WO1992003543A1 - Aldc derivative and use thereof - Google Patents

Aldc derivative and use thereof Download PDF

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Publication number
WO1992003543A1
WO1992003543A1 PCT/DK1991/000222 DK9100222W WO9203543A1 WO 1992003543 A1 WO1992003543 A1 WO 1992003543A1 DK 9100222 W DK9100222 W DK 9100222W WO 9203543 A1 WO9203543 A1 WO 9203543A1
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WO
WIPO (PCT)
Prior art keywords
aldc
glutaraldehyde
derivative
aldc derivative
immobilized
Prior art date
Application number
PCT/DK1991/000222
Other languages
French (fr)
Inventor
Sven Pedersen
Original Assignee
Novo Nordisk A/S
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Novo Nordisk A/S filed Critical Novo Nordisk A/S
Priority to EP91914849A priority Critical patent/EP0575323B1/en
Priority to CA002089498A priority patent/CA2089498C/en
Priority to DE69106896T priority patent/DE69106896T2/en
Priority to US07/976,983 priority patent/US5306634A/en
Priority to BR919106762A priority patent/BR9106762A/en
Publication of WO1992003543A1 publication Critical patent/WO1992003543A1/en
Priority to FI930654A priority patent/FI105696B/en
Priority to GR950400197T priority patent/GR3014933T3/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12C—BEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
    • C12C11/00—Fermentation processes for beer
    • C12C11/003—Fermentation of beerwort
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12C—BEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
    • C12C11/00—Fermentation processes for beer
    • C12C11/07—Continuous fermentation
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12C—BEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
    • C12C11/00—Fermentation processes for beer
    • C12C11/09—Fermentation with immobilised yeast
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12C—BEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
    • C12C5/00—Other raw materials for the preparation of beer
    • C12C5/004—Enzymes
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12C—BEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
    • C12C9/00—Methods specially adapted for the making of beerwort
    • C12C9/02—Beerwort treatment; Boiling with hops; Hop extraction
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/88—Lyases (4.)

