PH26060A

PH26060A - Alkaline cellulose K and CM case I

Info

Publication number: PH26060A
Application number: PH37390A
Authority: PH
Inventors: Susumo Ito; Kenzo Koike; Kikuhiko Okamoto; Yuichi-Ota; Akira Takei
Original assignee: Kao Corp
Priority date: 1986-10-28
Filing date: 1988-08-10
Publication date: 1992-01-29

Description

I ——— + -— — _—— — : 4 | 0 + 26060 . ’ BACKGROUND OF THE INVENTION ‘ i 1) Field of the Invention

This invention relates to a novel cellulase, a

CMCase isolated from the cellulase, and a microorganism capable of producing the cellulase. 2) Description of the Prior Art “o

Cellulases consist of a complicated enzymatic ’ system serving as a catalyst for an enzymatic reaction in which cellulose and similar polysaccharides are decomposed into glucose, cellobiose or celloligosaccharides. Cellulases are considered to be a general name for enzymes which are called, depending upon the mechanism of activity, cy enzyme, Cx enzyme and beta-glucosidase, or exo-beta-glucanase, endo-beta- glucanase, cellobiase and the like. Over a long term, cellulases have been studied mainly for the purpose of effectively utilizing. biomass resources. For instance, N . the source of cellulase supply has relied mainly on fungi belonging to the genera Trichoderma, Aspergillus,

Acremonium, and Humicola. However, the cellulases

3 F il . } 26000 driving its origin from microorganisms including the fungi involve a diversity of woking specificities and physicochemical properties of constituting enzyme groups, which have not been completely clarified yet.

Of these cellulases, those cellulases which have the high action on carboxymethyl cellulose (CMC) or

Cx enzymatic action are generally called CMCases. In recent years, novel industrial utility of cellulases including the CMCases have been developed, particularly, as an additive for use in detergent compositions for clothing. However, so far as cellulases produced by microorganism in the natural field and, particularly, the above-mentioned cellulases originating from microorganism are concerned, they are, in most cases, so unstable that their activity is lost in an alkaline pH range and are so-called acidic and neutral cellulases (whose optimum working pH is in the range of 4 to 6).

So-called alkaline cellulases which meet the requirement for detergent compositions for clothing, i.e. they have a maximum activity and are resistant in an alkaline range, are very small in number.

For instance, with regard to alkaline cellulases which are usable in detergent compositions for clothing, there are known only several methods of

Ag ul ’ 26060 i. | . producing alkaline cellulases originating from alkalophilic microorganisms. These method include a method in which microorganisms belonging to the genus

Bacillus are cultivated and cellulase A is collected from the medium (Japanese Patent publication No. 50- 28515), a method in which alkalophilic bacteria belonging to the genus Cellulomonas are cultivated to produce alkaline cellulase 301-A (Japanese Patent

Application Laid-open No. 58-224686), a method for oo producing CMCase by cultivation of alkalophilic Bacillus

No. 1139 (Horikoshi et al, J. Gen. Microbiol., Vol. 131, page 3339 (1985)), and a method of producing an alkaline cellulase using a strain belong to the genus

Streptomyces (Japanese Patent Application Laid-open No. © 61-19483).

Accordingly, there is a demand for an alkaline cellulase which has an optimum pH and a function as an enzyme for detergents for clothing in an alkaline range.

SUMMARY OF THE INVENTION

The present inventors made intensive studies to find, in the natural field, micoorganism capable of producing alkali cellulases and found that a microorganism collected from a sample of soil of Haga-

: ! . - =, ul . 26060 gun, Tochigi-ken, Japan and belonging to the genus : Bacillus was able to produce novel alkaline cellulase K effective as an additive for detergent compositions for i clothing. Moreover, it was also found that when the alkaline cellulase was further purified, novel CMCases I and II -were obtained as main components.

Accordingly, an object of the invention is to provide a novel alkaline cellulase K enzyme having an

So optimum pH at an alkaline side.

Another object of the invention is to provide novel CMCase I and II enzymes.

A further object of the invention is to provide a microorganism capable of producing these novel enzymes and a method for producing alkaline cellulase K by cultivating the microorganism and collecting the resulting alkaline cellulase K from the culture product.

BRIEF DESCRIPTION OF THE DRAWINGS

Fig. 1 is a graph showing a growth temperature range of Bacillus sp KSM 635;

Fig. 2 is a graph showing a growth pH range;

Fig. 3 is a graph showing a working pH range of CMCase of alkaline cellulase K;

Fig. 4 is a graph showing pH stability;

J —— ee

Co ge i 26060

Fig. 5 is a graph showing a working temeprature range of CMCase of alkaline cellulase K;

Fig. 6 is a graph showing thermal stability:

Fig. 7 is a graph showing the relation between elution fraction and activity in gel chromatography; : : Fig. 8 is a graph showing the relation between pH lat which CMCase I is reacted and relative activity:

Fig. 9 is a graph showing the relation between . pH at which CMCase I is treated and residual activity:

Fig. 10 is a graph showing the relation between reaction temperature (pH 9.0) of CMCase I and iJ relative activity:

Fig. 11 is a graph showing the relation between treating temperature of CMCase I (pH 9.0) and residual activity;

Fig. 12 is a UV absorption spectrum of CMCase 1 of the invention; : Fig. 13 is a graph showing the relation between reaction pH for CMCase II and relative activity:

Fig. 14 is a graph showing the relation between treating pH of CMCase II and residual activity:

Fig. 15 is a graph showing the relation between reaction temperature of CMCase II (pH 9.0) and relative activity:

: Co = : 26060

Fig. 16 is a graph showing the relation between treating temperature for CMCase II (pH 9.0) and residual activity;

Fig. 17 is a UV absorption spectrum of CMCase

II; and . Tig. 18 is a view showing the results of sodium dodecylsulfate electrophoresis of CMCases I and

II of the invention.

