OXIDATION STABLE ALPHA-AMYLASE VARIANTS

REFERENCE TO A SEQUENCE LISTING

This application contains a Sequence Listing in computer readable form, which is incorporated herein by reference.

BACKGROUND OF THE INVENTION

Field of the Invention

The present invention relates to oxidation stable alpha-amylase variants, polynucleotides encoding the variants, methods of producing the variants, and methods of using the variants.

Description of the Related Art

Alpha-amylases (alpha-1,4-glucan-4-glucanohydrolases, E.C. 3.2.1.1) constitute a group of enzymes, which catalyses hydrolysis of starch and other linear and branched 1,4-gluosidic oligo- and polysaccharides.

Alpha-amylase is a key enzyme for use in detergent compositions and its use has become increasingly important for removal of starchy stains during laundry washing or dishwashing.

Some detergents, in particular dishwashing detergents, comprise bleaching systems, bleach activators, and bleach catalysts which are all very destabilizing for the alpha-amylases due to oxidation of the molecules. Therefore, it is important to find alpha-amylase variants, which are stable, have high wash performance, stain removal effect and/or activity in detergents comprising various bleaching agents.

It is known in the art to stabilize alpha-amylases towards bleaching agents and oxidation by substituting the methionine at position 197 (using the amylase from B. licheniformis for numbering) with e.g. leucine. This has e.g. been disclosed in WO199418314. However, these prior art oxidation stable alpha-amylases have the disadvantage that the alpha-amylase activity is reduced.

Thus, it is an object of the present invention to provide alpha-amylase variants that exhibit a high level of stability in detergents, in particular in dishwashing detergents and other detergents comprising bleaching agents or systems but at the same time have improved wash performance compared to the parent alpha-amylase. It is a further object to provide alpha-amylase variants which have high performance, in particular high wash performance, in particular high dishwashing performance.

The present invention provides alpha-amylase variants with improved stability compared to its parent and improved activity compared to its parent.

SUMMARY OF THE INVENTION

The present invention relates to alpha-amylase variants of a parent alpha-amylase, wherein the variant comprises a substitution in one or more positions providing oxidation stability of the variant, wherein the variant has an improvement factor of >1.0 when compared to the parent alpha-amylase, and wherein the variant has alpha-amylase activity.

The present invention also relates to a composition comprising a variant according to the invention.

Further, the present invention also relates to polynucleotides encoding the variants, nucleic acid constructs, vectors, and host cells comprising the polynucleotides, and methods of producing the variants.

Conventions for Designation of Variants

For purposes of the present invention, the amino acid sequence as set forth in SEQ ID NO: 3 is used to determine the corresponding amino acid residue in another alpha-amylase. The amino acid sequence of another alpha-amylase is aligned with the amino acid sequence set forth in SEQ ID NO: 3, and based on the alignment, the amino acid position number corresponding to any amino acid residue in the amino acid sequence as set forth in SEQ ID NO: 3 is determined using the Needleman-Wunsch algorithm (Needleman and Wunsch, 1970, J. Mol. Biol. 48: 443-453) as implemented in the Needle program of the EMBOSS package (EMBOSS: The European Molecular Biology Open Software Suite, Rice et al., 2000, Trends

Genet. 16: 276-277), preferably version 5.0.0 or later. The parameters used are gap open penalty of 10, gap extension penalty of 0.5, and the EBLOSUM62 (EMBOSS version of BLOSUM62) substitution matrix.

Identification of the corresponding amino acid residue in another alpha-amylase may be determined by an alignment of multiple polypeptide sequences using several computer programs including, but not limited to, MUSCLE (multiple sequence comparison by log-expectation; version 3.5 or later; Edgar, 2004, Nucleic Acids Research 32: 1792-1797), MAFFT (version 6.857 or later; Katoh and Kuma, 2002, Nucleic Acids Research 30: 3059-3066; Katoh et al., 2005, Nucleic Acids Research 33: 511-518; Katoh and Toh, 2007, Bioinformatics 23: 372-374; Katoh et al., 2009, Methods in Molecular Biology 537:_39-64; Katoh and Toh, 2010, Bioinformatics 26: 1899-1900), and EMBOSS EMMA employing ClustalW (1.83 or later; Thompson et al., 1994, Nucleic Acids Research 22: 4673-4680), using their respective default parameters.

When the other enzyme has diverged from the amino acid sequence as set forth in SEQ ID NO: 3 such that traditional sequence-based comparison fails to detect their relationship (Lindahl and Elofsson, 2000, J. Mol. Biol. 295: 613-615), other pairwise sequence comparison algorithms can be used. Greater sensitivity in sequence-based searching can be attained using search programs that utilize probabilistic representations of polypeptide families (profiles) to search databases. For example, the PSI-BLAST program generates profiles through an iterative database search process and is capable of detecting remote homologs (Atschul et al., 1997, Nucleic Acids Res. 25: 3389-3402). Even greater sensitivity can be achieved if the family or superfamily for the polypeptide has one or more representatives in the protein structure databases. Programs such as GenTHREADER (Jones, 1999, J. Mol. Biol. 287: 797-815; McGuffin and Jones, 2003, Bioinformatics 19: 874-881) utilize information from a variety of sources (PSI-BLAST, secondary structure prediction, structural alignment profiles, and solvation potentials) as input to a neural network that predicts the structural fold for a query sequence. Similarly, the method of Gough et al., 2000, J. Mol. Biol. 313: 903-919, can be used to align a sequence of unknown structure with the superfamily models present in the SCOP database. These alignments can in turn be used to generate homology models for the polypeptide, and such models can be assessed for accuracy using a variety of tools developed for that purpose.

For proteins of known structure, several tools and resources are available for retrieving and generating structural alignments. For example the SCOP superfamilies of proteins have been structurally aligned, and those alignments are accessible and downloadable. Two or more protein structures can be aligned using a variety of algorithms such as the distance alignment matrix (Holm and Sander, 1998, Proteins 33: 88-96) or combinatorial extension (Shindyalov and Bourne, 1998, Protein Engineering 11: 739-747), and implementation of these algorithms can additionally be utilized to query structure databases with a structure of interest in order to discover possible structural homologs (e.g., Holm and Park, 2000, Bioinformatics 16: 566-567).

In describing the variants of the present invention, the nomenclature described below is adapted for ease of reference. The accepted IUPAC single letter or three letter amino acid abbreviation is employed.

Substitutions. For an amino acid substitution, the following nomenclature is used: Original amino acid, position, substituted amino acid. Accordingly, the substitution of threonine at position 226 with alanine is designated as “Thr226Ala” or “T226A”. Multiple mutations are separated by addition marks (“+”), e.g., “Gly205Arg+Ser411Phe” or “G205R+S411F”, representing substitutions at positions 205 and 411 of glycine (G) with arginine (R) and serine (S) with phenylalanine (F), respectively.

Deletions. For an amino acid deletion, the following nomenclature is used: Original amino acid, position, *. Accordingly, the deletion of glycine at position 195 is designated as “Glyl95*” or “G195*”. Multiple deletions are separated by addition marks (“+”), e.g., “Glyl95*+Ser411*” or “G195*+S411*”.

Multiple modifcations. Variants comprising multiple modifications are separated by addition marks (“+”), e.g., “Arg170Tyr+Glyl95Glu” or “R170Y+G195E” representing a substitution of arginine and glycine at positions 170 and 195 with tyrosine and glutamic acid, respectively.

Different modifications. Where different modifications may be introduced at a position, the different alterations are separated by a comma, e.g., “Arg170Tyr,Glu” represents a substitution of arginine at position 170 with tyrosine or glutamic acid. Thus, “Tyr167Gly,Ala +Arg170Gly,Ala” designates the following variants:

“Tyr167Gly+Arg170Gly”, “Tyr167Gly+Arg170Ala”, “Tyr167Ala+Arg170Gly”, and “Tyr167Ala+Arg170Ala”.
DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to a set of sequences. For ease, these are listed below;

SEQ ID NO: 1 is the mature nucleotide sequence of an alpha-amylase (AAI10)

SEQ ID NO: 2 is the full-length, i.e. including the signal peptide, amino acid sequence of the alpha-amylase (AAI10). The signal peptide is designated as amino acid number −29 to −1, and thus, the mature part of the alpha-amylase is designated as amino acid number 1 to 485.

SEQ ID NO: 3 is the mature amino acid sequence of the alpha-amylase (AAI10)

SEQ ID NO: 4 is the mature amino acid sequence of the alpha-amylase (AAI10) comprising a deletion of the amino acids corresponding to positions 182 and 183 of SEQ ID NO:

SEQ ID NO: 5 is the mature amino acid sequence of an alpha-amylase (SP707)

SEQ ID NO: 6 is the mature amino acid sequence of an alpha-amylase (AA560)

SEQ ID NO: 7 is the mature amino acid sequence of an alpha-amylase (K36)

SEQ ID NO: 8 is the mature amino acid sequence of a protease (Savinase)

SEQ ID NO: 9 is the mature amino acid sequence of an alpha-amylase (hybrid polypeptide)

SEQ ID NO: 10 is the mature amino acid sequence of an alpha-amylase (K38)

SEQ ID NO: 11 is the mature amino acid sequence of an alpha-amylase (KSM-AP1378)

SEQ ID NO: 12 is the mature amino acid sequence of an alpha-amylase (SP.7-7)

SEQ ID NO: 13 is the mature amino acid sequence of an alpha-amylase (AAI6)

Variants of the Invention

In one aspect, the present invention relates to variants of a parent polypeptide having alpha-amylase activity. Thus, in a particular aspect, the present invention relates to an alpha-amylase variant of a parent alpha-amylase, wherein the variant comprises a substitution in one or more positions providing oxidation stability of the variant, wherein the variant has an improvement factor of >1.0 as a measure for wash performance, when compared to the parent alpha-amylase, and wherein the variant has alpha-amylase activity.

The present inventors have found that a variant comprising an amino acid substitution in one or more positions providing oxidation stability does not compromise the wash performance of the variant, i.e. see the results of Example 3.

The term “alpha-amylase variant” as used herein, refers to a polypeptide having alpha-amylase activity comprising a modification, i.e., a substitution, insertion, and/or deletion, at one or more (e.g., several) positions. A substitution means replacement of the amino acid occupying a position with a different amino acid; a deletion means removal of the amino acid occupying a position; and an insertion means adding an amino acid adjacent to and immediately following the amino acid occupying a position, all as defined above. The variants of the present invention have at least 20%, e.g., at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 100% of the alpha-amylase activity of the amino acid sequences set forth in SEQ ID NOs: 3, 4, or the mature amino acid sequence of SEQ ID NO: 2.

The term “alpha-amylase activity” as used herein, refers to the activity of alpha-1,4-glucan-4-glucanohydrolases, E.C. 3.2.1.1, which constitute a group of enzymes, catalyzing hydrolysis of starch and other linear and branched 1,4-glucosidic oligo- and polysaccharides. The terms “alpha-amylase” and “amylase” may be used interchangeably and constitute the same meaning and purpose within the scope of the present invention. For purposes of the present invention, alpha-amylase activity is determined according to the procedure described in the Examples. In one embodiment, the variants of the present invention have at least 20%, e.g., at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 100% of the alpha-amylase activity of the amino acid sequence as set forth in SEQ ID NOs: 3 or 4; or the mature amino acid sequence as set forth in SEQ ID NO: 2.

The term “parent alpha-amylase” as used herein, refers to an alpha-amylase to which an alteration is made to produce alpha-amylase variants. An alpha-amylase having any of the amino acid sequences set forth in SEQ ID NOs: 3 and 4 may e.g. be a parent for the variants of the present invention. Any amino acid sequence having at least 80%, such as at least 85%, such at least 90%, such as at least 95%, such as at least 97%, such as at least 99%, sequence identity to any one of SEQ ID NOs: 3 and 4 may also be a parent alpha-amylase for the variants of the present invention.

The parent polypeptide may be obtained from microorganisms of any genus. For purposes of the present invention, the term “obtained from” as used herein in connection with a given source shall mean that the parent encoded by a polynucleotide is produced by the source or by a strain in which the polynucleotide from the source has been inserted.

In some aspects of the present invention, the parent alpha-amylase is Bacillus sp. alpha-amylase, e.g., the alpha-amylase of SEQ ID NO: 2, the mature polypeptide thereof, i.e. SEQ ID NO: 3 or 4.

In some aspects of the present invention, the parent alpha-amylase polypeptide is encoded by the nucleic acid sequence as set forth in SEQ ID NO: 1.

It will be understood that for the aforementioned species, the invention encompasses both the perfect and imperfect states, and other taxonomic equivalents, e.g., anamorphs, regardless of the species name by which they are known. Those skilled in the art will readily recognize the identity of appropriate equivalents.

Strains of this species are readily accessible to the public in a number of culture collections, such as the American Type Culture Collection (ATCC), Deutsche Sammlung von Mikroorganismen and Zellkulturen GmbH (DSMZ), Centraalbureau Voor Schimmelcultures (CBS), and Agricultural Research Service Patent Culture Collection, Northern Regional Research Center (NRRL).

The parent alpha-amylase may be identified and obtained from other sources including microorganisms isolated from nature (e.g., soil, composts, water, etc.) or DNA samples obtained directly from natural materials (e.g., soil, composts, water, etc.) using the above-mentioned probes. Techniques for isolating microorganisms and DNA directly from natural habitats are well known in the art. A polynucleotide encoding a parent polypeptide may then be obtained by similarly screening a genomic DNA or cDNA library of another microorganism or mixed DNA sample. Once a polynucleotide encoding a parent polypeptide has been detected with the probe(s), the polynucleotide can be isolated or cloned by utilizing techniques that are known to those of ordinary skill in the art (see, e.g., Sambrook et al., 1989, supra).

In one embodiment, the parent alpha-amylase comprises or consists of the amino acid sequence set forth in SEQ ID NO: 3 or 4. In another embodiment, the parent alpha-amylase comprises or consists of the full-length amino acid sequence as set forth in SEQ ID NO: 2. In particular, the parent alpha-amylase may comprise or consist of amino acids 1 to 485 of SEQ ID NO: 2.

In another embodiment, the parent alpha-amylase is a fragment of the amino acid sequence as set forth in SEQ ID NO: 3 or 4 containing at least 475 amino acid residues, e.g., at least 480 and at least 485 amino acid residues of SEQ ID NO: 3 or 4.

In another embodiment, the parent alpha-amylase is an allelic variant of the amino acid sequence as set forth in SEQ ID NO: 3 or 4. Accordingly, the parent alpha-amylase may comprise the amino acid sequence set forth in SEQ ID NO: 13.

The term “sequence identity” as used herein, refers to the relatedness between two amino acid sequences or between two nucleotide sequences. For purposes of the present invention, the sequence identity between two amino acid sequences is determined using the Needleman-Wunsch algorithm (Needleman and Wunsch, 1970, J. Mol. Biol. 48: 443-453) as implemented in the Needle program of the EMBOSS package (EMBOSS: The European Molecular Biology Open Software Suite, Rice et al., 2000, Trends Genet. 16: 276-277), preferably version 5.0.0 or later. The parameters used are gap open penalty of 10, gap extension penalty of 0.5, and the EBLOSUM62 (EMBOSS version of BLOSUM62) substitution matrix. The output of Needle labeled “longest identity” (obtained using the -nobrief option) is used as the percent identity and is calculated as follows:

(Identical Residues×100)/(Length of Alignment−Total Number of Gaps in Alignment)

For purposes of the present invention, the sequence identity between two deoxyribonucleotide sequences is determined using the Needleman-Wunsch algorithm (Needleman and Wunsch, 1970, supra) as implemented in the Needle program of the EMBOSS package (EMBOSS: The European Molecular Biology Open Software Suite, Rice et al., 2000, supra), preferably version 5.0.0 or later. The parameters used are gap open penalty of 10, gap extension penalty of 0.5, and the EDNAFULL (EMBOSS version of NCBI NUC4.4) substitution matrix. The output of Needle labeled “longest identity” (obtained using the -nobrief option) is used as the percent identity and is calculated as follows:

(Identical Deoxyribonucleotides×100)/(Length of Alignment−Total Number of Gaps in Alignment)

The term “oxidation stability” as used herein, refers to a property of a protein, such as an alpha-amylase variant according to the invention, which is not oxidized, i.e. protein degraded or made inactive, due to an active oxidation components of, e.g., a detergent composition comprising such oxidation components. The term “oxidation components” as used herein, refers to bleaching systems as defined elsewhere herein. Thus, a variant which is oxidation stable as the variants of the present invention remains active even in the presence of bleaching systems.

The term “wash performance” as used herein, refers to an enzyme's ability to remove starch or starch-containing stains present on the object to be cleaned during e.g. laundry or hard surface cleaning, such as dish wash. The term “wash performance” includes cleaning in general e.g. hard surface cleaning as in dish wash, but also wash performance on textiles such as laundry, and also industrial and institutional cleaning. The wash performance may be quantified by calculating the so-called Intensity value, and results may be displayed as “Improvement Factor” (IF). Wash performance may be determined as in described in the Examples herein.

The term “Intensity value” as used herein, refers to the wash performance measured as the brightness expressed as the intensity of the light reflected from the sample when illuminated with white light. When the sample is stained the intensity of the reflected light is lower, than that of a clean sample. Therefore the intensity of the reflected light can be used to measure wash performance, where a higher intensity value correlates with higher wash performance.

Color measurements are made with a professional flatbed scanner (Kodak iQsmart, Kodak) used to capture an image of the washed textile.

