, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 182, SEQ ID NO: 186, SEQ ID NO: 194, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 214, SEQ ID NO: 218, SEQ ID NO: 224, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 244, SEQ ID NO: 262, SEQ ID NO: 268, SEQ ID NO: 270, SEQ ID NO: 282, SEQ ID NO: 292, SEQ ID NO: 298, SEQ ID NO: 300, SEQ ID NO: 306, SEQ ID NO: 320, SEQ ID NO: 340, SEQ ID NO: 368, SEQ ID NO: 394, SEQ ID NO: 422, SEQ ID NO: 424, SEQ ID NO: 426, SEQ ID NO: 428, SEQ ID NO: 440, SEQ ID NO: 454, SEQ ID NO: 456, SEQ ID NO: 460, SEQ ID NO: 464, SEQ ID NO: 466, SEQ ID NO: 478, SEQ ID NO: 480, SEQ ID NO : 482, SEQ ID NO: 488, SEQ ID NO: 490, SEQ ID NO: 492, SEQ ID NO: 500, SEQ ID NO: 504, SEQ ID NO: 508, SEQ ID NO: 510, SEQ ID NO: 520, SEQ ID NO: 522, SEQ ID NO: 552, SEQ ID NO: 556, SEQ ID NO: 558, SEQ ID NO: 564, SEQ ID NO: 572, SEQ ID NO: 578, SEQ ID NO: 588, SEQ ID NO : 590, SEQ ID NO : 592, SEQ ID NO : 594, SEQ ID NO : 596, SEQ ID NO: 600, SEQ ID NO: 606, SEQ ID NO: 630, SEQ ID NO: 638, SEQ ID NO: 642, SEQ ID NO: 650, SEQ ID NO: 660, SEQ ID NO: 662, SEQ ID NO: 682, SEQ ID NO: 690, SEQ ID NO: 708, SEQ ID NO: 710, SEQ ID NO: 712, SEQ ID NO: 728, SEQ ID NO: 730, SEQ ID NO: 732, SEQ ID NO: 734, SEQ ID NO: 736, SEQ ID NO: 740, SEQ ID NO: 742, SEQ ID NO: 748, SEQ ID NO: 760, SEQ ID NO: 770, SEQ ID NO: 780, ID NO: 784, SEQ ID NO: 788, SEQ ID NO: 790, SEQ ID NO: 810, SEQ ID NO: 812, SEQ ID NO: 828, SEQ ID NO: 842, SEQ ID NO: 856, SEQ ID NO: 862, SEQ ID NO: 876, SEQ ID NO: 892, SEQ ID NO: 910, SEQ ID NO: 912, SEQ ID NO: 914, SEQ ID NO: 930, SEQ ID NO: 934, SEQ ID NO: 940 or SEQ ID NO: 952 or an enzymatically active fragment thereof having lipase activity; and
(iv) a lipase encoded by a nucleic acid sequence which hybridizes to the complement of the nu- cleic acid sequence according to any of SEQ ID NO: 955, SEQ ID NO: 3, SEQ ID NO: 15, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 75, SEQ ID NO: 99, SEQ ID NO: 1 13, SEQ ID NO: 141 , SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 155, SEQ ID NO: 159, SEQ ID NO: 161 , SEQ ID NO: 163, SEQ ID NO: 169, SEQ ID NO: 171 , SEQ ID NO: 181 , SEQ ID NO: 185, SEQ ID NO: 193, SEQ ID NO: 203, SEQ ID NO: 205, SEQ ID NO: 213, SEQ ID NO: 217, SEQ ID NO: 223, SEQ ID NO: 227, SEQ ID NO: 229, SEQ ID NO: 243, SEQ ID NO: 261 , SEQ ID NO: 267, SEQ ID NO: 269, SEQ ID NO: 281 , SEQ ID NO: 291 , SEQ ID NO: 297, SEQ ID NO: 299, SEQ ID NO: 305, SEQ ID NO: 319, SEQ ID NO: 339, SEQ ID NO: 367, SEQ ID NO: 393, SEQ ID NO: 421 , SEQ ID NO: 423, SEQ ID NO: 425, SEQ ID NO: 427, SEQ ID NO: 439, SEQ ID NO: 453, SEQ ID NO: 455, SEQ ID NO: 459, SEQ ID NO: 463, SEQ ID NO: 465, SEQ ID NO: 477, SEQ ID NO: 479, SEQ ID NO : 481 , SEQ ID NO: 487, SEQ ID NO: 489, SEQ ID NO: 491 , SEQ ID NO: 499, SEQ ID NO: 503, SEQ ID NO: 507, SEQ ID NO: 509, SEQ ID NO: 519, SEQ ID NO: 521 , SEQ ID NO: 551 , SEQ ID NO: 555, SEQ ID NO: 557, SEQ ID NO: 563, SEQ ID NO: 571 , SEQ ID NO: 577, SEQ ID NO: 587, SEQ ID NO: 589, SEQ ID NO: 591 , SEQ ID NO: 593, SEQ ID NO: 595, SEQ ID NO: 599, SEQ ID NO: 605, SEQ ID NO: 629, SEQ ID NO: 637, SEQ ID NO: 641 , SEQ ID NO: 649, SEQ ID NO: 659, SEQ ID NO: 661 , SEQ ID NO: 681 , SEQ ID NO: 689, SEQ ID NO: 707, SEQ ID NO: 709, SEQ ID NO: 711 , SEQ ID NO: 727, SEQ ID NO: 729, SEQ ID NO: 731 , SEQ ID NO: 733, SEQ ID NO: 735, SEQ ID NO: 739, SEQ ID NO: 741 , SEQ ID NO: 747, SEQ ID NO: 759, SEQ ID NO: 769, SEQ ID NO: 779, ID NO: 783, SEQ ID NO: 787, SEQ ID NO: 789, SEQ ID NO: 809, SEQ ID NO: 811 , SEQ ID NO: 827, SEQ ID NO: 841 , SEQ ID NO: 855, SEQ ID NO: 861 , SEQ ID NO: 875, SEQ ID NO: 891 , SEQ ID NO: 909, SEQ ID NO: 911 , SEQ ID NO: 913, SEQ ID NO: 929, SEQ ID NO: 933, SEQ ID NO: 939 or SEQ ID NO: 951 under stringent conditions.
Even more preferably, the lipase used in the context of the present invention is selected from the group consisting of:
(i) a lipase having the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 90, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100 or SEQ ID NO: 114 or an enzymatically active fragment thereof having lipase activity;
(ii) a lipase encoded by the nucleic acid sequence according to SEQ ID NO: 955, SEQ ID NO: 89, SEQ ID NO: 3, SEQ ID NO: 15, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 75, SEQ ID NO: 99 or SEQ ID NO: 113 or an enzymatically active frag- ment thereof having lipase activity;
(iii) a lipase having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 90, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100 or SEQ ID NO: 1 14 or an enzymatically active fragment thereof having lipase activity; and (iv) a lipase encoded by a nucleic acid sequence which hybridizes to the complement of the nu- cleic acid sequence according to SEQ ID NO: 955, SEQ ID NO: 89, SEQ ID NO: 3, SEQ ID NO: 15, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 75,
SEQ ID NO: 99 or SEQ ID NO: 113 under stringent conditions.
Particularly preferably, the lipase used in the context of the present invention is selected from the group consisting of:
(i) a lipase having the amino acid sequence according to SEQ ID NO: 956 or SEQ ID NO: 90 or an enzymatically active fragment thereof having lipase activity;
(ii) a lipase encoded by the nucleic acid sequence according to SEQ ID NO: 955 or SEQ ID NO: 89 or an enzymatically active fragment thereof having lipase activity;
(iii) a lipase having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956 or SEQ ID NO: 90 or an enzymatically active frag- ment thereof having lipase activity; and
(iv) a lipase encoded by a nucleic acid sequence which hybridizes to the complement of the nu- cleic acid sequence according to SEQ ID NO: 955 or SEQ ID NO: 89 under stringent condi- tions.
Most preferably, the lipase used in the context of the present invention is selected from the group consisting of:
(i) a lipase having the amino acid sequence according to SEQ ID NO: 956 or an enzymatically active fragment thereof having lipase activity;
(ii) a lipase encoded by the nucleic acid sequence according to SEQ ID NO: 955 or an enzymat- ically active fragment thereof having lipase activity;
(iii) a lipase having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956 or an enzymatically active fragment thereof having lipase activity; and
(iv) a lipase encoded by a nucleic acid sequence which hybridizes to the complement of the nu- cleic acid sequence according to any SEQ ID NO: 955 under stringent conditions.
An "enzymatically active fragment" of a lipase is understood to refer to a smaller part of the li- pase which consists of a contiguous amino acid sequence found in the amino acid sequence of the lipase and which has lipase activity. The skilled person knows that for a fragment to be en- zymatically active the fragment has to comprise at least the amino acids present in the catalytic centre of the lipase. These amino acids are either known for a given lipase or can easily be identified by the skilled person, for example by homology screening or mutagenesis. For exam- pie, an enzymatically active fragment of the lipase according to SEQ ID No. 956 comprises at least amino acid residues 87 to 285 of SEQ ID No.956, more preferably it comprises at least amino acid residues 61 to 291 of SEQ ID No. 956, even more preferably it comprises at least amino acid residues 41 to 301 of SEQ ID No. 956 and most preferably it comprises at least amino acid residues 11 to 311 of SEQ ID No. 956. A "fragment" of a nucleic acid sequence encoding an enzymatically active fragment of a lipase is understood to refer to a smaller part of the nucleic acid sequence which consists of a contigu- ous nucleic acid sequence found in the nucleic acid sequence of the lipase and which encodes a protein having lipase activity. The skilled person knows that for a fragment of an enzyme to be enzymatically active the fragment has to comprise at least the amino acids present in the cata- lytic centre of the lipase. These amino acids are either known for a given lipase or can easily be identified by the skilled person, for example by homology screening or mutagenesis. For exam- pie, the fragment of the nucleic acid sequence according to SEQ ID No. 955 encodes at least amino acid residues 87 to 285 of SEQ ID No. 956, more preferably it encodes at least amino acid residues 61 to 291 of SEQ ID No. 956, even more preferably it encodes at least amino acid residues 41 to 301 of SEQ ID No. 956 and most preferably it encodes at least amino acid resi- dues 11 to 311 of SEQ ID No. 956.
Within the present invention a lipase having an amino acid sequence with at least 70, 75 or 80 % sequence identity, preferably with at least 81 , 82, 83, 84, 85 or 86% sequence identity, more preferably with at least 87, 88, 89 or 90% sequence identity even more preferably with at least
91 , 92, 93, 94 or 95% sequence identity and most preferably with at least 96, 97, 98, 99 or 100% sequence identity to the complete sequence according to any one of SEQ ID NO: 956, SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56, SEQ ID NO: 58, SEQ ID NO: 60, SEQ ID NO: 62, SEQ ID NO: 64, SEQ ID NO: 66, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 72, SEQ ID NO: 74, SEQ ID NO: 76, SEQ ID NO: 78, SEQ ID NO: 80, SEQ ID NO: 82, SEQ ID NO: 84, SEQ ID NO: 86, SEQ ID NO: 88, SEQ ID NO: 90, SEQ ID NO:
92, SEQ ID NO: 94, SEQ ID NO: 96, SEQ ID NO: 98, SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, SEQ ID NO: 1 10, SEQ ID NO: 112, SEQ ID NO: 1 14, SEQ ID NO: 116, SEQ ID NO: 118, SEQ ID NO: 120, SEQ ID NO: 122, SEQ ID NO: 124, SEQ ID NO: 126, SEQ ID NO: 128, SEQ ID NO: 130, SEQ ID NO: 132, SEQ ID NO: 134, SEQ ID NO: 136, SEQ ID NO: 138, SEQ ID NO: 140, SEQ ID NO: 142, SEQ ID NO: 143, SEQ ID NO: 146, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 152, SEQ ID NO: 154, SEQ ID NO: 156, SEQ ID NO: 158, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 166, SEQ ID NO: 168, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 174, SEQ ID NO: 176, SEQ ID NO: 178, SEQ ID NO: 180, SEQ ID NO: 182, SEQ ID NO: 184, SEQ ID NO: 186, SEQ ID NO: 188, SEQ ID NO: 190, SEQ ID NO: 192, SEQ ID NO: 194, SEQ ID NO: 196, SEQ ID NO: 198, SEQ ID NO: 200, SEQ ID NO: 202, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 208, SEQ ID NO: 210, SEQ ID NO: 212, SEQ ID NO: 214, SEQ ID NO: 216, SEQ ID NO: 218, SEQ ID NO: 220, SEQ ID NO: 222, SEQ ID NO: 224, SEQ ID NO: 226, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 232, SEQ ID NO: 234, SEQ ID NO: 236, SEQ ID NO: 238, SEQ ID NO: 240, SEQ ID NO: 242, SEQ ID NO: 244, SEQ ID NO: 246, SEQ ID NO: 248, SEQ ID NO: 250, SEQ ID NO: 252, SEQ ID NO: 254, SEQ ID NO: 256, SEQ ID NO: 258, SEQ ID NO: 260, SEQ ID NO: 262, SEQ ID NO: 264, SEQ ID NO: 266, SEQ ID NO: 268, SEQ ID NO: 270, SEQ ID NO: 272, SEQ ID NO: 274, SEQ ID NO: 276, SEQ ID NO: 278, SEQ ID NO: 280, SEQ ID NO: 282, SEQ ID NO: 284, SEQ ID NO: 286, SEQ ID NO: 288, SEQ ID NO: 290, SEQ ID NO: 292, SEQ ID NO: 294, SEQ ID NO: 296, SEQ ID NO: 298, SEQ ID NO: 300, SEQ ID NO: 302, SEQ ID NO: 304, SEQ ID NO: 306, SEQ ID NO: 308, SEQ ID NO: 310, SEQ ID NO: 312, SEQ ID NO: 314, SEQ ID NO: 316, SEQ ID NO: 318, SEQ ID NO: 320, SEQ ID NO: 322, SEQ ID NO: 324, SEQ ID NO: 326, SEQ ID NO: 328, SEQ ID NO: 330, SEQ ID NO: 332, SEQ ID NO: 334, SEQ ID NO: 336, SEQ ID NO: 338, SEQ ID NO: 340, SEQ ID NO: 342, SEQ ID NO: 344, SEQ ID NO: 346, SEQ ID NO: 348, SEQ ID NO: 350, SEQ ID NO: 352, SEQ ID NO: 354, SEQ ID NO: 356, SEQ ID NO: 358, SEQ ID NO: 360, SEQ ID NO: 362, SEQ ID NO: 364, SEQ ID NO: 366, SEQ ID NO: 368, SEQ ID NO: 370, SEQ ID NO: 372, SEQ ID NO: 374, SEQ ID NO: 376, SEQ ID NO: 378, SEQ ID NO: 380, SEQ ID NO: 382, SEQ ID NO: 384, SEQ ID NO: 386, SEQ ID NO: 388, SEQ ID NO: 390, SEQ ID NO: 392, SEQ ID NO: 394, SEQ ID NO: 396, SEQ ID NO: 398, SEQ ID NO: 400, SEQ ID NO: 402, SEQ ID NO: 404, SEQ ID NO: 406, SEQ ID NO: 408, SEQ ID NO: 410, SEQ ID NO: 412, SEQ ID NO: 414, SEQ ID NO: 416, SEQ ID NO: 418, SEQ ID NO: 420, SEQ ID NO: 422, SEQ ID NO: 424, SEQ ID NO: 426, SEQ ID NO: 428, SEQ ID NO: 430, SEQ ID NO: 432, SEQ ID NO: 434, SEQ ID NO: 436, SEQ ID NO: 438, SEQ ID NO: 440, SEQ ID NO: 442, SEQ ID NO: 444, SEQ ID NO: 446, SEQ ID NO: 448, SEQ ID NO: 450, SEQ ID NO: 452, SEQ ID NO: 454, SEQ ID NO: 456, SEQ ID NO: 458, SEQ ID NO: 460, SEQ ID NO: 462, SEQ ID NO: 464, SEQ ID NO: 466, SEQ ID NO: 468, SEQ ID NO: 470, SEQ ID NO: 472, SEQ ID NO: 474, SEQ ID NO: 476, SEQ ID NO: 478, SEQ ID NO: 480, SEQ ID NO: 482, SEQ ID NO: 484, SEQ ID NO: 486, SEQ ID NO: 488, SEQ ID NO: 490, SEQ ID NO: 492, SEQ ID NO: 494, SEQ ID NO: 496, SEQ ID NO: 498, SEQ ID NO: 500, SEQ ID NO: 502, SEQ ID NO: 504, SEQ ID NO: 506, SEQ ID NO: 508, SEQ ID NO: 510, SEQ ID NO: 512, SEQ ID NO: 514, SEQ ID NO: 516, SEQ ID NO: 518, SEQ ID NO: 520, SEQ ID NO: 522, SEQ ID NO: 524, SEQ ID NO: 526, SEQ ID NO: 528, SEQ ID NO: 530, SEQ ID NO: 532, SEQ ID NO: 534, SEQ ID NO: 536, SEQ ID NO: 538, SEQ ID NO: 540, SEQ ID NO: 542, SEQ ID NO: 544, SEQ ID NO: 546, SEQ ID NO: 548, SEQ ID NO: 550, SEQ ID NO: 552, SEQ ID NO: 554, SEQ ID NO: 556, SEQ ID NO: 558, SEQ ID NO: 560, SEQ ID NO: 562, SEQ ID NO: 564, SEQ ID NO: 566, SEQ ID NO: 568, SEQ ID NO: 570, SEQ ID NO: 572, SEQ ID NO: 574, SEQ ID NO: 576, SEQ ID NO: 578, SEQ ID NO: 580, SEQ ID NO: 582, SEQ ID NO: 584, SEQ ID NO: 586, SEQ ID NO: 588, SEQ ID NO: 590, SEQ ID NO: 592, SEQ ID NO: 594, SEQ ID NO: 596, SEQ ID NO: 598, SEQ ID NO: 600, SEQ ID NO: 602, SEQ ID NO: 604, SEQ ID NO: 606, SEQ ID NO: 608, SEQ ID NO: 610, SEQ ID NO: 612, SEQ ID NO: 614, SEQ ID NO: 616, SEQ ID NO: 618, SEQ ID NO: 620, SEQ ID NO: 622, SEQ ID NO: 624, SEQ ID NO: 626, SEQ ID NO: 628, SEQ ID NO: 630, SEQ ID NO: 632, SEQ ID NO: 634, SEQ ID NO: 636, SEQ ID NO: 638, SEQ ID NO: 640, SEQ ID NO: 642, SEQ ID NO: 644, SEQ ID NO: 646, SEQ ID NO: 648, SEQ ID NO: 650, SEQ ID NO: 652, SEQ ID NO: 654, SEQ ID NO: 656, SEQ ID NO: 658, SEQ ID NO: 660, SEQ ID NO: 662, SEQ ID NO: 664, SEQ ID NO: 666, SEQ ID NO: 668, SEQ ID NO: 670, SEQ ID NO: 672, SEQ ID NO: 674, SEQ ID NO: 676, SEQ ID NO: 678, SEQ ID NO: 680, SEQ ID NO: 682, SEQ ID NO: 684, SEQ ID NO: 686, SEQ ID NO: 688, SEQ ID NO: 690, SEQ ID NO: 692, SEQ ID NO: 694, SEQ ID NO: 696, SEQ ID NO: 698, SEQ ID NO: 700, SEQ ID NO: 702, SEQ ID NO: 704, SEQ ID NO: 706, SEQ ID NO: 708, SEQ ID NO: 710, SEQ ID NO: 712, SEQ ID NO: 714, SEQ ID NO: 716, SEQ ID NO: 718, SEQ ID NO: 720, SEQ ID NO: 722, SEQ ID NO: 724, SEQ ID NO: 726, SEQ ID NO: 728, SEQ ID NO: 730, SEQ ID NO: 732, SEQ ID NO: 734, SEQ ID NO: 736, SEQ ID NO: 738, SEQ ID NO: 740, SEQ ID NO: 742, SEQ ID NO: 744, SEQ ID NO: 746, SEQ ID NO: 748, SEQ ID NO: 750, SEQ ID NO: 752, SEQ ID NO: 754, SEQ ID NO: 756, SEQ ID NO: 758, SEQ ID NO: 760, SEQ ID NO: 762, SEQ ID NO: 764, SEQ ID NO: 766, SEQ ID NO: 768, SEQ ID NO: 770, SEQ ID NO: 772, SEQ ID NO: 774, SEQ ID NO: 776, SEQ ID NO: 778, SEQ ID NO: 780, SEQ ID NO: 782, SEQ ID NO: 784, SEQ ID NO: 786, SEQ ID NO: 788, SEQ ID NO: 790, SEQ ID NO: 792, SEQ ID NO: 794, SEQ ID NO : 796, SEQ ID NO: 798, SEQ ID NO: 800, SEQ ID NO: 802, SEQ ID NO: 804, SEQ ID NO: 806, SEQ ID NO: 808, SEQ ID NO: 810, SEQ ID NO: 812, SEQ ID NO: 814, SEQ ID NO: 816, SEQ ID NO: 818, SEQ ID NO: 820, SEQ ID NO: 822, SEQ ID NO: 824, SEQ ID NO: 826, SEQ ID NO: 828, SEQ ID NO: 830, SEQ ID NO: 832, SEQ ID NO: 834, SEQ ID NO: 836, SEQ ID NO: 838, SEQ ID NO: 840, SEQ ID NO: 842, SEQ ID NO: 844, SEQ ID NO: 846, SEQ ID NO: 848, SEQ ID NO: 850, SEQ ID NO: 852, SEQ ID NO: 854, SEQ ID NO: 856, SEQ ID NO: 858, SEQ ID NO: 860, SEQ ID NO: 862, SEQ ID NO: 864, SEQ ID NO: 866, SEQ ID NO: 868, SEQ ID NO: 870, SEQ ID NO: 872, SEQ ID NO: 874, SEQ ID NO: 876, SEQ ID NO: 878, SEQ ID NO: 880, SEQ ID NO: 882, SEQ ID NO: 884, SEQ ID NO: 886, SEQ ID NO: 888, SEQ ID NO: 890, SEQ ID NO: 892, SEQ ID NO: 894, SEQ ID NO: 896, SEQ ID NO: 898, SEQ ID NO: 900, SEQ ID NO: 902, SEQ ID NO: 904, SEQ ID NO: 906, SEQ ID NO: 908, SEQ ID NO: 910, SEQ ID NO: 912, SEQ ID NO: 914, SEQ ID NO: 916, SEQ ID NO: 918, SEQ ID NO: 920, SEQ ID NO: 922, SEQ ID NO: 924, SEQ ID NO: 926, SEQ ID NO: 928, SEQ ID NO: 930, SEQ ID NO: 932, SEQ ID NO: 934, SEQ ID NO: 936, SEQ ID NO: 938, SEQ ID NO: 940, SEQ ID NO: 942, SEQ ID NO: 944, SEQ ID NO: 946, SEQ ID NO: 948, SEQ ID NO: 950, SEQ ID NO: 952 or SEQ ID NO: 954 or an enzymatically active fragment of any of these sequences having lipase activity may also be used. The lipases having the aforementioned sequence identity to the sequence according to SEQ ID No. 956 preferably comprise the amino acid serine on position 87 of SEQ ID No. 956, the amino acid aspartate on position 241 of SEQ ID No. 956 and the amino acid histidine on position 285 of SEQ ID No. 956.
In one embodiment a lipase with at least 70% sequence identity to the amino acid sequence ac- cording to SEQ ID NO: 956 is used which reduces the soil water repellency of non-wetting soils by at least 10% or 20%, preferably by at least 30% or 40%, more preferably by at least 50% or 60% and most preferably by at least 70% or 75%. In one embodiment a lipase with at least 80% sequence identity to the amino acid sequence according to SEQ ID NO: 956 is used which re- duces the soil water repellency of non-wetting soils by at least 10% or 20%, preferably by at least 30% or 40%, more preferably by at least 50% or 60% and most preferably by at least 70% or 75%. In one embodiment a lipase with at least 90% sequence identity to the amino acid se- quence according to SEQ ID NO: 956 is used which reduces the soil water repellency of non- wetting soils by at least 10% or 20%, preferably by at least 30% or 40%, more preferably by at least 50% or 60% and most preferably by at least 70% or 75%. In one embodiment a lipase with at least 95% sequence identity to the amino acid sequence according to SEQ ID NO: 956 is used which reduces the soil water repellency of non-wetting soils by at least 10% or 20%, pref- erably by at least 30% or 40%, more preferably by at least 50% or 60% and most preferably by at least 70% or 75%.
In one embodiment a lipase with at least 70% sequence identity to the amino acid sequence ac- cording to SEQ ID NO: 956 is used which increases the water holding capacity of non-wetting soils by at least 3% or 5%, preferably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15%. In one embodiment a lipase with at least 80% sequence identity to the amino acid sequence according to SEQ ID NO: 956 is used which increases the water holding capacity of non-wetting soils by at least 3% or 5%, preferably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15%. In one embodiment a lipase with at least 90% sequence identity to the amino acid sequence according to SEQ ID NO: 956 is used which increases the water holding capacity of non-wetting soils by at least 3% or 5%, preferably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15%. In one embodiment a lipase with at least 95% sequence identity to the amino acid sequence according to SEQ ID NO: 956 is used which increases the water holding capac- ity of non-wetting soils by at least 3% or 5%, preferably by at least 8% or 10%, more preferably by at least 12% and most preferably by at least 15%.
