LAUNDRY DETERGENT COMPOSITIONS WITH STAIN REMOVAL

FIELD OF THE INVENTION

Laundry detergent compositions, especially liquid laundry detergent compositions for cleaning mixed food stains.

BACKGROUND OF THE INVENTION

Laundry detergent compositions are formulated to provide good cleaning to fabrics: To keep white fabrics white, and to keep coloured fabrics bright. The laundry detergent compositions are also typically formulated to remove stains. A stain is a local discoloration that can be clearly distinguished on the fabric it is found upon. Since they result in a discoloration that strongly contrasts with the unstained fabrics, they are particularly noticeable on fabrics.

Certain mixed food stains, such as prepared sauces, remain challenging to remove, especially at low temperatures. Moreover, such stains have been found to redeposit on the fabric during laundering, despite the use of anti-redeposition aids. While improved removal of such stains can be achieved by increasing the levels of actives such as anti-redeposition aids, surfactants, and builders, this adds to the cost of the formulation and can lead to other issues such as stability.

Hence, a need remains for a laundry detergent composition which has improved efficacy against mixed food stains, such as prepared sauces, while being stable and without the need for high levels of stain treatment actives.

W02019/038059 relates to detergent compositions comprising endoglucanase variants and methods for use of said compositions. W02019/038060 relates to detergent compositions comprising xanthan lyase variants and methods for use of said compositions.

SUMMARY OF THE INVENTION

The present invention relates to a laundry detergent composition comprising: detersive surfactant, wherein the detersive surfactant comprises a combination of anionic and nonionic surfactant; an enzyme system comprising: a xanthan endoglucanase, wherein said xanthan endoglucanase comprises a polypeptide with at least 60% sequence identity to SEQ ID NO: 1; a xanthan lyase, wherein said xanthan lyase comprises a polypeptide with at least 60% sequence identity to SEQ ID NO: 2, and a mannanase, wherein said mannanase comprises a polypeptide with at least 85% sequence identity to residues 27- 331 of SEQ ID NO: 3 and/or at least 80% sequence identity to SEQ ID NO: 4.

The present invention further relates to a method of laundering fabric, preferably a fabric comprising a stain wherein the stain comprises a combination of mannans and polysaccharides, wherein the method comprises the steps of: providing a laundry detergent composition of the invention; diluting the laundry detergent composition to provide a wash liquor having a total surfactant concentration of greater than 300 ppm; and washing fabric in the wash liquor.

DETAILED DESCRIPTION OF THE INVENTION

It has surprisingly been found that the resiliency of certain mixed food stains, such as certain prepared sauces, is due to the combination of mannans and other polysaccharides. Such sauces can include chilli pastes, vinegar dressings, and some ice-creams. Examples of such mannans include locust bean, tara gum, guar gum, and the like, as well as mixtures thereof. Examples of polysaccharides include xanthan gum. It is believed that the combination of mannans and polysaccharides forms gels as the soil dries, resulting in hard to remove stains. In addition, the resiliency of such gels can be increased in the presence of greasy or oily residues such as animal fats (e.g. bacon grease, lard, shortening, butter) and vegetable oils (e.g. sunflower oil, rapeseed oil, cottonseed oil, olive oil, corn oil). In addition, even if the stain is removed, the gel-like structure results in the stains holding together in suspension during the wash cycle, resulting in greater redeposition. It is believed that the enzyme system of use in the present invention is better able to break down these gel structures, more effectively than mannanase alone or endoglucanases alone, even when the gel structures comprise greasy or oily residues, and hence results in improved removal of such stains. In addition, since the enzyme system is better able to break down such gel structures, reduced redeposition of the soils is also achieved.

Unless otherwise noted, all component or composition levels are in reference to the active portion of that component or composition, and are exclusive of impurities, for example, residual solvents or by-products, which may be present in commercially available sources of such components or compositions.

All percentages and ratios are calculated by weight unless otherwise indicated. All percentages and ratios are calculated based on the total composition unless otherwise indicated.

All measurements are performed at 25 °C unless otherwise specified. As used herein, the articles including“a” and“an” when used in a claim, are understood to mean one or more of what is claimed or described.

Laundry detergent composition:

The laundry detergent composition can be in any suitable form, such as liquid, paste, granular, solid, powder, or in conjunction with a carrier such as a substrate. Preferred laundry detergent compositions are either liquid or granular, with liquid being most preferred.

As used herein,“liquid detergent composition” refers to liquid detergent composition which is fluid, and preferably capable of wetting and cleaning a fabric, e.g., clothing in a domestic washing machine. As used herein,“laundry detergent composition” refers to compositions suitable for washing clothes. The composition can include solids or gases in suitably subdivided form, but the overall composition excludes product forms which are non-fluid overall, such as tablets or granules. The liquid laundry detergent composition preferably has a density in the range from 0.9 to 1.3 grams per cubic centimeter, more specifically from 1.00 to 1.10 grams per cubic centimeter, excluding any solid additives but including any bubbles, if present.

Aqueous liquid laundry detergent compositions are preferred. For such aqueous liquid laundry detergent compositions, the water content can be present at a level of from 5 % to 99 %, preferably from 15 % to 90 %, more preferably from 25 % to 80 % by weight of the liquid detergent composition.

The pH range of the detergent composition is from 6.0 to 8.9, preferably from pH 7 to 8.8.

The detergent composition can also be encapsulated in a water soluble film, to form a unit dose article. Such unit dose articles comprise a detergent composition of the present invention, wherein the detergent composition comprises less than 20%, preferably less than 15%, more preferably less than 10% by weight of water, and the detergent composition is enclosed in a water-soluble or dispersible film. Such unit-dose articles can be formed using any means known in the art.

