JPH11318442A - Ｄ―アミノアシラ―ゼ - Google Patents
Ｄ―アミノアシラ―ゼInfo
- Publication number
- JPH11318442A JPH11318442A JP11035620A JP3562099A JPH11318442A JP H11318442 A JPH11318442 A JP H11318442A JP 11035620 A JP11035620 A JP 11035620A JP 3562099 A JP3562099 A JP 3562099A JP H11318442 A JPH11318442 A JP H11318442A
- Authority
- JP
- Japan
- Prior art keywords
- acetyl
- aminoacylase
- valine
- methionine
- molecular weight
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- 101710097070 D-aminoacylase Proteins 0.000 title claims abstract description 57
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- XUYPXLNMDZIRQH-ZCFIWIBFSA-N N-acetyl-D-methionine Chemical compound CSCC[C@H](C(O)=O)NC(C)=O XUYPXLNMDZIRQH-ZCFIWIBFSA-N 0.000 claims abstract description 9
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- IHYJTAOFMMMOPX-LURJTMIESA-N N-acetyl-L-valine Chemical compound CC(C)[C@@H](C(O)=O)NC(C)=O IHYJTAOFMMMOPX-LURJTMIESA-N 0.000 claims abstract description 8
- IHYJTAOFMMMOPX-ZCFIWIBFSA-N (2r)-2-acetamido-3-methylbutanoic acid Chemical compound CC(C)[C@H](C(O)=O)NC(C)=O IHYJTAOFMMMOPX-ZCFIWIBFSA-N 0.000 claims abstract description 7
- WXNXCEHXYPACJF-SSDOTTSWSA-N N-acetyl-D-leucine Chemical compound CC(C)C[C@H](C(O)=O)NC(C)=O WXNXCEHXYPACJF-SSDOTTSWSA-N 0.000 claims abstract description 7
- XUYPXLNMDZIRQH-LURJTMIESA-N N-acetyl-L-methionine Chemical compound CSCC[C@@H](C(O)=O)NC(C)=O XUYPXLNMDZIRQH-LURJTMIESA-N 0.000 claims abstract description 7
- WXNXCEHXYPACJF-ZETCQYMHSA-M N-acetyl-L-leucinate Chemical compound CC(C)C[C@@H](C([O-])=O)NC(C)=O WXNXCEHXYPACJF-ZETCQYMHSA-M 0.000 claims abstract description 6
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- CBQJSKKFNMDLON-SNVBAGLBSA-N N-acetyl-D-phenylalanine Chemical compound CC(=O)N[C@@H](C(O)=O)CC1=CC=CC=C1 CBQJSKKFNMDLON-SNVBAGLBSA-N 0.000 claims description 6
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- IHYJTAOFMMMOPX-UHFFFAOYSA-N N-Acetyl-Valine Chemical compound CC(C)C(C(O)=O)NC(C)=O IHYJTAOFMMMOPX-UHFFFAOYSA-N 0.000 claims description 5
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- DZTHIGRZJZPRDV-UHFFFAOYSA-N N-acetyltryptophan Chemical compound C1=CC=C2C(CC(NC(=O)C)C(O)=O)=CNC2=C1 DZTHIGRZJZPRDV-UHFFFAOYSA-N 0.000 claims description 5
- KTHDTJVBEPMMGL-GSVOUGTGSA-N n-acetylalanine Chemical compound OC(=O)[C@@H](C)NC(C)=O KTHDTJVBEPMMGL-GSVOUGTGSA-N 0.000 claims description 5
- HXFOXFJUNFFYMO-UHFFFAOYSA-N 2-Acetamido-4-amino-4-oxobutanoic acid Chemical compound CC(=O)NC(C(O)=O)CC(N)=O HXFOXFJUNFFYMO-UHFFFAOYSA-N 0.000 claims description 4
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- KTHDTJVBEPMMGL-UHFFFAOYSA-N N-Acetyl-DL-alanine Chemical compound OC(=O)C(C)NC(C)=O KTHDTJVBEPMMGL-UHFFFAOYSA-N 0.000 claims description 4
- CBQJSKKFNMDLON-UHFFFAOYSA-N N-acetylphenylalanine Chemical compound CC(=O)NC(C(O)=O)CC1=CC=CC=C1 CBQJSKKFNMDLON-UHFFFAOYSA-N 0.000 claims description 4
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 claims description 3
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- 238000002425 crystallisation Methods 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 238000001212 derivatisation Methods 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 239000002532 enzyme inhibitor Substances 0.000 description 1
- 238000011067 equilibration Methods 0.000 description 1
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 229960002989 glutamic acid Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229940091173 hydantoin Drugs 0.000 description 1
- 150000001469 hydantoins Chemical class 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- JDNTWHVOXJZDSN-UHFFFAOYSA-N iodoacetic acid Chemical compound OC(=O)CI JDNTWHVOXJZDSN-UHFFFAOYSA-N 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 229960005190 phenylalanine Drugs 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 239000003910 polypeptide antibiotic agent Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229960002429 proline Drugs 0.000 description 1
