Technical Field
[0001] The present invention relates to heavy-duty liquid laundry detergent compositions
containing anionic synthetic surfactant, detergency builder, specific proteolytic
enzyme and calcium ion. The compositions provide improved cleaning performance, particularly
through-the-wash, of enzyme-sensitive stains such as grass, blood, gravy and chocolate
pudding.
[0002] Laundry detergents containing high levels of anionic surfactant and builder, and
capable of providing superior cleaning performance, are currently available. Some
of these compositions also contain enzymes to enhance removal of enzyme-sensitive
stains. However, it is believed that such compositions are enzyme-limited in that
they can denature and expose stains to enzymatic action faster than currently available
enzymes can cleave and break up the stains.
[0003] Enzyme performance can also be limited by a lack of adequate stability in liquid
detergents. The stabilization of enzymes is particularly difficult in built, heavy-duty
liquid detergents containing high levels of anionic surfactant and water. Anionic
surfactants, especially alkyl sulfates, tend to denature enzymes and render them inactive.
Detergent builders can sequester the calcium ion needed for enzyme activity andior
stability.
[0004] Thus, there is a continuing need for the development of new enzymes that provide
improved performance and better stability in liquid detergent compositions, particularly
those containing high levels of anionic surfactant and builder.
Background Art
[0005] U.S. Patent 4,261,868, Hora et al, issued April 14, 1981, discloses liquid detergents
containing enzymes and, as an enzyme-stabilizing system, 2-25% of a polyfunctional
amino compound selected from diethanolamine, triethanolamine, diisopropanolamine,
triisopropanolamine and tris-(hydroxymethyl) aminomethane, and 0.25-15% of a boron
compound selected from boric acid, boric oxide, borax, and sodium ortho-, meta-and
pyroborate. The compositions can contain 10-60% surfactant, including anionics, and
up to 40% builder.
[0006] U.S. Patent 4,404,115, Tai, issued September 13, 1983, discloses liquid cleaning
compositions, preferably built liquid detergents, containing enzyme, 1-15% alkali
metal pentaborate, 0-15% alkali metal sulfite, and 0-15% of a polyol having 2-6 hydroxy
groups. The compositions can contain 1-60% surfactant, preferably a mixture of anionic
and nonionic in a weight ratio of 6:1 to 1:1, with or without soap. The compositions
also preferably contain 5-50% builder.
[0007] U.S. Patent 4,318,818, Letton et at, issued March 9, 1982, discloses liquid detergents
containing enzymes and an enzyme-stabilizing system comprising calcium ion and a low
molecular weight carboxylic acid or salt, preferably a formate. The compositions preferably
contain from about 20% to 50% surfactant, which can be anionic. In a preferred embodiment,
the compositions contain about 3% to 15% of a saturated fatty acid. They are otherwise
substantially free of builders, but can contain minor amounts of sequestrants.
[0008] European Patent Application 130,756, published January 9, 1985, discloses the proteolytic
enzymes herein and methods for their preparation.
[0009] The enzymes are said to be useful in laundry detergents, both liquid and granular.
They can be combined with surfactants (including anionics), builders, bleach and/or
fluorescent whitening agents, but there is no disclosure of specific detergent compositions.
Summary of the Invention
[0010] This invention relates to heavy-duty liquid laundry detergent compositions comprising,
by weight:
(a) from about 7% to about 50% of an anionic synthetic surfactant; .
(b) from about 5% to about 40% of a detergency builder;
(c) from about 0.01% to about 5% of the proteolytic enzyme characterized by the following
amino acid sequence:


Leu lie Asn Val GIn Ala Ala Ala GIn, (hereinafter referred to as Protease A); or wherein
the Gly at position 166 is replaced with Asn, Ser, Lys, Arg, His, GIn, Ala or Glu;
the Gly at position 169 is replaced with Ser; the Met at position 222 is replaced
with GIn, Phe, Cys, His, Asn, Glu, Ala or Thr; the Gly at position 166 is replaced
with Lys and the Met at position 222 is replaced with Cys; or the Gly at 'position 169 is replaced with Ala and the Met at position 222 is replaced with Ala;
(d) from about 0.01 to about 50 millimoles of calcium ion per liter of composition;
and
(e) from about 10% to about 80% of water; said composition containing at least about
20% of (a) + (b) and having an initial pH of from about 6.5 to about 9.5 at a concentration
of about 0.2% in water at 20°C.
