Stabilized enzymes liquid detergent composition containing lipase and protease

Abstract

The invention relates to the stabilization of mixtures of proteolytic and lipolytic enzymes in a liquid medium such as a liquid detergent composition. By inclusion therein of a stabilizing system comprising a polyol and a boron compound which are capable of reacting with each other whereby the polyol has a first binding constant with the boron compound of at least 500 l/mole and a second binding constant of at least 1,000 l.sup.2 /mole.sup.2, the stability of the lipase in the presence of the protease is significantly improved.The lipase is preferably obtained from Humicola lanuginosa, and the stabilizing system preferably comprises a mixture of sorbitol and borax.

Description

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to enzymatic liquid detergent compositions comprising both lipolytic and proteolytic enzymes, wherein the storage stability of the lipolytic enzymes is improved by the inclusion in the composition of a particular enzyme-stabilizing system.

2. Description of the Related Art

Enzymatic liquid detergent compositions are well-known in the art. They mainly contain a proteolytic enzyme, or a mixture of a proteolytic enzyme and an amylolytic enzyme. One of the major problems which is encountered with such enzymatic liquid detergent compositions is that of ensuring a sufficient storage-stability of the enzymes in these compositions.

There have already been various proposals for the inclusion of a variety of special enzyme-stabilising systems in such enzymatic liquid detergent compositions. A number of these proposals are directed to the use of a combination of a polyol and a boron compound as an enzyme-stabilizing system. Thus, Canadian Pat. No. 1,092,036 (Hora et al.) discloses enzymatic liquid detergents comprising a proteolytic and/or an amylolytic enzyme and an enzyme stabilizing system containing a polyol such as 1,2-propanediol, ethyleneglycol, erythritan, glycerol, sorbitol, mannitol, glucose, fructose, lactose, and a boron compound such as boric acid, boric oxide borax, alkalimetal ortho-, meta- and pyroborates which is capable of reacting with the polyol. In U.S. Pat. No. 4,404,115 (Tai), the combination of an alkalimetal pentaborate, optionally with an alkalimetal sulphite and/or a polyol is described as an enzyme-stabilizing system in enzymatic liquid detergents comprising a protease and/or an amylase.

In Japanese patent application No. 72/35,192 (Nagase), laid open to public inspection on Nov. 24, 1972, the use of mixtures of a polyol such as sorbitol or glycerol and borax to stabilize proteolytic enzymes in liquid detergents is disclosed.

There are several references disclosing enzymatic liquid detergent compositions which include the combination of a polyol and a boron compound in an enzyme-stabilizing system, e.g. British Pat. No. 2,079,305 (Boskamp), European Pat. No. 80,223 (Boskamp) and U.S. Pat. No. 4,537,707 (Severson), wherein the enzyme is a proteolyotic and/or amylolytic enzyme.

In U.S. Pat. No. 4,465,619 (Boskamp) an enzymatic liquid detergent composition is described, which may contain proteases, amylases, cellulases or lipases, and an enzyme-stabilizing system comprising a mixture of a polyol and a boron compound. This composition may not contain more than about 2% by weight of the boron compound.

In European Patent Application No. 258,068 (NOVO) published on Mar. 2, 1988, a detergent lipase is described, which can be stabilized in an aqueous detergent composition by the inclusion therein of 1,2-propanediol, optionally together with a calcium salt. Sorbitol is stated to have only a slight stabilizing effect.

None of these prior proposals deal with enzyme-stabilizing systems to improve the stability of lipolytic enzymes in liquid detergent compositions which also include a proteolytic enzyme. It is therefore an object of the present invention to provide for an enzyme-stabilizing system which, when included in an enzymatic liquid detergent composition which includes both a lipase and a protease, would improve the storage stability of the lipase therein.