DETAILED DESCRIPTION OF THE INVENTION

AND PREFERRED EMBODIMENTS

The microorganism used for producing the novel enzymes according to the invention has the following mycological properties. The media used for classification of strains are those media 1 to 24 and contain a suitable amount of a sterilized 1.0 wt% sodium carbonate (NajCO3) solution unless otherwise indicated. : Compositions of Test Media for Classification (wt$)

Medium 1: Bacto peptone 0.5; meat extract 0.3; Bacto agar-agar 1.5

Medium 2: Bacto peptone 0.5; meat extract 0.3

Medium 3: Bacto peptone 0.5; meat extract 0.3; NaCl 7.0

Medium 4: Bacto peptone 0.5; meat extract 0.3; Bacto gelatin 20.0

} | 26060

Medium 5: Bacto litmus milk 10.5

Medium 6: Bacto peptone 0.5; meat extract 0.3; KNO3 0.1

Medium 7: Bacto peptone 0.7; glucose 0.5;

NaCl 0.5 . Medium 8: Bacto peptone 3.0; meat extract

J 0.3; sodium thiosulfate 0.005; cysteine hydrochloride 0.02; iron : ammounim citrate 0.05; Bacto agar- agar 0.5

Medium 9: Bacto peptone 1.5; meat extract } 0.4; lactose 1.0; sucrose 1.0; glucose 1.0; NaCl 0.5; sodium thiosulfate 0.008; sodium sulfite 0.04; ferrous sulfate 0.02; phenol red 0.002; Bacto agar-agar 1.5

Medium 10: Bacto peptone 1.5; yeast extract 0.5; soluble starch 2.0; KoHPO4 0.1; Bacto agar-agar 1.5;

MgSO4°7H20 0.02

Medium 11: ammonium phosphate 0.1; KCl 0.02; yeast extract 0.05; MgS0Oy4°7H20 0.02; sugars 1.0 (sterilized separately through filtration)

Medium 12: potassium monohydrogen phosphate 0.1; ammonium dihydrogen phosphate 0.1; sodium citrate 0.2;

MgS04°-7H20 0.03; salt 0.5;

Bromothymol Blue 0.0024; Bacto . agar-agar 1.5

Medium 13: yeast extract 0.05; cysteine hydrochloride 0.01; sodium citrate 0.3; NaCl 0.5; sodium thiosulfate 0.008; iron ammonium citrate 0.04; glucose 0.02; potassium dihydrogenphosphate 0.15; phenol red 0.0012; Bacto agar-agar 1.5

Medium 14: ammonium phosphate 0.1; potassium dihydrogenphosphate 0.05; sodium citrate 0.2; Bacto agar-agar 1.5;

MgS04+7Hy 0.02

Medium 15: yeast extract 0.05; Na3SO4 0.1;

KH2PO4 0.1; glucose 1.0; inorganic nitrogen sources suitable amounts* * Sodium nitrate was added in 0.25%, sodium nitrite was in 0.2025%, ammonium chloride was in 0.158%, and ammonium phosphate was -— 9 J oo | - [ i

AL oo 26060 in 0.195% (each corresponding to 0.0412 N%).

Medium 16: yeast extract 0.05; NazSO4 0.1; . KHpPO4 0.1; glucose 1.0; inorganic nitrogen sources suitable amounts**; CaClp°2H20 0.05;

MnSO4-4-6H20 0.001; FeS04°7H20 0.001 (sterilized separately : through filtration): MgSO04 + 7TH20 B 0.02 (sterilized separately through filtration) oo

J Sodium nitrate was added in an amount of 0.25%, sodium nitrite was in an amount of 0.2025%, ammonium chloride was added in an amount of 0.158%, and ammonium : phosphate was in an amount of 0.195% (each corresponding to 0.0412 N%).

Medium 17: King A medium "Eiken" (available from Eiken Chem Co., Ltd.), indicated amounts

Medium 18: King B med ium "Eiken" (available from Eiken Chem. Co., Ltd.), indicated amounts

EE ~ 7 Cb a i 9 6 ERP iN 0G0

Medium 19: potato dextrose agar-agar medium "Eiken" (Eiken Chem. Co., Ltd.), indicated amounts

Medium 20: Bacto peptone 0.25; salt 0.25; yeast extract 0.25; mannitol 0.5; . Bacto agar-agar 2.0

Medium 21: urea medium "Eiken" (available from Eiken Chem. Co., Ltd.),

B indicated amounts

Medium 22: Bacto peptone 0.1; NaCl 0.5;

KH7PO4 0.2; yeast extract 0.05; glucose 0.1; urea 2.0; phenol red 0.001

Medium 23: Bacto peptone 0.5; yeast extract 0.5; KpHPO4 0.1; glucose 1.0;

MgSO4+7H0 0.02

Medium 24: yeast extract 0.5; glucose 1.0; casein (Hammerstein, Merc Inc.) 0.5; KoHPOy4 0.1; MgSO4-7H20 0.02;

Bacto agar-agar 1.5 (Mycological Properties) . 1. Results of Microscopic Observation

The Bacillus has a size of 0.5 to 1.2 ym x 1.5 to 4.0 ym and make an endospore (0.7 to 1.2 ym x 1.0 to

SE ren ocd od i - 26060 2.0 um) at one end of the bacillus body. Periflagela

Motility: positive. Gram staining: positive. 2. The state of growth in various media (1) Meat broth and agar-agar medium (medium 1)

The colony is circular in shape and is flat on the surface thereof. The colony is white or yellow in color and is semi-transparent and glossy. (2) Meat broth liquid medium (medium 2)

Growing and becoming turbid. (3) 7% Salt meat broth liquid medium (medium 3)

Growing and becoming turbid. (4) Meat broth-gelatin stab culture (medium 4)

Not growing. (5) Litmus milk culture (medium 5) : Coagulation and peptonization of the milk: negative. Because of the alkalinity of the medium 5, no change in color of the litmus is recognized.

Va. Physiological Properties (1) Reduction of nitrates and denitrification ’ reaction

Reduction of nitric acid: positive.

Denitrification: negative (medium 6). (2) MR test (medium 7) :

Because of the alkalinity of the medium,

Co - “IT To . Fi Cond i

So i 26060

Methyl Red does not undergo any change, thus the juaghnent being impossible. (3) VP test (medium 7)

Positive. (4) Formation of indole (medium 8) ’ Negative with respect to the reaction against an indole-producing test filter paper ("Nissan", made by

Nissui Seiyaku K.K.) and also to the color change with

Kovacs' indole reagent. (5) Formation of hydrogen sulfide (medium 9)

Negative. (6) Hydrolysis of starch

A plate agar-agar medium, i.e. medium 10, which has been rendered acidic by the use of 4 N HCl is negative when determined by an ordinary detection method using the iodine reaction. In the liquid medium 11, formation of soluble starch is negative. (7) Utility of citric acid

Medium 11: positive.

Medium 12 (Koser's (Simons') citric acid/agar- agar plate medium): negative. A liquid medium which is obtained by eliminating agar-agar from the medium 12 and, instead, 0.05% of yeast extract is added, is positive.

a — — : = | = i} \ Bs id lL 26060

Medium 13 (Christensen's agar-agar plate medium): positive, but no change with phenol red is observed because of the alkalinity.

Medium 14: negative (not growing). Positive with respect to a liquid medium which is obtained by eliminating agar-agar from the medium 14 and adding 0.05% of yeast extract. (8) Utilization of inorganic nitrogen sources . Medium 15: negative to pseudopositive for all of nitric acid, nitrous acid and ammonia.

Medium 16: the present medium containing very small amounts of metal salts is positive with respect to nitric acid and nitrous acid. Ammonium chloride: pseudopositive. Ammonium phosphate: positive. (9) Formation of dyes

Not growing in the King A medium (medium 17) : and not possible to judge.