Suitable water soluble pouch materials include polymers, copolymers or derivatives thereof. Preferred polymers, copolymers or derivatives thereof can be selected from the group consisting of: polyvinyl alcohols, polyvinyl pyrrolidone, polyalkylene oxides, acrylamide, acrylic acid, cellulose, cellulose ethers, cellulose esters, cellulose amides, polyvinyl acetates, polycarboxylic acids and salts, polyaminoacids or peptides, polyamides, polyacrylamide, copolymers of maleic/acrylic acids, polysaccharides including starch and gelatin, natural gums such as xanthum and carragum. More preferred polymers are selected from polyacrylates and water-soluble acrylate copolymers, methylcellulose, carboxymethylcellulose sodium, dextrin, ethylcellulose, hydroxy ethyl cellulose, hydroxypropyl methylcellulose, maltodextrin, poly methacrylates, and most preferably selected from polyvinyl alcohols, polyvinyl alcohol copolymers and hydroxypropyl methyl cellulose (HPMC), and combinations thereof.

Detersive Surfactants

Detersive surfactant as used herein means surfactants or mixtures of surfactants that provide cleaning, stain removing, or laundering benefit to soiled material. Suitable detersive surfactants can be: anionic surfactant, nonionic surfactant, zwitterionic surfactant, and combinations thereof. The detersive surfactant comprises a combination of anionic and nonionic surfactant.

The laundry composition can comprises detersive surfactant at a level of from 3 wt % to 50 wt%, preferably from 10 wt % to 37.5 wt%, more preferably from 15 wt% to 30 wt%.

Suitable anionic surfactants can be selected from the group consisting of: alkyl sulphates, alkyl ethoxy sulphates, alkyl sulphonates, alkyl benzene sulphonates, fatty acids and their salts, and mixtures thereof. However, by nature, every anionic surfactant known in the art of detergent compositions may be used, such as disclosed in“Surfactant Science Series”, Vol. 7, edited by W. M. Linfield, Marcel Dekker. However, the composition preferably comprises at least a sulphonic acid surfactant, such as a linear alkyl benzene sulphonic acid, but water-soluble salt forms may also be used. Alkyl ethoxy sulphates, or mixtures thereof, are also preferred.

Anionic sulfonate or sulfonic acid surfactants suitable for use herein include the acid and salt forms of linear or branched alkylbenzene sulfonates, alkyl ester sulfonates, alkane sulfonates, alkyl sulfonated polycarboxylic acids, and mixtures thereof. Suitable anionic sulfonate or sulfonic acid surfactants include: C5-C20 alkylbenzene sulfonates, more preferably C10-C16 alkylbenzene sulfonates, more preferably C11-C13 alkylbenzene sulfonates, C5-C20 alkyl ester sulfonates, C6- C22 primary or secondary alkane sulfonates, C5-C20 sulfonated polycarboxylic acids, and any mixtures thereof, but preferably C11-C13 alkylbenzene sulfonates. The aforementioned surfactants can vary widely in their 2-phenyl isomer content. Such sulfonate or sulfonic acid surfactants can be present at a level of from 1.0% to 20%, more preferably from 5.0% to 15%, and most preferably from 6.5 to 12.5% by weight of the composition.

Anionic sulphate salts suitable for use in the compositions of the invention include the primary and secondary alkyl sulphates, having a linear or branched alkyl or alkenyl moiety having from 9 to 22 carbon atoms or more preferably 12 tol8 carbon atoms. Also useful are beta-branched alkyl sulphate surfactants or mixtures of commercial available materials, having a weight average (of the surfactant or the mixture) branching degree of at least 50%.

Other suitable anionic surfactants for use herein include fatty methyl ester sulphonates and/or alkyl alkoxylated sulphates such as alkyl ethoxy sulphates (AES) and/or alkyl polyalkoxylated carboxylates (AEC). When used, the alkyl alkoxylated sulphate surfactant is preferably a blend of one or more alkyl ethoxylated sulphates. Suitable alkyl alkoxylated sulphates include C10-C18 alkyl ethoxylate, more preferably C12-C15 alkyl ethoxylate, with a degree of ethoxylation of from 1 to 5, preferably from 2 to 3. Such alkyl alkoxylated sulphates are preferably present at a level of from 1.0% to 10%, more preferably from 2.0% to 7.5%, and most preferably from 3.0 to 5% by weight of the composition.

Suitable fatty acids include“natural” fatty acids, for example coconut, palm kernel, olive oil or tallow fatty acid and mixtures thereof. Such fatty acid surfactants can be present at a level of from 1.0% to 15%, more preferably from 2.0% to 12.5%, and most preferably from 5.0 to 10% by weight of the composition.

The anionic surfactants are typically present in the form of their salts with alkanolamines or alkali metals such as sodium and potassium.

The liquid detergent composition can comprise nonionic surfactant. The level of nonionic surfactant in the liquid detergent composition can be present at a level of from 1.0% to 20%, preferably from 2.5% to 15%, more preferably from 5.0% to 12.5% by weight of the composition. Suitable nonionic surfactants include, but are not limited to C12-C18 alkyl ethoxylates ("AE") including the so-called narrow peaked alkyl ethoxylates and C6-C12 alkyl phenol alkoxylates (especially ethoxylates and mixed ethoxy/propoxy), block alkylene oxide condensate of C6-C12 alkyl phenols, alkylene oxide condensates of C8-C22 alkanols and ethylene oxide/propylene oxide block polymers (Pluronic - BASF Corp.), as well as semi polar nonionics (e.g., amine oxides and phosphine oxides) can be used in the present compositions. An extensive disclosure of these types of surfactants is found in U.S. Pat. 3,929,678, Laughlin et al., issued December 30, 1975.

Alkylpolysaccharides such as disclosed in U.S. Pat. 4,565,647 Llenado are also useful nonionic surfactants in the compositions of the invention.

Also suitable are alkyl polyglucoside surfactants.

Nonionic surfactants of use include those of the formula R ₁ (OC ₂ H ₄ ) _n OH, wherein Ri is a C10-C16 alkyl group or a C8-C12 alkyl phenyl group, and n is from preferably 3 to 80. In some embodiments, the nonionic surfactants may be condensation products of C12-C15 alcohols with from 5 to 20 moles of ethylene oxide per mole of alcohol, e.g., C12-C13 alcohol condensed with 6.5 moles of ethylene oxide per mole of alcohol

Suitable amine oxide surfactants are amine oxides having the following formula : wherein R ₁ is an hydrocarbon chain comprising from 1 to 30 carbon atoms, preferably from 6 to 20, more preferably from 8 to 16 and wherein R ₂ and R ₃ are independently saturated or unsaturated, substituted or unsubstituted, linear or branched hydrocarbon chains comprising from 1 to 4 carbon atoms, preferably from 1 to 3 carbon atoms, and more preferably are methyl groups. R ₁ may be a saturated or unsaturated, substituted or unsubstituted linear or branched hydrocarbon chain. Suitable amine oxides for use herein are for instance preferably C ₁₂ -C ₁₄ dimethyl amine oxide, commercially available from Albright & Wilson, C ₁₂ -C ₁₄ amine oxides commercially available under the trade name Genaminox® LA from Clariant or AROMOX® DMC from AKZO Nobel. Additional suitable nonionic surfactants include polyhydroxy fatty acid amides of the formula: wherein R is a C9-17 alkyl or alkenyl, R1 is a methyl group and Z is glycidyl derived from a reduced sugar or alkoxylated derivative thereof. Examples are N-methyl N-l-deoxyglucityl cocoamide and N-methyl N-l-deoxyglucityl oleamide. Processes for making polyhydroxy fatty acid amides are known and can be found in Wilson, U.S. Patent 2,965,576 and Schwartz, U.S. Patent 2,703,798.

The liquid detergent composition can comprise a zwitterion. The zwitterion can be present at a level of from 0.1 wt% to 5 wt%, preferably from 0.2 wt% to 2 wt%, more preferably from 0.4 wt% to 1 wt %.

Suitable amphoteric or zwitterionic detersive surfactants include those which are known for use in hair care or other personal care cleansing. Non-limiting examples of suitable zwitterionic or amphoteric surfactants are described in U.S. Pat. Nos. 5,104,646 (Bolich Jr. et al.), 5,106,609 (Bolich Jr. et al.). Suitable amphoteric detersive surfactants include those surfactants broadly described as derivatives of aliphatic secondary and tertiary amines in which the aliphatic radical can be straight or branched chain and wherein one of the aliphatic substituents contains from 8 to 18 carbon atoms and one contains an anionic group such as carboxy, sulfonate, sulfate, phosphate, or phosphonate. Suitable amphoteric detersive surfactants for use in the present invention include, but are not limited to: cocoamphoacetate, cocoamphodiacetate, lauroamphoacetate, lauroamphodiacetate, and mixtures thereof.

Preferably surfactants comprising saturated alkyl chains are used.

The enzyme system

The laundry detergent composition of the present invention comprises an enzyme cocktail, wherein the enzyme cocktail comprises a xanthan endoglucanase, a xanthan lyase, and a mannanase.

Enzyme definitions

Parent: The term“parent” means an enzyme from which an alteration is made to produce the enzyme variants. The parent may be a naturally occurring (wild-type) polypeptide or a variant thereof.

Sequence Identity: The relatedness between two amino acid sequences or between two nucleotide sequences is described by the parameter“sequence identity”. For purposes of the present invention, the degree of 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 3.0.0 or later. The optional 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 x 100)/(Length of Alignment - Total Number of Gaps in Alignment) Alternatively, the parameters used may be 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 labelled“longest identity” (obtained using the -nobrief option) is used as the percent identity and is calculated as follows:

(Identical Deoxyribonucleotides x 100)/(Length of Alignment - Total Number of Gaps in Alignment)

Variant: The term “variant” means a polypeptide having enzyme activity comprising an alteration/mutation, i.e., a substitution, insertion, and/or deletion, at one or more (e.g. several) positions relative to the parent enzyme. A substitution means a replacement of an amino acid occupying a position with a different amino acid; a deletion means removal of an amino acid occupying a position; and an insertion means adding 1-3 amino acids adjacent to and immediately following an amino acid occupying a position. Alterations/mutations are typically described using single letter amino acid codes and notation that is familiar to those skilled in the art. For example, S23D defines a substation of a serine (S) residue at position 23 with aspartic acid (D); Y30* defines a deletion of the tyrosine residue at position 30. G34GW defines an insertion of a tryptophan residue after the glycine at position 34.

Wild-Type Enzyme: The term“wild-type” means an enzyme encoded by the DNA of a naturally occurring organism, such as a bacterium, yeast, or filamentous fungus found in nature.

The xanthan endoglucanase

As used herein, the term xanthan endoglucanase denotes an enzyme exhibiting endo-beta- 1 ,4- glucanase activity that is capable of catalysing hydrolysis of the 1 ,4-linked b-D-glucose polymeric backbone of xanthan gum in conjunction with a suitable xanthan lyase enzyme. The xanthan endoglucanase in accordance with the invention has endo-beta- 1,4-glucanase activity and a polypeptide having at least 60% identity to SEQ ID NO: 1. SEQ ID NO: 1 corresponds to the amino acid sequence of a xanthan endoglucanase endogenous to Paenibacillus sp-62047

In further embodiments of the invention, the xanthan endoglucanase is variant with at least 61 %, at least 62%, at least 63%, at least 64%, at least 65%, at least 66%, at least 67%, at least 68%, at least 69%, at least 70%, at least 71 %, at least 72%, at least 73%, at least 74%, at least 75%, at least 76%, at least 77%, at least 78%, at least 79%, at least 80%, at least 81 %, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91 %, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to SEQ ID NO: 1.

In further embodiments of the invention, the xanthan endoglucanase has substitutions at one or more of positions 17, 20, 51 , 53, 55, 56, 60, 63, 79, 87, 186, 192, 302, 31 1 , 313, 387, 388, 390, 403, 408, 410, 416, 448, 451 , 471 , 472, 476, 489, 507, 512, 515, 538, 598, 599, 602, 605, 609, 676, 688, 690, 694, 697, 698, 699, 71 1 , 719, 754, 756, 760, 781 , 786, 797, 833, 834, 835 and 1048 of SEQ ID NO: 1.