SUMMARY OF THE INVENTION

It has now surprisingly been found, that the above object of the invention can be achieved by using as an enzyme-stabilizing system a combination of a polyol and a boron compound, said polyol having predominantly vicinal hydroxyl groups and said boron compound being capable of reacting with said polyol, said polyol having a first binding constant to the boron compound of at least 500 l/mole and a second binding constant to the boron compound of at least 1,000 l.sup.2 /mole.sup.2 as determined at 25.degree. C. according to the method of Conner and Bulgrin, Journal of Inorganic Nuclear Chemistry, 1967, Vol. 29, pages 1953-1961.

Since lipases, being proteins, would be susceptible to proteolytic attack, it was unexpected to find that the above enzyme-stabilizing system, which embraces systems known to stabilize proteolytic enzymes, did not cause a decrease in the stability of the lipolytic enzyme on storage, but rather increased the storage stability of the lipolytic enzyme.

DETAILED DESCRIPTION OF THE INVENTION

The polyol, used in the present invention, should have vicinal hydroxyl groups and should be capable of forming a complex with the boron compound, having a first binding constant of at least 500 l/mole and a second binding constant of at least 1,000 l.sup.2 /mole.sup.2 when reacted with the boron compound as determined at 25.degree. C. according to the aforesaid method of Conner and Bulgrin, l.c.

The polyol should contain only C, H and O atoms and should contain at least two hydroxyl groups. Typical examples of suitable polyols for use in the present invention are D-mannitol, sorbitol and 1,2-benzenediol. Sorbitol is the preferred polyol.

In general, the polyol is used in the present invention in an amount of 1-20% by weight, preferably from 2-15% by weight of the final composition. The boron compound, used in the present invention, should be capable of forming a complex with the polyol. Typical examples of boron compounds, suitable in the present invention are boric acid, boric oxide, alkalimetal borates such as sodium and potassium ortho-, meta- and pyroborates, borax, and polyborates such as the alkalimetalpentaborates. Preferably the boron compound is sodium tetraborate 10.H.sub.2 O or 5.H.sub.2 O. In general, the boron compound is used in an amount of 1-10% by weight, preferably from 2-6% by weight of the final composition.

Although the weight ratio of the polyol to the boron compound may vary to some extent, it is preferred that this weight ratio ranges from 0.5 to 3, and is particularly greater than 1.0.

Naturally, mixtures of the above polyols and mixtures of the above boron compounds and their variations may be used.

The lipolytic enzyme used in the present invention is either a fungal lipase producible by Humicola lanuginosa and Thermomyces lanuginosus, or a bacterial lipase which show a positive immunological cross-reaction with the antibody of the lipase produced by the micro-organism Chromobacter viscosum var. lipolyticum NRRL B-3673. This micro-organism has been described in Dutch patent specification No. 154,269 of Toyo Jozo Kabushiki Kaisha and has been deposited with the Fermentation Research Institute, Agency of Industrial Science and Technology, Ministry of International Trade & Industry, Tokyo, Japan, and added to the permanent collection under nr. Ko Hatsu Ken Kin Ki 137 and is available to the public at the United States Department of Agriculture, Agricultural Research Service, Northern Utilization and Development Division at Peoria, Ill., U.S.A., under the nr. NRRL B-3673. The lipase produced by this micro-organism is commercially available from Toyo Jozo Co, Tagata, Japan, hereafter referred to as "TJ lipase". These bacterial lipases of the present invention should show a positive immunological cross-reaction with the TJ lipase antibody, using the standard and well-known immunodiffusion procedure according to Ouchterlony (Acta. Med. Scan., 133, pages 76-79 (1950).

The preparation of the antiserum is carried out as follows:

Equal volumes of 0.1 mg/ml antigen and of Freund's adjuvant (complete or incomplete) are mixed until an emulsion is obtained. Two female rabbits are injected with 2 ml samples of the emulsion according to the following scheme:

______________________________________day 0 antigen in complete Freund's adjuvantday 4 antigen in complete Freund's adjuvantday 32 antigen in incomplete Freund's adjuvantday 60 booster of antigen in incomplete Freund's adjuvant______________________________________ The serum containing the required antibody is prepared by centrifugation of clotted blood, taken on day 67.