To extract a value for the light intensity from the scanned images, 24-bit pixel values from the image are converted into values for red, green and blue (RGB). The intensity value (Int) is calculated by adding the RGB values together as vectors and then taking the length of the resulting vector:

Int=√{square root over (r²+g²+b²)}

The term “does not compromise the wash performance of the variant” as used herein, refers to a property of the variant according to the invention, wherein the modifications made in the variant does not have a negative or any effect on the wash performance.

In one embodiment, the oxidation stability is determined by an Automatic Mechanical Stress Assay (AMSA) wherein the variant is tested at 55° C. for 20 min, and wherein a detergent used in the AMSA comprises a bleaching system as described in Example 3.

The term “Automatic Mechanical Stress Assay (AMSA)” as used herein, refers to a specific assay which is used to assess the wash performance of an enzyme, such as an alpha-amylase. 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 opening. During the washing time, the plate, test solutions, textile and lidt are vigorously shaken to bring the test solution in contact with the textile and apply mechanical stress in a regular, periodic oscillating manner. For specific conditions under which wash performance may be determined, see the Example 3. Furthermore, the skilled person knows how to perform a general AMSA in order to evaluate wash performance of a variant.

The term “detergent” or “detergent solution” as used herein, refers to a composition which is considered applicable for use in detergents, such as laundry detergents. The terms “detergent” and “detergent solution” may be used interchangeably herein, and have the same meaning and purpose, unless otherwise explicitly stated by context.

The term “detergent used in the said AMSA” as used herein, refers to a specific detergent used in the AMSA performed. I.e. the detergent used may be such as the Model Z detergent as described in the Example 3.

The term “bleaching system” as used herein, refers to inorganic and organic bleaches suitable as cleaning actives. Inorganic bleaches include perhydrate salts such as perborate, percarbonate, perphosphate, persulfate and persilicate salts. The inorganic perhydrate salts are normally the alkali metal salts. The inorganic perhydrate salt may be included as the crystalline solid without additional protection. Alternatively, the salt can be coated.

Alkali metal percarbonates, particularly sodium percarbonate are preferred perhydrates for use herein. The percarbonate is most preferably incorporated into the products in a coated form which provides in-product stability. A suitable coating material providing in product stability comprises mixed salt of a water-soluble alkali metal sulphate and carbonate. Such coatings together with coating processes have previously been described in GB 1,466,799. The weight ratio of the mixed salt coating material to percarbonate lies in the range from 1:200 to 1:4, more preferably from 1:99 to 1:9, and most preferably from 1:49 to 1:19. Preferably, the mixed salt is of sodium sulphate and sodium carbonate which has the general formula Na2SO4.n.Na2CO3 wherein n is from 0.1 to 3, preferably n is from 0.3 to 1.0 and most preferably n is from 0.2 to 0.5.

Another suitable coating material providing in product stability, comprises sodium silicate of SiO₂: Na₂O ratio from 1.8:1 to 3.0:1, preferably 1.8:1 to 2.4:1, and/or sodium metasilicate, preferably applied at a level of from 2% to 10%, (normally from 3% to 5%) of SiO2 by weight of the inorganic perhydrate salt. Magnesium silicate can also be included in the coating. Coatings that comprise silicate and borate salts or boric acids or other inorganics are also suitable.

Other coatings which comprising waxes, oils, fatty soaps can also be used advantageously within the present invention.

Potassium peroxymonopersulfate is another inorganic perhydrate salt of utility herein. Typical organic bleaches are organic peroxyacids including diacyl and tetraacylperoxides, especially diperoxydodecanedioc acid, diperoxytetradecanedioc acid, and diperoxyhexadecanedioc acid. Dibenzoyl peroxide is a preferred organic peroxyacid herein. Mono- and diperazelaic acid, mono- and diperbrassylic acid, and Nphthaloylaminoperoxicaproic acid are also suitable herein. The diacyl peroxide, especially dibenzoyl peroxide, should preferably be present in the form of particles having a weight average diameter of from about 0.1 to about 100 microns, preferably from about 0.5 to about 30 microns, more preferably from about 1 to about 10 microns. Preferably, at least about 25%, more preferably at least about 50%, even more preferably at least about 75%, most preferably at least about 90%, of the particles are smaller than 10 microns, preferably smaller than 6 microns. Diacyl peroxides within the above particle size range have also been found to provide better stain removal especially from plastic dishware, while minimizing undesirable deposition and filming during use in automatic dishwashing machines, than larger diacyl peroxide particles. The preferred diacyl peroxide particle size thus allows the formulator to obtain good stain removal with a low level of diacyl peroxide, which reduces deposition and filming. Conversely, as diacyl peroxide particle size increases, more diacyl peroxide is needed for good stain removal, which increases deposition on surfaces encountered during the dishwashing process. Further typical organic bleaches include the peroxy acids, particular examples being the alkylperoxy acids and the arylperoxy acids. Preferred representatives are (a) peroxybenzoic acid and its ring-substituted derivatives, such as alkylperoxybenzoic acids, but also peroxy-[alpha]-naphthoic acid and magnesium monoperphthalate, (b) the aliphatic or substituted aliphatic peroxy acids, such as peroxylauric acid, peroxystearic acid, [epsilon]-phthalimidoperoxycaproic acid[phthaloiminoperoxyhexanoic acid (PAP)], o-carboxybenzamidoperoxycaproic acid, N-nonenylamidoperadipic acid and N-nonenylamidopersuccinates, and (c) aliphatic and araliphatic peroxydicarboxylic acids, such as 1,12-diperoxycarboxylic acid, 1,9-diperoxyazelaic acid, diperoxysebacic acid, diperoxybrassylic acid, the diperoxyphthalic acids, 2- decyldiperoxybutane-1,4-dioic acid, N,N-terephthaloyldi(6-aminopercaproic acid).

In a particular embodiment, the bleaching system is added in a concentration of at least 5 weight %, such as at least 8 weight %, such as at least 10 weight %, or such as at least 15 weight %.

The term “weight %” as used herein, refers to a component, such as a bleaching system, which is present in a percentage calculated based on weight rather than volume. The term is well-known to the skilled person, who is also able to calculate such weight % based on the knowledge of the components of a solution, such as a detergent solution.

In one embodiment, the bleaching system is sodium percarbonate. In one embodiment, the variant has an improvement factor of >1.5 wherein the IF has been determined in an AMSA wherein the conditions are a wash cycle of 20 min at 55° C. and wherein the variant is tested in the presence of a bleaching system, such as sodium percarbonate, at a concentration of 8 weight %.

In one embodiment, the parent alpha-amylase has an amino acid sequence as set forth in SEQ ID NO: 3, or has an amino acid sequence which is at least 80%, such as at least 85%, such as at least 90%, such as at least 95%, such as at least 98%, identical to the amino acid sequence as set forth in SEQ ID NO: 3.

In one embodiment, the parent alpha-amylase has an amino acid sequence as set forth in SEQ ID NO: 4, or has an amino acid sequence which is at least 80%, such as at least 85%, such as at least 90%, such as at least 95%, such as at least 98%, identical to the amino acid sequence as set forth in SEQ ID NO: 4.

In one embodiment, the parent alpha-amylase has an amino acid sequence as set forth in SEQ ID NO: 13, or has an amino acid sequence which is at least 80%, such as at least 85%, such as at least 90%, such as at least 95%, such as at least 98%, identical to the amino acid sequence as set forth in SEQ ID NO: 13.

In one embodiment, the parent alpha-amylase comprises or consists of the amino acid sequence as set forth in SEQ ID NO: 3.

In one embodiment, the parent alpha-amylase comprises or consists of the amino acid sequence as set forth in SEQ ID NO: 4.

In one embodiment, the parent alpha-amylase comprises or consists of the amino acid sequence as set forth in SEQ ID NO: 13.

In one embodiment, the parent alpha-amylase is a fragment of the polypeptide of SEQ ID NO: 3, wherein the fragment has alpha-amylase activity.

In one embodiment, the parent alpha-amylase is a fragment of the polypeptide of SEQ ID NO: 4, wherein the fragment has alpha-amylase activity.

In one embodiment, the parent alpha-amylase is a fragment of the polypeptide of SEQ ID NO: 13, wherein the fragment has alpha-amylase activity.

The term “fragment” as used herein, refers to a polypeptide having one or more (e.g., several) amino acids absent from the amino and/or carboxyl terminus of a mature polypeptide; wherein the fragment has alpha-amylase activity. In one embodiment, a fragment contains at least 480 amino acid residues, at least 481 amino acid residues, or at least 482 amino acid residues.

In one embodiment, the variant has a sequence identity of at least 80%, such as at least 85%, such as at least 90%, such as at least 95%, such as at least 98%, but less than 100% to the amino acid sequence as set forth in SEQ ID NO: 3.

The term “sequence identity” as used herein, refers to any definition already stated herein. Determination of the sequence identity may be performed as described elsewhere herein.

In one embodiment, the variant comprises a substitution in position 202, wherein said position corresponds to the amino acid position of the amino acid sequence as set forth in SEQ ID NO: 3.

Without being bound by any theory it is contemplated that any amino acid substitution but the naturally-occurring amino acid in the position corresponding to M202 of SEQ ID NO: 3, will provide an oxidation stable variant having an IF of at least 1.0 as a measure for wash performance.

Thus, in one embodiment, the substitution in position 202 is selected from any one of the following M202A, M202R, M202N, M202D, M202C, M202E, M202Q, M202G, M202H, M202I, M202L, M202K, M202F, M202P, M2025, M202T, M202W, M202Y, and M202V, preferably M202L, M2021, M202T, M202F, and M2025, wherein the position corresponds to the positions in the amino acid sequence as set forth in SEQ ID NO:3.

In one embodiment, the variant comprises a deletion in two or more positions corresponding to positions R181, G182, D183, and G184 of the amino acid sequence as set forth in SEQ ID NO: 3.

The term “deletion” as used herein, refers to the removal of an amino acid within a polypeptide, such as an enzyme. Such removal, i.e. deletion, of one or more amino acids may be done by site-directed mutagenesis or any other method known in the art and by the skilled person.

A variant according to the present invention comprising a deletion in two or more positions corresponding to positions R181, G182, D183, and G184 of SEQ ID NO: 3, provides stability to the variants as well as contribute to improving the wash performance of the variants. It is well-known that this particular part of alpha-amylases provides stability to alpha-amylase variants, i.e. as described in e.g. WO 1996/023873. The term “stability” as used in this context, refers to the stability of the alpha-amylase variants during wash. Such stability may be determined by measuring the activity of the variant after a wash cycle of e.g. 60 min in a detergent solution at 40-60° C. Providing variants comprising a deletion in two or more positions corresponding to positions R181, G182, D183, and G184 of SEQ ID NO: 3 and a substitution in one or more amino acids providing oxidation stability of a variant, lies within the scope of the present invention.

Thus, in one embodiment, the variant comprises a deletion in the positions corresponding to R181+G182; R181+D183; R181+G184; G182+D183; G182+G184; or D183+G184, wherein the positions correspond to the positions in the amino acid sequence as set forth in SEQ ID NO:3.

The variants may further comprise one or more additional modifications, e.g. substitutions, at one or more (e.g., several) other positions. The amino acid changes may be of a minor nature, that is conservative amino acid substitutions or insertions that do not significantly affect the folding and/or activity of the protein; small deletions, typically of 1-30 amino acids; small amino- or carboxyl-terminal extensions, such as an amino-terminal methionine residue; a small linker peptide of up to 20-25 residues; or a small extension that facilitates purification by changing net charge or another function, such as a poly-histidine tract, an antigenic epitope or a binding domain.

Examples of conservative substitutions are within the groups of basic amino acids (arginine, lysine and histidine), acidic amino acids (glutamic acid and aspartic acid), polar amino acids (glutamine and asparagine), hydrophobic amino acids (leucine, isoleucine and valine), aromatic amino acids (phenylalanine, tryptophan and tyrosine), and small amino acids (glycine, alanine, serine, threonine and methionine). Amino acid substitutions that do not generally alter specific activity are known in the art and are described, for example, by H. Neurath and R. L. Hill, 1979, In, The Proteins, Academic Press, New York. Common substitutions are Ala/Ser, Val/Ile, Asp/Glu, Thr/Ser, Ala/Gly, Ala/Thr, Ser/Asn, AlaNal, Ser/Gly, Tyr/Phe, Ala/Pro, Lys/Arg, Asp/Asn, Leu/Ile, Leu/Val, Ala/Glu, and Asp/Gly.

Alternatively, the amino acid changes are of such a nature that the physico-chemical properties of the polypeptides are altered. For example, amino acid changes may improve the thermal stability of the polypeptide, alter the substrate specificity, change the pH optimum, and the like.

Essential amino acids in a polypeptide can be identified according to procedures known in the art, such as site-directed mutagenesis or alanine-scanning mutagenesis (Cunningham and Wells, 1989, Science 244: 1081-1085). In the latter technique, single alanine mutations are introduced at every residue in the molecule, and the resultant mutant molecules are tested for alpha-amylase activity to identify amino acid residues that are critical to the activity of the molecule. See also, Hilton et al., 1996, J. Biol. Chem. 271: 4699-4708. The active site of the enzyme or other biological interaction can also be determined by physical analysis of structure, as determined by such techniques as nuclear magnetic resonance, crystallography, electron diffraction, or photoaffinity labeling, in conjunction with mutation of putative contact site amino acids. See, for example, de Vos et al., 1992, Science 255: 306-312; Smith et al., 1992, J. Mol. Biol. 224: 899-904; Wlodaver et al., 1992, FEBS Lett. 309: 59-64. The identity of essential amino acids can also be inferred from an alignment with a related polypeptide.

Thus, in one embodiment, the variant comprises 1 to 40 substitutions, such as 1 to 30, such as 1 to 20, such as 1 to 10, such as 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 substitutions.

In a particular embodiment, the number of substitutions is 1 to 20, e.g., 1 to 10 and 1 to 5, such as 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 substitutions.

In one embodiment, the variant further comprises further modifications.

The variants may consist of 430 to 490 amino acids, e.g., 440 to 485, 450 to 485, and 460 to 483 amino acids.

In one embodiment, the variant comprises or consists of the following modifications; G182*+D183*+M202L, wherein numbering is according to SEQ ID NO: 3.

In a particular embodiment, the variant comprises or consists of the following modifications; G182*+D183*+N195F+M202L, wherein numbering is according to SEQ ID NO: 3.

In one aspect, the present invention relates to a variant of a parent alpha-amylase, wherein the parent alpha-amylase comprises or consists of the amino acid sequence having at least 80%, such as at least 85%, such as at least 90%, such as at least 95%, or such as at least 98% sequence identity to an amino acid sequence as set forth in SEQ ID NO: 3, and wherein the variant consists of a substitution in a position corresponding to position M202 of SEQ ID NO: 3.

In a particular aspect, the present invention relates to a variant of a parent alpha-amylase consisting of the amino acid sequence as set forth in SEQ ID NO: 3, wherein the variant consists of a substitution in a position corresponding to position M202 of SEQ ID NO: 3.

In another aspect, the present invention relates to a variant of a parent alpha-amylase consisting of the amino acid sequence as set forth in SEQ ID NO: 3, wherein the variant consists of the modifications G182*+D183*+M202L, wherein numbering is according to SEQ ID NO: 3.

In another aspect, the present invention relates to a variant of a parent alpha-amylase consisting of the amino acid sequence as set forth in SEQ ID NO: 3, wherein the variant consists of the modifications G182*+D183*+N195F+M202L, wherein numbering is according to SEQ ID NO: 3.

Polynucleotides

The present invention also relates to polynucleotides encoding a variant of the present invention. Thus, in particular, the present invention relates to a polynucleotide encoding a variant comprising a substitution in one or more positions providing oxidation stability of the variant.

The term “polynucleotides encoding” as used herein, refers to a polynucleotide that encodes a mature polypeptide having alpha-amylase activity. In one aspect, the polypeptide coding sequence is the nucleotide sequence set forth in SEQ ID NO: 1.

In one embodiment, the polynucleotide encoding a variant according to the present invention as at least 80%, such as at least 85%, such as at least 90%, such as at least 95%, such as at least 96%, such as at least 97%, such as at least 98%, such as at least 99% but less than 100% sequence identity to the polynucleotide of SEQ ID NO: 1.

In one embodiment, the polynucleotide encodes a variant comprising a substitution and/or deletion in two, three, or four positions corresponding to positions R181, G182, D183, and G184 of the amino acid sequence as set forth in SEQ ID NO: 3, and a substitution in the position corresponding to position M202 of the amino acid sequence as set forth in SEQ ID NO: 3.

Nucleic Acid Constructs

The present invention also relates to nucleic acid constructs comprising a polynucleotide encoding a variant of the present invention operably linked to one or more control sequences that direct the expression of the coding sequence in a suitable host cell under conditions compatible with the control sequences. Thus, in particular, the present invention relates to a nucleic acid construct comprising a polynucleotide encoding a variant comprising a substitution in one or more positions providing oxidation stability of the variant, wherein the polynucleotide is operately linked to one or more control sequences.

The term “nucleic acid construct” as used herein, refers to a nucleic acid molecule, either single- or double-stranded, which is isolated from a naturally occurring gene or is modified to comprise segments of nucleic acids in a manner that would not otherwise exist in nature or which is synthetic, which comprises one or more control sequences.

The term “operably linked” as used herein, refers to a configuration in which a control sequence is placed at an appropriate position relative to the coding sequence of a polynucleotide such that the control sequence directs expression of the coding sequence.

The polynucleotide may be manipulated in a variety of ways to provide for expression of a variant. Manipulation of the polynucleotide prior to its insertion into a vector may be desirable or necessary depending on the expression vector. The techniques for modifying polynucleotides utilizing recombinant DNA methods are well known in the art.

