WO2005012340A1 - Proteines nematicides - Google Patents

Proteines nematicides Download PDF

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Publication number
WO2005012340A1
WO2005012340A1 PCT/GB2004/003231 GB2004003231W WO2005012340A1 WO 2005012340 A1 WO2005012340 A1 WO 2005012340A1 GB 2004003231 W GB2004003231 W GB 2004003231W WO 2005012340 A1 WO2005012340 A1 WO 2005012340A1
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WIPO (PCT)
Prior art keywords
protein
seq
polynucleotide
sequence
plant
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PCT/GB2004/003231
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English (en)
Inventor
Katrina Mackay
Daniel Fox
Jon Fletcher
Stuart Harrison
Elaine Mackay
Jacqueline Sheridan
Jane Cayley
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Syngenta Limited
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Priority to BRPI0413126-6A priority Critical patent/BRPI0413126A/pt
Priority to EP04743560A priority patent/EP1654274A1/fr
Publication of WO2005012340A1 publication Critical patent/WO2005012340A1/fr

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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
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8241—Phenotypically and genetically modified plants via recombinant DNA technology
    • C12N15/8261—Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield
    • C12N15/8271—Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield for stress resistance, e.g. heavy metal resistance
    • C12N15/8279—Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield for stress resistance, e.g. heavy metal resistance for biotic stress resistance, pathogen resistance, disease resistance
    • C12N15/8285—Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield for stress resistance, e.g. heavy metal resistance for biotic stress resistance, pathogen resistance, disease resistance for nematode resistance
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/37—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from fungi
    • C07K14/375—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from fungi from Basidiomycetes
    • 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
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8241—Phenotypically and genetically modified plants via recombinant DNA technology
    • C12N15/8261—Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield
    • C12N15/8271—Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield for stress resistance, e.g. heavy metal resistance
    • C12N15/8279—Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield for stress resistance, e.g. heavy metal resistance for biotic stress resistance, pathogen resistance, disease resistance
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A40/00—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
    • Y02A40/10—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in agriculture
    • Y02A40/146—Genetically Modified [GMO] plants, e.g. transgenic plants

Definitions

  • the present invention relates to inter alia, nematicidal, nucleic acid sequences encoding them and transformed plants containing them.
  • the invention relates to transformed crops having increased resistance and/or tolerance to nematodes.
  • Nematodes are essentially simple worms generally having cylindrical bodies that taper towards the head and tail.
  • Nematodes that are of agricultural importance can be subdivided into endoparasites, ectoparasites and ecto-endoparasites of plants. Some are sedentary and others remain mobile as they feed. All use a stylet to pierce plant cell walls and feed by removing plant cell contents before or after plant cell modification. More detail of particular important genera and species, their host ranges and economic importance are defined in well known standard texts.
  • Heterodera and Globodera cyst nematodes are important crop pests. They include H. glycines, (soybean cyst nematode) H. schachtii (beet cyst nematode), H. avenae (cereal cyst nematode) and potato cyst nematodes G. rostochiensis and G. pallida. Root-knot nematodes particularly the genus Meloidogyne, damage a wide range of crops. Examples are species M. javanica, M. hapla, M. arenaria and M. incognita. There are many other economically important nematodes.
  • Xiphinema the genera Xiphinema, Longidorus, Paralongidorus, Trichodorus and Paratrichodrus have distinctive importance. They cause damage to crops by their feeding but their economic status as crop pests is often due to roles as vectors of inter alia, NEPO and TOBRA plant viruses. Plant parasitic nematodes are reported to be responsible for the world-wide loss of billions of pounds worth of agricultural crops each year and so the professional agriculturist is constantly seeking ways to reduce these losses whilst maintaining a high quality commercial crop. The present invention therefore seeks to provide, ter alia, proteins that are active against nematode.
  • a nematicidal protein comprising or consisting of the sequence of SEQ LD NO: 1.
  • the present invention further provides a nematicidal protein having at least 70% identity to the protein of SEQ ID NO: 1.
  • said protein has at least 75% identity to the protein of SEQ ID NO: 1.
  • said protein has at least 80% identity to the protein of SEQ ID NO: 1.
  • said protein has at least 85% identity to the protein of SEQ ID NO: 1.
  • said protein has at least 90% identity to the protein of SEQ LD NO: 1.
  • said protein has at least 91% identity to the protein of SEQ ID NO: 1.
  • said protein has at least 92% identity to the protein of SEQ ID NO: 1. In a still further embodiment said protein has at least 93% identity to the protein of SEQ ID NO: 1. In a still further embodiment said protein has at least 94% identity to the protein of SEQ ID NO: 1. In a still further embodiment said protein has at least 95% identity to the protein of SEQ LD NO: 1. In a still further embodiment said protein has at least 96% identity to the protein of SEQ ID NO: 1. In a still further embodiment said protein has at least 97% identity to the protein of SEQ ID NO: 1. In a still further embodiment said protein has at least 98% identity to the protein of SEQ ID NO: 1.
  • said protein has at least 99% identity to the protein of SEQ ID NO: 1.
  • the percentage of sequence identity for proteins is determined by comparing two optimally aligned sequences over a comparison window, wherein the portion of the amino acid sequence in the comparison window may comprise additions or deletions (i.e. gaps) as compared to the initial reference sequence (which does not comprise additions or deletions) for optimal alignment of the two sequences. The percentage is calculated by determining the number of positions at which the identical amino acid residue occurs in both sequences to yield the number of match positions, dividing the number of match positions by the total number of positions in the window of comparison and multiplying the result by 100 to yield the percentage of sequence identity.
  • sequences may be aligned allowing for up to 3 gaps with the proviso that in respect of the gaps, a total of not more than 15 amino acid residues is affected.
  • Optimal alignment of sequences for comparison may also be conducted by computerised implementations of known algorithms.
  • the sequence identity is calculated using the FASTA version 3 algorithm which uses the method of Pearson and Lipman (Lipman, D.J. and Pearson, W.R. (1985) Rapid and sensitive protein similarity searches and Science. 227:1435-1441 and Pearson, W.R. and Lipman, D.J. (1988) Improved tools for biological sequence comparison. PNAS.
  • the protein may differ from the basic nematicidal protein of SEQ ID NO: 1 by conservative or non-conservative amino acid substitutions.
  • a conservative substitution is to be understood to mean that the amino acid is replaced with an amino acid with broadly similar chemical properties.