The titre of the anti-TJ-lipase antiserum is determined by the inspection of precipitation of serial dilutions of antigen and antiserum according to the Ouchterlony procedure. A 2.sup.5 dilution of antiserum was the dilution that still gave a visible precipitation with an antigen concentration of 0.1 mg/ml.

All bacterial lipase showing a positive immunological cross-reaction with the TJ-lipase antibody as hereabove described are lipases suitable in the present invention. Typical examples thereof are the lipase ex Pseudomonas fluorescens IAM 1057 available from Amano Pharmaceutical Co, Nagoya, Japan, under the trade-name Amano-P lipase, the lipase ex Pseudomonas fragi FERM P 1339 (available under the trade-name Amano-B), the lipase ex Pseudcmonas nitroreducens var. lipolyticum FERM P 1338, the lipase ex Pseudomonas sp. available under the trade name Amano CES, the lipase ex Pseudomonas cepacia, lipases ex Chromobacter viscosum, e.g. Chromobacter viscosum var. lipolyticum NRRL B-3673, commercially available from Toyo Jozo Co., Tagata, Japan; and further Chromobacter viscosum lipases from U.S. Biochemical Corp., U.S.A. and Diosynth Co., The Netherlands, and lipases ex Pseudomonas gladioli.

An example of a fungal lipase as defined above is the lipase ex Humicola lanuginosa, available from Amano under the trade-name Aaano CE; the lipase ex Humicola lanuginosa as described in the aforesaid European Patent Application No. 0258,068 (NOVO), as well as the lipase obtained by cloning the gene from Humicola lanuginosa and expressing this gene in Aspergillus oryzae, commercially available from NOVO Industri A/S under the trade name "Lipolase". This Lipolase is a preferred lipase for use in the present invention.

The lipases of the present invention are included in the liquid detergent composition in such an amount that the final composition has a lipolytic enzyme activity of from 100 to 0.005 LU/mg, preferably 25 to 0.05 LU/mg of the composition.

A Lipase Unit (LU) is that amount of lipase which produces 1 .mu.mol of titratable fatty acid per minute in a pH stat. under the following conditions: temperature 30.degree. C.; pH=9.0; substrate is an emulsion of 3.3 wt. % of olive oil and 3.3% gum arabic, in the presence of 13 mmol/l Ca.sup.2+ and 20 mmol/l NaCl in 5 mmol/l Tris-buffer.

Naturally, mixtures of the above lipases can be used. The lipases can be used in their non-purified form or in a purified form, e.g. purified with the aid of well-known adsorption methods, such as phenyl sepharose adsorption techniques.

The proteolytic enzyme, used in the present invention, can be of vegetable, animal or microorganism origin. Preferably it is of the latter origin, which includes yeasts, fungi, molds and bacteria. Particularly preferred are bacterial subtilisin type proteases, obtained from e.g. particular strains of B. subtilis and B. licheniformis. Examples of suitable commercially available proteases are Alcalase, Savinase, Esperase, all of NOVO Industri A/S; Maxatase and Maxacal of Gist-Brocades; Kazusase of Showa Denko; BPN and BPN' proteases and so on. The amount of proteolytic enzyme, included in the composition, ranges from 0.1-50 GU/mg, based on the final composition. Naturally, mixtures of different proteolytic enzymes may be used.

A GU is a glycine unit, which is the amount of proteolytic enzyme which under standard incubation conditions produces an amount of terminal NH.sub.2 -groups equivalent to 1 microgramme/ml of glycine.

