JP2007325553A - METHOD FOR ACTIVATING alpha-AMYLASE - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an activation method for remarkably enhancing enzyme activity of α-amylase by a simple operation. <P>SOLUTION: The method for activating α-amylase comprises arranging (B) an oxidizing agent or a particle containing the same in the vicinity of (A) an α-amylase or a particle containing the same in a noncontact state. The detergent composition having an improved enzyme effect is obtained, after the treatment, by mixing the obtained α-amylase with a detergent base. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention relates to an α-amylase activation method and an α-amylase activated by the method.

  α-Amylase (1,4-α-D-glucan glucohydrolase [EC 3.2.1.1]) is an endo-type enzyme that randomly cleaves α-1,4 glucoside bonds such as starch and glycogen. Industrially, it is widely used for starch processing, food processing, fiber processing, brewing, medicine, clinical testing, detergents, etc., and its origins range widely from microorganisms, plants and animals.

  This industrially important enzyme has not always been satisfactory in terms of its activity and price, and as a means for solving this, high production of enzymes by enzyme recombination and protein engineering techniques and enzymes Studies have been made on how to enhance the catalytic ability and how to improve the reaction rate of the enzyme in the enzyme reaction system, that is, how to activate the enzyme reaction.

  Enzyme activation methods include those obtained by adding a specific polymer to an enzyme reaction system (Patent Document 1), and those obtained by adding chloride ions to a specific amylase (Non-Patent Document 1). , Which enhances enzyme activity using a reversed-phase micelle system obtained by adding Tween 20 (polyoxyethylene sorbitan monolaurate) to n-hexane (Non-patent Document 2), a specific alkyl chain length in the enzyme reaction system It has been reported that an enzyme activity is enhanced by adding an alkyl sulfate and / or an alkyl sulfonate having a salt (Patent Document 2). Moreover, the method of activating an enzyme by melt | dissolving an enzyme in an exothermic inorganic salt (patent document 3) which dissolves an enzyme in electrogenerated water beforehand, and activating an enzyme in the pre-stage of an enzyme reaction (patent document 3) Patent Document 4) has been reported.

In addition, as a method for producing a detergent composition containing an enzyme, many literatures have reported that an enzyme or a bleaching agent is separately after-blended with a detergent base obtained by various granulation operations. Yes.
Special table hei 5-507615 JP-A-8-256768 JP 2000-245453 A JP 2000-37186 A Clin. Biochem. 16, 224-228 (1983) Biotechnol. Bioeng. , 29, 901-902 (1987)

  However, although these activation methods can increase the reaction rate of the enzyme to some extent, the activation power is still not sufficient. In addition, these methods require a step of separating the enzyme and the enzyme reaction activator, and sometimes there are problems such as mixing into the final product and lowering its product value, and it is widely used as a general-purpose technology. There was a problem in doing.

  The subject of this invention is providing the activation method which raises the enzyme activity of (alpha) -amylase notably by simple operation. Or it is providing the detergent composition containing the alpha-amylase obtained according to this activation method.

  Therefore, as a result of continual studies on the activation method of α-amylase, the present inventors have made α-amylase and an oxidizing agent close to each other and brought into a non-contact state as a pretreatment method for the enzyme reaction. It has been found that the enzyme activity is remarkably activated, and the present invention has been completed.

  The present invention relates to a method for activating α-amylase, comprising the step of A) arranging an oxidizing agent or a particle containing the same in the non-contact state in the vicinity of α-amylase or the particle containing the same.

  The present invention also provides an activated α-amylase having a step of A) arranging an oxidizing agent or a particle containing the same in a non-contact state in the vicinity of the α-amylase or the particle containing the same. It relates to a manufacturing method.

  The present invention also relates to an α-amylase obtained according to the method of the present invention, and a detergent composition containing the α-amylase.

  Furthermore, the present invention contains A) α-amylase that is mixed with a detergent base after B) an oxidizing agent or particles containing the same is arranged in a non-contact state in the vicinity of A) α-amylase or particles containing the same. The present invention relates to a method for producing a cleaning composition.

  Hereinafter, α-amylase may include particles containing α-amylase, and oxidant may include particles containing an oxidant.