The control sequence may be a promoter, a polynucleotide which is recognized by a host cell for expression of the polynucleotide. The promoter comprises transcriptional control sequences that mediate the expression of the variant. The promoter may be any polynucleotide that shows transcriptional activity in the host cell including mutant, truncated, and hybrid promoters, and may be obtained from genes encoding extracellular or intracellular polypeptides either homologous or heterologous to the host cell.

In one embodiment, the nucleic acid construct comprises a polynucleotide encoding a variant comprising a substitution and/or deletion in two, three, or four positions corresponding to positions R181, G182, D183, and G184 of the amino acid sequence as set forth in SEQ ID NO: 3, and a substitution in the position corresponding to position M202 of the amino acid sequence as set forth in SEQ ID NO: 3, wherein the polynucleotide is operately linked to one or more control sequences.

Expression Vectors

The present invention also relates to recombinant expression vectors comprising a polynucleotide encoding a variant of the present invention, a promoter, and transcriptional and translational stop signals. Thus, the present invention relates to an expression vector, optionally a recombinant expression vector, comprising a polynucleotide encoding a variant comprising a substitution in one or more positions providing oxidation stability of the variant, a promoter, and transcriptional and translational stop signals.

The term “expression vector” as used herein, refers to a linear or circular DNA molecule that comprises a polynucleotide encoding a variant and is operably linked to control sequences that provide for its expression.

In one embodiment, the expression vector comprises a polynucleotide encoding a variant comprising a substitution and/or deletion in two, three, or four positions corresponding to positions R181, G182, D183, and G184 of the amino acid sequence as set forth in SEQ ID NO: 3, and a substitution in the position corresponding to position M202 of the amino acid sequence as set forth in SEQ ID NO: 3, and wherein the expression vector further comprises a promoter, and transcriptional and translational stop signals.

The various nucleotide and control sequences may be joined together to produce a recombinant expression vector that may include one or more convenient restriction sites to allow for insertion or substitution of the polynucleotide encoding the variant at such sites.

Alternatively, the polynucleotide may be expressed by inserting the polynucleotide or a nucleic acid construct comprising the polynucleotide into an appropriate vector for expression. In creating the expression vector, the coding sequence is located in the vector so that the coding sequence is operably linked with the appropriate control sequences for expression.

The recombinant expression vector may be any vector (e.g., a plasmid or virus) that can be conveniently subjected to recombinant DNA procedures and can bring about expression of the polynucleotide. The choice of the vector will typically depend on the compatibility of the vector with the host cell into which the vector is to be introduced.

The vector may be an autonomously replicating vector, i.e., a vector that exists as an extrachromosomal entity, the replication of which is independent of chromosomal replication, e.g., a plasmid, an extrachromosomal element, a minichromosome, or an artificial chromosome. The vector may comprise any means for assuring self-replication. Alternatively, the vector may be one that, when introduced into the host cell, is integrated into the genome and replicated together with the chromosome(s) into which it has been integrated. Furthermore, a single vector or plasmid or two or more vectors or plasmids that together contain the total DNA to be introduced into the genome of the host cell, or a transposon, may be used.

The vector preferably comprises one or more selectable markers that permit easy selection of transformed, transfected, transduced, or the like cells. A selectable marker is a gene the product of which provides for biocide or viral resistance, resistance to heavy metals, prototrophy to auxotrophs, and the like.

The skilled person would know which expression vector is the most suitable for specific expression systems. Thus, the present invention is not limited to any specific expression vector, but any expression vector comprising the polynucleotide encoding a variant according to the invention is considered part of the present invention.

Host Cells

The present invention also relates to recombinant host cells, comprising a polynucleotide encoding a variant of the present invention operably linked to one or more control sequences that direct the production of a variant of the present invention. Thus, the present invention relates to a host cell, optionally a recombinant host cell, comprising polynucleotide encoding a variant comprising a substitution in one or more positions providing oxidation stability of the variant, operably linked to one or more control sequences that direct the production of the variant.

The term “host cell” as used herein, refers to any cell type that is susceptible to transformation, transfection, transduction, or the like with a nucleic acid construct or expression vector comprising a polynucleotide of the present invention. The term “host cell” encompasses any progeny of a parent cell that is not identical to the parent cell due to mutations that occur during replication.

In one embodiment, the host cell comprises a polynucleotide encoding a variant comprising a substitution and/or deletion in two, three, or four positions corresponding to positions R181, G182, D183, and G184 of the amino acid sequence as set forth in SEQ ID NO: 3, and a substitution in the position corresponding to position M202 of the amino acid sequence as set forth in SEQ ID NO: 3, the polynucleotide operately linked to one or more control sequences that direct the production of the variant.

A construct or vector comprising a polynucleotide is introduced into a host cell so that the construct or vector is maintained as a chromosomal integrant or as a self-replicating extra-chromosomal vector as described earlier. The term “host cell” encompasses any progeny of a parent cell that is not identical to the parent cell due to mutations that occur during replication. The choice of a host cell will to a large extent depend upon the gene encoding the variant and its source.

The host cell may be any cell useful in the recombinant production of a variant, e.g., a prokaryote or a eukaryote.

The prokaryotic host cell may be any Gram-positive or Gram-negative bacterium. Gram-positive bacteria include, but are not limited to, Bacillus, Clostridium, Enterococcus, Geobacillus, Lactobacillus, Lactococcus, Oceanobacillus, Staphylococcus, Streptococcus, and Streptomyces. Gram-negative bacteria include, but are not limited to, Campylobacter, E. coli, Flavobacterium, Fusobacterium, Helicobacter, Ilyobacter, Neisseria, Pseudomonas, Salmonella, and Ureaplasma.

Methods of the Invention

The present invention also relates to methods of producing a variant, comprising: (a) cultivating a host cell of the present invention under conditions suitable for expression of the variant; and (b) recovering the variant. Thus, the present invention relates to a method of producing a variant comprising a substitution in one or more positions providing oxidation stability of the variant, wherein the method comprises the steps of a) cultivating the host cell according to the invention under conditions suitable for expression of the variant, and b) recovering the variant.

The term “conditions suitable for expression” as used herein, refers to which settings the host cell expressing the variant according to the invention, are cultivated in. These conditions (or settings) may depend on the type of host cell. I.e. conditions suitable to cultivate yeast host cells are different than from those of cultivate bacterial host cells. It is within the knowledge of the skilled person to determine which conditions are the most optimal, i.e. suitable, for the specific host cells.

In one embodiment, the method of producing a variant comprising a substitution and/or deletion in two, three, or four positions corresponding to positions R181, G182, D183, and G184 of the amino acid sequence as set forth in SEQ ID NO: 3, and a substitution in the position corresponding to position M202 of the amino acid sequence as set forth in SEQ ID NO: 3, comprises the steps of a) cultivating the host cell according to the invention under conditions suitable for expression of the variant, and b) recovering the variant.

The host cells are cultivated in a nutrient medium suitable for production of the variant using methods known in the art. For example, the cell may be cultivated by shake flask cultivation, or small-scale or large-scale fermentation (including continuous, batch, fed-batch, or solid state fermentations) in laboratory or industrial fermentors performed in a suitable medium and under conditions allowing the variant to be expressed and/or isolated. The cultivation takes place in a suitable nutrient medium comprising carbon and nitrogen sources and inorganic salts, using procedures known in the art. Suitable media are available from commercial suppliers or may be prepared according to published compositions (e.g., in catalogues of the American Type Culture Collection). If the variant is secreted into the nutrient medium, the variant can be recovered directly from the medium. If the variant is not secreted, it can be recovered from cell lysates.

The variant may be detected using methods known in the art that are specific for the variants having alpha-amylase activity. These detection methods include, but are not limited to, use of specific antibodies, formation of an enzyme product, or disappearance of an enzyme substrate. For example, an enzyme assay may be used to determine the activity of the variant.

The variant may be recovered using methods known in the art. For example, the variant may be recovered from the nutrient medium by conventional procedures including, but not limited to, collection, centrifugation, filtration, extraction, spray-drying, evaporation, or precipitation.

The variant may be purified by a variety of procedures known in the art including, but not limited to, chromatography (e.g., ion exchange, affinity, hydrophobic, chromatofocusing, and size exclusion), electrophoretic procedures (e.g., preparative isoelectric focusing), differential solubility (e.g., ammonium sulfate precipitation), SDS-PAGE, or extraction (see, e.g., Protein Purification, Janson and Ryden, editors, VCH Publishers, New York, 1989) to obtain substantially pure variants.

In an alternative aspect, the variant is not recovered, but rather a host cell of the present invention expressing the variant is used as a source of the variant.

In a further aspect, the present invention relates to methods for obtaining a variant, comprising introducing into a parent alpha-amylase a substitution in position M202 wherein the position correspond to the position of the amino acid sequence as set forth in SEQ ID NO: 3; b) optionally, introducing a deletion in two or more positions corresponding to positions R181, G182, D183, and G184 of the amino acid sequence as set forth in SEQ ID NO: 3; and c) recovering the variant.

The variants can be prepared using any mutagenesis procedure known in the art, such as site-directed mutagenesis, synthetic gene construction, semi-synthetic gene construction, random mutagenesis, shuffling, etc.

Site-directed mutagenesis is a technique in which one or more (e.g., several) mutations are introduced at one or more defined sites in a polynucleotide encoding the parent.

Site-directed mutagenesis can be accomplished in vitro by PCR involving the use of oligonucleotide primers containing the desired mutation. Site-directed mutagenesis can also be performed in vitro by cassette mutagenesis involving the cleavage by a restriction enzyme at a site in the plasmid comprising a polynucleotide encoding the parent and subsequent ligation of an oligonucleotide containing the mutation in the polynucleotide. Usually the restriction enzyme that digests the plasmid and the oligonucleotide is the same, permitting sticky ends of the plasmid and the insert to ligate to one another. See, e.g., Scherer and Davis, 1979, Proc. Natl. Acad. Sci. USA 76: 4949-4955; and Barton et al., 1990, Nucleic Acids Res. 18: 7349-4966.

Site-directed mutagenesis can also be accomplished in vivo by methods known in the art. See, e.g., U.S. Patent Application Publication No. 2004/0171154; Storici et al., 2001, Nature Biotechnol. 19: 773-776; Kren et al., 1998, Nat. Med. 4: 285-290; and Calissano and Macino, 1996, Fungal Genet. Newslett. 43: 15-16.

Any site-directed mutagenesis procedure can be used in the present invention. There are many commercial kits available that can be used to prepare variants. Synthetic gene construction entails in vitro synthesis of a designed polynucleotide molecule to encode a polypeptide of interest. Gene synthesis can be performed utilizing a number of techniques, such as the multiplex microchip-based technology described by Tian et al. (2004, Nature 432: 1050-1054) and similar technologies wherein oligonucleotides are synthesized and assembled upon photo-programmable microfluidic chips.

Single or multiple amino acid substitutions, deletions, and/or insertions can be made and tested using known methods of mutagenesis, recombination, and/or shuffling, followed by a relevant screening procedure, such as those disclosed by Reidhaar-Olson and Sauer, 1988, Science 241: 53-57; Bowie and Sauer, 1989, Proc. Natl. Acad. Sci. USA 86: 2152-2156; WO 95/17413; or WO 95/22625. Other methods that can be used include error-prone PCR, phage display (e.g., Lowman et al., 1991, Biochemistry 30: 10832-10837; U.S. Pat. No. 5,223,409; WO 92/06204) and region-directed mutagenesis (Derbyshire et al., 1986, Gene 46: 145; Ner et al., 1988, DNA 7: 127).

Mutagenesis/shuffling methods can be combined with high-throughput, automated screening methods to detect activity of cloned, mutagenized polypeptides expressed by host cells (Ness et al., 1999, Nature Biotechnology 17: 893-896). Mutagenized DNA molecules that encode active polypeptides can be recovered from the host cells and rapidly sequenced using standard methods in the art. These methods allow the rapid determination of the importance of individual amino acid residues in a polypeptide.

Semi-synthetic gene construction is accomplished by combining aspects of synthetic gene construction, and/or site-directed mutagenesis, and/or random mutagenesis, and/or shuffling. Semi-synthetic construction is typified by a process utilizing polynucleotide fragments that are synthesized, in combination with PCR techniques. Defined regions of genes may thus be synthesized de novo, while other regions may be amplified using site-specific mutagenic primers, while yet other regions may be subjected to error-prone PCR or non-error prone PCR amplification. Polynucleotide subsequences may then be shuffled.

The present invention also relates to a method of improving oxidation stability of a parent alpha-amylase having the amino acid sequence of SEQ ID NO: 3 or 4, or having at least 80% sequence identity thereto, wherein the method comprises the steps of;

a) introducing a substitution in one or more positions providing oxidation stability in the parent alpha-amylase; and

b) optionally, introducing a substitution and/or deletion of two, three, or four positions corresponding to positions R181, G182, D183, and G184 of the amino acid sequence as set forth in SEQ ID NO: 3,

wherein the variant has at least 80%, such as at least 85%, such as at least 90%, such as at least 95%, such as at least 98%, such as at least 99%, but less than 100% sequence identity with the amino acid sequence as set forth in SEQ ID NO: 3, and wherein the variant has alpha-amylase activity and improved oxidation stability compared to the parent alpha-amylase.

In one embodiment, the method of improving oxidation stability of a parent alpha-amylase having the amino acid sequence of SEQ ID NO: 3 or 4, or having at least 80% sequence identity thereto, wherein the method comprises the steps of;

a) introducing a substitution in the position corresponding to position M202 of the amino acid sequence as set forth in SEQ ID NO: 3; and

b) introducing a substitution and/or deletion of two, three, or four positions corresponding to positions R181, G182, D183, and G184 of the amino acid sequence as set forth in SEQ ID NO: 3,

In one embodiment, the variant has at least 50%, such as at least 60%, or at least 70%, or at least 80%, or at least 90%, or at least 100% of the activity of the parent polypeptide having the amino acid sequence of SEQ ID NO: 4.

In another embodiment, the variant has at least 50%, such as at least 60%, or at least 70%, or at least 80%, or at least 90%, or at least 100% of the activity of the parent polypeptide having the amino acid sequence of SEQ ID NO: 3.

In one embodiment, the activity is determined according to a Phadebas assay.

The alpha-amylase activity may be determined by a method using the Phadebas substrate (from for example Magle Life Sciences, Lund, Sweden). A Phadebas tablet includes interlinked starch polymers that are in the form of globular microspheres that are insoluble in water. A blue dye is covalently bound to these microspheres. The interlinked starch polymers in the microsphere are degraded at a speed that is proportional to the alpha-amylase activity. When the alpha-amylase degrades the starch polymers, the released blue dye is water soluble and concentration of dye can be determined by measuring absorbance at 620 nm. The concentration of blue is proportional to the alpha-amylase activity in the sample.

The variant sample to be analyzed is diluted in activity buffer with the desired pH. Two substrate tablets are suspended in 5 mL activity buffer and mixed on magnetic stirrer. During mixing of substrate transfer 150 μl to microtiter plate (MTP) or PCR-MTP. Add 30 μl diluted amylase sample to 150 μl substrate and mix. Incubate for 15 minutes at 37° C. The reaction is stopped by adding 30 μl M NaOH and mix. Centrifuge MTP for 5 minutes at 4000× g. Transfer 100p1 to new MTP and measure absorbance at 620nm.

The alpha-amylase sample should be diluted so that the absorbance at 620 nm is between 0 and 2.2, and is within the linear range of the activity assay.

Thus, in one embodiment, the activity is determined by a method comprising the steps of;

a) incubating an alpha-amylase variant according to the invention with a dyed amylose substrate for 15 minute at 37° C.; and

b) measuring the absorption at OD 620 nm.

In a further embodiment, the activity is determined by a method comprising the steps of;

a) incubating an alpha-amylase variant according to the invention with a dyed amylose substrate for 15 minute at 37° C.; and

b) centrifuging the sample;

c) transferring the supernatant to reader plate, and measuring the absorption at OD 620 nm.

In another embodiment, the activity is determined according to the pNP-G7 assay as described in Example 2.

Fermentation Broth Formulations or Cell Compositions

The present invention also relates to a fermentation broth formulation or a cell composition comprising a variant of the present invention. Thus, in one embodiment, the fermentation broth formulation or cell composition comprises a variant comprising a substitution in one or more positions providing oxidation stability of the variant. In another embodiment, the fermentation broth formulation or cell composition comprises a polynucleotide encoding a variant comprising a substitution in one or more positions providing oxidation stability of the variant, nucleic acid construct encoding a variant comprising a substitution in one or more positions providing oxidation stability of the variant, or an expression vector encoding a variant comprising a substitution in one or more positions providing oxidation stability of the variant. The fermentation broth product may further comprise additional ingredients used in the fermentation process, such as, for example, cells (including, the host cells containing the gene encoding the polypeptide of the present invention which are used to produce the polypeptide of interest), cell debris, biomass, fermentation media and/or fermentation products. In some embodiments, the composition is a cell-killed whole broth containing organic acid(s), killed cells and/or cell debris, and culture medium.

The term “fermentation broth” as used herein refers to a preparation produced by cellular fermentation that undergoes no or minimal recovery and/or purification. For example, fermentation broths are produced when microbial cultures are grown to saturation, incubated under carbon-limiting conditions to allow protein synthesis (e.g., expression of enzymes by host cells) and secretion into cell culture medium. The fermentation broth may comprise unfractionated or fractionated contents of the fermentation materials derived at the end of the fermentation. Typically, the fermentation broth is unfractionated and comprises the spent culture medium and cell debris present after the microbial cells (e.g., filamentous fungal cells) are removed, e.g., by centrifugation. In some embodiments, the fermentation broth comprises spent cell culture medium, extracellular enzymes, and viable and/or nonviable microbial cells.