The compositions of the invention furthermore may comprise one or more detergent-active materials such as soaps, synthetic anionic, nonionic, amphoteric or zwitterionic detergent materials or mixtures thereof. These materials are all well-known in the art. Preferably the compositions contain a nonionic detergent or a mixture of a nonionic and an anionic detergent. Nonionic detergents are well-known in the art. They are normally reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example aliphatic alcohols, acids, amides or alkylphenols with alkylene oxides, especially ethylene oxide either alone or with propylene oxide. Typical examples of suitable nonionic detergents are alkyl (C.sub.6 -C.sub.22) phenol-ethylene oxide condensation products, with generally 5-25 moles of ethylene oxide per mole of alkylphenol, the condensation products of aliphatic C.sub.8 -C.sub.18 primary or secondary, linear or branched chain alcohols with generally 5-40 moles of ethylene oxide, and products made by condensation of ethylene oxide and propylene oxide with ethylenediamine. Other nonionic detergents include the block copolymers of ethylene oxide and propylene oxide, alkylpolyglycosides, tertiary amine-oxides and dialkylsulphoxides. The condensation products of the alcohols with ethylene oxide are the preferred nonionic detergents.

Anionic detergents, suitable for inclusion in the compositions of the present invention include the C.sub.10 -C.sub.24 alkylbenzenesulphonates, the C.sub.10 -C.sub.18 alkanesulphonates, the C.sub.10 -C.sub.24 alkylethersulphates with 1-10 moles of ethylene and/or propyleneoxide in the ether variety and so on.

In general, the compositions may contain the detergent-active compounds in an amount of 5-90, usually 1-70 and preferably 15-50% by weight.

The liquid detergent compositions of the present invention can furthermore contain one or more other, optional ingredients. Such optional ingredients are e.g. perfumes, including deoperfumes, colouring materials, opacifiers, soil-suspending agents, soil-release agents, solvents such as ethanol, ethyleneglycol, propylene glycol, hydrotropes such as sodium cumene-, toluene- and xylenesulphonate as well as urea, alkaline materials such as mono-, di- or triethanol-amine, clays, fabric-softening agents and so on.

The liquid detergent composition may be unbuilt or built, and may be aqueous or non-aqueous. If a built liquid detergent composition is required, the composition may contain from 1-60%, preferably 5-30% by weight of one or more organic and/or inorganic builder. Typical examples of such builders are the alkalimetal ortho-, pyro- and tri- polyphosphates, alkalimetal carbonates, either alone or in admixture with calcite, alkalimetal citrates, alkalimetal nitrilotriacetates, carboxyethyloxy succinates, zeolites, polyacetal carboxylates and so on.

The compositions may furthermore comprise lather boosters, foam depressors, anti-corrosion agents, chelating agents, anti-soil redeposition agents, bleaching agents, other stabilizing agents for the enzymes such as glycerol, sodium formate, calcium salts and the like, activators for the bleaching agents and so on. They may also comprise enzymes other than the proteases and lipases, such as amylases, oxidases and cellulases. In general, the compositions may comprise such other enzymes in an amount of 0.01-10% by weight.

When the liquid detergent composition is an aqueous composition, the balance of the formulation consists of an aqueous medium. When it is in the form of a non-aqueous composition, the above ingredients together with the essential ingredients make up for the whole formulation.

The invention will further be illustrated by way of Example.

EXAMPLE I

The storage stability of Lipolase in water was accessed at 37.degree. C. The Lipolase was present in an amount of 7500 LU/ml, and Savinase was present in an amount of 15,000 GU/ml. The pH of the solution was 7. The following Table represents the results of this assessment.

______________________________________ Lipase Stability @37.degree. C. (% Left) DaysSolution Composition 1 2 8 15 34______________________________________Distilled water (pH7) + Savinase 28 9 0 -- --Distilled water + 6% Sodium Tetra- 100 100 49 19 7borate (10 H.sub.2 O) + 7% Sorbitol +Savinase (pH7)______________________________________

EXAMPLE II

The following citrate-built formulations were prepared.