“Sequence Identity,”“% sequence identity.”“% identity,” or“sequence alignment” means a com- parison of a first amino acid sequence to a second amino acid sequence, or a comparison of a first nucleic acid sequence to a second nucleic acid sequence and is calculated as a percentage based on the comparison. The result of this calculation can be described as“percent identical” or “percent ID.”
Generally, a sequence alignment can be used to calculate the sequence identity by one of two different approaches. In the first approach, both, mismatches at a single position and gaps at a single position are counted as non-identical positions in final sequence identity calculation. In the second approach, mismatches at a single position are counted as non-identical positions in final sequence identity calculation; however, gaps at a single position are not counted (ignored) as non-identical positions in final sequence identity calculation. In other words, in the second ap- proach gaps are ignored in final sequence identity calculation. The differences between these two approaches, counting gaps as non-identical positions vs ignoring gaps, at a single position can lead to variability in sequence identity value between two sequences.
In an embodiment of this disclosure, sequence identity is determined by a program, which pro- duces an alignment, and calculates identity counting both mismatches at a single position and gaps at a single position as non-identical positions in final sequence identity calculation. For ex- ample program Needle (EMBOS), which has implemented the algorithm of Needleman and Wun- sch (Needleman and Wunsch (1970) J. Mol. Biol. 48: 443-453), and which calculates sequence identity by first producing an alignment between a first sequence and a second sequence over the full length of these sequences, then counting the number of identical positions over the length of the alignment, then dividing the number of identical residues by the length of an alignment, and then multiplying this number by 100 to generate the % sequence identity [% sequence identity = (# of Identical residues / length of alignment) x 100)].
In another embodiment of this disclosure, sequence identity can be calculated from a pairwise alignment showing only a local region of the first sequence or the second sequence (“Local Iden- tity”). For example, program Blast (NCBI) produces such alignments; % sequence identity = (# of identical residues / length of alignment) x 100)]. In a preferred embodiment, a sequence alignment is calculated with mismatches at a single po- sition being counted as non-identical positions in final sequence identity calculation; however, gaps at a single position are not counted (i.e. they are ignored) as non-identical positions in final sequence identity calculation. The sequence alignment is generated by using the algorithm of Needleman and Wunsch (J. Mol. Biol. (1979) 48, p. 443-453). Preferably, the program“NEEDLE” (The European Molecular Biology Open Software Suite (EMBOSS)) is used for the purposes of the current invention, with using the programs default parameter (gap open=10.0, gap extend=0.5 and matrix=EBLOSUM62). Then, a sequence identity can be calculated from the alignment show- ing both sequences over the full length, so showing the first sequence and the second sequence in their full length (“Global sequence identity”). For example,; % sequence identity = (# of identical residues / length of alignment) x 100)].
The nucleic acid sequence hybridizing under stringent conditions with a complementary se- quence of a nucleic acid sequence according to SEQ ID No. 2 or an enzymatically active frag- ment thereof encodes a protein having lipase activity.
The term "hybridizing under stringent conditions" denotes in the context of the present invention that the hybridization is implemented in vitro under conditions which are stringent enough to en- sure a specific hybridization. Stringent in vitro hybridization conditions are known to those skilled in the art and may be taken from the literature (e.g. Sambrook and Russell (2001 ) Molec ular Cloning: A Laboratory Manual, 3rd edition, Cold Spring Harbour Laboratory Press, Cold Spring Harbour, NY). The term "specific hybridization" refers to the circumstance that a mole- cule, under stringent conditions, preferably binds to a certain nucleic acid sequence, i.e. the tar- get sequence, if the same is part of a complex mixture of, e.g. DNA or RNA molecules, but does not, or at least very rarely, bind to other sequences.
Stringent conditions depend on the circumstances. Longer sequences hybridize specifically at higher temperatures. In general, stringent conditions are chosen such that the hybridization temperature is about 5°C below the melting point (Tm) of the specific sequence at a defined ionic strength and at a defined pH value. Tm is the temperature (at a defined pH value, a defined ionic strength and a defined nucleic acid concentration), at which 50% of the molecules comple- mentary to the target sequence hybridize to the target sequence in the state of equilibrium. Typ- ically, stringent conditions are conditions, where the salt concentration has a sodium ion con- centration (or concentration of a different salt) of at least about 0.01 to 1 .0 M at a pH value be- tween 7.0 and 8.3, and the temperature is at least 30°C for small molecules (i.e. 10 to 50 nucle- otides, for example). In addition, stringent conditions may include the addition of substances, such as, e. g., formamide, which destabilise the hybrids. At hybridization under stringent condi- tions, as used herein, normally nucleotide sequences which are at least 60% homologous to each other hybridize to each other. Preferably, said stringent conditions are chosen such that sequences which are about 65%, preferably at least about 70%, and especially preferably at least about 75% or higher homologous to each other, normally remain hybridized to each other. A preferred but non-limiting example of stringent hybridization conditions is hybridizations in 6 x sodium chloride/sodium citrate (SSC) at about 45°C, followed by one or more washing steps in 0.2 x SSC, 0.1 % SDS at 50 to 65°C. The temperature depends on the type of the nucleic acid and is between 42°C and 58°C in an aqueous buffer having a concentration of 0.1 to 5 x SSC (pH value 7.2).
If an organic solvent, e.g. 50% formamide, is present in the above-mentioned buffer, the tem- perature is about 42°C under standard conditions. Preferably, the hybridisation conditions for DNA:DNA hybrids are, for example, 0.1 x SSC and 20°C to 45°C, preferably 30°C to 45°C. Pref- erably, the hybridisation conditions for DNA:RNA hybrids are, for example, 0.1 x SSC and 30°C to 55°C, preferably between 45°C and 55°C. The above-mentioned hybridization temperatures are determined, for example, for a nucleic acid which is 100 base pairs long and has a G/C con- tent of 50% in the absence of formamide. Those skilled in the art know how to determine the re- quired hybridization conditions using text books such as those mentioned above or the following textbooks: Current Protocols in Molecular Biology, John Wiley & Sons, N.Y. (1989), Hames and Higgins (publ.) 1985, Nucleic Acids Hybridization: A Practical Approach, IRL Press at Oxford University Press, Oxford; Brown (publ.) 1991 , Essential Molecular Biology: A Practical Ap- proach, IRL Press at Oxford University Press, Oxford.
Typical hybridization and washing buffers for example have the following composition:
Pre-hybridization solution. 0.5 % SDS
5x SSC
50 mM sodium phosphate, pH 6.8
0.1 % sodium pyrophosphate
5x Denhardt's solution
100 pg/mL salmon sperm DNA
Hybridization solution: pre-hybridization solution
1x106 cpm/mL probe (5 - 10 min 95 °C)
20x SSC: 3 M NaCI
0.3 M sodium citrate
ad pH 7 with HCI
50x Denhardt's reagent: 5 g Ficoll
5 g polyvinylpyrrolidone
5 g bovine serum albumin
ad 500 mL aqua destillata
A typical procedure for hybridization is as follows:
Optional: wash blot 30 min in 1x SSC/ 0.1 % SDS at 65 °C
Pre-hybridization: at least 2 h at 50 - 55 °C Hybridization: over night at 55 - 60 °C
Washing: 5 min 2x SSC/ 0.1 % SDS hybridization temp
30 min 2x SSC/ 0.1 % SDS hybridization temp
30 min 1x SSC/ 0.1 % SDS hybridization temp.
45 min 0.2x SSC/ 0.1 % SDS 65 °C
5 min O.lx SSC room temperature
Those skilled in the art know that the given solutions and the presented protocol may be modi- fied or have to be modified, depending on the application.
The proteins encoded by the nucleic acid sequence hybridizing under stringent conditions to the complement of the sequence according to SEQ ID No. 955 preferably comprise the amino acid serine on position 87 of SEQ ID No. 956, the amino acid aspartate on position 241 of SEQ ID No. 1 and the amino acid histidine on position 285 of SEQ ID No. 956.
The proteins having the abovementioned sequence identity to the sequence according to any one of SEQ ID NO: 956, SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56, SEQ ID NO: 58, SEQ ID NO: 60, SEQ ID NO: 62, SEQ ID NO: 64, SEQ ID NO: 66, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 72, SEQ ID NO: 74, SEQ ID NO: 76, SEQ ID NO: 78, SEQ ID NO: 80, SEQ ID NO: 82, SEQ ID NO: 84, SEQ ID NO: 86, SEQ ID NO: 88, SEQ ID NO: 90, SEQ ID NO: 92, SEQ ID NO: 94, SEQ ID NO: 96, SEQ ID NO: 98, SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, SEQ ID NO: 110, SEQ ID NO: 1 12, SEQ ID NO: 114, SEQ ID NO: 116, SEQ ID NO: 1 18, SEQ ID NO: 120, SEQ ID NO: 122, SEQ ID NO: 124, SEQ ID NO: 126, SEQ ID NO: 128, SEQ ID NO: 130, SEQ ID NO: 132, SEQ ID NO: 134, SEQ ID NO: 136, SEQ ID NO: 138, SEQ ID NO: 140, SEQ ID NO: 142, SEQ ID NO: 143, SEQ ID NO: 146, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 152, SEQ ID NO: 154, SEQ ID NO: 156, SEQ ID NO: 158, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 166, SEQ ID NO: 168, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 174, SEQ ID NO: 176, SEQ ID NO: 178, SEQ ID NO: 180, SEQ ID NO: 182, SEQ ID NO: 184, SEQ ID NO: 186, SEQ ID NO: 188, SEQ ID NO: 190, SEQ ID NO: 192, SEQ ID NO: 194, SEQ ID NO: 196, SEQ ID NO: 198, SEQ ID NO: 200, SEQ ID NO: 202, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 208, SEQ ID NO: 210, SEQ ID NO: 212, SEQ ID NO: 214, SEQ ID NO: 216, SEQ ID NO: 218, SEQ ID NO: 220, SEQ ID NO: 222, SEQ ID NO: 224, SEQ ID NO: 226, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 232, SEQ ID NO: 234, SEQ ID NO: 236, SEQ ID NO: 238, SEQ ID NO: 240, SEQ ID NO: 242, SEQ ID NO: 244, SEQ ID NO: 246, SEQ ID NO: 248, SEQ ID NO: 250, SEQ ID NO: 252, SEQ ID NO: 254, SEQ ID NO: 256, SEQ ID NO: 258, SEQ ID NO: 260, SEQ ID NO: 262, SEQ ID NO: 264, SEQ ID NO: 266, SEQ ID NO: 268, SEQ ID NO: 270, SEQ ID NO: 272, SEQ ID NO: 274, SEQ ID NO: 276, SEQ ID NO: 278, SEQ ID NO: 280, SEQ ID NO: 282, SEQ ID NO: 284, SEQ ID NO: 286, SEQ ID NO: 288, SEQ ID NO: 290, SEQ ID NO: 292, SEQ ID NO: 294, SEQ ID NO: 296, SEQ ID NO: 298, SEQ ID NO: 300, SEQ ID NO: 302, SEQ ID NO: 304, SEQ ID NO: 306, SEQ ID NO: 308, SEQ ID NO: 310, SEQ ID NO: 312, SEQ ID NO: 314, SEQ ID NO: 316, SEQ ID NO: 318, SEQ ID NO: 320, SEQ ID NO: 322, SEQ ID NO: 324, SEQ ID NO: 326, SEQ ID NO: 328, SEQ ID NO: 330, SEQ ID NO: 332, SEQ ID NO: 334, SEQ ID NO: 336, SEQ ID NO: 338, SEQ ID NO: 340, SEQ ID NO: 342, SEQ ID NO: 344, SEQ ID NO: 346, SEQ ID NO: 348, SEQ ID NO: 350, SEQ ID NO: 352, SEQ ID NO: 354, SEQ ID NO: 356, SEQ ID NO: 358, SEQ ID NO: 360, SEQ ID NO: 362, SEQ ID NO: 364, SEQ ID NO: 366, SEQ ID NO: 368, SEQ ID NO: 370, SEQ ID NO: 372, SEQ ID NO: 374, SEQ ID NO: 376, SEQ ID NO: 378, SEQ ID NO: 380, SEQ ID NO: 382, SEQ ID NO: 384, SEQ ID NO: 386, SEQ ID NO: 388, SEQ ID NO: 390, SEQ ID NO: 392, SEQ ID NO: 394, SEQ ID NO: 396, SEQ ID NO: 398, SEQ ID NO: 400, SEQ ID NO: 402, SEQ ID NO: 404, SEQ ID NO: 406, SEQ ID NO: 408, SEQ ID NO: 410, SEQ ID NO: 412, SEQ ID NO: 414, SEQ ID NO: 416, SEQ ID NO: 418, SEQ ID NO: 420, SEQ ID NO: 422, SEQ ID NO: 424, SEQ ID NO: 426, SEQ ID NO: 428, SEQ ID NO: 430, SEQ ID NO: 432, SEQ ID NO: 434, SEQ ID NO: 436, SEQ ID NO: 438, SEQ ID NO: 440, SEQ ID NO: 442, SEQ ID NO: 444, SEQ ID NO: 446, SEQ ID NO: 448, SEQ ID NO: 450, SEQ ID NO: 452, SEQ ID NO: 454, SEQ ID NO: 456, SEQ ID NO: 458, SEQ ID NO: 460, SEQ ID NO: 462, SEQ ID NO: 464, SEQ ID NO: 466, SEQ ID NO: 468, SEQ ID NO: 470, SEQ ID NO: 472, SEQ ID NO: 474, SEQ ID NO: 476, SEQ ID NO: 478, SEQ ID NO: 480, SEQ ID NO: 482, SEQ ID NO: 484, SEQ ID NO: 486, SEQ ID NO: 488, SEQ ID NO: 490, SEQ ID NO: 492, SEQ ID NO: 494, SEQ ID NO: 496, SEQ ID NO: 498, SEQ ID NO: 500, SEQ ID NO: 502, SEQ ID NO: 504, SEQ ID NO: 506, SEQ ID NO: 508, SEQ ID NO: 510, SEQ ID NO: 512, SEQ ID NO: 514, SEQ ID NO: 516, SEQ ID NO: 518, SEQ ID NO: 520, SEQ ID NO: 522, SEQ ID NO: 524, SEQ ID NO: 526, SEQ ID NO: 528, SEQ ID NO: 530, SEQ ID NO: 532, SEQ ID NO: 534, SEQ ID NO: 536, SEQ ID NO: 538, SEQ ID NO: 540, SEQ ID NO: 542, SEQ ID NO: 544, SEQ ID NO: 546, SEQ ID NO: 548, SEQ ID NO: 550, SEQ ID NO: 552, SEQ ID NO: 554, SEQ ID NO: 556, SEQ ID NO: 558, SEQ ID NO: 560, SEQ ID NO: 562, SEQ ID NO: 564, SEQ ID NO: 566, SEQ ID NO: 568, SEQ ID NO: 570, SEQ ID NO: 572, SEQ ID NO: 574, SEQ ID NO: 576, SEQ ID NO: 578, SEQ ID NO: 580, SEQ ID NO: 582, SEQ ID NO: 584, SEQ ID NO: 586, SEQ ID NO: 588, SEQ ID NO: 590, SEQ ID NO: 592, SEQ ID NO: 594, SEQ ID NO: 596, SEQ ID NO: 598, SEQ ID NO: 600, SEQ ID NO: 602, SEQ ID NO: 604, SEQ ID NO: 606, SEQ ID NO: 608, SEQ ID NO: 610, SEQ ID NO: 612, SEQ ID NO: 614, SEQ ID NO: 616, SEQ ID NO: 618, SEQ ID NO: 620, SEQ ID NO: 622, SEQ ID NO: 624, SEQ ID NO: 626, SEQ ID NO: 628, SEQ ID NO: 630, SEQ ID NO: 632, SEQ ID NO: 634, SEQ ID NO: 636, SEQ ID NO: 638, SEQ ID NO: 640, SEQ ID NO: 642, SEQ ID NO: 644, SEQ ID NO: 646, SEQ ID NO: 648, SEQ ID NO: 650, SEQ ID NO: 652, SEQ ID NO: 654, SEQ ID NO: 656, SEQ ID NO: 658, SEQ ID NO: 660, SEQ ID NO: 662, SEQ ID NO: 664, SEQ ID NO: 666, SEQ ID NO: 668, SEQ ID NO: 670, SEQ ID NO: 672, SEQ ID NO: 674, SEQ ID NO: 676, SEQ ID NO: 678, SEQ ID NO: 680, SEQ ID NO: 682, SEQ ID NO: 684, SEQ ID NO: 686, SEQ ID NO: 688, SEQ ID NO: 690, SEQ ID NO: 692, SEQ ID NO: 694, SEQ ID NO: 696, SEQ ID NO: 698, SEQ ID NO: 700, SEQ ID NO: 702, SEQ ID NO: 704, SEQ ID NO: 706, SEQ ID NO: 708, SEQ ID NO: 710, SEQ ID NO: 712, SEQ ID NO: 714, SEQ ID NO: 716, SEQ ID NO: 718, SEQ ID NO: 720, SEQ ID NO: 722, SEQ ID NO: 724, SEQ ID NO: 726, SEQ ID NO: 728, SEQ ID NO: 730, SEQ ID NO: 732, SEQ ID NO: 734, SEQ ID NO: 736, SEQ ID NO: 738, SEQ ID NO: 740, SEQ ID NO: 742, SEQ ID NO: 744, SEQ ID NO: 746, SEQ ID NO: 748, SEQ ID NO: 750, SEQ ID NO: 752, SEQ ID NO: 754, SEQ ID NO: 756, SEQ ID NO: 758, SEQ ID NO: 760, SEQ ID NO: 762, SEQ ID NO: 764, SEQ ID NO: 766, SEQ ID NO: 768, SEQ ID NO: 770, SEQ ID NO: 772, SEQ ID NO: 774, SEQ ID NO: 776, SEQ ID NO: 778, SEQ ID NO: 780, SEQ ID NO: 782, SEQ ID NO: 784, SEQ ID NO: 786, SEQ ID NO: 788, SEQ ID NO: 790, SEQ ID NO: 792, SEQ ID NO: 794, SEQ ID NO : 796, SEQ ID NO: 798, SEQ ID NO: 800, SEQ ID NO: 802, SEQ ID NO: 804, SEQ ID NO: 806, SEQ ID NO: 808, SEQ ID NO: 810, SEQ ID NO: 812, SEQ ID NO: 814, SEQ ID NO: 816, SEQ ID NO: 818, SEQ ID NO: 820, SEQ ID NO: 822, SEQ ID NO: 824, SEQ ID NO: 826, SEQ ID NO: 828, SEQ ID NO: 830, SEQ ID NO: 832, SEQ ID NO: 834, SEQ ID NO: 836, SEQ ID NO: 838, SEQ ID NO: 840, SEQ ID NO: 842, SEQ ID NO: 844, SEQ ID NO: 846, SEQ ID NO: 848, SEQ ID NO: 850, SEQ ID NO: 852, SEQ ID NO: 854, SEQ ID NO: 856, SEQ ID NO: 858, SEQ ID NO: 860, SEQ ID NO: 862, SEQ ID NO: 864, SEQ ID NO: 866, SEQ ID NO: 868, SEQ ID NO: 870, SEQ ID NO: 872, SEQ ID NO: 874, SEQ ID NO: 876, SEQ ID NO: 878, SEQ ID NO: 880, SEQ ID NO: 882, SEQ ID NO: 884, SEQ ID NO: 886, SEQ ID NO: 888, SEQ ID NO: 890, SEQ ID NO: 892, SEQ ID NO: 894, SEQ ID NO: 896, SEQ ID NO: 898, SEQ ID NO: 900, SEQ ID NO: 902, SEQ ID NO: 904, SEQ ID NO: 906, SEQ ID NO: 908, SEQ ID NO: 910, SEQ ID NO: 912, SEQ ID NO: 914, SEQ ID NO: 916, SEQ ID NO: 918, SEQ ID NO: 920, SEQ ID NO: 922, SEQ ID NO: 924, SEQ ID NO: 926, SEQ ID NO: 928, SEQ ID NO: 930, SEQ ID NO: 932, SEQ ID NO: 934, SEQ ID NO: 936, SEQ ID NO: 938, SEQ ID NO: 940, SEQ ID NO: 942, SEQ ID NO: 944, SEQ ID NO: 946, SEQ ID NO: 948, SEQ ID NO: 950, SEQ ID NO: 952 or SEQ ID NO: 954 and the proteins encoded by the nucleic acid sequence hybridizing under stringent conditions to the complement of the sequence according to any one of SEQ ID NO: 955, SEQ ID NO: 1 , SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 1 1 , SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 19, SEQ ID NO: 21 , SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 27, SEQ ID NO: 29, SEQ ID NO: 31 , SEQ ID NO: 33, SEQ ID NO: 35, SEQ ID NO: 37, SEQ ID NO: 39, SEQ ID NO: 41 , SEQ ID NO: 43, SEQ ID NO: 45, SEQ ID NO: 47, SEQ ID NO: 49, SEQ ID NO: 51 , SEQ ID NO: 53, SEQ ID NO: 55, SEQ ID NO: 57, SEQ ID NO: 59, SEQ ID NO: 61 , SEQ ID NO: 63, SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 71 , SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 77, SEQ ID NO: 79, SEQ ID NO: 81 , SEQ ID NO: 83, SEQ ID NO: 85, SEQ ID NO: 87, SEQ ID NO: 89, SEQ ID NO: 91 , SEQ ID NO: 93, SEQ ID NO: 95, SEQ ID NO: 97, SEQ ID NO: 99, SEQ ID NO: 101 , SEQ ID NO: 103, SEQ ID NO: 105, SEQ ID NO: 107, SEQ ID NO: 109, SEQ ID NO: 11 1 , SEQ ID NO: 1 13, SEQ ID NO: 115, SEQ ID NO: 1 17, SEQ ID NO: 119, SEQ ID NO: 121 , SEQ ID NO: 123, SEQ ID NO: 125, SEQ ID NO: 127, SEQ ID NO: 129, SEQ ID NO: 131 , SEQ ID NO: 133, SEQ ID NO: 135, SEQ ID NO: 137, SEQ ID NO: 139, SEQ ID NO: 141 , SEQ ID NO: 143, SEQ ID NO: 145, SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 151 , SEQ ID NO: 153, SEQ ID NO: 155, SEQ ID NO: 157, SEQ ID NO: 159, SEQ ID NO: 161 , SEQ ID NO: 163, SEQ ID NO: 165, SEQ ID NO: 167, SEQ ID NO: 169, SEQ ID NO: 171 , SEQ ID NO: 173, SEQ ID NO: 175, SEQ ID NO: 177, SEQ ID NO: 179, SEQ ID NO: 181 , SEQ ID NO: 183, SEQ ID NO: 185, SEQ ID NO: 187, SEQ ID NO: 189, SEQ ID NO: 191 , SEQ ID NO: 193, SEQ ID NO: 195, SEQ ID NO: 197, SEQ ID NO: 199, SEQ ID NO: 201 , SEQ ID NO: 203, SEQ ID NO: 205, SEQ ID NO: 207, SEQ ID NO: 209, SEQ ID NO: 211 , SEQ ID NO: 213, SEQ ID NO: 215, SEQ ID NO: 217, SEQ ID NO: 219, SEQ ID NO: 221 , SEQ ID NO: 223, SEQ ID NO: 225, SEQ ID NO: 227, SEQ ID NO: 229, SEQ ID NO: 231 , SEQ ID NO: 233, SEQ ID NO: 235, SEQ ID NO: 237, SEQ ID NO: 239, SEQ ID NO: 241 , SEQ ID NO: 243, SEQ ID NO: 245, SEQ ID NO: 247, SEQ ID NO: 249, SEQ ID NO: 251 , SEQ ID NO: 253, SEQ ID NO: 255, SEQ ID NO: 257, SEQ ID NO: 259, SEQ ID NO: 261 , SEQ ID NO: 263, SEQ ID NO: 265, SEQ ID NO: 267, SEQ ID NO: 269, SEQ ID NO: 271 , SEQ ID NO: 273, SEQ ID NO: 275, SEQ ID NO: 277, SEQ ID NO: 279, SEQ ID NO: 281 , SEQ ID NO: 283, SEQ ID NO: 285, SEQ ID NO: 287, SEQ ID NO: 289, SEQ ID NO: 291 , SEQ ID NO: 293, SEQ ID NO: 295, SEQ ID NO: 297, SEQ ID NO: 299, SEQ ID NO: 301 , SEQ ID NO: 303, SEQ ID NO: 305, SEQ ID NO: 307, SEQ ID NO: 309, SEQ ID NO: 31 1 , SEQ ID NO: 313, SEQ ID NO: 315, SEQ ID NO: 317, SEQ ID NO: 319, SEQ ID NO: 321 , SEQ ID NO: 323, SEQ ID NO: 325, SEQ ID NO: 327, SEQ ID NO: 329, SEQ ID NO: 331 , SEQ ID NO: 333, SEQ ID NO: 335, SEQ ID NO: 337, SEQ ID NO: 339, SEQ ID NO: 341 , SEQ ID NO: 343, SEQ ID NO: 345, SEQ ID NO: 347, SEQ ID NO: 349, SEQ ID NO: 351 , SEQ ID NO: 353, SEQ ID NO: 355, SEQ ID NO: 357, SEQ ID NO: 359, SEQ ID NO: 361 , SEQ ID NO: 363, SEQ ID NO: 365, SEQ ID NO: 367, SEQ ID NO: 369, SEQ ID NO: 371 , SEQ ID NO: 373, SEQ ID NO: 375, SEQ ID NO: 377, SEQ ID NO: 379, SEQ ID NO: 381 , SEQ ID NO: 383, SEQ ID NO: 385, SEQ ID NO: 387, SEQ ID NO: 389, SEQ ID NO: 391 , SEQ ID NO: 393, SEQ ID NO: 395, SEQ ID NO: 397, SEQ ID NO: 399, SEQ ID NO: 401 , SEQ ID NO: 403, SEQ ID NO: 405, SEQ ID NO: 407, SEQ ID NO: 409, SEQ ID NO: 41 1 , SEQ ID NO: 413, SEQ ID NO: 415, SEQ ID NO: 417, SEQ ID NO: 419, SEQ ID NO: 421 , SEQ ID NO: 423, SEQ ID NO: 425, SEQ ID NO: 427, SEQ ID NO: 429, SEQ ID NO: 431 , SEQ ID NO: 433, SEQ ID NO: 435, SEQ ID NO: 437, SEQ ID NO: 439, SEQ ID NO: 441 , SEQ ID NO: 443, SEQ ID NO: 445, SEQ ID NO: 447, SEQ ID NO: 449, SEQ ID NO: 451 , SEQ ID NO: 453, SEQ ID NO: 455, SEQ ID NO: 457, SEQ ID NO: 459, SEQ ID NO: 461 , SEQ ID NO: 463, SEQ ID NO: 465, SEQ ID NO: 467, SEQ ID NO: 469, SEQ ID NO: 471 , SEQ ID NO: 473, SEQ ID NO: 475, SEQ ID NO: 477, SEQ ID. NO: 479, SEQ ID NO: 481 , SEQ ID NO: 483, SEQ ID NO: 485, SEQ ID NO: 487, SEQ ID NO: 489, SEQ ID NO: 491 , SEQ ID NO: 493, SEQ ID NO: 495, SEQ ID NO: 497, SEQ ID NO: 499, SEQ ID NO: 501 , SEQ ID NO: 503, SEQ ID NO: 505, SEQ ID NO: 507, SEQ ID NO: 509, SEQ ID NO: 51 1 , SEQ ID NO: 513, SEQ ID NO: 515, SEQ ID NO: 517, SEQ ID NO: 519, SEQ ID NO: 521 , SEQ ID NO: 523, SEQ ID NO: 525, SEQ ID NO: 527, SEQ ID NO: 529, SEQ ID NO: 531 , SEQ ID NO: 533, SEQ ID NO: 535, SEQ ID NO: 537, SEQ ID NO: 539, SEQ ID NO: 541 , SEQ ID NO: 543, SEQ ID NO: 545, SEQ ID NO: 547, SEQ ID NO: 549, SEQ ID NO: 551 , SEQ ID NO: 553, SEQ ID NO: 555, SEQ ID NO: 557, SEQ ID NO: 559, SEQ ID NO: 561 , SEQ ID NO: 563, SEQ ID NO: 565, SEQ ID NO: 567, SEQ ID NO: 569, SEQ ID NO: 571 , SEQ ID NO: 573, SEQ ID NO: 575, SEQ ID NO: 577, SEQ ID NO: 579, SEQ ID NO: 581 , SEQ ID NO: 583, SEQ ID NO: 585, SEQ ID NO: 587, SEQ ID NO: 589, SEQ ID NO: 591 , SEQ ID NO: 593, SEQ ID NO: 595, SEQ ID NO: 597, SEQ ID NO: 599, SEQ ID NO: 601 , SEQ ID NO: 603, SEQ ID NO: 605, SEQ ID NO: 607, SEQ ID NO: 609, SEQ ID NO: 61 1 , SEQ ID NO: 613, SEQ ID NO: 615, SEQ ID NO: 617, SEQ ID NO: 619, SEQ ID NO: 621 , SEQ ID NO: 623, SEQ ID NO: 625, SEQ ID NO: 627, SEQ ID NO: 629, SEQ ID NO: 631 , SEQ ID NO: 633, SEQ ID NO: 635, SEQ ID NO: 637, SEQ ID NO: 639, SEQ ID NO: 641 , SEQ ID NO: 643, SEQ ID NO: 645, SEQ ID NO: 647, SEQ ID NO: 649, SEQ ID NO: 651 , SEQ ID NO: 653, SEQ ID NO: 655, SEQ ID NO: 657, SEQ ID NO: 659, SEQ ID NO: 661 , SEQ ID NO: 663, SEQ ID NO: 665, SEQ ID NO: 667, SEQ ID NO: 669, SEQ ID NO: 671 , SEQ ID NO: 673, SEQ ID NO: 675, SEQ ID NO: 677, SEQ ID NO: 679, SEQ ID NO: 681 , SEQ ID NO: 683, SEQ ID NO: 685, SEQ ID NO: 687, SEQ ID NO: 689, SEQ ID NO: 691 , SEQ ID NO: 693, SEQ ID NO: 695, SEQ ID NO: 697, SEQ ID NO: 699, SEQ ID NO: 701 , SEQ ID NO: 703, SEQ ID NO: 705, SEQ ID NO: 707, SEQ ID NO: 709, SEQ ID NO: 71 1 , SEQ ID NO: 713, SEQ ID NO: 715, SEQ ID NO: 717, SEQ ID NO: 719, SEQ ID NO: 721 , SEQ ID NO: 723, SEQ ID NO: 725, SEQ ID NO: 727, SEQ ID NO: 729, SEQ ID NO: 731 , SEQ ID NO: 733, SEQ ID NO: 735, SEQ ID NO: 737, SEQ ID NO: 739, SEQ ID NO: 741 , SEQ ID NO: 743, SEQ ID NO: 745, SEQ ID NO: 747, SEQ ID NO: 749, SEQ ID NO: 751 , SEQ ID NO: 753, SEQ ID NO: 755, SEQ ID NO: 757, SEQ ID NO: 759, SEQ ID NO: 761 , SEQ ID NO: 763, SEQ ID NO: 765, SEQ ID NO : 767, SEQ ID NO : 769, SEQ ID NO : 771 , SEQ ID NO: 773, SEQ ID NO: 775, SEQ ID NO: 777, SEQ ID NO: 779, SEQ ID NO: 781 , SEQ ID NO: 783, SEQ ID NO: 785, SEQ ID NO: 787, SEQ ID NO: 789, SEQ ID NO: 791 , SEQ ID NO: 793, SEQ ID NO: 795, SEQ ID NO: 797, SEQ ID NO: 799, SEQ ID NO: 801 , SEQ ID NO: 803, SEQ ID NO: 805, SEQ ID NO: 807, SEQ ID NO: 809, SEQ ID NO: 81 1 , SEQ ID NO: 813, SEQ ID NO: 815, SEQ ID NO: 817, SEQ ID NO: 819, SEQ ID NO: 821 , SEQ ID NO: 823, SEQ ID NO: 825, SEQ ID NO: 827, SEQ ID NO: 829, SEQ ID NO: 831 , SEQ ID NO: 833, SEQ ID NO: 835, SEQ ID NO: 837, SEQ ID NO: 839, SEQ ID NO: 841 , SEQ ID NO: 843, SEQ ID NO: 845, SEQ ID NO: 847, SEQ ID NO: 849, SEQ ID NO: 851 , SEQ ID NO: 853, SEQ ID NO: 855, SEQ ID NO: 857, SEQ ID NO: 859, SEQ ID NO: 861 , SEQ ID NO: 863, SEQ ID NO: 865, SEQ ID NO: 867, SEQ ID NO: 869, SEQ ID NO: 871 , SEQ ID NO: 873, SEQ ID NO: 875, SEQ ID NO: 877, SEQ ID NO: 879, SEQ ID NO: 881 , SEQ ID NO: 883, SEQ ID NO: 885, SEQ ID NO: 887, SEQ ID NO: 889, SEQ ID NO: 891 , SEQ ID NO: 893, SEQ ID NO: 895, SEQ ID NO: 897, SEQ ID NO: 899, SEQ ID NO: 901 , SEQ ID NO: 903, SEQ ID NO: 905, SEQ ID NO: 907, SEQ ID NO: 909, SEQ ID NO: 91 1 , SEQ ID NO: 913, SEQ ID NO: 915, SEQ ID NO: 917, SEQ ID NO: 919, SEQ ID NO: 921 , SEQ ID NO: 923, SEQ ID NO: 925, SEQ ID NO: 927, SEQ ID NO: 929, SEQ ID NO: 931 , SEQ ID NO: 933, SEQ ID NO: 935, SEQ ID NO: 937, SEQ ID NO: 939, SEQ ID NO: 941 , SEQ ID NO: 943, SEQ ID NO: 945, SEQ ID NO: 947, SEQ ID NO: 949, SEQ ID NO: 951 or SEQ ID NO: 953 are called variants of this protein.
These variants have lipase activity, i.e. the ability to cleave a suitable lipid substrate. Preferably, the variants of the lipase have essentially the same lipase activity as the wild-type lipase char- acterized by any of the specific sequences disclosed herein, i.e. the activity of the variants is at least 50% or 60%, preferably at least 70% or 80%, more preferably 85% or 90% and most pref- erably at least 95% or 98% of the activity of the wild-type lipase characterized by the corre- sponding sequences according to any one of the specific sequences disclosed herein.
The activity of the variants can be compared with the activity of the corresponding wild-type li- pase by incubating the variant and the wild-type lipase with a suitable substrate under suitable conditions and detecting the amount of the cleavage products of the variant and the wild-type lipase. A suitable substrate for the lipase according to SEQ ID NO. 956 is osra-nitrophenyl pal- mitate ( >NPP) (Winkler and Stuckmann (1979) J. Bacteriol. 138: 663-670). Alternatively, an ol- ive oil emulsion may be used (Frenken et al. (1992) Appl. Environm. Microbiol. 58(12): 3787- 3791 ).
The lipase or an enzymatically active variant thereof as described herein is preferably recombi- nantly produced using a bacteria, fungi, or yeast expression system.“Expression system” also means a host microorganism, expression hosts, host cell, production organism, or production strain and each of these terms can be used interchangeably for this disclosure. Examples of expression systems include but are not limited to: Aspergillus niger, Aspergillus oryzae, Han- senula polymorpha, Thermomyces lanuginosus, Fusarium oxysporum, Fusarium heterosporum, Escherichia coH, Bacillus, preferably Bacillus subti/is, or Bacillus Hcheniformis, Pseudomonas, preferably Pseudomonas fluorescens, Pichia pastoris (also known as Komagataella phaffii), My- celiopthora thermophile ( C1 '), Schizosaccharomyces pombe, Trichoderma, preferably Tricho- derma reesei and Saccharomyces, preferably Saccharomyces cerevisiae. In an embodiment the lipase or an enzymatically active variant thereof as described herein is produced using one of the expression systems listed above. Suitable vectors for expressing the lipase and cultivation con- ditions for producing the lipase are known to the skilled person.
The lipase or an enzymatically active variant thereof as described herein may be isolated from the host microorganism by well-known methods including centrifugation and filtration which re- move most of the host cell components. If a higher degree of purity is desired, the lipase may be subjected to further purification steps such as anion or cation exchange chromatography, hy- drophobic interaction chromatography, mixed mode chromatography or hydroxyapatite chroma- tography. The isolated lipase may be used directly or it may be subjected to a drying step such as a spray-drying step. If the isolated lipase is dried, e.g. spray-dried or lyophilized, it has to be dissolved in a suitable solvent, before it is applied to the soil.
The lipase or an enzymatically active variant thereof as described above may be used in combi- nation with another enzyme which may be useful in reducing soil water repellency or enhancing water holding capacity. This other enzyme may be selected from the group consisting of amyl- ases, cellulases, chitinases, esterases, beta-glucosidases, laccases, pectinases, proteases and xylanases. Preferably, the lipase or a variant thereof is used in combination with a chitinase, a laccase, a pectinase and/or a protease. The chitinase may be from Streptomyces griseus. The laccase may be from Pycnoporus sp. SYBC-L3. The pectinase may be from Aspergillus niger and the protease may be from Aspergillus oryzae.
The lipase may be used in a composition with at least one auxiliary. The at least one auxiliary may be a liquid carrier which may be selected from the group of water and organic solvents.
The at least one auxiliary may be a solid carrier selected from the group of phytogels, hydro- gels, mineral earths, meal, cellulose powder, fumed silica or precipitated silica, polysaccharides, or compost.
The lipase may be used in combination with at least one soil additive. The soil additive may be selected from the group consisting of surfactants, fertilizers, nitrification inhibitors and/or pesti- cides.
"Surfactant" (synonymously used herein with“surface active agent” and "wetting agent") means an organic chemical that, when added to a liquid, changes the properties of that liquid at an in- terface. According to its ionic charge, a surfactant is called non-ionic, anionic, cationic, or am- photeric. Other examples of surfactants include block polymers and polyelectrolytes. Non-limiting examples of surfactants are disclosed McCutcheon's 2016 Detergents and Emulsi fiers, and McCutcheon's 2016 Functional Materials, both North American and International Edi- tion, MC Publishing Co, 2016 edition. Further useful examples are disclosed in earlier editions of the same publications which are known to those skilled in the art.
Non-ionic surfactant means a surfactant that contains neither positively nor negatively charged (i.e. ionic) functional groups. In contrast to anionic and cationic surfactants, non-ionic surfac- tants do not ionize in solution. Mixtures of two or more different non-ionic surfactants may also be used. Examples provided below for surfactants of any kind are to be understood to be non- limiting.
Non-ionic surfactants may be compounds of the general formulae (la) and (lb):
Figure imgf000048_0001
The variables of the general formulae (la) and (lb) are defined as follows:
R1 is selected from C1-C23 alkyl and C2-C23 alkenyl, wherein alkyl and/or alkenyl are linear or branched; examples are n-C7Hi5, n-CgH-ig, n-CnH23, n-Ci3H27, n-C-isHs-i, n-C F s, i-CgH-ig, i- C12H25.
R2 is selected from H, C1-C20 alkyl and C2-C20 alkenyl, wherein alkyl and/or alkenyl are linear or branched.
R3 and R4, each independently selected from C1-C16 alkyl, wherein alkyl is linear or branched; examples are methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, sec-pentyl, neopentyl, 1 ,2-dimethylpropyl, isoamyl, n-hexyl, isohexyl, sec-hexyl, n- heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl, isodecyl.
R5 is selected from H and C1-C18 alkyl, wherein alkyl is linear or branched.
The integers of the general formulae (la) and (lb) are defined as follows:
m is in the range of zero to 200, preferably 1 -80, more preferably 3-20; n and o, each inde- pendently in the range of zero to 100; n preferably is in the range of 1 to 10, more preferably 1 to 6; o preferably is in the range of 1 to 50, more preferably 4 to 25. The sum of m, n and o is at least one, preferably the sum of m, n and o is in the range of 5 to 100, more preferably in the range of from 9 to 50.
The non-ionic surfactants of the general formula (I) may be of any structure, is it block or ran- dom structure, and is not limited to the displayed sequence of formula (I). Non-ionic surfactants may further be compounds of the general formula (II), which might be called alkyl-polyglycosides (APG):
Figure imgf000049_0001
The variables of the general formula (II) are defined as follows:
R1 is selected from C1-C17 alkyl and C2-C17 alkenyl, wherein alkyl and/or alkenyl are linear or branched; examples are n-C7Hi5, n-CgH-ig, n-CnH23, n-Ci3H27, n-CisH3i, n-C^Hss, i-CgH-ig, i- C12H25.
R2 is selected from H, C1-C17 alkyl and C2-C17 alkenyl, wherein alkyl and/or alkenyl are linear or branched.
G1 is selected from monosaccharides with 4 to 6 carbon atoms, such as glucose and xylose. The integer w of the general formula (II) is in the range of from 1.1 to 4, w being an average number.
Non-ionic surfactants may further be compounds of general formula (III):
Figure imgf000049_0002
The variables of the general formula (III) are defined as follows:
AO is selected from ethylene oxide (EO), propylene oxide (PO), butylene oxide (BO), and mix- tures thereof.
R6 is selected from C5-C17 alkyl and C5-C17 alkenyl, wherein alkyl and/or alkenyl are linear or branched.
R7 is selected from H, Ci-Cie-alkyl, wherein alkyl is linear or branched.
The integer y of the general formula (III) is a number in the range of 1 to 70, preferably 7 to 15. Non-ionic surfactants may further be selected from sorbitan esters and/or ethoxylated or propoxylated sorbitan esters. Non-limiting examples are products sold under the trade names
SPAN and TWEEN.
Non-ionic surfactants may further be selected from alkoxylated mono- or di-alkylamines, fatty acid monoethanolamides (FAMA), fatty acid diethanolamides (FADA), ethoxylated fatty acid monoethanolamides (EFAM), propoxylated fatty acid monoethanolamides (PFAM), polyhydroxy alkyl fatty acid amides, or N-acyl N-alkyl derivatives of glucosamine (glucamides, GA, or fatty acid glucamide, FAGA), and combinations thereof.
Amphoteric surfactants are those, depending on pH, which can be either cationic, zwitterionic or anionic. Mixtures of two or more different amphoteric surfactants may also be used. Surfactants may be compounds comprising amphoteric structures of general formula (IV), which might be called modified amino acids (proteinogenic as well as non-proteinogenic):
Figure imgf000050_0001
The variables in general formula (IV) are defined as follows:
R8 is selected from H, C1-C4 alkyl, C2-C4 alkenyl, wherein alkyl and/or are linear or branched.
R9 is selected from C1-C22- alkyl, C2-C22- alkenyl, C10-C22 alkylcarbonyl, and C10-C22 alkenylcar- bonyl.
R10 is selected from H, methyl, -(CH2)3NHC(NH)NH2, -CH2C(0)NH2, -CH2C(0)0H, - (CH2)2C(0)NH2, -(CH2)2C(0)0H, (imidazole-4-yl)-methyl, -CH(CH3)C2H5, -CH2CH(CH3)2, - (CH2)4NH2, benzyl, hydroxymethyl, -CH(OH)CH3, (indole-3-yl)-methyl, (4-hydroxy-phenyl)-me- thyl, isopropyl, -(CH2)2SCH3, and -CH2SH.
Rx is selected from H and Ci-C4-alkyl.
Surfactants may further be compounds comprising amphoteric structures of general formulae (Va), (Vb), or (Vc), which might be called betaines and/or sulfobetaines:
Figure imgf000050_0003
The variables in general formulae (Va), (Vb) and (Vc) are defined as follows:
R11 is selected from linear or branched C7-C22 alkyl and linear or branched C7-C22 alkenyl. R12 are each independently selected from linear C1-C4 alkyl.
R13 is selected from C1-C5 alkyl and hydroxy C1-C5 alkyl; for example 2-hydroxypropyl.
A- is selected from carboxylate and sulfonate.
The integer r in general formulae (Va), (Vb), and (Vc) is in the range of 2 to 6.
Surfactants may further be compounds comprising amphoteric structures of general formula (VI), which might be called alkyl-amphocarboxylates:
Figure imgf000050_0002
The variables in general formula (VI) are defined as follows:
R11 is selected from C7-C22 alkyl and C7-C22 alkenyl, wherein alkyl and/or alkenyl are linear or branched, preferably linear. R14 is selected from -CH2C(0)0-M+, -CH2CH2C(0)0-M+ and -CH2CH(0H)CH2S03-M+.
R15 is selected from H and -CH2C(0)O
The integer r in general formula (VI) is in the range of 2 to 6.
Non-limiting examples of further suitable alkyl-amphocarboxylates include sodium cocoampho- acetate, sodium lauroamphoacetate, sodium capryloamphoacetate, disodium cocoamphodiace- tate, disodium lauroamphodiacetate, disodium caprylamphodiacetate, disodium capryloam- phodiacetate, disodium cocoamphodipropionate, disodium lauroamphodipropionate, disodium caprylamphodipropionate, and disodium capryloamphodipropionate.
Surfactants may further be compounds comprising amphoteric structures of general formula (VII), which might be called amine oxides (AO):
Figure imgf000051_0001
The variables in general formula (VII) are defined as follows:
R16 is selected from Cs-C-is linear or branched alkyl, hydroxy Cs-C-is alkyl, acylamidopropoyl and C8-C18 alkyl phenyl group; wherein alkyl and/or alkenyl are linear or branched.
R17 is selected from C2-C3 alkylene, hydroxy C2-C3 alkylene, and mixtures thereof.
R18: each residue can be independently selected from Ci-C3 alkyl and hydroxy Ci-C3; R15 groups can be attached to each other, e.g., through an oxygen or nitrogen atom, to form a ring structure.
The integer x in general formula (VII) is in the range of 0 to 5, preferably from 0 to 3, most pref- erably 0.
Non-limiting examples of further suitable amine oxides include C10-C18 alkyl dimethyl amine ox- ides and C8-C18 alkoxy ethyl dihydroxyethyl amine oxides. Examples of such materials include dimethyloctyl amine oxide, diethyldecyl amine oxide, bis-(2-hydroxyethyl)dodecyl amine oxide, dimethyldodecylamine oxide, dipropyltetradecyl amine oxide, methylethylhexadecyl amine ox ide, dodecylamidopropyl dimethyl amine oxide, cetyl dimethyl amine oxide, stearyl dimethyl amine oxide, tallow dimethyl amine oxide and dimethyl-2-hydroxyoctadecyl amine oxide. A fur- ther example of a suitable amine oxide is cocamidylpropyl dimethylaminoxide, sometimes also called cocamidopropylamine oxide.
Anionic surfactant means a surfactant with a negatively charged ionic group. Anionic surfactants include, but are not limited to, surface-active compounds that contain a hydrophobic group and at least one water-solubilizing anionic group, usually selected from sulfates, sulfonate, and car- boxylates to form a water-soluble compound. Mixtures of two or more different anionic surfac- tants may also be used. Mixtures of non-ionic and/or amphoteric and/or anionic surfactants may also be used.
Anionic surfactants may be compounds of general formula (VIII), which might be called (fatty) alcohol/alkyl (ethoxy/ether) sulfates [(F)A(E)S] when A- is S03-, (fatty) alcohol/alkyl (eth- oxy/ether) carboxylate [(F)A(E)C] when A- is -RCOO:
Figure imgf000052_0001
(VI I lb)
The variables in general formulae (Villa and Vlllb) are defined as follows:
R1 is selected from Ci-C23-alkyl (such as 1 -, 2-, 3-, 4- Ci-C23-alkyl) and C2-C23-alkenyl, wherein alkyl and/or alkenyl are linear or branched, and wherein 2-, 3-, or 4-alkyl; examples are n-CzHis, n-CgH-ig, n-CnH23, n-Ci3H27, n-CisH3i, n-C-^Ftas, i-CgH-ig, i-Ci2H25.
R2 is selected from H, Ci-C2o-alkyl and C2-C2o-alkenyl, wherein alkyl and/or alkenyl are linear or branched.
R3 and R4, each independently selected from Ci-Ci6-alkyl, wherein alkyl is linear or branched; examples are methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, sec-pentyl, neopentyl, 1 ,2-dimethylpropyl, isoamyl, n-hexyl, isohexyl, sec-hexyl, n- heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl, isodecyl.
A- is selected from -RCOO, -SO3 and RSO3 , wherein R is selected from linear or branched C1- Ce-alkyl, and C1-C4 hydroxyalkyl, wherein alkyl is.
M+ is selected from H and salt forming cations. Salt forming cations may be monovalent or multi- valent; hence M+ equals 1/v Mv+. Examples include but are not limited to sodium, potassium, magnesium, calcium, ammonium, and the ammonium salt of mono-, di, and triethanolamine.
The integers of the general formulae (Villa) and (Vlllb) are defined as follows:
m is in the range of zero to 200, preferably 1 -80, more preferably 3-20; n and o, each inde- pendently in the range of zero to 100; n preferably is in the range of 1 to 10, more preferably 1 to 6; o preferably is in the range of 1 to 50, more preferably 4 to 25. The sum of m, n and o is at least one, preferably the sum of m, n and o is in the range of 5 to 100, more preferably in the range of from 9 to 50.
Anionic surfactants of the general formula (VIII) may be of any structure, block copolymers or random copolymers.
Further suitable anionic surfactants include salts (M+) of C12-C18 sulfo fatty acid alkyl esters (such as C12-C18 sulfo fatty acid methyl esters), Cio-C-i8-alkylarylsulfonic acids (such as n-C-io- Cis-alkylbenzene sulfonic acids) and C10-C18 alkyl alkoxy carboxylates.
M+ in all cases is selected from salt forming cations. Salt forming cations may be monovalent or multivalent; hence M+ equals 1/v Mv+. Examples include but are not limited to sodium, potas- sium, magnesium, calcium, ammonium, and the ammonium salt of mono-, di, and triethanola- mine. Non-limiting examples of further suitable anionic surfactants include branched alkylbenzenesul- fonates (BABS), phenylalkanesulfonates, alpha-olefinsulfonates (AOS), olefin sulfonates, al- kene sulfonates, alkane-2, 3-diylbis(sulfates), hydroxyalkanesulfonates and disulfonates, sec- ondary alkanesulfonates (SAS), paraffin sulfonates (PS), sulfonated fatty acid glycerol esters, alkyl- or alkenylsuccinic acid, fatty acid derivatives of amino acids, diesters and monoesters of sulfo-succinic acid.