  According to the present invention, when α-amylase is activated, it does not include a step of contacting with an oxidizing agent, and thus activated α-amylase containing no impurities is widely used as a component for various industrial processes and detergents. can do. The α-amylase activated by the present invention is effective in reducing the amount of enzyme used or shortening the reaction time. Moreover, the oxidizing agent used for activation in the present invention can be used repeatedly. Therefore, the present invention brings about an advantageous effect in terms of economy in the enzyme reaction using α-amylase and its applied technology.

  Examples of the α-amylase targeted by the present invention include Bacillus subtilis Marburg, Bacillus subtilis natto, Bacillus subilis chillis, Bacteria such as Bacillus cereus, Bacillus macerans, Pseudomonas stutzeri, Klebusella aerogenes, Streptomyces glyceus Actinomycetes such as (Streptomyces griseus), molds such as Aspergillus oryzae, Aspergillus niger, seeds of grasses and legumes, digestive glands of animals such as humans and pigs What is obtained can be used.

  The α-amylase used in the present invention is an anabolic carbon that transforms a host cell or the like transformed with a recombinant vector having a DNA sequence encoding the microorganism or a mutant thereof, or the enzyme or a mutant thereof. It can be obtained by inoculating a medium containing a source, a nitrogen source and other essential nutrients, cultivating according to a conventional method, and following a general enzyme collection and purification method. The enzyme solution thus obtained can be used as it is, but further purified, crystallized, powdered or granulated by a known method (for example, Japanese Examined Patent Publication No. 58-26315, Special Table No. 7-500013, No. 62-255990 and JP-A-9-48996) can be used.

  The form of α-amylase used in the present invention is not particularly limited, and a dried product of enzyme protein, particles containing enzyme protein, and liquid containing enzyme protein) can be used.

  The oxidizing agent used in the present invention is preferably a solid, and if it is solid, it can be used in any form of powder, granule, and granulated particles (in the case of a liquid, the humidity of the atmosphere becomes high and adversely affects the enzyme activity). To affect). Examples of the oxidizing agent include one or more selected from the group consisting of percarbonate, perborate, persulfate, permanganate, and perchlorate.

Specifically, sodium percarbonate, sodium perborate, sodium tartrate hydrogen peroxide adduct, urea hydrogen peroxide adduct, sodium tripolyphosphate hydrogen peroxide adduct, sodium pyrophosphate hydrogen peroxide adduct, 4Na ₂ SO ₄ · 2H ₂ O ₂ · NaCl double salt, sodium peroxide, calcium peroxide, sodium persulfate, potassium persulfate, ammonium persulfate, and those that produce sulfate ion radical and mixtures of these compounds, potassium permanganate, perchloric Examples thereof include sodium acid and sodium hypochlorite.

  Among these, sodium percarbonate, sodium perborate, and sodium perchlorate are preferable in view of safety and ease of handling when used. These can be used alone or in combination of two or more. Percarbonate is from Wako Pure Chemical Industries, Ltd., Mitsubishi Gas Chemical Co., Ltd., Nippon Peroxide Co., Ltd., Asahi Denka Kogyo Co., Ltd., and perborate is Wako Pure Chemical Industries, Ltd., Mitsubishi Gas Chemical Co., Ltd. Co., Ltd., Degussa-Huels Co. , Shaoxing Sino-USA (Meihua) Home Solution Co. , Ltd., Ltd. Therefore, as the perchlorate, those commercially available from Wako Pure Chemical Industries, Ltd., Mitsubishi Gas Chemical Co., Ltd. and the like can be used.

  In particular, α-amylase is preferably 1 IU to 500 million IU (international unit), more preferably 100 IU to 50 million IU of α-amylase with respect to an oxidizing agent corresponding to 1 g of available oxygen.

  Here, the activity of α-amylase is measured by the Fadebas method shown in the Examples described later.

  Further, the effective oxygen amount of the oxidant can be obtained by measuring by the following iodometry method.

(Measurement method of effective oxygen content)
The oxidizing agent was dissolved in a 0.5% by weight sulfuric acid aqueous solution, 10 ml of this was sampled into a screw tube (manufactured by Marum Co., Ltd., No. 8), 10 ml of a 20% by weight sulfuric acid aqueous solution was added, and then 10% by weight iodide. After adding 10 ml of potassium and sealing, it was allowed to stand at 40 ° C. for a certain time in a light-shielded state. The mixture is allowed to cool to room temperature and titrated with a sodium thiosulfate standard solution. The effective oxygen amount per gram of sample defined by the following formula is measured. The standing time at 40 ° C. until titration with the sodium thiosulfate standard solution is the time until the variation of the effective oxygen amount is within ± 10%.