Detailed Description of the Invention
[0011] The liquid detergents of the present invention contain, as essential components,
anionic synthetic surfactant, detergency builder, specific proteolytic enzyme, calcium
ion, and water. The compositions herein provide improved cleaning performance, particularly
through-the-wash, on enzyme-sensitive stains such as grass, blood, gravy and chocolate
pudding.
[0012] While not intending to be limited by theory, it is believed that the relatively high
level of anionic surfactant and builder in the present compositions provides an effective
matrix for denaturing stains and exposing sites to enzymatic action. The anionic surfactant
is believed to be the primary denaturing agent, whereas the builder controls water
hardness that would otherwise complex the anionic surfactant and interfere with its
denaturing action. Once the stains are denatured, enzymes bind to the exposed sites
and clip chemical bonds before returning to solution to begin the cycle again. After
a sufficient number of clips are made, the stained fragments are removed and/or solubilized
by the surfactants. However, it is believed that the surfactant and builder matrix
herein can denature and expose more sites on stains than currently available enzymes
can cleave during the washing process. This is particularly true at low washing temperatures
(e.g., in the range of 15°C to 35°C) where enzymes are catalytically slow. The present
proteolytic enzymes appear to be superior to other proteases in catalytic efficiency.
They thus can take advantage of the stain denaturing power of the compositions herein
and provide significant stain removal benefits. In contrast, they provide little or
no benefits in detergent compositions containing less anionic surfactant and builder.
Anionic Synthetic Surfactant
[0013] The compositions of the present invention contain from about 7% to about 50%, preferably
from about 10% to about 40%, and most preferably from about 15% to about 30%, by weight
of an anionic synthetic surfactant. Suitable anionic synthetic surfactants are disclosed
in U.S. Patent 4,285,841, Barrat et al, issued August 25, 1981, and in U.S. Patent
3,929,678, Laughlin et a1, issued December 30, 1975, both incorporated herein by reference.
[0014] Useful anionic surfactants include the water- soluble salts, particularly the alkali
metal, ammonium and alkylolammonium (e.g., monoethanolammonium or triethanolammonium)
salts, of organic sulfuric reaction products having in their molecular structure an
alkyl group containing from about 10 to about 20 carbon atoms and a sulfonic acid
or sulfuric acid ester group. (Included in the term "alkyl" is the alkyl portion of
aryl groups.) Examples of this group of synthetic surfactants are. the alkyl sulfates,
especially those obtained by sulfating the higher alcohols (C,-C,
s carbon atoms) such as those produced by reducing the glycerides of tallow or coconut
oil; and the alkylbenzene sulfonates in which the alkyl group contains from about
9 to about 15 carbon atoms, in straight chain or branched chain configuration, e.g.,
those of the type described in U. S. Patents 2,220,099 and 2,477,383. Especially valuable
are linear straight chain alkylbenzene sulfonates in which the average number of carbon
atoms in the alkyl group is from about 11 to 14.
[0015] Other anionic surfactants herein are the water- soluble salts of: paraffin sulfonates
containing from about 8 to about 24 (preferably about 12 to 18) carbon atoms; alkyl
glyceryl ether sulfonates, especially those ethers of C ε.
iε alcohols (e.g., those derived from tallow and coconut oil); alkyl phenol ethylene
oxide ether sulfates containing from about 1 to 4 units of ethylene oxide per molecule
and from about 8 to about 12 carbon atoms in the alkyl group; and alkyl ethylene oxide
ether sulfates containing about 1 to about 4 units of ethylene oxide per molecule
and from about 10 to about 20 carbon atoms in the alkyl group.