In one embodiment, the fermentation broth formulation and cell compositions comprise a first organic acid component comprising at least one 1-5 carbon organic acid and/or a salt thereof and a second organic acid component comprising at least one 6 or more carbon organic acid and/or a salt thereof. In a particular embodiment, the first organic acid component is acetic acid, formic acid, propionic acid, a salt thereof, or a mixture of two or more of the foregoing and the second organic acid component is benzoic acid, cyclohexanecarboxylic acid, 4-methylvaleric acid, phenylacetic acid, a salt thereof, or a mixture of two or more of the foregoing.

In one embodiment, the composition comprises an organic acid(s), and optionally further comprises killed cells and/or cell debris. In one embodiment, the killed cells and/or cell debris are removed from a cell-killed whole broth to provide a composition that is free of these components.

The fermentation broth formulations or cell compositions may further comprise a preservative and/or anti-microbial (e.g., bacteriostatic) agent, including, but not limited to, sorbitol, sodium chloride, potassium sorbate, and others known in the art.

The cell-killed whole broth or composition may comprise the unfractionated contents of the fermentation materials derived at the end of the fermentation. Typically, the cell-killed whole broth or composition comprises the spent culture medium and cell debris present after the microbial cells (e.g., filamentous fungal cells) are grown to saturation, incubated under carbon-limiting conditions to allow protein synthesis. In some embodiments, the cell-killed whole broth or composition comprises the spent cell culture medium, extracellular enzymes, and killed filamentous fungal cells. In some embodiments, the microbial cells present in the cell-killed whole broth or composition may be permeabilized and/or lysed using methods known in the art.

A whole broth or cell composition as described herein is typically a liquid, but may comprise insoluble components, such as killed cells, cell debris, culture media components, and/or insoluble enzyme(s). In some embodiments, insoluble components may be removed to provide a clarified liquid composition.

The whole broth formulations and cell compositions of the present invention may be produced by a method described in WO 90/15861 or WO 2010/096673.

Compositions

The present invention also relates to compositions comprising a variant according to the invention. Thus, the invention relates to a composition comprising a variant comprising a substitution in one or more positions providing oxidation stability of the variant. Preferably, the compositions are enriched in such a variant. The term “enriched” means that the alpha-amylase activity of the composition has been increased, e.g., with an enrichment factor of 1.1.

In one embodiment, the composition comprises a variant comprising a substitution in the position corresponding to position M202 of the amino acid sequence as set forth in SEQ ID NO: 3, and a substitution and/or deletion of two, three, or four positions corresponding to positions R181, G182, D183, and G184 of the amino acid sequence as set forth in SEQ ID NO: 3.

The compositions may be prepared in accordance with methods known in the art and may be in the form of a liquid or a dry composition. For instance, the composition may be in the form of a granulate or a microgranulate. The variant may be stabilized in accordance with methods known in the art.

Accordingly, in one embodiment, the composition is a liquid laundry or liquid dish wash composition, such as an Automatic Dish Wash (ADW) liquid detergent composition, or a powder laundry, such as a soap bar, or powder dish wash composition, such as an ADW detergent composition.

In one embodiment, the composition further comprises one or more surfactants, one or more sulfonated polymers, one or more chelators, one or more bleaching systems, and/or one or more builders.

The choice of additional components is within the skills of the skilled person in the art and includes conventional ingredients, including the exemplary non-limiting components set forth below. The choice of components may include, for fabric care, the consideration of the type of fabric to be cleaned, the type and/or degree of soiling, the temperature at which cleaning is to take place, and the formulation of the detergent product. Although components mentioned below are categorized by general header according to a particular functionality, this is not to be construed as a limitation, as a component may comprise additional functionalities as will be appreciated by the skilled artisan.

In one embodiment of the present invention, the variant of the present invention may be added to a detergent composition in an amount corresponding to 0.001-100 mg of protein, such as 0.01-100 mg of protein, preferably 0.005-50 mg of protein, more preferably 0.01-25 mg of protein, even more preferably 0.05-10 mg of protein, most preferably 0.05-5 mg of protein, and even most preferably 0.01-1 mg of protein per liter of wash liquor. The term “protein” in this context is contemplated to be understood to include a variant according to the present invention.

A composition for use in automatic dish wash (ADW), for example, may include 0.0001%-50%, such as 0.001%-20%, such as 0.01%-10%, such as 0.05-5% of enzyme protein by weight of the composition.

A composition for use in laundry granulation, for example, may include 0.0001%-50%, such as 0.001%-20%, such as 0.01%-10%, such as 0.05%-5% of enzyme protein by weight of the composition.

A composition for use in laundry liquid, for example, may include 0.0001%-10%, such as 0.001-7%, such as 0.1%-5% of enzyme protein by weight of the composition.

The variants of the invention as well as the further active components, such as additional enzymes, 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, for example, WO92/19709 and WO92/19708.

In certain markets different wash conditions and, as such, different types of detergents are used. This is disclosed in e.g. EP 1 025 240. For example, in Asia (Japan) a low detergent concentration system is used, while the United States uses a medium detergent concentration system, and Europe uses a high detergent concentration system.

A low detergent concentration system includes detergents where less than about 800 ppm of detergent components are present in the wash water. Japanese detergents are typically considered low detergent concentration system as they have approximately 667 ppm of detergent components present in the wash water.

A medium detergent concentration includes detergents where between about 800 ppm and about 2000 ppm of detergent components are present in the wash water. North American detergents are generally considered to be medium detergent concentration systems as they have approximately 975 ppm of detergent components present in the wash water.

A high detergent concentration system includes detergents where greater than about 2000 ppm of detergent components are present in the wash water. European detergents are generally considered to be high detergent concentration systems as they have approximately 4500-5000 ppm of detergent components in the wash water.

Latin American detergents are generally high suds phosphate builder detergents and the range of detergents used in Latin America can fall in both the medium and high detergent concentrations as they range from 1500 ppm to 6000 ppm of detergent components in the wash water. Such detergent compositions are all embodiments of the invention.

A variant of the present invention may also be incorporated in the detergent formulations disclosed in WO97/07202, which is hereby incorporated by reference.

Examples are given herein of preferred uses of the compositions of the present invention. The dosage of the composition and other conditions under which the composition is used may be determined on the basis of methods known in the art.

In one embodiment, the composition further comprises a bleaching system.

The term “bleaching system” as used herein, refers to inorganic and organic bleaches suitable cleaning actives. The terms “bleaching system” and “bleaches” may be used interchangeably herein and constitute the same meaning and purpose, unless explicitly stated otherwise. Inorganic bleaches include perhydrate salts such as perborate, percarbonate, perphosphate, persulfate and persilicate salts. The inorganic perhydrate salts are normally the alkali metal salts. The inorganic perhydrate salt may be included as the crystalline solid without additional protection. Alternatively, the salt can be coated.

Another suitable coating material providing in product stability, comprises sodium silicate of SiO₂:Na₂O ratio from 1.8:1 to 3.0:1, preferably 1.8:1 to 2.4:1, and/or sodium metasilicate, preferably applied at a level of from 2% to 10%, (normally from 3% to 5%) of SiO2 by weight of the inorganic perhydrate salt. Magnesium silicate can also be included in the coating. Coatings that comprise silicate and borate salts or boric acids or other inorganics are also suitable.

Other coatings which comprise waxes, oils, fatty soaps can also be used advantageously within the present invention.

Further typical organic bleaches include the peroxy acids, particular examples being the alkylperoxy acids and the arylperoxy acids. Preferred representatives are (a) peroxybenzoic acid and its ring-substituted derivatives, such as alkylperoxybenzoic acids, but also peroxy-[alpha]-naphthoic acid and magnesium monoperphthalate, (b) the aliphatic or substituted aliphatic peroxy acids, such as peroxylauric acid, peroxystearic acid, [epsilon]-phthalimidoperoxycaproic acid[phthaloiminoperoxyhexanoic acid (PAP)], o-carboxybenzamidoperoxycaproic acid, N- nonenylamidoperadipic acid and N-nonenylamidopersuccinates, and (c) aliphatic and araliphatic peroxydicarboxylic acids, such as 1,12-diperoxycarboxylic acid, 1,9-diperoxyazelaic acid, diperoxysebacic acid, diperoxybrassylic acid, the diperoxyphthalic acids, 2-decyldiperoxybutane-1,4-dioic acid, N,N-terephthaloyldi(6-aminopercaproic acid).

In one embodiment, the composition further comprises a bleach activator, bleach catalyst, silicate and/or metal care agent(s).

The term “bleach activators” as used herein, refers to a typically organic peracid precursor which enhances the bleaching action in the course of cleaning at temperatures of 60° C. and below. Bleach activators suitable for use herein include compounds which, under perhydrolysis conditions, give aliphatic peroxoycarboxylic acids having preferably from 1 to 10 carbon atoms, in particular from 2 to 4 carbon atoms, and/or optionally substituted perbenzoic acid. Suitable substances bear 0-acyl and/or N-acyl groups of the number of carbon atoms specified and/or optionally substituted benzoyl groups. Preference is given to polyacylated alkylenediamines, in particular tetraacetylethylenediamine (TAED), acylated triazine derivatives, in particular 1,5-diacetyl-2,4- dioxohexahydro-1,3,5-triazine (DADHT), acylated glycolurils, in particular tetraacetylglycoluril (TAGU), N-acylimides, in particular N-nonanoylsuccinimide (NOSI), acylated phenolsulfonates, in particular n-nonanoyl- or isononanoyloxybenzenesulfonate (n- or iso-NOBS), carboxylic anhydrides, in particular phthalic anhydride, acylated polyhydric alcohols, in particular triacetin, ethylene glycol diacetate and 2,5-diacetoxy-2,5-dihydrofuran and also triethylacetyl citrate (TEAC). Bleach activators if included in the compositions of the invention are in a level of from about 0.1 to about 10%, preferably from about 0.5 to about 2% by weight of the composition.

The term “bleach catalysts” as used herein, refers to manganese triazacyclononane and related complexes (U.S. Pat. No. 4,246,612, U.S. Pat. No. 5,227,084); Co, Cu, Mn and Fe bispyridylamine and related complexes (U.S. Pat. No. 5,114,611); and pentamine acetate cobalt(III) and related complexes (U.S. Pat. No. 4,810,410). A complete description of bleach catalysts suitable for use herein can be found in WO 99/06521, pages 34, line 26 to page 40, line 16. Bleach catalyst if included in the compositions of the invention are in a level of from about 0.1 to about 10%, preferably from about 0.5 to about 2% by weight of the composition.

Oxidoreductases, for example oxidases, oxygenases, catalases, peroxidases such as halo-, chloro-, bromo-, lignin, glucose, or manganese peroxidases, dioxygenases, or laccases (phenoloxidases, polyphenoloxidases), can also be used according to the present invention to intensify the bleaching effect. Advantageously, preferably organic, particularly preferably aromatic compounds that interact with the enzymes are additionally added in order to enhance the activity of the relevant oxidoreductases (enhancers) or, if there is a large difference in redox potentials between the oxidizing enzymes and the stains, to ensure electron flow (mediators).

The term “silicates” as used herein, refers to sodium silicates such as sodium disilicate, sodium metasilicate and crystalline phyllosilicates. Silicates if present are at a level of from about 1 to about 20%, preferably from about 5 to about 15% by weight of composition.

The term “metal care agents” as used herein, refers to prevention or reduction of tarnishing, corrosion or oxidation of metals, including aluminium, stainless steel and non-ferrous metals, such as silver and copper. Suitable examples include one or more of the following: (

a) benzatriazoles, including benzotriazole or bis-benzotriazole and substituted derivatives thereof. Benzotriazole derivatives are those compounds in which the available substitution sites on the aromatic ring are partially or completely substituted. Suitable substituents include linear or branch-chain Ci-C20-alkyl groups and hydroxyl, thio, phenyl or halogen such as fluorine, chlorine, bromine and iodine.

(b) metal salts and complexes chosen from the group consisting of zinc, manganese, titanium, zirconium, hafnium, vanadium, cobalt, gallium and cerium salts and/or complexes, the metals being in one of the oxidation states II, Ill, IV, V or VI. In one aspect, suitable metal salts and/or metal complexes may be chosen from the group consisting of Mn(II) sulphate, Mn(II) citrate, Mn(II) stearate, Mn(II) acetylacetonate, KATiF6, KAZrF6, CoSO4, Co(NOs)2 and Ce(NOs)3, zinc salts, for example zinc sulphate, hydrozincite or zinc acetate.; (c) silicates, including sodium or potassium silicate, sodium disilicate, sodium metasilicate, crystalline phyllosilicate and mixtures thereof.

Further suitable organic and inorganic redox-active substances that act as silver/copper corrosion inhibitors are disclosed in WO 94/26860 and WO 94/26859. Preferably the composition of the invention comprises from 0.1 to 5% by weight of the composition of a metal care agent, preferably the metal care agent is a zinc salt.

In one embodiment, the composition further comprises a surfactant.

The term “surfactant” as used herein, refers in particular to a dish washing component, which is a non-ionic compound. Suitable nonionic surfactants include, but are not limited to low-foaming nonionic (LFNI) surfactants. A LFNI surfactant is most typically used in an automatic dishwashing composition because of the improved water- sheeting action (especially from glassware) which they confer to the automatic dishwashing composition. They also may encompass non-silicone, phosphate or nonphosphate polymeric materials which are known to defoam food soils encountered in automatic dishwashing. The LFNI surfactant may have a relatively low cloud point and a high hydrophilic-lipophilic balance (HLB). Cloud points of 1% solutions in water are typically below about 32° C. and alternatively lower, e.g., 0° C., for optimum control of sudsing throughout a full range of water temperatures. If desired, a biodegradable LFNI surfactant having the above properties may be used.

An LFNI surfactant may include, but is not limited to: alkoxylated surfactants, especially ethoxylates derived from primary alcohols, and blends thereof with more sophisticated surfactants, such as the polyoxypropylene/polyoxyethylene/polyoxypropylene reverse block polymers. Suitable block polyoxyethylene-polyoxypropylene polymeric compounds that meet the requirements may include those based on ethylene glycol, propylene glycol, glycerol, trimethylolpropane and ethylenediamine, and mixtures thereof. Polymeric compounds made from a sequential ethoxylation and propoxylation of initiator compounds with a single reactive hydrogen atom, such as C12- is aliphatic alcohols, do not generally provide satisfactory suds control in Automatic dishwashing compositions. However, certain of the block polymer surfactant compounds designated as PLURONIC(R) and TETRONIC(R) by the BASF-Wyandotte Corp., Wyandotte, Mich., are suitable in Automatic dishwashing compositions. The LFNI surfactant can optionally include a propylene oxide in an amount up to about 15% by weight. Other LFNI surfactants can be prepared by the processes described in U.S. Pat. No. 4,223,163. The LFNI surfactant may also be derived from a straight chain fatty alcohol containing from about 16 to about 20 carbon atoms (C16-C20 alcohol), alternatively a Ci8 alcohol, condensed with an average of from about 6 to about 15 moles, or from about 7 to about 12 moles, and alternatively, from about 7 to about 9 moles of ethylene oxide per mole of alcohol. The ethoxylated nonionic surfactant so derived may have a narrow ethoxylate distribution relative to the average.

In certain embodiments, a LFNI surfactant having a cloud point below 30° C. may be present in an amount from about 0.01% to about 60%, or from about 0.5% to about 10% by weight, and alternatively, from about 1% to about 5% by weight of the composition

In preferred embodiments, the surfactant is a non-ionic surfactant or a non-ionic surfactant system having a phase inversion temperature, as measured at a concentration of 1% in distilled water, between 40 and 70° C., preferably between 45 and 65° C. By a “non-ionic surfactant system” is meant herein a mixture of two or more non-ionic surfactants. Preferred for use herein are non-ionic surfactant systems. They seem to have improved cleaning and finishing properties and stability in product than single non-ionic surfactants. Suitable nonionic surfactants include: i) ethoxylated non-ionic surfactants prepared by the reaction of a monohydroxy alkanol or alkyphenol with 6 to 20 carbon atoms with preferably at least 12 moles particularly preferred at least 16 moles, and still more preferred at least 20 moles of ethylene oxide per mole of alcohol or alkylphenol; ii) alcohol alkoxylated surfactants having a from 6 to 20 carbon atoms and at least one ethoxy and propoxy group. Preferred for use herein are mixtures of surfactants i) and ii).

Another suitable non-ionic surfactants are epoxy-capped poly(oxyalkylated) alcohols represented by the formula:

R₁O[CH₂CH(CH₃)O]_x[CH₂CH₂O]_y[CH₂CH(OH)R₂] (I)

wherein R₁is a linear or branched, aliphatic hydrocarbon radical having from 4 to 18 carbon atoms; R₂is a linear or branched aliphatic hydrocarbon radical having from 2 to 26 carbon atoms; x is an integer having an average value of from 0.5 to 1.5, more preferably about 1; and y is an integer having a value of at least 15, more preferably at least 20.

Preferably, the surfactant of formula I has at least about 10 carbon atoms in the terminal epoxide unit [CH₂CH(OH)R₂]. Suitable surfactants of formula I are Olin Corporation's POLY-TERGENT(R) SLF-18B nonionic surfactants, as described, for example, in WO 94/22800, published Oct. 13, 1994 by Olin Corporation.

