EP1563064A2 - Variantes de subtilase - Google Patents
Variantes de subtilaseInfo
- Publication number
- EP1563064A2 EP1563064A2 EP03769258A EP03769258A EP1563064A2 EP 1563064 A2 EP1563064 A2 EP 1563064A2 EP 03769258 A EP03769258 A EP 03769258A EP 03769258 A EP03769258 A EP 03769258A EP 1563064 A2 EP1563064 A2 EP 1563064A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- variant
- subtilase
- variants
- s99sd
- enzyme
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
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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)
- C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
- C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
- C12N9/52—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from bacteria or Archaea
- C12N9/54—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from bacteria or Archaea bacteria being Bacillus
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
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- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
Definitions
- the present invention relates to novel subtilase variants exhibiting alterations relative to the parent subtilase in one or more properties including: Wash performance, thermal stability, storage stability or catalytic activity.
- the variants of the invention are suitable for use in e.g. cleaning or detergent compositions, such as laundry detergent compositions and dish wash compositions, including automatic dish wash compositions.
- the present invention also relates to isolated DNA sequences encoding the variants, expression vectors, host cells, and methods for producing and using the variants of the invention. Further, the present invention relates to cleaning and detergent compositions comprising the variants of the invention.
- Enzymes used in such formulations comprise proteases, lipases, amyiases, cellulases, as well as other enzymes, or mixtures thereof. Commercially the most important enzymes are proteases.
- proteases protein engineered variants of naturally occurring wild type proteases, e.g. Durazym ® , Relase ® , Alcalase ® , Savinase ® , Primase ® , Duralase ® , Esperase ® , Ovozyme ® and Kannase ® (Novozymes A/S), MaxataseTM, MaxacalTM, MaxapemTM, ProperaseTM, PurafectTM, Purafect OxPTM, FN2TM, FN3TM and FN4TM (Genencor International, Inc.). Further, a number of protease variants are described in the art. A thorough list of prior art protease variants is given in WO 99/27082.
- an object of the present invention is to provide improved subtilase variants for such purposes.
- the present invention relates to a subtilase variant comprising at least a) an insertion, substitution or deletion of one of the amino acid residues K,H,R,E,D,Q,N,C,V,L,I,P,M,F,W,Y,G,A,S,T in one or more of the positions
- N173D A174V; M175L,I,V,A,S,T; N183D; N184D.S; N185S.D; R186L,C,H; S188G; S190A;
- modification(s) comprise(s): deletion, insertion and/or substitution of an amino acid residue selected from the group consisting of K,H,R,E,D,Q,N,C,V,L,I,P, ,F,W,Y,GAS and T.
- the present invention relates to a subtilase variant comprising a) the combination of one or more of the modifications X62D,XD,XE,XG,DE
- the present invention relates to a subtilase variant comprising at least one of the alterations disclosed in Table I below:
- subtilase variants of the inventions having one or more of the alterations:
- each position corresponds to a position of the amino acid sequence of subtilisin B PN', shown in Figure 1 and SEQ ID NO: 1.
- the present invention relates to an isolated polynucleotide encoding a subtilase variant of the invention.
- the present invention relates to an expression vector comprising the isolated polynucleotide of the invention.
- the present invention relates to a microbial host cell transformed with the expression vector of the invention.
- the present invention relates to a method for producing a subtilase variant according to the invention, wherein a host according to the invention is cultured under conditions conducive to the expression and secretion of the variant, and the variant is recovered.
- the present invention relates to a cleaning or detergent composition, preferably a laundry or dish wash composition, comprising the variant of the invention.
- the present invention relates to a subtilase variant comprising at least one of the alterations disclosed in Table II below:
- subtilase variants of the inventions having one or more of the alterations:
- each position corresponds to a position of the amino acid sequence of subtilisin B PN', shown in Figure 1 and SEQ ID NO: 1.
- the present invention relates to a subtilase variant comprising one of the alterations N252D and N252M.
- the present invention relates to a subtilase variant comprising one or more of the alterations M119L, I, V, A, S; M175L, I, V, A, S and M222L, I, V, A, S in combination with the subtilase variants listed in tables I and II above.
- Fig. 1 shows an alignment between subtilisin BPN'(a) (BASBPN) and subtilisin 309 (b) (BLSAVI). This alignment is in this patent application used as a reference for numbering the residues.
- a frame of reference is first defined by aligning the isolated or parent enzyme with subtilisin BPN' (BASBPN).
- Another method is to use known recognized alignments between subtilases, such as the alignment indicated in WO 91/00345. In most cases the differences will not be of any importance.
- subtilisin 309 SEQ ID NO.2
- subtilisin 309 SEQ ID NO.2
- Enzymes cleaving the amide linkages in protein substrates are classified as proteases, or (interchangeably) peptidases (see Walsh, 1979, Enzymatic Reaction Mechanisms. W.H. Freeman and Company, San Francisco, Chapter 3).
- subtilase BPN subtilase BPN' (BASBPN) sequence.
- BPN' sequence see Fig. 1 , SEQ ID NO:1 or Siezen et al., Protein Engng. 4 (1991) 719-737.
- a serine protease is an enzyme which catalyzes the hydrolysis of peptide bonds, and in which there is an essential serine residue at the active site (White, Handler and Smith, 1973 "Principles of Biochemistry," Fifth Edition, McGraw-Hill Book Company, NY, pp. 271-272).
- the bacterial serine proteases have molecular weights in the 20,000 to 45,000 Dalton range. They are inhibited by diisopropylfluorophosphate. They hydrolyze simple terminal esters and are similar in activity to eukaryotic chymotrypsin, also a serine protease.
- alkaline protease covering a sub-group, reflects the high pH optimum of some of the serine proteases, from pH 9.0 to 11.0 (for review, see Priest (1977) Bacteriological Rev. 41 711-753).
- subtilases A sub-group of the serine proteases tentatively designated subtilases has been proposed by Siezen et al., Protein Engng. 4 (1991) 719-737 and Siezen et al. Protein Science 6 (1997) 501-523. They are defined by homology analysis of more than 170 amino acid sequences of serine proteases previously referred to as subtilisin-like proteases. A subtilisin was previously often defined as a serine protease produced by Gram-positive bacteria or fungi, and according to Siezen et al. now is a subgroup of the subtilases. A wide variety of subtilases have been identified, and the amino acid sequence of a number of subtilases has been determined. For a more detailed description of such subtilases and their amino acid sequences reference is made to Siezen et al. (1997).
- subtilisin 168 subtilisin 168
- subtilisin BPN subtilisin BPN
- subtilisin Carlsberg ALCALASE ®
- NOVOZYMES A/S subtilisin Carlsberg
- subtilisin DY subtilisin DY
- subtilases I-S2 or high alkaline subtilisins
- Sub-group I-S2 proteases are described as highly alkaline subtilisins and comprises enzymes such as subtilisin PB92 (BAALKP) (MAXACAL ® , Genencor International Inc.), subtilisin 309 (SAVINASE ® , NOVOZYMES A/S), subtilisin 147 (BLS147) (ESPERASE ® , NOVOZYMES A S), and alkaline elastase YaB (BSEYAB).
- SAVINASE® is marketed by NOVOZYMES A/S. It is subtilisin 309 from B. Lentus and differs from BAALKP only in one position (N87S). SAVINASE® has the amino acid sequence designated b) in Fig. 1 and in SEQ ID NO:2.
- parent subtilase describes a subtilase defined according to Siezen et al. (1991 and 1997). For further details see description of "Subtilases” above.
- a parent subtilase may also be a subtilase isolated from a natural source, wherein subsequent modifications have been made while retaining the characteristic of a subtilase.
- a parent subtilase may be a subtilase which has been prepared by the DNA shuffling technique, such as described by J.E. Ness et al., Nature Biotechnology, 17, 893-896 (1999). Alternatively the term "parent subtilase” may be termed "wild type subtilase".
- Modification(s) of a subtilase variant The term "modification(s)" used herein is defined to include chemical modification of a subtilase as well as genetic manipulation of the DNA encoding a subtilase.
- the modification(s) can be replacement(s) of the amino acid side chain(s), substitution(s), deletion(s) and/or insertions in or at the amino acid(s) of interest.
- subtilase variant or mutated subtilase means a subtilase that has been produced by an organism which is expressing a mutant gene derived from a parent microorganism which possessed an original or parent gene and which produced a corresponding parent enzyme, the parent gene having been mutated in order to produce the mutant gene from which said mutated subtilase protease is produced when expressed in a suitable host.
- GCG package version 9.1 can be applied (infra) using the same settings.
- the output from the routine is besides the amino acid alignment the calculation of the "Percent Identity" between the two sequences.
- isolated when applied to a polynucleotide, denotes that the polynucleotide has been removed from its natural genetic milieu and is thus free of other extraneous or unwanted coding sequences, and is in a form suitable for use within genetically engineered protein production systems.
- isolated molecules are those that are separated from their natural environment and include cDNA and genomic clones.
- Isolated DNA molecules of the present invention are free of other genes with which they are ordinarily associated, but may include naturally occurring 5' and 3" untranslated regions such as promoters and terminators. The identification of associated regions will be evident to one of ordinary skill in the art (see for example, Dynan and Tijan, Nature 316:774-78, 1985).
- the term "an isolated polynucleotide” may alternatively be termed "a cloned polynucleotide”.
- the term “isolated” indicates that the protein has been removed from its native environment.
- the isolated protein is substantially free of other proteins, particularly other homologous proteins (i.e. "homologous impurities” (see below)).
- An isolated protein is more than 10% pure, preferably more than 20% pure, more preferably more than 30% pure, as determined by SDS-PAGE. Further it is preferred to provide the protein in a highly purified form, i.e., more than 40% pure, more than 60% pure, more than
- isolated protein may alternatively be termed “purified protein”.
- homologous impurities means any impurity (e.g. another polypeptide than the subtilase of the invention), which originate from the homologous cell where the subtilase of the invention is originally obtained from.
- the term "obtained from” as used herein in connection with a specific microbial source means that the polynucleotide and/or subtilase produced by the specific source, or by a cell in which a gene from the source has been inserted.
- substrate used in connection with a substrate for a protease should be interpreted in its broadest form as comprising a compound containing at least one peptide (amide) bond susceptible to hydrolysis by a subtilisin protease.
- product used in connection with a product derived from a protease enzymatic reaction should, in the context of the present invention, be interpreted to include the products of a hydrolysis reaction involving a subtilase protease.
- a product may be the substrate in a subsequent hydrolysis reaction.
- wash performance is used as an enzyme's ability to remove proteinaceous or organic stains present on the object to be cleaned during e.g. wash or hard surface cleaning. See also the wash performance test in Example 3 herein.
- Fig. 1 shows an alignment between subtilisin BPN' (a) and Savinase®(b) using the GAP routine mentioned above.
- the present invention relates to novel subtilase variants exhibiting alterations relative to the parent subtilase in one or more properties including: Wash performance, thermal stability, storage stability or catalytic activity.
- variants which are contemplated as being part of the invention are such variants where, when compared to the wild-type subtilase, one or more amino acid residues has been substituted, deleted or inserted, said variants comprising at least
- modification(s) comprise(s): deletion, insertion and/or substitution of an amino acid residue selected from the group consisting of K,H,R,E,D,Q,N,C,V,L,I,P,M,F,W,Y,G,A,S and T.
- variants of the present invention comprises at least one or more of the alterations indicated in Table I and II, wherein
- a subtilase variant of the first aspect of the invention may be a parent or wild-type subtilase identified and isolated from nature. Such a parent wild-type subtilase may be specifically screened for by standard techniques known in the art.
- One preferred way of doing this may be by specifically PCR amplify conserved DNA regions of interest from subtilases from numerous different microorganism, preferably different Bacillus strains.
- Subtilases are a group of conserved enzymes, in the sense that their DNA and amino acid sequences are homologous. Accordingly it is possible to construct relatively specific primers flanking the polynucleotide sequences of interest.
- subtilase variants of the invention is predominantly a variant of a parent subtilase.
- a subtilase variant suitable for the uses described herein may be constructed by standard techniques known in the art such as by site-directed/random mutagenesis or by DNA shuffling of different subtilase sequences. See the "Material and Methods" section and Example 1 herein (vide infra) for further details.
- variants described herein may comprise one or more further modifications, in particular one or more further substitutions or insertions.