In further embodiments of the invention, the xanthan endoglucanase has substitutions at one or more of positions S17A, F20P, F20N, F20G, F20Y, K51Q, K51H, E53P, E53G, Y55M, V56M, Y60F, S63F, T87R, A186P, K192N, I320D, I302H, I302V, I302M, H311N, S313D, I387T, K388R, K390Q, I403Y, E408D, E408S, E408P, E408A, E408G, E408N, P410G, Q416S, Q416D, A448E, A448W, A448S, K451S, G471S, S472Y, D476R, Q489P, K507R, K512P, S515V, S538C, Y579W, S598Q, A599S, I602T, I602D, V603P, S605T, G609E, D676H, A688G, Y690F, T694A, T697G, R698W, T699A, T711V, T711Y, W719R, K754R, V756H, V756Y, S760G, T781M, N786K, T797S, A824D, N833D, Q834E, S835D and F1048W

Examples of suitable xanthan endoglucanases in accordance with the invention are listed below, wherein the substitutions correspond to positions in SEQ ID NO: 1:

The xanthan lyase

As used herein, the term“xanthan lyase” denotes an enzyme that cleaves the b-D-mannosyl-b-D- 1 ,4-glucuronosyl bond of xanthan and have been described in the literature. Xanthan lyases are classified according to the Enzyme Nomenclature as EC 4.2.2.12, and are known to be produced by many xanthan-degrading bacteria including Bacillus,

Corynebacterium and Paenibacillus species. The xanthan lyase in accordance with the invention has xanthan lyase activity and comprises a polypeptide having at least 60% identity to SEQ ID NO: 2. SEQ ID NO: 2 corresponds to the amino acid sequence of a xanthan lyase endogenous to a Paenibacillus sp.

In further embodiments of the invention, the xanthan lyase is a variant with at least 61 %, at least 62%, at least 63%, at least 64%, at least 65%, at least 66%, at least 67%, at least 68%, at least 69%, at least 70%, at least 71 %, at least 72%, at least 73%, at least 74%, at least 75%, at least 76%, at least 77%, at least 78%, at least 79%, at least 80%, at least 81 %, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91 %, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to SEQ ID NO: 2.

In another embodiment of the invention, the xanthan lyase is a variant with alterations at one or more positions selected from the group consisting of positions: 9, 15, 46, 58, 66, 89, 95, 100, 106, 109, 183, 188, 190, 203, 204, 221 , 229, 234, 238, 240, 242, 243, 257, 258, 291 , 293, 316, 320, 324, 329, 333, 339, 341 , 352, 354, 360, 377, 399, 400, 419, 440, 450, 451 , 454, 458, 481 , 492, 567, 568, 578, 579, 582, 664, 672, 703, 728, 843, 855, 887, 892, 1008 and 1016 of SEQ ID NO: 2.

In another embodiment of the invention, the xanthan lyase is a variant with alterations at one or more positions selected from the group consisting of positions 624, 631, 635, 649, 656, 752, 752, 754, 757, 769, 775, 777, 800, 801, 875, 911, and 915 of SEQ ID NO: 2.

In another embodiment of the invention, the xanthan lyase is a variant with one or more substitutions selected from the group consisting of: K9R, N15T, L46D, A58L, S66H, Q89Y, K95E, S100D, N106Y, Q109R, Q109D, Q109F, Q109K, Q109A, K183Q, K183R, V188I, A190Q, A203P, K204R, A221 P, E229N, E229S, I234V, I238W, I238L, I238M, I240W, N242S, G243V, Y257W, R258E, K291 R, A293G, A293P, K316R, K320R, L324Q, K329R, K333R, L339M, 1341 P, V352I, S354P, K360G, K360R, F377Y, N399K, K400R, F419Y, N440K, D450P, K451 E, K451 R, A454V, D458S, K481 R, A492L, A492H, K567R, G568A, S578K, S578R, S579R, S579K, S582K, A624E, T631 N, S635E, T649K, I656V, T664K, N672D, I703L, M728V, G738L, P752K, P752R, G753E, S754E, S754R, S757D, A769D, L775A, D777R, V800P, D801 G, A843P, K855R, K875T, K887R, N892Y, N892W, N892F, A911V, T915A, N1008D and K1016T of SEQ ID NO: 2.

In another embodiment of the invention, the xanthan lyase is a variant with one of the following sets of substitutions, based on SEQ ID NO: 2.

The mannanase

As used herein, the term "mannanase" or "galactomannanase" denotes a mannanase enzyme defined according to that known in the art as mannan endo-l,4-beta-mannosidase and having the alternative names beta-mannanase and endo-l,4-mannanase and catalysing hydrolysis of 1,4-beta- D-mannosidic linkages in mannans, galactomannans, glucomannans, and galactoglucomannans. Mannanases are classified according to the Enzyme Nomenclature as EC 3.2.1.78.

Suitable mannanase can be selected from the group consisting of:

a) mannanase having mannanase activity and a polypeptide having at least 85% sequence identity to residues 27- 331 of SEQ ID NO: 3. SEQ ID NO: 3 corresponds to the full-length amino acid sequence of the Man7 mannanase endogenous to Bacillus hemicellulosilyticus including a signal sequence; b) mannanase has mannanase activity and a polypeptide having at least 60% identity to SEQ ID NO: 4. In one embodiment of the invention, the mannanase has mannanase activity and a polypeptide having at least 80% identity to SEQ ID NO: 4. SEQ ID NO: 4 corresponds to the full-length amino acid sequence of the Man4 mannanase endogenous to Paenibacillus sp;

c) and mixtures thereof.

As such, suitable mannanase can have mannanase activity and a polypeptide having at least 85% sequence identity to residues 27- 331 of SEQ ID NO: 3. SEQ ID NO: 3 corresponds to the full- length amino acid sequence of the Man7 mannanase endogenous to Bacillus hemicellulosilyticus including a signal sequence. In one embodiment of the invention, the mannanase has at least 90% sequence identity to residues 27-331 of SEQ ID NO: 3. In another embodiment of the invention, the mannanase is a variant of SEQ ID NO: 3 comprising at least one substitution at positions 123, 158, 180, 272, 285, or 307 or a combination thereof. In another embodiment of the invention, the mannanase is a variant of SEQ ID NO: 3 comprising at least one substitution at positions M123, A158, F180, G272, T285, or T307 or a combination thereof. In another embodiment of the invention, the mannanase is a variant of SEQ ID NO: 3 comprising at least one substitution at positions M123, A158, F180, G272, T307, or L316, or a combination thereof. In an embodiment the variant comprises one further substitution, two further substitutions, three further substitutions or four further substitutions.