______________________________________ Wt % in FormulationIngredeients 2.1 2.2 2.3 2.4 2.5______________________________________C.sub.10 -C.sub.13 Alkylpolyglycoside (ex 17 17 17 17 17Horizon 1:1 blend of APG 400& 500)C.sub.12 -C.sub.15 Alcohol Ethoxylate 7 7 7 7 7with 9 moles ofethylene oxideSodium Citrate Dihydrate 7 7 7 7 7Sodium Formate -- 3 -- 3 --Sorbitol 7.1 7.1 -- -- --Sodium Tetra borate 4 4 -- 4 4DecahydrateSavinase 16.0/L 0.375 0.375 0.375 0.375 0.375Lipolase 7,500 LU per gramWater to 100%______________________________________ The formulation 2.3 was adjusted to pH 7 with HCl.

The stability of Lipolase in these formulations at 37.degree. C. was found to be as follows:

______________________________________ % Lipase Activity Remaining DaysFormulation 1 2 4 7 15______________________________________2.1 97 88 89 70 262.2 97 92 86 68 292.3 68 49 30 15 02.4 73 42 18 9 02.5 68 40 19 3 0______________________________________

EXAMPLE III

The liquid detergent compositions given below were prepared. Each of the compositions contained Lipolase at a level delivering 15 LU/ml when the formulations were diluted to 2 gm/l.

______________________________________ Wt % in FormulationIngredients 3.1 3.2 3.3 3.4______________________________________C.sub.12 -C.sub.15 alcohol ethoxylate with 17 17 17 179 moles of ethylene oxideSodium C.sub.11 alkylbenzene Sulfonate 7 7 7 7Sodium Xylene Sulfonate 4 4 4 4Sodium Tetra Borate Decahydrate 4 4 4 4Glycerol 6 6 6 6Sorbitol 2.7 -- 2.7 --Savinase 16L 0.375 0.375Alcalase 2.5L -- -- 0.75 0.75Water Water to 100%______________________________________ The stability of Lipolase in these formulations at 37.degree. C. is given below. ______________________________________ DaysFormulation 1 2 4 7 15______________________________________3.1 89 77 63 43 33.2 69 59 35 12 03.3 64 27 5 0 03.4 28 9 0 0 0______________________________________

EXAMPLE IV

The liquid detergent compositions given below were prepared. Each of the compositions contained Lipolase at a level delivering 15 LU/ml when the Formulations were diluted to 2 gm/l.

__________________________________________________________________________ wt. % in FormulationIngredients 4.1 4.2 4.3 4.4 4.5 4.6 4.7__________________________________________________________________________C.sub.12 -C.sub.15 alcohol ethoxylate 17 17 17 17 17 17 17with 9 moles of ethylene oxideSodium C.sub.11 alkylbenzene sulfonate 7 7 7 7 7 7 7Sodium xylene sulfonate 5 5 5 5 5 5 5Sodium tetraborate decahydrate -- 4 -- 4 4 4 4propylene glycol -- -- -- -- 5.9 -- 5.3sorbitol -- -- 5.9 5.9 -- 5.3 --sodium formate -- -- -- -- -- 1.5 1.5calcium chloride dihydrate -- -- -- -- -- 0.5 0.5Savinase 16L 0.375 0.375 0.375 0.375 0.375 0.375 0.375water water to 100%__________________________________________________________________________

The stability of Lipolase in these formulations at 37.degree. C. is given below.

______________________________________ DaysFormulation 1 2 3 5 6 8 9______________________________________4.1 54 32 19 -- 3 -- --4.2 17 9 -- -- -- -- --4.3 61 33 23 -- 8 -- --4.4 86 66 53 -- 34 -- 124.5 71 39 -- 11 -- -- --4.6 81 68 60 -- 41 -- 184.7 71 49 37 -- 14 -- 4______________________________________

EXAMPLE V

The following formulations were prepared, all containing the same amount of Lipolase as in Example III.