- the variants described herein may encompass mutation at more than just one position.
- the variant according to the invention may contain mutations at one position, two positions, three positions or more than three positions, such as four to eight positions.
- the parent subtilase belongs to the subgroups I-S1 or I-S2, especially subgroup I-S2, both for enzymes from nature or from the artificial creation of diversity, and for designing and producing variants from a parent subtilase.
- subtilase In relation to variants from subgroup I-S1 , it is preferred to select a parent subtilase from the group consisting of BSS168 (BSSAS, BSAPRJ, BSAPRN, BMSAMP), BASBPN, BSSDY, BLSCAR (BLKERA, BLSCA1 , BLSCA2, BLSCA3), BSSPRC, and BSSPRD, or functional variants thereof having retained the characteristic of sub-group I-S1.
- subtilase In relation to variants from subgroup I-S2 it is preferred to select a parent subtilase from the group consisting of BSAPRQ, BLS147 (BSAPRM, BAH 101 ), BLSAVI (BSKSMK, BAALKP, BLSUBL), BYSYAB, BAPB92, TVTHER, and BSAPRS, or functional variants thereof having retained the characteristic of sub-group I-S2.
- the parent subtilase is BLSAVI (Savinase®, NOVOZYMES A/S), and a preferred subtilase variant of the invention is accordingly a variant of Savinase®.
- the present invention also encompasses any of the a bove m entioned s ubtilase variants i n combination with any other modification to the amino acid sequence thereof. Especially com- binations with other modifications known in the art to provide improved properties to the enzyme are envisaged.
- the art describes a number of subtilase variants with different improved properties and a number of those are mentioned in the "Background of the invention" section herein (vide supra). Those references are disclosed here as references to identify a subtilase variant, which advantageously can be combined with a subtilase variant described herein.
- subtilase variant described herein may advantageously be combined with one or more modification(s) in any of the positions:
- a particular interesting variant is a variant, which, in addition to modifications according to the invention, contains the following substitutions:
- subtilase variants of the main aspect(s) of the invention are preferably combined with one or more modification(s) in any of the positions 129, 131 and 194, preferably as 129K, 131H and 194P modifications, and most preferably as P129K, P131H and A194P modifications. Any of those modification(s) are expected to provide a higher expression level of the subtilase variant in the production thereof.
- the wash performance of a selected variant of the invention may be tested in the wash performance test disclosed in Example 3 herein.
- the wash performance test may be employed to assess the ability of a variant, when incorporated in a standard or commercial detergent composition, to remove proteinaceous stains from a standard textile as compared to a reference system, namely the parent subtilase or a similar subtilase exhibiting an even better wash performance (incorporated in the same detergent system and tested under identical conditions).
- the enzyme variants of the present application were tested using the Automatic Mechanical Stress Assay (AMSA). With the AMSA test the wash performance of a large quantity of small volume enzyme-detergent solutions can be examined rapidly. Using this test, the wash performance of a selected variant can be initially investigated, the rationale being that if a selected variant does not show a significant improvement in the test compared to the parent subtilase, it is normally not necessary to carry out further test experiments.
- AMSA Automatic Mechanical Stress Assay
- variants which are particularly interesting for the purposes described herein are such variants which, when tested in a commercial detergent composition such as a US type detergent, an Asian type, a European type or a Latin American type detergent as described in the wash performance test (Example 3), shows an improved wash performance as compared to the parent subtilase tested under identical conditions.
- a commercial detergent composition such as a US type detergent, an Asian type, a European type or a Latin American type detergent as described in the wash performance test (Example 3)
- the improvement in the wash performance may be quantified by calculating the so-called intensity value (Int) defined in Example 3, herein.
- the variant of the invention when tested in the wash performance test has a Performance Score (S) of at least 1 , preferably a
- S (1) variant performs better than the reference at one or two concentrations.
- the variant of the invention fulfils the above criteria on at least the stated lowest level, more preferably at the stated highest level.
- subtilase genes Many methods for cloning a subtilase and for introducing substitutions, deletions or insertions into genes (e.g. subtilase genes) are well known in the art.
- subtilase variant of the invention In general standard procedures for cloning of genes and introducing mutations (random and/or site directed) into said genes may be used in order to obtain a subtilase variant of the invention.
- suitable techniques reference is made to Example 1 herein (vide infra) and (Sambrook et al. (1989) Molecular cloning: A laboratory manual, Cold Spring Harbor lab., Cold Spring Harbor, NY; Ausubel, F. M. et al. (eds.) "Current protocols in Molecular Biology”. John Wiley and Sons, 1995; Harwood, C. R., and Cutting, S. M. (eds.) "Molecular Biological Methods for Bacillus”. John Wiley and Sons, 1990), and WO 96/34946.
- subtilase variant may be constructed by standard techniques for artificial creation of diversity, such as by DNA shuffling of different subtilase genes (WO 95/22625; Stemmer WPC, Nature 370:389-91 (1994)). DNA shuffling of e.g. the gene encoding Savinase® with one or more partial subtilase sequences identified in nature, will after subsequent screening for improved wash performance variants, provide subtilase variants suitable for the purposes described herein.
- a recombinant expression vector comprising a DNA construct encoding the e nzyme o f t he invention may be any vector that may conveniently be subjected to recombinant D NA p rocedures.
- the vector may be an autonomously replicating vector, i.e. a vector that exists as an extra- chromosomal entity, the replication of which is independent of chromosomal replication, e.g. a plasmid.
- the vector may be one that on introduction into a host cell is integrated into the host cell genome in part or in its entirety and replicated together with the chromosome(s) into which it has been integrated.
- the vector is preferably an expression vector in which the DNA sequence encoding the enzyme of the invention is operably linked to additional segments required for transcription of the DNA.
- the expression vector is derived from plasmid or viral DNA, or may contain elements of both.
- operably linked indicates that the segments are arranged so that they function in concert for their intended purposes, e.g. transcription initiates in a promoter and proceeds through the DNA sequence coding for the enzyme.
- the promoter may be any DNA sequence that shows transcriptional activity in the host cell of choice and may be derived from genes encoding proteins either homologous or heterologous to the host cell.
- suitable promoters for use in bacterial host cells include the promoter of the Bacillus stearothermophilus maltogenic amylase gene, the Bacillus licheniformis alpha- amylase gene, the Bacillus amyloliquefaciens alpha-amylase gene, the Bacillus subtilis alkaline protease gene, or the Bacillus pumilus xylosidase gene, or the phage Lambda P R or PL promoters or the E. coli lac, trp or tac promoters.
- the DNA sequence encoding the enzyme of the invention may also, if necessary, be operably connected to a suitable terminator.
- the recombinant vector of the invention may further comprise a DNA sequence enabling the vector to replicate in the host cell in question.
- the vector may also comprise a selectable marker, e.g. a gene the product of which complements a defect in the host cell, or a gene encoding resistance to e.g. antibiotics like kanamycin, chloramphenicol, erythromycin, tetracycline, spectinomycine, or the like, or resistance to heavy metals or herbicides.
- a secretory signal sequence (also known as a leader sequence, prepro sequence or pre sequence) may be provided in the recombinant vector.
- the secretory signal sequence is joined to the DNA sequence encoding the enzyme in the correct reading frame.
- Secretory signal s equences a re commonly positioned 5' to the DNA sequence encoding the enzyme.
- the secretory signal sequence may be that normally associated with the enzyme or may be from a gene encoding another secreted protein.
- the DNA sequence encoding the present enzyme introduced into the host cell may be either homologous or heterologous to the host in question. If homologous to the host cell, i.e. produced by the host cell in nature, it will typically be operably connected to another promoter sequence or, if applicable, another secretory signal sequence and/or terminator sequence than in its natural environment.
- the term "homologous” is intended to include a DNA sequence encoding an enzyme native to the host organism in question.
- heterologous is intended to include a DNA sequence not expressed by the host cell in nature. Thus, the DNA sequence m ay b e f rom a nother o rganism, o r it may b e a synthetic sequence.
- the host cell into which the DNA construct or the recombinant vector of the invention is introduced may be any cell that is capable of producing the present enzyme and includes bacteria, yeast, fungi and higher eukaryotic cells including plants.
- Examples of bacterial host cells which, on cultivation, are capable of producing the enzyme of the invention are gram-positive bacteria such as strains of Bacillus, such as strains of B. subtilis, B. licheniformis, B. lentus, B. brevis, B. stearothermophilus, B. alkalophilus, B. amyloliquefaciens, B. coagulans, B. circulans, B. lautus, B. megaterium or ⁇ . thuringiensis, or strains of Streptomyces, such as S. lividans or S. murinus, or gram-negative bacteria such as Escherichia coli.
- Bacillus such as strains of B. subtilis, B. licheniformis, B. lentus, B. brevis, B. stearothermophilus, B. alkalophilus, B. amyloliquefaciens, B. coagulans, B. circulans, B. lautus, B. megaterium or
- the transformation of the bacteria may be effected by protoplast transformation, electroporation, conjugation, or by using competent cells in a manner known per se (cf. Sambrook et al., supra).
- the enzyme When expressing the enzyme in bacteria such as E. coli, the enzyme may be retained in the cytoplasm, typically as insoluble granules (known as inclusion bodies), or may be directed to the periplasmic space by a bacterial secretion sequence. In the former case, the cells a re lysed and the granules are recovered and denatured after which the enzyme is refolded by diluting the denaturing agent. In the latter case, the enzyme may be recovered from the periplasmic space by disrupting the cells, e.g. by sonication or osmotic shock, to release the contents of the periplasmic space and recovering the enzyme.
- the enzyme When expressing the enzyme in gram-positive bacteria such as Bacillus or Streptomyces strains, the enzyme may be retained in the cytoplasm, or may be directed to the extracellular medium by a bacterial secretion sequence. In the latter case, the enzyme may be recovered from the medium as described below.
- the present invention provides a method of producing an isolated enzyme according to the invention, wherein a suitable host cell, which has been transformed with a DNA sequence encoding the enzyme, is cultured under conditions permitting the production of the enzyme, and the resulting enzyme is recovered from the culture.
- the medium used to culture the transformed host cells may be any conventional medium suitable for growing the host cells in question.
- the expressed subtilase may conveniently be secreted into the culture medium and may be recovered there-from by well-known procedures including separating the cells from the medium by centrifugation or filtration, precipitating proteinaceous components of the medium by means of a salt such as ammonium sulfate, followed by chromatographic procedures such as ion exchange chromatography, affinity chromatography, or the like.
- the enzyme of the invention may be added to and thus become a component of a detergent composition.
- cleaning and detergent compositions are well described in the art and reference is made to WO 96/34946; WO 97/07202; WO 95/30011 for further description of suitable cleaning and detergent compositions.
- the detergent composition of the invention may for example be formulated as a hand or machine laundry detergent composition including a laundry additive composition suitable for pre-treatment of stained fabrics and a rinse added fabric softener composition, or be formulated as a detergent composition for use in general h ousehold h ard s urface cleaning operations, or be formulated for hand or machine dishwashing operations.
- the invention provides a detergent additive comprising the enzyme of the invention.
- the detergent additive as well as the detergent composition may comprise one or more other enzymes such as a protease, a lipase, a cutinase, an amylase, a carbohydrase, a cellulase, a pectinase, a mannanase, an arabinase, a galactanase, a xylanase, an oxidase, e.g., a laccase, and/or a peroxidase.
- enzymes such as a protease, a lipase, a cutinase, an amylase, a carbohydrase, a cellulase, a pectinase, a mannanase, an arabinase, a galactanase, a xylanase, an oxidas
- the properties of the chosen enzyme(s) should be compatible with the selected detergent, (i.e. pH-optimum, compatibility with other enzymatic and non-enzymatic ingredients, etc.), and the enzyme(s) should be present in effective amounts.
- proteases include those of animal, vegetable or microbial origin. Microbial origin is preferred. Chemically modified or protein engineered mutants are included.
- the protease may be a serine protease or a metallo protease, preferably an alkaline microbial protease or a trypsin-like protease.
- alkaline proteases are subtilisins, especially those derived from Bacillus, e.g., subtilisin Novo, subtilisin Carlsberg, subtilisin 309, subtilisin 147 a nd s ubtilisin 168 (described in WO 89/06279).
- trypsin-like proteases are trypsin (e.g. of porcine or bovine origin) and the Fusarium protease described in WO 89/06270 and WO 94/25583.