Definitions

  • the invention comprises an ALDC derivative and a use thereof.
  • ALDC is an abbreviation for acetolactate decarboxylase.
  • carbohydrate containing substances e.g. wort or grape juice
  • various by-products may be formed by processes other than the wanted alcoholic fermentation.
  • an unwanted by-product is diacetyl.
  • ALDC may be chemically modified to shift the optimum activity to lower pH values, reference being made to Biochem., vol. 11 , No. 22, 1972 (p. 4022-4084).
  • the modification methods mentioned in the Biochem. article comprise growing poly(ornithyl) side chains on chymotrypsin; the Biochem. article thus does not offer any suggestions for modification of ALDC.
  • the prior art modification method for shifting the optimum activity to lower pH values is not suitable for industrial application, and furthermore it is not known, if the poly(ornithyl) method can be transferred from chymotrypsin to ALDC. Finally, it does not appear from the Biochem. article, if the stability at low pH of the prior art modified chymotrypsin is satisfactory.
  • the purpose of the invention is the provision of an ALDC derivative which can be used with advantage in industry, and which exhibits a satisfactory stability at low pH.
  • the ALDC derivative according to the invention can be provided both as a soluble and an immobilized derivative, as will be explained later.
  • the ALDC derivative according to the invention is characterized by the fact that ALDC in an aqueous medium is treated with glutaraldehyde in a concentration corresponding to between 0.1 and 5 g of glutaraldehyde per g of pure ALDC protein, preferably corresponding to between 0,25 and 2 g of glutaraldehyde per g of pure ALDC protein. It has been found that this ALDC derivative is soluble, if not further treated and that it can be produced in a high activity yield. In Biotechnology Letters Vol. 10 No. 5 325-330 (1988) it is described that crosslinking of 0-glucosidase with glutaraldehyde provides a derivative with improved thermal stability. In Adv. Biochem. Eng. 12, p.
  • ALDC enzymes i.e. ALDCs produced from any microorganism
  • Preferred ALDC' ⁇ are from Bacillus brevis and Bacillus licheniformis.
  • a preferred embodiment of the ALDC derivative according to the invention is characterized by the fact that the ALDC derivative indicated in the previous paragraph is immobilized. The immobilization can take place in any known manner, e.g. by adsorption. In this manner the advantage comprising a beer without any ALDC is obtained.
  • EP 131125 describes a special inorganic carrier, on which enzymes, e.g. ALDC, are immobilized by adsorption and crosslinking with glutaraldehyde.
  • This EP does not describe the shift of the pH of the pH-activity curve of the ALDC, which is one of the main features of the present invention.
  • Another main feature of the present invention which is not described in the EP, is the treatment of the ALDC with glutaraldehyde in a defined small concentration before the optional immobilization.
  • the invention comprises a use of the ALDC derivative according to the invention in beer fermentation.
  • a preferred embodiment of the use according to the invention is characterized by the fact that the soluble ALDC derivative is used together with ordinary yeast in a batch fermentation. This is the simplest way of using the ALDC derivative according to the invention.
  • a preferred embodiment of the use according to the invention is characterized by the fact that the immobilized ALDC derivative is used together with ordinary yeast in a batch fermentation. This embodiment offers the advantage that no ALDC will appear in the final product.
  • a preferred embodiment of the use according to the invention is characterized by the fact that the immobilized ALDC derivative is used together with immobilized yeast in a continuous fermentation.
  • This provides the advantage comprising the immediate removal of the diacetyl precursor ⁇ -acetolactate.
  • the invention will be illustrated by means of the following examples. In these examples an ALDC preparation will be used, produced by cultivation of a Bacillus subtilis strain containing a gene encoding and expressing the ALDC of Bacillus brevis with properties described in DK 149335B.
  • AF 278/1 -GB available on request from Novo Nordisk A/S, Novo Alle, DK-2880 Bagsvaerd
  • pH adjusted in the substrates to values ranging from 3.6 to 6.0.
  • the pH-activity curves are shown in Fig. 1.
  • the stability of ALDC and the derivatized sample was measured in a normal, pasteurized Danish beer (HOF). 20 ADU was added per ml beer in which pH was adjusted to 4.0 and 6.0, respectively. Samples from the beers were taken each day, and the residual ALDC activity measured at pH 6.0. The results are shown
  • the fermentations were carried out with brewery malt wort (FAXE) and the same wort with added amounts (10, 20, 30 and 40% w/w) of adjunct (sucrose). 5 2.5 g of yeast was added per litre of wort. ALDC was added together with the yeast
  • a glutaraldehyde treated ALDC prepared as described in Example 1 (1100 ADU/ml) is added to 1 g of carrier (a silica carrier from Grace described in Biocatalyst Supports SG BC 1E / June 1987, Grade 500 MP). pH was adjusted to 4.5 and the carrier and the ALDC solution is slowly agitated for 20 hours by rotation at 5°C followed by vacuum filtration.
  • 0.5 ml of a 3% solution of polyazetidine (Kymene, Hercules BV) is added to the particles with adsorbed ALDC and the mixture is vacuum dried.
  • the activity of the immobilized ALDC is 589 ADU/g at pH 6.0 and 331 ADU/g at pH 3.8.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Genetics & Genomics (AREA)
  • Wood Science & Technology (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Food Science & Technology (AREA)
  • Microbiology (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • Biotechnology (AREA)
  • Medicinal Chemistry (AREA)
  • Mycology (AREA)
  • Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Analysing Materials By The Use Of Radiation (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

The ALDC derivative is produced by treating ALDC in an aqueous medium with glutaraldehyde in defined proportions with optional subsequent immobilization. The ALDC derivative which is used in beer fermentation exhibits a satisfactory stability at low pH.