Light yellow (involving no fluorescence) in the King B medium (medium 18). Growing in a potato/dextrose/agar-agar medium (medium 19) and in a mannitol/yeast extract/agar-agar medium (medium 20) but negative with respect to the formation of dyes. (10) Urease

Medium 21: not growing. Negative when the

. . = } Fit

A Co = i ’ ® : 26060 formation ammonia with Nessler's reagent was confirmed after removal of phenol red from the medium 21 and cultivation of the present organism.

Medium 22 (Christensen's urea medium to which yeast extract is added): negative when the formation of ammonia with Nessler's reagent was confirmed after removal of phenol red from the medium and cultivation of the present organism. Negative when tested by changing the urea concentration in the medium 22 to 0.1, 0.2, 0.5, 1.0 and 2.0% on the presupposition of cytotoxin. (11) Oxidase "Positive" or "negative" is not clear. ) (12) Catalase

Positive. : (13) Range of Growth (medium 23)

A temperature gradient incubator was used for shaking culture in an L-type test tube for 3 days. The drowing temperature range was from 20 to 45°C and an : optimum growing temperature range was from 29 to 37°C (Fig. 1).

In order to determine a pH range for growth, a test was conducted in which the concentration of NapCOj3 in the medium 23 was changed to change an initial pH of the medium. As a result it was found that the growing oo 7 hie 26na0 pH range was from 8 to ll and an optimum growing pH range of from 9.5 to 10.2 (Fig. 2). On the other hand, when the pH of the medium was controlled by the use of

KoCO3, it was found that the growing amount was very small and the optimum growing pH was about 9. (14) Behavior on oxygen

Aerobic. ~ (15) O-F test

Undergoing no change in color because of the alkalinity and growing only in an aerobic condition. (16) Utility of Sugars (medium 11)

Utilizable carbon sources: D-ribose, L- arabinose, D-xylose, D-glucose, D-mannose, D-fructose, maltose, sucrose, trehalose, mannitol, inositol, and glycerin.

Non-utilizable carbon sources: D-galactose, ] lactose, sorbitol, starch, dextrin, and raffinose.

N17) Hydrolysis of casein (medium 24)

Microorganism was grown up in an agar-agar plate culture, into which 30% trichloroacetic acid was poured for judgement, revealing that any transparent zone was not formed around the bacillus colonies, from which it was judged as negative. (18) Requirement for nutrients

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As is shown in Table 1, biotin (desthiobiotin) is essential for the growth.

Table 1 . -—

Concentration of Vitamin Degree of Growth of (Ug/m1l) Bacillus sp KSM-635

Biotin Desthiobiotin (Absorbance, 600 nm/6 days) -_— 0.001 0 4.6 0.01 0 : 4.6 0 0.001 4.3 0 0.01 4.4 nil 0.0 _—

Reference is made to Bergey's Mannual of

Determinative Bacteriology, eighth edition, with respect to the above mycological properties, with the result + that the present strain is considered as a spore-forming } microorganism belonging the genus Bacillus. However, since the present strain does not grow in a neutral pH but grows well only at a highly alkaline pH range, it \ can be provisionally determined as an alkalophilic microorganism, which has been recently reported by 7

Horikoshi and Akiba in "Alkalophilic Microorganisms",

. ! yo o | Ulf 26060

Japan Scientific Society Press (Tokyo), 1982, and is distinguished from known bacilli growing in neutrality. bf Because the mycological properties of the

Pore ! present strain do not coincide with those of known

WM alkalophilic bacilli, the present strain has been

NC (x7 determined as a novel strain and named Bacillus sp KSM- a 635, and ig now deposited as FERM No. 8872 at the

Fermentation Research Institute of Japan.

For the production of alkaline cellulase K by the use of the above novel microorganism, Bacillus sp

KSM-635, the strain of Bacillus sp KSM-635 or its variant is cultivated in a medium to produce alkaline cellulase K. This product is subjected to an ordinary enzyme purification method to isolate and purify it.

For the production by fermentation of alkaline cellulase K, a suitable medium is sterilized such as by heating and the strain of Bacillus sp KSM-635 (FERM BP- , 1485) is inoculated in the medium, followed by shaking 2 or aeration spinner cultivation at 22 to 40°C, ? preferably from 26 to 37°C, for 1 to 4 days. Good - pr results are obtained when the pH is adjusted to 8 to 11.

Since the production-by-fermentation medium is alkaline in nature, it may sometimes be expanded, which will be solved by the addition of a suitable amount of an antifoamer at suitable times.

Fo ORIGINAL J \etiasa—

, vo Yond \ iif . p : Lo 26060

The production of the alkaline cellulase K requires a suitable combination of nitrégen sources and carbon sources contained in a culture medium. These nutrient sources are not critical. For instance, nitrogen sources include inorganic sources such as ammonium nitrate, ammonium sulfate, ammonium chloride, ammonium phosphate, sodium nitrate and the like, and corn gluten meal, bean flour, corn steep liquor, casamino acid, yeast extract, Pharmamedia, sardine meal, meat extract, peptone, Hypro, Ajipower, corn soybean meal, coffee grounds, cotton seed oil meal, Cultivater,

Amiflex, Ajipron, Zest, Ajix, and the like. Examples of the carbon sources include plant fibers such as chaff, bran, filter paper, ordinary papers, sawdust and the like, and waste molasses, invert sugar, CMC, Avicel, cellulosic cotton, xylan, pectin and the like. Further utilizable carbon sources include, for example, ribose, arabionse, xylose, glucose, mannose, fructose, maltose, sucrose, trehalose, mannitol, inositol, glycerin and the like, and organic acids such.as ztetic acid, citric acid and the like. Any media using combinations of these nitrogen and carbon sources may be used and the nutrient sources should not be limited to any specific ones.

Aside from these ingredients, phosphoric acid and i id Ui ~ . 26060 - Co, inorganic salts such as of Mg?t, cat, Mn2t, an2t, cot,

Na’, xt and the like, and, if necessary, inorganic and organic trace nutrient sources may be suitably added to the medium.

The alkaline cellulase K may be obtained from the thus obtained culture product according to any known techniques of collection and purification of ordinary enzymes as will be particularly described in examples appearing hereinafter.

For instance, the culture product may be subjected to centrifugal separation or ultrafiltration to separate the bacillus cells. The resultant culture broth are subjected to ordinary isolation methods including, for example, salting-out, isoelectric precipitation, solvent precipitation (using methanol, ethanol, isopropanol or the like), thereby separating the protein as a precipitate. Alternatively, ultrafiltration (e.g. Diaflow Membrane YC, available from Amicon Co., Ltd.) may be used for concentration to obtain alkaline cellulase K. . After precipitation in ammonium sulfate (30 to 70% saturated fraction) for the salting-out method or 75% ethanol for the solvent precipitation method, the enzyme may be filtered, centrifugally separated or desalted to obtain a freeze-

oo BE = i .