[0016] Other useful anionic surfactants include the watersoluble salts of esters of alpha-sulfonated
fatty acids containing from about 6 to 20 carbon atoms in the fatty acid group and
from about 1 to 10 carbon atoms in the ester group; water-soluble salts of 2-acyloxy-alkane-1-sulfonic
acids containing from about 2 to 9 carbon atoms in the acyl group and from about 9
to about 23 carbon atoms in the alkane moiety; water-soluble salts of olefin sulfonates
containing from about 12 to 24 carbon atoms; and beta-alkyloxy alkane sulfonates containing
from about 1 to 3 carbon atoms in the alkyl group and from about 8 to 20 carbon atoms
in the alkane moiety.
[0017] Preferred anionic surfactants are the C,o-C,s alkyl sulfates and alkyl ethoxy sulfates
containing an average of up to about 4 ethylene oxide units per mole of alkyl sulfate,
C
11-C
13 linear alkylbenzene sulfonates, and mixtures thereof.
[0018] The compositions preferably contain from about 1% to about 5%, more preferably from
about 2% to about 4%, by weight of unethoxylated alkyl sulfate. These alkyl sulfates
are desired for best detergency performance, in part because they are very denaturing
to stains.
[0019] The compositions herein can optionally contain other synthetic surfactants known
in the art, such as the nonionic, cationic, zwitterionic, and ampholytic surfactants
described in the above-cited Barrat et al and Laughlin et al patents.
[0020] A preferred cosurfactant, used at a level of from about 1% to about 25%, preferably
from about 3% to about 15%, by weight of the composition, is an ethoxylated nonionic
surfactant of the formula R
1(OC
2H
4)
nOH, wherein R' is a C
10-C
16 alkyl group or a C
8-C
12 alkyl phenyl group, n is from about 3 to about 9, and said nonionic surfactant has
an HLB (hydrophile-lipophile balance) of from about 6 to about 14, preferably from
about 10 to about 13. These surfactants are more fully described in U.S. Patents 4,285,841,
Barrat et al, issued August 25, 1981, and 4,284,532, Leikhim et al, issued August
18, 1981, both incorporated herein by reference. Particularly preferred are condensation
products of C
12-C
15 alcohols with from about 3 to about 8 moles of ethylene oxide per mole of alcohol,
e.g., C
12-C
13 alcohol condensed with about 6.5 moles of ethylene oxide per mole of alcohol.
[0021] Preferred cosurfactants for use with the above ethoxylated nonionic surfactants are
amides of the formula

wherein R' is an alkyl, hydroxyalkyl or alkenyl radical containing from about 8 to
about 20 carbon atoms, and R
2 and R
3 are selected from the group consisting of hydrogen, methyl, ethyl, propyl, isopropyl,
2-hydroxyethyl, 2-hydroxypropyl, 3-hydroxypropyl, and said radicals additionally containing
up to about 5 ethylene oxide units, provided at least one of R
2 and R' contains a hydroxyl group.
[0022] Preferred amides are the C
.-C
20 fatty acid alkylol amides in which each alkylol group contains from 1 to 3 carbon
atoms, and additionally can contain up to about 2 ethylene oxide units. Particularly
preferred are the C,2-C,f, fatty acid monoethanol and diethanol amides.
[0023] Certain compositions herein preferably contain from about 5% to about 20%, preferably
from about 6% to about 15%, more preferably from about 7% to about 12%, by weight
of a mixture of the above ethoxylated nonionic surfactant and amide surfactant in
a weight ratio of from about 4:1 to 1:4, preferably from about 3:1 to about 1:3, more
preferably from about 2:1 to about 1:2. In addition, the weight ratio of anionic synthetic
surfactant (on an acid basis) to the total nonionic surfactant (both the ethoxylated
nonionic and the amide) should be from about 2:1 to about 4:1, preferably from about
2.5:1 to about 3.5:1, to ensure that formation and adsorption of sufficient hardness
surfactants at the oilrwater interface to provide good greasy/oily soil removal.