Anionic surfactants may be compounds of general formula (IX), which might be called N-acyl amino acid surfactants:
Figure imgf000053_0001
The variables in general formula (IX) are defined as follows:
R19 is selected from linear or branched C6-C22-alkyl and linear or branched C6-C22-alkenyl such as oleyl.
R20 is selected from H and Ci-C4-alkyl.
R21 is selected from H, methyl, -(CH2)3NHC(NH)NH2, -CH2C(0)NH2, -CH2C(0)0H, - (CH2)2C(0)NH2, -(CH2)2C(0)0H, (imidazole-4-yl)-methyl, -CH(CH3)C2H5, -CH2CH(CH3)2, - (CH2)4NH2, benzyl, hydroxymethyl, -CH(OH)CH3, (indole-3-yl)-methyl, (4-hydroxy-phenyl)-me- thyl, isopropyl, -(CH2)2SCH3, and -CH2SH.
R22 is selected from -COOX and -CH2S03X, wherein X is selected from Li+, Na+ and K+.
Non-limiting examples of suitable N-acyl amino acid surfactants are the mono- and di-carbox- ylate salts (e.g., sodium, potassium, ammonium and ammonium salt of mono-, di, and triethano- lamine) of N-acylated glutamic acid, for example, sodium cocoyl glutamate, sodium lauroyl glu tamate, sodium myristoyl glutamate, sodium palmitoyl glutamate, sodium stearoyl glutamate, disodium cocoyl glutamate, disodium stearoyl glutamate, potassium cocoyl glutamate, potas- sium lauroyl glutamate, and potassium myristoyl glutamate; the carboxylate salts (e.g., sodium, potassium, ammonium and ammonium salt of mono-, di, and triethanolamine) of N-acylated ala- nine, for example, sodium cocoyl alaninate, and triethanolamine lauroyl alaninate; the carbox- ylate salts (e.g., sodium, potassium, ammonium and ammonium salt of mono-, di, and triethano- lamine) of N-acylated glycine, for example, sodium cocoyl glycinate, and potassium cocoyl glycinate; the carboxylate salts (e.g., sodium, potassium, ammonium and ammonium salt of mono-, di, and triethanolamine) of N-acylated sarcosine, for example, sodium lauroyl sar- cosinate, sodium cocoyl sarcosinate, sodium myristoyl sarcosinate, sodium oleoyl sarcosinate, and ammonium lauroyl sarcosinate.
Anionic surfactants may further be selected from the group of soaps. Suitable are salts (M+) of saturated and unsaturated C12-C18 fatty acids, such as lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, oleic acid, (hydrated) erucic acid. M+ is selected from salt forming cat- ions. Salt forming cations may be monovalent or multivalent; hence M+ equals 1/v Mv+. Exam- pies include but are not limited to sodium, potassium, magnesium, calcium, ammonium, and the ammonium salt of mono-, di, and triethanolamine. Further non-limiting examples of suitable soaps include soap mixtures derived from natural fatty acids such as tallow, coconut oil, palm kernel oil, laurel oil, olive oil, or canola oil. Such soap mixtures comprise soaps of lauric acid and/or myristic acid and/or palmitic acid and/or stearic acid and/or oleic acid and/or linoleic acid in different amounts, depending on the natural fatty ac- ids from which the soaps are derived.
Further non-limiting examples of suitable anionic surfactants include salts (M+) of sulfates, sul- fonates or carboxylates derived from natural fatty acids such as tallow, coconut oil, palm kernel oil, laurel oil, olive oil, or canola oil. Such anionic surfactants comprise sulfates, sulfonates or carboxylates of lauric acid and/or myristic acid and/or palmitic acid and/or stearic acid and/or oleic acid and/or linoleic acid in different amounts, depending on the natural fatty acids from which the soaps are derived.
Cationic surfactant means a surfactant with a positively charged ionic group. Typically, these cationic moieties are nitrogen containing groups such as quaternary ammonium or protonated amino groups. The cationic protonated amines can be primary, secondary, or tertiary amines.
Cationic surfactants may be compounds of the general formula (X) which might be called qua- ternary ammonium compounds (quats):
Figure imgf000054_0001
The variables in general formula (X) are defined as follows:
R23 is selected from H, C1-C4 alkyl (such as methyl) and C2-C4 alkenyl, wherein alkyl and/or alkenyl is linear or branched.
R24 is selected from C1-C4 alkyl (such as methyl), C2-C4 alkenyl and C1-C4 hydroxyalkyl (such as hydroxyethyl), wherein alkyl and/or alkenyl is linear or branched.
R25 is selected from C1-C22 alkyl (such as methyl, C18 alkyl), C2-C4 alkenyl, C12-C22 alkylcarbon- yloxymethyl and C12-C22 alkylcarbonyloxyethyl (such as C16-C18 alkylcarbonyloxyethyl), wherein alkyl and/or alkenyl is linear or branched.
R26 is selected from C12-C18 alkyl, C2-C4 alkenyl, C12-C22 alkylcarbonyloxymethyl, C12-C22 alkyl- carbonyloxyethyl and 3-(Ci2-C22 alkylcarbonyloxy)-2(Ci2-C22 alkylcarbonyloxy)-propyl.
X is selected from halogenid, such as Ch or Br.
Non-limiting examples of further cationic surfactants include, amines such as primary, second- ary and tertiary monoamines with C18 alkyl or alkenyl chains, ethoxylated alkylamines, alkox- ylates of ethylenediamine, imidazoles (such as 1-(2-hydroxyethyl)-2-imidazoline, 2-alkyl-1-(2- hydroxyethyl)-2-imidazoline, and the like), quaternary ammonium salts like alkylquaternary am- monium chloride surfactants such as n-alkyl(Ci2-Ci8)dimethylbenzyl ammonium chloride, n- tetradecyldimethylbenzylammonium chloride monohydrate, and a naphthylene-substituted qua- ternary ammonium chloride such as dimethyl-1 -naphthylmethylammonium chloride.
Particularly suitable cationic surfactants that may be:
N,N-dimethyl-N-(hydroxy-C7-C25-alkyl)ammonium salts;
mono- and di(C7-C25-alkyl)dimethylammonium compounds quaternized with alkylat- ing agents; ester quats, in particular quaternary esterified mono-, di- and trialkanolamines which are esterified with C8-C22-carboxylic acids;
imidazoline quats, in particular 1-alkylimidazolinium salts of formulae XI or XII
Figure imgf000055_0001
The variables in formulae (XI) and (XII) are defined as follows:
R27 is selected from Ci-C25-alkyl and C2-C25-alkenyl;
R28 is selected from Ci-C4-alkyl and hydroxy-Ci-C4-alkyl;
R29 is selected from Ci-C4-alkyl, hydroxy-Ci -Chalky I and a R*-(CO)-R30-(CH2)r radical, wherein R* is selected from Ci-C2i-alkyl and C2-C2i-alkenyl; R30 is selected from-O- and -NH-; j is 2 or 3.
Suitable block polymers are block polymers of the A-B or A-B-A type comprising blocks of poly- ethylene oxide and polypropylene oxide or higher alkylene oxide or of the A-B-C type compris- ing alkanol, polyethylene oxide and polypropylene oxide or higher alkylene oxide. Preferably, the surfactant is an ethylene oxide-propylene oxide block copolymer (EO/PO) or a blend of alkyl polyglycoside and ethylene oxide-propylene oxide block copolymer (APG-EO/PO). Such surfac- tants are marketed as ACA 1853 (EO/PO) and ACA 1848 (APG-EO/PO), respectively.
Suitable polyelectrolytes are polyacids or polybases. Examples of polyacids are alkali salts of polyacrylic acid or polyacid comb polymers. Examples of polybases are polyvinylamines or poly- ethyleneamines.
Several surfactants are commercially available for reducing soil water repellency. These in- clude, but are not limited to, Kick® (available from Compo), Clearing (available from Collier Turf Care), Primer®604 (available from Plant Products) and Aqueduct®, Revolution®, ACA 1853 and ACA 1848 (all available from Aquatrols).
In a preferred embodiment the surfactant comprises a block polymer (P) comprising at least one polyethyleneoxide moiety and at least one polypropyleneoxide moiety, an alcohol alkoxylate (E) and/or an alcohol ethoxylate (L) of the general formula (XIII)
R3-0-(C2H40)s-H (XIII) wherein R3 is linear or branched Cs to C20 alkyl, and
s has a value of from 1 to 40.
The block polymer (P) is preferably a triblock polymer comprising one polyethyleneoxide moiety and two polypropyleneoxide moieties, or two polyethyleneoxide moieties and one polypropylene- oxide moiety. In another preferred embodiment, the block polymer (P) is a pentablock polymer comprising two polyethyleneoxide moieties and three polypropyleneoxide moieties, or three polyethyleneoxide moieties and two polypropyleneoxide moieties.
In another preferred embodiment, the block polymer (P) comprises
A1.1) a (EO-PO-EO) triblock polymer of the general formula (Q1 )
H0(CH2-CH20HCH(CH3)-CH20]g-(CH2-CH20)h-H (Q1 ) wherein f, g and h may denote the degree of polymerization and thus determine the mo- lecular weight,
and/or
A1.2) a (EO-PO-EO-PO-EO) pentablock polymer of the general formula (Q2)
H0(CH2-CH20)a-[CH(CH3)-CH20]b-(CH2-CH20)c-[CH(CH3)-CH20]d-(CH2-CH20)e-H
(Q2) wherein a, b, c, d and e may denote the degree of polymerization and thus determine the molecular weight.
In a particularly preferred embodiment, the block polymer (P) is or comprises a polyethyleneox- ide polypropyleneoxide polyethyleneoxide (EO-PO-EO) triblock polymer. The polypropyleneox- ide moiety in the EO-PO-EO triblock polymer may have a molar mass of 250 to 5000 g/mol, preferably from 400 to 3000 g/mol, and in particular from 600 to 1500 g/mol. The EO-PO-EO triblock polymer may contain 3 to 90 mol%, preferably 25 to 85 mol%, and in particular 50 to 80 mol% of the polypropyleneoxide moiety.
In a particularly preferred embodiment, the block polymer (P) is or comprises a polyethyleneox- ide polypropyleneoxide polyethyleneoxide polypropyleneoxide polyethyleneoxide (EO-PO-EO- PO-EO) pentablock polymer. The polypropyleneoxide moiety in the EO-PO-EO-PO-EO pen- tablock polymer may have a molar mass of 500 to 5000 g/mol, preferably from 750 to 3500 g/mol, and in particular from 1000 to 2500 g/mol. The EO-PO-EO triblock polymer may contain 3 to 90 mol%, preferably 25 to 80 mol%, and in particular 50 to 70 mol% of the polypropylene- oxide moiety.
The alcohol alkoxylate (E) is selected in particular among alcohol alkoxylates of the formula (XIV)
R-0-(CmH2m0)x-(CnH2n0)y-(CpH2p0)z-H (XIV) in which
R is branched C5-C3o-alkyl; m, n, p independently of one another are an integer from 2 to 16, preferably 2, 3, 4 or 5;
x+y+z have a value of 1 to 100.
In an especially preferred embodiment, m is 2, x is from 5.0 to 5.5, n = 3, y is from 4.5 to 5.0, p =2, and z is from 2 to 2.5.
In accordance with a particular embodiment, alcohol alkoxylates of the formula (I) are used in which m=2 and the value of x is greater than 0. These are alcohol alkoxylates of the EO type, which include mainly alcohol ethoxylates (m=2; x>0; y, z=0) and alcohol alkoxylates with an EO block bonded to the alcohol moiety (m=2; x>0; y and/or z>0). Substances which must be men- tioned among the alcohol alkoxylates with an EO block bonded to the alcohol moiety are mainly EO/PO block alkoxylates (m=2; x>0; y>0; n=3; z=0), and EO/PO/EO block alkoxylates (m, p=2; x, z>0; y>0; n=3).
Preferred substances are EO/PO block alcohol alkoxylates in which the EO:PO ratio is 1 : 1 to 4:1 , in particular 1.3:1 to 3:1. In this context, the degree of ethoxylation is, as a rule, 1 to 20, preferably 2 to 15, in particular 4 to 10, and the degree of propoxylation is, as a rule, 1 to 20, preferably 1 to 8, in particular 2 to 6. The total degree of alkoxylation, i.e. the total of EO and PO units, is, as a rule, 2 to 40, preferably 3.to 25, in particular 6 to 15.
In accordance with a further particular embodiment, alcohol alkoxylates of the formula (I) are used in which n=2, the values of x and y are both greater than 0 and z=0. Again, these alcohol alkoxylates take the form of the EO type, with the EO block being bonded terminally, however. These include mainly PO/EO block alcohol alkoxylates (n=2; x>0; y>0; m=3; z=0).
Preferred PO/EO block alcohol alkoxylates are those in which the PO:EO ratio is 1 :10 to 3:1 , in particular 1 :6 to 1.5:1. In this context, the degree of ethoxylation is, as a rule, 1 to 20, preferably 2 to 15, in particular 4 to 10, and the degree of propoxylation is, as a rule, 0.5 to 10, preferably 0.5 to 8, in particular 1 to 6. The total degree of alkoxylation, i.e. the total of EO and PO units given as an average number, is, as a rule, 1.5 to 30, preferably 2.5 to 21 , in particular 5 to 16.
In accordance with a preferred embodiment, the alcohol alkoxylates (E) are based on primary, alpha-branched alcohols of the general formula (XV)
Figure imgf000057_0001
in which
R1, R2 independently of one another are hydrogen or Ci-C26-alkyl.
Preferably, R1 and R2 independently of one another are Ci-C6-alkyl, in particular C2-C4-alkyl, for example C3-alkyl. Very especially preferred are alcohol alkoxylates which are based on 2-propylheptanol. These include, in particular, alcohol alkoxylates of the formula (XIV) in which R is a 2-propylheptyl radi cal, i.e. R1 and R2 in formula (XV) are in each case n-propyl.
Such alcohols are also referred to as Guerbet alcohols. They can be obtained for example by dimerization of corresponding primary alcohols (for example R1·2 CH2CH20H) at elevated tem- perature, for example 180 to 300°C, in the presence of an alkaline condensing agent such as potassium hydroxide.
Alkoxylates which are employed for the purposes of this preferred embodiment, which is based on Guebert alcohols, are mainly alkoxylates of the EO type. Particularly preferred are ethox- ylates with a degree of ethoxylation of 1 to 50, preferably 2 to 20, in particular approximately 3 to 10. The correspondingly ethoxylated 2-propylheptanols may be mentioned especially among these.
In accordance with a further preferred embodiment, the alcohol alkoxylates to be used are based on C13-oxo alcohols.
As a rule, the term "C13-oxo alcohol" refers to an alcohol mixture whose main component is formed by at least one branched C13-alcohol (isotridecanol). Such C13-alcohols include, in par- ticular, tetramethylnonanols, for example 2,4,6,8-tetramethyM -nonanol or 3,4,6,8-tetramethyM - nonanol and furthermore ethyldimethylnonanols such as 5-ethyl-4,7-dimethyl-1 -nonanol.
Suitable C13-alcohol mixtures can generally be obtained by hydrogenation of hydroformylated trimeric butane, as described in US2005/0170968. In particular, it is possible to proceed as fol- lows:
a) butenes are brought into contact with a suitable catalyst for oligomerization,
b) a C12-olefin fraction is isolated from the reaction mixture,
c) the C12-olefin fraction is hydroformylated by reacton with carbon monoxide and hydrogen in the presence of a suitable catalyst, and
d) hydrogenated.
Advantageous C13-alcohol mixtures are essentially free from halogens, i.e. they contain less than 3 ppm by weight, in particular less than 1 ppm by weight, of halogen, in particular chlorine.
Further suitable C13-alcohol mixtures can be obtained by proceeding as follows:
a) subjecting a C4-olefin mixture to metathesis,
b) separating olefins having 6 C atoms from the metathesis mixture,
c) subjecting the olefins which have been separated off, individually or as a mixture, to a dimeri- zation to give olefins mixtures having 12 C atoms, and
d) subjecting the resulting olefin mixture, if appropriate after fractionation, to derivatization to give a C13-oxo alcohol mixture. The alcohol alkoxylates (E) may have an average molecular weight of preferably at least 200 g/mol, more preferably at least 300 g/mol, most preferably at least 400 g/mol, particularly prefer- ably at least 500 g/mol, particularly more preferably at least 600 g/mol, particularly most prefera- bly at least 650 g/mol. The alcohol alkoxylates (E) may have an average molecular weight of preferably up to 10000 g/mol, more preferably up to 5000 g/mol, most preferably up to 3000 g/mol, particularly preferably up to 2000 g/mol, particularly more preferably up to 1500 g/mol, particularly most preferably up to 1200 g/mol, particularly up to 1000 g/mol, for example up to 850 g/mol. The alcohol alkoxylates (E) may have an average molecular weight of from 300 to 2000 g/mol, preferably from 400 to 1000 g/mol, and particularly from 650 to 850 g/mol.
In another embodiment, an alcohol ethoxylate (L) of the general formula (XIII)
R3-0-(C2H40)s-H (XIII) wherein R3 is linear or branched Cs to C20 alkyl, and
s has a value of from 1 to 40
may be used.
In the formula (XIII) of the alcohol ethoxylate (L), R3 is preferably branched C10 to C15 alkyl, more preferably branched C12 to C14 alkyl, most preferably isotridecyl.
In the formula (XIII) of the alcohol ethoxylate (L), s has a value of from 1 to 40, preferably 2 to 30, more preferably 3 to 20, most preferably 4 to 15, particularly preferably 5 to 10, particularly preferably 7 to 9, for example 8.
Suitable C13-alcohol mixtures, for example isotridecanol mixtures, as precursor for alcohol eth- oxylate (L), can generally be obtained by hydrogenation of hydroformylated trimeric butene. In particular, it is possible to proceed as follows:
a) butenes are brought into contact with a suitable catalyst for oligomerization,
b) a C12-olefin fraction is isolated from the reaction mixture,
c) the C12-olefin fraction is hydroformylated by reacton with carbon monoxide and hydrogen in the presence of a suitable catalyst, and
d) hydrogenated.
The synthesis of alcohol ethoxylates (L) is also described in US2005/170968.
As a rule, C13-alcohol mixtures, for example isotridecanol mixtures, as precursor for alcohol ethoxylate (L), have a mean degree of branching of from 1 to 4, preferably from 2 to 3, in partic- ular from 2.3 to 2.7. The degree of branching is defined as the number of methyl groups in one molecule of the alcohol minus 1. The mean degree of branching is the statistical mean of the degrees of branching of the molecules of a sample. The mean number of methyl groups in the molecules of a sample can be determined readily by 'H-NMR spectroscopy. For this purpose, the signal area corresponding to the methyl protons in the 'H-NMR spectrum of a sample is di- vided by three and then divided by the signal area of the methylene protons if the CHn— OH group divided by two. The alcohol ethoxylate (L) may have an average molecular weight of preferably at least 200 g/mol, more preferably at least 300 g/mol, most preferably at least 350 g/mol, particularly prefer- ably at least 400 g/mol, particularly more preferably at least 450 g/mol, particularly most prefera- bly at least 500 g/mol. The alcohol alkoxylates (E) may have an average molecular weight of preferably up to 2000 g/mol, more preferably up to 1500 g/mol, most preferably up to 1000 g/mol, particularly preferably up to 800 g/mol, particularly more preferably up to 700 g/mol, par- ticularly most preferably up to 650 g/mol, particularly up to 600 g/mol. The alcohol ethoxylate (L) may have an average molecular weight of from 200 to 2000 g/mol, preferably from 400 to 1000 g/mol, and particularly from 500 to 600 g/mol.
In a preferred embodiment the surfactant is a composition (A) comprising a block polymer (P) comprising at least one polyethyleneoxide moiety and at least one polypropyleneoxide moiety, and an alcohol alkoxylate (E) as discussed above.
In a preferred embodiment, the block polymer (P) is contained in an amount of from 4 wt.-% to 96 wt.-%, more preferably from 8 wt.-% to 92 wt.-%, most preferably from 12 wt.-% to 88 wt.-%, particularly preferably from 16 w.-% to 84 wt.-%, particularly more preferably from 20 wt.-% to 80 wt.-%, particularly even more preferably from 24 wt.-% to 76 wt.-%, particularly most prefera- bly from 28 wt.-% to 72 wt.-%, for example preferably from 32 wt.-% to 68 wt.-%, for example more preferably from 36 wt.-% to 64 wt.-%, for example even more preferably from 40 wt.-% to 60 wt.-%, for example most preferably from 44 wt.-% to 56 wt.-%, for example from 48 wt.-% to 52 wt.-%, based on the total weight of the composition A.
In a preferred embodiment, the alcohol alkoxylate (E) is contained in an amount of from 4 wt.-% to 96 wt.-%, more preferably from 8 wt.-% to 92 wt.-%, most preferably from 12 wt.-% to 88 wt- %, particularly preferably from 16 w.-% to 84 wt.-%, particularly more preferably from 20 wt.-% to 80 wt.-%, particularly even more preferably from 24 wt.-% to 76 wt.-%, particularly most pref- erably from 28 wt.-% to 72 wt.-%, for example preferably from 32 wt.-% to 68 wt.-%, for example more preferably from 36 wt.-% to 64 wt.-%, for example even more preferably from 40 wt.-% to 60 wt.-%, for example most preferably from 44 wt.-% to 56 wt.-%, for example from 48 wt.-% to 52 wt.-%, based on the total weight of the composition A.
In another preferred embodiment the surfactant is a composition (B) comprising an alcohol eth- oxylate (L) of the general formula (XIII)
R3-0-(C2H40)s-H (XIII)
wherein R3 is linear or branched Cs to C20 alkyl, and
s has a value of from 1 to 40,
and an alcohol alkoxylate (E) as discussed above.
In a preferred embodiment, the alcohol ethoxylate (L) is contained in an amount of from 4 wt.-% to 96 wt.-%, more preferably from 8 wt.-% to 92 wt.-%, most preferably from 12 wt.-% to 88 wt- %, particularly preferably from 16 w.-% to 84 wt.-%, particularly more preferably from 20 wt.-% to 80 wt.-%, particularly even more preferably from 24 wt.-% to 76 wt.-%, particularly most pref- erably from 28 wt.-% to 72 wt.-%, for example preferably from 32 wt.-% to 68 wt.-%, for example more preferably from 36 wt.-% to 64 wt.-%, for example even more preferably from 40 wt.-% to 60 wt.-%, for example most preferably from 44 wt.-% to 56 wt.-%, for example from 48 wt.-% to 52 wt.-%, based on the total weight of the composition B.
In another embodiment the surfactant comprises sodium-di-ethyl-hexyl-sulfosucccinate and an iso C13-alcohol ethoxylate.
In still another embodiment the surfactant comprises a mixture of ethylenoxide-propyleneoxide block copolymer, 2-propylheptanol and a triblock polymer of ethylenoxide-propyleneoxide-eth- ylenoxide. Preferably, the surfactant comprises a mixture of equal volumes of (a) ethylenoxide- propyleneoxide block copolymer; and (b) 2-propylheptanol and a triblock polymer of ethylenox- ide-propyleneoxide-ethylenoxide.
In accordance with the invention solvents or liquid carriers, solid carriers, surfactants, adjuvants, dispersants, emulsifiers, wetters, adjuvants, solubilizers, penetration enhancers, protective col- loids, adhesion agents, thickeners, humectants, compatibilizers, bactericides, anti-freezing agents, anti-foaming agents, colorants, tackifiers, binders, preservatives, antioxidants, and odorants may be used in addition to the lipase.
Suitable solvents and liquid carriers are water and organic solvents, such as mineral oil frac- tions of medium to high boiling point, e.g. kerosene, diesel oil; oils of vegetable or animal origin; aliphatic, cyclic and aromatic hydrocarbons, e. g. toluene, paraffin, tetrahydronaphthalene, alkyl- ated naphthalenes; alcohols, e.g. ethanol, propanol, butanol, cyclohexanol; glycols; DMSO; ke- tones, e.g. cyclohexanone; esters, e.g. lactates, carbonates, fatty acid esters, gammabutyrolac- tone; fatty acids; phosphonates; amines; amides, e.g. N-methylpyrrolidone, fatty acid dimethyla- mides; and mixtures thereof. Preferably, the solvent is water.
Suitable solid carriers or fillers are mineral earths, e.g. silicates, silica gels, talc, kaolins, lime- stone, lime, chalk, clays, dolomite, diatomaceous earth, bentonite, calcium sulfate, magnesium sulfate, magnesium oxide; polysaccharides, e.g. cellulose, starch; fertilizers, e.g. ammonium sulfate, ammonium phosphate, ammonium nitrate, urea; products of vegetable origin, e.g. ce- real meal, tree bark meal, wood meal, nutshell meal, and mixtures thereof.
Suitable thickeners are polysaccharides (e.g. starch, xanthan gum, carboxymethylcellulose), anorganic clays (organically modified or unmodified), polycarboxylates, superabsorbent poly- mers and silicates.
Suitable bactericides are bronopol and isothiazolinone derivatives such as alkylisothiazolinones and benzisothiazolinones.