Preferably non-ionic surfactants and/or system herein have a Draves wetting time of less than 360 seconds, preferably less than 200 seconds, more preferably less than 100 seconds and especially less than 60 seconds as measured by the Draves wetting method (standard method ISO 8022 using the following conditions; 3-g hook, 5-g cotton skein, 0.1% by weight aqueous solution at a temperature of 25 ° C.). Amine oxides surfactants are also useful in the present invention as anti-redeposition surfactants include linear and branched compounds having the formula:

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wherein R³is selected from an alkyl, hydroxyalkyl, acylamidopropoyl and alkyl phenyl group, or mixtures thereof, containing from 8 to 26 carbon atoms, preferably 8 to 18 carbon atoms; R⁴is an alkylene or hydroxyalkylene group containing from 2 to 3 carbon atoms, preferably 2 carbon atoms, or mixtures thereof; x is from 0 to 5, preferably from 0 to 3; and each R⁵is an alkyl or hydroxyalkyl group containing from 1 to 3, preferably from 1 to 2 carbon atoms, or a polyethylene oxide group containing from 1 to 3, preferable 1, ethylene oxide groups. The R⁵groups can be attached to each other, e.g., through an oxygen or nitrogen atom, to form a ring structure.

These amine oxide surfactants in particular include C₁₀-C₁₈alkyl dimethyl amine oxides and C₈-C₁₈alkoxy ethyl dihydroxyethyl amine oxides. Examples of such materials include dimethyloctylamine oxide, diethyldecylamine oxide, bis-(2-hydroxyethyl)dodecylamine oxide, dimethyldodecylamine oxide, dipropyltetradecylamine oxide, methylethylhexadecylamine oxide, dodecylamidopropyl dimethylamine oxide, cetyl dimethylamine oxide, stearyl dimethylamine oxide, tallow dimethylamine oxide and dimethyl-2-hydroxyoctadecylamine oxide. Preferred are C₁₀-C₁₈alkyl dimethylamine oxide, and C₁₀-C₁₈acylamido alkyl dimethylamine oxide. Surfactants and especially non-ionic surfactants may be present in amounts from 0 to 10% by weight, preferably from 0.1% to 10%, and most preferably from 0.25% to 6%.

In one embodiment, the composition further comprises a sulfonated polymer.

The term “sulfonated polymer” as used herein, refers to polymers containing sulfonic acid or sulfonate functional groups.

The polymer, if used, is used in any suitable amount from about 0.1% to about 20%, preferably from 1% to about 15%, more preferably from 2% to 10% by weight of the composition. Sulfonated/carboxylated polymers are particularly suitable for the compositions contained in the pouch of the invention.

Suitable sulfonated/carboxylated polymers described herein may have a weight average molecular weight of less than or equal to about 100,000 Da, or less than or equal to about 75,000 Da, or less than or equal to about 50,000 Da, or from about 3,000 Da to about 50,000, preferably from about 5,000 Da to about 45,000 Da.

As noted herein, the sulfonated/carboxylated polymers may comprise (a) at least one structural unit derived from at least one carboxylic acid monomer having the general formula (I):

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wherein R¹to R⁴are independently hydrogen, methyl, carboxylic acid group or CH₂COOH and wherein the carboxylic acid groups can be neutralized; (b) optionally, one or more structural units derived from at least one nonionic monomer having the general formula (II):

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wherein R⁵i is hydrogen, C₁to C₆alkyl, or C₁to C₆hydroxyalkyl, and X is either aromatic (with R⁵being hydrogen or methyl when X is aromatic) or X is of the general formula (III):

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wherein R⁶is (independently of R⁵) hydrogen, C₁to C₆alkyl, or C₁to C₆hydroxyalkyl, and Y is 0 or N; and at least one structural unit derived from at least one sulfonic acid monomer having the general formula (IV):

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wherein R⁷is a group comprising at least one sp²bond, A is O, N, P, S or an amido or ester linkage, B is a mono- or polycyclic aromatic group or an aliphatic group, each t is independently 0 or 1 , and M⁺is a cation. In one aspect, R⁷is a C₂to C₆alkene. In another aspect, R⁷is ethene, butene or propene.

Preferred carboxylic acid monomers include one or more of the following: acrylic acid, maleic acid, itaconic acid, methacrylic acid, or ethoxylate esters of acrylic acids, acrylic and methacrylic acids being more preferred. Preferred sulfonated monomers include one or more of the following: sodium (meth) allyl sulfonate, vinyl sulfonate, sodium phenyl (meth) allyl ether sulfonate, or 2-acrylamido-methyl propane sulfonic acid. Preferred non-ionic monomers include one or more of the following: methyl (meth) acrylate, ethyl (meth) acrylate, t-butyl (meth) acrylate, methyl (meth) acrylamide, ethyl (meth) acrylamide, t-butyl (meth) acrylamide, styrene, or [alpha]-methyl styrene.

Preferably, the polymer comprises the following levels of monomers: from about 40 to about 90%, preferably from about 60 to about 90% by weight of the polymer of one or more carboxylic acid monomer; from about 5 to about 50%, preferably from about 10 to about 40% by weight of the polymer of one or more sulfonic acid monomer; and optionally from about 1% to about 30%, preferably from about 2 to about 20% by weight of the polymer of one or more non-ionic monomer. An especially preferred polymer comprises about 70% to about 80% by weight of the polymer of at least one carboxylic acid monomer and from about 20% to about 30% by weight of the polymer of at least one sulfonic acid monomer.

The carboxylic acid is preferably (meth)acrylic acid. The sulfonic acid monomer is preferably one of the following: 2-acrylamido methyl- 1-propanesulfonic acid, 2-methacrylamido-2-methyl- 1-propanesulfonic acid, 3-methacrylamido-2-hydroxypropanesulfonic acid, allysulfonic acid, methallysulfonic acid, allyloxybenzenesulfonic acid, methallyloxybenzensulfonic acid, 2-hydrocy-3 3-(2-propenyloxy)propanesulfonic acid, 2-methyl-2-propene-1-sulfonic acid, styrene sulfonic acid, vinylsulfonic acid, 3-sulfopropyl acrylate, 3-sulfopropyl methacrylate, sulfomethylacrylamid, sulfomethylmethacrylamide, and water soluble salts thereof. The unsaturated sulfonic acid monomer is most preferably 2-acrylamido-2-propanesulfonic acid (AMPS).

Preferred commercial available polymers include: Alcosperse 240, Aquatreat AR 540 and Aquatreat MPS supplied by Alco Chemical; Acumer 3100, Acumer 2000, Acusol 587G and Acusol 588G supplied by Rohm & Haas; Goodrich K-798, K-775 and K-797 supplied by BF Goodrich; and ACP 1042 supplied by ISP technologies Inc. Particularly preferred polymers are Acusol 587G and Acusol 588G supplied by Rohm & Haas.

In the polymers, all or some of the carboxylic or sulfonic acid groups may be present in neutralized form, i.e. the acidic hydrogen atom of the carboxylic and/or sulfonic acid group in some or all acid groups can be replaced with metal ions, preferably alkali metal ions and in particular with sodium ions.

In one embodiment, the composition further comprises a hydrotrope.

The term “hydrotrope” as used herein, refers to a compound that solubilises hydrophobic compounds in aqueous solutions (or oppositely, polar substances in a non-polar environment). Typically, hydrotropes have both hydrophilic and a hydrophobic character (so-called amphiphilic properties as known from surfactants); however the molecular structure of hydrotropes generally do not favor spontaneous self-aggregation, see e.g. review by Hodgdon and Kaler (2007), Current Opinion in Colloid & Interface Science 12: 121-128. Hydrotropes do not display a critical concentration above which self-aggregation occurs as found for surfactants and lipids forming miceller, lamellar or other well defined meso-phases. Instead, many hydrotropes show a continuous-type aggregation process where the sizes of aggregates grow as concentration increases. However, many hydrotropes alter the phase behavior, stability, and colloidal properties of systems containing substances of polar and non-polar character, including mixtures of water, oil, surfactants, and polymers. Hydrotropes are classically used across industries from pharma, personal care, food, to technical applications. Use of hydrotropes in detergent compositions allow for example more concentrated formulations of surfactants (as in the process of compacting liquid detergents by removing water) without inducing undesired phenomena such as phase separation or high viscosity.

The detergent may contain 0-10% by weight, for example 0-5% by weight, such as about 0.5 to about 5%, or about 3% to about 5%, of a hydrotrope. Any hydrotrope known in the art for use in detergents may be utilized. Non-limiting examples of hydrotropes include sodium benzenesulfonate, sodium p-toluene sulfonate (STS), sodium xylene sulfonate (SXS), sodium cumene sulfonate (SCS), sodium cymene sulfonate, amine oxides, alcohols and polyglycolethers, sodium hydroxynaphthoate, sodium hydroxynaphthalene sulfonate, sodium ethylhexyl sulfate, and combinations thereof.

In particular, a composition according to the present invention further comprises a chelator.

The term “chelator” as used herein, refers to chemicals which form molecules with certain metal ions, inactivating the ions so that they cannot react with other elements. Thus, a chelator may be defined as a binding agent that suppresses chemical activity by forming chelates. Chelation is the formation or presence of two or more separate bindings between a ligand and a single central atom. The ligand may be any organic compound, a silicate or a phosphate. In the present context the term “chelating agents” comprises chelants, chelating agent, chelating agents, complexing agents, or sequestering agents that forms water-soluble complexes with metal ions such as calcium and magnesium. The chelate effect describes the enhanced affinity of chelating ligands for a metal ion compared to the affinity of a collection of similar non-chelating ligands for the same metal. Chelating agents having binding capacity with metal ions, in particular calcium (Ca2+) ions, and has been used widely in detergents and compositions in general for wash, such as laundry or dish wash. Chelating agents have however shown themselves to inhibit enzymatic activity. The term chelating agent is used in the present application interchangeably with “complexing agent” or “chelating agent” or “chelant”.

Since most alpha-amylases are calcium sensitive the presence of chelating agents these may impair the enzyme activity. The calcium sensitivity of alpha-amylases may be determined by incubating a given alpha-amylase in the presence of a strong chelating agent and analyze the impact of this incubation on the activity of the alpha-amylase in question. A calcium sensitive alpha-amylase will lose a major part or all of its activity during the incubation. Chelating agent may be present in the composition in an amount from 0.0001 wt % to 20wt %, preferably from 0.01 to 10 wt %, more preferably from 0.1 to 5wt %.

Non-limiting examples of chelating agents are; EDTA, DTMPA, HEDP, EDDS, and citrate. Thus, in one embodiment, the composition comprises a variant according to the invention and a chelating agent, such as EDTA, DTMPA, HEDP, EDDS, or citrate.

The term “EDTA” as used herein, refers to ethylene-diamine-tetra-acetic acid which falls under the definition of “strong chelating agents”.

The term “DTMPA” as used herein, refers to diethylenetriamine penta(methylene phosphonic acid). DTMPA can inhibit the scale formation of carbonate, sulfate and phosphate.

The term “HEDP” as used herein, refers to hydroxy-ethane diphosphonic acid, which falls under the definition of “strong chelating agents”.

The term “EDDS” as used herein, refers to an aminopolycarboxylic acid, which falls under the definition of “strong chelating agents”.

The chelate effect or the chelating effect describes the enhanced affinity of chelating ligands for a metal ion compared to the affinity of a collection of similar nonchelating ligands for the same metal. However, the strength of this chelate effect can be determined by various types of assays or measure methods thereby differentiating or ranking the chelating agents according to their chelating effect (or strength).

In an assay the chelating agents may be characterized by their ability to reduce the concentration of free calcium ions (Ca2+) from 2.0 mM to 0.10 mM or less at pH 8.0, e.g. by using a test based on the method described by M. K. Nagarajan et al., JAOCS, Vol. 61, no. 9 (September 1984), pp. 1475-1478.

For reference, a chelator having the same ability to reduce the concentration of free calcium ions (Ca2+) from 2.0 mM to 0.10 mM at pH as EDTA at equal concentrations of the chelator are said to be strong chelators.

The composition of the present invention may be in any convenient form, e.g., a bar, a homogenous tablet, a tablet having two or more layers, a pouch having one or more compartments, a regular or compact powder, a granule, a paste, a gel, or a regular, compact or concentrated liquid. There are a number of detergent formulation forms such as layers (same or different phases), pouches, as well as forms for machine dosing unit.

Pouches can be configured as single or multicompartments. It can be of any form, shape and material which is suitable for hold the composition, e.g. without allowing the release of the composition from the pouch prior to water contact. The pouch is made from water soluble film which encloses an inner volume. Said inner volume can be divided into compartments of the pouch. Preferred films are polymeric materials preferably polymers which are formed into a film or sheet. Preferred polymers, copolymers or derivatives thereof are selected polyacrylates, and water soluble acrylate copolymers, methyl cellulose, carboxy methyl cellulose, sodium dextrin, ethyl cellulose, hydroxyethyl cellulose, hydroxypropyl methyl cellulose, malto dextrin, poly methacrylates, most preferably polyvinyl alcohol copolymers and, hydroxyprpyl methyl cellulose (HPMC). Preferably the level of polymer in the film for example PVA is at least about 60%. Preferred average molecular weight will typically be about 20,000 to about 150,000. Films can also be of blend compositions comprising hydrolytically degradable and water soluble polymer blends such as polyactide and polyvinyl alcohol (known under the Trade reference M8630 as sold by Chris Craft In. Prod. Of Gary, Ind., US) plus plasticisers like glycerol, ethylene glycerol, Propylene glycol, sorbitol and mixtures thereof. The pouches can comprise a solid laundry cleaning composition or part components and/or a liquid cleaning composition or part components separated by the water soluble film. The compartment for liquid components can be different in composition than compartments containing solids. Ref: (US2009/0011970 A1).

Detergent ingredients may be separated physically from each other by compartments in water dissolvable pouches or in different layers of tablets. Thereby negative storage interaction between components may be avoided. Different dissolution profiles of each of the compartments can also give rise to delayed dissolution of selected components in the wash solution.

A liquid or gel detergent, which is not unit dosed, may be aqueous, typically containing at least 20% by weight and up to 95% water, such as up to about 70% water, up to about 65% water, up to about 55% water, up to about 45% water, up to about 35% water. Other types of liquids, including without limitation, alkanols, amines, diols, ethers and polyols may be included in an aqueous liquid or gel. An aqueous liquid or gel detergent may contain from 0-30% organic solvent. A liquid or gel detergent may be non-aqueous.

Another form of composition is in the form of a soap bar, such as a laundry soap bar, and may be used for hand washing laundry, fabrics and/or textiles. The term “soap bar” as used herein, refers to includes laundry bars, soap bars, combo bars, syndet bars and detergent bars. The types of bar usually differ in the type of surfactant they contain, and the term laundry soap bar includes those containing soaps from fatty acids and/or synthetic soaps. The laundry soap bar has a physical form which is solid and not a liquid, gel or a powder at room temperature. The term “solid” as used herein, refers to a physical form which does not significantly change over time, i.e. if a solid object (e.g. laundry soap bar) is placed inside a container, the solid object does not change to fill the container it is placed in. The bar is a solid typically in bar form but can be in other solid shapes such as round or oval.

The soap bar may also comprise complexing agents like EDTA and HEDP, perfumes and/or different type of fillers, surfactants e.g. anionic synthetic surfactants, builders, polymeric soil release agents, detergent chelators, stabilizing agents, fillers, dyes, colorants, dye transfer inhibitors, alkoxylated polycarbonates, suds suppressers, structurants, binders, leaching agents, bleaching activators, clay soil removal agents, anti-redeposition agents, polymeric dispersing agents, brighteners, fabric softeners, perfumes and/or other compounds known in the art.

The soap bar may be processed in conventional laundry soap bar making equipment such as but not limited to: mixers, plodders, e.g. a two stage vacuum plodder, extruders, cutters, logo-stampers, cooling tunnels and wrappers. The invention is not limited to preparing the soap bars by any single method. The premix of the invention may be added to the soap at different stages of the process. For example, the premix comprising a soap, an enzyme, optionally one or more additional enzymes, a protease inhibitor, and a salt of a monovalent cation and an organic anion may be prepared and the mixture may then plodded. The enzyme and optional additional enzymes may be added at the same time as an enzyme inhibitor, e.g. a protease inhibitor, for example in liquid form. Besides the mixing step and the plodding step, the process may further comprise the steps of milling, extruding, cutting, stamping, cooling and/or wrapping.

In one embodiment, the composition comprises a builder and/or a co-builder.

The term “builder” as used herein, refers to specific type of a chelating agent. Accordingly, the composition may comprise about 0-65% by weight, such as about 5% to about 50% of a detergent builder or co-builder, or a mixture thereof. In a dish wash detergent, the level of builder is typically 40-65%, particularly 50-65%. The builder and/or co-builder may particularly be a chelating agent that forms water-soluble complexes with Ca and Mg. Any builder and/or co-builder known in the art for use in ADW detergents may be utilized. Non-limiting examples of builders include zeolites, diphosphates (pyrophosphates), triphosphates such as sodium triphosphate (STP or STPP), carbonates such as sodium carbonate, soluble silicates such as sodium metasilicate, layered silicates (e.g., SKS-6 from Hoechst), ethanolamines such as 2-aminoethan-1-ol (MEA), diethanolamine (DEA, also known as 2,2′-iminodiethan-1-ol), triethanolamine (TEA, also known as 2,2′,2″-nitrilotriethan-1-ol), and (carboxymethyl)inulin (CMI), and combinations thereof.