[0024] Other preferred cosurfactants, used at a level of from about 0.5% to about 3%, preferably
from about 0.7% to about 2%, by weight are the quaternary ammonium, amine or amine
oxide surfactants described in U.S. Patent 4,507,219, Hughes, issued March 26, 1985,
incorporated herein by reference.
[0025] While the compositions herein can contain di- long chain quaternary ammonium cationic
surfactants (e.g., those having 2 chains, each containing an average of from about
16 to about 22 carbon atoms), such as disclosed in British Patent 2,041,968, Murphy,
published September 19, 1979, incoroporated herein by reference, the compositions
preferably contain less than about 2%, more preferably less than about 1%, by weight
of such surfactants. Most preferably, the compositions are substantially free of such
surfactants because they appear to be detrimental to the stability of the proteolytic
enzymes herein.
Detergency Builder
[0026] The compsitions herein contain from about 5% to about 40%, preferably from about
8% to about 30%, more preferably from about 10% to about 25%, by weight of a detergent
builder material. In addition, the composition should contain at least about 20%,
preferably from about 25% to about 60%, more preferably from about 30% to about 50%,
by weight.of the anionic synthetic surfactant and builder. Since the proteolytic enzymes
herein appear to provide optimum performance benefits versus other enzymes when the
builder to water hardness ratio is close to one, the compositions preferably contain
sufficient builder to sequester from about 2 to about 10, preferably from about 3
to about 8, grains per gallon of hardness.
[0027] Useful builders are fatty acids containing from about 10 to about 22 carbon atoms.
Preferred are saturated fatty acids containing from about 10 to about 18, preferably
from about 10 to about 14, carbon atoms. When present, the fatty acid preferably represents
about 5% to about 20%, more preferably from about 8% to about 16%, by weight of the
composition.
[0028] Suitable saturated fatty acids can be obtained from natural sources such as plant
or animal esters (e.g., palm kernel oil, palm oil and coconut oil) or synthetically
prepared (e.g., via the oxidation of petroleum or by hydrogenation of carbon monoxide
via the Fisher-Tropsch process). Examples of suitable saturated fatty acids for use
in the compositions of this invention include capric, lauric, myristic, cocnut and
palm kernel fatty acid. Preferred are saturated coconut fatty acids; from about 5:1
to 1:1 (preferably about 3:1) weight ratio mixtures of lauric and myristic acid; mixtures
of the above with minor amounts (e.g., 1 %-30% of total fatty acid) of oleic acid;
and palm kernel fatty acid.
[0029] Detergent builders useful herein also include the polycarboxylate, polyphosphonate
and polyphosphate builders described in U.S. Patent 4,284,532, Leikhim et aI, issued
August 18, 1981, incorporated herein by reference. Water-soluble polycarboxylate builders,
particularly citrates, are preferred of this group. Polycarboxylate builders preferably
represent from about 1 % to about 20% by weight of the composition.
[0030] Suitable polycarboxylate builders include the various aminopolycarboxylates, cycloalkane
polycarboxylates, ether polycarboxylates, alkyl polycarboxylates, epoxy polycarboxylates,
tetrahydrofuran polycarboxylates, benzene polycarboxylates, and polyacetal polycarboxylates.
[0031] Examples of such polycarboxylate builders are sodium and- potassium ethylenediaminetetraacetate;
sodium and potassium nitrilotriacetate; the water-soluble salts of phytic acid, e.g.,
sodium and potassium phytates, disclosed in U.S. Patent 1,739,942, Eckey, issued March
27, 1956, incorporated herein by reference; the polycarboxylate materials described
in U.S. Patent 3,364,103, incorporated herein by reference; and the water-soluble
salts of polycarboxylate polymers and copolymers described in U.S. Patent 3,308,067,
Diehl, issued March 7, 1967, incorporated herein by reference.