  In addition, the time for maintaining the oxidizing agent in the non-contact state in the vicinity of α-amylase is preferably 30 seconds or longer, and more preferably 5 minutes to 2 months.

  Moreover, the temperature at the time of arrange | positioning an oxidizing agent in the non-contact state in the vicinity of (alpha) -amylase is 5 to 80 degreeC, Furthermore, 20 to 50 degreeC is preferable. This temperature is the ambient temperature of both components.

Further, the absolute humidity in placing an oxidizing agent in a non-contact state in the vicinity of the α- ^{amylase, 0.5g / m 3 ~1000g / m} 3, preferably further 1.5g / m ³ ~200g / m ³ . This humidity is the ambient humidity of both components.

  Arranging the α-amylase and the oxidizing agent in a non-contact state means that they are in spatial communication. For example, the method of accommodating (alpha) -amylase and an oxidizing agent in the container which each has an opening part, Preferably arrange | positioning in the closed space is mentioned. In addition, a method of moving α-amylase in the vicinity of a large number of fixed oxidants (for example, transporting α-amylase by a belt conveyor in a space filled with oxidants) can be mentioned. In the present invention, it is also preferable to flow and stir the ambient atmosphere of α-amylase and the oxidizing agent by blowing air or the like. Moreover, the aspect which accommodates (alpha) -amylase and an oxidizing agent separately in a permeable packaging material, a container, etc., and arrange | positions it maintaining spatial communication is also included. Examples of the packaging material that can permeate the ambient atmosphere components of α-amylase and oxidant include polymer membranes such as dense membranes, homogeneous membranes, and porous membranes, and inorganic membranes such as ceramic membranes and zeolite membranes. These membrane types are selected according to the form of α-amylase, and are not particularly limited when the form of α-amylase is a dried product or particles, but in the case of liquid α-amylase, a dehumidifying membrane, oxygen An enriched film, a nitrogen-enriched film, an organic gas permeable film, a carbon film and the like are preferable.

  In the present invention, the terms “near” and “close” do not indicate a critical range, but indicate that it is preferable that the two approach each other in a non-contact state. For example, when both are present in a closed space, the amount of α-amylase per liter of space volume is 0.001 g or more and less than 900 g, preferably 0.1 g or more and less than 900 g. On the other hand, since the effect is reduced in the case of an open system, the amount of α-amylase per 1 L of the space volume is 0.1 g or more and less than 900 g, preferably 1 g or more and less than 900 g. As long as the effect of the present invention is manifested, the distance between the α-amylase and the oxidizing agent may be arbitrary. In this case, the case where the distance between the two is relatively close can be regarded as “near” or “close”.

  The detergent composition containing α-amylase obtained according to the activation method described above has higher cleaning performance than that containing untreated α-amylase.

  Below, the measuring method [phadebas method] of the alpha-amylase activity used in the Example is shown.

<Method for measuring α-amylase activity>
(1) Measurement of absorbance of sample 5 mL of buffer (Britton-Robinson Buffer, pH 8.5, 50 mM (Author: Anan Koichi et al. Basic Biochemical Experimental Method 6. P277, Maruzen Co., Ltd.)) Add 1 tablet of amylase test “Daiichi” [obtained from Daiichi Chemical Co., Ltd., product number 701501-005], stir for about 10 seconds, and then add 1 mL of enzyme solution diluted with 2 mM aqueous calcium chloride solution. And reacted at 50 ° C. for 15 minutes. The reaction was stopped by adding 1 mL of 0.5 N aqueous sodium hydroxide and stirring, and then insoluble components were precipitated by centrifugation (400 × g, 5 minutes). Absorbance was measured.

(2) Absorbance measurement of blank 5 mL of buffer solution (Britton-Robinson Buffer, pH 8.5, 50 mM (authored by Koichi Anan et al., Basic Biochemical Experimental Method 6. P277. Maruzen Co., Ltd.)) One tablet of amylase test “Daiichi” was added and stirred for about 10 seconds. 1 ml of 0.5N sodium hydroxide aqueous solution was added and stirred, 1 ml of enzyme solution was added thereto, incubated at 50 ° C. for 15 minutes, and then centrifuged (400 × g, 5 minutes). The absorbance at 620 nm of the obtained centrifugal supernatant was measured.