The detergent composition may also comprise 0-50% by weight, such as about 5% to about 30%, of a detergent co-builder. The detergent composition may include a co-builder alone, or in combination with a builder, for example a zeolite builder. Non-limiting examples of co-builders include homopolymers of polyacrylates or copolymers thereof, such as poly(acrylic acid) (PAA) or copoly(acrylic acid/maleic acid) (PAA/PMA). Further non-limiting examples include citrate, chelators such as aminocarboxylates, aminopolycarboxylates and phosphonates, and alkyl- or alkenylsuccinic acid. Additional specific examples include 2,2′,2″-nitrilotriacetic acid (NTA), ethylenediaminetetraacetic acid (EDTA), diethylenetriaminepentaacetic acid (DTPA), iminodisuccinic acid (IDS), ethylenediamine-N,N′-disuccinic acid (EDDS), methylglycinediacetic acid (MGDA), glutamic acid-N,N-diacetic acid (GLDA), 1-hydroxyethane-1,1-diphosphonic acid (HEDP), ethylenediaminetetra(methylenephosphonic acid) (EDTMPA), diethylenetriaminepentakis(methylenephosphonic acid) (DTMPA or DTPMPA), N-(2-hydroxyethyl)iminodiacetic acid (EDG), aspartic acid-N-monoacetic acid (ASMA), aspartic acid-N,N-diacetic acid (ASDA), aspartic acid-N-monopropionic acid (ASMP), iminodisuccinic acid (IDA), N-(2-sulfomethyl)-aspartic acid (SMAS), N-(2-sulfoethyl)-aspartic acid (SEAS), N-(2-sulfomethyl)-glutamic acid (SMGL), N-(2-sulfoethyl)-glutamic acid (SEGL), N-methyliminodiacetic acid (MIDA), α-alanine-N,N-diacetic acid (α-ALDA), serine-N,N-diacetic acid (SEDA), isoserine-N,N-diacetic acid (ISDA), phenylalanine-N,N-diacetic acid (PHDA), anthranilic acid-N,N-diacetic acid (ANDA), sulfanilic acid-N,N-diacetic acid (SLDA) , taurine-N,N-diacetic acid (TUDA) and sulfomethyl-N,N-diacetic acid (SMDA), N-(2-hydroxyethyl)ethylenediamine-N,N,N″-triacetic acid (HEDTA), diethanolglycine (DEG), diethylenetriamine penta(methylenephosphonic acid) (DTPMP), aminotris(methylenephosphonic acid) (ATMP), and combinations and salts thereof. Further exemplary builders and/or co-builders are described in, e.g., WO 09/102854, US 5977053.

In one embodiment, the composition comprises a polymer. The composition may comprise 0-10% by weight, such as 0.5-5%, 2-5%, 0.5-2% or 0.2-1% of a polymer. Any polymer known in the art for use in detergents may be utilized. The polymer may function as a co-builder as mentioned above, or may provide antiredeposition, fiber protection, soil release, dye transfer inhibition, grease cleaning and/or anti-foaming properties. Some polymers may have more than one of the above-mentioned properties and/or more than one of the below-mentioned motifs. Exemplary polymers include (carboxymethyl)cellulose (CMC), poly(vinyl alcohol) (PVA), poly(vinylpyrrolidone) (PVP), poly(ethyleneglycol) or poly(ethylene oxide) (PEG), ethoxylated poly(ethyleneimine), carboxymethyl inulin (CMI), and polycarboxylates such as PAA, PAA/PMA, poly-aspartic acid, and lauryl methacrylate/acrylic acid copolymers , hydrophobically modified CMC (HM-CMC) and silicones, copolymers of terephthalic acid and oligomeric glycols, copolymers of poly(ethylene terephthalate) and poly(oxyethene terephthalate) (PET-POET), PVP, poly(vinylimidazole) (PVI), poly(vinylpyridine-N-oxide) (PVPO or PVPNO) and polyvinylpyrrolidone-vinylimidazole (PVPVI). Further exemplary polymers include sulfonated polycarboxylates, polyethylene oxide and polypropylene oxide (PEO-PPO) and diquaternium ethoxy sulfate. Other exemplary polymers are disclosed in, e.g., WO 2006/130575. Salts of the above-mentioned polymers are also contemplated.

The compositions according to the present invention may comprise a variant of the present invention as the major enzymatic component, e.g., a mono-component composition. In another embodiment, the composition comprises at least one additional enzyme, such as a protease, lipase, cellulose, pectate lyase, and/or mannanase. Thus, the compositions may comprise multiple enzymatic activities, such as one or more (e.g., several) enzymes selected from the group consisting of hydrolase, isomerase, ligase, lyase, oxidoreductase, or transferase, e.g., an alpha-galactosidase, alpha-glucosidase, aminopeptidase, amylase, beta-galactosidase, beta-glucosidase, beta-xylosidase, carbohydrase, carboxypeptidase, catalase, cellobiohydrolase, cellulase, chitinase, cutinase, cyclodextrin glycosyltransferase, deoxyribonuclease, endoglucanase, esterase, glucoamylase, invertase, laccase, lipase, mannosidase, mutanase, oxidase, pectinolytic enzyme, peroxidase, phytase, polyphenoloxidase, proteolytic enzyme, ribonuclease, transglutaminase, or xylanase.

In a particular embodiment, the composition further comprises one or more additional enzymes selected from the following group:

(i) an alpha-amylase comprising a modifications in the following position: 202 as compared with the alpha-amylase in SEQ ID NO:5;

(ii) an alpha-amylase comprising one or more modifications in the following positions: 9, 118, 149, 182, 186, 195, 202, 257, 295, 299, 320, 323, 339, 345, and 458 as compared with the alpha-amylase in SEQ ID NO:6;

(iii) an alpha-amylase comprising one or more modification in the following positions: 405, 421, 422, and 428 as compared with the alpha-amylase in SEQ ID NO: 9;

(iv) an alpha-amylase comprising any one the amino acid sequences set forth in SEQ ID NO: 7, 10, 11, and 12; and/or

(v) a protease comprising one or more modifications in the following positions: 32, 33, 48-54, 58-62, 94-107, 116, 123-133, 150, 152-156, 158-161, 164, 169, 175-186, 197, 198, 203-216 as compared with the protease in SEQ ID NO:8.

In general the properties of the selected 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.

In one embodiment, the composition comprises or consists of an alpha-amylase variant comprising or consisting of the following modifications; G182*+D183*+M202L, wherein numbering is according to SEQ ID NO: 3 and an alpha-amylase comprising a modification in the following position: 202 as compared with the alpha-amylase in SEQ ID NO:5.

In one embodiment, the composition comprises or consists of an alpha-amylase variant comprising or consisting of the following modifications; G182*+D183*+N195F+M202L, wherein numbering is according to SEQ ID NO: 3 and an alpha-amylase comprising a modifications in the following position: 202 as compared with the alpha-amylase in SEQ ID NO:5.

In one embodiment, the composition comprises or consists of an alpha-amylase variant comprising or consisting of the following modifications; G182*+D183*+M202L, wherein numbering is according to SEQ ID NO: 3 and an alpha-amylase comprising one or more modifications in the following positions: 9, 118, 149, 182, 186, 195, 202, 257, 295, 299, 320, 323, 339, 345, and 458 as compared with the alpha-amylase in SEQ ID NO:6.

In one embodiment, the composition comprises or consists of an alpha-amylase variant comprising or consisting of the following modifications; G182*+D183*+N195F+M202L, wherein numbering is according to SEQ ID NO: 3 and an alpha-amylase comprising one or more modifications in the following positions: 9, 118, 149, 182, 186, 195, 202, 257, 295, 299, 320, 323, 339, 345, and 458 as compared with the alpha-amylase in SEQ ID NO:6.

In one embodiment, the composition comprises or consists of an alpha-amylase variant comprising or consisting of the following modifications; G182*+D183*+M202L, wherein numbering is according to SEQ ID NO: 3 and an alpha-amylase comprising one or more modification in the following positions: 405, 421, 422, and 428 as compared with the alpha-amylase in SEQ ID NO: 9.

In one embodiment, the composition comprises or consists of an alpha-amylase variant comprising or consisting of the following modifications; G182*+D183*+N195F+M202L, wherein numbering is according to SEQ ID NO: 3 and an alpha-amylase comprising one or more modification in the following positions: 405, 421, 422, and 428 as compared with the alpha-amylase in SEQ ID NO: 9.

In one embodiment, the composition comprises or consists of an alpha-amylase variant comprising or consisting of the following modifications; G182*+D183*+M202L, wherein numbering is according to SEQ ID NO: 3 and an alpha-amylase comprising any one the amino acid sequences set forth in SEQ ID NO: 7, 10, 11, and 12.

In one embodiment, the composition comprises or consists of an alpha-amylase variant comprising or consisting of the following modifications; G182*+D183*+N195F+M202L, wherein numbering is according to SEQ ID NO: 3 and an alpha-amylase comprising any one the amino acid sequences set forth in SEQ ID NO: 7, 10, 11, and 12.

In one embodiment, the composition comprises or consists of an alpha-amylase variant comprising or consisting of the following modifications; G182*+D183*+M202L, wherein numbering is according to SEQ ID NO: 3 and a protease comprising one or more modifications in the following positions: 32, 33, 48-54, 58-62, 94-107, 116, 123-133, 150, 152-156, 158-161, 164, 169, 175-186, 197, 198, 203-216 as compared with the protease in SEQ ID NO:8.

In one embodiment, the composition comprises or consists of an alpha-amylase variant comprising or consisting of the following modifications; G182*+D183*+N195F+M202L, wherein numbering is according to SEQ ID NO: 3 and a protease comprising one or more modifications in the following positions: 32, 33, 48-54, 58-62, 94-107, 116, 123-133, 150, 152-156, 158-161, 164, 169, 175-186, 197, 198, 203-216 as compared with the protease in SEQ ID NO:8.

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 U.S. Pat. No. 4,435,307, U.S. Pat. No. 5,648,263, U.S. Pat. No. 5,691,178, U.S. Pat. No. 5,776,757 and WO 89/09259.

Especially suitable cellulases are the alkaline or neutral cellulases having color care benefits. Examples of such cellulases are cellulases described in EP 0 495 257, EP 0 531 372,

WO 96/11262, WO 96/29397, WO 98/08940. Other examples are cellulase variants such as those described in WO 94/07998, EP 0 531 315, U.S. Pat. No. 5,457,046, U.S. Pat. No. 5,686,593, U.S. Pat. No. 5,763,254, WO 95/24471, WO 98/12307 and PCT/DK98/00299.

Example of cellulases exhibiting endo-beta-1,4-glucanase activity (EC 3.2.1.4) are those having described in WO02/099091.

Other examples of cellulases include the family 45 cellulases described in WO96/29397, and especially variants thereof having substitution, insertion and/or deletion at one or more of the positions corresponding to the following positions in SEQ ID NO: 8 of WO 02/099091: 2, 4, 7, 8, 10, 13, 15, 19, 20, 21, 25, 26, 29, 32, 33, 34, 35, 37, 40, 42, 42a, 43, 44, 48, 53, 54, 55, 58, 59, 63, 64, 65, 66, 67, 70, 72, 76, 79, 80, 82, 84, 86, 88, 90, 91, 93, 95, 95d, 95h, 95j, 97, 100, 101, 102, 103, 113, 114, 117, 119, 121, 133, 136, 137, 138, 139, 140a, 141, 143a, 145, 146, 147, 150e, 150j, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160c, 160e, 160k, 161, 162, 164, 165, 168, 170, 171, 172, 173, 175, 176, 178, 181, 183, 184, 185, 186, 188, 191, 192, 195, 196, 200, and/or 20, preferably selected among P19A, G20K, Q44K, N48E, Q119H or Q146 R.

Commercially available cellulases include Celluzyme, and Carezyme (Novozymes NS), Clazinase, and Puradax HA (Genencor International Inc.), and KAC-500(B) (Kao Corporation).

Suitable lipases and cutinases include those of bacterial or fungal origin. Chemically modified or protein engineered mutant enzymes are included. Examples include lipase from Thermomyces, e.g. from T. lanuginosus (previously named Humicola lanuginosa) as described in EP258068 and EP305216, cutinase from Humicola, e.g. H. insolens (WO96/13580), lipase from strains of Pseudomonas (some of these now renamed to Burkholderia), e.g. P. alcaligenes or P. pseudoalcaligenes (EP218272), P. cepacia (EP331376), P. sp. strain SD705 (WO95/06720 & WO96/27002), P. wisconsinensis (W096/12012), GDSL-type Streptomyces lipases (WO10/065455), cutinase from Magnaporthe grisea (WO10/107560), cutinase from Pseudomonas mendocina (U.S. Pat. No. 5,389,536), lipase from Thermobifida fusca (WO11/084412), Geobacillus stearothermophilus lipase (WO11/084417), lipase from Bacillus subtilis (WO11/084599), and lipase from Streptomyces griseus (WO11/150157) and S. pristinaespiralis (WO12/137147).

Further examples are lipases sometimes referred to as acyltransferases or perhydrolases, e.g. acyltransferases with homology to Candida antarctica lipase A (WO010/111143), acyltransferase from Mycobacterium smegmatis (WO005/56782), perhydrolases from the CE 7 family (WO009/67279), and variants of the M. smegmatis perhydrolase in particular the S54V variant used in the commercial product Gentle Power Bleach from Huntsman Textile Effects Pte Ltd (WO010/100028).

Other examples are lipase variants such as those described in EP407225, WO92/05249, WO94/01541, WO94/25578, WO95/14783, WO95/30744, WO95/35381, WO95/22615, WO96/00292, WO97/04079, WO97/07202, WO00/34450, WO00/60063, WO01/92502, WO07/87508 and WO09/109500.

Preferred commercial lipase products include Lipolase™, Lipex™; Lipolex™ and Lipoclean™ (Novozymes NS), Lumafast (originally from Genencor) and Lipomax (originally from Gist-Brocades).

Suitable 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 NS).

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, for example, as a granulate, liquid, 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 U.S. Pat. Nos. 4,106,991 and 4,661,452 and may optionally be coated by methods known in the art. Examples of 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. Examples of film-forming coating materials suitable for application by fluid bed techniques are given in GB 1483591. 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 compositions may be prepared in accordance with methods known in the art and may be in the form of a liquid or a dry composition. The compositions may be stabilized in accordance with methods known in the art.

Any detergent components known in the art for use in ADW detergents may also be utilized. Other optional detergent components include anti-corrosion agents, anti-shrink agents, anti-soil redeposition agents, anti-wrinkling agents, bactericides, binders, corrosion inhibitors, disintegrants/disintegration agents, dyes, enzyme stabilizers (including boric acid, borates, CMC, and/or polyols such as propylene glycol), fabric conditioners including clays, fillers/processing aids, fluorescent whitening agents/optical brighteners, foam boosters, foam (suds) regulators, perfumes, soil-suspending agents, softeners, suds suppressors, tarnish inhibitors, and wicking agents, either alone or in combination. Any ingredient known in the art for use ADW detergents may be utilized. The choice of such ingredients is well within the skill of the artisan.

The compositions of the present invention may also comprise dispersants. In particular powdered detergents may comprise dispersants. Suitable water-soluble organic materials include the homo- or co-polymeric acids or their salts, in which the polycarboxylic acid comprises at least two carboxyl radicals separated from each other by not more than two carbon atoms. Suitable dispersants are for example described in Powdered Detergents, Surfactant science series volume 71, Marcel Dekker, Inc.

The compositions of the present invention may also comprise one or more dye transfer inhibiting agents. Suitable polymeric dye transfer inhibiting agents include, but are not limited to, polyvinylpyrrolidone polymers, polyamine N-oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinyloxazolidones and polyvinylimidazoles or mixtures thereof. When present in a subject composition, the dye transfer inhibiting agents may be present at levels from about 0.0001% to about 10%, from about 0.01% to about 5% or even from about 0.1% to about 3% by weight of the composition.

The compositions of the present invention will preferably also contain additional components that may tint articles being cleaned, such as fluorescent whitening agent or optical brighteners. Where present the brightener is preferably at a level of about 0.01% to about 0.5%. Any fluorescent whitening agent suitable for use in a laundry detergent composition may be used in the composition of the present invention. The most commonly used fluorescent whitening agents are those belonging to the classes of diaminostilbene-sulfonic acid derivatives, diarylpyrazoline derivatives and bisphenyl-distyryl derivatives. Examples of the diaminostilbene-sulfonic acid derivative type of fluorescent whitening agents include the sodium salts of: 4,4′-bis-(2-diethanolamino-4-anilino-s-triazin-6-ylamino) stilbene-2,2′-disulfonate, 4,4′-bis-(2,4-dianilino-s-triazin-6-ylamino) stilbene-2.2′-disulfonate, 4,4′-bis-(2-anilino-4-(N-methyl-N-2-hydroxy-ethylamino)-s-triazin-6-ylamino) stilbene-2,2′-disulfonate, 4,4′-bis-(4-phenyl-1,2,3-triazol-2-yl)stilbene-2,2′-disulfonate and sodium 5-(2H-naphtho[1,2-d][1,2,3]triazol-2-yl)-2-[(E)-2-phenylvinyl]benzenesulfonate. Preferred fluorescent whitening agents are Tinopal DMS and Tinopal CBS available from Ciba-Geigy AG, Basel, Switzerland. Tinopal DMS is the disodium salt of 4,4′-bis-(2-morpholino-4-anilino-s-triazin-6-ylamino) stilbene-2,2′-disulfonate. Tinopal CBS is the disodium salt of 2,2′-bis-(phenyl-styryl)-disulfonate. Also preferred are fluorescent whitening agents is the commercially available Parawhite KX, supplied by Paramount Minerals and Chemicals, Mumbai, India. Other fluorescers suitable for use in the invention include the 1-3-diary) pyrazolines and the 7-alkylaminocoumarins. Suitable fluorescent brightener levels include lower levels of from about 0.01, from 0.05, from about 0.1 or even from about 0.2 wt % to upper levels of 0.5 or even 0.75 wt %.