[0032] Useful detergent builders also include the . water-soluble salts of polymeric aliphatic
polycarboxylic acids having the following structural and physical characteristics:
(a) a minimum molecular weight of about 350 calculated as to the acid form; (b) an
equivalent weight of about 50 to about 80 calculated as to acid form; (3) at least
45 mole percent of the monomeric species having at least two carboxyl radicals separated
from each other by not more than two carbon atoms: (d) the site of attachment of the
polymer chain of any carboxyl- containing radical being separated by not more than
three carbon atoms along the polymer chain from the site of attachment of the next
carboxyl- containing radical. Specific examples of such builders are the polymers
and copolymers of itaconic acid, aconitic acid, maleic acid, mesaconic acid, fumaric
acid, methylene malonic acid, and citraconic acid.
[0033] Other suitable polycarboxylate builders include the water-soluble salts, especially
the sodium and potassium salts, of mellitic acid, citric acid, pyromellitic acid,
benzene pentacarboxylic acid, oxydiacetic acid, carboxymethyloxysuccinic acid, carboxymethyloxymalonic
acid, cis-cyclohex- anehexacarboxylic acid, cis-cyclopentanetetracarboxylic acid and
oxydisuccinic acid..
[0034] Other polycarboxylates for use herein are the polyacetal carboxylates described in
U.S. Patent 4,144,226, issued March 13, 1979 to Crutchfield et al, and U.S. Patent
4,146,495, issued March 27, 1979 to Crutchfield et al, both incorporated herein by
reference.
[0035] Other detergent builders useful herein include the aluminosilicate ion exchange material
described in U.S. Patent 4,405,483, Kuzel et al, issued September 20, 1983, incorporated
herein by reference.
[0036] As part of the builder system, the compositions herein preferably contain from about
0.1 % to about 1 %, more preferably from about 0.2% to about 0.6%, by weight of water-soluble
salts of ethylenediamine tetramethylenephosphonic acid, diethylenetriamine pentamethylenephosphonic
acid, ethylenediamine tetraacetic acid, or diethylenetriamine pentaacetic acid to
enhance cleaning performance when pretreating fabrics.
Proteolytic Enzyme
[0037] The compositions of the present invention contain from about 0.01% to about 5%, preferably
from about 0.1% to about 2%, by weight of the composition of Protease A as previously
defined, or variants thereof in which the Gly at position 166 is replaced with Asn,
Ser, Lys, Arg, His, Gln, Ala or Glu; the Gly at position 169 is replaced with Ser;
the Met at position 222 is replaced with Gin, Phe, Cys, His, Asn, Glu, Ala or Thr;
the Gly at position 166 is replaced with Lys and the Met at position 222 is replaced
with Cys; or the Gly at position 169 is replaced with Ala and the Met at position
222 is replaced with Ala.
[0038] These proteases, and methods for their preparation, are described in European Patent
Application 130,756, published January 9, 1985, incorporated herein by reference.
[0039] The above enzyme is preferably included in an amount sufficient to provide an activity
of from about 0.001 to about 0.1, more preferably from about 0.005 to about 0.07,
most preferably from about 0.01 to about 0.04, Anson units per gram of composition.
[0040] The proteases herein are preferably purified, prior to incorporation in the finished
composition, so that they have no detectable odor at a concentration of less than
about 0.002 Anson units per gram in distilled water. They preferably have no detectable
odor at a concentration of less than about 0.0025, more preferably less than about
0.003, Anson units per gram of distilled water.
[0041] Proteases herein can be odor purified by any method known in the art. Examples include
the solvent precipitation methods described in Preci
pi-tation of the Enzymes and Their Stability in High Alcohol Concentrations by Bauer
et al in the Israel J. Chem. 5(3), pages 117-20 (1967) and Enzyme Preparations by
Sugiura et al and Yakusaigaku 1967, Volume 27(2), pages 135-9.
[0042] Solvent initiated precipitation of a crude commercial enzyme solution results in
most of the enzymatic activity being precipitated from solution and most of the odor
and color impurities remaining in the supernatant liquid. Decantation or centrifugation
of the supernatant liquid from the precipitated enzyme results in an enzyme fraction
with enriched enzymatic activity/gram and improved odor and color.