- useful proteases are the variants described in WO 92/19729, WO 98/20115, WO 98/20116, and WO 98/34946, especially the variants with substitutions in one or more of the following positions: 27, 36, 57, 76, 87, 97, 101 , 104, 120, 123, 167, 170, 194, 206, 218, 222, 224, 235 and 274.
- Preferred commercially available protease enzymes include Durazym ® , Relase ® , Alcalase ® , Savinase ® , Primase ® , Duralase ® , Esperase ® , Ovozyme ® and Kannase ® (Novozymes A S), MaxataseTM, MaxacalTM, MaxapemTM, ProperaseTM, PurafectTM, Purafect OxPTM, FN2TM, FN3TM and FN4TM (Genencor International, Inc.).
- Lipases S Amble I ipases i nclude t hose o f b acterial o r f ungal o rigin. C hemically m odified or protein engineered mutants are included. Examples of useful lipases include lipases from Humicola (synonym Thermomyces), e.g. from H. lanuginosa (T. lanuginosus) as described in EP 258 068 and EP 305 216 or from H. insolens as described in WO 96/13580, a Pseudomonas lipase, e.g. from P. alcaligenes or P. pseudoalcaligenes (EP 218 272), P.
- Humicola semomyces
- H. lanuginosa T. lanuginosus
- Pseudomonas lipase e.g. from P. alcaligenes or P. pseudoalcaligenes (EP
- cepacia EP 331 376
- P. stutzeri GB 1 ,372,034
- P. fluorescens Pseudomonas sp. strain SD 705 (WO 95/06720 and WO 96/27002)
- P. wisconsinensis WO 96/12012
- Bacillus lipase e.g. from B. subtilis (Dartois et al. (1993), Biochemica et Biophysica Acta, 1131 , 253-360), B. stearothermophilus (JP 64/744992) or ⁇ . pumilus (WO 91/16422).
- lipase variants such as those described in WO 92/05249, WO 94/01541 , EP 407 225, EP 260 105, WO 95/35381 , WO 96/00292, WO 95/30744, WO 94/25578, WO 95/14783, WO 95/22615, WO 97/04079 and WO 97/07202.
- Lipex ® Lipex ®
- Lipolase ® Lipolase Ultra ®
- Amyiases include those of bacterial or fungal origin.
- Amyiases include, for example, ⁇ -amylases obtained from Bacillus, e.g. a special strain of B. licheniformis, described in more detail in GB 1 ,296,839.
- amyiases examples include the variants described in WO 94/02597, WO 94/18314, WO 96/23873, and WO 97/43424, especially the variants with substitutions in one or more of the following positions: 15, 23, 105, 106, 124, 128, 133, 154, 156, 181 , 188, 190, 197, 202, 208,
- amyiases are Duramyl ® , Termamyl ® , Fungamyl ® and BAN ®
- Suitable cellulases include those of bacterial or fungal origin. Chemically modified or protein engineered mutants are included. Suitable cellulases include cellulases from the genera Bacillus, Pseudomonas, Humicola, Fusarium, Thielavia, Acremonium, e.g. the fungal cellulases produced from Humicola insolens, Myceliophthora thermophila and Fusarium oxysporum disclosed in US 4,435,307, US 5,648,263, US 5,691 ,178, US 5,776,757 and WO 89/09259. Especially suitable cellulases are the alkaline or neutral cellulases having colour care benefits.
- cellulases examples include cellulases described in EP 0 495 257, EP 0 531 372, WO 96/11262, WO 96/29397, WO 98/08940.
- cellulase variants such as those described in WO 94/07998, EP 0 531 315, US 5,457,046, US 5,686,593, US 5,763,254, WO 95/24471 , WO 98/12307 and PCT/DK98/00299.
- cellulases include Celluzyme ® , and Carezyme ® (Novozymes A/S), ClazinaseTM, and Puradax HATM (Genencor International Inc.), and KAC-500(B)TM (Kao Corporation).
- Peroxidases/Oxidases include those of plant, bacterial or fungal origin. Chemically modified or protein engineered mutants are included. Examples of useful peroxidases include peroxidases from Coprinus, e.g. from C. cinereus, and variants thereof as those described in WO 93/24618, WO 95/10602, and WO 98/15257. Commercially available peroxidases include Guardzyme ® (Novozymes A/S).
- the detergent enzyme(s) may be included in a detergent composition by adding separate additives containing one or more enzymes, or by adding a combined additive comprising all of these enzymes.
- a detergent additive of the invention i.e. a separate additive or a combined additive, can be formulated e.g. as a granulate, a liquid, a slurry, etc.
- Preferred detergent additive formulations are granulates, in particular non-dusting granulates, liquids, in particular stabilized liquids, or slurries.
- Non-dusting granulates may be produced, e.g., as disclosed in US 4,106,991 and 4,661 ,452 and may optionally be coated by methods known in the art.
- waxy coating materials are poly(ethylene oxide) products (polyethyleneglycol, PEG) with mean molar weights of 1000 to 20000; ethoxylated nonylphenols having from 16 to 50 ethylene oxide units; ethoxylated fatty alcohols in which the alcohol contains from 12 to 20 carbon atoms and in which there are 15 to 80 ethylene oxide units; fatty alcohols; fatty acids; and mono- and di- and triglycerides of fatty acids.
- Liquid enzyme preparations may, for instance, be stabilized by adding a polyol such as propylene glycol, a sugar or sugar alcohol, lactic acid or boric acid according to established methods.
- Protected enzymes may be prepared according to the method disclosed in EP 238,216.
- the detergent composition of the invention may be in any convenient form, e.g., a bar, a tablet, a powder, a granule, a paste or a liquid.
- a liquid detergent may be aqueous, typically containing up to 70 % water and 0-30 % organic solvent, or non-aqueous.
- the detergent composition comprises one or more surfactants, which may be non-ionic including semi-polar and/or anionic and/or cationic and/or zwitterionic.
- the surfactants are typically present at a level of from 0.1% to 60% by weight.
- the detergent When included therein the detergent will usually contain from about 1 % to about 40% of an anionic surfactant such as linear alkylbenzenesulfonate, alpha-olefinsulfonate, a lkyl s ulfate (fatty alcohol sulfate), alcohol ethoxysulfate, secondary alkanesulfonate, alpha-sulfo fatty acid methyl ester, alkyl- or alkenylsuccinic acid or soap.
- an anionic surfactant such as linear alkylbenzenesulfonate, alpha-olefinsulfonate, a lkyl s ulfate (fatty alcohol sulfate), alcohol ethoxysulfate, secondary alkanesulfonate, alpha-sulfo fatty acid methyl ester, alkyl- or alkenylsuccinic acid or soap.
- the detergent When included therein the detergent will usually contain from about 0.2% to about 40% of a non-ionic surfactant such as alcohol ethoxylate, nonylphenol ethoxylate, alkylpolyglycoside, alkyldimethylamineoxide, ethoxylated fatty acid monoethanolamide, fatty acid monoethanol- amide, polyhydroxy alkyl fatty acid amide, or N-acyl N-alkyl derivatives of glucosamine (“glucamides").
- a non-ionic surfactant such as alcohol ethoxylate, nonylphenol ethoxylate, alkylpolyglycoside, alkyldimethylamineoxide, ethoxylated fatty acid monoethanolamide, fatty acid monoethanol- amide, polyhydroxy alkyl fatty acid amide, or N-acyl N-alkyl derivatives of glucosamine (“glucamides”).
- glucamides N-acyl N-alkyl derivatives of glucosamine
- the detergent may contain 0-65 % of a detergent builder or complexing agent such as zeolite, diphosphate, triphosphate, phosphonate, carbonate, citrate, nitrilotriacetic acid, ethylene- diaminetetraacetic acid, diethylenetriaminepentaacetic acid, alkyl- or alkenyl-succinic acid, soluble silicates or layered silicates (e.g. SKS-6 from Hoechst).
- a detergent builder or complexing agent such as zeolite, diphosphate, triphosphate, phosphonate, carbonate, citrate, nitrilotriacetic acid, ethylene- diaminetetraacetic acid, diethylenetriaminepentaacetic acid, alkyl- or alkenyl-succinic acid, soluble silicates or layered silicates (e.g. SKS-6 from Hoechst).
- the detergent may comprise one or more polymers.
- examples are carboxymethyl-cellulose, poly(vinylpyrrolidone), poly (ethylene glycol), poly(vinyl alcohol), poly(vinyl-pyridine-N-oxide), poly(vinylimidazole), polycarboxylates such as poly-acrylates, maleic/acrylic acid copolymers and lauryl methacrylate/acrylic acid copolymers.
- the detergent may contain a bleaching system which may comprise a H 2 O 2 source such as perborate or percarbonate which may be combined with a p eracid-forming b leach a ctivator such as tetraacetylethylenediamine or nonanoyloxybenzenesulfonate.
- a bleaching system may comprise peroxyacids of e.g. the amide, imide, or sulfone type.
- the detergent may also contain other conventional detergent ingredients such as e.g. fabric conditioners including clays, foam boosters, suds suppressors, anti-corrosion agents, soil- suspending agents, anti-soil redeposition agents, dyes, bactericides, optical brighteners, hydrotropes, tarnish inhibitors, or perfumes.
- fabric conditioners including clays, foam boosters, suds suppressors, anti-corrosion agents, soil- suspending agents, anti-soil redeposition agents, dyes, bactericides, optical brighteners, hydrotropes, tarnish inhibitors, or perfumes.
- Detergent Examples 1 and 2 provide ranges for the composition of a typical Latin American detergent and a typical European powder detergent respectively.
- Detergent Example 1 Typical Latin American detergent composition.
- the enzyme(s) of the detergent composition of the invention may be stabilized using conventional stabilizing agents, e.g., a polyol such as propylene glycol or glycerol, a sugar or sugar alcohol, lactic acid, boric acid, or a boric acid derivative, e.g., an aromatic borate ester, or a phenyl boronic acid derivative such as 4-formylphenyl boronic acid, and the composition may be formulated as described in e.g. WO 92/19709 and WO 92/19708.
- a polyol such as propylene glycol or glycerol
- a sugar or sugar alcohol lactic acid, boric acid, or a boric acid derivative, e.g., an aromatic borate ester, or a phenyl boronic acid derivative such as 4-formylphenyl boronic acid
- any single enzyme in particular the enzyme of the invention, may be added in an amount corresponding to 0.01-200 mg of enzyme protein per liter of wash liqour, preferably 0.05-50 mg of enzyme protein per liter of wash liqour, in particular 0.1-10 mg of enzyme protein per liter of wash liqour.
- the enzyme of the invention may additionally be incorporated in the detergent formulations disclosed in WO 97/07202 which is hereby incorporated as reference.
- Standard textile pieces are obtained from EMPA St. Gallen, Lerchfeldstrasse 5, CH-9014 St. Gallen, Switzerland. Especially type EMPA116 (cotton textile stained with blood, milk and ink) and EMPA117 (polyester/cotton textile stained with blood, milk and ink).
- Bacillus lentus strain 309 is deposited with the NCIB and accorded the accession number NCIB 10309, and described in US Patent No. 3,723,250 incorporated by reference herein.
- the parent subtilase 309 or Savinase® can be obtained from Strain 309.
- the expression host organism is Bacillus subtilis.
- the plasmid pSX222 is used as E. coli - B. subtilis shuttle vector and B. subtilis expression vector (as described in WO 96/34946).
- Fermentations for the production of subtilase enzymes are performed at pH 7.3 and 37°C on a rotary s haking table at 225 rpm. i n 50 ml tubes containing 15 ml double TY media for 2-3 days.
- the s ubtilase variant s ecreted from the h ost cells may conveniently be recovered from the culture medium by well-known procedures, including separating the cells from the medium by centrifugation or filtration, and precipitating proteinaceous components of the medium by means of a salt such as ammonium sulfate, followed by the use of chromatographic procedures such as ion exchange chromatography, affinity chromatography, or the like.
- WASH PERFORMANCE TEST In order to asses the wash performance of selected subtilase variants in detergent compositions, washing experiments are performed. The enzyme variants of the present application is tested using the Automatic Mechanical Stress Assay (AMSA). With the AMSA test the wash performance of a large quantity of small volume enzyme-detergent solutions can be examined.