Uses

The present invention further relates to the use of a variant according to the present invention in a cleaning process such as laundry or hard surface cleaning including automated dish wash and industrial cleaning. The soils and stains that are important for cleaning are composed of many different substances, and a range of different enzymes, all with different substrate specificities, have been developed for use in detergents both in relation to laundry and hard surface cleaning, such as dishwashing. These enzymes are considered to provide an enzyme detergency benefit, since they specifically improve stain removal in the cleaning process that they are used in, compared to the same process without enzymes. Stain removing enzymes that are known in the art include enzymes such as proteases, amylases, lipases, cutinases, cellulases, endoglucanases, xyloglucanases, pectinases, pectin lyases, xanthanases, peroxidaes, haloperoxygenases, catalases and mannanases.

In one embodiment, the invention relates the use of variants of the present invention in detergent compositions, for use in cleaning hard-surfaces, such as dish wash, or in laundering or for stain removal. In another embodiment, the invention relates to the use of a variant according to the invention in a cleaning process such as laundry or hard surface cleaning including, but not limited to, dish wash and industrial cleaning. Thus, in one embodiment, the invention relates to the use of a variant comprising a substitution in one or more positions providing oxidation stability of the variant.

In a particular embodiment, the variant comprising a substitution in the position corresponding to position M202 of the amino acid sequence as set forth in SEQ ID NO: 3, and a substitution and/or deletion of two, three, or four positions corresponding to positions R181, G182, D183, and G184 of the amino acid sequence as set forth in SEQ ID NO: 3.

In one embodiment of the invention relates the use of a composition according to the invention comprising a variant of the present invention together with one or more surfactants and optionally one or more detergent components, selected from the list comprising of hydrotropes, builders and co-builders, bleaching systems, polymers, fabric hueing agents and adjunct materials, or any mixture thereof in detergent compositions and in detergent applications.

A further embodiment is the use of the composition according to the invention comprising a variant of the present invention together with one or more surfactants, and one or more additional enzymes selected from the group comprising of proteases, lipases, cutinases, cellulases, endoglucanases, xyloglucanases, pectinases, pectin lyases, xanthanases, peroxidaes, haloperoxygenases, catalases and mannanases, or any mixture thereof in detergent compositions and in detergent applications.

In another aspect, the invention relates to a laundering process which may be for household laundering as well as industrial laundering. Furthermore, the invention relates to a process for the laundering of textiles (e.g. fabrics, garments, cloths etc.) where the process comprises treating the textile with a washing solution containing a detergent composition and an alpha-amylase of the present invention. The laundering can for example be carried out using a household or an industrial washing machine or be carried out by hand using a detergent composition containing a glucoamylase of the invention.

In another aspect, the invention relates to a dish wash process which may be for household dish wash as well as industrial dish wash. The term “dish wash” as used herein, refers to both manual dish wash and automated dish wash. Furthermore, the invention relates to a process for the washing of hard surfaces (e.g. cutlery such as knives, forks, spoons; crockery such as plates, glasses, bowls; and pans) where the process comprises treating the hard surface with a washing solution containing a detergent composition and an alpha-amylase variant of the present invention. The hard surface washing can for example be carried out using a household or an industrial dishwasher or be carried out by hand using a detergent composition containing an alpha-amylase of the invention, optionally together with one or more further enzymes selected from the group comprising of proteases, amylases, lipases, cutinases, cellulases, endoglucanases, xyloglucanases, pectinases, pectin lyases, xanthanases, peroxidaes, haloperoxygenases, catalases, mannanases, or any mixture thereof.

In a further aspect, the invention relates to a method for removing a stain from a surface comprising contacting the surface with a composition comprising an alpha-amylase of the present invention together with one or more surfactants and optionally one or more detergent components selected from the list comprising of hydrotropes, builders and co-builders, bleaching systems, polymers, fabric hueing agents and adjunct materials, or any mixture thereof in detergent compositions and in detergent applications. A further aspect is a method for removing a stain from a surface comprising contacting the surface with a composition comprising an alpha-amylase variant of the present invention together with one or more surfactants, one or more additional enzymes selected from the group comprising of proteases, lipases, cutinases, cellulases, endoglucanases, xyloglucanases, pectinases, pectin lyases, xanthanases, peroxidaes, haloperoxygenases, catalases and mannanases, or any mixture thereof in detergent compositions and in detergent applications.

The present invention is further described by the following examples that should not be construed as limiting the scope of the invention.

EXAMPLES
Example 1
Generation of Variants

Using the parent alpha-amylase having the amino acid sequence as set forth in SEQ ID NO: 4, the variants of the present invention were constructed. The variants were prepared by standard procedures, which in brief is; introducing an amino acid substitution in the position corresponding to position M200 of the amino acid sequence as set forth in SEQ ID NO: 4 (if numbering is according to SEQ ID NO: 3, the amino acid position is M202), by site-directed mutagenesis into the gene, transforming Bacillus subtilis host cells with the mutated gene, fermenting the transformed cells (e.g. as described in Example 1 of WO 2004/111220), and purifying the variants from the fermentation broth. The reference amylase, i.e. the parent alpha-amylase, having the amino acid sequence as set forth in SEQ ID NO: 3 or 4, respectively, were produced recombinantly in Bacillus subtilis in a similar manner.

Example 2
Determination of Amylolytic Activity (Alpha-Amylase Activity)

The variants generated as described in Example 1 were tested for alpha-amylase activity by a pNP-G7 assay.

The alpha-amylase activity was determined by employing the pNP-G7 substrate (PNP-G7 the abbreviation for 4,6-ethylidene(G7)-p-nitrophenyl(G1)-α,D-maltoheptaoside, a blocked oligosaccharide which is cleaved by an endo-amylase, such as an alpha-amylase).

An antibody was diluted in Phosphate buffered saline (PBS) (0.010 M Phosphate buffer pH7.4, 0.0027M KCl, 0.14M NaCl) buffer to concentration of 10 μg/ml. A maxisorp microtiter plate was coated with antibody by adding 100 μl diluted antibody (10 μg/ml) to each well and incubated for 1 h at room temperature (RT) and mixing at 800 rpm. After incubation the microtiter plate was washed (using Bio-Tek ELx405 ELISA washer) with 3×200 μl Phosphate buffered saline with 0.05% Tween (PBST) (0.010 M Phosphate buffer pH7.4, 0.0027M KCl, 0.14M NaCl, 0.05% Tween 20) buffer.

Microtiter plates with the alpha-amylase variants culture broths were spun down and supernatants transferred to new microtiter plates and diluted 4× in PBST buffer. 100 μl diluted supernatant was transferred to antibody coated maxisorp microtiter plate and incubated for 1 h at RT and mixing at 800rpm. After incubation microtiter plates were washed in PBST buffer (3×200 μl, ELISA washer).

Upon the cleavage of the pNP-G7 substrate, the alpha-Glucosidase included in the kit used is digested and the hydrolysed substrate liberates a free pNP molecule which has a yellow color and thus can be measured by visible spectophometry at Abs=405nm (400-420 nm.). Kits containing pNP-G7 substrate and alpha-Glucosidase are manufactured by Roche/Hitachi (cat. No. 11876473). 100p1 pNP-G7 substrate was added to all wells and mixed for 1 minute before measuring absorbance at 405nm. The slope (absorbance per minute) is determined and only the linear range of curve is used.

Results were compared to a reference sample and samples with an activity on par or higher were considered to have a maintained alpha-amylase activity. Such variants were further evaluated for oxidation stability, as described in Example 3.

The specific alpha-amylase activity may also be determined by other activity assays, such as amylazyme activity assay, Phadebas activity assay, or reducing sugar activity assay as described below.

Amylazyme activity assay (from Megazyme, Ireland): An Amylazyme tablet includes interlinked amylose polymers that are in the form of globular microspheres that are insoluble in water. A blue dye is covalently bound to these microspheres. The interlinked amylose polymers in the microsphere are degraded at a speed that is proportional to the alpha-amylase activity. When the alpha-amylase degrades the amylose polymers, the released blue dye is water soluble and concentration of dye can be determined by measuring absorbance at 650 nm. The concentration of blue is proportional to the alpha-amylase activity in the sample.

The amylase sample to be analysed is diluted in activity buffer with the desired pH. One substrate tablet is suspended in 5 mL activity buffer and mixed on magnetic stirrer. During mixing of substrate transfer 150 μl to microtiter plate (MTP). Add 30 μl diluted amylase sample to 150 μl substrate and mix. Incubate for 15 minutes at 37° C. The reaction is stopped by adding 30 μl M NaOH and mix. Centrifuge MTP for 5 minutes at 4000× g. Transfer 100 μl to new MTP and measure absorbance at 620 nm.

The amylase sample should be diluted so that the absorbance at 650 nm is between 0 and 2.2, and is within the linear range of the activity assay.

Phadebas activity assay (from for example Magle Life Sciences, Lund, Sweden): A Phadebas tablet includes interlinked starch polymers that are in the form of globular microspheres that are insoluble in water. A blue dye is covalently bound to these microspheres. The interlinked starch polymers in the microsphere are degraded at a speed that is proportional to the alpha-amylase activity. When the alpha-amylase degrades the starch polymers, the released blue dye is water soluble and concentration of dye can be determined by measuring absorbance at 650 nm. The concentration of blue is proportional to the alpha-amylase activity in the sample.

The amylase sample should be diluted so that the absorbance at 650 nm is between 0 and 2.2, and is within the linear range of the activity assay.

Reducing sugar activity assay: The number of reducing ends formed by the alpha-amylase hydrolysing the alpha-1,4-glycosidic linkages in starch is determined by reaction with p-Hydroxybenzoic acid hydrazide (PHBAH). After reaction with PHBAH the number of reducing ends can be measured by absorbance at 405 nm and the concentration of reducing ends is proportional to the alpha-amylase activity in the sample.

The corns starch substrate (3 mg/ml) is solubilised by cooking for 5 minutes in milliQ water and cooled down before assay. For the stop solution prepare a Ka-Na-tartrate/NaOH solution (K-Na-tartrate (Merck 8087) 50 g/l, NaOH 20 g/l) and prepare freshly the stop solution by adding p-Hydroxybenzoic acid hydrazide (PHBAH, Sigma H9882) to Ka-Na-tartrate/NaOH solution to 15 mg/ml.

In PCR-MTP 50 μl activity buffer is mixed with 50 μl substrate. Add 50 μl diluted enzyme and mix. Incubate at the desired temperature in PCR machine for 5 minutes. Reaction is stopped by adding 75 μl stop solution (Ka-Na-tartrate/NaOH/PH BAH). Incubate in PCR machine for 10 minutes at 95° C. Transfer 150 μl to new MTP and measure absorbance at 405nm.

The amylase sample should be diluted so that the absorbance at 405 nm is between 0 and 2.2, and is within the linear range of the activity assay.

Example 3
Oxidation Stability Verified by AMSA

In order to assess the oxidation stability of the variants generated as described in Example 1, the wash performance of the variants in a detergent composition comprising an oxidizing agent, such as a bleaching system, was determined by using Automatic Mechanical

Stress Assay (AMSA). A variant which is oxidation stable will have a maintained wash performance, and even may have an improved wash performance.

The variants of the present invention were, thus, tested for the wash performance. By use of 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 in a regular, periodic oscillating manner. For further description see WO 02/42740, especially the paragraph “Special method embodiments” at page 23-24.

General Wash Performance Description

The detergent solution used for the AMSA test comprising water (15° dH), 8.67 g/L Model Z detergent composition and the enzyme of the invention at concentration of 0, 0.1 or 0.2 mg enzyme protein/L, was prepared. Fabrics stained with starch (CS-28 from Center For Test materials BV, P.O. Box 120, 3133 KT, Vlaardingen, The Netherlands) was added and washed for 20 minutes at 55° C. After thorough rinse under running tap water and drying in the dark, the light intensity values of the stained fabrics were subsequently measured as a measure for wash performance. The test with 0 mg enzyme protein/L is used as a blank and corresponds to the contribution from the detergent composition. The mechanical action was applied during the wash step, e.g. in the form of shaking, rotating or stirring the wash solution with the fabrics. The AMSA wash performance experiments were conducted under the experimental conditions specified below:

TABLE 1

Experimental condition

Detergent
Model detergent Z (see Table 2)

Detergent dosage
8.67
g/L

Test solution volume
160
micro L

pH
pH 10.4-10.5

Wash time
20
minutes

Temperature
55°
C.

Water hardness
15°
dH

Enzyme concentration in test
0.1 or 0.2
mg/L

Test material
CS-28 (Rice starch cotton)

TABLE 2

Model detergent Z with bleach

Content of
% active

compound
component

Compound
(% w/w)
(% w/w)

LAS, sodium salt
7.03
6.0

Soap
1.08
1.0

AEO*
1.51
1.5

Sodium carbonate
20.10
20.0

Sodium (di)silicate
9.99
8.0

Zeolite A
5.00
4.0

HEDP-Na4
0.24
0.2

Sodium citrate
2.01
2.0

Polycarboxylate (PCA)
1.09
1.0

Sodium paercarbonate
9.33
8.0

TAED
1.09
1.0

Na₂SO₄
41.54
41.5

*AEO is added separately before wash.

Notice the balance up to 100% and extra contributions to sodium carbonate and sodium sulphate. The balance is water 5 ca. 2.6% (from LAS ca. 0.1%; from Sodium (di)silicate ca. 1.6%; from Zeolite A ca. 0.8%; from Polycarboxylate ca. 0.1%); sodium sulfate 5 ca. 0.9% (from LAS, sodium salt probably ca. 0.8%; from Zeolite A ca. 0.1%); sodium carbonate probably ca. 1.1% from Sodium percarbonate; and CMC (carboxymethylcellulose, sodium salt), ca. 0.2% from TAED.

Water hardness was adjusted to 15° dH by addition of CaCl₂, MgCl₂, and NaHCO₃

(Ca²⁺:Mg²⁺:HCO³⁻=4:1:7.5) to the test system. After washing the textiles were flushed in tap water and dried.

Relative Performance to Parent alpha-amylase in AMSA 20 min 55° C. model detergent Z with bleach

0.1 mg
0.2 mg

Mutations
enzyme/L
enzyme/L

Blank
−0.2
0.0

G182* + D183*
1.0
1.0

G182* + D183* + N195F
0.9
1.1

G182* + D183* + N195F + M202L
1.8
1.6

Specifically, the variants of the present invention is considered to be particularly efficient in the ADW use. Thus, in order to further evaluate this, an AMSA for ADW performance may be performed. Such an AMSA for ADW may be performed under the following conditions;

A test solution comprising water (15° dH), 8.67 g/L detergent, e.g. Liquid model detergent containing phosphate, as described below, and the variants of the invention at concentration of 0 or 0.5 mg enzyme protein/L, may be prepared. Melamine plates stained with mixed starch (DM-177 from Center For Test materials BV, P.O. Box 120, 3133 KT, Vlaardingen, The Netherlands) can be added and washed for 20 minutes at 55° C. After short rinse under running tap water and drying in the dark, the light intensity values of the stained plates are subsequently measured as a measure for wash performance. The test with 0 mg enzyme protein/L may be used as a blank and corresponds to the contribution from the detergent. Preferably mechanical action is applied during the wash step, e.g. in the form of shaking, rotating or stirring the wash solution with the plates. The AMSA automatic dish wash performance experiments may be conducted under the experimental conditions specified below:

TABLE 3

Experimental condition

Detergent
Liquid model detergent containing

phosphate (see Table 4)

Detergent dosage
5
mL/L

Test solution volume
160
micro L

pH
~8

Wash time
20
minutes

Temperature
50°
C.

Water hardness
21°
dH

Enzyme concentration in test
0.01-0.24
mg/L

Test material
Melamine plates (Mixed Starch)

TABLE 4

Liquid model automatic dish wash detergent containing phosphate

Content of

compound

Compound
(% w/w)

STPP
50.0

Sodium carbonate
20.0

Sodium percarbonate
10.0

Sodium disilicate
5.0

TAED
2.0

Sokalan CP5 (39.5%)
5.0

Surfac 23-6.5 (100%)
2.0

Sodium Sulfate
6.0

Water hardness was adjusted to 21° dH by addition of CaCl₂, MgCl₂, and NaHCO₃(Ca²⁺:Mg²⁺:HCO₃⁻=2:1:10) to the test system. After washing the plates were flushed in tap water and dried.

TABLE 5

Experimental condition

Detergent
Powder model detergent

A (see Table 6)

Detergent dosage
3.94
g/L

Test solution volume
160
micro L

pH
9.9

Wash time
20
minutes

Temperature
50°
C.

Water hardness
21°
dH

Enzyme concentration in test
0.01-0.24
mg/L

Test material
Melamine plates (Mixed Starch)

TABLE 6

Powder automatic dish wash model detergent

Content of
% active

ingredient
component

Compound
(% w/w)
(% w/w)

MGDA
28.9
20

Sodium citrate
17.1
20

Sodium carbonate
17.1
20

Sodium percarbonate
9.7
10

Sodium Silicate
5.3
5

Sodium sulfate
10.2
12

Acusol 588G
4.6
5

TAED
2.8
3

Surfac 23-6.5 (liq)
4.3
5

* Surfac 23-6.5 (liq) is added separately before wash

Evaluation of wash performance

The wash performance is measured as the brightness expressed as the intensity of the light reflected from the sample when illuminated with white light. When the sample is stained the intensity of the reflected light is lower, than that of a clean sample. Therefore the intensity of the reflected light can be used to measure wash performance.