Description

ALDC DERIVATIVE AND USE THEREOF
The invention comprises an ALDC derivative and a use thereof. ALDC is an abbreviation for acetolactate decarboxylase.
By fermentation of carbohydrate containing substances, e.g. wort or grape juice, various by-products may be formed by processes other than the wanted alcoholic fermentation. Thus, an unwanted by-product is diacetyl.
It appears from EP 46066 that ALDC can be used as an enzyme, which prevents the formation of diacetyl. However, the pH optimum of most naturally occurring ALDC's is around 6, and the activity at pH 3.8-4.7, which is the pH of the fermenting wort, is too low for practical purposes, especially at pH below 4, which is a usual pH of fermenting worts with low malt content. For that reason, the process of preventing the formation of diacetyl from fermenting beer or wine has not yet found its way into the practical industrial production on any larger scale. It is stated in the EP 46066 that the ALDC may be immobilized. In the EP 46066 it is also stated that ALDC may be chemically modified to shift the optimum activity to lower pH values, reference being made to Biochem., vol. 11 , No. 22, 1972 (p. 4022-4084). The modification methods mentioned in the Biochem. article comprise growing poly(ornithyl) side chains on chymotrypsin; the Biochem. article thus does not offer any suggestions for modification of ALDC. The prior art modification method for shifting the optimum activity to lower pH values is not suitable for industrial application, and furthermore it is not known, if the poly(ornithyl) method can be transferred from chymotrypsin to ALDC. Finally, it does not appear from the Biochem. article, if the stability at low pH of the prior art modified chymotrypsin is satisfactory. Thus, the purpose of the invention is the provision of an ALDC derivative which can be used with advantage in industry, and which exhibits a satisfactory stability at low pH.
Surprisingly, it has been found that treatment of ALDC with glutaraldehyde provides a modified ALDC, which in the first place exhibits the wanted pH profile, which in the second place is cheap and easily manufactured, and which in the third place exhibits a satisfactory stability. Also, the ALDC derivative according to the invention can be provided both as a soluble and an immobilized derivative, as will be explained later.
Thus, the ALDC derivative according to the invention is characterized by the fact that ALDC in an aqueous medium is treated with glutaraldehyde in a concentration corresponding to between 0.1 and 5 g of glutaraldehyde per g of pure ALDC protein, preferably corresponding to between 0,25 and 2 g of glutaraldehyde per g of pure ALDC protein. It has been found that this ALDC derivative is soluble, if not further treated and that it can be produced in a high activity yield. In Biotechnology Letters Vol. 10 No. 5 325-330 (1988) it is described that crosslinking of 0-glucosidase with glutaraldehyde provides a derivative with improved thermal stability. In Adv. Biochem. Eng. 12, p. 41-118, 1979, Rolf D. Schmid describes that crosslinking of different enzymes, e.g. papain, glucose oxidase, catalase and uricase, but not ALDC, provides enzyme derivatives with improved thermal stability. Thus, the prior art does not point to glutaraldehyde as an agent which could fulfil the purpose of the invention.
It is to be understood that all ALDC enzymes, i.e. ALDCs produced from any microorganism, can be used according to the invention. Preferred ALDC'ε are from Bacillus brevis and Bacillus licheniformis. A preferred embodiment of the ALDC derivative according to the invention is characterized by the fact that the ALDC derivative indicated in the previous paragraph is immobilized. The immobilization can take place in any known manner, e.g. by adsorption. In this manner the advantage comprising a beer without any ALDC is obtained. Reference can be made to EP 131125, which describes a special inorganic carrier, on which enzymes, e.g. ALDC, are immobilized by adsorption and crosslinking with glutaraldehyde. This EP, however, does not describe the shift of the pH of the pH-activity curve of the ALDC, which is one of the main features of the present invention. Another main feature of the present invention, which is not described in the EP, is the treatment of the ALDC with glutaraldehyde in a defined small concentration before the optional immobilization. Also, the invention comprises a use of the ALDC derivative according to the invention in beer fermentation.
A preferred embodiment of the use according to the invention is characterized by the fact that the soluble ALDC derivative is used together with ordinary yeast in a batch fermentation. This is the simplest way of using the ALDC derivative according to the invention.
A preferred embodiment of the use according to the invention is characterized by the fact that the immobilized ALDC derivative is used together with ordinary yeast in a batch fermentation. This embodiment offers the advantage that no ALDC will appear in the final product.
A preferred embodiment of the use according to the invention is characterized by the fact that the immobilized ALDC derivative is used together with immobilized yeast in a continuous fermentation. This provides the advantage comprising the immediate removal of the diacetyl precursor α-acetolactate. The invention will be illustrated by means of the following examples. In these examples an ALDC preparation will be used, produced by cultivation of a Bacillus subtilis strain containing a gene encoding and expressing the ALDC of Bacillus brevis with properties described in DK 149335B.
EXAMPLE 1
100 ml of ALDC solution (batch EDF 212, which is the fermentation liquor centrifugate with an ALDC activity of 1700 ADU/ml) was mixed with 2.5 ml of a 2% glutaraldehyde solution (final glutaraldehyde concentration 0.05% (w/w, corresponding to 0.5 g of glutaraldehyde/g of ALDC). The reaction mixture was cooled with ice for three hours. pH was constantly adjusted to 7.5. The ALDC activity (ADU/ml) was measured by Novo Analysis method
AF 278/1 -GB (available on request from Novo Nordisk A/S, Novo Alle, DK-2880 Bagsvaerd) with pH adjusted in the substrates to values ranging from 3.6 to 6.0. The pH-activity curves are shown in Fig. 1. The stability of ALDC and the derivatized sample was measured in a normal, pasteurized Danish beer (HOF). 20 ADU was added per ml beer in which pH was adjusted to 4.0 and 6.0, respectively. Samples from the beers were taken each day, and the residual ALDC activity measured at pH 6.0. The results are shown
5 in Figs. 2 and 3.
It is concluded that treatment with glutaraldehyde improves both the activity and the stability at pH 4.0 of ALDC.
EXAMPLE 2
Testing of derivatized ALDC in a traditional batch fermentation o ALDC (batch EDF 212, 1700 ADU/ml) (preparation 1 ) and a glutaralde¬ hyde treated ALDC (preparation 2) prepared as described in Example 1 (1100
ADU/ml) were used.
The fermentations were carried out with brewery malt wort (FAXE) and the same wort with added amounts (10, 20, 30 and 40% w/w) of adjunct (sucrose). 5 2.5 g of yeast was added per litre of wort. ALDC was added together with the yeast
(46 ADU per litre). The fermentations were carried out at 12°C and lasted for 7 days. pH (Fig. 4), ALDC residual activity (Fig. 5) and total diacetyl (α-acetolactid acid + diacetyl) (Figs. 6 - 9) were measured each day.
The results show that the reduction of total diacetyl is larger when the 0 derivatized ALDC (prep. 2) is used than when untreated ALDC is used, and that the derivatized preparation is more stable. EXAMPLE 3
3 ml of a glutaraldehyde treated ALDC prepared as described in Example 1 (1100 ADU/ml) is added to 1 g of carrier (a silica carrier from Grace described in Biocatalyst Supports SG BC 1E / June 1987, Grade 500 MP). pH was adjusted to 4.5 and the carrier and the ALDC solution is slowly agitated for 20 hours by rotation at 5°C followed by vacuum filtration. 0.5 ml of a 3% solution of polyazetidine (Kymene, Hercules BV) is added to the particles with adsorbed ALDC and the mixture is vacuum dried. The activity of the immobilized ALDC is 589 ADU/g at pH 6.0 and 331 ADU/g at pH 3.8.