Alternatively, or in addition, suitable mannanase can have mannanase activity and a polypeptide having at least 60% identity to SEQ ID NO: 4. In one embodiment of the invention, the mannanase has mannanase activity and a polypeptide having at least 80% identity to SEQ ID NO: 4. SEQ ID NO: 4 corresponds to the full-length amino acid sequence of the Man4 mannanase endogenous to Paenibacillus sp.

The mannanase can be a variant of SEQ ID NO: 4 comprising one, two, three, four, five, six, seven or more variations versus SEQ ID NO: 4 selected from:

(i) N10Q/T, P19E/V, S30T, T38E/I/L/M/Q/R/V, S59D/G/K/N/Q/T, L60F/M/V, T62E/I/Q/V, K63L, L66C/T/V, N67A/D/E/G/P/Q/S/V, A68L/M/R/S/W, K70R/V, N71D/H, N74E/C/Q/V, V75I, Q78A/D/L/M, N79E/F/W, K80Q/T, N97E/L/P/Q, V103I, Y129M, T131P, S135A/C/Q, A136E, K143Q/R, F167L/S/W/Y, P168A/E/G/L/M/S/T, Q184D/F/H/L/M/P, N213E, K214C/Q, G225A/C/P/W, T228A/G/H/I/K/S/V/Y, Y235G/I/L/Q/S/V, Q242S/E,

K244A/C/G/L/M/P/S , S258A/D/E/G/M/N/P/T, G259A/E/R/S/W,

N261I/M/P/Q/R/S/T/V/W/Y, and D283G/H/T; or (ii) P19E/V, T38E/I/L/M/Q/R/V, N67A/D/E/G/P/Q/S/V, N97E/L/P/Q, Y129M, K143Q/R,

P 168 A/E/G/L/M/S/T, Q184D/F/H/L/M/P, G225A/C/P/W, T228A/G/H/I/K/S/V/Y, Y235G/I/L/Q/S/V, K244A/C/G/L/M/P/S, S258A/D/E/G/M/N/P/T, and

N261I/M/P/Q/R/S/T/V/W/Y ; or

(iii) P19E/V, T38E/I/L/M/Q/R/V, N67A/D/E/G/P/Q/S/V, L85L, Y129M,

PI 68 A/E/G/L/M/S/T, Q184D/F/H/L/M/P, G225A/C/P W, K244A/C/G/L/M/P/S,

S258 A/D/E/G/M/N/P/T, and N261I/M/P/Q/R S/T/V/W/Y; or

(iv) P19E, S30T, T38E, S59V, L60Q, K63R, N67D, N97D, V103I, Y129M, F167Y, P168S, Q184L, G225C, T228V, Y235L, K244L, S258D, and N261R;

with the proviso that one or more of said variations is non-naturally occurring; and wherein the amino acid positions of said mannanase variant or recombinant polypeptide or active fragment thereof are numbered by correspondence with the amino acid sequence of SEQ ID NO:4.

Alternatively, or in addition, the mannanase can be a variant of SEQ ID NO: 4 comprising a combination of variations to SEQ ID NO:4 selected from P19E-T38E-N67D-N97D-Y129M- P168S-Q184L-K244L-S258D-N261R; N10T-P19E-G28S-S30T-T38E-N67D-N71D-N97D-

Y129M-P168S-Q184L-G225C-Y235L-K244L-S258D-N261R-F297FQ; P19E-S30T-T38E-

S59V-L60Q-K63R-N67D-N97D-V103I-Y129M-F167Y-Q184L-G225C-T2 28V-Y235L-K244L- S258D-N261R-F297FQ; N10T-P19E-S30T-T38E-S59V-L60Q-K63R-N67D-N97D-Y129M-

K143Q-P168S-Q184L-G225C-T228V-Y235L-K244L-S258D-N261R-F29 7FQ; N10T-P19E-

S30T-T38E-S59V-L60Q-K63R-N67D-N97D-Y129M-K143Q-P168S-Q184 L-G225P-T228V- Y235L-K244L-S258D-N261R-F297FQ; N10T-P19E-S30T-T38E-S59V-L60Q-K63R-N67D-

N71D-N97D-V103I-Y129M-K143Q-P168S-Q184L-G225P-T228V-Y235L -K244L-S258D- N261R-F297FQ; A2S-P19E-G28S-S30T-T38E-K63R-N67D-N71D-N74E-K93R-N97D-

Y129M-N150T-P168S-Q184L-N213A-G225C-Y235L-K244L-S258D-N26 1Q-F297FQ; T3R- N10T-P19E-G28A-S30T-T38E-T62E-N67D-N71D-K93R-N97L-E111S-Y129 M-D139M- P168S-Q184L-G225C-Y235L-K244L-S258D-N261Q-F297FQ; and N10T-P19E-G28A-S30T- T38E-S59D-N67D-A68S-N71D-K93R-N97D-Y129M-K143Q-P168S-Q184D-G 225C-Y235L- K244L-S258D-N261R-T284E-F297FQ; and wherein the amino acid positions of said mannanase variant are numbered by correspondence with the amino acid sequence of SEQ ID NO:4.

Mannanase activity can be confimed using readily available assay kits, including those commercially available from Megazyme, Bray, Ireland and Glycospot, Spborg, Denmark. Lipase

The enzyme system preferably further comprises a lipase. The presence of oils and/or grease can further increase the resiliency of stains comprising mannans and other polysaccharides. As such, the presence of lipase in the enzyme package can further improve the removal of such stains. Suitable lipases include those of bacterial, fungal or synthetic origin, and variants thereof. Chemically modified or protein engineered mutants are also suitable. Examples of suitable lipases include lipases from Humicola (synonym Thermomyces), e.g., from H. lanuginosa (T. lanuginosus).