RB B

26060 dried powder. The desalting may be effected by an ordinary procedure such as dialysis or gel filtration using Sephadex G-25 or the like. Moreover, the purification of the enzyme is possible by a suitable combination of, for example, a hydroxy apatite chromatography, an ion exchange chromatography using

DEAE-Sephadex or DEAE-cellulose and a molecular sieve gel chromatography using Sephadex or Bio-gel. : The resultant alkaline cellulase K of the invention have the following physical and chemical properties. (1) Activity

The present enzyme has a Cx enzymatic activity of acting on CMC. However, it also acts on phosphoric acid-swollen cellulose and has such action specificities as exhibiting an activity as an enzyme acting on crystalline cellulose (cellulosic cotton) or Avicel which is cellulose having high crystallinity (i.e.

Avicelase), and an activity of a Cj; enzyme typical of which is a filterpaper-degrading activity (FPDase), and a beta-glucosidase activity on cellobiose and cellooligosaccharide. In addition, the enzyme slightly acts on the artificial substrate of PNPC to liberate p- nitrophenol.

’ : ; * Ty, TL " si . ! 2 3. il (2) Substrate specificity

The alkaline cellulase K has no degradation activity on xylan, amylose, dextrin, pectin, inulin and cardolan. The Avicelase and FPPase activities are about 0.3% of the CMCase activity. The degradation activity on the artificial substrate of p-nitrophenyl cellobloside (PNEC) was about 1.5 to 1.8% of the CMCase “YL activity (Pabel 2). : Table 2 —

Action of Enzyme Specifc Activity (units/g of enzyme) ee — 3-Glucosidase 0.7

PNPCase” 5.2

CMCase : 298

FPDase 1.2

Avicelase 1.1 ee ere er rt meee re eee eet Ath terme =® * PNPC degrading activity (3) Working pH and optimum working pH

The working pH of the present enzyme is from 4 to 12 and the optimum working pH is approximately from 9 to 10. At about a pH of 10.5, there appears a shoulder (Feg. 3).

R uli 26060 (4) pH stability

Stable pH values, which are determined by allowing to stand in buffer solutions of different pHs at 40°C for 10 minutes and 30 minutes, are, respectively, from 4.5 to 10.5 and 6.8 to 10 (Fig. 4).

When allowed to stand at 5°C, the pH is 4 to 11 and is stable over at least one month. : (5) Working temperature range and working optimum temperature

The present enzyme works in a wide temperature range of from 10°C to 65°C. When the reaction is effected in a glycine buffer solution (pH 9) for 20 minutes, the working optimum temperature is found to be about 40°C (Fig. 5). (6) Thermal stability

When thermally treated in a glycine buffer solution (pH 9) at different temperatures for 20 minutes, the present enzyme is not inactivated at all at about 40°C, and has a residual activity of about 50% at 60°C and about 25% at 70°C (Fig. 6). (7) Measuring methods of enzymatic activities and proteins (i) CMCase activity 0.1 ml of an enzyme solution was added to a substrate solution composed of 0.2 ml of CMC (2.5%), 0.1 oo . = | 0 . 5,

Bb i 2606 ml of a 0.5M glycine buffer solution (pH 9.0) and 0.1 ml of deionized water, followed by reaction at(a0°c for 20 minutes. After completion of the reaction, reducing sugar was quantitatively determined by a 3,5-dinitro- salicylic acid (DNS) method. More specifically, 1 ml of a DNS reagent was added to 0.5 ml of the reaction solution and heated at 100°C for 5 minutes for color development, followed by cooling and dilution with 4.5 . ml of deionized water. This was subjected to colorimetry at an absorbance of 535 nm. The enzyme titer determined as one unit is an amount of the enzyme which is capable of producing reducing sugar corresponding to 1 pmol of glucose in one minute under the above-described conditions. (ii) Decomposition activity of PNPC

A suitable amount of CMCase was acted at 30°C on 1.0 ml of a reaction solution containing 100 ymol of a phosphate buffer solution (pH 7.0) and 0.1 ymol of

PNPC (Sigma Co., Ltd.) after which 0.3 ml of 1 M NayCOj3 and 1.7 ml of deionized water were added in this order, followed by subjecting the resultant free p-nitrophenol v to colorimetry at 400 nm. The amount of the enzyme capable of liberating 1 Amol of free p-nitrophenol in one minute under the above conditions was determined as one unit.

Toy ?

Fe id i : | 26060 (iii) Avicelase and FPDase activities 2 ml of a reaction solution for measurement of the CMCase activity was provided, in which there was used, instead of the CMC substrate, 20 mg of Avicel (Merk Inc.) or a bulk piece of a filter paper having a width of 0.5 cm and a length of 5 cm (filter paper for determination of cellulase activity, Toyo No. 51- } Specific), thereby determining Avicelase and FPDase activities. An amount of the enzyme capable of liberating 1 {mol of reducing sugar, calculated as glucose, in one minute under the above conditions was determined as one unit. (iv) The quntitative determination of proteins was effected by the use of Bio Lad Protein

Assay Kit (Bio Lad Co., Ltd.) and bovine serum albumin was used for calculation as a standard protein. (8) Influence of chelating agents

The resistance of an enzyme for detergents to chelating agents in a builder used as a reaction composition is the most important factor. Alkaline cellulase K was pretreated with EDTA (0.5 mM), EGTA (0.5 mM) , NTA (0.5 mM), sodium tripolyphosphate (STPP, 50 mg/ml) and zeolite (5 mg/ml) to determine a residual ’ activity, but any influence was not recognized.

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X ) i £55) ait a ui 26086 (9) Influence of proteinases

Proteinases function to improve the detergency of detergent compositions. Accordingly, it is a matter a. course to further improve the detergency by adding cellulases to proteinase-containing detergents. For this purpose, it is necessary to satisfy the requirement that cellulases for detergents are not hydrolyzed by proteinase and can stably maintain the activity.

Alkaline cellulase K has a good resistance to actually employed proteinases for detergents (e.g. API-21,

Maxatase, Alkalase and the like) and ordinary proteinases (e.g. pronase) (Table 3).