(3) Calculation of enzyme activity Neo. The amylase activity was calculated by applying the difference in absorbance between (1) and (2) to the calibration curve of the international unit enclosed in the amylase test “Daiichi”.

Example 1
As particles containing α-amylase, Duramyl 60T commercially available from Novozymes was used, and 200 mg thereof was put in a Petri dish (Asahi Techno Glass, outside diameter 30 mm × height 15 mm). Moreover, 2g of percarbonate type oxidizing agent SPC-D which can be obtained from Mitsubishi Gas Chemical Co., Ltd. was put into another Petri dish (Asahi techno glass, outside diameter 30mm x height 15mm). These petri dishes were placed in a deep petri dish (Tokyo Glassware Co., Ltd., diameter 90 mm, height 60 mm, product code 0132-02-15-32), the lid was closed, and the ambient temperatures in Table 1 (deep type) The enzyme activity was measured by the method described above after a predetermined time shown in Table 1 at a temperature outside the petri dish, the same applies hereinafter. The enzyme in which the oxidizing agent was allowed to coexist in a non-contact manner had higher activity than the enzyme that was not allowed to coexist (Table 1). The ambient humidity at this time (humidity outside the deep petri dish, hereinafter the same) was 8 g / m ³ . Moreover, when 1 g of oxidizing agent SPC-D (b1) was converted into an effective oxygen amount, it was 0.12 g, and Duramil 60T had an enzyme activity before contact of 12000 IU / g.

* Relative activity: Enzyme activity when the enzyme activity of the enzyme that did not coexist with non-oxidizing agent (control product) was taken as 100% (hereinafter the same)

Example 2
As particles containing α-amylase, Duramyl 60T commercially available from Novozymes was used, and 200 mg thereof was put in a Petri dish (Asahi Techno Glass, outside diameter 30 mm × height 15 mm). In another Petri dish (Asahi Techno Glass, outside diameter 30 mm x height 15 mm), a percarbonate-based oxidizing agent SPC-D, which can be obtained from Mitsubishi Gas Chemical Co., Ltd., in a weight ratio (enzyme / oxidizing agent) So as to be 100/1, 10/1, and 1/10. Put the Petri dish with the enzyme / oxidant combination in a deep petri dish (Tokyo Glassware Co., Ltd., diameter 90 mm, height 60 mm, product code 0132-02-15-32), and after closing the lid, 1 hour later Enzyme activity was measured by the method described above. The enzyme in which the oxidizing agent was allowed to coexist in a non-contact manner had higher activity than the enzyme that was not allowed to coexist (Table 2). At this time, the ambient temperature was 25 ° C., and the ambient humidity was 8 g / m ³ .

Example 3 Kind of oxidizing agent As particles containing α-amylase, Duramyl 60T commercially available from Novozymes was used, and 200 mg thereof was placed in a Petri dish (Asahi Techno Glass, outside diameter 30 mm × height 15 mm). Moreover, sodium perborate tetrahydrate (product number 28-3630-5 manufactured by Wako Pure Chemical Industries, Ltd.) or sodium perchlorate monohydrate in another Petri dish (Asahi Techno Glass, outside diameter 30 mm x height 15 mm) 2 g of a Japanese product (product number 193-08065, manufactured by Wako Pure Chemical Industries, Ltd.) was added. Put the Petri dish with the enzyme / oxidant combination in a deep petri dish (Tokyo Glassware Co., Ltd., diameter 90 mm, height 60 mm, product code 0132-02-15-32), and after closing the lid, 1 hour later When the enzyme activity was measured by the method described above, the product of the present invention had higher activity than the enzyme enzyme (control product) in which the oxidizing agent was not allowed to coexist without contact (Table 3). At this time, the ambient temperature was 25 ° C., and the ambient humidity was 8 g / m ³ .