The lipase may be a "first cycle lipase", e.g. such as those described in W006/090335 and WO 13/ 116261. In one aspect, the lipase is a first-wash lipase, preferably a variant of the wild- type lipase from Thermomyces lanuginosus comprising T231R and/or N233R mutations.

Preferred lipases include those sold under the tradenames Lipex®, Lipolex® and Lipoclean® by Novozymes, Bagsvaerd, Denmark.

Other suitable lipases include: Liprl 139, e.g. as described in WO2013/171241; TfuLip2, e.g. as described in WO2011/084412 and WO2013/033318; Pseudomonas stutzeri lipase, e.g. as described in WO2018228880; Microbulbifer thermotolerans lipase, e.g. as described in WO2018228881; Sulfobacillus acidocaldarius lipase, e.g. as described in EP3299457; LIP062 lipase e.g. as described in WO2018209026; PinLip lipase e.g. as described in W02017036901 and Absidia sp. lipase e.g. as described in W02017005798. A suitable lipase is a variant of SEQ ID NO:5 comprising:

(a) substitution T231R

and

(b) substitution N233R or N233C

and

(c) at least three further substitutions selected from E1C, D27R, N33Q, G38A, F51V, G91Q, D96E, K98L, K98I, D111A, G163K, H198S, E210Q, Y220F, D254S, I255A, and P256T;

where the positions correspond to the positions of SEQ ID NO:5 and wherein the lipase variant has at least 90% but less than 100% sequence identity to the polypeptide having the amino acid sequence of SEQ ID NO: 5 and wherein the variant has lipase activity.

One preferred lipase is a variant of SEQ ID NO: 5 comprising the following substitutions: T231R, N233R, D27R, G38A, D96E, D111A, G163K, D254S and P256T One preferred lipase is a variant of SEQ ID NO: 5 comprising the following substitutions: T231R, N233R, N33Q, G91Q, E210Q, I255A.

Suitable lipases are commercially available from Novozymes, for example as Lipex Evity 100L, Lipex Evity 200L (both liquid raw materials) and Lipex Evity 105T (a granulate). These lipases have different structures to the products Lipex 100L, Lipex 100T and Lipex Evity 100T which are outside the scope of the invention.

Other enzymes

The enzyme system can comprise other enzymes. Suitable enzymes provide cleaning performance and/or fabric care benefits. Examples of other suitable enzymes include, but are not limited to, hemicellulases, peroxidases, proteases, cellulases, xylanases, lipases, phospholipases, esterases, cutinases, pectinases, keratanases, reductases, oxidases, phenoloxidases, lipoxygenases, ligninases, pullulanases, tannases, pentosanases, malanases, b-glucanases, arabinosidases, hyaluronidase, chondroitinase, laccase, and known amylases, or combinations thereof. A preferred enzyme system further comprises a cocktail of conventional detersive enzymes such as protease, lipase, cutinase and/or cellulase in conjunction with amylase. Detersive enzymes are described in greater detail in U.S. Patent No. 6,579,839.

Optional Ingredients

The detergent composition may additionally comprise one or more of the following optional ingredients: external structurant or thickener, enzymes, enzyme stabilizers, cleaning polymers, bleaching systems, optical brighteners, hueing dyes, particulate material, perfume and other odour control agents, hydrotropes, suds suppressors, fabric care benefit agents, pH adjusting agents, dye transfer inhibiting agents, preservatives, non-fabric substantive dyes and mixtures thereof. In more preferred embodiments, the laundry detergent composition does not comprise a bleach.

External structurant or thickener: Preferred external structurants and thickeners are those that do not rely on charge - charge interactions for providing a structuring benefit. As such, particularly preferred external structurants are uncharged external structurants, such as those selected from the group consisting of: non-polymeric crystalline, hydroxyl functional structurants, such as hydrogenated castor oil; microfibrillated cellulose; uncharged hydroxyethyl cellulose; uncharged hydrophobically modified hydroxyethyl cellulose; hydrophobically modified ethoxylated urethanes; hydrophobically modified non- ionic polyols; and mixtures thereof.

Suitable polymeric structurants include naturally derived and/or synthetic polymeric structurants. Examples of naturally derived polymeric structurants of use in the present invention include: microfibrillated cellulose, hydroxyethyl cellulose, hydrophobically modified hydroxyethyl cellulose, carboxymethyl cellulose, polysaccharide derivatives and mixtures thereof. Non-limiting examples of microfibrillated cellulose are described in WO 2009/101545 Al. Suitable polysaccharide derivatives include: pectine, alginate, arabinogalactan (gum Arabic), carrageenan, gellan gum, xanthan gum, guar gum and mixtures thereof.

Examples of synthetic polymeric structurants or thickeners of use in the present invention include: polycarboxylates, hydrophobically modified ethoxylated urethanes (HEUr), hydrophobically modified non-ionic polyols and mixtures thereof.

Preferably, the aqueous liquid detergent composition has a viscosity of 50 to 5,000, preferably 75 to 1,000, more preferably 100 to 500 mPa.s, when measured at a shear rate of 100 s-1, at a temperature of 20°C. For improved phase stability, and also improved stability of suspended ingredients, the aqueous liquid detergent composition has a viscosity of 50 to 250,000, preferably 5,000 to 125,000, more preferably 10,000 to 35,000 mPa.s, when measured at a shear rate of 0.05 s-1, at a temperature of 20°C.

Cleaning polymers: The detergent composition preferably comprises a cleaning polymer. Such cleaning polymers are believed to at least partially lift the stain from the textile fibres and enable the enzyme system to more effectively break up the complexes comprising mannan and other polysaccharide. Suitable cleaning polymers provide for broad-range soil cleaning of surfaces and fabrics and/or suspension of the soils. Non-limiting examples of suitable cleaning polymers include: amphiphilic alkoxylated grease cleaning polymers; clay soil cleaning polymers; soil release polymers; and soil suspending polymers. A preferred cleaning polymer is obtainable by free-radical copolymerization of at least one compound of formula (I),

in which n is equal to or greater than 3 for a number,

with at least one compound of formula (II),

in which A- represents an anion, in particular selected from halides such as fluoride, chloride, bromide, iodide, sulfate, hydrogen sulfate, alkyl sulfate such as methyl sulfate, and mixtures thereof. Such polymers are further described in EP3196283A1.