Suitable anti-freezing agents are ethylene glycol, propylene glycol, urea and glycerin.
Suitable anti-foaming agents are silicones, long chain alcohols, and salts of fatty acids. Suitable colorants (e.g. in red, blue, or green) are pigments of low water solubility and water- soluble dyes. Examples are
- inorganic colorants, such as iron oxide, titan oxide, iron hexacyanoferrate,
- metal-complex dyes such as chromium-complex dyes, for example Orasol Yellow 141 ,
- organic colorants such as alizarin-, azo- and phthalocyanine colorants.
Preferred colorants are metal-complex dyes, more preferably chromium-complex dyes
Suitable tackifiers or binders are polyvinylpyrrolidones, polyvinylacetates, polyvinyl alcohols, polyacrylates, biological or synthetic waxes, and cellulose ethers.
Suitable preservatives include e.g. sodium benzoate, benzoic acid, sorbic acid, and derivatives thereof.
Suitable antioxidants include sulfites, ascorbic acid, tocopherol, tocopherol acetate, tocotrienol, melatonin, carotene, beta-carotene, ubiquinol, and derivatives thereof. Tocophercol acetate is preferred as antioxidant.
In addition, compounds which stabilize the lipase enzyme may be used, such as buffers, chela- tors, anti-oxidants, non-ionic surfactants, sugars, proteins (e.g. BSA) and heavy metal and phe- nol scavengers.
In accordance with the invention fertilizers and/or nitrification inhibitors and/or urease inhibitors may be used in addition to the lipase or a variant thereof as defined herein.
As used herein, the term“fertilizer” includes any chemical compound that improves the levels of available plant nutrients and/or the chemical and physical properties of soil, thereby directly or indirectly promoting plant growth, yield, and quality. Fertilizers are typically applied either through the soil (for uptake by plant roots) or by foliar feeding (for uptake through leaves). The term "fertilizer" can be subdivided into two major categories: a) organic fertilizers (composed of decayed plant/animal matter) and b) inorganic fertilizers (composed of chemicals and minerals). Inorganic fertilizers are usually manufactured through chemical processes (such as the Haber- Bosch process), also using naturally occurring deposits, while chemically altering them (e.g. concentrated triple superphosphate). Naturally occurring water soluble inorganic fertilizers in- clude Chilean sodium nitrate.
The fertilizer is preferably a urea-containing fertilizer, and/or P-containing fertilizer, and/or a K fertilizer (potassium-containing fertilizer), and/or a N fertilizer (nitrogen-containing fertilizer), and/or a NK fertilizer (nitrogen-potassium fertilizer), and/or a NPK (nitrogen-phosphorous-potas- sium fertilizer), and/or a single or dual element fertilizer containing S, Ca, Mg, Fe, Mn, Cu, Zn, Mo, B, Ni, Cl, or a combination thereof. As used herein, a“urea-containing fertilizer” is defined as a fertilizer comprising at least one component selected from the group consisting of urea, urea ammonium nitrate (UAN), and sus- pensions of isobutylidene diurea (IBDU), crotonylidene diurea (CDU) and urea formaldehyde (UF), urea-acetaldehyde, and ureaglyoxal condensates.
In a preferred embodiment of the invention, the urea-containing fertilizer is urea or urea ammo- nium nitrate (UAN).
In customary commercial fertilizer quality, the urea has a purity of at least 90%, and may for ex- ample be in crystalline, granulated, compacted, prilled or ground form.
The urea-containing fertilizer may be used together with a urease inhibitor. Urease is an en- zyme which hydrolyzes urea to ammonia and carbon dioxide. In agriculture, high urease activity during treatment with urea-containing fertilizers causes significant environmental and economic problems due to the release of ammonia which may be toxic to the plants and which deprives the plants of urea. Accordingly, it is desirable to inhibit the action of urease. Inhibitors of urease activity may comprise (i) substrate structural analogs of urea as e.g. hydroxyurea or hydroxamic acid or (ii) inhibitors which affect the mechanism of the urease reaction. The later may be di- vided in the four groups of (i) phosphorodiamidates or phosphorotriamidiates as e.g. N-(n-bu- tyl)thiophosphoric triamide, (ii) thiols as e.g. cysteamine, (iii) hydroxamic acids and its deriva- tives as e.g. acetohydroxamic acid, and (iv) ligands and chelators of the nickel ion in the active center of ureases as e.g. fluoride ions. Urease inhibitors are also discussed in Upadhyay (2012) Ind. J. Biotechnol. 1 1 : 381-388 and in "Improving Efficiency of Urea Fertlizers by Inhibition of Soil Urease Activity" by Kiss and Simihaian (2002), Springer Netherlands, ISBN 978-1-4020- 0493-3.
As used herein, the“P-containing fertilizer” is any fertilizer providing any form of the chemical element phosphorus (P) or containing any chemical compounds incorporating the chemical ele- ment phosphorus (P), including but not limited to phosphate-containing fertilizers or fertilizers containing P. Preferably, the P-containing fertilizer is selected from the group consisting of a NPK fertilizer, a NP fertilizer, a PK fertilizer, or a P fertilizer. Most preferably, the P-containing fertilizer is a NPK fertilizer. Of course, also combinations of these fertilizers may be used as ad- ditional P-containing fertilizer.
P fertilizers, K fertilizers, and N fertilizers are straight fertilizers, i.e. fertilizers that contain only one of the nutritive elements P, K, and N. It is to be understood, however, that these fertilizers may additionally comprise at least one additional nutritive element selected from S, Ca, Mg, Fe, Mn, Cu, Zn, Mo, B, Ni, and Cl.
NPK fertilizers, NP fertilizers, and PK fertilizers are multinutrient fertilizers, i.e. fertilizers that comprise combinations of the nutritive elements P, K, and N as indicated by the terms“NPK”, “NP”, and“PK”. It is to be understood, however, that these fertilizers may additionally comprise at least one additional nutritive element selected from S, Ca, Mg, Fe, Mn, Cu, Zn, Mo, B, Ni and Cl. The NPK fertilizers, NP fertilizers, and PK fertilizers may be provided as complex fertilizers or bulk-blend or blended fertilizers. The term complex fertilizer refers to a compound fertilizer formed by mixing ingredients that react chemically. In bulk-blend or blended fertilizers, two or more granular fertilizers of similar size are mixed to form a compound fertilizer.
Dual element fertilizers are preferably dual element fertilizers with Ca, Mg, Fe, Mn, Zn or Ni which may be applied as soluble salts of chloride, sulfate, nitrate or in chelated form (e.g.
MnEDTA, Fe EDTA, FeEDDHA).
Single or dual element fertilizers of Mo are available as salts of molybdate, B as boric acid or borates.
Ammonium (NH4 +) compounds present in nitrogen-containing fertilizers are converted by soil microorganisms to nitrates (NO3 ) in a relatively short time in a process known as nitrification. The nitrification process typically leads to nitrogen leakage and environmental pollution. As a result of the various losses, approximately 50% of the applied nitrogen fertilizers are lost during the year following fertilizer addition (see Nelson and Huber; Nitrification inhibitors for corn pro- duction (2001 ), National Corn Handbook, Iowa State University).
As countermeasure, nitrification inhibitors, mostly together with fertilizers, can be used. Suitable nitrification inhibitors include linoleic acid, alpha-linolenic acid, methyl p-coumarate, methyl feru- late, methyl 3-(4-hydroxyphenyl) propionate (MHPP), Karanjin, brachialacton, p-benzoquinone sorgoleone, 2-chloro-6-(trichloromethyl)-pyridine (nitrapyrin or N-serve), dicyandiamide (DCD, DIDIN), 3,4-dimethyl pyrazole phosphate (DMPP, ENTEC), 4-amino-1 ,2,4-triazole hydrochloride (ATC), 1 -amido-2 -thiourea (ASU), 2-amino-4-chloro-6-methylpyrimidine (AM), 2-mercapto-ben- zothiazole (MBT), 5-ethoxy-3-trichloromethyl-1 ,2,4-thiodiazole (terrazole, etridiazole), 2-sulfanil- amidothiazole (ST), ammoniumthiosulfate (ATU), 3-methylpyrazol (3-MP), 3,5-dimethylpyrazole (DMP), 1 ,2,4-triazol thiourea (TU), N-(1 H-pyrazolyl-methyl)acetamides such as N-((3(5)-methyl- 1 H-pyrazole-1 -yl)methyl)acetamide, and N-(1 H-pyrazolyl-methyl)formamides such as N-((3(5)- methyl-1 H-pyrazole-1 -yl)methyl formamide, N-(4-chloro-3(5)-methyl-pyrazole-1 -ylmethyl)-forma- mide, N-(3(5),4-dimethyl-pyrazole-1 -ylmethyl)-formamide, neem, products based on ingredients of neem, cyan amide, melamine, zeolite powder, catechol, benzoquinone, sodium terta board and zinc sulfate.
Pesticides are substances which aim to control pests and include herbicides, insecticides, ne- maticides, mollluscicides, piscicides, avicdes, rodenticides, bactericides, insect repellents, ani- mal repellents, antimicrobials and fungicides.
If the water-repellent soil is a fairy ring caused by basidiomycetes, preferably a fungicide is used in combination with the lipase. More preferably, the fungizide is a fungizide which can be ap- plied through the soil. Hence, the present invention also relates to the use of (a) an isolated polypeptide having lipase activity; and (b) at least one fungicide for the treatment of at least one fairy ring.
The present invention also relates to a method for treating at least one fairy ring comprising ap- plying (a) an isolated polypeptide having lipase activity; (b) at least one fungicide to an area of groundcover.
Preferably, the lipase is one of the specific lipases disclosed herein and more preferably it is the lipase according to SEQ ID No. 956 or an enzymatically active variant thereof.
Suitable fungicides include strobilurins, carboximides, oxidizing agents, polyoxins and sterol de- methylation inhibitors. Specific examples include, but are not limited to, Azoxystrobin, Triflox- istrobin, Picoxystrobin, Pyraclostrobin, Sedaxane, Penthiopyrad, Penflufe, Fluopyram, Fluxapy- roxad, Boscalid, Oxathiapiprolin, Metalaxyl, Metalaxyl-M, Ethaboxam, DMM, Cyproconazole, Difenoconazole, Prothioconazole, Flutriafol, Thiabendazole, Ipconazole, Tebuconazole, Triad- imenol, Prochloraz, Fluquinconazole, TTZ, Fludioxinil, Carboxin, Silthiofarm, Ziram, Thiram, Carbendazim, TPM, Valifenalate, Oxathiapiprolin analague of BCS, Pydiflumetofen (Adepydin), Fluindapyr, Mandestrobin, Inpyrfuxam, Imazalil and Picarbutrazox. Preferably, a fungizide se- lected from Azoxystrobin, Trifloxistrobin, Picoxystrobin, Pyraclostrobin, Sedaxane, Penthiopy- rad, Penflufe, Fluxapyroxad, Boscalid, Oxathiapiprolin, Metalaxyl-M, Ethaboxam, DMM, Difeno- conazole, Prothioconazole, Flutriafol, Ipconazole, TTZ, Fludioxinil, Carboxin, Silthiofarm and Valifenalate is used in combination with the lipase.
Examples of suitable fungicides which are marketed for the treatment of fairy rings and which may be used in combination with the lipase include azoxystrobin (marketed under the name Heritage®), flutolanil (marketed under the name Prostar®), hydrogen dioxide (marketed under the name Zerotol®), polyoxin D (marketed under the name Endorse®), triadimefon (marketed un- der the name Bayleton® FLO), pyraclostrobin (marketed under the name Insignia®), a mixture of pyraclostrobin and triticonazole (marketed under the name Pillar® G Intrinsic), a mixture of azoxystrobin and propiconazole (marketed under the name Headway®) and a mixture of triad- imefon and trifloxystrobin (marketed under the name Tartan® Stressgard®).
Insecticides which may be used in combination with the lipase include, but are not limited to, Fipronil, BAS 450, IL-39, Clothianidin, Thiamethoxam, Acetamiprid, Dinotefuran, Imidacloprid, Thiacloprid, Sulfoxaflor, Methiocarb, Tefluthrin, Bifenthrin, Cypermethrin, Alphacypermethrin, Spinosad, Cyazypyr, Rynaxapyr, Thiodicarb, Triflumezopyrim (Mesoionic), Acephate, Chlorpyri- phos, Flupyradifurone, Tetraniliprole, IL-101 , S-1587, Oxazosulfyl, Cyclaniliprole and Fluxamet- amide. Preferably, an insecticide selected from the group consisting of Fipronil, BAS 450, IL-39, Clothianidin, Thiamethoxam, Imidacloprid, Thiacloprid, Sulfoxaflor, Tefluthrin, Spinosad, Cyazypyr, Rynaxapyr, Triflumezopyrim (Mesoionic), Acephate and Chlorpyriphos is used in combination with the lipase.
Nematicides which may be used in combination with the lipase include, but are not limited to, Thiodicarb, Abamectin, Tioxazafen, Bacillus firmus and Pasteuria nishizawae. The polypeptide having lipase activity may be applied to the groundcover in a concentration of between 0.001 kg to 60 kg of polypeptide per hectare, preferably of between 0.016 kg to 10 kg per hectare, more preferably of between 0.06 kg to 2 kg per hectare, most preferably of be- tween 0.1 kg to 0.5 kg per hectare.
The polypeptide having lipase activity may be applied to the groundcover in a concentration of between 0.01 kg to 600 kg of polypeptide per hectare, preferably of between 0.16 kg to 100 kg per hectare, more preferably of between 0.6 kg to 20 kg per hectare, most preferably of be- tween 1 kg to 5 kg per hectare.
In one embodiment the lipase is dissolved in water in a concentration of 0.001 % to 5% or 3% w/v, preferably of 0.002% to 2% or 1 % w/v, more preferably of 0.003% to 0.08 or 0.06% w/v, even more preferably of 0.004% to 0.04% or 0.03% w/v and most preferably of 0.005% to 0.01 %. One particularly preferred concentration of the lipase is 0.006% w/v.
In one embodiment the lipase is dissolved in water in a concentration of 0.01 % to 50% or 30% w/v, preferably of 0.02% to 20% or 10% w/v, more preferably of 0.03% to 0.8 or 0.6% w/v, even more preferably of 0.04% to 0.4% or 0.3% w/v and most preferably of 0.05% to 0.1 %. One par- ticularly preferred concentration of the lipase is 0.06% w/v.
Typically, for large volume applications the lipase is dissolved in water in a concentration of 0.001 % to 0.01 % w/v, preferably of 0.002% to 0.008% w/v, more preferably of 0.003% to 0.007% and most preferably of 0.006% (w/v). Typically, for small volume applications the lipase is dissolved in water in a concentration of 0.1 % to 5% w/v, preferably of 0.5% to 3% w/v, more preferably of 0.8% to 2% and most preferably of 1 % (w/v). In large volume applications the li- pase is dissolved in a great volume of water for application to a great area of soil. In small vol- ume applications the lipase is dissolved in a small volume of water for application to a small area.
Typically, for large volume applications the lipase is dissolved in water in a concentration of 0.01 % to 0.1 % w/v, preferably of 0.02% to 0.08% w/v, more preferably of 0.03% to 0.07% and most preferably of 0.06% (w/v). Typically, for small volume applications the lipase is dissolved in water in a concentration of 1 % to 50% w/v, preferably of 5% to 30% w/v, more preferably of 8% to 20% and most preferably of 10% (w/v). In large volume applications the lipase is dissolved in a great volume of water for application to a great area of soil. In small volume applications the lipase is dissolved in a small volume of water for application to a small area.
The lipase may be supplied as a concentrated suspension and diluted to the concentrations in- dicated above before the application to soil. The lipase may also be supplied in powder form and either dissolved before the application to soil or applied to the soil in powder form. If the li- pase is applied to the soil in powder form, it is washed into the soil by rain or irrigation water with a volume of 0.5 L to 15 L, preferably with a volume of 1 L to 10 L per square meter, more preferably with a volume of 4 to 8 L per square meter shortly after application. In the use and method of the present invention the lipase is applied to an area of groundcover.
The term“groundcover” as used herein includes, but is not limited to, soil, natural soil, potting soil, sand, silt, clay, turfgrasses and other plants and forms of vegetation used to cover and pro- tect the soil, as well as composites of organic materials that form within or as part of such groundcovers, such as thatch and mat layers, and also includes potting mixes.
Preferably, groundcover is soil, more preferably, groundcover is water-repellent or non-wetting soil. In another preferred embodiment, groundcover is potting mix. Potting mix, which is also re- ferred to potting soil, is typically a soilless blend of ingredients that is used to grow plants, pref- erably, the potting mix comprises a combination of peat moss, vermiculite, coir fiber, perlite, pine bark, sand, compost, and further ingredients. The potting mix may also comprise native soil.
The term "applying" includes any activity by which the lipase come into contact with the area of groundcover. The lipase can be dissolved in water and applied as a solution. Alternatively, a granulate can be prepared from the lipase and the granulate is then applied to the groundcover in solid form which is dissolved when water is applied to the soil.
In one embodiment, the lipase is applied in irrigation water. In one embodiment the lipase is ap- plied extensively and non-directional to turfgrass soil. In one embodiment the lipase is applied extensively and non-directional to turfgrass soil in irrigation water. In one embodiment the lipase is applied directional to turfgrass soil using a watering can.
In one embodiment the lipase is applied to turfgrass soil as part of a topdressing which corn- prises particles to which the lipase is coupled. Topdressing refers to a material applied to the top of a ground covering, usually in order to obtain a desirable effect on the groundcover, and includes sand or other particulate material.
In another embodiment the application of the lipase serves to prepare a non-wetting soil for the seeding of crops. In one embodiment the lipase is applied selectively to those locations of the non-wetting soil where the seeds will be placed, e.g. the seeding row, so that they can prepare the soil for seed uptake. In another embodiment, the lipase is applied non-selectively to the en- tire application site (so-called blanket application).
It was also found that lipases and in particular the lipase according to SEQ ID NO: 956 can be used for promoting plant growth. The term "promoting plant growth" means that upon applica- tion of a lipase to the plant, the dry weight of the plant increases within a period of 10 to 20 days, preferably of 12 to 18 days and most preferably a period of 14 days by at least 5%, prefer- ably by at least 10%, 15% or 20%, more preferably by at least 25%, 30% or 35% even more preferably by at least 40% or 45% and most preferably by at least 50%. In one embodiment, the term "promoting plant growth" means that upon application of a lipase to the plant, the dry weight of the plant increases within a period of 10 to 20 days, preferably within a period of 12 to 18 days and most preferably within a period of 14 days by 5% to 70%, preferably by 10% to 65%, more preferably by 20% to 60% and most preferably by 40 to 50%.
The term "plant" is intended to comprise any plant including dicotyledonous and monocotyle- donous plants. Preferably, the plant is a monocotyledonous plant and more preferably it is turf grass.
The following examples are provided for illustrative purposes. It is thus understood that the ex- amples are not to be construed as limiting. The skilled person will clearly be able to envisage further modifications of the principles laid out herein.
EXAMPLES
Example 1
Soil was sampled freshly. Harvested soils were a wetting soil from Limburgerhof, serving as a control, and two non-wetting soils from Western Australia: Peter Black and South Stirling. The harvested soil samples were dried and subsequently sieved through a 500 pm sieve. Approxi- mately 3 g dry sample soil, 4 g dry silica sand, and 10 mg cotton wool were placed into a 5 mL syringe as column filling, with the cotton wool forming the bottom layer on the narrow end of the syringe, the silica sand forming the middle layer, and the soil sample forming the topmost layer on the wide end of the syringe (see Figure 1 A). Columns prepared in this way were weighed to determine the dry weight.
Next, 0.06% (w/v) lipase solution was prepared by dissolving powdered, lyophilized lipase ac- cording to SEQ ID No. 956 (also designated as "Lipase BP" or "Lipase BP 2015") in pure dis- tilled water (DW). The prepared columns were then treated with either 1 mL lipase solution (0.06%) or with 1 mL distilled water (DW) as a control, applied to the top of the sample soil layer. The columns were left to incubate for 24 hours at room temperature (RT) followed by rins- ing with 2 mL DW and drying at 45°C for 48 hours.
The water droplet penetration time (WDPT) was measured by adding 20 pL of DW to the dried columns and recording the time needed for the entirety of the 20 pL volume to penetrate into the sample soil layer. Thereafter, water infiltration time was measured next by adding 2 mL DW to the top of the sample soil layer and recording the time needed for the entirety of the 2 mL vol- ume to infiltrate into the column. Finally, 2 hours after measuring infiltration time, the columns were weighed again (Figure 1 B). Any increase in weight over the initially measured dry weight was due to water retention in the column layers and could be correlated to the water volume re- tained, thereby providing the water holding capacity.
Lipase treatment markedly reduced WDPT in the non-wetting Peter Black and South Stirling soils, which had much higher WDPT compared to the control wetting Limburgerhof soil when untreated (see Figure 2A). Likewise, the water infiltration time is reduced in these non-wetting soils upon lipase treatment, while no difference in infiltration time is observed in the control wet- ting Limburgerhof soil (see Figure 2B).
Clearly, lipase treatment of non-wetting soils overcomes soil water repellency (reduced WDPT and water infiltration time), i.e. lipase treatment improves water availability to the soil.
Example 2
In order to assess concentration dependency of the effect of lipase treatment on the non-wetting soils, the same experimental set up described in Example 1 was used for South Stirling or Peter Black soil, and the concentration of the lipase according to SEQ ID No. 956 (also called "Lipase BP" or "Lipase BP 2015") was varied from 0.02% - 0.06% w/v in the applied lipase solution.
WDPT was markedly reduced by lipase treatment at concentrations as low as 0.02% w/v (see Figure 3A). Similarly, water infiltration time was reduced upon treatment with as little as 0.02% lipase, although higher lipase concentrations led to a greater effect, especially in South Stirling soil (see Figure 3B). The water holding capacity of both soils increased linearly with increasing concentration of lipase (see Figure 3C).
Example 3
Plastic pots (upper diameter 13 cm) were filled with exactly 1000 g of previously dried soil Lim- burgerhof and placed in a growth chamber with 16 h light and 8 h dark period at 20 °C ( ± 2 °C). The main characteristics of soil Limburgerhof are pH(CaCl2) 6.8, with a mineral content of 73% sand, 24% silt, and 3 % clay, classified according to FAO as sandy loam.
At day zero the two treatments were tap water (120 mL/per pot) or 120 mL tap water with 0.06% (w/v) of the lipase according to SEQ ID No. 956. For each treatment the amount of 120 mL wa- ter was divided into 6 x 20 mL doses . Per treatment n = 7 pots were used and the 14 pots were randomly placed central in the growth chamber. The pots were covered and allowed to stand for 24 h. Then each pot received in total 130 mL of deionized water split up over an hour into 7 pro- portions simulating rain, which exceeded the water holding capacity of the pots. The amount of water leached was collected in saucers and weighed (see Figure 4A). The lower amount of wa- ter leached from the pots treated with lipase indicates an increased water holding capacity due to the treatment with the lipase.
For another 8 days the weighed pots after leaching received no more water and were then weighed again. The loss in weight at this time-point corresponds to the evaporation of water from the pots. The lower loss in weight by the lipase treated pots by on average 5% reflects a lower evaporation rate due to the lipase treatment (see Figure 4B).
Thereafter the pots could dry further for another 4 days and at day 13 after the lipase treatment each pot was watered to exactly 55% of its maximum water holding capacity and seeded with 15 wheat seeds per pot. Up to day 19 each pot was watered daily up to 55% of its WHC. Then, at day 19 each pot received uniformly 80 mL of water Thereafter, the plants were singled out to uniformly 10 emerged plants per pot and each pot was individually watered to 55% WHC.
From day 19 onwards no more water was applied and the wheat plants could grow until harvest at day 25 after the experiment had started, which was 12 days after seeding.
To harvest the plants were cut 5 mm above ground with scissors and the fresh weight of the10 plant per pot recorded. To determine the shoot dry weight per pot the shoots were dried until constant weight at 80 °C in a forced-air oven. The plants grown in soil treated with lipase had a slightly higher weight of the fresh and dry shoots (see Figure 4C) and the plants did not show any kind of damage, necrosis or chlorosis.
Example 4
The influence of enzyme treatment on the water contact angle of a water-repellent sandy soil from South Stirling, a wheat growing area of Western Australia, having a MED of 4.0 and free of residual organic matter, was measured. The enzymes evaluated were: Lipase (from BASF SE) and Laccase and Chitinase (Sigma Aldrich).
Enzyme treatment of the South Stirling soil used the following quantities of enzyme: Lipase, 0.0015 g/g soil, Laccase, 8U/g soil, and Chitinase, 0.11 1 U/g soil. Enzyme pre-treatment was carried out by adding 10 ml aqueous enzyme solution to 10 grams of soil particles (sieved to <2 mm) in a 50 ml capacity polypropylene container which was then placed in a roller mixer for 24 hr incubation time. Soil particles were then separated by centrifuging followed by thorough washing with doubly distilled water to remove excess enzyme. Finally the soil particles were dried at 80° C.
One control sample was subjected to the same pre-treatment procedure, but incubated with doubly distilled water, and in another control the soil fraction was left untreated.