Example 4
As particles containing α-amylase, Termamyl 60T and Steinzyme 12T commercially available from Novozymes, Purastar OxAm4000E 200 mg commercially available from Genencor, Amylase A (manufactured by SIGMA, product number A 6380, derived from Bacillus species), or amylase B (manufactured by SIGMA, product number A-0273, derived from Apsergillus orizae) was placed in a separate Petri dish (Asahi Techno Glass, outer diameter 30 mm × height 15 mm). Moreover, 2g of percarbonate type oxidizing agent SPC-D which can be obtained from Mitsubishi Gas Chemical Co., Ltd. was put into another Petri dish (Asahi techno glass, outside diameter 30mm x height 15mm). Put the Petri dish with the enzyme / oxidizer combination in a deep petri dish (Tokyo Glassware Co., Ltd., diameter 90 mm, height 60 mm, product code 0132-02-15-32), and after closing the lid, 30 minutes later Enzyme activity was measured by the method described above. The enzyme in which the oxidizing agent was allowed to coexist in a non-contact manner had higher activity than the enzyme that was not allowed to coexist (Table 4). At this time, the ambient temperature was 25 ° C. and the ambient humidity was 8 g / m ³ . The enzyme activities of Termamyl60T, Stainzyme12T, Purastar OxAm4000E, Amylase A, and Amylase B before treatment were 10,000 IU / g, 180000 IU / g, 37000 IU / g, 1430,000 IU / g, and 840 IU / g, respectively.

Example 5
As particles containing α-amylase, Duramyl 300L commercially available from Novozymes was used, and 200 mg thereof was put in a Petri dish (Asahi Techno Glass, outside diameter 30 mm × height 15 mm). Moreover, 2g of percarbonate type oxidizing agent SPC-D which can be obtained from Mitsubishi Gas Chemical Co., Ltd. was put into another Petri dish (Asahi techno glass, outside diameter 30mm x height 15mm). These petri dishes were put into a deep petri dish (Tokyo Glassware Co., Ltd., diameter 90 mm, height 60 mm, product code 0132-02-15-32), the lid was closed, and 30 minutes later, the enzyme was prepared by the method described above. Activity was measured. The enzyme in which the oxidizing agent was allowed to coexist in a non-contact manner had 15% higher activity than the enzyme that was not allowed to coexist. At this time, the ambient temperature was 25 ° C., and the ambient humidity was 8 g / m ³ .

Example 6
In the detergent base 99% by weight described in Example 2 in Table 1 of JP-A No. 2001-152199, the oxidizing agent in Example 1 at a weight ratio of 10/1 (enzyme / oxidizing agent) was contacted without contact. A detergent composition was prepared by blending 0.5% by weight of Stainzyme 12T and 0.5% by weight of a fragrance. This detergent composition was dissolved in 1 L of tap water adjusted to 30 ° C. at a concentration of 0.07% by mass, and transferred to a stainless beaker for a targotometer (manufactured by Ueshima Seisakusho). Five pieces of starch / dye-stained cloth (EMPA162) (6 cm square) were placed in the detergent solution and washed with stirring at 80 rpm for 10 minutes. After rinsing under running water, it was iron-pressed and subjected to reflectance measurement. The reflectance of the base cloth of the contaminated cloth and the artificially contaminated cloth before and after washing was measured at 460 nm with a self-recording color difference meter (Shimadzu Corporation), and the washing rate (%) was measured. As a result, a high cleaning effect was confirmed in the stainzyme 12T in which the oxidizing agent was allowed to coexist without contact.

Claims (8)

A) Activation method of (alpha) -amylase which has the process of arrange | positioning the oxidizing agent or particle | grains containing this in the non-contact state in the vicinity of (A) (alpha) -amylase or particle | grains containing this. A) The manufacturing method of activated alpha-amylase which has the process of arrange | positioning the oxidizing agent or particle | grains containing this in the non-contact state in the vicinity of alpha-amylase or particle | grains containing this. The method according to claim 1 or 2, wherein the state in which component B) is disposed in a non-contact manner in the vicinity of component A) is maintained for 30 seconds or more. The method according to any one of claims 1 to 3, wherein the oxidizing agent is selected from the group consisting of percarbonate, perborate, persulfate, perchlorate, and permanganate. The method according to any one of claims 1 to 4, wherein 1 to 500 million IU (international units) of α-amylase is used for an oxidizing agent corresponding to 1 g of available oxygen. The alpha-amylase obtained according to the method of any one of Claims 1-5. A detergent composition comprising the α-amylase according to claim 6. A) A detergent composition containing an α-amylase which is placed in the vicinity of α-amylase or a particle containing the same and B) an oxidizing agent or a particle containing the same in a non-contact state and then mixed with the detergent base. Production method.