SRI Re 26040

Table 3

Added Proteinase Concentration Relative Residual (Wt$) Activity (%)*

API-21 0.002 98 (Showa Denko) 0.02 100 0.2 114

Maxatase 0.002 113 (Gist) 0.02 99 : 0.2 99

Alkalase 0.002 110 (Novo) 0.02 108 0.2 99

Pronase 0.002 99 (Sigma) 0.02 98 0.2 102 *Treated with the respective proteinases at 15°C for 12 hours. The activity of an enzyme preparation not treated was taken as 100% and the activity of the respective treated preparations was indicated as an index to the non-treated preparation. (10) Influence of metals . , 2+ 2+ ,

Divalent metal ions (Hg™ , Cu and the like) at|a suitable concentration give an effect of

Co. “ i ) il 0 26080 inhibition. A slight degree of inhibition is experienced by means of monoiodoacetic acid and p- chloromercuribenzoate. (11) Influence of surface active agents

Alkaline cellulase K suffers little inhibition of activity by means of various surface active agents such as, for example, LAS, AS, ES, AOS, alpha-SFE, SAS, polyoxyethylene secondary alkyl ethers, fatty acid salts (sodium salts), and dimethyldialkylammonium chloride. (12) Molecular weight (gel chromatography using Sephadex G100)

Having a maximum peak at 180,000 + 10,000 (Fig. 7).

The alkaline cellulase K of the invention as compared with known cellulases has the following properties.

The present alkaline cellulase has an optimum . pH in a high pH range and is thus clearly

Se distinguishable from cellulases, which have an optimum i | pH in an acidic range, of molds or germs belonging to . | the genera Trichoderma, Penicillium, Aspergillus \ ("Cellulases" by Kazutoshi Nishizawa, Tokyo Nankodo,

Shy 1974), Acremonium (Japanese Patent Publication No. 59- iN \ 166081), Humicola (Japanese Patent Publication No. 61- 16316) and the like.

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Gd Ul 260R()

When compared with the alkaline cellulase disclosed in Japanese Patent Publication No. 50-28515, the present alkaline cellulase has a molecular weight having a maximum peak at 180,000 + 10,000. On the other , hand, the known cellulase has a molecular weight of 15,000 to 30,000. The cellulase of Bacillus No. 1139 had a molecular weight of 92,000. Moreover, other physical and chemical properties are different from ’ those of these known cellulases. Thus, the present cellulase is clearly distinguishable from these ~ cellulases. :

For obtaining CMCase I and CMCase II from the alkaline cellulase K, the alkaline cellulase K is purified by means of a preparative high performance liquid chromatography, a hydroxy apatite chromatography and a DEAE-Toyopearl chromatography and the like, thereby isolating the respective constituents. CMCase I and CMCase II have different molecular weights and electrically charging properties slightly. For instance, they can be separated from each other by elution using a linear concentration gradient of NaCl in the DEAE-Toyopearl chromatography.

The thus obtained CMCase I and CMCase II have the following properties.

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CMCase I: (1) Activity

The present enzyme has a Cx enzymatic activity of acting on CMC. The enzyme has also acts on phosphoric acid-swollen cellulose and has such activity specificities as exhibiting the activity of an enzyme (Avicelase) acting on crystalline cellulose (cellulosic cotton) and Avicel which is a high crystallinity, and activity of a Cj; enzyme such as a filter paper degrading activity (FPDase) and a beta-glucosidase activity of acting on cellobiose and cellooligosaccharides.

Furthermore, it slightly acts on PNPC which is an artificial substrate to liberate p-nitrophenol. : (2) Substrate specificity

The main activity of the present enzyme is the

CMCase activity and has about 0.3%, based on the main activity, of avicellase and FPDase activities (C3 activity). The artificial PNPC substrate degrading activity is about 1.5 to 1.8% (Table 4). On the other hand, it has not any degrading activity on xylan, : amylose, dextrin, pectin, inulin and curdlan.

: TN [71 i. 25. 26000

Table 4 oo -

Substrate to be Reacted Enzymatic Activity (specific activity, units/mg of protein) of

CMCase I _——

CMC ’ 6.56

Filter Paper 0.020

Avicel 0.019

Cellobiose 0.010

PNPC 0.099 —— (3) Working pH and optimum working pH

The working pH of the present enzyme is from 3 to 12.5 and the optimum working pH is from 6 to 11.5 (Fig. 8). The pH at which the working is the highest is about 9.5.

The working pH range with respect to PNPC is from 4 to 11 and the optimum pH is about 7. (4) pH stability

Stable pH values were determined by allowing the present enzyme to stand at different pH values at 30°C for 1 hour and measuring a residual activity. As a result, the enzyme was very stable at a pH of from 5 to 12 and was not inactivated (Fig. 9).

(5) Measuring methods of enzymatic activities and protein /The CMCase activity, PNPC degrading activity,

Avicelase and FPDase activity, and the content of proteins were measured in the same method as with the alkaline cellulase K. (6) Working temperature range and working oo optimum temperature

The working temperature range of CMCase I is in the range of from 10 to 60°C. The preferable temperature range is from 22 to 53°C. The optimum working temperature of the present enzyme is 40°C. The present enzyme has a good resistance at low temperature and has about 50% of the activity at a low temperature of 20°C (Fig. 10). (7) Thermal stability

When thermally treated at 50°C for 30 minutes, the enzyme has residual activity of about 50% (in glycine buffer solution: pH 9.0). (8) Influences of metals

Metals and ions give influences on the physicochemical properties, particularly a viscosity, of

CMC. It will be apparent that when the activity of the enzymatic components of the present invention is

. Sp :

A i 2600 measured using a CMC substrate, the factors of the . reaction kinetics of the alkaline cellulose K are not correctly reflected.

Accordingly, on the basis of the indication that the CMCase I has the decomposition activity on

PNPC, influengdces of metals on the enzymatic activity were determined. As a result, it was found that Zn2+,

Co2+, Ni2+, Cu2+ and Hg2+ inhibited the activity of the

CMCase I. On the other hand, Mn2t and Ba2+ promoted to activate slightly. (9) Influence of chelating agents

When CMC was used as a substrate, CMCase I suffered no inhibition with EDTA, EGTA, NTA, STPP and zeolite. (10) Influence of sugars

Similar to (8), PNPC was used as a substrate for the CMCase I to determine the influences of various sugars. Cellobiose inhibited both enzymatic components and thus exhibited the mode of product inhibition, but other disaccharides, e.g. lactose and maltose, gave no influence. The activity was not inhibited with monosaccharides including glucosamine, N- acetylglucosamine, ribose, arabinose, sorbose, xylose, fructose, galactose, glucose, and their derivatives such idl il : } 26060 as 3-0-methyl-beta-D-glucose, alpha-methyl-beta-D- glucose, alpha-methyl-D-glucoside, alpha-methyl-beta- mannoside and 2-deoxyglucose, and other saccharides such as rhamnose. (11) Influence of salt concentration © © A phosphate buffer solution, a bicine-Na buffer solution and a tris-HCl were used and salt (0 to 250 mM) was used as lan ion-strength adjusting agent.