For similar reasons, polyester based soil release polymers, such as SRA300, supplied by Clariant are also particularly preferred.

Other useful cleaning polymers are described in USPN 2009/0124528A1. The detergent composition may comprise amphiphilic alkoxylated grease cleaning polymers, which may have balanced hydrophilic and hydrophobic properties such that they remove grease particles from fabrics and surfaces. The amphiphilic alkoxylated grease cleaning polymers may comprise a core structure and a plurality of alkoxylate groups attached to that core structure. These may comprise alkoxylated polyalkyleneimines, for example. Such compounds may comprise, but are not limited to, ethoxylated polyethyleneimine, ethoxylated hexamethylene diamine, and sulfated versions thereof. Polypropoxylated derivatives may also be included. A wide variety of amines and polyalklyeneimines can be alkoxylated to various degrees. A useful example is 600g/mol polyethyleneimine core ethoxylated to 20 EO groups per NH and is available from BASF. The alkoxylated polyalkyleneimines may have an inner polyethylene oxide block and an outer polypropylene oxide block. The detergent compositions may comprise from 0.1% to 10%, preferably, from 0.1% to 8%, more preferably from 0.1% to 2%, by weight of the detergent composition, of the cleaning polymer.

Dye transfer inhibitor: The detergent composition can comprise a dye transfer inhibitor. Suitable dye transfer inhibitors can be selected from the group consisting of polyvinylpyrrolidone (PVP), polyvinylimidazole (PVI), copolymers of vinylpyrrolidone and vinylimidazole (PVP/PVI), polyvinyl pyridine-N-oxide, poly-N-carboxymethyl-4-vinylpyridiumchloride, and mixtures thereof, with polyvinylpyrrolidone (PVP), polyvinylimidazole (PVI), copolymers of vinylpyrrolidone and vinylimidazole (PVP/PVI), and mixtures thereof being particularly preferred. The dye transfer inhibitor can be present at a level of from 0.05% to 5%, preferably from 0.1% to 3%, and more preferably from 0.2% to 2.5%, by weight of the detergent composition. Polymer Deposition Aid: The laundry detergent composition can comprise from 0.1% to 7%, more preferably from 0.2% to 3%, of a polymer deposition aid. As used herein,“polymer deposition aid” refers to any cationic polymer or combination of cationic polymers that significantly enhance deposition of a fabric care benefit agent onto the fabric during laundering. Suitable polymer deposition aids can comprise a cationic polysaccharide and/or a copolymer, with cationic polysaccharide being preferred and polyquatemium 7 being most preferred.“Fabric care benefit agent” as used herein refers to any material that can provide fabric care benefits. Non-limiting examples of fabric care benefit agents include: silicone derivatives, oily sugar derivatives, dispersible polyolefins, polymer latexes, cationic surfactants and combinations thereof. Preferably, the deposition aid is a cationic or amphoteric polymer. The cationic charge density of the polymer preferably ranges from 0.05 milliequivalents/g to 6 milliequivalents/g. The charge density is calculated by dividing the number of net charge per repeating unit by the molecular weight of the repeating unit. In one embodiment, the charge density varies from 0.1 milliequivalents/g to 3 milliequivalents/g. The positive charges could be on the backbone of the polymers or the side chains of polymers.

Organic builder and/or chelant: The laundry detergent composition can comprise from 0.6% to 10%, preferably from 2 to 7% by weight of one or more organic builder and/or chelants. Suitable organic builders and/or chelants are selected from the group consisting of: MEA citrate, citric acid, aminoalkylenepoly(alkylene phosphonates), alkali metal ethane 1-hydroxy disphosphonates, and nitrilotrimethylene, phosphonates, diethylene triamine penta (methylene phosphonic acid) (DTPMP), ethylene diamine tetra(methylene phosphonic acid) (DDTMP), hexamethylene diamine tetra(methylene phosphonic acid), hydroxy- ethylene 1,1 diphosphonic acid (HEDP), hydroxyethane dimethylene phosphonic acid, ethylene di-amine di-succinic acid (EDDS), ethylene diamine tetraacetic acid (EDTA), hydroxy ethylethylenediamine triacetate (HEDTA), nitrilotriacetate (NTA), methylglycinediacetate (MGDA), iminodisuccinate (IDS), hydroxy ethyliminodisuccinate (HIDS), hydroxy ethyliminodiacetate (HEIDA), glycine diacetate (GLDA), diethylene triamine pentaacetic acid (DTP A), catechol sulfonates such as Tiron™ and mixtures thereof.

Enzyme stabiliser: Enzymes can be stabilized using any known stabilizer system such as calcium and/or magnesium compounds, boron compounds and substituted boric acids, aromatic borate esters, peptides and peptide derivatives, polyols, low molecular weight carboxylates, relatively hydrophobic organic compounds [e.g. certain esters, diakyl glycol ethers, alcohols or alcohol alkoxylates], alkyl ether carboxylate in addition to a calcium ion source, benzamidine hypochlorite, lower aliphatic alcohols and carboxylic acids, N,N-bis(carboxymethyl) serine salts; (meth)acrylic acid-(meth)acrylic acid ester copolymer and PEG; lignin compound, polyamide oligomer, glycolic acid or its salts; poly hexa methylene bi guanide or N,N-bis-3-amino-propyl- dodecyl amine or salt; and mixtures thereof.

Hueing dyes: The detergent composition may comprise fabric hueing agent (sometimes referred to as shading, bluing, or whitening agents). Typically the hueing agent provides a blue or violet shade to fabric. Hueing agents can be used either alone or in combination to create a specific shade of hueing and/or to shade different fabric types. This may be provided for example by mixing a red and green-blue dye to yield a blue or violet shade. Hueing agents may be selected from any known chemical class of dye, including but not limited to acridine, anthraquinone (including polycyclic quinones), azine, azo (e.g., monoazo, disazo, trisazo, tetrakisazo, polyazo), including premetallized azo, benzodifurane and benzodifuranone, carotenoid, coumarin, cyanine, diazahemicyanine, diphenylmethane, formazan, hemicyanine, indigoids, methane, naphthalimides, naphthoquinone, nitro and nitroso, oxazine, phthalocyanine, pyrazoles, stilbene, styryl, triarylmethane, triphenylmethane, xanthenes and combinations thereof.