  • conservative substitutions may be made between amino acids within the following groups: (i) Alanine and Glycine; (ii) Serine and Threonine; (ii) Glutamic acid and Aspartic acid; (iii) Arginine and Lysine; (iv) Asparagine and Glutamine; (v) Isoleucine and Leucine, (vi) Valine and Methionine; (vii) Phenylalanine and Tryptophan.
  • more conservative than non-conservative substitutions will be possible without destroying the nematicidal properties of the proteins. Suitable variants may be determined by testing nematicidal properties of the peptide using routine methods that are well known to the person skilled in the art.
  • the nematicidal protein of the invention is processed to remove the N-terminal methionine residue.
  • the processed protein is modified, for example, by acetylation at the N-terminus.
  • the present invention still further provides a nematicidal protein as described above having a specific lactose binding ability.
  • the present invention still further provides a nematicidal protein as described above having the ability to cleave disaccharides and/or polysaccharides.
  • the protein is a mannanase.
  • the nematicidal protein described above is obtainable from Lepista nuda.
  • the present invention further provides a polynucleotide which encodes a protein as described above.
  • the person skilled in the art will appreciate that there are a number of polynucleotides which can encode each protein due to the degeneracy of the genetic code.
  • the polynucleotide comprises or consists of the sequence of SEQ ID NO: 2.
  • the present invention further provides a polynucleotide which is the complement of one which hybridises to a sequence as described above under stringent conditions and wherein said polynucleotide still encodes a protein which is nematicidal.
  • Such stringent conditions are well known to the person skilled in the art and comprise, for example: hybridisation at a temperature of about 65 °C in a solution containing 6 x SSC, 0.01% SDS and 0.25% skimmed milk powder, followed by rinsing at the same temperature in a solution containing 0.2 x SSC and 0.1% SDS followed by confirmation that the polynucleotide so identified still encodes a nematicidal protein according to the invention.
  • the skilled man may alternatively select the following hybridisation conditions viz., hybridisation at a temperature of between 60°C and 65°C in 0.3 strength citrate buffered saline containing 0.1% SDS followed by rinsing at the same temperature with 0.3 strength citrate buffered saline containing 0.1% SDS followed by confirmation that the polynucleotide so identified, still encodes a nematicidal protein according to the present invention.
  • Further polynucleotides according to the present invention may be identified from nucleic acid libraries.
  • Suitable oligonucleotide probes may be constructed on the basis of the amino acid sequence information of the proteins according to the present invention and used to screen any such nucleic acid library for the identification of further polynucleotides encoding proteins according to the invention.
  • the a polynucleotide selected from the group consisiting of SEQ ID NOs: 2, 30, 32, 34, 36 and 37 may be used for the construction of oligonucleotide probes by the skilled person.
  • the person skilled in the art is well versed in methods for the production and screening of nucleic acid libraries and the necessary techniques for the subsequent identification, isolation and sequence determination of polynucleotides which encode further nematicidal proteins in accordance with the present invention.
  • the polynucleotide described above is obtainable from Lepista nuda.
  • the present invention still further provides a polynucleotide having a first region encoding a protein as described above and a second region encoding a further protein. The regions may be separated by a region which provides for a self-processing polypeptide which is capable of separating the proteins such as the self-processing polypeptide described in US Patent No.
  • the regions may be separated by a sequence which acts as a target site for an external element which is capable of separating the protein sequences.
  • the polynucleotide may provide for a polyprotein which comprises a plurality of protein functions.
  • the proteins of the polyprotein may be arranged in tandem. These polyproteins may comprise the proteins according to the present invention and optionally further proteins such as those encoding any desired agronomic trait, for example, a further agronomic trait selected from the group consisting of herbicide resistance, insect resistance, fungus resistance, nematode resistance, altered stress tolerance, altered yield and altered nutritional content.
  • the further agronomic trait provides resistance to a herbicide which comprises glyphosate acid or agriculturally acceptable salt thereof.
  • the polynucleotide may be used to provide the proteins and proteins compositions of the present invention that are described herein.
  • the present invention still further provides a method of evolving a polynucleotide which encodes a protein having nematicidal properties comprising: (a) providing a population of variants of said polynucleotide and further polynucleotides which encode further proteins, at least one of which is in cell free form; and (b) shuffling said variants and further polynucleotides to form recombinant polynucleotides; and (c) selecting or screening for recombinant polynucleotides which have evolved towards the said nematicidal properties; and (d) repeating steps (b) and (c) with the recombinant polynucleotides according to step (c) until an evolved polynucleotide which encodes a protein having nematicidal properties has been acquired wherein said population of variants in part (a) contains at least one polynucleotide as described in the preceding paragraphs.
  • the methods for evolving a polynucleotide as described above are well known to the person skilled in the art and are described inter alia, in US Patent No. 5,811,238.
  • the present invention still further provides a construct comprising a polynucleotide as described above.
  • the construct comprises a polynucleotide as described above operably linked to a transcription initiation region and a transcription termination region.
  • the transcriptional initiation region and/or the transcription termination region are operable in plants.
  • the construct may further comprise a region which provides for the targeting of the protein product to a particular location.
  • an extracellular targeting sequence may be ligated to the polynucleotide encoding the protein of the present invention.
  • Other examples of targeting include targeting to a specific intracellular organelle or compartment.
  • the construct may further comprise a region which provides for the retention of the protein at a specific location such as a particular organelle or compartment.
  • the KDEL endoplasmic reticulum retention sequence may be used.
  • the present invention still further provides a construct as described above which further comprises a region which provides for the production of a selectable marker.
  • the selectable marker is provided by the mannose isomerase (Positech ⁇ ) selection system.
  • the selectable marker may, in particular, confer resistance to kanamycin, hygromycin or gentamycin.
  • Further suitable selectable markers include genes that confer resistance to toxins such as eutypine or that confer resistance to herbicides such as protoporphyrinogen oxidase (PPO) inhibitor-based herbicides or glyphosate-based herbicides.
  • the gene may be a mutated PPO such as the ones described in PCT Publication No. WO 97/32011 and PCT Publication No. WO 95/34659 and found, for example, in AcuronTM technology.
  • Other forms of selection are also available such as hormone based selection systems such as the Multi Auto Transformation (MAT) system of Hiroyrasu
  • the present invention still further provides a construct as described above wherein the plant operable promoter is selected from the group consisting of: CaMV35S, FMN35S, ⁇ OS, OCS, Patatin, E9, alcA/alcR switch, GST switch, RMS switch, oleosin, ribulose bisphosphate carboxylase-oxygenase small sub-unit, actin 7, Cestrum or root specific promoters including MR7 promoter (maize), Gos 9 (rice), GOS2 promoters, a superMas promoter as described in PCT Publication No. WO 95/14098 and US Patent No.