The decomposition activity of PNPC was used as an index to determine an effect of the ion strength on the CMCase

I. As a result, it was found that the ion strength had no relation to the enzymatic activity with respect to the promotion or inhibition. (12) Influence of surface active agents

The activity was little inhibited by means of

LAS, AS, ES, AOS, alpha-SFE, SAS, polyoxyethylene secondary alkyl ethers, fatty acid salts (sodium salts), dimethyldialkylammonium chloride, and taurocholic acid. (13) Molecular weight

The molecular weight determined by gel chromatography (Toyopearl 55S, available from Toyo Soda

Co., Ltd.) was 145,000 + 10,000. (14) UV absorption spectrum

The present enzyme was dissolved in a bicine-

: } i Ar gn ik 26060 sodium buffer solution and subjected to measurement of a

UV absorption spectrum, revealing that it had a maximum absorption at about 280 nm with the existence of a shoulder absorption at 290 nm being found by checking a differential absorption spectrum (Fig. 12). ’ (15) Detection of sugars

The purified enzyme protein was subjected to a color development test using a phenol/sulfuric acid method, with the result that a maximum absorption appeared at 480 nm. This result means that the present enzyme contains a sugar. The sugar was detected by gas chromatography using an Alditol/acetic acid method, indicating that (N-acetyl)glucosamine was contained as a sugar. The present enzyme had a content of the sugar of from 1.3 to 4.0 wts%. (16) Resistance to proteinases

Proteinases for detergents, e.g. API (showa

Denko), Maxatase (Gist Co., Ltd.) and .Alkalase (Nobo

Co., Ltd.) (0.0002 to 0.1 wt%) were used in coexistence with the present enzyme and the residual activity of the preparations pre-incubated at 15°C for 12 hours was measured. Inactivation was not recognized. Thus, the present enzyme was found to have a strong resistance to the proteinases (Table 5).

Ce on ome oa

Ea [1] ’ To or it Ui

HRS

Table 5 ee ————————————————————————

Added Proteinase Concentration Relative Residual {wts) Activity (3%) of

CMCase I ee —— rrr rrr ————

Reference (no addition) - 100

API-21 0.1 IE 99 (Showa Denko) 0.01 112

Maxatase 0.1 102 (Gist) 0.01 108

Alkalase 0.1 111 (Novo) 0.01 116

CMCase II: (1) Activity

The present enzyme has a Cx enzymatic activity of acting on CMC. The enzyme has also acts on phosphoric acid-swollen cellulose and has such activity specificities as exhibiting the activity of an enzyme (Avicelase) acting on crystalline cellulose (cellulosic cotton) and Avicel which is a high crystallinity, and

1 fy : i IL

Yoo (a " blr — wit 26060 activity of a Cj) enzyme such as FPDase and a beta- glucosidase activity on cellobiose and cellooligosaccharides. Furthermore, it slightly acts on

PNPC which is an artificial substrate to liberate p- nitrophenol. ’ / (2) Substrate specificity

The main activity of the present enzyme is the

CMCase activity and has about 0.3%, based on the main activity, of avicellase and FPDase activities (Ci activity). The artificial substrate PNPC degrading activity is about 1.5 to 2.0% (Table 6). On the other hand, it has not any degrading activity on xylan, amylose, dextrin, pectin, inulin and curdlan.

Table 6

Substrate to be Reracted Enzyme Activity (specific acitivity, units/mg of protein) of

CMCase II

CMC 7.06

Filter Paper 0.022

Avicel 0.020

Cellobiose 0.010

PNPC 0.140

0 ER Il : 2600 (3) Working pH and optimum working pH

The working pH of the present enzyme is from 3 to 12 and the optimum working pH is from 6 to 11.5 (Fig. 13). The pH at which the working is the highest is about 9.5. ’ The working pH range of the present enzyme with respect to PNPC is from 4 to 11 and the optimum pH ~ is about 7. (4) pH stability “ stable pH values were determined by allowing the present enzyme to stand at different pH values at 30°C for 1 hour and measuring a residual activity. As a result, the enzyme was very stable at a pH of from 5 to 12 and was not deactivated (Fig. 14). - (5) Measuring methods of enzymatic activities and proteins

The CMCase activity, PNPC degrading activity, : Avicelase and FPDase activity, and the content of proteins were measured in the same manner as with the alkaline cellulase K. (6) Working temperature range and working optimum temperature

The working temperature range of CMCase II is in the range of from 5 to 58°C. The preferable

= Ul 26060 temperature range is from 14 to 45°C. The optimum working temperature of the present enzyme is 30 to 40°C.

At 15°C, the present enzyme has an activity of about 50% of the case of 30 to 40°C where the maximum activity is shown (Fig. 15). . (7) Thermal stability

When thermally treated at 40°C for 30 minutes, the enzyme has a residual activity of about 75% (in glycine buffer solution: pH 9.0) (Fig. 16). (8) Influences of metals

CMC. It will be apparent that when the activity of the enzymatic components of the present invention is measured using a CMC substrate, the factors of the reaction kinetics of the alkaline cellulase K are not correctly reflected. Accordingly, on the basis of the indication that the CMCase II has the decomposition activity on PNPC, influences of metals on the enzymatic activity were determined. As a result, it was found that zn", colt, NiZ2+, cut, Hg2* and cat inhibited the activity. On the other hand, Mg2t, Mn2*t, cat, Bat,

Felt, Lit, kt, and Na’ promoted to active the present enzyme to 1.1 to 2.4 times the original activity.

= [i

LL Ii 2606 () (9) Influence of chelating agents

When CMC was used as a substrate, the present . enzyme suffered no inhibition with EDTA, EGTA, NTA, STPP and zeolite. (10) Influence of sugars . Similar to (8), PNPC was used as a substrate for the CMCase II to determine the influences of various sugars. Cellobiose inhibited both enzymatic components and thus exhibited the mode of product inhibition, but other disaccharides, e.g. lactose and maltose, gave no influence. The activity was not inhibited by monosaccharides including glucosamine, N- acetylglucosamine, ribose, arabinose, sorbose, xylose, fructose, galactose, glucose, and their derivatives such as 3-O-methyl-beta-D-glucose, alpha-methyl-beta-D- glucose, alpha-methyl-D-glucoside, alpha-methyl-beta- mannoside and 2-deoxyglucose, and other saccharides such as rhamnose. (11) Influence of salt concentration

A phosphate buffer solution, a bicine-Na buffer solution and a tris-HCl were used and salt (0 to 250 mM) was used as an ion-strength adjusting agent.