A flat adhesive surface was prepared by covering a microscope glass slide with a double sided adhesive polyimide tape. Enzyme modified soil particles prepared according to the method above were uniformly distributed over a 2 cm by 1 cm adhesive area and a uniform load of 250 g was applied over this particulate surface for 30 s after which, the slide was carefully tapped to remove any excess particles. This yielded a compactly packed monolayer of particles, repre- senting a soil surface containing hierarchical roughness where the particle surface nanoscale topology was superimposed onto the microscale packing roughness, analogous to a wetting front within a particulate bed (Truong et al. (2014) Journal of Colloid and Interface Science 460: 61-70).
The sessile drop method was used for measuring static water contact angles under ambient conditions (20 °C, 40 % RH) using a Contact Angle Goniometer equipped with a nanodispenser (model FTA1000c, First Ten Angstroms, Inc., Portsmouth, VA, USA). The droplet volume used was 1.0 pL and 10 replicate the contact angles were evaluated by recording 50 images over 2 s with a Pelcomodel PCHM 575-4 camera and measuring contact angles after the droplet had rested on the surface for a period of 2 s (Truong et al. (2014) Journal of Colloid and Interface Science 460: 61-70).
Dynamic spreading of the water droplets on enzyme modified soil surfaces was recorded in the first 60 seconds of contact using a Prosilica Model Navitar 444037 camera at a speed of 2 frames per second. The contact angle was determined by image analysis using the FTA Win- dows Mode 32 software.
Fig. 5 shows the dynamic water contact angles for South Stirling soil which was originally se- verely hydrophobic (MED 4.0) after treatment with the three enzymes plus the two controls (wa- ter treated and untreated soil). Here it can clearly be seen that lipase enzyme treatment pro- duces the highest wettability of the soil particle surfaces. After lipase treatment South Stirling soil became only moderately hydrophobic having a MED <1.0.
The relative equilibrium contact angles for the three enzymes and controls are given in Table 1.
Table 1 : Water contact angles for enzyme modified soil particulate surfaces and their compari- son with untreated and water treated counterparts.
Figure imgf000071_0001
Example 5
Putting greens established with grass seed mixture Penn A-4 showing both symptoms of local- ized dry spot or not were sampled from a golf club near Mannheim, Germany. Soil cores were taken with an auger 8.5 cm in diameter and 10 cm in depth. Transported in firmly packed plastic bags to keep the cores intact, they were segmented with a knife into 0 - 2 cm, 2 - 4 cm, 4 - 6 cm, and 6- 8 cm sections. The soil sections were then air dried at room temperature and there- after passed through a 4 mm sieve and then through a 2 mm sieve and stored at room tempera- ture until testing. All soil samples 0 - 2 cm and 2 - 4 cm had contact angles > 90, and all sam- ples from 4 - 6 and 6 -8 cm soil depth had contact angles < 90° measured according to Bach- mann eta I. (2000) J. of Hydrology 231 : 66-75. According to conventional classification contact angles > 90° indicate hydrophobicity, whereas contact angles below 90° indicate wettability of a soil sample. The pH (0.01 M CaCh) of the samples was in the range between 6.4 to 6.8.
The experimental set up (Figure 6A) was the same as in Example 1 with the difference that the columns were filled with 6.000 g turf soil and the Water Droplet Penetration Time (WDPT) test was performed with 15 pL demineralized water and that the final weighing was done 24 h after soil saturation with water. There were 5 replications per treatment. The lipase according to SEQ ID No. 956 was applied at a concentration of 0.04% (w/v) dissolved in water and the wetting agent KICK was applied at a concentration of 0.42 % (w/v). Figures 6B and 6D show that both the lipase and the wetting agent decreased the water infiltra tion time at a soil depth of 0 to 4 cm compared to water. Figure 6C shows that the application of both lipase and wetting agent decreased the water droplet penetration time (WDPT) at a soil depth of 0 to 6 cm compared to water. Figure 6E shows that both lipase and wetting agent in- crease the water holding capacity of soil at a soil depth of 0 to 6 cm compared to water.
Example 6
To see how water infiltration time and water availability of the treated soils from Example 5 be- have long term, the columns from Example 5 where“weathered” by addition of water and stored for a longer period of time to dry and then again tested for water availability (water infiltration time, water holding capacity) thereafter (Figure 7A). Only turf soil from the layer 0 - 2 cm was used. For each weathering period 2 mL + 2 mL + 2 mL water equivalent to a simulated rain ap- plication of 53 mm were applied. To measure water infiltration time to all columns 2 mL of water were applied (Figure 1C).
Initially, both the surfactant and the lipase treatment increased both water infiltration time (Fig. 7B) and water holding capacity (Fig. 7C) significantly over the water control. However, upon longer term treatment the wetting agent lost its activity and at the third measurement the water infiltration time and water holding capacity was the same as for the control, while the soil treated with lipase still had a significantly lower water infiltration time and a higher water holding capac- ity compared to the water control.
Example 7
Putting green with grass mixture R.S.M 4.1.2 (15% Agrostis stolonifera, 45% Festuca rubra commutate, 40% Festuca rubra trichophytta) was used from a golf club near Ludwigshafen, Germany. The solutions were applied at a rate of 8 L/m2 on confined areas by filling the solu- tions into rings pressed to turf until infiltration was completed. Lipase according to SEQ ID No. 956 was applied at a concentration of 0.03% (w/v) dissolved in water. Four replications were used for water controls and two replications for the Lipase solution. After 14 days of growth with daily watering the application rings were located again at the marked application sites. With scissors the grass was cut, and with a battery-powered table vacuum cleaner the clipping was collected from the confined application areas. After drying to constant weight at 80° C the dry matter of the clippings was determined.
Figure 8 shows that treatment with lipase increases the dry weight of the putting green by about 50% compared to the water control.

Claims

Claims
1. Use of an isolated polypeptide having lipase activity for increasing the water availability in soil.
2. Use according to claim 1 , wherein the soil water repellency of non-wetting soil is reduced and/or the water holding capacity of non-wetting soils is increased.
3. Use according to claim 1 , wherein the water holding capacity of wetting soil is increased and/or the evaporation from wetting soil is decreased.
4. Use according to any one of the preceding claims, wherein the isolated polypeptide hav- ing lipase activity is selected from the group consisting of:
(i) a polypeptide having the amino acid sequence according to any one of SEQ ID NOs: SEQ ID NO: 956, SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22,
SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56,
SEQ ID NO: 58, SEQ ID NO: 60, SEQ ID NO: 62, SEQ ID NO: 64, SEQ ID NO: 66, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 72, SEQ ID NO: 74, SEQ ID NO: 76, SEQ ID NO: 78, SEQ ID NO: 80, SEQ ID NO: 82, SEQ ID NO: 84, SEQ ID NO: 86, SEQ ID NO: 88, SEQ ID NO: 90,
SEQ ID NO: 92, SEQ ID NO: 94, SEQ ID NO: 96, SEQ ID NO: 98, SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, SEQ ID NO: 110, SEQ ID NO: 1 12, SEQ ID NO: 1 14, SEQ ID NO: 116, SEQ ID NO: 1 18, SEQ ID NO: 120, SEQ ID NO: 122, SEQ ID NO: 124, SEQ ID NO: 126, SEQ ID NO: 128, SEQ ID NO: 130, SEQ ID NO: 132, SEQ ID NO: 134, SEQ ID NO: 136, SEQ ID NO: 138, SEQ ID NO: 140, SEQ ID NO: 142, SEQ ID NO: 143, SEQ ID NO: 146, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 152, SEQ ID NO: 154, SEQ ID NO: 156, SEQ ID NO: 158, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 166, SEQ ID NO: 168, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 174, SEQ ID NO: 176, SEQ ID NO: 178, SEQ ID NO: 180, SEQ ID NO: 182, SEQ ID NO: 184, SEQ ID NO: 186, SEQ ID NO: 188, SEQ ID NO: 190, SEQ ID NO: 192, SEQ ID NO: 194, SEQ ID NO: 196, SEQ ID NO: 198, SEQ ID NO: 200, SEQ ID NO: 202, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 208, SEQ ID NO: 210, SEQ ID NO: 212, SEQ ID NO: 214, SEQ ID NO: 216, SEQ ID NO: 218, SEQ ID NO: 220, SEQ ID NO: 222, SEQ ID NO: 224, SEQ ID NO: 226, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 232, SEQ ID NO: 234, SEQ ID NO: 236, SEQ ID NO: 238, SEQ ID NO: 240, SEQ ID NO: 242, SEQ ID NO: 244, SEQ ID NO: 246, SEQ ID NO: 248, SEQ ID NO: 250, SEQ ID NO: 252, SEQ ID NO: 254, SEQ ID NO: 256, SEQ ID NO: 258, SEQ ID NO: 260, SEQ ID NO: 262, SEQ ID NO: 264, SEQ ID NO: 266, SEQ ID NO: 268, SEQ ID NO: 270, SEQ ID NO: 272, SEQ ID NO: 274, SEQ ID NO: 276, SEQ ID NO: 278, SEQ ID NO: 280, SEQ ID NO: 282, SEQ ID NO: 284, SEQ ID NO: 286, SEQ ID NO: 288, SEQ ID NO: 290, SEQ ID NO: 292, SEQ ID NO: 294, SEQ ID NO: 296, SEQ ID NO: 298, SEQ ID NO: 300, SEQ ID NO: 302, SEQ ID NO: 304, SEQ ID NO: 306, SEQ ID NO: 308, SEQ ID NO: 310, SEQ ID NO: 312, SEQ ID NO: 314, SEQ ID NO: 316, SEQ ID NO: 318, SEQ ID NO: 320, SEQ ID NO: 322, SEQ ID NO: 324, SEQ ID NO: 326, SEQ ID NO: 328, SEQ ID NO: 330, SEQ ID NO: 332, SEQ ID NO: 334, SEQ ID NO: 336, SEQ ID NO: 338, SEQ ID NO: 340, SEQ ID NO: 342, SEQ ID NO: 344, SEQ ID NO: 346, SEQ ID NO: 348, SEQ ID NO: 350, SEQ ID NO: 352, SEQ ID NO: 354, SEQ ID NO: 356, SEQ ID NO: 358, SEQ ID NO: 360, SEQ ID NO: 362, SEQ ID NO: 364, SEQ ID NO: 366, SEQ ID NO: 368, SEQ ID NO: 370, SEQ ID NO: 372, SEQ ID NO: 374, SEQ ID NO: 376, SEQ ID NO: 378, SEQ ID NO: 380, SEQ ID NO: 382, SEQ ID NO: 384, SEQ ID NO: 386, SEQ ID NO: 388, SEQ ID NO: 390, SEQ ID NO: 392, SEQ ID NO: 394, SEQ ID NO: 396, SEQ ID NO: 398, SEQ ID NO: 400, SEQ ID NO: 402, SEQ ID NO: 404, SEQ ID NO: 406, SEQ ID NO: 408, SEQ ID NO: 410, SEQ ID NO: 412, SEQ ID NO: 414, SEQ ID NO: 416, SEQ ID NO: 418, SEQ ID NO: 420, SEQ ID NO: 422, SEQ ID NO: 424, SEQ ID NO: 426, SEQ ID NO: 428, SEQ ID NO: 430, SEQ ID NO: 432, SEQ ID NO: 434, SEQ ID NO: 436, SEQ ID NO: 438, SEQ ID NO: 440, SEQ ID NO: 442, SEQ ID NO: 444, SEQ ID NO: 446, SEQ ID NO: 448, SEQ ID NO: 450, SEQ ID NO: 452, SEQ ID NO: 454, SEQ ID NO: 456, SEQ ID NO: 458, SEQ ID NO: 460, SEQ ID NO: 462, SEQ ID NO: 464, SEQ ID NO: 466, SEQ ID NO: 468, SEQ ID NO: 470, SEQ ID NO: 472, SEQ ID NO: 474, SEQ ID NO: 476, SEQ ID NO: 478, SEQ ID NO: 480, SEQ ID NO: 482, SEQ ID NO: 484, SEQ ID NO: 486, SEQ ID NO: 488, SEQ ID NO: 490, SEQ ID NO: 492, SEQ ID NO: 494, SEQ ID NO: 496, SEQ ID NO: 498, SEQ ID NO: 500, SEQ ID NO: 502, SEQ ID NO: 504, SEQ ID NO: 506, SEQ ID NO: 508, SEQ ID NO: 510, SEQ ID NO: 512, SEQ ID NO: 514, SEQ ID NO: 516, SEQ ID NO: 518, SEQ ID NO: 520, SEQ ID NO: 522, SEQ ID NO: 524, SEQ ID NO: 526, SEQ ID NO: 528, SEQ ID NO: 530, SEQ ID NO: 532, SEQ ID NO: 534, SEQ ID NO: 536, SEQ ID NO: 538, SEQ ID NO: 540, SEQ ID NO: 542, SEQ ID NO: 544, SEQ ID NO: 546, SEQ ID NO: 548, SEQ ID NO: 550, SEQ ID NO: 552, SEQ ID NO: 554, SEQ ID NO: 556, SEQ ID NO: 558, SEQ ID NO: 560, SEQ ID NO: 562, SEQ ID NO: 564, SEQ ID NO: 566, SEQ ID NO: 568, SEQ ID NO: 570, SEQ ID NO: 572, SEQ ID NO: 574, SEQ ID NO: 576, SEQ ID NO: 578, SEQ ID NO: 580, SEQ ID NO: 582, SEQ ID NO: 584, SEQ ID NO: 586, SEQ ID NO: 588, SEQ ID NO: 590, SEQ ID NO: 592, SEQ ID NO: 594, SEQ ID NO: 596, SEQ ID NO: 598, SEQ ID NO: 600, SEQ ID NO: 602, SEQ ID NO: 604, SEQ ID NO: 606, SEQ ID NO: 608, SEQ ID NO: 610, SEQ ID NO: 612, SEQ ID NO: 614, SEQ ID NO: 616, SEQ ID NO: 618, SEQ ID NO: 620, SEQ ID NO: 622, SEQ ID NO: 624, SEQ ID NO: 626, SEQ ID NO: 628, SEQ ID NO: 630, SEQ ID NO: 632, SEQ ID NO: 634, SEQ ID NO: 636, SEQ ID NO: 638, SEQ ID NO: 640, SEQ ID NO: 642, SEQ ID NO: 644, SEQ ID NO: 646, SEQ ID NO: 648, SEQ ID NO: 650, SEQ ID NO: 652, SEQ ID NO: 654, SEQ ID NO: 656, SEQ ID NO: 658, SEQ ID NO: 660, SEQ ID NO: 662, SEQ ID NO: 664, SEQ ID NO: 666, SEQ ID NO: 668, SEQ ID NO: 670, SEQ ID NO: 672, SEQ ID NO: 674, SEQ ID NO: 676, SEQ ID NO: 678, SEQ ID NO: 680, SEQ ID NO: 682, SEQ ID NO: 684, SEQ ID NO: 686, SEQ ID NO: 688, SEQ ID NO: 690, SEQ ID NO: 692, SEQ ID NO: 694, SEQ ID NO: 696, SEQ ID NO: 698, SEQ ID NO: 700, SEQ ID NO: 702, SEQ ID NO: 704, SEQ ID NO: 706, SEQ ID NO: 708, SEQ ID NO: 710, SEQ ID NO: 712, SEQ ID NO: 714, SEQ ID NO: 716, SEQ ID NO: 718, SEQ ID NO: 720, SEQ ID NO: 722, SEQ ID NO: 724, SEQ ID NO: 726, SEQ ID NO: 728, SEQ ID NO: 730, SEQ ID NO: 732, SEQ ID NO: 734, SEQ ID NO: 736, SEQ ID NO: 738, SEQ ID NO: 740, SEQ ID NO: 742, SEQ ID NO: 744, SEQ ID NO: 746, SEQ ID NO: 748, SEQ ID NO: 750, SEQ ID NO: 752, SEQ ID NO: 754, SEQ ID NO: 756, SEQ ID NO: 758, SEQ ID NO: 760, SEQ ID NO: 762, SEQ ID NO: 764, SEQ ID NO: 766, SEQ ID NO: 768, SEQ ID NO: 770, SEQ ID NO: 772, SEQ ID NO: 774, SEQ ID NO: 776, SEQ ID NO: 778, SEQ ID NO: 780, SEQ ID NO: 782, SEQ ID NO: 784, SEQ ID NO: 786, SEQ ID NO: 788, SEQ ID NO: 790, SEQ ID NO: 792, SEQ ID NO: 794, SEQ ID NO : 796, SEQ ID NO: 798, SEQ ID NO: 800, SEQ ID NO: 802, SEQ ID NO: 804, SEQ ID NO: 806, SEQ ID NO: 808, SEQ ID NO: 810, SEQ ID NO: 812, SEQ ID NO: 814, SEQ ID NO: 816, SEQ ID NO: 818, SEQ ID NO: 820, SEQ ID NO: 822, SEQ ID NO: 824, SEQ ID NO: 826, SEQ ID NO: 828, SEQ ID NO: 830, SEQ ID NO: 832, SEQ ID NO: 834, SEQ ID NO: 836, SEQ ID NO: 838, SEQ ID NO: 840, SEQ ID NO: 842, SEQ ID NO: 844, SEQ ID NO: 846, SEQ ID NO: 848, SEQ ID NO: 850, SEQ ID NO: 852, SEQ ID NO: 854, SEQ ID NO: 856, SEQ ID NO: 858, SEQ ID NO: 860, SEQ ID NO: 862, SEQ ID NO: 864, SEQ ID NO: 866, SEQ ID NO: 868, SEQ ID NO: 870, SEQ ID NO: 872, SEQ ID NO: 874, SEQ ID NO: 876, SEQ ID NO: 878, SEQ ID NO: 880, SEQ ID NO: 882, SEQ ID NO: 884, SEQ ID NO: 886, SEQ ID NO: 888, SEQ ID NO: 890, SEQ ID NO: 892, SEQ ID NO: 894, SEQ ID NO: 896, SEQ ID NO: 898, SEQ ID NO: 900, SEQ ID NO: 902, SEQ ID NO: 904, SEQ ID NO: 906, SEQ ID NO: 908, SEQ ID NO: 910, SEQ ID NO: 912, SEQ ID NO: 914, SEQ ID NO: 916, SEQ ID NO: 918, SEQ ID NO: 920, SEQ ID NO: 922, SEQ ID NO: 924, SEQ ID NO: 926, SEQ ID NO: 928, SEQ ID NO: 930, SEQ ID NO: 932, SEQ ID NO: 934, SEQ ID NO: 936, SEQ ID NO: 938, SEQ ID NO: 940, SEQ ID NO: 942, SEQ ID NO: 944, SEQ ID NO: 946, SEQ ID NO: 948, SEQ ID NO: 950, SEQ ID NO: 952 or SEQ ID NO: 954 or an enzymatically active fragment thereof having lipase activity;