  • the plant operable promoter is selected from the group consisting of: CaMV35S, FMN35S, ⁇ OS, OCS, Patatin, E9, alcA/alcR switch, GST switch, RMS switch, oleosin, ribulose bisphosphate carboxylase-oxygenase small sub-unit, actin 7, Cestrum or root
  • Terminators that can be used in the constructs according to the present invention include Nos, proteinase inhibitor JJ, CaMV35S and the terminator of a gene of alpha-tubulin (European Patent Application, Publication No. EP 0652 286 A).
  • transcriptional or translational enhancers for example, tobacco etch virus (TEV) translation activator described in PCT Publication No. WO 87/07644, figwort mosaic virus (FMV) enhancer (as described in PCT Publication No. WO 00/66748) and cauliflower mosaic virus (CaMV) 35S enhancer (Fang et al. 1989. The Plant Cell Vol. 1 pp 141 -150). It is also possible to use, in association with the promoter regulation sequence, other regulation sequences such as introns.
  • TMV tobacco etch virus
  • FMV figwort mosaic virus
  • CaMV cauliflower mosaic virus
  • the polynucleotide encoding the nematicidal protein according to the invention may also be codon-optimised, or otherwise altered to enhance, for example, transcription once it is incorporated into plant material. Such codon optimisation may also be used to alter the predicted secondary structure of the RNA transcript produced in any transformed cell, or to destroy cryptic RNA instability elements present in the unaltered transcript, thereby increasing the stability and/or availability of the transcript in the transformed cell (Abler and Green. 1996. Plant Molecular Biology (32) pp63-78). Table 1 below shows exemplary codon usage preferences for soyabean. Table 1. Codon-usage preferences for Soyabean
  • the present invention still further provides a host cell comprising a polynucleotide or a construct as described above.
  • Suitable host cells include micro-organisms or cultured cells. Suitable micro-organisms include Escherichia coli and Pseudomonas.
  • Suitable cultured cells include cultured insect cells, cultured mammalian cells and plant cells.
  • the proteins expressed in the host cells described above may be used in the aspects and embodiments of the invention described herein. In addition, these proteins may be used in the production of antibodies using techniques well known in the art. Antibodies produced using the proteins of the invention are suitable for use in screening assays, for example.
  • the present invention still further provides a transgenic plant comprising a polynucleotide or a construct as described above.
  • the present invention still further provides a method of providing a plant or plant part with a nematicidal protein comprising: (a) inserting into the genome of the plant or of plant material a polynucleotide or a construct as described above; and (b) regenerating plants or plant parts therefrom; and (c) selecting those plants or plant parts having said protein.
  • the said polynucleotide or construct may be incorporated into the cells by plant transformation techniques that are well known to the person skilled in the art.
  • Such techniques include but are not limited to particle mediated biolistic transformation, Agrobacterium-mediated transformation, protoplast transformation (optionally in the presence of polyethylene glycols); sonication of plant tissues, cells or protoplasts in a medium comprising the polynucleotide or vector; micro-insertion of the polynucleotide or vector into totipotent plant material (optionally employing the known silicon carbide "whiskers” technique), electroporation and the like.
  • the present invention still further provides plants or plant parts obtained according to the method of the preceding paragraph.
  • plant parts include, but are not limited to, protoplasts, cells, seeds, fruits, leaves, flowers and the like and any other part of the plant that can be reproduced either sexually, asexually or both.
  • the plants or plant parts of the present invention are selected from the group consisting of: melon, mango, soybean, cotton, tobacco, sugar beet, oilseed rape, canola, flax, sunflower, potato, tomato, alfalfa, lettuce, maize, wheat, sorghum, rye, banana, barley, oat, turf grass, forage grass, sugar cane, pea, field bean, rice, pine, poplar, apple, peach, grape, strawberry, carrot, cabbage, onion, citrus, cereal or nut plants or any other horticultural crops.
  • Plants and plant parts in accordance with the present invention show improved resistance or enhanced tolerance to a nematode pest when compared to control-like or wild-type plants. Resistance may vary from a slight increase in tolerance to the pest to total resistance so that the plant is unaffected by the presence of pest (where the pest is severely inhibited or killed).
  • the invention still further provides plants or plant parts as described above which comprise a further agronomic trait selected from the group consisting of herbicide resistance, insect resistance, fungus resistance, nematode resistance, altered stress tolerance, altered yield, altered nutritional content and any other desired agronomic trait.
  • the further agronomic trait provides resistance to a herbicide which comprises glyphosate acid or agriculturally acceptable salt thereof.
  • the invention still further provides plants or plant parts as described above which comprise a pharmaceutical trait.
  • the present invention still further provides the use of a polynucleotide or a construct as described above in a method of producing plants which are resistant and/or tolerant to nematodes.
  • the present invention still further provides the use of at least one protein as described above as an active ingredient in the production of a nematicide.
  • the nematicide further comprises an agriculturally acceptable carrier and/or a diluent and/or a nemtatode attractant and may be formulated for use as a spray.
  • the present invention still further provides a method of controlling nematodes comprising providing at a locus where said nematodes feed at least one protein as described above.
  • the present invention still further provides a method of controlling nematodes comprising providing at a locus where said nematodes feed a mannanase.
  • the present invention still further provides a composition comprising a nematicidally effective amount of at least one protein as described above and an agriculturally acceptable carrier and/or a diluent and/or a nematode attractant.
  • the composition comprises a combination of at least two of the proteins described above.
  • the present invention still further provides a composition comprising a nematicidally effective amount of at least one protein as described above and at least one further protein and an agriculturally acceptable carrier and or a diluent and/or a nematode attractant.
  • the further protein may be a herbicidal protein, a fungicidal protein, an insectidal protein or another nematicidal protein.
  • the nematicidal proteins according to the present invention may also be combined in application with other agrochemicals such as herbicides, fungicides, insecticides and nematicides.
  • mixture partners include insecticidal and nematicidal lectins, insecticidal protease inhibitors and insecticidal proteins derived from species of the Bacillus thurigiensis, Xenorhabdus nematophilus, or Photorabdus luminescens and other chemicals for example pyrethroids, carbamates, imidacloprid, organochlorines, macromolecules such as spinosad abamectin or emamectin.
  • the present invention still further provides a recombinant micro-organism which provides for production of a protein as described above.
  • the recombinant micro-organism is an endophyte or a Pseudomonas sp.