II. As a result, it was found that the ion strength had no relation to the enzymatic activity with respect to the promotion or inhibition. (12) Influence of surface active agents

The activity was little inhibited by means of

LAS, AS, ES, AOS, alpha-SFE, SAS, polyoxyethylene secondary alkyl ethers, fatty acid salts (sodium salts), dimethyldialkylammonium chloride, and taurocholic acid. (13) Molecular weight <

Co., Ltd.) was 170,000 + 20,000. } (14) UV absorption spectrum

The present enzyme was dissolved in a bicine- sodium buffer solution and subjected to measurement of a

UV absorption spectrum, revealing that it had a maximum absorption at about 280 nm with the existence of a shoulder absorption at 290 nm being found by checking a differential absorption spectrum (Fig. 17). (15) Detection of sugars

The purified enzyme protein was subjected to a color development test using a phenol/sulfuric acid method, with the result that a maximum absorption appeared at 480 nm. This result revealed that the ’

oo 26060 present enzyme contains a sugar. The sugar was detected by gas chromatography using an Aldeytol/acetic acid method, indicating that (N-acetyl)glucosamine was contained as a sugar. The present enzyme had a content of the sugar of from 1.3 to 4.0 wts. ’ (16) Resistance to proteinases

Proteinases for detergents, e.g. API (Showa

Denko), Maxatase (Gist Co., Ltd.) and Alkalase (Novo

Co., Ltd.) (0.0002 to 0.1 wt%) were used in coexistence with the present enzyme and the residual activity of the preparations pre-incubated at 15°C for 12 hours was measured. Inactivation was not recognized. Thus, the present enzyme was found to have a strong resistance to the proteinases (Table 7).

a = i Sis 0 3 if ie li

Table 7 0 6 0

Added Proteinase Concentration Relative Residual (wt) Activity (%) of

CMCase II

Reference (no addition) - 100

API-21 0.1 102 (Showa Denko) 0.01 115

Maxatase 0.1 100 (Gist) 0.01 102

Alkalase 0.1 104 (Novo) 0.01 108

The comparison in properties between CMCases I and II and those of a known cellulase is as follows.

The present enzymes have an optimum pH in a high pH range and are thus clearly distinguishable from cellulases, which have an optimum pH in an acidic range, ¢ of molds or germs belonging to the genera Trichoderma,

Penicillium, Aspergillus ("Cellulases" by Kazutoshi

Nishizawa, Tokyo Nankodo, 1974), Acremonium (Japanese

Patent Publication No. 59-166081), Humicola (Japanese

Patent Publication No. 61-16316) and the like.

oo . . con 72 . 26060 when compared with the cellulase disclosed in

Japanese Patent Publication No. 50-28515 and the cellulase reported in J. Gen. Microbiol., Vol. 131, page 3339 (1985), it will be found that the CMCase I has a molecular weight of 145,000 + 10,000 and the CMCase II has a molecular weight of 170,000 + 20,000, whereas the alkali cellulase of Japanese Patent Publication No. 50- 28515 has a molecular weight of 15,000 to 30,000 and the a molecular weight of Bacillus No. 1139 is 92,000.

Moreover, the enzymes of the present invention apparently differ from these known cellulases in various reaction kinetic properties and the existence of the : sugar therein.

The alkaline cellulase K and CMCases I and II obtained according to the invention are specific enzymes which stably work in a wide range including an alkaline side.

For instance, the alkaline cellulase K has, at a pH of 11, a relative activity of about 75 to 80% based on the activity at the optimum pH. Although the optimum pH is at a strongly alkaline side, the activity is shown at a strongly acidic side of about a pH 4 or lower.

Likewise, the CMCase I has a relative activity of about 75 to 80% at a pH of 11 based on the activity

7 I

A a oo 26060 at an optimum pH and exhibits an activity even at a pH of (about 3.5. The CMCase II has a relative activity of about 70% at a pH of 11, based on the activity at an optimum pH and exhibits an activity at a pH of about 3.

As will be apparent from the above, the alkaline cellulase K and the CMCases I and II of the present invention are enzyme groups which shown good activity at the most strongly alkaline side among hitherto known alkaline cellulases.

Moreover, these enzymes has the features that their activity is shown even at low temperatures and that they have a strong resistance to surface active agents, chelating agents and proteinases. Accordingly, the alkaline cellulase K and the CMCases I and II of the invention can be effectively utilized not only as an additive for clothing detergents, but also as a biomass and in other fields.

The present invention is described in more detail by way of references and examples.

Keemere 1

A soil collected at Ichikai-machi, Haga-gun,

Tochigi-ken, Japan as suspended in a sterilized saline solution and thermally treated at 80°C for 30 minutes.

- aime 26060

The thermally treated solution was suitably diluted and spread plated on a master plate (composed of 1% of a meat extract (Oxoid Co., Ltd.), 1% of Bacto peptone (Difco Co., Ltd.), 1% of NaCl, 0.1% of KH2PO4, 0.5% of

NayCO3 (separately sterilized) and 1.5% of Bacto agar- agar), followed by cultivation at 30°C for 3 days, thereby forming colonies. Tranplantation on a 2% CMC- containing master plate according to a replica method was effected to again form colonies, followed by pouring a Congo Red dye solution to obtain colonies whose periphery was transparent. The thus obtained colonies were collected from the plate and high titer CMC-ase- producing bacilli were screened.

By the above procedure, Bacillus sp KSM-635 (FERM BP-1485) of the invention was isolated. aoe 2

The strain of Bacillus sp KSM-635 (FERM BP- 1485) was aerobic cultivated in a liquid medium consisting of 1.5% of meat extract, 0.5% of yeast extract, 1% of CMC, 0.1% of KH2PO4 and 0.75% of NajsCO3 at 34°C for 2 days. 3 liters of cooled ethanol (-10°C) were gradually added to 1 liter of a supernatant liquid of the culture product to cause proteins to precipitate.

aE 5 : E ot]

LY od oll

The precipitate was dissolved in a minimum amount of sterilized deionized water and neutralized with diluted acetic acid, followed by dialysis with running water for hours and freeze-drying to obtain 8.2 g of alkaline cellulase K. The thus obtained cellulase K had the — a following enzymatic activities shown in Table 8. :

Table 8

Kind of Enzyme Specific Activity (units/g of enzyme powder) 3-Glucosidase 0.6

PNPCase* 7

CMCase 325

FPDase 1.2

Avicelase 1.1 : * PNPC degrading activity ample 3

A Hundred ml of a medium (pH 8.4 to 8.6) containing 1% of CMC, 2% of polypeptone, 0.1% of KH2PO4, 0.1% of yeast extract and 0.75% of NajCO3 was placed in a 500 ml Erlenmeyer flask and sterilized by a usual manner, followed by inoculation of the strain of

Ea i 2606

Bacillus sp KSM-635 (FERM BP-1485) and shaking culture at 30°C for 4 days. After completion of the culture, the bacillus cells were centrifugally removed and the resultant supernatant liquid was subjected to measurement of the CMCase activity. The activity was ——— found to be 3,100 units/liter. This supernatant liquid was treated in the same manner as in Example 2 to obtain 9.2 g of alkaline cellulase K.

Example 4

The strain of Bacillus sp KSM-635 (FERM BP- 1485) was inoculated in a medium of Example 2 in which 1.5 % of meat extract was added instead of Bacto peptone, followed by shaking culture at 30°C for 3 days.