______________________________________ Wt % in FormulationIngredients 4.1 4.2 4.3 4.4 4.5 4.6______________________________________C.sub.12 -C.sub.15 alcohol ethoxylate 17 17 17 17 17 17with 9 moles of ethylene oxideSodium C.sub.11 alkylbenzene 7 7 7 7 7 7Sulfonate (Sodium Salt)Sodium Xylene Sulfonate 4 4 4 4 4 4Sodium Tetraborate (10 H.sub.2 O) 4 -- 4 -- 4 --Glycerol 6 6 6 6 6 6Sorbitol 2.7 -- 2.7 -- 2.7 --Savinase 16.0L 0.375 0.375 -- -- -- --Alcalase 2.5L -- -- 0.75 0.75 -- --Lipolase (7500 LU/g) .sqroot. .sqroot. .sqroot. .sqroot. .sqroot. .sqroot.Water to 100%______________________________________ The detergent performance of these formulations in cleaning two types of test fabrics was carried out. Testing cloth A comprised a complex soil containing proteinaceous and fatty components; Test cloth B contained a fatty/particulate type of soil.

The detergency procedure was as follows: The soiled clothes (4 type A 2 type B) were washed for 14 minutes at 40.degree. C. in a Tergo-Tometer (United State Testing) in the presence of one liter of the test detergent solution at a concentration of 2 gm/liter. The agitation was set at 100 RPM and the wash solution contained 120 ppm hardness (as calcium carbonate, Ca/Mg 2:1). After the wash, the clothes were rinsed for five minute in tap water (100 ppm Ca/Mg 2:1) and dried. The extent of cleaning was determined from the change in reflectance measured with a Gardener colormeter Model No. 05. All measurements were done in duplicate.

Results of these detergency evaluations are given below.

______________________________________Change in Reflectance After Washing Delta RFormulation Test Cloth A Test Cloth B______________________________________4.1 18.0 16.24.2 10.8 11.04.3 19.1 16.54.4 14.6 10.84.5 5.2 15.04.6 5.5 10.4______________________________________ The above results demonstrate the improvement which the incorporation of the higher polyol/borate has on detergency performance of the protease/lipase containing formulations. In the absence of protease the incorporation of sorbitol/borate does not have a perceptible effect on performance of the Type A cloth which contains a proteinaceous soil.

Claims

1. An enzymatic liquid detergent and cleaning composition comprising, in a liquid medium, from 0-90% by weight of a detergent-active compound, a proteolytic enzyme and a lipolytic enzyme, said lipolytic enzyme being selected from the group consisting of fungal lipases obtainable from Humicola lanuginosa and Thermomyces lanuginosus, and bacterial lipases which show a positive immunological cross-reaction with the antibody of the lipase, produced by Chromobacter viscosum var. lipolyticum NRRL-B3673, and an enzyme stabilizing system comprising a mixture of a polyol containing only C, H and O atoms and containing at least two hydroxyl groups and a boron compound which is capable of reacting with said polyol, wherein said polyol has a first binding constant with said boron compound of at least 500 l/mole and a second binding constant of at least 1,000 l.sup.2 /mole.sup.2, and wherein the weight ratio of said polyol to said boron compound is greater than 1.0.

2. The composition of claim 1, wherein the lipase is a lipase, obtained by cloning the gene from Humicola lanuginosa and expressing this gene in Aspergillus oryzae.

3. The composition of claim 1, wherein the polyol is sorbitol or 1,2-benzenediol.

4. The composition of claim 1, wherein the boron compound is sodium tetraborate.

5. The composition of claim 1, wherein the proteolytic enzyme is a bacterial subtilisin protease.

6. The composition of claim 1, comprising, in a liquid medium, from 5-90% by weight of the detergent-active compound, from 0.1-50 GU per milligramme of the final composition of the proteolytic enzyme, from 0.005-100 LU per milligramme of the final composition of the lipolytic enzyme, from 1-20% by weight of the polyol, and from 1-10% by weight of the boron compound.