- the AMSA plate has a number of slots for test solutions and a lid firmly squeezing the textile swatch to be washed against all the slot openings. During the washing time, the plate, test solutions, textile and lid are vigorously shaken to bring the test solution in contact with the textile and apply mechanical stress.
- WO 02/42740 especially the paragraph "Special method embodiments" at page 23-24.
- Detergents for wash performance tests of the subtilase enzymes of the invention can be obtained by purchasing fully formulated commercial detergents at the market and subsequently inactivate the enzymatic components by heat treatment (5 minutes at 85°C in aqueous solution). Moreover a commercial detergent base without enzymes can be purchased directly from the manufacturer. Further a suitable model detergent can be composed according to the provisions at page 19-24 herein and used for wash performance tests.
- Subtilisin 309 (Savinase ® ) site-directed variants of the invention comprising specific insertions/deletions/substitutions are made by traditional cloning of DNA fragments (Sambrook et al., Molecular Cloning: A Laboratory Manual, 2nd Ed., Cold Spring Harbor, 1989) produced by PCR with oligos containing the desired mutations.
- the template plasmid DNA may be pSX222, or an analogue of this containing a variant of subtilisin 309. Mutations are introduced by oligo directed mutagenesis to the construction of variants.
- the subtilisin 309 variants are transformed into E. coli.
- DNA purified from an over night culture of t hese t ransformants is transformed i nto ⁇ . subtilis by restriction endonuclease digestion, purification of DNA fragments, ligation, transformation of B. subtilis. Transformation of B. subtilis is performed as described by Dubnau et al., 1971 , J. Mol. Biol. 56, pp. 209-221.
- SITE-DIRECTED MUTAGENESIS IN ORDER TO INTRODUCE MUTATIONS IN A SPECIFIC REGION
- Mutagenic primers are synthesized corresponding to the DNA sequence flanking the sites of mutation, separated by the DNA base pairs defining the insertions / deletions / substitutions.
- the resulting mutagenic primers are used in a PCR reaction with the modified plasmid pSX222.
- the resulting PCR fragment is purified and extended in a second PCR- reaction, the resulting PCR product is purified and extended in a third PCR-reaction before being digested by endonucleases and cloned into the E. coli - B. subtilis shuttle vector pSX222.
- the PCR reactions are performed under normal conditions.
- the plasmid DNA is transformed into E. coli by well-known techniques and one E. coli colony is sequenced to confirm the mutation designed.
- subtilase variants of the invention can be constructed as described above.
- the pSX222 expression plasmid comprising a variant of the invention was transformed into a competent ⁇ . subtilis strain and fermented as described above.
- HCIC Hydrophobic Charge Induction Chromatography
- the HCIC uses a cellulose matrix to which 4-Mercapto-Ethyl-Pyridine (4-MEP) is bound.
- Beads of the cellulose matrix sized 80-100 ⁇ m are mixed with a media containing yeast extract and the transformed ⁇ . subtilis capable of secreting the subtilisin variants and incubated at pH
- the concentration of the purified subtilisin enzyme variants is assessed by active site titration (AST).
- the purified enzyme is incubated with the high affinity inhibitor CI-2A at different concentrations to inhibit a varying amount of the active sites.
- the protease and inhibitor binds to each other at a 1 :1 ratio and accordingly the enzyme concentration can be directly related to the concentration of inhibitor, at which all protease is inactive.
- a substrate 0.6 mM Suc-Ala-Ala-Pro-Phe-pNA in Tris/HCI buffer
- a substrate 0.6 mM Suc-Ala-Ala-Pro-Phe-pNA in Tris/HCI buffer
- p NA paranitrophenol
- the performance of the enzyme variant is measured as the brightness of the colour of the textile samples washed with that specific enzyme variant. Brightness can also be expressed as the intensity of the light reflected from the textile sample when luminated with white light.
- the intensity of the reflected light can be used to measure wash performance of an enzyme variant.
- Colour measurements are made with a professional flatbed scanner (PFU DL2400pro), which is used to capture an image of the washed textile samples.
- the scans are made with a resolution of 200 dpi and with an output colour dept of 24 bits.
- the scanner is frequently calibrated with a Kodak reflective IT8 target.
- a special designed software application is used (Novozymes Color Vector Analyzer).
- the program retrieves the 24 bit pixel values from the image and converts them into values for red, green and blue (RGB).
- RGB red, green and blue
- T he intensity value (Int) is calculated by adding the RGB values together as vectors and then taking the length of the resulting vector:
- wash performance (P) of the variants was calculated in accordance with the below formula:
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Abstract
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP10183162.6A EP2399992A3 (fr) | 2002-11-06 | 2003-11-05 | Variantes de subtilase |
EP09172028.4A EP2138574B1 (fr) | 2002-11-06 | 2003-11-05 | Variantes de subtilase |
EP20100180046 EP2284258A3 (fr) | 2002-11-06 | 2003-11-05 | Variantes de subtilase |
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DK200201705 | 2002-11-06 | ||
DKPA200201705 | 2002-11-06 | ||
DKPA200201933 | 2002-12-18 | ||
DK200201933 | 2002-12-18 | ||
US50753703P | 2003-10-01 | 2003-10-01 | |
US507537P | 2003-10-01 | ||
PCT/DK2003/000756 WO2004041979A2 (fr) | 2002-11-06 | 2003-11-05 | Variantes de subtilase |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP09172028.4A Division EP2138574B1 (fr) | 2002-11-06 | 2003-11-05 | Variantes de subtilase |
Publications (1)
Publication Number | Publication Date |
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EP1563064A2 true EP1563064A2 (fr) | 2005-08-17 |
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EP09172028.4A Expired - Lifetime EP2138574B1 (fr) | 2002-11-06 | 2003-11-05 | Variantes de subtilase |
EP20100180046 Ceased EP2284258A3 (fr) | 2002-11-06 | 2003-11-05 | Variantes de subtilase |
EP10183162.6A Withdrawn EP2399992A3 (fr) | 2002-11-06 | 2003-11-05 | Variantes de subtilase |
EP03769258A Withdrawn EP1563064A2 (fr) | 2002-11-06 | 2003-11-05 | Variantes de subtilase |
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EP09172028.4A Expired - Lifetime EP2138574B1 (fr) | 2002-11-06 | 2003-11-05 | Variantes de subtilase |
EP20100180046 Ceased EP2284258A3 (fr) | 2002-11-06 | 2003-11-05 | Variantes de subtilase |
EP10183162.6A Withdrawn EP2399992A3 (fr) | 2002-11-06 | 2003-11-05 | Variantes de subtilase |
Country Status (13)
Country | Link |
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EP (4) | EP2138574B1 (fr) |
JP (3) | JP4694964B2 (fr) |
KR (4) | KR20140021051A (fr) |
CN (3) | CN103397010B (fr) |
AR (2) | AR041993A1 (fr) |
AU (1) | AU2003277836B2 (fr) |
BR (1) | BR0315916A (fr) |
CA (1) | CA2503965C (fr) |
CL (1) | CL2010000493A1 (fr) |
MX (1) | MXPA05004755A (fr) |
MY (1) | MY140915A (fr) |
TW (1) | TWI319007B (fr) |
WO (1) | WO2004041979A2 (fr) |
Families Citing this family (263)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7888093B2 (en) | 2002-11-06 | 2011-02-15 | Novozymes A/S | Subtilase variants |
TWI319007B (en) * | 2002-11-06 | 2010-01-01 | Novozymes As | Subtilase variants |
ATE529505T1 (de) * | 2005-07-08 | 2011-11-15 | Novozymes As | Subtilase varianten |
US20070161531A1 (en) | 2005-07-08 | 2007-07-12 | Novozymes A/S | Subtilase variants |
EP2013339B1 (fr) | 2006-04-20 | 2013-09-11 | Novozymes A/S | Variants de savinase offrant une meilleure efficacité de lavage contre les taches d'oeuf |
EP2059591B1 (fr) * | 2006-07-18 | 2012-09-05 | Danisco US Inc. | Composition pour lavage de vaisselle contenant de variantes de protéases |
US20080221008A1 (en) * | 2006-10-06 | 2008-09-11 | Novozymes A/S | Detergent compositions and the use of enzyme combinations therein |
EP2102335B1 (fr) * | 2007-01-04 | 2012-02-22 | Crucell Holland B.V. | Purification de facteur xi |
JP2011524166A (ja) * | 2008-06-06 | 2011-09-01 | ダニスコ・ユーエス・インク | 変異体微生物プロテアーゼを含む組成物及び方法 |
GB0915572D0 (en) * | 2009-09-07 | 2009-10-07 | Reckitt Benckiser Nv | Detergent composition |
CN102648273B (zh) * | 2009-09-25 | 2017-04-26 | 诺维信公司 | 枯草蛋白酶变体 |
CN104946427A (zh) | 2009-09-25 | 2015-09-30 | 诺维信公司 | 蛋白酶变体的用途 |
PL2566960T3 (pl) * | 2010-05-06 | 2017-08-31 | The Procter And Gamble Company | Produkty konsumenckie z odmianami proteaz |
FI123942B (fi) | 2010-10-29 | 2013-12-31 | Ab Enzymes Oy | Sieniperäisen seriiniproteaasin variantteja |
TR201901382T4 (tr) * | 2011-05-05 | 2019-02-21 | Danisco Inc | Serin proteaz varyantlarını içeren bileşimler ve yöntemler. |
EP2705145B1 (fr) * | 2011-05-05 | 2020-06-17 | The Procter and Gamble Company | Compositions et procédés comportant des variants de protéases à sérine |
US20140342433A1 (en) | 2011-11-25 | 2014-11-20 | Novozymes A/S | Subtilase Variants and Polynucleotides Encoding Same |
EP2607468A1 (fr) * | 2011-12-20 | 2013-06-26 | Henkel AG & Co. KGaA | Compositions détergentes comprenant des variants de subtilase |
WO2013092635A1 (fr) | 2011-12-20 | 2013-06-27 | Novozymes A/S | Variants de subtilase et polynucléotides codant pour ceux-ci |
CN104114698A (zh) | 2012-02-17 | 2014-10-22 | 诺维信公司 | 枯草杆菌蛋白酶变体以及编码它们的多核苷酸 |
EP2628785B1 (fr) | 2012-02-17 | 2016-05-18 | Henkel AG & Co. KGaA | Compositions détergentes comprenant des variants de subtilase |