[0043] Various solvents or solvent pair combinations can be used to effect the desired precipitation.
For example, methanol, ethanol, acetone, other organic solvents, and combinations
of organic solvents with and without water can be used. A highly preferred solvent
is a combination of water and 30-70% by weight ethanol. This appears to be optimal
to prevent enzyme deactivation and maximum recovery of activity.
[0044] Purfication of protease enzymes also provide benefits in the area of product color
stability.
Calcium Ion
[0045] The composition also contains from about 0.01 to about 50, preferably from about
0.1 to about 30, more preferably from about 1 to about 20, millimoles of calcium ion
per liter. The level of calcium ion should be selected so that there is always some
minimum level available for the enzyme, after allowing for complexation with builders,
etc., in the composition. Any water-soluble calcium salt can be used as the source
of calcium ion, including calcium chloride, calcium formate, and calcium acetate.
A small amount of calcium ion, generally from about 0.05 to about 0.4 millimoles per
liter, is often also present in the composition due to calcium in the enzyme slurry
and formula water.
Water
[0046] Finally, the compositions herein contain from about 10% to about 80%, preferably
from about 20% to about 60%-, more preferably from about 30% to about 50%, by weight
of water.
Optional Components
[0047] The compositions of the present invention can also contain other materials known
in the art to enhance enzyme stability. Preferably the compositions herein contain
from about 0.1% to about 10%, more preferably from about 0.25% to about 5%, most preferably
from about 0.5% to about 3%, by weight of boric acid or a compound capable of forming
boric acid in the composition (calculated on the basis of the boric acid). Boric acid
is preferred, although other compounds such as boric oxide, borax and other alkali
metal borates (e.g., sodium ortho-, meta-and pyroborate, and sodium pentaborate) are
suitable. Substituted boric acids - (e.g., phenylboronic acid, butane boronic acid,
and p-bromo phenylboronic acid) can also be used in place of boric acid.
[0048] Other preferred enzyme stabilizers are polyols containing only carbon, hydrogen and
oxygen atoms. They preferably contain from 2 to 6 carbon atoms and from 2 to 6 hydroxy
groups. Examples include propylene glycol (especially 1,2 propane diol, which is preferred),
ethylene, glycol, glycerol, sorbitol, mannitol, and glucose. The polyol generally
represents from about 1% to about 15%, preferably from about 1.5% to about 10%, by
weight of the composition. Preferably, the weight ratio of polyol to boric acid is
at least 1, more preferably at least about 1.3.
[0049] The compositions can also contain the water- soluble, short chain carboxylates described
in U.S. Patent 4,318,818, Letton et al, issued March 9, 1982, incorporated herein
by reference. The for- mates are preferred and can be used at levels of from about
0.05% to about 5%, preferably from about 0.2% to about 2%, most preferably from about
0.4% to about 1.5%, by weight of the composition.
[0050] The compositions herein have an initial pH of from about 6.5 to about 9.5, preferably
from about 7 to about 8.5, most preferably from about 7.2 to about 8.0, at a concentration
of 0.2% by weight in distilled water at 20°C. Preferred pH buffers include monoethanolamine
and triethanolamine. Monoethanolamine and triethanolamine also further enhance enzyme
stability, and preferably are included at levels of from about 0.5% to about 10%,
preferably from about 1 % to about 4%, by weight of the composition.
[0051] Other optional components for use in the Iiquid _ detergents herein include soil
removal agents, antiredeposition agents, suds regulants, hydrotropes, opacifiers,
antioxidants, bactericides, dyes, perfumes, and brighteners known in the art. Such
optional components generally represent less than about 15%, preferably from about
1% to about 10%, by weight of the composition.
[0052] Particularly preferred stable isotropic liquid detergents herein are described in
U.S. Patent 4,507,219, Hughes, issued March 26, 1985, incorporated herein by reference.