  • An endophyte is generally accepted within the art as a micro-organism having the ability to enter into non-pathogenic endosymbiotic relationships with a plant host.
  • a method of endophyte-enhanced protection of plants has been described in a series of patent applications by Crop Genetics International Corporation (for example, PCT Publication No. WO 90/13224, European Patent Publication No. EP 0 125 468 Bl , PCT Publication No. WO 91/10363, PCT Publication No. WO 87/03303).
  • WO 94/16076 describes the use of endophytes which have been genetically modified to express a plant-derived insecticidal peptide.
  • the present invention also envisages that the proteins of the invention are active against nematodes which infect animals or humans.
  • a pharmaceutical composition comprising at least one protein as described above and a pharmaceutically acceptable carrier.
  • a protein as described above for use as a pharmaceutical or a vaccine.
  • the present invention provides for the use of a protein as described above in the manufacture of a medicament for vaccination against or treatment of animal or human nematode infection.
  • the nematodes to be controlled by the proteins of the present invention may include but are not limited to: Heterodera sp.; H. schachtii; H. glycines; H. avenae; Meliodogyne sp.; M. incognita; M. javanica; M. hapla; M. arenaria; Globodera sp. including G. rostochiensis; G.
  • Figure 1 Sequence of clone pLnuda-cl8 (SEQ ID NO: 30) aligned with the corresponding peptide sequence (SEQ ID NO: 31).
  • the nucleotide is shown as a double stranded polynucleotide sequence (SEQ LD NO: 30 and its complement, SEQ ID NO: 38) with the corresponding translated peptide sequence (SEQ ID NO: 31) aligned above the coding region.
  • the positions of the L. nuda tryptic peptide sequences (SEQ ID NOs: 3, 4, 5 and 6) and the 5' UTR are indicated.
  • Figure 2 Consensus sequence of six 5' RACE cDNA clones (Lnuda-c25, c26, c27, c30, c31 and c32; SEQ ID NO: 32) aligned with the corresponding peptide sequence (SEQ LD NO: 33).
  • the nucleotide is shown as a double stranded polynucleotide sequence (SEQ ID NO: 32 and its complement, SEQ ID NO: 39) with the corresponding translated peptide sequence (SEQ ID NO: 33) aligned above the coding region. The positions of the translation start codon and the 5' UTR are indicated.
  • Figure 3 Consensus sequence of seven 3' RACE cDNA clones (Lnuda-c37, c38, c40, c41, c42, c47 and c48; SEQ ID NO: 34) aligned with the corresponding peptide sequence (SEQ LD NO: 35).
  • the nucleotide is shown as a double stranded polynucleotide sequence (SEQ LD NO: 34 and its complement, SEQ ED NO: 40) with the corresponding translated peptide sequence aligned above the coding region.
  • the positions of three polymorphisms, the translation stop codon, the 3' UTR and the poly A tail are indicated.
  • Figure 4 Sequence of full-length cDNA clone Lnuda-c57 (SEQ LD NO: 36) aligned with the corresponding protein sequence (SEQ LD NO: 1).
  • the nucleotide is shown as a double stranded polynucleotide sequence (SEQ ID NO: 36 and its complement, SEQ ID NO: 41) with the corresponding translated protein sequence aligned above the coding region.
  • the positions of three polymorphisms, the translation start codon and the translation stop codon are indicated.
  • Figure 5 Schematic representation of the positions of the translation start and stop codons and the four introns and four exons of the on a full-length gDNA map of the L.nuda gene for the nematicidal protein of SEQ ID NO: 1.
  • the translation start and stop codons are indicated by vertical black bars, the exons by striped arrows, the introns by a transparent bar and flanking regions (the 5' and 3' UTRs) by a horizontal black bar.
  • Figure 6 Consensus sequence of twenty full-length gDNA clones (SEQ ID NO: 37) aligned with the correseponding protein sequence (SEQ ID NO: 1).
  • the nucleotide is shown as a double stranded polynucleotide sequence (SEQ ED NO: 37 and its complement, SEQ ID NO: 42) with the corresponding translated protein sequence aligned above the coding region. The positions of the translation start and stop codons and the introns and exons are indicated.
  • SEQ LD NO: 1 is an exemplary nematicidal protein of the invention.
  • SEQ LD NO: 2 is a polynucleotide encoding the protein of SEQ ID NO: 1.
  • SEQ LD NO: 3 to SEQ ID NO: 11 are protein fragments identified by de novo protein sequencing.
  • SEQ LD NO: 12 to SEQ ID NO: 29 are primers used in the present invention.
  • SEQ LD NO: 30 is the sequence of clone pLnuda-cl8.
  • SEQ ED NO: 31 is the peptide sequence corresponding to SEQ LD NO: 30.
  • SEQ ID NO: 32 is the sequence identified in six 5' RACE cDNA clones (Lnuda-c25, c26, c27, c30, c31 and c32).
  • SEQ ID NO: 33 is the peptide sequence corresponding to SEQ ID NO: 32.
  • SEQ LD NO: 34 is the sequence identified in seven 3' RACE cDNA clones (Lnuda-c37, c38, c40, c41, c42, c47 and c48).
  • SEQ ID NO: 35 is the peptide sequence corresponding to SEQ ID NO: 34.
  • SEQ ID NO: 36 is the sequence of full-length cDNA clone Lnuda-c57.
  • SEQ TD NO: 37 is the consensus sequence of 20 full-length gDNA clones.
  • SEQ LD NO: 38 to SEQ ID NO: 42 are complementary sequences to SEQ ID NO: 30, 32, 34, 36 and 37, respectively.
  • SEQ ED NO: 43 is a protein fragment identified by de novo protein sequencing.
  • Example 1 Protein sequencing a) De novo protein sequencing of L. nuda (15kDa band) A crude extract from L. nuda was shown to have nematicidal activity using the method of Example 6. A 15kDa protein band was purified from this extract using the method of Example 5. Tryptic peptides from this protein sample were prepared for nanaospray MS/MS sequencing by digestion using trypsin of either solution or polyacrylamide gel slices containing the protein sample. After digestion with trypsin the peptides were desalted using C )8 zip tips TM. The peptides were eluted from the zip tips using 50:50:0.1 acetonitrile: water: formic acid and directly transferred into a nano electrospray needle.
  • Mass spectrometry of the desalted peptides was carried out using a micromass Q-TOF 2 mass spectrometer.
  • the mass spectrometer was calibrated using the product ions from the fragmentation of the doubly charged ion of glu-fibrinopeptide B in 50:50:0.1 acetonitrile: water: formic acid at 500fmol/ ⁇ l.