CN104302753A (zh) | 2012-05-16 | 2015-01-21 | 诺维信公司 | 包括脂肪酶的组合物及其使用方法 |
AU2013279440B2 (en) | 2012-06-20 | 2016-10-06 | Novozymes A/S | Use of polypeptides having protease activity in animal feed and detergents |
EP2888358A1 (fr) | 2012-08-22 | 2015-07-01 | Novozymes A/S | Compositions détergentes comprenant des métalloprotéases |
CN104619838A (zh) | 2012-08-22 | 2015-05-13 | 诺维信公司 | 来自微小杆菌属的金属蛋白酶 |
US9315791B2 (en) | 2012-08-22 | 2016-04-19 | Novozymes A/S | Metalloproteases from alicyclobacillus |
TR201910918T4 (tr) | 2012-12-07 | 2019-08-21 | Novozymes As | Bakterilerin yapışmasının önlenmesi. |
US9551042B2 (en) | 2012-12-21 | 2017-01-24 | Novozymes A/S | Polypeptides having protease activity and polynucleotides encoding same |
WO2014106593A1 (fr) | 2013-01-03 | 2014-07-10 | Novozymes A/S | Variants d'alpha-amylase et polynucléotides les codant |
MY192746A (en) | 2013-05-14 | 2022-09-06 | Novozymes As | Detergent compositions |
CN105209613A (zh) | 2013-05-17 | 2015-12-30 | 诺维信公司 | 具有α淀粉酶活性的多肽 |
EP3004315A2 (fr) | 2013-06-06 | 2016-04-13 | Novozymes A/S | Variants d'alpha-amylase et polynucléotides les codant |
WO2014207228A1 (fr) | 2013-06-27 | 2014-12-31 | Novozymes A/S | Variants de subtilase et polynucléotides codant pour ceux-ci |
CN105874067A (zh) | 2013-06-27 | 2016-08-17 | 诺维信公司 | 枯草杆菌酶变体以及编码它们的多核苷酸 |
EP3013955A1 (fr) | 2013-06-27 | 2016-05-04 | Novozymes A/S | Variants de subtilase et polynucléotides codant pour ceux-ci |
US20160152925A1 (en) | 2013-07-04 | 2016-06-02 | Novozymes A/S | Polypeptides Having Anti-Redeposition Effect and Polynucleotides Encoding Same |
CN105339492A (zh) | 2013-07-09 | 2016-02-17 | 诺维信公司 | 具有脂肪酶活性的多肽和编码它们的多核苷酸 |
WO2015014790A2 (fr) | 2013-07-29 | 2015-02-05 | Novozymes A/S | Variants de protéase et polynucléotides les codant |
WO2015014803A1 (fr) | 2013-07-29 | 2015-02-05 | Novozymes A/S | Variants de protéases et polynucléotides les codant |
WO2015049370A1 (fr) | 2013-10-03 | 2015-04-09 | Novozymes A/S | Composition détergente et utilisation de celle-ci |
US10030239B2 (en) | 2013-12-20 | 2018-07-24 | Novozymes A/S | Polypeptides having protease activity and polynucleotides encoding same |
US10208297B2 (en) | 2014-01-22 | 2019-02-19 | Novozymes A/S | Polypeptides with lipase activity and polynucleotides encoding same for cleaning |
WO2015134729A1 (fr) | 2014-03-05 | 2015-09-11 | Novozymes A/S | Compositions et procédés destinés à améliorer les propriétés de matériaux textiles non-cellulosiques par l'utilisation d'endo-xyloglucane transférase |
WO2015134737A1 (fr) | 2014-03-05 | 2015-09-11 | Novozymes A/S | Compositions et procédés pour améliorer les propriétés de matières textiles cellulosiques avec une xyloglucane endotransglycosylase |
EP3117001B1 (fr) | 2014-03-12 | 2019-02-20 | Novozymes A/S | Polypeptides à activité lipase et polynucléotides codant pour ceux-ci |
EP3126479A1 (fr) | 2014-04-01 | 2017-02-08 | Novozymes A/S | Polypeptides présentant une activité alpha-amylase |
DK3129457T3 (en) | 2014-04-11 | 2018-09-17 | Novozymes As | detergent |
US10030215B2 (en) | 2014-04-15 | 2018-07-24 | Novozymes A/S | Polypeptides with lipase activity and polynucleotides encoding same |
AR100606A1 (es) | 2014-05-27 | 2016-10-19 | Novozymes As | Variantes de lipasas y polinucleótidos que las codifican |
EP3878957A1 (fr) | 2014-05-27 | 2021-09-15 | Novozymes A/S | Procédés de production de lipases |
EP3155097A1 (fr) | 2014-06-12 | 2017-04-19 | Novozymes A/S | Variants d'alpha-amylase et polynucléotides codant pour ces derniers |
BR112017000102B1 (pt) | 2014-07-04 | 2023-11-07 | Novozymes A/S | Variantes de subtilase de uma subtilase progenitora, composição detergente, uso da mesma e método para a produção de uma variante de subtilase que tem atividade de protease |
WO2016001450A2 (fr) * | 2014-07-04 | 2016-01-07 | Novozymes A/S | Variants de subtilase et polynucléotides codant pour ceux-ci |
WO2016079110A2 (fr) | 2014-11-19 | 2016-05-26 | Novozymes A/S | Utilisation d'enzymes pour le nettoyage |
EP4067485A3 (fr) | 2014-12-05 | 2023-01-04 | Novozymes A/S | Variantes de la lipase et polynucléotides les codant |
US10760036B2 (en) | 2014-12-15 | 2020-09-01 | Henkel Ag & Co. Kgaa | Detergent composition comprising subtilase variants |
CN107002058A (zh) | 2014-12-15 | 2017-08-01 | 诺维信公司 | 枯草杆菌酶变体 |
WO2016096996A1 (fr) | 2014-12-16 | 2016-06-23 | Novozymes A/S | Polypeptides ayant une activité n-acétylglucosamine oxydase |
WO2016097352A1 (fr) | 2014-12-19 | 2016-06-23 | Novozymes A/S | Variants de protéase et polynucléotides les codant |
ES2813727T3 (es) | 2014-12-19 | 2021-03-24 | Novozymes As | Variantes de proteasa y polinucleótidos que las codifican |
US20180105772A1 (en) | 2015-04-10 | 2018-04-19 | Novozymes A/S | Detergent composition |
EP3280791A1 (fr) | 2015-04-10 | 2018-02-14 | Novozymes A/S | Procédé de lavage de linge, utilisation d'adnase et composition détergente |
CN107835853B (zh) | 2015-05-19 | 2021-04-20 | 诺维信公司 | 气味减少 |
BR112017025607B1 (pt) | 2015-06-02 | 2022-08-30 | Unilever Ip Holdings B.V. | Composição de detergente para lavagem de roupas e método doméstico de tratamento de um tecido |
EP3101108B1 (fr) | 2015-06-04 | 2018-01-31 | The Procter and Gamble Company | Composition de détergent liquide pour lavage de la vaisselle à la main |
ES2670044T3 (es) | 2015-06-04 | 2018-05-29 | The Procter & Gamble Company | Composición detergente líquida para lavado de vajillas a mano |
EP3101107B1 (fr) | 2015-06-05 | 2019-04-24 | The Procter and Gamble Company | Composition de detergent liquide compacte pour blanchisserie |
EP3101100B1 (fr) | 2015-06-05 | 2018-02-07 | The Procter and Gamble Company | Composition détergente liquide concentrée pour le lavage du linge |
EP3101102B2 (fr) | 2015-06-05 | 2023-12-13 | The Procter & Gamble Company | Composition de detergent liquide compacte pour blanchisserie |
WO2016198262A1 (fr) | 2015-06-11 | 2016-12-15 | Unilever Plc | Composition détergente pour lessive |
US10858637B2 (en) | 2015-06-16 | 2020-12-08 | Novozymes A/S | Polypeptides with lipase activity and polynucleotides encoding same |
US10717576B2 (en) | 2015-06-17 | 2020-07-21 | Novozymes A/S | Container for polypeptide |
WO2016202839A2 (fr) | 2015-06-18 | 2016-12-22 | Novozymes A/S | Variants de subtilase et polynucléotides codant pour ceux-ci |
EP3106508B1 (fr) | 2015-06-18 | 2019-11-20 | Henkel AG & Co. KGaA | Composition détergente comprenant des variantes de subtilase |
CN107810260B (zh) | 2015-06-26 | 2020-07-17 | 荷兰联合利华有限公司 | 洗衣洗涤剂组合物 |
CN107922896A (zh) | 2015-06-30 | 2018-04-17 | 诺维信公司 | 衣物洗涤剂组合物、用于洗涤的方法和组合物的用途 |
CA3175255A1 (fr) | 2015-07-01 | 2017-01-05 | Novozymes A/S | Procedes de reduction d'odeur |
EP3320089B1 (fr) | 2015-07-06 | 2021-06-16 | Novozymes A/S | Variantes de la lipase et polynucleotides les codant |
US20180171269A1 (en) * | 2015-09-01 | 2018-06-21 | Novozymes A/S | Laundry method |
AU2016323412B2 (en) | 2015-09-17 | 2021-04-01 | Henkel Ag & Co. Kgaa | Detergent compositions comprising polypeptides having xanthan degrading activity |
CA2991114A1 (fr) | 2015-09-17 | 2017-03-23 | Novozymes A/S | Polypeptides presentant une activite de degradation de xylanase et polynucleotides codant pour ceux-ci |
EP3356504B1 (fr) | 2015-10-01 | 2019-08-14 | Unilever PLC | Composition détergente en poudre pour linge |
EP3359658A2 (fr) | 2015-10-07 | 2018-08-15 | Novozymes A/S | Polypeptides |
WO2017064269A1 (fr) | 2015-10-14 | 2017-04-20 | Novozymes A/S | Variants polypeptidiques |
US20180171318A1 (en) | 2015-10-14 | 2018-06-21 | Novozymes A/S | Polypeptides Having Protease Activity and Polynucleotides Encoding Same |
US10675589B2 (en) | 2015-10-14 | 2020-06-09 | Novozymes A/S | Cleaning of water filtration membranes |
US11028346B2 (en) | 2015-10-28 | 2021-06-08 | Novozymes A/S | Detergent composition comprising protease and amylase variants |
CN108473974A (zh) | 2015-11-24 | 2018-08-31 | 诺维信公司 | 具有蛋白酶活性的多肽以及编码其的多核苷酸 |
CN108431217B (zh) | 2015-12-01 | 2022-06-21 | 诺维信公司 | 用于产生脂肪酶的方法 |
CA3003536A1 (fr) | 2015-12-07 | 2017-06-15 | Novozymes A/S | Polypeptides ayant une activite beta-glucanase, polynucleotides codant pour celles-ci et utilisations de ceux-ci dans des compositions nettoyantes et detergentes |
US20210171927A1 (en) | 2016-01-29 | 2021-06-10 | Novozymes A/S | Beta-glucanase variants and polynucleotides encoding same |
EP3417040B1 (fr) | 2016-02-17 | 2019-09-04 | Unilever PLC | Composition de blanchiment |
BR112018068068B1 (pt) | 2016-03-21 | 2023-04-18 | Unilever Ip Holdings B.V. | Composição aquosa líquida de detergente para lavagem de roupas e método doméstico de tratamento de um tecido |
BR112018069220A2 (pt) | 2016-03-23 | 2019-01-22 | Novozymes As | uso de polipeptídeo que tem atividade de dnase para tratamento de tecidos |
CN109312270B (zh) | 2016-04-08 | 2022-01-28 | 诺维信公司 | 洗涤剂组合物及其用途 |
BR112018070468B1 (pt) | 2016-04-08 | 2022-07-12 | Unilever Ip Holdings B.V | Composição de detergente líquida aquosa para lavagem de roupas e método doméstico de tratamento de um tecido |
EP3693449A1 (fr) | 2016-04-29 | 2020-08-12 | Novozymes A/S | Compositions détergentes et leurs utilisations |
EP3845642B1 (fr) * | 2016-05-05 | 2023-08-09 | Danisco US Inc. | Variantes de protéase et leurs utilisations |
CN109563450A (zh) | 2016-05-31 | 2019-04-02 | 诺维信公司 | 稳定的液体过氧化物组合物 |
EP3475404A1 (fr) | 2016-06-23 | 2019-05-01 | Novozymes A/S | Utilisation d'enzymes, composition et procédé d'élimination de salissures |
CN117721095A (zh) | 2016-06-30 | 2024-03-19 | 诺维信公司 | 脂肪酶变体及包含表面活性剂和脂肪酶变体的组合物 |
WO2018002261A1 (fr) | 2016-07-01 | 2018-01-04 | Novozymes A/S | Compositions détergentes |