Claims

1. ALDC derivative, wherein ALDC in an aqueous medium is treated with glutaraldehyde in a concentration corresponding to between 0.1 and 5 g of glutaraldehyde per g of pure ALDC protein, preferably corresponding to between 0.25 and 2 g of glutaraldehyde per g of pure ALDC protein.
2. ALDC derivative according to Claim 1 , wherein the glutaraldehyde treated ALDC derivative is immobilized.
3. Use of the ALDC derivative according to Claims 1 - 2 in beer fermentation.
4. Use according to Claim 3, wherein an ALDC derivative according to
Claim 1 is used together with ordinary yeast in a batch fermentation.
5. Use according to Claim 3, wherein an ALDC derivative according to Claim 2 is used together with ordinary yeast in a batch fermentation.
6. Use according to Claim 3, wherein an ALDC derivative according to Claim 2 is used together with immobilized yeast in a continuous fermentation.
PCT/DK1991/000222 1990-08-16 1991-08-09 Aldc derivative and use thereof WO1992003543A1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
EP91914849A EP0575323B1 (en) 1990-08-16 1991-08-09 Soluble aldc derivative and use thereof
CA002089498A CA2089498C (en) 1990-08-16 1991-08-09 Soluble aldc derivative and use thereof
DE69106896T DE69106896T2 (en) 1990-08-16 1991-08-09 SOLUBLE DERIVATIVE OF ACETOLACTATE DECARBOXYLASE AND ITS USE.
US07/976,983 US5306634A (en) 1990-08-16 1991-08-09 Soluble ALDC derivative and use thereof
BR919106762A BR9106762A (en) 1990-08-16 1991-08-09 ALDC DERIVATIVE AND USE OF THE SAME
FI930654A FI105696B (en) 1990-08-16 1993-02-15 Soluble ALDC derivative and its use
GR950400197T GR3014933T3 (en) 1990-08-16 1995-02-01 Soluble aldc derivative and use thereof.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DK1949/90 1990-08-16
DK194990A DK194990D0 (en) 1990-08-16 1990-08-16 ALDC DERIVATIVES AND USE THEREOF

Publications (1)

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WO1992003543A1 true WO1992003543A1 (en) 1992-03-05

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Country Status (14)

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US (1) US5306634A (en)
EP (1) EP0575323B1 (en)
JP (1) JP3126730B2 (en)
CN (2) CN1054638C (en)
AT (1) ATE117368T1 (en)
AU (1) AU645343B2 (en)
BR (1) BR9106762A (en)
CA (1) CA2089498C (en)
DE (1) DE69106896T2 (en)
DK (2) DK194990D0 (en)
FI (1) FI105696B (en)
GR (1) GR3014933T3 (en)
MX (1) MX9100626A (en)
WO (1) WO1992003543A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011091084A2 (en) 2010-01-19 2011-07-28 Basf Corporation Stabilized proteases for use in skin care