After the culture, a centrifugally separated supernatant liquid was subjected to measurement of the CMCase activity. As a result, the activity was found to be 3,200 units/liter. ~~ Example 5 /

One liter of the supernatant liquid obtained in Example 4 was purified according to the following procedure to obtain CMCases I and II. The purification was conducted by (1) treatment with streptomycin, (2) fractionation with ammonium sulfate (30 to 75% saturated precipitation fraction), (3) a preparative high performance liquid chromatography (e.g. SW 3000 G column (Toyo Soda Co., Ltd.)), (4) DEAE-Toyopearl (Toyo Soda

Co., Ltd.) chromatography, (5) hydroxy apatite (Seikagaku Ind. Co., Ltd.) chromatography, and (6) DEAE-

Toyopearl chromatography. At the sixth stage of the purification, when elution by a NaCl linear concentration gradient (from 0.25 M NaCl to 0.35 M NaCl)

Sd Jl 26060 was effected, CMCase I and CMCase II were eluted — according to the order of the elution speed to obtain 24 mg of CMCase I and 15 mg of CMCase II. The thus obtained CMCases I and II were subjected to . electrophoresis according to the Davis method (Davis p.J., Ann. N.Y. Acad. Sci., Vol. 121, page 404 (1964)), : followed by dyeing with Coomassie Brilliant Blue. As a © result, it was found that a single band was obtained for the respective enzymes. Co ample 6

The CMCases I and II obtained Example 5 were subjected to electrophoresis using sodium dodecylsulfate "according to a usal procedure. The results are shown in

Fig. 18. From the results, it was found that the :

CMCases I and II were association products of different molecule species having a lowest molecular weight of 30,000 + 2,000 and a highest molecular weight of 120,000 + 15,000. The CMCases I and II are assumed to be associated products of enzyme proteins which are strongly associated by some physical and chemical interactions and have a lowest molecular weight of 30,000 + 2,000. However, how the protein is associated is not known at present. It is considered that the main

} -— oo 2606 protein species of the CMCase I has a molecular weight of from 55,000 to 65,000 and the CMCase II has a ‘molecular weight of from 95,000 to 120,000.

Accordingly, the products obtained in this example are merely an example of the results of the sodium- dodecylsulfate electrphoresis and should not be construed as limiting exact subunit structures of the

CMCases I and II.

Claims

: | LE : = ol ls 2606 ( WHAT IS CLAIMED IS: .

1. Alkaline cellulase K having the following physicochemical properties. (1) Activity Having a Cx enzymatic activity of acting on carboxymethyl cellulose (CMC) along with a weak Cj enzymatic activity and a weak beta-glucosidase activity. (2) Specificity on Substrates ioroeggteline wld Acting on CMC, crystalline cellulose, Avieel, cellobiose, and p-nitrophenyl cellobioside (PNPC). (3) Working pH and Optimum pH Cu Having a working pH in the range of 4 to 12 and an optimum pH in the range of 9 to 10. (4) Stable pH o) Having stable pH values of 4.5 to 10.5 and 6.8 A to 10 when allowed to stand at 40°C for 10 minutes and . \y 30 minutes, respectively. (5) Working Temperature Range and Working Optimum Temperature Working in a wide temperature range of from 10 Ao 65°C with an optimum temperature being recognized at about 40°C. (6) Influences of Chelating Agents -

g ul 2d 2606 0 The activity not impeded with ethylenediamine tetraacetic acid (EDTA), ethyleneglycol-bis-(f- aminoethylether) N,N,N',N"-tetraacetic acid (EGTA), N,N- bis(carboxymethyl)glycine (nitrilotriacetic acid) (NTA), sodium tripolyphosphate (STPP) and zeolite. (7) Influences of Surface Active Agents Undergoing little inhibition of activity by Co means of surface active agents such as sodium linear alkylbenzenesulfonates (LAS), sodium alkylsulfates (AS), sodium polyoxyethylene alkylsulfates (ES), sodium alpha- olefinsulfonates (AOS), sodium alpha-sulfonated aliphatic acid esters (alpha-SFE), sodium alkylsulfonates (SAS), polyoxyethylene secondary alkyl ethers, fatty acid salts (sodium salts), and dimethyldialkylammonium chloride. . (8) Influences of Proteinases Having a strong resistance to proteinases. (9) Molecular Weight (determined by gel chromatography) Having a maximum peak at 180,000 + 10,000.

2. Alkaline cellulase K according to claim 1, which is obtained by isolation from a culture product of Bacillus sp KSM-635.

=: ol FRAY 26060

3. A method for producing alkaline cellulase K which comprises cultivating alkaline cellulase “e pant -U35) producing bacteria belonging to the genus Bacillus, and collecting alkaline cellulase K from the resulting culture product. : Q-2

&

4. CMCase I having the following physico- chemical properties. Co (1) Activity Having a Cx enzymatic activity of acting on CMC along with a weak Cj enzymatic activity and a weak beta-glucosidase activity. (2) Specificity on Substrates microetgtaline alludes Acting on CMC, crystalline cellulose, Awicael, A cellobiose, and PNEC. = ) (3) Working pH and Optimum pH : - Having a working pH in the range of 3 to 12.5 and an optimum pH in the range of 6 to 11.5. (4) Stable pH Not inactivated at a pH of 5 to 12 when allowed to stand at 30°C for 1 hour. (5) Working Temperature and Working Optimum Temperature Working in a temperature range of from 10 to

- | . oo = a no ; bo 26060 60°C with an optimum temperature being at 22 to 53°C. ' (6) Influences of Chelating Agents The activity not impeded with EDTA, EGTA, NTA, STPP and zeolite. (7) Influences of Surface Active Agents ; "Undergoing little inhibition of activity by means of LAS, AS, ES, AOS, alpha-SFE, sas, polyoxyethylene secondary alkyl ethers, fatty acid salts (sodium salts), dimethyldialkylammonium chloride, and taurocholic acid. f (8) Resistance to Proteinases Co Having a strong resistance to proteinases. (9) Molecular Weight (determined by gel chromatography) Having a molecular weight of this enzyme of ! 145,000 + 10,000. (10) UV Absorption Spectrum This enzyme has a maximum absorption at 280 nm and a soulder absorption at 290 nm, thus sugar components being contained.

/

5. CMCase I according to Claim 4, which is - obtained by isolation from a culture product of Bacillus : sp KSM-635. | | oo

Cd 26060 ABSTRACT OF THE DISCLOSURE Bh i.

Novel alkaline cellulase K, CMCase I and Te “ ~ CMCase II are obtained by isolation from a culture ’ product of Bacillus sp KSM-635. These enzymes stably work in a wide range including an alkaline side, and their activity is shown even at low temperatures.

Further, they have a strong resistance to surfce active agents, chelating agents and : proteinases.

Therefore, they can be effectively } utilized not on.; as an additive for clothing detergents, but also as a biomass and. in other fields.

E