WO2018007573A1 (fr) | 2016-07-08 | 2018-01-11 | Novozymes A/S | Compositions détergentes contenant de la galactanase |
WO2018011276A1 (fr) | 2016-07-13 | 2018-01-18 | The Procter & Gamble Company | Variants dnase de bacillus cibi et leurs utilisations |
US11326152B2 (en) | 2016-07-18 | 2022-05-10 | Novozymes A/S | Lipase variants, polynucleotides encoding same and the use thereof |
US20190177665A1 (en) | 2016-08-08 | 2019-06-13 | Basf Se | Liquid laundry formulation |
EP3284805B1 (fr) | 2016-08-17 | 2020-02-19 | The Procter & Gamble Company | Composition de nettoyage |
CN109790491B (zh) | 2016-09-27 | 2021-02-23 | 荷兰联合利华有限公司 | 家用洗衣方法 |
WO2018060216A1 (fr) | 2016-09-29 | 2018-04-05 | Novozymes A/S | Utilisation d'enzyme pour le lavage, procédé de lavage et composition pour laver la vaisselle |
WO2018060475A1 (fr) | 2016-09-29 | 2018-04-05 | Novozymes A/S | Granule contenant des spores |
EP3532592A1 (fr) | 2016-10-25 | 2019-09-04 | Novozymes A/S | Compositions détergentes |
US11753605B2 (en) | 2016-11-01 | 2023-09-12 | Novozymes A/S | Multi-core granules |
KR20190086540A (ko) | 2016-12-01 | 2019-07-22 | 바스프 에스이 | 조성물 중 효소의 안정화 |
EP3551740B1 (fr) | 2016-12-12 | 2021-08-11 | Novozymes A/S | Utilisation de polypeptides |
CN110023469A (zh) | 2016-12-15 | 2019-07-16 | 荷兰联合利华有限公司 | 洗衣洗涤剂组合物 |
WO2018178061A1 (fr) | 2017-03-31 | 2018-10-04 | Novozymes A/S | Polypeptides présentant une activité de rnase |
US11208639B2 (en) | 2017-03-31 | 2021-12-28 | Novozymes A/S | Polypeptides having DNase activity |
EP3601549A1 (fr) | 2017-03-31 | 2020-02-05 | Novozymes A/S | Polypeptides ayant une activité dnase |
EP3607039A1 (fr) | 2017-04-04 | 2020-02-12 | Novozymes A/S | Polypeptides |
WO2018185152A1 (fr) | 2017-04-04 | 2018-10-11 | Novozymes A/S | Compositions de poypeptides et utilisations associées |
WO2018185181A1 (fr) | 2017-04-04 | 2018-10-11 | Novozymes A/S | Glycosyl hydrolases |
EP3385362A1 (fr) | 2017-04-05 | 2018-10-10 | Henkel AG & Co. KGaA | Compositions détergentes comprenant des mannanases fongiques |
DK3385361T3 (da) | 2017-04-05 | 2019-06-03 | Ab Enzymes Gmbh | Detergentsammensætninger omfattende bakterielle mannanaser |
US10968416B2 (en) | 2017-04-06 | 2021-04-06 | Novozymes A/S | Cleaning compositions and uses thereof |
WO2018184818A1 (fr) | 2017-04-06 | 2018-10-11 | Novozymes A/S | Compositions de nettoyage et leurs utilisations |
US20200190437A1 (en) | 2017-04-06 | 2020-06-18 | Novozymes A/S | Cleaning compositions and uses thereof |
EP3967756A1 (fr) | 2017-04-06 | 2022-03-16 | Novozymes A/S | Compositions détergentes et leurs utilisations |
EP3607043A1 (fr) | 2017-04-06 | 2020-02-12 | Novozymes A/S | Compositions de nettoyage et leurs utilisations |
EP3607042A1 (fr) | 2017-04-06 | 2020-02-12 | Novozymes A/S | Compositions de nettoyage et leurs utilisations |
EP3626809A1 (fr) | 2017-04-06 | 2020-03-25 | Novozymes A/S | Compositions détergentes et leurs utilisations |
WO2018202846A1 (fr) | 2017-05-05 | 2018-11-08 | Novozymes A/S | Compositions comprenant une lipase et un sulfite |
WO2018224544A1 (fr) | 2017-06-08 | 2018-12-13 | Novozymes A/S | Compositions comprenant des polypeptides ayant une activité cellulase et une activité amylase et leurs utilisations dans des compositions de nettoyage et détergentes |
WO2019002356A1 (fr) | 2017-06-30 | 2019-01-03 | Novozymes A/S | Composition de suspension enzymatique |
US20200277553A1 (en) | 2017-09-20 | 2020-09-03 | Novozymes A/S | Use of Enzymes for Improving Water Absorption And/Or Whiteness |
EP3684899A1 (fr) | 2017-09-22 | 2020-07-29 | Novozymes A/S | Nouveaux polypeptides |
CA3073362A1 (fr) | 2017-09-27 | 2019-04-04 | Novozymes A/S | Variants de lipase et compositions de microcapsules comprenant de tels variants de lipase |
US11286443B2 (en) | 2017-09-27 | 2022-03-29 | The Procter & Gamble Company | Detergent compositions comprising lipases |
US11732221B2 (en) | 2017-10-02 | 2023-08-22 | Novozymes A/S | Polypeptides having mannanase activity and polynucleotides encoding same |
US11746310B2 (en) | 2017-10-02 | 2023-09-05 | Novozymes A/S | Polypeptides having mannanase activity and polynucleotides encoding same |
EP3697881A1 (fr) | 2017-10-16 | 2020-08-26 | Novozymes A/S | Granules libérant une faible quantité poussière |
WO2019076834A1 (fr) | 2017-10-16 | 2019-04-25 | Novozymes A/S | Granulés à faible teneur en poussière |
WO2019076800A1 (fr) | 2017-10-16 | 2019-04-25 | Novozymes A/S | Compositions de nettoyage et leurs utilisations |
WO2019081515A1 (fr) | 2017-10-24 | 2019-05-02 | Novozymes A/S | Compositions comprenant des polypeptides présentant une activité mannanase |
US10781408B2 (en) | 2017-10-27 | 2020-09-22 | The Procter & Gamble Company | Detergent compositions comprising polypeptide variants |
US11441136B2 (en) | 2017-10-27 | 2022-09-13 | Novozymes A/S | DNase variants |
WO2019086532A1 (fr) | 2017-11-01 | 2019-05-09 | Novozymes A/S | Procédés de nettoyage de dispositifs médicaux |
DE102017125560A1 (de) | 2017-11-01 | 2019-05-02 | Henkel Ag & Co. Kgaa | Reinigungszusammensetzungen, die dispersine iii enthalten |
EP3704219B1 (fr) | 2017-11-01 | 2024-01-10 | Novozymes A/S | Polypeptides et compositions comprenant de tels polypeptides |
DE102017125559A1 (de) | 2017-11-01 | 2019-05-02 | Henkel Ag & Co. Kgaa | Reinigungszusammensetzungen, die dispersine ii enthalten |
DE102017125558A1 (de) | 2017-11-01 | 2019-05-02 | Henkel Ag & Co. Kgaa | Reinigungszusammensetzungen, die dispersine i enthalten |
CN111479919A (zh) | 2017-11-01 | 2020-07-31 | 诺维信公司 | 多肽以及包含此类多肽的组合物 |
WO2019105781A1 (fr) | 2017-11-29 | 2019-06-06 | Basf Se | Préparations d'enzyme stables au stockage, leur production et utilisation |
WO2019110462A1 (fr) | 2017-12-04 | 2019-06-13 | Novozymes A/S | Variants de lipases et polynucléotides codant pour ces derniers |
EP3749760A1 (fr) | 2018-02-08 | 2020-12-16 | Novozymes A/S | Variants de lipase et compositions en comprenant |
CN111868239A (zh) | 2018-02-08 | 2020-10-30 | 诺维信公司 | 脂肪酶、脂肪酶变体及其组合物 |
CN112262207B (zh) | 2018-04-17 | 2024-01-23 | 诺维信公司 | 洗涤剂组合物中包含碳水化合物结合活性的多肽及其在减少纺织品或织物中的褶皱的用途 |
US11661592B2 (en) | 2018-04-19 | 2023-05-30 | Novozymes A/S | Stabilized endoglucanase variants |
US11566239B2 (en) | 2018-04-19 | 2023-01-31 | Novozymes A/S | Stabilized cellulase variants |
CN112368375A (zh) | 2018-04-26 | 2021-02-12 | 巴斯夫欧洲公司 | 脂肪酶 |
US20210115422A1 (en) | 2018-05-03 | 2021-04-22 | Basf Se | Amylase enzymes |
WO2019238761A1 (fr) | 2018-06-15 | 2019-12-19 | Basf Se | Films multicouches hydrosolubles contenant des produits chimiques et des enzymes actifs de lavage |
EP3814472A1 (fr) | 2018-06-28 | 2021-05-05 | Novozymes A/S | Compositions détergentes et leurs utilisations |
WO2020002608A1 (fr) | 2018-06-29 | 2020-01-02 | Novozymes A/S | Compositions détergentes et leurs utilisations |
EP3818139A1 (fr) | 2018-07-02 | 2021-05-12 | Novozymes A/S | Compositions de nettoyage et leurs utilisations |
WO2020007875A1 (fr) | 2018-07-03 | 2020-01-09 | Novozymes A/S | Compositions de nettoyage et leurs utilisations |
WO2020008024A1 (fr) | 2018-07-06 | 2020-01-09 | Novozymes A/S | Compositions de nettoyage et leurs utilisations |
WO2020030623A1 (fr) | 2018-08-10 | 2020-02-13 | Basf Se | Unité d'emballage comprenant une composition détergente contenant une enzyme et au moins un agent chélatant |
WO2020070063A2 (fr) | 2018-10-01 | 2020-04-09 | Novozymes A/S | Compositions détergentes et leurs utilisations |
EP3861110A1 (fr) | 2018-10-02 | 2021-08-11 | Novozymes A/S | Ribonucléases d'endonucléase 1 pour le nettoyage |
WO2020070209A1 (fr) | 2018-10-02 | 2020-04-09 | Novozymes A/S | Composition de nettoyage |
WO2020070014A1 (fr) | 2018-10-02 | 2020-04-09 | Novozymes A/S | Composition de nettoyage comprenant un tensioactif anionique et un polypeptide ayant une activité rnase |
EP3861094A1 (fr) | 2018-10-02 | 2021-08-11 | Novozymes A/S | Composition de nettoyage |
WO2020070249A1 (fr) | 2018-10-03 | 2020-04-09 | Novozymes A/S | Compositions de nettoyage |
WO2020070199A1 (fr) | 2018-10-03 | 2020-04-09 | Novozymes A/S | Polypeptides ayant une activité de dégradation de l'alpha-mannane et polynucléotides codant pour ceux-ci |
BR112021006317A2 (pt) | 2018-10-05 | 2021-07-06 | Basf Se | preparação de enzima, processo para preparar uma preparação de enzima estável, métodos para reduzir perda da atividade amiolítica, de preparação de uma formulação detergente, para remover manchas sensíveis à amilase e para aumentar a estabilidade no armazenamento de uma formulação detergente líquida, usos de um composto e da preparação de enzima, e, formulação detergente |
US20210395651A1 (en) | 2018-10-05 | 2021-12-23 | Basf Se | Compounds stabilizing hydrolases in liquids |
MX2021003930A (es) | 2018-10-05 | 2021-06-04 | Basf Se | Compuestos estabilizadores de hidrolasas en liquidos. |
EP3677676A1 (fr) | 2019-01-03 | 2020-07-08 | Basf Se | Composés de stabilisation d'amylases dans des liquides |
CN112996894A (zh) | 2018-10-11 | 2021-06-18 | 诺维信公司 | 清洁组合物及其用途 |
EP3647398B1 (fr) | 2018-10-31 | 2024-05-15 | Henkel AG & Co. KGaA | Compositions de nettoyage contenant des dispersines v |
EP3647397A1 (fr) | 2018-10-31 | 2020-05-06 | Henkel AG & Co. KGaA | Compositions de nettoyage contenant des dispersions iv |
WO2020104231A1 (fr) | 2018-11-19 | 2020-05-28 | Basf Se | Poudres et granulés contenant un agent chélatant et une enzyme |
US20220017844A1 (en) | 2018-12-03 | 2022-01-20 | Novozymes A/S | Low pH Powder Detergent Composition |
CN113366103A (zh) | 2018-12-21 | 2021-09-07 | 诺维信公司 | 具有肽聚糖降解活性的多肽以及编码其的多核苷酸 |
EP3898919A1 (fr) | 2018-12-21 | 2021-10-27 | Novozymes A/S | Sachet de détergent comprenant des métalloprotéases |