  • Ions from the nanospray needle were detected in the Q-TOF mass spectrometer running in survey mode. Multiply charged ions were then selected one at a time and fragmented by collision with argon gas to form fragment ions.
  • the fragment ion spectra obtained are referred to as MS/MS spectra.
  • E(Q/K)ELN(Q/K)SG(Q/K)TYLLTNAK (SEQ ED NO: 3) LVAVTTPVEWHLWHDEVDHT(366.21) (SEQ ID NO: 4) WSSEMYLGLNGSPSDGTK (SEQ ED NO: 5) AVTTPVEWHLWHDEVD(623.23) (SEQ LD NO: 6) SGNLGLYF or FYLGLNGS (SEQ ID NO: 7 and SEQ LD NO: 8, respectively) (243.19)TVDLS(1304.65) (SEQ ED NO: 9) (1716.75)(Q/K)SAAPGSSHTTGEYTWK (SEQ ID NO: 10) (3821.49)NSVYTWK (SEQ LD NO: 1 1)
  • L means Leucine or Isoleucine (Q/K) means Glutamine or a Lysine at this position (623.23) means unable to assign remaining 623.23 dalton fragment
  • F means Phenylalanine or oxidized Methionine at this position
  • Example 2 Cloning of cDNA and gDNA a. Cloning of Partial cDNA Nested degenerate oligonucleotides were designed to proposed tryptic peptide sequences generated from MS/MS derived data as detailed in Example 1. The following tryptic peptide sequences were used:
  • Peptide 2 (SEQ ED NO: 4) LVAVTTPVEWHLWHDEVDHT(366.21) m.wt. - 2749.36
  • a 418 bp PCR product was amplified from an amplified L. nuda cultivated mushroom cDNA library in ⁇ ZapII (Stratagene #200400/200401/200450) using nested degenerate Lnuda primers in combination with nested T3 promoter specific primers, as follows:
  • PCR amplification reactions were run using puRe TaqTMReady-To-GoTMPCR Beads (Amersham Biosciences #27-9558-01) incorporating 300ng of degenerate primer, lOOng of specific primer and l ⁇ l of cDNA library template under the following conditions: 95°C for 5 minutes, 35 cycles of 95°C for 30 seconds, 50°C for 30 seconds, 72°C for 90 seconds, then 72°C for 6 minutes (Techne Progene thermal cycler), l ⁇ l of primary PCR was used as template for secondary PCR.
  • the 418 bp PCR amplicon was cloned directly into pCR ® 2.1 TOPO ® using TOPO TA Cloning Kit (Invitrogen 45-0641) and sequenced by automated cycle sequencing from Ml 3 forward (GTAAAACGACGGCCAG; SEQ ID NO: 22) and reverse (CAGGASAACAGCTATGAC; SEQ ED NO: 23) primers.
  • the sequence of the 418 bp L.nuda PCR amplicon (clone pLnuda-cl8) was determined to be:
  • nucleotide sequence when translated from the open reading frame starting at the ATG codon at nucleotides 144 to 146, corresponds to the following peptide sequence:
  • Figure 1 shows this nucleotide sequence (pLnuda-cl8; SEQ ID NO: 30) aligned with the corresponding peptide sequence (SEQ LD NO: 31).
  • the nucleotide is shown as a double stranded polynucleotide sequence (SEQ ED NO: 30 and its complement, SEQ ED NO: 38) with the corresponding translated peptide sequence (SEQ LD NO: 31) aligned above the coding region.
  • the positions of the L. nuda tryptic peptide sequences (SEQ LD NOs: 3, 4, 5 and 6) and the 5' UTR are indicated. All major tryptic peptides are represented on the 418bp cDNA clone thereby confirming authenticity.
  • b. Cloning of L. nuda 5' & 3' cDNA ends L. nuda gene specific nested forward and reverse primers were designed in order to
  • L.nuda 5' RACE consensus sequence Six 5' RACE cDNA clones were identified (Lnuda-c25, c26, c27, c30, c31 and c32) having the following consensus sequence:
  • This nucleotide sequence corresponds to the following peptide sequence; the ATG translation start codon being found at nucleotides 46 to 48: O 2005/012340 - 18 -
  • Figure 2 shows the consensus sequence of the six 5' RACE cDNA clones (Lnuda- c25, c26, c27, c30, c31 and c32; SEQ ID NO: 32) aligned with the corresponding peptide sequence (SEQ ED NO: 33).
  • the nucleotide is shown as a double stranded polynucleotide sequence (SEQ ID NO: 32 and its complement, SEQ LD NO: 39) with the corresponding translated peptide sequence (SEQ ID NO: 33) aligned above the coding region.
  • the positions of the translation start codon and the 5' UTR are indicated.
  • L.nuda 3' RACE consensus sequence Seven 3' RACE cDNA clones were identified (Lnuda-c37, c38, c40, c41, c42, c47 and c48) having the following consensus sequence.
  • This nucleotide sequence corresponds to the following peptide sequence, translation being carried out starting from the GTT codon at positions 3 to 5 and finishing at the TAG codon at positions 362 to 364:
  • FIG. 3 shows the consensus sequence of the seven 3' RACE cDNA clones (Lnuda-c37, c38, c40, c41, c42, c47 and c48; SEQ ED NO: 34) aligned with the O 2005/012340 - 19 - corresponding peptide sequence (SEQ ED NO: 35).
  • the nucleotide is shown as a double stranded polynucleotide sequence (SEQ ID NO: 34 and its complement, SEQ ID NO: 40) with the corresponding translated peptide sequence aligned above the coding region. The positions of three polymorphisms, the translation stop codon, the 3' UTR and the poly A tail are indicated.
  • SEQ ID NO: 34 and its complement, SEQ ID NO: 40 The positions of three polymorphisms, the translation stop codon, the 3' UTR and the poly A tail are indicated.
  • c Cloning of full-length L. nuda cDNA L. nuda gene specific primers were designed to conserved 5' and 3' UTR regions in order to PCR amplify full-length clones using cDNA template as generated by the RLM- RACE Kit:
  • Lnuda-S5 TCTCTTCCAGTTTCTACCATG (SEQ ID NO: 28) Lnuda-S6 ACAAATTACATCCGAAACCTG (SEQ ED NO: 29) 25 ⁇ l PCR amplification reactions were run using puRe TaqTMReady-To-GoTMPCR
  • the L. nuda gene is comprised of a 429 bp open reading frame (SEQ ID NO: 2), encoding 142 amino acids (SEQ ED NO: 1), thereby giving a predicted molecular weight of 15962.85 Daltons.