(ii) a polypeptide encoded by the nucleic acid sequence according to any one of SEQ ID Nos. SEQ ID NO: 955, SEQ ID NO: 1 , SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 1 1 , SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 19, SEQ ID NO: 21 , SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 27, SEQ ID NO: 29, SEQ ID NO: 31 , SEQ ID NO: 33, SEQ ID NO: 35, SEQ ID NO: 37, SEQ ID NO: 39, SEQ ID NO: 41 , SEQ ID NO: 43, SEQ ID NO: 45, SEQ ID NO: 47, SEQ ID NO: 49, SEQ ID NO: 51 , SEQ ID NO: 53, SEQ ID NO: 55, SEQ ID NO: 57, SEQ ID NO: 59, SEQ ID NO: 61 , SEQ ID NO: 63, SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 71 , SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 77, SEQ ID NO: 79, SEQ ID NO: 81 , SEQ ID NO: 83, SEQ ID NO: 85, SEQ ID NO: 87, SEQ ID NO: 89, SEQ ID NO: 91 , SEQ ID NO: 93, SEQ ID NO: 95, SEQ ID NO: 97, SEQ ID NO: 99, SEQ ID NO: 101 , SEQ ID NO: 103, SEQ ID NO: 105, SEQ ID NO: 107, SEQ ID NO: 109, SEQ ID NO: 1 11 , SEQ ID NO: 1 13, SEQ ID NO: 115, SEQ ID NO: 1 17, SEQ ID NO: 119, SEQ ID NO: 121 , SEQ ID NO: 123, SEQ ID NO: 125, SEQ ID NO: 127, SEQ ID NO: 129, SEQ ID NO: 131 , SEQ ID NO: 133, SEQ ID NO: 135, SEQ ID NO: 137, SEQ ID NO: 139, SEQ ID NO: 141 , SEQ ID NO: 143, SEQ ID NO: 145, SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 151 , SEQ ID NO: 153, SEQ ID NO: 155, SEQ ID NO: 157, SEQ ID NO: 159, SEQ ID NO: 161 , SEQ ID NO: 163, SEQ ID NO: 165, SEQ ID NO: 167, SEQ ID NO: 169, SEQ ID NO: 171 , SEQ ID NO: 173, SEQ ID NO: 175, SEQ ID NO: 177, SEQ ID NO: 179, SEQ ID NO: 181 , SEQ ID NO: 183, SEQ ID NO: 185, SEQ ID NO: 187, SEQ ID NO: 189, SEQ ID NO: 191 , SEQ ID NO: 193, SEQ ID NO: 195, SEQ ID NO: 197, SEQ ID NO: 199, SEQ ID NO: 201 , SEQ ID NO: 203, SEQ ID NO: 205, SEQ ID NO: 207, SEQ ID NO: 209, SEQ ID NO: 21 1 , SEQ ID NO: 213, SEQ ID NO: 215, SEQ ID NO: 217, SEQ ID NO: 219, SEQ ID NO: 221 , SEQ ID NO: 223, SEQ ID NO: 225, SEQ ID NO: 227, SEQ ID NO: 229, SEQ ID NO: 231 , SEQ ID NO: 233, SEQ ID NO: 235, SEQ ID NO: 237, SEQ ID NO: 239, SEQ ID NO: 241 , SEQ ID NO: 243, SEQ ID NO: 245, SEQ ID NO: 247, SEQ ID NO: 249, SEQ ID NO: 251 , SEQ ID NO: 253, SEQ ID NO: 255, SEQ ID NO: 257, SEQ ID NO: 259, SEQ ID NO: 261 , SEQ ID NO: 263, SEQ ID NO: 265, SEQ ID NO: 267, SEQ ID NO: 269, SEQ ID NO: 271 , SEQ ID NO: 273, SEQ ID NO: 275, SEQ ID NO: 277, SEQ ID NO: 279, SEQ ID NO: 281 , SEQ ID NO: 283, SEQ ID NO: 285, SEQ ID NO: 287, SEQ ID NO: 289, SEQ ID NO: 291 , SEQ ID NO: 293, SEQ ID NO: 295, SEQ ID NO: 297, SEQ ID NO: 299, SEQ ID NO: 301 , SEQ ID NO: 303, SEQ ID NO: 305, SEQ ID NO: 307, SEQ ID NO: 309, SEQ ID NO: 31 1 , SEQ ID NO: 313, SEQ ID NO: 315, SEQ ID NO: 317, SEQ ID NO: 319, SEQ ID NO: 321 , SEQ ID NO: 323, SEQ ID NO: 325, SEQ ID NO: 327, SEQ ID NO: 329, SEQ ID NO: 331 , SEQ ID NO: 333, SEQ ID NO: 335, SEQ ID NO: 337, SEQ ID NO: 339, SEQ ID NO: 341 , SEQ ID NO: 343, SEQ ID NO: 345, SEQ ID NO: 347, SEQ ID NO: 349, SEQ ID NO: 351 , SEQ ID NO: 353, SEQ ID NO: 355, SEQ ID NO: 357, SEQ ID NO: 359, SEQ ID NO: 361 , SEQ ID NO: 363, SEQ ID NO: 365, SEQ ID NO: 367, SEQ ID NO: 369, SEQ ID NO: 371 , SEQ ID NO: 373, SEQ ID NO: 375, SEQ ID NO: 377, SEQ ID NO: 379, SEQ ID NO: 381 , SEQ ID NO: 383, SEQ ID NO: 385, SEQ ID NO: 387, SEQ ID NO: 389, SEQ ID NO: 391 , SEQ ID NO: 393, SEQ ID NO: 395, SEQ ID NO: 397, SEQ ID NO: 399, SEQ ID NO: 401 , SEQ ID NO: 403, SEQ ID NO: 405, SEQ ID NO: 407, SEQ ID NO: 409, SEQ ID NO: 41 1 , SEQ ID NO: 413, SEQ ID NO: 415, SEQ ID NO: 417, SEQ ID NO: 419, SEQ ID NO: 421 , SEQ ID NO: 423, SEQ ID NO: 425, SEQ ID NO: 427, SEQ ID NO: 429, SEQ ID NO: 431 , SEQ ID NO: 433, SEQ ID NO: 435, SEQ ID NO: 437, SEQ ID NO: 439, SEQ ID NO: 441 , SEQ ID NO: 443, SEQ ID NO: 445, SEQ ID NO: 447, SEQ ID NO: 449, SEQ ID NO: 451 , SEQ ID NO: 453, SEQ ID NO: 455, SEQ ID NO: 457, SEQ ID NO: 459, SEQ ID NO: 461 , SEQ ID NO: 463, SEQ ID NO: 465, SEQ ID NO: 467, SEQ ID NO: 469, SEQ ID NO: 471 , SEQ ID NO: 473, SEQ ID NO: 475, SEQ ID NO: 477, SEQ ID. NO: 479, SEQ ID NO: 481 , SEQ ID NO: 483, SEQ ID NO: 485, SEQ ID NO: 487, SEQ ID NO: 489, SEQ ID NO: 491 , SEQ ID NO: 493, SEQ ID NO: 495, SEQ ID NO: 497, SEQ ID NO: 499, SEQ ID NO: 501 , SEQ ID NO: 503, SEQ ID NO: 505, SEQ ID NO: 507, SEQ ID NO: 509, SEQ ID NO: 51 1 , SEQ ID NO: 513, SEQ ID NO: 515, SEQ ID NO: 517, SEQ ID NO: 519, SEQ ID NO: 521 , SEQ ID NO: 523, SEQ ID NO: 525, SEQ ID NO: 527, SEQ ID NO: 529, SEQ ID NO: 531 , SEQ ID NO: 533, SEQ ID NO: 535, SEQ ID NO: 537, SEQ ID NO: 539, SEQ ID NO: 541 , SEQ ID NO: 543, SEQ ID NO: 545, SEQ ID NO: 547, SEQ ID NO: 549, SEQ ID NO: 551 , SEQ ID NO: 553, SEQ ID NO: 555, SEQ ID NO: 557, SEQ ID NO: 559, SEQ ID NO: 561 , SEQ ID NO: 563, SEQ ID NO: 565, SEQ ID NO: 567, SEQ ID NO: 569, SEQ ID NO: 571 , SEQ ID NO: 573, SEQ ID NO: 575, SEQ ID NO: 577, SEQ ID NO: 579, SEQ ID NO: 581 , SEQ ID NO: 583, SEQ ID NO: 585, SEQ ID NO: 587, SEQ ID NO: 589, SEQ ID NO: 591 , SEQ ID NO: 593, SEQ ID NO: 595, SEQ ID NO: 597, SEQ ID NO: 599, SEQ ID NO: 601 , SEQ ID NO: 603, SEQ ID NO: 605, SEQ ID NO: 607, SEQ ID NO: 609, SEQ ID NO: 61 1 , SEQ ID NO: 613, SEQ ID NO: 615, SEQ ID NO: 617, SEQ ID NO: 619, SEQ ID NO: 621 , SEQ ID NO: 623, SEQ ID NO: 625, SEQ ID NO: 627, SEQ ID NO: 629, SEQ ID NO: 631 , SEQ ID NO: 633, SEQ ID NO: 635, SEQ ID NO: 637, SEQ ID NO: 639, SEQ ID NO: 641 , SEQ ID NO: 643, SEQ ID NO: 645, SEQ ID NO: 647, SEQ ID NO: 649, SEQ ID NO: 651 , SEQ ID NO: 653, SEQ ID NO: 655, SEQ ID NO: 657, SEQ ID NO: 659, SEQ ID NO: 661 , SEQ ID NO: 663, SEQ ID NO: 665, SEQ ID NO: 667, SEQ ID NO: 669, SEQ ID NO: 671 , SEQ ID NO: 673, SEQ ID NO: 675, SEQ ID NO: 677, SEQ ID NO: 679, SEQ ID NO: 681 , SEQ ID NO: 683, SEQ ID NO: 685, SEQ ID NO: 687, SEQ ID NO: 689, SEQ ID NO: 691 , SEQ ID NO: 693, SEQ ID NO: 695, SEQ ID NO: 697, SEQ ID NO: 699, SEQ ID NO: 701 , SEQ ID NO: 703, SEQ ID NO: 705, SEQ ID NO: 707, SEQ ID NO: 709, SEQ ID NO: 71 1 , SEQ ID NO: 713, SEQ ID NO: 715, SEQ ID NO: 717, SEQ ID NO: 719, SEQ ID NO: 721 , SEQ ID NO: 723, SEQ ID NO: 725, SEQ ID NO: 727, SEQ ID NO: 729, SEQ ID NO: 731 , SEQ ID NO: 733, SEQ ID NO: 735, SEQ ID NO: 737, SEQ ID NO: 739, SEQ ID NO: 741 , SEQ ID NO: 743, SEQ ID NO: 745, SEQ ID NO: 747, SEQ ID NO : 749, SEQ ID NO: 751 , SEQ ID NO : 753, SEQ ID NO : 755, SEQ ID NO: 757, SEQ ID NO: 759, SEQ ID NO: 761 , SEQ ID NO: 763, SEQ ID NO: 765, SEQ ID NO : 767, SEQ ID NO : 769, SEQ ID NO : 771 , SEQ ID NO: 773, SEQ ID NO: 775, SEQ ID NO: 777, SEQ ID NO: 779, SEQ ID NO: 781 , SEQ ID NO: 783, SEQ ID NO: 785, SEQ ID NO: 787, SEQ ID NO: 789, SEQ ID NO: 791 , SEQ ID NO: 793, SEQ ID NO: 795, SEQ ID NO: 797, SEQ ID NO: 799, SEQ ID NO: 801 , SEQ ID NO: 803, SEQ ID NO: 805, SEQ ID NO: 807, SEQ ID NO: 809, SEQ ID NO: 811 , SEQ ID NO: 813, SEQ ID NO: 815, SEQ ID NO: 817, SEQ ID NO: 819, SEQ ID NO: 821 , SEQ ID NO: 823, SEQ ID NO: 825, SEQ ID NO: 827, SEQ ID NO: 829, SEQ ID NO: 831 , SEQ ID NO: 833, SEQ ID NO: 835, SEQ ID NO: 837, SEQ ID NO: 839, SEQ ID NO: 841 , SEQ ID NO: 843, SEQ ID NO: 845, SEQ ID NO: 847, SEQ ID NO: 849, SEQ ID NO: 851 , SEQ ID NO: 853, SEQ ID NO: 855, SEQ ID NO: 857, SEQ ID NO: 859, SEQ ID NO: 861 , SEQ ID NO: 863, SEQ ID NO: 865, SEQ ID NO: 867, SEQ ID NO: 869, SEQ ID NO: 871 , SEQ ID NO: 873, SEQ ID NO: 875, SEQ ID NO: 877, SEQ ID NO: 879, SEQ ID NO: 881 , SEQ ID NO: 883, SEQ ID NO: 885, SEQ ID NO: 887, SEQ ID NO: 889, SEQ ID NO: 891 , SEQ ID NO: 893, SEQ ID NO: 895, SEQ ID NO: 897, SEQ ID NO: 899, SEQ ID NO: 901 , SEQ ID NO: 903, SEQ ID NO: 905, SEQ ID NO: 907, SEQ ID NO: 909, SEQ ID NO: 911 , SEQ ID NO: 913, SEQ ID NO: 915, SEQ ID NO: 917, SEQ ID NO: 919, SEQ ID NO: 921 , SEQ ID NO: 923, SEQ ID NO: 925, SEQ ID NO: 927, SEQ ID NO: 929, SEQ ID NO: 931 , SEQ ID NO: 933, SEQ ID NO: 935, SEQ ID NO: 937, SEQ ID NO: 939, SEQ ID NO: 941 , SEQ ID NO: 943, SEQ ID NO: 945, SEQ ID NO: 947, SEQ ID NO: 949, SEQ ID NO: 951 or SEQ ID NO: 953 or an enzymatically active fragment thereof having lipase activity;
(iii) a polypeptide having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28,
SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56, SEQ ID NO: 58, SEQ ID NO: 60, SEQ ID NO: 62,
SEQ ID NO: 64, SEQ ID NO: 66, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 72, SEQ ID NO: 74, SEQ ID NO: 76, SEQ ID NO: 78, SEQ ID NO: 80, SEQ ID NO: 82, SEQ ID NO: 84, SEQ ID NO: 86, SEQ ID NO: 88, SEQ ID NO: 90, SEQ ID NO: 92, SEQ ID NO: 94, SEQ ID NO: 96,
SEQ ID NO: 98, SEQ ID NO: 100, SEQ ID NO: 102, SEQ ID NO: 104, SEQ ID NO: 106, SEQ ID NO: 108, SEQ ID NO: 1 10, SEQ ID NO: 1 12, SEQ ID NO: 1 14, SEQ ID NO: 116, SEQ ID NO: 1 18, SEQ ID NO: 120, SEQ ID NO: 122, SEQ ID NO: 124, SEQ ID NO: 126, SEQ ID NO: 128, SEQ ID NO: 130, SEQ ID NO: 132, SEQ ID NO: 134, SEQ ID NO: 136, SEQ ID NO: 138, SEQ ID NO: 140, SEQ ID NO: 142, SEQ ID NO: 143, SEQ ID NO: 146, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 152, SEQ ID NO: 154, SEQ ID NO: 156, SEQ ID NO: 158, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 166, SEQ ID NO: 168, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 174, SEQ ID NO: 176, SEQ ID NO: 178, SEQ ID NO: 180, SEQ ID NO: 182, SEQ ID NO: 184, SEQ ID NO: 186, SEQ ID NO: 188, SEQ ID NO: 190, SEQ ID NO: 192, SEQ ID NO: 194, SEQ ID NO: 196, SEQ ID NO: 198, SEQ ID NO: 200, SEQ ID NO: 202, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 208, SEQ ID NO: 210, SEQ ID NO: 212, SEQ ID NO: 214, SEQ ID NO: 216, SEQ ID NO: 218, SEQ ID NO: 220, SEQ ID NO: 222, SEQ ID NO: 224, SEQ ID NO: 226, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 232, SEQ ID NO: 234, SEQ ID NO: 236, SEQ ID NO: 238, SEQ ID NO: 240, SEQ ID NO: 242, SEQ ID NO: 244, SEQ ID NO: 246, SEQ ID NO: 248, SEQ ID NO: 250, SEQ ID NO: 252, SEQ ID NO: 254, SEQ ID NO: 256, SEQ ID NO: 258, SEQ ID NO: 260, SEQ ID NO: 262, SEQ ID NO: 264, SEQ ID NO: 266, SEQ ID NO: 268, SEQ ID NO: 270, SEQ ID NO: 272, SEQ ID NO: 274, SEQ ID NO: 276, SEQ ID NO: 278, SEQ ID NO: 280, SEQ ID NO: 282, SEQ ID NO: 284, SEQ ID NO: 286, SEQ ID NO: 288, SEQ ID NO: 290, SEQ ID NO: 292, SEQ ID NO: 294, SEQ ID NO: 296, SEQ ID NO: 298, SEQ ID NO: 300, SEQ ID NO: 302, SEQ ID NO: 304, SEQ ID NO: 306, SEQ ID NO: 308, SEQ ID NO: 310, SEQ ID NO: 312, SEQ ID NO: 314, SEQ ID NO: 316, SEQ ID NO: 318, SEQ ID NO: 320, SEQ ID NO: 322, SEQ ID NO: 324, SEQ ID NO: 326, SEQ ID NO: 328, SEQ ID NO: 330, SEQ ID NO: 332, SEQ ID NO: 334, SEQ ID NO: 336, SEQ ID NO: 338, SEQ ID NO: 340, SEQ ID NO: 342, SEQ ID NO: 344, SEQ ID NO: 346, SEQ ID NO: 348, SEQ ID NO: 350, SEQ ID NO: 352, SEQ ID NO: 354, SEQ ID NO: 356, SEQ ID NO: 358, SEQ ID NO: 360, SEQ ID NO: 362, SEQ ID NO: 364, SEQ ID NO: 366, SEQ ID NO: 368, SEQ ID NO: 370, SEQ ID NO: 372, SEQ ID NO: 374, SEQ ID NO: 376, SEQ ID NO: 378, SEQ ID NO: 380, SEQ ID NO: 382, SEQ ID NO: 384, SEQ ID NO: 386, SEQ ID NO: 388, SEQ ID NO: 390, SEQ ID NO: 392, SEQ ID NO: 394, SEQ ID NO: 396, SEQ ID NO: 398, SEQ ID NO: 400, SEQ ID NO: 402, SEQ ID NO: 404, SEQ ID NO: 406, SEQ ID NO: 408, SEQ ID NO: 410, SEQ ID NO: 412, SEQ ID NO: 414, SEQ ID NO: 416, SEQ ID NO: 418, SEQ ID NO: 420, SEQ ID NO: 422, SEQ ID NO: 424, SEQ ID NO: 426, SEQ ID NO: 428, SEQ ID NO: 430, SEQ ID NO: 432, SEQ ID NO: 434, SEQ ID NO: 436, SEQ ID NO: 438, SEQ ID NO: 440, SEQ ID NO: 442, SEQ ID NO: 444, SEQ ID NO: 446, SEQ ID NO: 448, SEQ ID NO: 450, SEQ ID NO: 452, SEQ ID NO: 454, SEQ ID NO: 456, SEQ ID NO: 458, SEQ ID NO: 460, SEQ ID NO: 462, SEQ ID NO: 464, SEQ ID NO: 466, SEQ ID NO: 468, SEQ ID NO: 470, SEQ ID NO: 472, SEQ ID NO: 474, SEQ ID NO: 476, SEQ ID NO: 478, SEQ ID NO: 480, SEQ ID NO: 482, SEQ ID NO: 484, SEQ ID NO: 486, SEQ ID NO: 488, SEQ ID NO: 490, SEQ ID NO: 492, SEQ ID NO: 494, SEQ ID NO: 496, SEQ ID NO: 498, SEQ ID NO: 500, SEQ ID NO: 502, SEQ ID NO: 504, SEQ ID NO: 506, SEQ ID NO: 508, SEQ ID NO: 510, SEQ ID NO: 512, SEQ ID NO: 514, SEQ ID NO: 516, SEQ ID NO: 518, SEQ ID NO: 520, SEQ ID NO: 522, SEQ ID NO: 524, SEQ ID NO: 526, SEQ ID NO: 528, SEQ ID NO: 530, SEQ ID NO: 532, SEQ ID NO: 534, SEQ ID NO: 536, SEQ ID NO: 538, SEQ ID NO: 540, SEQ ID NO: 542, SEQ ID NO: 544, SEQ ID NO: 546, SEQ ID NO: 548, SEQ ID NO: 550, SEQ ID NO: 552, SEQ ID NO: 554, SEQ ID NO: 556, SEQ ID NO: 558, SEQ ID NO: 560, SEQ ID NO: 562, SEQ ID NO: 564, SEQ ID NO: 566, SEQ ID NO: 568, SEQ ID NO: 570, SEQ ID NO: 572, SEQ ID NO: 574, SEQ ID NO: 576, SEQ ID NO: 578, SEQ ID NO: 580, SEQ ID NO: 582, SEQ ID NO: 584, SEQ ID NO: 586, SEQ ID NO: 588, SEQ ID NO: 590, SEQ ID NO: 592, SEQ ID NO: 594, SEQ ID NO: 596, SEQ ID NO: 598, SEQ ID NO: 600, SEQ ID NO: 602, SEQ ID NO: 604, SEQ ID NO: 606, SEQ ID NO: 608, SEQ ID NO: 610, SEQ ID NO: 612, SEQ ID NO: 614, SEQ ID NO: 616, SEQ ID NO: 618, SEQ ID NO: 620, SEQ ID NO: 622, SEQ ID NO: 624, SEQ ID NO: 626, SEQ ID NO: 628, SEQ ID NO: 630, SEQ ID NO: 632, SEQ ID NO: 634, SEQ ID NO: 636, SEQ ID NO: 638, SEQ ID NO: 640, SEQ ID NO: 642, SEQ ID NO: 644, SEQ ID NO: 646, SEQ ID NO: 648, SEQ ID NO: 650, SEQ ID NO: 652, SEQ ID NO: 654, SEQ ID NO: 656, SEQ ID NO: 658, SEQ ID NO: 660, SEQ ID NO: 662, SEQ ID NO: 664, SEQ ID NO: 666, SEQ ID NO: 668, SEQ ID NO: 670, SEQ ID NO: 672, SEQ ID NO: 674, SEQ ID NO: 676, SEQ ID NO: 678, SEQ ID NO: 680, SEQ ID NO: 682, SEQ ID NO: 684, SEQ ID NO: 686, SEQ ID NO: 688, SEQ ID NO: 690, SEQ ID NO: 692, SEQ ID NO: 694, SEQ ID NO: 696, SEQ ID NO: 698, SEQ ID NO: 700, SEQ ID NO: 702, SEQ ID NO: 704, SEQ ID NO: 706, SEQ ID NO: 708, SEQ ID NO: 710, SEQ ID NO: 712, SEQ ID NO: 714, SEQ ID NO: 716, SEQ ID NO: 718, SEQ ID NO: 720, SEQ ID NO: 722, SEQ ID NO: 724, SEQ ID NO: 726, SEQ ID NO: 728, SEQ ID NO: 730, SEQ ID NO: 732, SEQ ID NO: 734, SEQ ID NO: 736, SEQ ID NO: 738, SEQ ID NO: 740, SEQ ID NO: 742, SEQ ID NO: 744, SEQ ID NO: 746, SEQ ID NO: 748, SEQ ID NO: 750, SEQ ID NO: 752, SEQ ID NO: 754, SEQ ID NO: 756, SEQ ID NO: 758, SEQ ID NO: 760, SEQ ID NO: 762, SEQ ID NO: 764, SEQ ID NO: 766, SEQ ID NO: 768, SEQ ID NO: 770, SEQ ID NO: 772, SEQ ID NO: 774, SEQ ID NO: 776, SEQ ID NO: 778, SEQ ID NO: 780, SEQ ID NO: 782, SEQ ID NO: 784, SEQ ID NO: 786, SEQ ID NO: 788, SEQ ID NO: 790, SEQ ID NO: 792, SEQ ID NO: 794, SEQ ID NO : 796, SEQ ID NO: 798, SEQ ID NO: 800, SEQ ID NO: 802, SEQ ID NO: 804, SEQ ID NO: 806, SEQ ID NO: 808, SEQ ID NO: 810, SEQ ID NO: 812, SEQ ID NO: 814, SEQ ID NO: 816, SEQ ID NO: 818, SEQ ID NO: 820, SEQ ID NO: 822, SEQ ID NO: 824, SEQ ID NO: 826, SEQ ID NO: 828, SEQ ID NO: 830, SEQ ID NO: 832, SEQ ID NO: 834, SEQ ID NO: 836, SEQ ID NO: 838, SEQ ID NO: 840, SEQ ID NO: 842, SEQ ID NO: 844, SEQ ID NO: 846, SEQ ID NO: 848, SEQ ID NO: 850, SEQ ID NO: 852, SEQ ID NO: 854, SEQ ID NO: 856, SEQ ID NO: 858, SEQ ID NO: 860, SEQ ID NO: 862, SEQ ID NO: 864, SEQ ID NO: 866, SEQ ID NO: 868, SEQ ID NO: 870, SEQ ID NO: 872, SEQ ID NO: 874, SEQ ID NO: 876, SEQ ID NO: 878, SEQ ID NO: 880, SEQ ID NO: 882, SEQ ID NO: 884, SEQ ID NO: 886, SEQ ID NO: 888, SEQ ID NO: 890, SEQ ID NO: 892, SEQ ID NO: 894, SEQ ID NO: 896, SEQ ID NO: 898, SEQ ID NO: 900, SEQ ID NO: 902, SEQ ID NO: 904, SEQ ID NO: 906, SEQ ID NO: 908, SEQ ID NO: 910, SEQ ID NO: 912, SEQ ID NO: 914, SEQ ID NO: 916, SEQ ID NO: 918, SEQ ID NO: 920, SEQ ID NO: 922, SEQ ID NO: 924, SEQ ID NO: 926, SEQ ID NO: 928, SEQ ID NO: 930, SEQ ID NO: 932, SEQ ID NO: 934, SEQ ID NO: 936, SEQ ID NO: 938, SEQ ID NO: 940, SEQ ID NO: 942, SEQ ID NO: 944, SEQ ID NO: 946, SEQ ID NO: 948, SEQ ID NO: 950, SEQ ID NO: 952 or SEQ ID NO: 954 or an enzymatically active fragment thereof having lipase activity; and
(iv) a polypeptide encoded by a nucleic acid sequence which hybridizes to the complement of the nucleic acid sequence according to any of SEQ ID NO: 955, SEQ ID NO: 1 , SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11 , SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 19, SEQ ID NO: 21 , SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 27, SEQ ID NO: 29, SEQ ID NO: 31 , SEQ ID NO: 33, SEQ ID NO: 35, SEQ ID NO: 37, SEQ ID NO: 39, SEQ ID NO: 41 , SEQ ID NO: 43, SEQ ID NO: 45, SEQ ID NO: 47, SEQ ID NO: 49,
SEQ ID NO: 51 , SEQ ID NO: 53, SEQ ID NO: 55, SEQ ID NO: 57, SEQ ID NO: 59, SEQ ID NO: 61 , SEQ ID NO: 63, SEQ ID NO: 65, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 71 , SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 77, SEQ ID NO: 79, SEQ ID NO: 81 , SEQ ID NO: 83,
SEQ ID NO: 85, SEQ ID NO: 87, SEQ ID NO: 89, SEQ ID NO: 91 , SEQ ID NO: 93, SEQ ID NO: 95, SEQ ID NO: 97, SEQ ID NO: 99, SEQ ID NO: 101 , SEQ ID NO: 103, SEQ ID NO: 105, SEQ ID NO: 107, SEQ ID NO: 109, SEQ ID NO: 11 1 , SEQ ID NO: 1 13, SEQ ID NO: 115, SEQ ID NO: 1 17, SEQ ID NO: 1 19, SEQ ID NO: 121 , SEQ ID NO: 123, SEQ ID NO: 125, SEQ ID NO: 127, SEQ ID NO: 129, SEQ ID NO: 131 , SEQ ID NO: 133, SEQ ID NO: 135, SEQ ID NO: 137, SEQ ID NO: 139, SEQ ID NO: 141 , SEQ ID NO: 143, SEQ ID NO: 145, SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 151 , SEQ ID NO: 153, SEQ ID NO: 155, SEQ ID NO: 157, SEQ ID NO: 159, SEQ ID NO: 161 , SEQ ID NO: 163, SEQ ID NO: 165, SEQ ID NO: 167, SEQ ID NO: 169, SEQ ID NO: 171 , SEQ ID NO: 173, SEQ ID NO: 175, SEQ ID NO: 177, SEQ ID NO: 179, SEQ ID NO: 181 , SEQ ID NO: 183, SEQ ID NO: 185, SEQ ID NO: 187, SEQ ID NO: 189, SEQ ID NO: 191 , SEQ ID NO: 193, SEQ ID NO: 195, SEQ ID NO: 197, SEQ ID NO: 199, SEQ ID NO: 201 , SEQ ID NO: 203, SEQ ID NO: 205, SEQ ID NO: 207, SEQ ID NO: 209, SEQ ID NO: 21 1 , SEQ ID NO: 213, SEQ ID NO: 215, SEQ ID NO: 217, SEQ ID NO: 219, SEQ ID NO: 221 , SEQ ID NO: 223, SEQ ID NO: 225, SEQ ID NO: 227, SEQ ID NO: 229, SEQ ID NO: 231 , SEQ ID NO: 233, SEQ ID NO: 235, SEQ ID NO: 237, SEQ ID NO: 239, SEQ ID NO: 241 , SEQ ID NO: 243, SEQ ID NO: 245, SEQ ID NO: 247, SEQ ID NO: 249, SEQ ID NO: 251 , SEQ ID NO: 253, SEQ ID NO: 255, SEQ ID NO: 257, SEQ ID NO: 259, SEQ ID NO: 261 , SEQ ID NO: 263, SEQ ID NO: 265, SEQ ID NO: 267, SEQ ID NO: 269, SEQ ID NO: 271 , SEQ ID NO: 273, SEQ ID NO: 275, SEQ ID NO: 277, SEQ ID NO: 279, SEQ ID NO: 281 , SEQ ID NO: 283, SEQ ID NO: 285, SEQ ID NO: 287, SEQ ID NO: 289, SEQ ID NO: 291 , SEQ ID NO: 293, SEQ ID NO: 295, SEQ ID NO: 297, SEQ ID NO: 299, SEQ ID NO: 301 , SEQ ID NO: 303, SEQ ID NO: 305, SEQ ID NO: 307, SEQ ID NO: 309, SEQ ID NO: 31 1 , SEQ ID NO: 313, SEQ ID NO: 315, SEQ ID NO: 317, SEQ ID NO: 319, SEQ ID NO: 321 , SEQ ID NO: 323, SEQ ID NO: 325, SEQ ID NO: 327, SEQ ID NO: 329, SEQ ID NO: 331 , SEQ ID NO: 333, SEQ ID NO: 335, SEQ ID NO: 337, SEQ ID NO: 339, SEQ ID NO: 341 , SEQ ID NO: 343, SEQ ID NO: 345, SEQ ID NO: 347, SEQ ID NO: 349, SEQ ID NO: 351 , SEQ ID NO: 353, SEQ ID NO: 355, SEQ ID NO: 357, SEQ ID NO: 359, SEQ ID NO: 361 , SEQ ID NO: 363, SEQ ID NO: 365, SEQ ID NO: 367, SEQ ID NO: 369, SEQ ID NO: 371 , SEQ ID NO: 373, SEQ ID NO: 375, SEQ ID NO: 377, SEQ ID NO: 379, SEQ ID NO: 381 , SEQ ID NO: 383, SEQ ID NO: 385, SEQ ID NO: 387, SEQ ID NO: 389, SEQ ID NO: 391 , SEQ ID NO: 393, SEQ ID NO: 395, SEQ ID NO: 397, SEQ ID NO: 399, SEQ ID NO: 401 , SEQ ID NO: 403, SEQ ID NO: 