JP7489393B2 (ja) | 2019-01-28 | 2024-05-23 | ノボザイムス アクティーゼルスカブ | スブチラーゼ変異体及びスブチラーゼ変異体を含む組成物 |
US20220186234A1 (en) | 2019-02-20 | 2022-06-16 | Basf Se | Industrial Fermentation Process for Bacillus Using Defined Medium and Trace Element Feed |
EP3927837A1 (fr) | 2019-02-20 | 2021-12-29 | Basf Se | Procédé de fermentation industrielle pour bacillus utilisant un milieu défini et une alimentation en magnésium |
US20220235341A1 (en) | 2019-03-21 | 2022-07-28 | Novozymes A/S | Alpha-amylase variants and polynucleotides encoding same |
MX2021011981A (es) | 2019-04-03 | 2021-11-03 | Novozymes As | Polipeptidos que tienen actividad de beta-glucanasa, polinucleotidos que los codifican y usos de los mismos en composiciones de limpieza y de detergente. |
EP3953462A1 (fr) | 2019-04-10 | 2022-02-16 | Novozymes A/S | Variants polypeptidiques |
EP3953463A1 (fr) | 2019-04-12 | 2022-02-16 | Novozymes A/S | Variants stabilisés d'un glycoside hydrolase |
WO2020229480A1 (fr) | 2019-05-14 | 2020-11-19 | Basf Se | Composés stabilisant des hydrolases dans des liquides |
MX2021015364A (es) | 2019-06-13 | 2022-01-24 | Basf Se | Metodo de recuperacion de una proteina de un caldo de fermentacion mediante el uso de un cation divalente. |
WO2021001244A1 (fr) | 2019-07-01 | 2021-01-07 | Basf Se | Acétals peptidiques pour stabiliser des enzymes |
EP3994255A1 (fr) | 2019-07-02 | 2022-05-11 | Novozymes A/S | Variants de lipase et compositions de ceux-ci |
WO2021001297A1 (fr) | 2019-07-02 | 2021-01-07 | Basf Se | Procédé de préparation d'un milieu de fermentation |
WO2021004830A1 (fr) | 2019-07-05 | 2021-01-14 | Basf Se | Procédé de fermentation industrielle pour cellules microbiennes à l'aide d'une pré-culture par lots |
EP3997202A1 (fr) | 2019-07-12 | 2022-05-18 | Novozymes A/S | Émulsions enzymatiques pour détergents |
WO2021030400A1 (fr) | 2019-08-13 | 2021-02-18 | Novozymes Bioag A/S | Combinaisons pesticides de yersinia et de protéases |
WO2021037878A1 (fr) | 2019-08-27 | 2021-03-04 | Novozymes A/S | Composition comprenant une lipase |
US20220325204A1 (en) | 2019-08-27 | 2022-10-13 | Novozymes A/S | Detergent composition |
WO2021053127A1 (fr) | 2019-09-19 | 2021-03-25 | Novozymes A/S | Composition détergente |
WO2021064068A1 (fr) | 2019-10-03 | 2021-04-08 | Novozymes A/S | Polypeptides comprenant au moins deux domaines de liaison aux hydrates de carbone |
BR112022006082A2 (pt) | 2019-10-18 | 2022-06-21 | Basf Se | Preparação enzimática, formulação de detergente, e, uso de pelo menos um diol |
CN113891931A (zh) | 2019-11-29 | 2022-01-04 | 巴斯夫欧洲公司 | 组合物和可以用于该类组合物的聚合物 |
WO2021115912A1 (fr) | 2019-12-09 | 2021-06-17 | Basf Se | Formulations comprenant une polyéthylèneimine modifiée de manière hydrophobe et une ou plusieurs enzymes |
EP4077620A1 (fr) | 2019-12-20 | 2022-10-26 | Henkel AG & Co. KGaA | Compositions de nettoyage comprenant des dispersines vi |
WO2021122121A1 (fr) | 2019-12-20 | 2021-06-24 | Henkel Ag & Co. Kgaa | Compositions de nettoyage comprenant des dispersines ix |
KR20220121235A (ko) | 2019-12-20 | 2022-08-31 | 헨켈 아게 운트 코. 카게아아 | 디스페르신 및 카르보히드라제를 포함하는 세정 조성물 |
CN114929848A (zh) | 2019-12-20 | 2022-08-19 | 诺维信公司 | 稳定的液体无硼酶组合物 |
WO2021123307A2 (fr) | 2019-12-20 | 2021-06-24 | Novozymes A/S | Polypeptides présentant une activité protéolytique et leur utilisation |
BR112022015120A2 (pt) | 2020-01-29 | 2022-12-13 | Unilever Ip Holdings B V | Recipiente plástico transparente e processo de fabricação de recipiente plástico transparente |
EP4097226A1 (fr) | 2020-01-31 | 2022-12-07 | Novozymes A/S | Variants de mannanase et polynucléotides codant pour ceux-ci |
JP2023511739A (ja) | 2020-01-31 | 2023-03-22 | ノボザイムス アクティーゼルスカブ | マンナナーゼバリアント及びそれをコードするポリヌクレオチド |
WO2021160818A1 (fr) | 2020-02-14 | 2021-08-19 | Basf Se | Variants de la mannanase |
EP3892708A1 (fr) | 2020-04-06 | 2021-10-13 | Henkel AG & Co. KGaA | Compositions de nettoyage comprenant des variantes de dispersine |
JP2023520312A (ja) | 2020-04-08 | 2023-05-17 | ノボザイムス アクティーゼルスカブ | 炭水化物結合モジュールバリアント |
WO2021214059A1 (fr) | 2020-04-21 | 2021-10-28 | Novozymes A/S | Compositions de nettoyage comprenant des polypeptides ayant une activité de dégradation de fructane |
MX2022014895A (es) | 2020-06-18 | 2023-01-04 | Basf Se | Composiciones y su uso. |
WO2021259099A1 (fr) | 2020-06-24 | 2021-12-30 | Novozymes A/S | Utilisation de cellulases pour retirer d'un textile les acariens de la poussière |
EP3936593A1 (fr) | 2020-07-08 | 2022-01-12 | Henkel AG & Co. KGaA | Compositions de nettoyage et leurs utilisations |
EP4179053B1 (fr) | 2020-07-09 | 2024-04-03 | Basf Se | Compositions et leurs applications |
WO2022008732A1 (fr) | 2020-07-10 | 2022-01-13 | Basf Se | Amélioration de l'activité de conservateurs antimicrobiens |
EP4189051B1 (fr) | 2020-07-27 | 2024-02-28 | Unilever IP Holdings B.V. | Utilisation d'une enzyme et d'un tensioactif pour inhiber les microorganismes |
JP2023538740A (ja) | 2020-08-25 | 2023-09-11 | ノボザイムス アクティーゼルスカブ | ファミリー44キシログルカナーゼの変異体 |
EP4213641A1 (fr) | 2020-09-15 | 2023-07-26 | Novozymes A/S | Aliment pour animaux comprenant des insectes ou de la farine d'insectes |
EP4225905A2 (fr) | 2020-10-07 | 2023-08-16 | Novozymes A/S | Variants d'alpha-amylase |
WO2022083949A1 (fr) | 2020-10-20 | 2022-04-28 | Basf Se | Compositions et leur utilisation |
WO2022084303A2 (fr) | 2020-10-20 | 2022-04-28 | Novozymes A/S | Utilisation de polypeptides ayant une activité de dnase |
US20230399588A1 (en) | 2020-10-28 | 2023-12-14 | Novozymes A/S | Use of lipoxygenase |
EP4237552A2 (fr) | 2020-10-29 | 2023-09-06 | Novozymes A/S | Variants de lipase et compositions comprenant de tels variants de lipase |
CN116670261A (zh) | 2020-11-13 | 2023-08-29 | 诺维信公司 | 包含脂肪酶的洗涤剂组合物 |
WO2022106400A1 (fr) | 2020-11-18 | 2022-05-27 | Novozymes A/S | Combinaison de protéases immunochimiquement différentes |
EP4032966A1 (fr) | 2021-01-22 | 2022-07-27 | Novozymes A/S | Composition enzymatique liquide avec piégeur de sulfite |
WO2022162043A1 (fr) | 2021-01-28 | 2022-08-04 | Novozymes A/S | Lipase à faible génération de mauvaises odeurs |
WO2022171780A2 (fr) | 2021-02-12 | 2022-08-18 | Novozymes A/S | Variants d'alpha-amylase |
WO2022171872A1 (fr) | 2021-02-12 | 2022-08-18 | Novozymes A/S | Détergents biologiques stabilisés |
EP4305146A1 (fr) | 2021-03-12 | 2024-01-17 | Novozymes A/S | Variants polypeptidiques |
EP4060036A1 (fr) | 2021-03-15 | 2022-09-21 | Novozymes A/S | Variantes de polypeptides |
US20240060061A1 (en) | 2021-03-15 | 2024-02-22 | Novozymes A/S | Dnase variants |
CN117083370A (zh) | 2021-03-26 | 2023-11-17 | 诺维信公司 | 聚合物含量降低的洗涤剂组合物 |
EP4359518A1 (fr) | 2021-06-23 | 2024-05-01 | Novozymes A/S | Polypeptides d'alpha-amylase |
WO2023061827A1 (fr) | 2021-10-13 | 2023-04-20 | Basf Se | Compositions comprenant des polymères, polymères et leur utilisation |
WO2023066741A1 (fr) | 2021-10-20 | 2023-04-27 | Basf Se | Composition sans phosphate et leurs procédés de fabrication et leur utilisation |
WO2023088776A1 (fr) | 2021-11-22 | 2023-05-25 | Basf Se | Compositions comprenant des polymères, polymères et leur utilisation |
WO2023088761A1 (fr) | 2021-11-22 | 2023-05-25 | Basf Se | Compositions comprenant des polymères, polymères et leur utilisation |
WO2023110599A2 (fr) | 2021-12-17 | 2023-06-22 | Basf Se | Compositions et applications associées |
WO2023116569A1 (fr) | 2021-12-21 | 2023-06-29 | Novozymes A/S | Composition comprenant une lipase et un renforçateur |
WO2023117950A1 (fr) | 2021-12-21 | 2023-06-29 | Basf Se | Produit chimique avec attributs environnementaux |
EP4206309A1 (fr) | 2021-12-30 | 2023-07-05 | Novozymes A/S | Particules de protéines à blancheur améliorée |
EP4234664A1 (fr) | 2022-02-24 | 2023-08-30 | Evonik Operations GmbH | Composition comprenant des glucolipides et des enzymes |
WO2023165507A1 (fr) | 2022-03-02 | 2023-09-07 | Novozymes A/S | Utilisation de xyloglucanase pour l'amélioration de la durabilité de détergents |
WO2023165950A1 (fr) | 2022-03-04 | 2023-09-07 | Novozymes A/S | Variants de dnase et compositions |
WO2023194204A1 (fr) | 2022-04-08 | 2023-10-12 | Novozymes A/S | Variants et compositions d'hexosaminidase |
WO2023233025A1 (fr) | 2022-06-03 | 2023-12-07 | Unilever Ip Holdings B.V. | Produit détergent liquide |
WO2023247348A1 (fr) | 2022-06-21 | 2023-12-28 | Novozymes A/S | Variants de mannanase et polynucléotides codant pour ceux-ci |
WO2023247664A2 (fr) | 2022-06-24 | 2023-12-28 | Novozymes A/S | Variants de lipase et compositions comprenant de tels variants de lipase |
WO2024012894A1 (fr) | 2022-07-15 | 2024-01-18 | Basf Se | Formiates d'alcanolamine pour la stabilisation d'enzymes dans des formulations liquides |
WO2024083589A1 (fr) | 2022-10-18 | 2024-04-25 | Basf Se | Compositions détergentes, polymères et leurs procédés de fabrication |
WO2024121058A1 (fr) | 2022-12-05 | 2024-06-13 | Novozymes A/S | Composition comprenant une lipase et un peptide |
WO2024126483A1 (fr) | 2022-12-14 | 2024-06-20 | Novozymes A/S | Variants de lipase gcl1 améliorés |
EP4389864A1 (fr) | 2022-12-20 | 2024-06-26 | Basf Se | Cutinases |
Family Cites Families (81)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE80993C (fr) | 1894-09-03 | |||
GB1234445A (fr) | 1967-10-03 | 1971-06-03 | ||
GB1296839A (fr) | 1969-05-29 | 1972-11-22 | ||
GB1372034A (en) | 1970-12-31 | 1974-10-30 | Unilever Ltd | Detergent compositions |
GB1483591A (en) | 1973-07-23 | 1977-08-24 | Novo Industri As | Process for coating water soluble or water dispersible particles by means of the fluid bed technique |
GB1590432A (en) | 1976-07-07 | 1981-06-03 | Novo Industri As | Process for the production of an enzyme granulate and the enzyme granuate thus produced |