[0053] The following examples illustrate the compositions of the present invention.
[0054] All parts, percentages and ratios used herein are by weight unless otherwise specified.
EXAMPLE I
[0055] The following detergent compositions were prepared.

in which about 20% by weight of the material has a value of u higher than 5 is dissolved
at about 15% level in anhydrous ethanol; cooled to about 10°C; the insoluble portion
(~ 20%) is filtered; and enough ethanol is distilled to reduce the ethanol level to
within the level in the formula
[0056] When used in Compositions A and B (which were tested at a concentration of 2000 parts
per million [ppm] in water), Protease A of the present invention provided significantly
better through-the-wash cleaning of enzyme-sensitive stains such as grass, blood,
gravy, and/or chocolate pudding than did equivalent amounts (providing either 0.0012,
0.015 or 0.03 Anson units of activity per gram of composition) of the commercially
available proteolytic enzymes Alcalase® (Novo Industries A.S.), Maxtase® (Gist-Brocades
N.V.) and Maxacal@ - (Gist-Brocades N.V.). With pretreatment, Protease A provided
smaller, generally directional benefits, but with some losses, versus Alcalase on
enzyme-sensitive stains. Protease A also provided similar benefits relative to Alcalase
when the pH of Composition A in the wash solution was adjusted from 7.5 to 7.1, 7.3,
8.0 and 8.5. Protease A provided similar benefits relative to Maxatase when the pH
of Composition B in the wash solution was adjusted to 8.0 and 8.5. Significant advantages
on grass and chocolate pudding for Protease A were also obtained when the solution
pH of Composition B was adjusted to 9.0 to 9.5, although the magnitude of the benefit
was reduced at these higher pH's.
[0057] In Compositions C (which was tested at a concentration of 900 ppm in water) and D
(tested at a concentration of 2000 ppm in water), both of which are not within the
scope of the invention, Protease A exhibited little or no benefit overall, and some
negatives, on enzyme-sensitive stains, both through-the-wash and with pre-treatment,
when compared with Alcalase.
[0058] Protease A was also significantly less effective than Maxacal on certain grass, blood,
gravy and chocolate pudding stains when used in a granular detergent (which is not
within the scope of the invention) containing 14.5% anionic surfactant, 33.7% sodium
tripolyphosphate and 10.5% sodium carbonate builder, and which provided a pH of 10.0
at its usage concentration of 1500 ppm by weight in water at 20°C. Protease A was
generally equivalent to Alcalase in the same test, except for significant advantages
on some blood stains. When the solution pH of the granular detergent was reduced to
8.0 and 8.5, Protease A was significantly less effective than Maxatase on grass, blood,
gravy and chocolate pudding stains.
[0059] When the C
12.
14 fatty acid and citric acid of Composition A were added at a level of 260 ppm and
80 ppm, respectively, to wash water containing 900 ppm of Composition C (thereby providing
a composition which would have been within the . scope of the invention if the fatty
acid and citric acid were added directly to Composition C), Protease A provided better
overall cleaning and significant advantages on some stains when compared with Alcalase.
Similar results were obtained when 260 ppm of the fatty acid and 60 ppm of citric
acid were added to a wash solution containing 1800 ppm of Composition C (also thereby
providing a composition which would have been within the scope of the invention if
the acids were added directly to Composition C).
[0060] Variants of Protease A in which the Gly at position 166 is replaced with Asn, Ser,
Lys, Arg, His, Gin, Ala or Glu; the Gly at position 169 is replaced with Ser; the
Met at position 222 is replaced with Gin, Phe, Cys, His, Asn, Glu, Ala or Thr; the
Gly at position 166 is replaced with Lys and the Met at position 222 is replaced with
Cys; or the Gly at position 169 is replaced with Ala and the Met at position 222 is
replaced with Ala, all provided better stain removal than Alcalase when tested in
Composition A.
[0061] Preferred Composition E of the present invention contains 0.75% of a slurry of Protease
A, providing an activity of 0.015 Anson units per gram of composition.