  • SEQ ID NO: 2 The confirmed protein sequence coded for by SEQ ID NO: 2, and nucleotides 19 to 447 of SEQ LD NO: 35, is as follows:
  • This protein is a non-secretory protein as predicted by SignalP.
  • BlastP searched there was only one significant match: 55% identity to an Agaricus bisporus putative mannanase. Over the full protein length, there is 52.1% identity to the A.bisporus putative mannanase.
  • Figure 4 shows the sequence of the full-length cDNA clone Lnuda-c57 (SEQ ID NO: 36) aligned with the co ⁇ esponding protein sequence (SEQ ED NO: 1).
  • the nucleotide is shown as a double stranded polynucleotide sequence (SEQ ED NO: 36 and its complement, SEQ ED NO: 41) with the corresponding translated protein sequence aligned above the coding region. The positions of three polymorphisms, the translation start codon and the translation stop codon are indicated. O 2005/012340 - 21 - d. Cloning of full-length L.nuda gDNA Primers Lnuda-S5 and Lnuda-S6 were used to PCR amplify the full-length coding region from L.nuda cultivated mushroom genomic DNA (gDNA). Amplification conditions were as described above. A resulting 706 bp amplicon was TOPO TA cloned and sequenced, as previously described. The consensus sequence for 20 positive clones is shown below:
  • Figure 5 shows a schematic representation of the positions of the translation start and stop codons and the four introns and four exons on a full-length gDNA map of the L.nuda gene encoding for the nematicidal protein of SEQ ID NO: 1.
  • Figure 6 shows the consensus sequence of the twenty full-length gDNA clones (SEQ LD NO: 37) aligned with the correseponding protein sequence (SEQ ID NO: 1).
  • the nucleotide is shown as a double stranded polynucleotide sequence (SEQ LD NO: 37 and its complement, SEQ LD NO: 42) with the corresponding translated protein sequence aligned above the coding region. The positions of the translation start and stop codons and the introns and exons are indicated.
  • Example 3 Construction of vectors.
  • the person skilled in the art is capable of producing the polynucleotides and polynucleotide sequences according to the invention utilising standard molecular biology cloning techniques.
  • various polynucleotides based on the sequence information as listed in the Sequence Listing and described above can be synthesised chemically using standard techniques well known to the person skilled in the art.
  • Basic vectors are available or may be constructed which are suitable for assembling the polynucleotides and polynucleotide sequences according to the invention.
  • the component parts of the polynucleotides may be synthesised or may be cloned from other vectors or libraries containing said sequences.
  • the person skilled in the art may generate probes based on the information presented in the Sequence Listing to isolate the sequences according to the invention also using standard techniques.
  • the vectors may be used for DNA work (sequencing, mutagenesis), for in vitro production and for plant transformation, following methods well known in the art.
  • sequences according to the invention are inserted between the border regions of a single T-DNA region.
  • Agrobacterium may be transformed in accordance with methods which are well known to the person skilled in the art.
  • Example 4 Transformation The vectors are transformed into plant cells using standard procedures. Any transformation method suitable for the target plant or plant cells may be employed, including, but not limited to, Agrobacterium-mediated transformation (for example, infection by Agrobacterium tumefaciens containing recombinant Ti plasmids, infection with Agrobacterium rhizogenes transformed with binary vectors to produce transgenic hairy root cultures (Cho FI-J et al.
  • Agrobacterium-mediated transformation for example, infection by Agrobacterium tumefaciens containing recombinant Ti plasmids, infection with Agrobacterium rhizogenes transformed with binary vectors to produce transgenic hairy root cultures (Cho FI-J et al.
  • Planta 210, 195-204) particle mediated biolistic transformation, protoplast transformation (optionally in the presence of polyethylene glycols), electroporation, sonication of plant tissues, cells or protoplasts in a medium comprising the polynucleotide or vector, microinjection of plant cells and protoplasts, bacterial bombardment, micro-insertion of the polynucleotide or vector into totipotent plant material (optionally employing the known silicon carbide "fibre” or "whisker” method) and pollen tube transformation.
  • the transformed cells may then in suitable cases be regenerated into whole plants in which the new nuclear material is stably incorporated into the genome. Both transformed monocot and dicot plants may be obtained in this way.
  • Full details of the methods of transformation are known to the person skilled in the art.
  • Example 5 Protein purification from L. nuda Approximately 100 gram quantities of L. nuda were frozen in liquid nitrogen and ground using a pestle and mortar. Ground mushroom was placed into a flat-bottomed dish with plastic, perforated lid and was then freeze dried for two days until all moisture had been removed from the sample. The lyophilised mushroom was removed from the container and weighed. 20mls of extraction buffer was added for every lg of lyophilised mushroom.
  • Protease inhibitor cocktail containing a mixture of water-soluble protease inhibitors with broad specificity for the inhibition of serine, cysteine, aspartic, and metallo-pro teases (containing 4-(2- aminoethyl) benzenesulfonyl fluoride (AEBSF), E-64, bestatin, leupeptin, aprotinin, and sodium EDTA) was added (1 pot of protease inhibitor cocktail was made up to 100ml with the addition of ultra pure water). 1ml of protease inhibitor cocktail was used for every 100ml of mushroom extract. The extract was incubated overnight at 4°C with stirring to ensure the full extraction of all proteins. The particulates were then removed by centrifugation.
  • AEBSF 4-(2- aminoethyl) benzenesulfonyl fluoride
  • E-64 bestatin
  • leupeptin leupeptin
  • aprotinin sodium EDTA
  • Extract was centrifuged at as high a speed as the rotor allowed, and the supernatant removed. The supernatant was then filtered to ensure all particulates were removed. In order to concentrate and remove other contaminants, ammonium sulphate was added to the extract to 90% saturation. This was incubated at 4°C with rolling for 1 hour. The protein was then spun down using ss34 rotor at 20,000 rpm for 20mins. The supernatant was removed and the precipitated protein was re-solubilised in 20mM Tris (pH 8.0) in order to give to solution some buffering capacity.
  • the resuspended extract was dialysed into Lactosyl Agarose Buffer A (PBS pH 7.5) using 3kDa dialysis membrane. This ensured removal of the remaining ammonium sulphate and allowed further purification using lactosyl agarose.