DK187280A (da) | 1980-04-30 | 1981-10-31 | Novo Industri As | Ruhedsreducerende middel til et fuldvaskemiddel fuldvaskemiddel og fuldvaskemetode |
DK263584D0 (da) | 1984-05-29 | 1984-05-29 | Novo Industri As | Enzymholdige granulater anvendt som detergentadditiver |
EP0218272B1 (fr) | 1985-08-09 | 1992-03-18 | Gist-Brocades N.V. | Enzymes lipolytiques et leur usage dans des compositions détergentes |
EG18543A (en) | 1986-02-20 | 1993-07-30 | Albright & Wilson | Protected enzyme systems |
DE3750450T2 (de) | 1986-08-29 | 1995-01-05 | Novo Industri As | Enzymhaltiger Reinigungsmittelzusatz. |
NZ221627A (en) | 1986-09-09 | 1993-04-28 | Genencor Inc | Preparation of enzymes, modifications, catalytic triads to alter ratios or transesterification/hydrolysis ratios |
ATE125865T1 (de) | 1987-08-28 | 1995-08-15 | Novo Nordisk As | Rekombinante humicola-lipase und verfahren zur herstellung von rekombinanten humicola-lipasen. |
DK6488D0 (da) | 1988-01-07 | 1988-01-07 | Novo Industri As | Enzymer |
DE68924654T2 (de) | 1988-01-07 | 1996-04-04 | Novonordisk As | Spezifische Protease. |
JP3079276B2 (ja) | 1988-02-28 | 2000-08-21 | 天野製薬株式会社 | 組換え体dna、それを含むシュードモナス属菌及びそれを用いたリパーゼの製造法 |
US5648263A (en) | 1988-03-24 | 1997-07-15 | Novo Nordisk A/S | Methods for reducing the harshness of a cotton-containing fabric |
DE68911131T2 (de) | 1988-03-24 | 1994-03-31 | Novonordisk As | Cellulosezubereitung. |
DK316989D0 (da) | 1989-06-26 | 1989-06-26 | Novo Nordisk As | Enzymer |
EP0405902A1 (fr) * | 1989-06-26 | 1991-01-02 | Unilever Plc | Compositions détergentes enzymatiques |
GB8915658D0 (en) | 1989-07-07 | 1989-08-23 | Unilever Plc | Enzymes,their production and use |
JP3112937B2 (ja) | 1990-04-14 | 2000-11-27 | カリ―ヒエミー アクチエンゲゼルシヤフト | アルカリ性バチルスーリパーゼ、これをコード化するdna配列およびこのリパーゼを生産するバチルス |
DK115890D0 (da) | 1990-05-09 | 1990-05-09 | Novo Nordisk As | Enzym |
WO1991017243A1 (fr) | 1990-05-09 | 1991-11-14 | Novo Nordisk A/S | Preparation de cellulase comprenant un enzyme d'endoglucanase |
DE69129988T2 (de) | 1990-09-13 | 1999-03-18 | Novo Nordisk As | Lipase-varianten |
ES2174820T3 (es) | 1991-01-16 | 2002-11-16 | Procter & Gamble | Composiciones detergentes compactas con celulasa de alta actividad. |
EP0511456A1 (fr) | 1991-04-30 | 1992-11-04 | The Procter & Gamble Company | Détergents liquides contenant un ester aromatique de l'acide borique pour inhibition d'enzyme protéolitique |
DE69209500T2 (de) | 1991-04-30 | 1996-10-31 | Procter & Gamble | Gerüstsubstanzhaltige flüssigwaschmittel mit borsäure-polyolkomplex zur ptoteolytischen enzyminhibierung |
DE69226182T2 (de) | 1991-05-01 | 1999-01-21 | Novo Nordisk As | Stabilisierte enzyme und waschmittelzusammensetzungen |
DK72992D0 (da) | 1992-06-01 | 1992-06-01 | Novo Nordisk As | Enzym |
DK88892D0 (da) | 1992-07-06 | 1992-07-06 | Novo Nordisk As | Forbindelse |
DE69334295D1 (de) | 1992-07-23 | 2009-11-12 | Novo Nordisk As | MUTIERTE -g(a)-AMYLASE, WASCHMITTEL UND GESCHIRRSPÜLMITTEL |
WO1994007998A1 (fr) | 1992-10-06 | 1994-04-14 | Novo Nordisk A/S | Variantes de cellulase |
AU3235893A (en) * | 1992-12-04 | 1994-07-04 | Me Medical Enzymes Ag | Genetically engineered glutaminase and its use in antiviral and anticancer therapy |
EP0867504B2 (fr) | 1993-02-11 | 2011-05-18 | Genencor International, Inc. | Alpha-amylase stable à l'oxydation |
KR950702240A (ko) | 1993-04-27 | 1995-06-19 | 한스 발터 라벤 | 세제로의 이용을 위한 새로운 리파제 변형체 |
DK52393D0 (fr) | 1993-05-05 | 1993-05-05 | Novo Nordisk As | |
JP2859520B2 (ja) | 1993-08-30 | 1999-02-17 | ノボ ノルディスク アクティーゼルスカブ | リパーゼ及びそれを生産する微生物及びリパーゼ製造方法及びリパーゼ含有洗剤組成物 |
US6436690B1 (en) * | 1993-09-15 | 2002-08-20 | The Procter & Gamble Company | BPN′ variants having decreased adsorption and increased hydrolysis wherein one or more loop regions are substituted |
AU7853194A (en) | 1993-10-13 | 1995-05-04 | Novo Nordisk A/S | H2o2-stable peroxidase variants |
JPH07143883A (ja) | 1993-11-24 | 1995-06-06 | Showa Denko Kk | リパーゼ遺伝子及び変異体リパーゼ |
US5605793A (en) | 1994-02-17 | 1997-02-25 | Affymax Technologies N.V. | Methods for in vitro recombination |
AU1806795A (en) | 1994-02-22 | 1995-09-04 | Novo Nordisk A/S | A method of preparing a variant of a lipolytic enzyme |
ES2251717T3 (es) | 1994-03-08 | 2006-05-01 | Novozymes A/S | Nuevas celulasas alcalinas. |
US6599730B1 (en) | 1994-05-02 | 2003-07-29 | Procter & Gamble Company | Subtilisin 309 variants having decreased adsorption and increased hydrolysis |
ZA952220B (en) * | 1994-05-02 | 1995-12-14 | Procter & Gamble | Bpn' variants having decreased adsorption and increased hydrolysis wherein one or more loop regions are substituted |
CA2189441C (fr) | 1994-05-04 | 2009-06-30 | Wolfgang Aehle | Lipases a resistance aux tensioactifs amelioree |
WO1995035381A1 (fr) | 1994-06-20 | 1995-12-28 | Unilever N.V. | Lipases modifiees provenant de pseudomonas et leur utilisation |
WO1996000292A1 (fr) | 1994-06-23 | 1996-01-04 | Unilever N.V. | Pseudomonas lipases modifiees et leur utilisation |
AU3604595A (en) | 1994-10-06 | 1996-05-02 | Novo Nordisk A/S | An enzyme and enzyme preparation with endoglucanase activity |
BE1008998A3 (fr) | 1994-10-14 | 1996-10-01 | Solvay | Lipase, microorganisme la produisant, procede de preparation de cette lipase et utilisations de celle-ci. |
CN1167503A (zh) | 1994-10-26 | 1997-12-10 | 诺沃挪第克公司 | 一种具有脂解活性的酶 |
AR000862A1 (es) | 1995-02-03 | 1997-08-06 | Novozymes As | Variantes de una ó-amilasa madre, un metodo para producir la misma, una estructura de adn y un vector de expresion, una celula transformada por dichaestructura de adn y vector, un aditivo para detergente, composicion detergente, una composicion para lavado de ropa y una composicion para la eliminacion del |
JPH08228778A (ja) | 1995-02-27 | 1996-09-10 | Showa Denko Kk | 新規なリパーゼ遺伝子及びそれを用いたリパーゼの製造方法 |
US5837516A (en) * | 1995-03-03 | 1998-11-17 | Genentech, Inc. | Subtilisin variants capable of cleaving substrates containing basic residues |
CN1182451A (zh) | 1995-03-17 | 1998-05-20 | 诺沃挪第克公司 | 新的内切葡聚糖酶 |
EP0824585B1 (fr) | 1995-05-05 | 2009-04-22 | Novozymes A/S | Variantes du type protease et compositions |
JP4307549B2 (ja) | 1995-07-14 | 2009-08-05 | ノボザイムス アクティーゼルスカブ | 脂肪分解活性を有する修飾された酵素 |
ES2221934T3 (es) | 1995-08-11 | 2005-01-16 | Novozymes A/S | Nuevas enzimas lipoliticas. |
US5763385A (en) | 1996-05-14 | 1998-06-09 | Genencor International, Inc. | Modified α-amylases having altered calcium binding properties |
WO1998008940A1 (fr) | 1996-08-26 | 1998-03-05 | Novo Nordisk A/S | Nouvelle endoglucanase |
CN100362100C (zh) | 1996-09-17 | 2008-01-16 | 诺沃奇梅兹有限公司 | 纤维素酶变体 |
AU730286B2 (en) | 1996-10-08 | 2001-03-01 | Novo Nordisk A/S | Diaminobenzoic acid derivatives as dye precursors |
EP0948610B1 (fr) | 1996-11-04 | 2011-05-25 | Novozymes A/S | Variants et compositions de subtilase |
US6300116B1 (en) | 1996-11-04 | 2001-10-09 | Novozymes A/S | Modified protease having improved autoproteolytic stability |
US6159731A (en) | 1997-02-12 | 2000-12-12 | Massachusetts Institute Of Technology | Daxx, a Fas-binding protein that activates JNK and apoptosis |
EP0913458B1 (fr) * | 1997-10-22 | 2004-06-16 | The Procter & Gamble Company | Compositions détergentes liquide pour surfaces dures |
AR015977A1 (es) * | 1997-10-23 | 2001-05-30 | Genencor Int | Variantes de proteasa multiplemente substituida con carga neta alterada para su empleo en detergentes |
KR100762164B1 (ko) | 1997-11-21 | 2007-10-01 | 노보자임스 에이/에스 | 프로테아제 변이체 및 조성물 |
JP2003512012A (ja) * | 1998-10-23 | 2003-04-02 | ザ、プロクター、エンド、ギャンブル、カンパニー | 洗剤組成物に用いられるプロテアーゼ変異体のスクリーニング法 |
KR100660818B1 (ko) * | 1998-12-18 | 2006-12-26 | 노보자임스 에이/에스 | 활성부위 루프 영역에 추가적 아미노산 잔기를 가지는서브그룹 i-s1과 i-s2의 서브틸라제 효소 |
ATE342965T1 (de) * | 1998-12-18 | 2006-11-15 | Novozymes As | Subtilase enzyme der i-s1 und is2 untergruppen, mit einem zusätzlichen aminosaürerest in einer aktiven schleifenregion |
DK1141335T3 (da) * | 1998-12-21 | 2009-11-09 | Genencor Int | Kemisk modificerede enzymer med multipelt ladede varianter |
EP1183338B2 (fr) * | 1999-05-20 | 2012-06-13 | Novozymes A/S | Enzymes subtilases des sous-groupes i-s1 et i-s2 possedant au moins un residu d'acide amine supplementaire entre les positions 97 et 98 |
WO2000071691A1 (fr) | 1999-05-20 | 2000-11-30 | Novozymes A/S | Enzymes de subtilase des sous-groupes i-s1 et i-s2 possedant au moins un residu supplementaire d'acide amine entre les positions 125 et 126 |
WO2001044452A1 (fr) * | 1999-12-15 | 2001-06-21 | Novozymes A/S | Variants de subtilase a performance de nettoyage amelioree sur des taches d'oeuf |
US6541234B1 (en) * | 2000-09-11 | 2003-04-01 | University Of Maryland Biotechnology Institute | Calcium free subtilisin mutants |
EP1326966B2 (fr) * | 2000-10-13 | 2015-03-18 | Novozymes A/S | Variants de subtilase |
AU2302002A (en) | 2000-11-27 | 2002-06-03 | Novozymes As | Automated mechanical stress assay for screening cleaning ingredients |
DK200101090A (da) * | 2001-07-12 | 2001-08-16 | Novozymes As | Subtilase variants |
TWI319007B (en) * | 2002-11-06 | 2010-01-01 | Novozymes As | Subtilase variants |
-
2003
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- 2003-11-05 EP EP03769258A patent/EP1563064A2/fr not_active Withdrawn
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- 2003-11-05 WO PCT/DK2003/000756 patent/WO2004041979A2/fr active Application Filing
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-
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- 2013-04-30 JP JP2013095728A patent/JP5806255B2/ja not_active Expired - Lifetime
Non-Patent Citations (1)
Title |
---|
See references of WO2004041979A2 * |
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