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5917166B2 (en) * 2012-01-25 2016-05-11 アサヒビール株式会社 Method for producing fermented malt beverage
US20170121741A1 (en) 2014-04-01 2017-05-04 Dupont Nutrition Biosciences Aps Method for increasing crude palm oil yields
WO2016097266A1 (en) 2014-12-19 2016-06-23 Dupont Nutrition Biosciences Aps Method of improving palm oil yields from palm fruit or palm fruit liquid
WO2016191169A1 (en) * 2015-05-22 2016-12-01 Dupont Nutrition Biosciences Aps Acetolactate decarboxylase

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4241185A (en) * 1979-02-23 1980-12-23 The Great Western Sugar Company Method of stabilizing α-galactosidase
EP0128714A2 (en) * 1983-06-03 1984-12-19 Novo Nordisk A/S Alpha-acetolactate decarboxylase enzyme and preparation thereof
EP0131251A1 (en) * 1983-07-08 1985-01-16 Superfos a/s Immobilized enzyme composition and process for the preparation thereof

Family Cites Families (4)

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Publication number Priority date Publication date Assignee Title
DK145502C (en) * 1980-08-07 1983-05-02 Forenede Bryggerier As PROCEDURE FOR THE PREPARATION OF FERMENTED ALCOHOLIC PRODUCTS
JPH0614865B2 (en) * 1985-12-13 1994-03-02 麒麟麦酒株式会社 DNA chain encoding α-acetolactate decarboxylase and yeast transformed with this DNA chain
FI92333C (en) * 1987-03-17 1994-10-25 Panimolaboratorio Bryggerilabo DNA sequence encoding an enzyme having acetolactate decarboxylase activity and its use in the construction of yeast strains suitable for accelerated brewing
US5043276A (en) * 1988-04-22 1991-08-27 Kirin Beer Kabushiki Kaisha DNA strand coding for alpha-acetolactate decarboxylase and yeast transformed with the DNA strand

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4241185A (en) * 1979-02-23 1980-12-23 The Great Western Sugar Company Method of stabilizing α-galactosidase
EP0128714A2 (en) * 1983-06-03 1984-12-19 Novo Nordisk A/S Alpha-acetolactate decarboxylase enzyme and preparation thereof
EP0131251A1 (en) * 1983-07-08 1985-01-16 Superfos a/s Immobilized enzyme composition and process for the preparation thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Biotechnology Letters, Vol. 10, No. 5, 1988, J.O. BAKER et al.: "Thermal stabilization of fungal beta-glucosidase through glutaraldehyde crosslinking", see page 325 - page 330. *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011091084A2 (en) 2010-01-19 2011-07-28 Basf Corporation Stabilized proteases for use in skin care
EP2525828A2 (en) * 2010-01-19 2012-11-28 BASF Corporation Stabilized proteases for use in skin care
EP2525828A4 (en) * 2010-01-19 2013-07-31 Basf Corp Stabilized proteases for use in skin care
US8778336B2 (en) 2010-01-19 2014-07-15 Basf Corporation Stabilized proteases that have been immobilized and further crosslinked for use in skin care

Also Published As

Publication number Publication date
EP0575323A1 (en) 1993-12-29
FI930654A (en) 1993-02-15
JP3126730B2 (en) 2001-01-22
CN1113093C (en) 2003-07-02
CN1054638C (en) 2000-07-19
DK194990D0 (en) 1990-08-16
CA2089498A1 (en) 1992-02-17
FI930654A0 (en) 1993-02-15
CN1059168A (en) 1992-03-04
BR9106762A (en) 1993-07-20
FI105696B (en) 2000-09-29
DK0575323T3 (en) 1995-05-01
DE69106896T2 (en) 1995-06-14
ATE117368T1 (en) 1995-02-15
EP0575323B1 (en) 1995-01-18
CN1257913A (en) 2000-06-28
JPH06500013A (en) 1994-01-06
AU645343B2 (en) 1994-01-13
CA2089498C (en) 2002-07-16
GR3014933T3 (en) 1995-05-31
DE69106896D1 (en) 1995-03-02
MX9100626A (en) 1992-04-01
US5306634A (en) 1994-04-26
AU8390891A (en) 1992-03-17

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