Optical brighteners: The detergent composition may comprise, based on the total detergent composition weight, from 0.005 to 2 %, preferably 0.01 to 0.1 % of a fluorescent agent (optical brightener). Fluorescent agents are well known and many fluorescent agents are available commercially. Usually, these fluorescent agents are supplied and used in the form of their alkali metal salts, for example, the sodium salts. Preferred classes of fluorescent agent are: Di-styryl biphenyl compounds, e.g. Tinopal (Trade Mark) CBS-X, Di -amine stilbene di-sulphonic acid compounds, e.g. Tinopal DMS pure Xtra and Blankophor (Trade Mark) HRH, and Pyrazoline compounds, e.g. Blankophor SN. Preferred fluorescers are: sodium 2-(4-styryl-3-sulfophenyl)-2H- napthol[l ,2-d]trazole, disodium 4,4'-bis{ [(4-anilino-6-(N methyl-N-2 hydroxyethyl) amino 1 ,3 ,5-triazin-2-yl)]amino } stilbene-2-2' disulfonate, disodium 4,4'-bis { [(4-anilino-6-morpholino- 1 ,3,5-triazin-2-yl)]annino} stilbene-2-2' disulfonate, and disodium 4,4'-bis(2-sulfoslyryl)biphenyl. Hydrotrope: The detergent composition may comprise, based on the total detergent composition weight, from 0 to 30%, preferably from 0.5 to 5%, more preferably from 1.0 to 3.0%, which can prevent liquid crystal formation. The addition of the hydrotrope thus aids the clarity /transparency of the composition. Suitable hydrotropes comprise but are not limited to urea, salts of benzene sulphonate, toluene sulphonate, xylene sulphonate or cumene sulphonate. Preferably, the hydrotrope is selected from the group consisting of propylene glycol, xylene sulfonate, ethanol, and urea to provide optimum performance.

Particles: The composition can also comprise particles, especially when the composition further comprises a structurant or thickener. The composition may comprise, based on the total composition weight, from 0.02% to 10%, preferably from 0.1% to 4%, more preferably from 0.25% to 2.5% of particles. Said particles include beads, pearlescent agents, microcapsules, and mixtures thereof.

Microcapsules: Suitable capsules are typically formed by at least partially, preferably fully, surrounding a benefit agent with a wall material. Preferably, the capsule is a perfume capsule, wherein said benefit agent comprises one or more perfume raw materials. The capsule wall material may comprise: melamine, polyacrylamide, silicones, silica, polystyrene, polyurea, polyurethanes, polyacrylate based materials, polyacrylate esters based materials, gelatin, styrene malic anhydride, polyamides, aromatic alcohols, polyvinyl alcohol, resorcinol-based materials, poly-isocyanate-based materials, acetals (such as 1,3,5-triol-benzene-gluteraldehyde and 1,3,5- triol-benzene melamine), starch, cellulose acetate phthalate and mixtures thereof. Preferably, the capsule wall comprises melamine and/or a polyacrylate based material. The perfume capsule may be coated with a deposition aid, a cationic polymer, a non-ionic polymer, an anionic polymer, or mixtures thereof. Preferably, the perfume capsules have a volume weighted mean particle size from 0.1 microns to 100 microns, preferably from 0.5 microns to 60 microns. Especially where the composition comprises capsules having a shell formed at least partially from formaldehyde, the composition can additionally comprise one or more formaldehyde scavengers.

Process of making the laundry detergent composition:

The laundry detergent compositions can be made using any suitable process known to the skilled person. Typically, the ingredients are blended together in any suitable order. Preferably, the detersive surfactants are added as part of a concentrated premix, to which are added the other optional ingredients. Preferably, the solvent is added either last, or if an external structurant is added, immediately before the external structurant, with the external structurant being added as the last ingredient.

Method of laundering fabrics:

The laundry detergent compositions of the present invention can be used to launder fabrics. In such methods, the laundry detergent composition is diluted to provide a wash liquor having a total surfactant concentration of greater than 300 ppm, preferably from 400 ppm to 2,500 ppm, more preferably from 600 ppm to 1000 ppm. The fabric is then washed in the wash liquor, and preferably rinsed.

The method of the present invention is particularly suited for removing stains, particularly when the stain comprises a combination of mannans and other polysaccharides, and especially when the stains further comprises oils and/or greases such as natural oils and/or natural greases, such as animal fat, vegetable fat, and mixtures thereof. METHODS:

A) pH measurement:

The pH is measured, at 25°C, using a Santarius PT-10P pH meter with gel-filled probe (such as the Toledo probe, part number 52 000 100), calibrated according to the instructions manual. The pH is measured in a 10% dilution in demineralised water (i.e. 1 part laundry detergent composition and 9 parts demineralised water).

B) Method of measuring viscosity:

The viscosity is measured using an AR 2000 rheometer from TA instruments using a cone and plate geometry with a 40 mm diameter and an angle of 1°. The viscosity at the different shear rates is measured via a logarithmic shear rate sweep from 0.1 s ^-1 to 1200 s ^-1 in 3 minutes time at 20°C. Low shear viscosity is measured at a continuous shear rate of 0.05 s ^-1 .

EXAMPLES:

The following are examples of liquid laundry detergent compositions of the present invention.

The following is a low-water liquid laundry detergent composition which can be encapsulated in a water-soluble film in order to provide a water-soluble unit dose article of the present invention. Typically, 24g of the low-water liquid laundry detergent composition can be encapsulated in polyvinyl alcohol film, in order to provide the water-soluble unit dose article. The enzyme levels are given in mg active enzyme protein per lOOg finished product.

The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as“40 mm” is intended to mean“about 40 mm”.