  • This purification was carried out as follows. 2mls of 50% lactosyl-agarose shrrry (lactosyl agarose from Sigma in 0.15M NaCl and 0.01M sodium phosphate, pH 6.8) was pipetted into 15ml Falcon tube. The beads were washed 4 times with lOmls of PBS.
  • the beads were pelleted by spinning at 3500 rpm for 4mins (speed is important as higher speeds may disrupt the integrity of the beads) and as much supernatant as possible was removed without disturbing the beads.
  • lOmls of mushroom extract was added to the tube which was then incubated overnight to allow lectin binding. The beads were then pelleted again and the supernatant is removed as Unbound fraction. The beads were then washed and pelleted again three times with 1 Omls of PBS solution to remove the remaining unbound proteins.
  • lOmls of 0.4M ⁇ -lactose was then added and the tube was incubated at 4°C with rolling for 1 hour. The beads were pelleted and the supernatant removed as Bound fraction.
  • Example 6 Recombinant protein production
  • the cDNA sequence (SEQ ID NO: 2) operably linked to appropriate regulatory regions, was cloned into plasmid pET24a (Novagen) to allow expression of protein with sequence identical to SEQ ID NO: 1 and the construct was transformed into E . coli BL21(DE3) (Invitrogen) competent cells using standard methods. It is noted that the protein as expressed in E. coli lacks the N-terminal methionine residue, which has been cleaved to give the mature protein.
  • the pET24a construct was also subjected to mutagenesis to allow expression of SEQ LD NO: 1 with an additional glycine residue encoded after the start methionine, to potentially mimic amino-terminal acetylation of the mature protein (referred to hereinafter as L. nuda G).
  • Recombinant protein expression was induced at 20°C by addition of EPTG and the resultant protein was purified from soluble extract by binding to lactosyl-agarose and elution with ⁇ -lactose as described in Example 5.
  • the purified protein was concentrated and dialysed into lOmM Tris-HCl, pH 7.5 for assay of nematocidal effect on H. schachtii as detailed in Example 7.
  • Example 7 Nematicidal effect on Heterodera schachtii in plants A micro-injection screen was developed to assess nematicidal effects of a range of test samples (including crude extracts containing proteins and polypeptides, partially purified proteins or polypeptides, purified proteins or polypeptides and recombinantly expressed proteins or polypeptides). These test samples are delivered directly to feeding sites induced by Heterodera schachtii juveniles feeding on Arabidopsis thaliana roots.
  • Nematode median bulb pumping Nematode moulting/development Evidence of vacuolation inside nematode
  • Example 2 a crude extract from L. nuda (as referred to in Example 1), protein purified from L. nuda using the method of Example 5 (sample refe ⁇ ed to in Example 5, after loading on superdex 70) and recombinant L. nuda protein (prepared using the procedure of Example 6) was tested for nematicidal activity.
  • Table 2 Nematidal activity of native and recombinant L. nuda protein
  • the crude extract, purified protein and both forms of recombinant protein showed activity equivalent or better than that shown the positive control (2% arsenic acid).
  • Example 8 Transformation of soybean (Glycine max) Soybean cotyledon explants are harvested and wounded with a scalpel dipped in a culture of A. rhizogenes containing binary vectors as described in Example 3 and grown overnight in LB medium containing 150mg/l kanamycin. After wounding, the explants are dried on sterile filter paper and transfe ⁇ ed onto co-cultivation media for 3 days. The explants are then transferred onto hormone-free media supplemented with 500 mg/1 carbenicillin and 200 mg/1 kanamycin. About 10-14 days after root emergence, l-2cm long root tips are transferred onto fresh new media and regularly sub-cultured every 5-6 weeks. Transgenic hairy roots may be used in feeding assays with nematodes.
  • Example 9 Transformation of tobacco (Nicotiana tobacum ssp.) Tobacco was transformed by co-cultivation of plant tissue with an Agrobacterium tumefaciens strain containing binary vectors as described in Example 3. The person skilled in the art will appreciate that alternative binary vectors may be used in association with the present invention. Transformation was carried out using co-cultivation of tobacco leaf segments from 4 week old plants. Transgenic plants were regenerated from shoots that grew on selection medium (containing kanamycin), rooted and transferred to germination medium or soil. Young plants were then grown to maturity and allowed to self-pollinate and set seed or used in feeding assays with nematodes.
  • Example 10 Transformation of other plants Other plants, including, but not limited to, Arabidopsis, sugarbeet, potato and tomato, are transformed using methods well known to those skilled in the art.
  • Example 11 Analysis of transgenic hairy roots for susceptibility to plant parasitic nematodes fPPN) Eggs are obtained from females of H. glycines collected from soybean plants grown in a greenhouse. Eggs are washed by centrifugation in sterile distilled water, surface sterilized and washed again. About 200 eggs are added to recently sub-cultured transformed root cultures (about 200mg fresh weight). Cultures are incubated at 25°C and about 4-5 weeks after inoculation, scored for presence of female cysts.
  • Example 12 Analysis of transgenic tobacco plants for susceptibility to PPN
  • Transgenic tobacco plants prepared using the method of Example 9 were assayed in soil for resistance against M. incognita.
  • Transgenic plants from tissue culture were transferred into 3 inch pots and acclimatised in the greenhouse for 7 days.
  • Two holes were made in the soil on either side of the stem, approximately 1 cm from the stem and 2 cm deep.
  • 1500 infective second stage juvenile (J2) M. incognita in liquid were inoculated into the holes. Root knots were counted approximately 3 weeks post-inoculation.
  • Example 13 In planta expression. Events were tested for protein expression by western blot analysis. Protein was extracted from root samples of soybean and tobacco hairy roots transformed as in Examples 8 and 9 and lO ⁇ g protein subjected to SDS-polyacrylamide gel electrophoresis alongside 25ng recombinant protein (as prepared in Example 6), and western blot analysis performed. The filter was incubated with antibody raised in rabbit against recombinant protein, washed, then incubated with goat anti rabbit- ⁇ RP (Sigma) secondary antibody and binding detected by enhanced chemiluminescence.
  • Soybean hairy root events 19B1, 21E3, 26B2, 26D3, 27C1, 28E1 and 83C2 and tobacco events 9824, 9825, 9826, 9827, 9828 and 9829 showed expression of L.nuda recombinant protein as detected by this method.
  • Example 14 Tobacco/Meloidogyne incognita promoter activity assays Feeding assays to determine promoter activity upon nematode infection were carried out on transgenic tobacco transformed via Agrobacterium tumefaciens with a construct containing cestrum yellow leaf curling virus promoter driving GUS reporter gene. Transgenic plants from tissue culture were transferred into 3 inch pots and acclimatised in the greenhouse for 7 days.