- 230000017854 proteolysis Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- IFGCUJZIWBUILZ-UHFFFAOYSA-N sodium 2-[[2-[[hydroxy-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphosphoryl]amino]-4-methylpentanoyl]amino]-3-(1H-indol-3-yl)propanoic acid Chemical compound [Na+].C=1NC2=CC=CC=C2C=1CC(C(O)=O)NC(=O)C(CC(C)C)NP(O)(=O)OC1OC(C)C(O)C(O)C1O IFGCUJZIWBUILZ-UHFFFAOYSA-N 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 230000003390 teratogenic effect Effects 0.000 description 1
- 229960003433 thalidomide Drugs 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 229960004295 valine Drugs 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
- C12P41/006—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures
- C12P41/007—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures by reactions involving acyl derivatives of racemic amines
-
- 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
- C12N9/14—Hydrolases (3)
- C12N9/78—Hydrolases (3) acting on carbon to nitrogen bonds other than peptide bonds (3.5)
- C12N9/80—Hydrolases (3) acting on carbon to nitrogen bonds other than peptide bonds (3.5) acting on amide bonds in linear amides (3.5.1)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/04—Alpha- or beta- amino acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Analytical Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Enzymes And Modification Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11035620A JPH11318442A (ja) | 1998-03-17 | 1999-02-15 | Ｄ―アミノアシラ―ゼ |
| US09/268,941 US6030823A (en) | 1998-03-17 | 1999-03-16 | D-aminoacylase |
| DE69905636T DE69905636T2 (de) | 1998-03-17 | 1999-03-17 | D-Aminoacylase aus Sebekia benihana |
| EP99104069A EP0950706B1 (en) | 1998-03-17 | 1999-03-17 | D-aminoacylase from Sebekia benihana |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10-89246 | 1998-03-17 | ||
| JP8924698 | 1998-03-17 | ||
| JP11035620A JPH11318442A (ja) | 1998-03-17 | 1999-02-15 | Ｄ―アミノアシラ―ゼ |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH11318442A true JPH11318442A (ja) | 1999-11-24 |
| JPH11318442A5 JPH11318442A5 (enExample) | 2005-12-08 |
Family
ID=26374604
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11035620A Pending JPH11318442A (ja) | 1998-03-17 | 1999-02-15 | Ｄ―アミノアシラ―ゼ |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US6030823A (enExample) |
| EP (1) | EP0950706B1 (enExample) |
| JP (1) | JPH11318442A (enExample) |
| DE (1) | DE69905636T2 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000041684A (ja) * | 1998-07-29 | 2000-02-15 | Daicel Chem Ind Ltd | 新規なｄ−アミノアシラーゼおよびその製造方法、並びに該ｄ−アミノアシラーゼを利用したｄ−アミノ酸の製造方法 |
| JP4327301B2 (ja) * | 1999-06-17 | 2009-09-09 | 天野エンザイム株式会社 | 形質転換微生物、ｄ−アミノアシラーゼの製造方法 |
| ES2272372T3 (es) | 2000-04-19 | 2007-05-01 | Basilea Pharmaceutica Ag | Procedimiento para la preparacion de derivados de asparagina. |
| JP4502295B2 (ja) * | 2000-08-02 | 2010-07-14 | ダイセル化学工業株式会社 | 耐熱性ｄ−アミノアシラーゼ |
| US20060172375A1 (en) * | 2002-12-18 | 2006-08-03 | Daiichi Pure Chemicals Co., Ltd | D-aminoacylase |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0783711B2 (ja) * | 1987-06-29 | 1995-09-13 | ダイセル化学工業株式会社 | 新規なｄ―アミノアシラーゼの製造法 |
| US5206162A (en) * | 1991-10-17 | 1993-04-27 | National Science Council Of Republic Of China | Process for making D-aminoacylase |
-
1999
- 1999-02-15 JP JP11035620A patent/JPH11318442A/ja active Pending
- 1999-03-16 US US09/268,941 patent/US6030823A/en not_active Expired - Fee Related
- 1999-03-17 EP EP99104069A patent/EP0950706B1/en not_active Expired - Lifetime
- 1999-03-17 DE DE69905636T patent/DE69905636T2/de not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DE69905636T2 (de) | 2003-12-18 |
| EP0950706B1 (en) | 2003-03-05 |
| US6030823A (en) | 2000-02-29 |
| DE69905636D1 (de) | 2003-04-10 |
| EP0950706A3 (en) | 1999-12-15 |
| EP0950706A2 (en) | 1999-10-20 |
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