405, SEQ ID NO: 407, SEQ ID NO: 409, SEQ ID NO: 41 1 , SEQ ID NO: 413, SEQ ID NO: 415, SEQ ID NO: 417, SEQ ID NO: 419, SEQ ID NO: 421 , SEQ ID NO: 423, SEQ ID NO: 425, SEQ ID NO: 427, SEQ ID NO: 429, SEQ ID NO: 431 , SEQ ID NO: 433, SEQ ID NO: 435, SEQ ID NO: 437, SEQ ID NO: 439, SEQ ID NO: 441 , SEQ ID NO: 443, SEQ ID NO: 445, SEQ ID NO: 447, SEQ ID NO: 449, SEQ ID NO: 451 , SEQ ID NO: 453, SEQ ID NO: 455, SEQ ID NO: 457, SEQ ID NO: 459, SEQ ID NO: 461 , SEQ ID NO: 463, SEQ ID NO: 465, SEQ ID NO: 467, SEQ ID NO: 469, SEQ ID NO: 471 , SEQ ID NO: 473, SEQ ID NO: 475, SEQ ID NO: 477, SEQ ID. NO: 479, SEQ ID NO: 481 , SEQ ID NO: 483, SEQ ID NO: 485, SEQ ID NO: 487, SEQ ID NO: 489, SEQ ID NO: 491 , SEQ ID NO: 493, SEQ ID NO: 495, SEQ ID NO: 497, SEQ ID NO: 499, SEQ ID NO: 501 , SEQ ID NO: 503, SEQ ID NO: 505, SEQ ID NO: 507, SEQ ID NO: 509, SEQ ID NO: 51 1 , SEQ ID NO: 513, SEQ ID NO: 515, SEQ ID NO: 517, SEQ ID NO: 519, SEQ ID NO: 521 , SEQ ID NO: 523, SEQ ID NO: 525, SEQ ID NO: 527, SEQ ID NO: 529, SEQ ID NO: 531 , SEQ ID NO: 533, SEQ ID NO: 535, SEQ ID NO: 537, SEQ ID NO: 539, SEQ ID NO: 541 , SEQ ID NO: 543, SEQ ID NO: 545, SEQ ID NO: 547, SEQ ID NO: 549, SEQ ID NO: 551 , SEQ ID NO: 553, SEQ ID NO: 555, SEQ ID NO: 557, SEQ ID NO: 559, SEQ ID NO: 561 , SEQ ID NO: 563, SEQ ID NO: 565, SEQ ID NO: 567, SEQ ID NO: 569, SEQ ID NO: 571 , SEQ ID NO: 573, SEQ ID NO: 575, SEQ ID NO: 577, SEQ ID NO: 579, SEQ ID NO: 581 , SEQ ID NO: 583, SEQ ID NO: 585, SEQ ID NO: 587, SEQ ID NO: 589, SEQ ID NO: 591 , SEQ ID NO: 593, SEQ ID NO: 595, SEQ ID NO: 597, SEQ ID NO: 599, SEQ ID NO: 601 , SEQ ID NO: 603, SEQ ID NO: 605, SEQ ID NO: 607, SEQ ID NO: 609, SEQ ID NO: 61 1 , SEQ ID NO: 613, SEQ ID NO: 615, SEQ ID NO: 617, SEQ ID NO: 619, SEQ ID NO: 621 , SEQ ID NO: 623, SEQ ID NO: 625, SEQ ID NO: 627, SEQ ID NO: 629, SEQ ID NO: 631 , SEQ ID NO: 633, SEQ ID NO: 635, SEQ ID NO: 637, SEQ ID NO: 639, SEQ ID NO: 641 , SEQ ID NO: 643, SEQ ID NO: 645, SEQ ID NO: 647, SEQ ID NO: 649, SEQ ID NO: 651 , SEQ ID NO: 653, SEQ ID NO: 655, SEQ ID NO: 657, SEQ ID NO: 659, SEQ ID NO: 661 , SEQ ID NO: 663, SEQ ID NO: 665, SEQ ID NO: 667, SEQ ID NO: 669, SEQ ID NO: 671 , SEQ ID NO: 673, SEQ ID NO: 675, SEQ ID NO: 677, SEQ ID NO: 679, SEQ ID NO: 681 , SEQ ID NO: 683, SEQ ID NO: 685, SEQ ID NO: 687, SEQ ID NO: 689, SEQ ID NO: 691 , SEQ ID NO: 693, SEQ ID NO: 695, SEQ ID NO: 697, SEQ ID NO: 699, SEQ ID NO: 701 , SEQ ID NO: 703, SEQ ID NO: 705, SEQ ID NO: 707, SEQ ID NO: 709, SEQ ID NO: 711 , SEQ ID NO: 713, SEQ ID NO: 715, SEQ ID NO: 717, SEQ ID NO: 719, SEQ ID NO: 721 , SEQ ID NO: 723, SEQ ID NO: 725, SEQ ID NO: 727, SEQ ID NO: 729, SEQ ID NO: 731 , SEQ ID NO: 733, SEQ ID NO: 735, SEQ ID NO: 737, SEQ ID NO: 739, SEQ ID NO: 741 , SEQ ID NO: 743, SEQ ID NO: 745, SEQ ID NO: 747, SEQ ID NO: 749, SEQ ID NO: 751 , SEQ ID NO: 753, SEQ ID NO: 755, SEQ ID NO: 757, SEQ ID NO: 759, SEQ ID NO: 761 , SEQ ID NO: 763, SEQ ID NO: 765, SEQ ID NO : 767, SEQ ID NO : 769, SEQ ID NO : 771 , SEQ ID NO: 773, SEQ ID NO: 775, SEQ ID NO: 777, SEQ ID NO: 779, SEQ ID NO: 781 , SEQ ID NO: 783, SEQ ID NO: 785, SEQ ID NO: 787, SEQ ID NO: 789, SEQ ID NO: 791 , SEQ ID NO: 793, SEQ ID NO: 795, SEQ ID NO: 797, SEQ ID NO: 799, SEQ ID NO: 801 , SEQ ID NO: 803, SEQ ID NO: 805, SEQ ID NO: 807, SEQ ID NO: 809, SEQ ID NO: 811 , SEQ ID NO: 813, SEQ ID NO: 815, SEQ ID NO: 817, SEQ ID NO: 819, SEQ ID NO: 821 , SEQ ID NO: 823, SEQ ID NO: 825, SEQ ID NO: 827, SEQ ID NO: 829, SEQ ID NO: 831 , SEQ ID NO: 833, SEQ ID NO: 835, SEQ ID NO: 837, SEQ ID NO: 839, SEQ ID NO: 841 , SEQ ID NO: 843, SEQ ID NO: 845, SEQ ID NO: 847, SEQ ID NO: 849, SEQ ID NO: 851 , SEQ ID NO: 853, SEQ ID NO: 855, SEQ ID NO: 857, SEQ ID NO: 859, SEQ ID NO: 861 , SEQ ID NO: 863, SEQ ID NO: 865, SEQ ID NO: 867, SEQ ID NO: 869, SEQ ID NO: 871 , SEQ ID NO: 873, SEQ ID NO: 875, SEQ ID NO: 877, SEQ ID NO: 879, SEQ ID NO: 881 , SEQ ID NO: 883, SEQ ID NO: 885, SEQ ID NO: 887, SEQ ID NO: 889, SEQ ID NO: 891 , SEQ ID NO: 893, SEQ ID NO: 895, SEQ ID NO: 897, SEQ ID NO: 899, SEQ ID NO: 901 , SEQ ID NO: 903, SEQ ID NO: 905, SEQ ID NO: 907, SEQ ID NO: 909, SEQ ID NO: 911 , SEQ ID NO: 913, SEQ ID NO: 915, SEQ ID NO: 917, SEQ ID NO: 919, SEQ ID NO: 921 , SEQ ID NO: 923, SEQ ID NO: 925, SEQ ID NO: 927, SEQ ID NO: 929, SEQ ID NO: 931 , SEQ ID NO: 933, SEQ ID NO: 935, SEQ ID NO: 937, SEQ ID NO: 939, SEQ ID NO: 941 , SEQ ID NO: 943, SEQ ID NO: 945, SEQ ID NO: 947, SEQ ID NO: 949, SEQ ID NO: 951 or SEQ ID NO: 953 under stringent conditions.
5. The use according to any one of claims 1 to 3, wherein the polypeptide having lipase ac- tivity is selected from the group consisting of
(i) a polypeptide having the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100, SEQ ID NO: 1 14, SEQ ID NO: 142, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 156, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 182, SEQ ID NO: 186, SEQ ID NO: 194, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 214, SEQ ID NO: 218, SEQ ID NO: 224, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 244, SEQ ID NO: 262, SEQ ID NO: 268, SEQ ID NO: 270, SEQ ID NO: 282, SEQ ID NO: 292, SEQ ID NO: 298, SEQ ID NO: 300, SEQ ID NO: 306, SEQ ID NO: 320, SEQ ID NO: 340, SEQ ID NO: 368, SEQ ID NO: 394, SEQ ID NO: 422, SEQ ID NO: 424, SEQ ID NO: 426, SEQ ID NO: 428, SEQ ID NO: 440, SEQ ID NO: 454, SEQ ID NO: 456, SEQ ID NO: 460, SEQ ID NO: 464, SEQ ID NO: 466, SEQ ID NO: 478, SEQ ID NO: 480, SEQ ID NO : 482, SEQ ID NO: 488, SEQ ID NO: 490, SEQ ID NO: 492, SEQ ID NO: 500, SEQ ID NO: 504, SEQ ID NO: 508, SEQ ID NO: 510, SEQ ID NO: 520, SEQ ID NO: 522, SEQ ID NO: 552, SEQ ID NO: 556, SEQ ID NO: 558, SEQ ID NO: 564, SEQ ID NO: 572, SEQ ID NO: 578, SEQ ID NO: 588, SEQ ID NO : 590, SEQ ID NO : 592, SEQ ID NO : 594, SEQ ID NO : 596, SEQ ID NO: 600, SEQ ID NO: 606, SEQ ID NO: 630, SEQ ID NO: 638, SEQ ID NO: 642, SEQ ID NO: 650, SEQ ID NO: 660, SEQ ID NO: 662, SEQ ID NO: 682, SEQ ID NO: 690, SEQ ID NO: 708, SEQ ID NO: 710, SEQ ID NO: 712, SEQ ID NO: 728, SEQ ID NO: 730, SEQ ID NO: 732, SEQ ID NO: 734, SEQ ID NO: 736, SEQ ID NO: 740, SEQ ID NO: 742, SEQ ID NO: 748, SEQ ID NO: 760, SEQ ID NO: 770, SEQ ID NO: 780, ID NO: 784, SEQ ID NO: 788, SEQ ID NO: 790, SEQ ID NO: 810, SEQ ID NO: 812, SEQ ID NO: 828, SEQ ID NO: 842, SEQ ID NO: 856, SEQ ID NO: 862, SEQ ID NO: 876, SEQ ID NO: 892, SEQ ID NO: 910, SEQ ID NO: 912, SEQ ID NO: 914, SEQ ID NO: 930, SEQ ID NO: 934, SEQ ID NO: 940 or SEQ ID NO: 952, or an enzymati- cally active fragment thereof having lipase activity;
(ii) a polypeptide encoded by the nucleic acid sequence according to SEQ ID NO: 955, SEQ ID NO: 3, SEQ ID NO: 15, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 75, SEQ ID NO: 99, SEQ ID NO: 113, SEQ ID NO: 141 , SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 155, SEQ ID NO: 159, SEQ ID NO: 161 , SEQ ID NO: 163, SEQ ID NO: 169, SEQ ID NO: 171 , SEQ ID NO: 181 , SEQ ID NO: 185, SEQ ID NO: 193, SEQ ID NO: 203, SEQ ID NO: 205, SEQ ID NO: 213, SEQ ID NO: 217, SEQ ID NO: 223, SEQ ID NO: 227, SEQ ID NO: 229, SEQ ID NO: 243, SEQ ID NO: 261 , SEQ ID NO: 267, SEQ ID NO: 269, SEQ ID NO: 281 , SEQ ID NO: 291 , SEQ ID NO: 297, SEQ ID NO: 299, SEQ ID NO: 305, SEQ ID NO: 319, SEQ ID NO: 339, SEQ ID NO: 367, SEQ ID NO: 393, SEQ ID NO: 421 , SEQ ID NO: 423, SEQ ID NO: 425, SEQ ID NO: 427, SEQ ID NO: 439, SEQ ID NO: 453, SEQ ID NO: 455, SEQ ID NO: 459, SEQ ID NO: 463, SEQ ID NO: 465, SEQ ID NO: 477, SEQ ID NO: 479, SEQ ID NO : 481 , SEQ ID NO: 487, SEQ ID NO: 489, SEQ ID NO: 491 , SEQ ID NO: 499, SEQ ID NO: 503, SEQ ID NO: 507, SEQ ID NO: 509, SEQ ID NO: 519, SEQ ID NO: 521 , SEQ ID NO: 551 , SEQ ID NO: 555, SEQ ID NO: 557, SEQ ID NO: 563, SEQ ID NO: 571 , SEQ ID NO: 577, SEQ ID NO: 587, SEQ ID NO: 589, SEQ ID NO: 591 , SEQ ID NO: 593, SEQ ID NO: 595, SEQ ID NO: 599, SEQ ID NO: 605, SEQ ID NO: 629, SEQ ID NO: 637, SEQ ID NO: 641 , SEQ ID NO: 649, SEQ ID NO: 659, SEQ ID NO: 661 , SEQ ID NO: 681 , SEQ ID NO: 689, SEQ ID NO: 707, SEQ ID NO: 709, SEQ ID NO: 711 , SEQ ID NO: 727, SEQ ID NO: 729, SEQ ID NO: 731 , SEQ ID NO: 733, SEQ ID NO: 735, SEQ ID NO: 739, SEQ ID NO: 741 , SEQ ID NO: 747, SEQ ID NO: 759, SEQ ID NO: 769, SEQ ID NO: 779, ID NO: 783, SEQ ID NO: 787, SEQ ID NO: 789, SEQ ID NO: 809, SEQ ID NO: 811 , SEQ ID NO: 827, SEQ ID NO: 841 , SEQ ID NO: 855, SEQ ID NO: 861 , SEQ ID NO: 875, SEQ ID NO: 891 , SEQ ID NO: 909, SEQ ID NO: 91 1 , SEQ ID NO: 913, SEQ ID NO: 929, SEQ ID NO: 933, SEQ ID NO: 939 or SEQ ID NO: 951 or an enzymati- cally active fragment thereof having lipase activity;
(iii) a polypeptide having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100, SEQ ID NO: 1 14, SEQ ID NO: 142, SEQ ID NO: 148, SEQ ID NO: 150, SEQ ID NO: 156, SEQ ID NO: 160, SEQ ID NO: 162, SEQ ID NO: 164, SEQ ID NO: 170, SEQ ID NO: 172, SEQ ID NO: 182, SEQ ID NO: 186, SEQ ID NO: 194, SEQ ID NO: 204, SEQ ID NO: 206, SEQ ID NO: 214, SEQ ID NO: 218, SEQ ID NO: 224, SEQ ID NO: 228, SEQ ID NO: 230, SEQ ID NO: 244, SEQ ID NO: 262, SEQ ID NO: 268, SEQ ID NO: 270, SEQ ID NO: 282, SEQ ID NO: 292, SEQ ID NO: 298, SEQ ID NO: 300, SEQ ID NO: 306, SEQ ID NO: 320, SEQ ID NO: 340, SEQ ID NO: 368, SEQ ID NO: 394, SEQ ID NO: 422, SEQ ID NO: 424, SEQ ID NO: 426, SEQ ID NO: 428, SEQ ID NO: 440, SEQ ID NO: 454, SEQ ID NO: 456, SEQ ID NO: 460, SEQ ID NO: 464, SEQ ID NO: 466, SEQ ID NO: 478, SEQ ID NO: 480, SEQ ID NO : 482, SEQ ID NO: 488, SEQ ID NO: 490, SEQ ID NO: 492, SEQ ID NO: 500, SEQ ID NO: 504, SEQ ID NO: 508, SEQ ID NO: 510, SEQ ID NO: 520, SEQ ID NO: 522, SEQ ID NO: 552, SEQ ID NO: 556, SEQ ID NO: 558, SEQ ID NO: 564, SEQ ID NO: 572, SEQ ID NO: 578, SEQ ID NO: 588, SEQ ID NO : 590, SEQ ID NO : 592, SEQ ID NO : 594, SEQ ID NO : 596, SEQ ID NO: 600, SEQ ID NO: 606,
SEQ ID NO: 630, SEQ ID NO: 638, SEQ ID NO: 642, SEQ ID NO: 650, SEQ ID NO: 660, SEQ ID NO: 662, SEQ ID NO: 682, SEQ ID NO: 690, SEQ ID NO: 708, SEQ ID NO: 710, SEQ ID NO: 712, SEQ ID NO: 728, SEQ ID NO: 730, SEQ ID NO: 732, SEQ ID NO: 734, SEQ ID NO: 736, SEQ ID NO: 740, SEQ ID NO: 742, SEQ ID NO: 748, SEQ ID NO: 760, SEQ ID NO: 770, SEQ ID NO: 780, ID NO: 784, SEQ ID NO: 788, SEQ ID NO: 790, SEQ ID NO: 810, SEQ ID NO: 812, SEQ ID NO: 828, SEQ ID NO: 842, SEQ ID NO: 856, SEQ ID NO: 862, SEQ ID NO: 876, SEQ ID NO: 892, SEQ ID NO: 910, SEQ ID NO: 912, SEQ ID NO: 914, SEQ ID NO: 930, SEQ ID NO: 934, SEQ ID NO: 940 or SEQ ID NO: 952 or an enzymatically active fragment thereof having lipase activity; and
(iv) a polypeptide encoded by a nucleic acid sequence which hybridizes to the complement of the nucleic acid sequence according to any of SEQ ID NO: 955, SEQ ID NO: 3, SEQ ID NO: 15, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 75, SEQ ID NO: 99, SEQ ID NO: 113, SEQ ID NO: 141 , SEQ ID NO: 147, SEQ ID NO: 149, SEQ ID NO: 155, SEQ ID NO: 159, SEQ ID NO: 161 , SEQ ID NO: 163, SEQ ID NO: 169, SEQ ID NO: 171 , SEQ ID NO: 181 , SEQ ID NO: 185, SEQ ID NO: 193, SEQ ID NO: 203, SEQ ID NO: 205, SEQ ID NO: 213, SEQ ID NO: 217, SEQ ID NO: 223, SEQ ID NO: 227, SEQ ID NO: 229, SEQ ID NO: 243, SEQ ID NO: 261 , SEQ ID NO: 267, SEQ ID NO: 269, SEQ ID NO: 281 , SEQ ID NO: 291 , SEQ ID NO: 297, SEQ ID NO: 299, SEQ ID NO: 305, SEQ ID NO: 319, SEQ ID NO: 339, SEQ ID NO: 367, SEQ ID NO: 393, SEQ ID NO: 421 , SEQ ID NO: 423, SEQ ID NO: 425, SEQ ID NO: 427, SEQ ID NO: 439, SEQ ID NO: 453, SEQ ID NO: 455, SEQ ID NO: 459, SEQ ID NO: 463, SEQ ID NO: 465, SEQ ID NO: 477, SEQ ID NO: 479, SEQ ID NO : 481 , SEQ ID NO: 487, SEQ ID NO: 489, SEQ ID NO: 491 , SEQ ID NO: 499, SEQ ID NO: 503, SEQ ID NO: 507, SEQ ID NO: 509, SEQ ID NO: 519, SEQ ID NO: 521 , SEQ ID NO: 551 , SEQ ID NO: 555, SEQ ID NO: 557, SEQ ID NO: 563, SEQ ID NO: 571 , SEQ ID NO: 577, SEQ ID NO: 587, SEQ ID NO: 589, SEQ ID NO: 591 , SEQ ID NO: 593, SEQ ID NO: 595, SEQ ID NO: 599, SEQ ID NO: 605, SEQ ID NO: 629, SEQ ID NO: 637, SEQ ID NO: 641 , SEQ ID NO: 649, SEQ ID NO: 659, SEQ ID NO: 661 , SEQ ID NO: 681 , SEQ ID NO: 689, SEQ ID NO: 707, SEQ ID NO: 709, SEQ ID NO: 711 , SEQ ID NO: 727, SEQ ID NO: 729, SEQ ID NO: 731 , SEQ ID NO: 733, SEQ ID NO: 735, SEQ ID NO: 739, SEQ ID NO: 741 , SEQ ID NO: 747, SEQ ID NO: 759, SEQ ID NO: 769, SEQ ID NO: 779, ID NO: 783, SEQ ID NO: 787, SEQ ID NO: 789, SEQ ID NO: 809, SEQ ID NO: 811 , SEQ ID NO: 827, SEQ ID NO: 841 , SEQ ID NO: 855, SEQ ID NO: 861 , SEQ ID NO: 875, SEQ ID NO: 891 , SEQ ID NO: 909, SEQ ID NO: 91 1 , SEQ ID NO: 913, SEQ ID NO: 929, SEQ ID NO: 933, SEQ ID NO: 939 or SEQ ID NO: 951 under stringent conditions.
6. The use according to any one of claims 1 to 3, wherein the polypeptide having lipase ac- tivity is selected from the group consisting of:
(i) a polypeptide having the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO:
90, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76, SEQ ID NO: 100 or SEQ ID NO: 114 or an enzymatically active frag- ment thereof having lipase activity;
(ii) a polypeptide encoded by the nucleic acid sequence according to SEQ ID NO: 955, SEQ ID NO: 89, SEQ ID NO: 3, SEQ ID NO: 15, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 75, SEQ ID NO: 99 or SEQ ID NO: 113 or an enzymatically active frag- ment thereof having lipase activity;
(iii) a polypeptide having an amino acid sequence with at least 70% sequence identity to the amino acid sequence according to SEQ ID NO: 956, SEQ ID NO: 90, SEQ ID NO: 4, SEQ ID NO: 16, SEQ ID NO: 26, SEQ ID NO: 40, SEQ ID NO: 68, SEQ ID NO: 70, SEQ ID NO: 76,
SEQ ID NO: 100 or SEQ ID NO: 114 or an enzymatically active fragment thereof having lipase activity; and
(iv) a polypeptide encoded by a nucleic acid sequence which hybridizes to the complement of the nucleic acid sequence according to any SEQ ID NO: 955, SEQ ID NO: 89, SEQ ID NO: 3, SEQ ID NO: 15, SEQ ID NO: 25, SEQ ID NO: 39, SEQ ID NO: 67, SEQ ID NO: 69, SEQ ID NO: 75, SEQ ID NO: 99 or SEQ ID NO: 113 under stringent conditions.
7. The use according to any one of the preceding claims, wherein the polypeptide having li- pase activity is used in combination with at least one soil additive, preferably selected from the group of surfactants, fertilizers, nitrification inhibitors and/or pesticides, preferably fungicides.
8. The use according to any one of the preceding claims, wherein the polypeptide having li- pase activity is applied in a concentration of between 0.01 kg to 600 kg of polypeptide per hec- tare, preferably of between 0.16 kg to 100 kg per hectare, more preferably of between 0.6 kg to 20 kg per hectare, most preferably of between 1 kg to 5 kg per hectare.
9. The use according to any one of the preceding claims, wherein the soil is selected from agricultural land, pasture, coastal dune sands, forest, shrub lands, parks, turfgrass soils, no-till agriculture, and soils irrigated with treated wastewater.
10. A method for increasing the water availability in soil comprising treating an area of ground- cover with an isolated polypeptide having lipase activity.
1 1. Method according to claim 10, wherein the soil water repellency of non-wetting soil is re- duced and/or the water holding capacity of non-wetting soil is increased.
12. Method according to claim 10, wherein the water holding capacity of wetting soil is in- creased and/or the evaporation from wetting soil is decreased.
13. Method according to any one of claims 10 to 12, wherein the polypeptide having lipase ac- tivity is as defined in any one of claims 4 to 6.
14. Method according to any one of claims 10 to 13, wherein the polypeptide or an enzymati- cally active fragment thereof having lipase activity is used in combination with at least one soil additive, preferably selected from the group of surfactants, fertilizers, nitrification inhibitors and/or pesticides, preferably fungicides.
15. The method according to any one of claims 10 to 14, wherein the polypeptide or an enzy- matically active fragment thereof having lipase activity is applied in a concentration of between 0.01 kg to 600 kg of polypeptide per hectare, preferably of between 0.16 kg to 100 kg per hec- tare, more preferably of between 0.6 kg to 20 kg per hectare, most preferably of between 1 kg to 5 kg per hectare.
16. Use of an isolated polypeptide having lipase activity for promoting plant growth.
17. The use according to claim 16, wherein the polypeptide having lipase activity is as defined in any one of claims 4 to 6.
18. The use according to claim 16 or 17, wherein the polypeptide having lipase activity is ap- plied in a concentration of between 0.01 kg to 600 kg of polypeptide per hectare, preferably of between 0.16 kg to 100 kg per hectare, more preferably of between 0.6 kg to 20 kg per hectare, most preferably of between 1 kg to 5 kg per hectare.
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