  • Example 15 Arabidopsis/Hetero-fera schachtii promoter activity assays Feeding assays to determine promoter activity upon nematode infection were carried out on transgenic Arabidopsis thaliana (ecotype WS) transformed via Agrobacterium tumefaciens with a construct containing cestrum yellow leaf curling virus promoter driving GUS reporter gene. T3 seeds were sown onto agar. These seeds had been sterilised by washing in 70% EtOI (2 mins), soaking in 4% Na-hypochlorite (15 mins), and washing in sterile water (3 rinses then extended washes of 3 mins each).
  • the seeds were dried overnight in a sterile cabinet before being sown onto 7ml knop agar in 9cm petri dishes (6 seeds per petri, 4 petris pe transgenic line). Petris were sealed with parafilm then stored vertically in a Sanyo growth cabinet (25°C, 16 hr photoperiod). At 14 days after sowing, the root systems of the seedlings were infected with 50 sterile J2 H. schachtii per seedling. For each transgenic line seedlings on one petri dish were left uninfected.
  • GUS staining was carried out in the following way at 10 days post infection: Shoots were removed from plants grown on agar plates prior to staining whole roots directly using 5ml GUS stain solution (0.1M sodium phosphate (p ⁇ 7), ImM potassium ferrocyanide, ImM potassium ferrocyanide, lOmM EDTA, 0.1% Triton, 0.1% X- GlcA) with incubation overnight at 37°C. The stain solution was rinsed away and replaced wit! 70% ethanob Stained roots were stored at 4°C prior to examination or examined immediately.
  • GUS stain solution 0.1M sodium phosphate (p ⁇ 7), ImM potassium ferrocyanide, ImM potassium ferrocyanide, lOmM EDTA, 0.1% Triton, 0.1% X- GlcA
  • GUS + no change in staining compared to surrounding root
  • GUS +/- decrease in staining, or patchy staining, compared to surrounding root
  • GUS - no GUS staining present in feeding site

Abstract

La présente invention a trait, entre autres, à des protéines nématicides. Dans un mode de réalisation particulier, la protéine comporte la séquence désignée SEQ ID NO: 1. L'invention a également trait à un polynucléotide codant pour la protéine de SEQ ID NO: 1. L'invention a trait en outre à des cellules hôtes et à des plantes contenant un polynucléotide codant pour la protéine de SEQ ID NO: 1.
PCT/GB2004/003231 2003-08-01 2004-07-26 Proteines nematicides WO2005012340A1 (fr)

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BRPI0413126-6A BRPI0413126A (pt) 2003-08-01 2004-07-26 proteìna nematicida, polinucleotìdeo, construção, célula hospedeira, planta transgênica, método para dotar uma planta ou uma parte da planta com uma proteìna nematicida, plantas ou partes das plantas, usos de um polinucleotìdeos ou de uma construção e de uma proteìna, método para controlar nematódeos, e, composição
EP04743560A EP1654274A1 (fr) 2003-08-01 2004-07-26 Proteines nematicides provenant de lepista nuda

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012038480A2 (fr) 2010-09-22 2012-03-29 Bayer Cropscience Ag Utilisation d'agents de lutte biologique ou chimique pour la lutte contre les insectes et les nématodes dans des cultures résistantes
EP2460406A1 (fr) 2010-12-01 2012-06-06 Bayer CropScience AG Utilisation de fluopyram pour contrôler les nématodes dans les cultures résistant aux nématodes
WO2013092519A1 (fr) 2011-12-19 2013-06-27 Bayer Cropscience Ag Utilisation de dérivés de diamide d'acide anthranilique pour lutter contre les organismes nuisibles dans des cultures transgéniques
EP2622961A1 (fr) 2012-02-02 2013-08-07 Bayer CropScience AG Combinaisons de composés actifs
WO2014004064A1 (fr) 2012-06-29 2014-01-03 E. I. Du Pont De Nemours And Company Carboxamides hétérocycliques fongicides
WO2014090765A1 (fr) 2012-12-12 2014-06-19 Bayer Cropscience Ag Utilisation de 1-[2-fluoro-4-méthyle-5-(2,2,2- trifluoroéthylsulfinyl)phényl]-5-amino-3-trifluorométhyl)-1 h-1,2,4 tfia zole à des fins de régulation des nématodes dans les cultures résistantes aux nématodes

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WO2001000840A1 (fr) * 1999-06-24 2001-01-04 Syngenta Limited Proteines insecticides et nematicides

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MORALES PORFIRIO ET AL: "Efficient isolation of genes differentially expressed on cellulose by suppression subtractive hybridization in Agaricus bisporus.", MYCOLOGICAL RESEARCH, vol. 107, no. 4, April 2003 (2003-04-01), pages 401 - 407, XP008036383, ISSN: 0953-7562 *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012038480A2 (fr) 2010-09-22 2012-03-29 Bayer Cropscience Ag Utilisation d'agents de lutte biologique ou chimique pour la lutte contre les insectes et les nématodes dans des cultures résistantes
WO2012038476A1 (fr) 2010-09-22 2012-03-29 Bayer Cropscience Ag Utilisation de principes actifs pour lutter contre les nématodes dans des cultures résistant aux nématodes
EP2460406A1 (fr) 2010-12-01 2012-06-06 Bayer CropScience AG Utilisation de fluopyram pour contrôler les nématodes dans les cultures résistant aux nématodes
WO2013092519A1 (fr) 2011-12-19 2013-06-27 Bayer Cropscience Ag Utilisation de dérivés de diamide d'acide anthranilique pour lutter contre les organismes nuisibles dans des cultures transgéniques
EP2622961A1 (fr) 2012-02-02 2013-08-07 Bayer CropScience AG Combinaisons de composés actifs
WO2013113742A1 (fr) 2012-02-02 2013-08-08 Bayer Intellectual Property Gmbh Combinaisons de composés actifs
WO2014004064A1 (fr) 2012-06-29 2014-01-03 E. I. Du Pont De Nemours And Company Carboxamides hétérocycliques fongicides
WO2014090765A1 (fr) 2012-12-12 2014-06-19 Bayer Cropscience Ag Utilisation de 1-[2-fluoro-4-méthyle-5-(2,2,2- trifluoroéthylsulfinyl)phényl]-5-amino-3-trifluorométhyl)-1 h-1,2,4 tfia zole à des fins de régulation des nématodes dans les cultures résistantes aux nématodes

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