Color measurements are made with a professional flatbed scanner (EPSON EXPRESSION 10000XL) used to capture an image of the washed textile and with a controlled digital imaging system (ColorVectorAnalyzer) for capture an image of the washed melamine plates.

To extract a value for the light intensity from the scanned images, from the image are converted into values for red, green and blue (RGB). The intensity value (Int) is calculated by adding the RGB values together as vectors and then taking the length of the resulting vector:

Int=√{square root over (r²+g²+b²)}

Table of sequences referred to in the present

application

SEQ ID
Sequence

NO: 1
CATCACGATGGGACGAACGGAACGATTATGCAGTATTTTGAAT

GGAACGTTCCGAATGATGGACAACATTGGAACCGCTTACACAA

CAACGCTCAAAATTTAAAAAATGCCGGAATTACAGCAATCTGG

ATTCCACCTGCGTGGAAAGGAACGAGCCAAAATGATGTAGGCT

ACGGTGCGTATGACCTTTATGACCTTGGTGAATTTAACCAAAA

AGGAACGGTCCGTACGAAATATGGAACAAAAGCAGAATTAGAA

CGAGCGATTCGTTCGTTAAAGGCGAACGGGATTCAAGTGTATG

GCGATGTTGTTATGAACCATAAAGGCGGAGCTGATTTCACCGA

GCGTGTTCAAGCGGTTGAAGTGAACCCGCAAAACCGAAACCAA

GAAGTGTCTGGCACTTATCAAATCGAAGCATGGACAGGGTTCA

ATTTTCCTGGACGTGGCAATCAACATTCTTCGTTTAAATGGCG

CTGGTATCATTTCGATGGGACGGATTGGGACCAGTCTCGCCAA

CTCGCAAATCGTATTTATAAGTTTAGAGGAGACGGAAAAGCAT

GGGACTGGGAAGTTGACACTGAAAATGGGAACTATGATTACTT

AATGTATGCAGACGTTGACATGGATCATCCAGAAGTGATTAAC

GAACTAAACCGTTGGGGCGTCTGGTACGCGAATACCCTTAATT

TAGACGGCTTCCGACTGGATGCAGTGAAACATATTAAATTTAG

CTTCATGCGTGATTGGTTAGGGCATGTTCGCGGGCAAACGGGC

AAGAATCTTTTTGCCGTTGCAGAGTATTGGAAGAATGACCTAG

GGGCTTTAGAAAATTATTTAAGCAAAACAAATTGGACGATGAG

CGCCTTTGATGTTCCGCTTCATTACAACCTTTATCAAGCGTCA

AATAGTAGCGGAAATTACGACATGAGAAACTTGTTAAATGGAA

CACTCGTTCAACGTCATCCGAGCCATGCGGTTACGTTTGTCGA

TAACCACGACACACAGCCTGGAGAAGCCCTCGAATCGTTCGTT

CAAGGCTGGTTTAAACCACTAGCTTATGCAACGATTCTTACGA

GAGAGCAAGGCTACCCACAAGTGTTTTACGGCGATTATTATGG

CATCCCAAGTGACGGTGTTCCAAGCTACCGTCAACAGATCGAC

CCACTTTTAAAAGCTCGTCAACAATATGCTTATGGTAGACAGC

ACGATTACTTTGATCATTGGGATGTAATTGGCTGGACACGTGA

AGGAAACGCATCTCACCCGAACTCAGGACTTGCAACCATTATG

TCTGATGGTCCAGGTGGATCAAAATGGATGTATGTTGGCCGTC

AGAAAGCTGGCGAAGTGTGGCATGACATGACTGGAAACCGCAG

TGGCACTGTGACAATTAATCAAGACGGCTGGGGACACTTTTTT

GTCAACGGCGGCTCTGTCTCCGTATGGGTGAAACGATAA

2

MNRWKAAFSWMLSLALVFTLFYTPSSASAHHDGTNGTIMQYFE

WNVPNDGQHWNRLHNNAQNLKNAGITAIWIPPAWKGTSQNDVG

YGAYDLYDLGEFNQKGTVRTKYGTKAELERAIRSLKANGIQVY

GDVVMNHKGGADFTERVQAVEVNPQNRNQEVSGTYQIEAWTGF

NFPGRGNQHSSFKWRWYHFDGTDWDQSRQLANRIYKFRGDGKA

WDWEVDTENGNYDYLMYADVDMDHPEVINELNRWGVWYANTLN

LDGFRLDAVKHIKFSFMRDWLGHVRGQTGKNLFAVAEYWKNDL

GALENYLSKTNWTMSAFDVPLHYNLYQASNSSGNYDMRNLLNG

TLVQRHPSHAVTFVDNHDTQPGEALESFVQGWFKPLAYATILT

REQGYPQVFYGDYYGIPSDGVPSYRQQIDPLLKARQQYAYGRQ

HDYFDHWDVIGWTREGNASHPNSGLATIMSDGPGGSKWMYVGR

QKAGEVWHDMTGNRSGTVTINQDGWGHFFVNGGSVSVWVKR

3
HHDGTNGTIMQYFEWNVPNDGQHWNRLHNNAQNLKNAGITAIW

IPPAWKGTSQNDVGYGAYDLYDLGEFNQKGTVRTKYGTKAELE

RAIRSLKANGIQVYGDVVMNHKGGADFTERVQAVEVNPQNRNQ

EVSGTYQIEAWTGFNFPGRGNQHSSFKWRWYHFDGTDWDQSRQ

LANRIYKFRGDGKAWDWEVDTENGNYDYLMYADVDMDHPEVIN

ELNRWGVVVYANTLNLDGFRLDAVKHIKFSFMRDWLGHVRGQT

GKNLFAVAEYWKNDLGALENYLSKTNWTMSAFDVPLHYNLYQA

SNSSGNYDMRNLLNGTLVQRHPSHAVTFVDNHDTQPGEALESF

VQGWFKPLAYATILTREQGYPQVFYGDYYGIPSDGVPSYRQQI

DPLLKARQQYAYGRQHDYFDHWDVIGWTREGNASHPNSGLATI

MSDGPGGSKWMYVGRQKAGEVWHDMTGNRSGTVTINQDGWGHF

FVNGGSVSVWVKR

4
HHDGTNGTIMQYFEWNVPNDGQHWNRLHNNAQNLKNAGITAIW

IPPAWKGTSQNDVGYGAYDLYDLGEFNQKGTVRTKYGTKAELE

RAIRSLKANGIQVYGDVVMNHKGGADFTERVQAVEVNPQNRNQ

EVSGTYQIEAWTGFNFPGRGNQHSSFKWRWYHFDGTDWDQSRQ

LANRIYKFRGKAWDWEVDTENGNYDYLMYADVDMDHPEVINEL

NRWGVWYANTLNLDGFRLDAVKHIKFSFMRDWLGHVRGQTGKN

LFAVAEYWKNDLGALENYLSKTNWTMSAFDVPLHYNLYQASNS

SGNYDMRNLLNGTLVQRHPSHAVTFVDNHDTQPGEALESFVQG

WFKPLAYATILTREQGYPQVFYGDYYGIPSDGVPSYRQQIDPL

LKARQQYAYGRQHDYFDHWDVIGWTREGNASHPNSGLATIMSD

GPGGSKWMYVGRQKAGEVWHDMTGNRSGTVTINQDGWGHFFVN

GGSVSVWVKR

5
HHNGTNGTMMQYFEWYLPNDGNHWNRLNSDASNLKSKGITAVW

IPPAWKGASQNDVGYGAYDLYDLGEFNQKGTVRTKYGTRSQLQ

AAVTSLKNNGIQVYGDVVMNHKGGADATEMVRAVEVNPNNRNQ

EVTGEYTIEAWTRFDFPGRGNTHSSFKWRWYHFDGVDWDQSRR

LNNRIYKFRGHGKAWDWEVDTENGNYDYLMYADIDMDHPEVVN

ELRNWGVWYTNTLGLDGFRIDAVKHIKYSFTRDWINHVRSATG

KNMFAVAEFWKNDLGAIENYLQKTNWNHSVFDVPLHYNLYNAS

KSGGNYDMRNIFNGTVVQRHPSHAVTFVDNHDSQPEEALESFV

EEWFKPLAYALTLTREQGYPSVFYGDYYGIPTHGVPAMRSKID

PILEARQKYAYGKQNDYLDHHNIIGWTREGNTAHPNSGLATIM

SDGAGGSKWMFVGRNKAGQVWSDITGNRTGTVTINADGWGNFS

VNGGSVSIWVNK

6
HHNGTNGTMMQYFEWYLPNDGNHWNRLRSDASNLKDKGISAVW

IPPAWKGASQNDVGYGAYDLYDLGEFNQKGTIRTKYGTRNQLQ

AAVNALKSNGIQVYGDVVMNHKGGADATEMVRAVEVNPNNRNQ

EVSGEYTIEAWTKFDFPGRGNTHSNFKWRWYHFDGVDWDQSRK

LNNRIYKFRGDGKGWDWEVDTENGNYDYLMYADIDMDHPEVVN

ELRNWGVWYTNTLGLDGFRIDAVKHIKYSFTRDWINHVRSATG

KNMFAVAEFWKNDLGAIENYLNKTNWNHSVFDVPLHYNLYNAS

KSGGNYDMRQIFNGTVVQRHPMHAVTFVDNHDSQPEEALESFV

EEWFKPLAYALTLTREQGYPSVFYGDYYGIPTHGVPAMKSKID

PILEARQKYAYGRQNDYLDHHNIIGWTREGNTAHPNSGLATIM

SDGAGGNKWMFVGRNKAGQVWTDITGNRAGTVTINADGWGNFS

VNGGSVSIWVNK

7
MKRWVVAMLAVLFLFPSVVVADGLNGTMMQYYEWHLENDGQHW

NRLHDDAEALSNAGITAIWIPPAYKGNSQADVGYGAYDLYDLG

EFNQKGTVRTKYGTKAQLERAIGSLKSNDINVYGDVVMNHKLG

ADFTEAVQAVQVNPSNRWQDISGVYTIDAWTGFDFPGRNNAYS

DFKWRWFHFNGVDWDQRYQENHLFRFANTNWNWRVDEENGNYD

YLLGSNIDFSHPEVQEELKDWGSWFTDELDLDGYRLDAIKHIP

FWYTSDWVRHQRSEADQDLFVVGEYWKDDVGALEFYLDEMNWE

MSLFDVPLNYNFYRASKQGGSYDMRNILRGSLVEAHPIHAVTF

VDNHDTQPGESLESWVADWFKPLAYATILTREGGYPNVFYGDY

YGIPNDNISAKKDMIDELLDARQNYAYGTQHDYFDHWDIVGWT

REGTSSRPNSGLATIMSNGPGGSKWMYVGQQHAGQTWTDLTGN

HAASVTINGDGWGEFFTNGGSVSVYVNQ

8
AQSVPWGISRVQAPAAHNRGLTGSGVKVAVLDTGISTHPDLNI

RGGASFVPGEPSTQDGNGHGTHVAGTIAALNNSIGVLGVAPSA

ELYAVKVLGASGSGSVSSIAQGLEWAGNNGMHVANLSLGSPSP

SATLEQAVNSATSRGVLVVAASGNSGAGSISYPARYANAMAVG

ATDQNNNRASFSQYGAGLDIVAPGVNVQSTYPGSTYASLNGTS

MATPHVAGAAALVKQKNPSWSNVQIRNHLKNTATSLGSTNLYG

SGLVNAEAATR

9
HHNGTNGTMMQYFEWYLPNDGNHWNRLNSDASNLKSKGITAVW

IPPAWKGASQNDVGYGAYDLYDLGEFNQKGTVRTKYGTRSQLQ

AAVTSLKNNGIQVYGDVVMNHKGGADATEMVRAVEVNPNNRNQ

EVTGEYTIEAWTRFDFPGRGNTHSSFKWRWYHFDGVDWDQSRR

LNNRIYKFRGKAWDWEVDTENGNYDYLMYADIDMDHPEVVNEL

RNWGVWYTNTLGLDGFRIDAVKHIKYSFTRDWINHVRSATGKN

MFAVAEFWKNDLGAIENYLQKTNWNHSVFDVPLHYNLYNASKS

GGNYDMRNIFNGTVVQRHPSHAVTFVDNHDSQPEEALESFVEE

WFKPLAYALTLTREQGYPSVFYGDYYGIPTHGVPAMRSKIDPI

LEARQKYAYGPQHDYLDHPDVIGWTREGDSSHPKSGLATLITD

GPGGSKRMYAGLKNAGETWYDITGNRSDTVKIGSDGWGEFHVN

DGSVSIYVQK

10
DGLNGTMMQYYEWHLENDGQHWNRLHDDAAALSDAGITAIWIP

PAYKGNSQADVGYGAYDLYDLGEFNQKGTVRTKYGTKAQLERA

IGSLKSNDINVYGDVVMNHKMGADFTEAVQAVQVNPTNRWQDI

SGAYTIDAWTGFDFSGRNNAYSDFKWRWFHFNGVDWDQRYQEN

HIFRFANTNWNWRVDEENGNYDYLLGSNIDFSHPEVQDELKDW

GSWFTDELDLDGYRLDAIKHIPFWYTSDWVRHQRNEADQDLFV

VGEYWKDDVGALEFYLDEMNWEMSLFDVPLNYNFYRASQQGGS

YDMRNILRGSLVEAHPMHAVTFVDNHDTQPGESLESWVADWFK

PLAYATILTREGGYPNVFYGDYYGIPNDNISAKKDMIDELLDA

RQNYAYGTQHDYFDHWDVVGWTREGSSSRPNSGLATIMSNGPG

GSKWMYVGRQNAGQTWTDLTGNNGASVTINGDGWGEFFTNGGS

VSVYVNQ

11
HHNGTNGTMMQYFEWHLPNDGNHWNRLRDDAANLKSKGITAVW

IPPAWKGTSQNDVGYGAYDLYDLGEFNQKGTVRTKYGTRSQLQ

GAVTSLKNNGIQVYGDVVMNHKGGADGTEMVNAVEVNRSNRNQ

EISGEYTIEAWTKFDFPGRGNTHSNFKWRWYHFDGTDWDQSRQ

LQNKIYKFRGTGKAWDWEVDIENGNYDYLMYADIDMDHPEVIN

ELRNWGVWYTNTLNLDGFRIDAVKHIKYSYTRDWLTHVRNTTG

KPMFAVAEFWKNDLAAIENYLNKTSWNHSVFDVPLHYNLYNAS

NSGGYFDMRNILNGSVVQKHPIHAVTFVDNHDSQPGEALESFV

QSWFKPLAYALILTREQGYPSVFYGDYYGIPTHGVPSMKSKID

PLLQARQTYAYGTQHDYFDHHDIIGWTREGDSSHPNSGLATIM

SDGPGGNKWMYVGKHKAGQVWRDITGNRSGTVTINADGWGNFT

VNGGAVSVWVKQ

12
HHNGTNGTMMQYFEWYLPNDGNHWNRLRSDASNLKDKGITAVW

IPPAWKGASQNDVGYGAYDLYDLGEFNQKGTVRTKYGTRNQLQ

AAVTALKSNGIQVYGDVVMNHKGGADATEWVRAVEVNPSNRNQ

EVSGDYTIEAWTKFDFPGRGNTHSNFKWRWYHFDGVDWDQSRQ

LQNRIYKFRGDGKGWDWEVDTENGNYDYLMYADIDMDHPEVVN

ELRNWGVWYTNTLGLDGFRIDAVKHIKYSFTRDWLTHVRNTTG

KNMFAVAEFWKNDIGAIENYLSKTNWNHSVFDVPLHYNLYNAS

RSGGNYDMRQIFNGTVVQRHPTHAVTFVDNHDSQPEEALESFV

EEWFKPLACALTLTRDQGYPSVFYGDYYGIPTHGVPAMKSKID

PILEARQKYAYGKQNDYLDHHNMIGWTREGNTAHPNSGLATIM

SDGPGGNKWMYVGRNKAGQVWRDITGNRSGTVTINADGWGNFS

VNGGSVSIWVNN

13
HHDGTNGTIMQYFEWNVPNDGQHWNRLHNNAQNLKNAGITAIW

IPPAWKGTSQNDVGYGAYDLYDLGEFNQKGTVRTKYGTKAELE

RAIRSLKANGIQVYGDVVMNHKGGADFTERVQAVEVNPQNRNQ

EVSGTYEIEAWTGFNFPGRGNQHSSFKWRWYHFDGTDWDQSRQ

LSNRIYKFRGDGKAWDWEVDTENGNYDYLMYADVDMNHPEVIN

ELNRWGVWYANTLNLDGFRLDAVKHIQFSFMRNWLGHVRGQTG

KNLFAVAEYWKNDLGALENYLSKTNWTMSAFDVPLHYNLYQAS

NSGGNYDMRNLLNGTLVQRHPSHAVTFVDNHDTQPGEALESFV

QGWFKPLAYATILTREQGYPQVFYGDYYGIPSDGVPSYRQQID

PLLKARQQYAYGRQHDYFDHWDVIGWTREGNASHPNSGLATIM

SDGPGGSKWMYVGRQKAGEVWHDITGNRSGTVTINQDGWGQFF

VNGGSVSVWVKR

The invention described and claimed herein is not to be limited in scope by the specific aspects herein disclosed, since these aspects are intended as illustrations of several aspects of the invention. Any equivalent aspects are intended to be within the scope of this invention. Indeed, various modifications of the invention in addition to those shown and described herein will become apparent to those skilled in the art from the foregoing description. Such modifications are also intended to fall within the scope of the appended claims. In the case of conflict, the present disclosure including definitions will control.

OXIDATION STABLE ALPHA-AMYLASE VARIANTS

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