JPH0449399B2 - - Google Patents

Info

Publication number: JPH0449399B2
Authority: JP; Japan
Prior art keywords: nad; nadh; reaction; hydrogen; present
Prior art date: 1984-03-09
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.): Expired

Application number

JP4619684A

Other languages

English (en)

Japanese (ja)

Other versions

JPS60188091A (ja

Inventor

Tadashi Matsunaga

Naoki Matsunaga

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Unitika Ltd

Original Assignee

Unitika Ltd

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.)

1984-03-09

Filing date

1984-03-09

Publication date

1992-08-11

1984-03-09 Application filed by Unitika Ltd filed Critical Unitika Ltd

1984-03-09 Priority to JP4619684A priority Critical patent/JPS60188091A/ja

1985-09-25 Publication of JPS60188091A publication Critical patent/JPS60188091A/ja

1992-08-11 Publication of JPH0449399B2 publication Critical patent/JPH0449399B2/ja

Status Granted legal-status Critical Current

Links

BAWFJGJZGIEFAR-NNYOXOHSSA-N NAD zwitterion Chemical compound NC(=O)C1=CC=C[N+]([C@H]2[C@@H]([C@H](O)[C@@H](COP([O-])(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 BAWFJGJZGIEFAR-NNYOXOHSSA-N 0.000 claims description 29
229950006238 nadide Drugs 0.000 claims description 29
229930027945 nicotinamide-adenine dinucleotide Natural products 0.000 claims description 28
229910052739 hydrogen Inorganic materials 0.000 claims description 13
239000001257 hydrogen Substances 0.000 claims description 13
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
238000000034 method Methods 0.000 claims description 9
241000193403 Clostridium Species 0.000 claims description 8
244000005700 microbiome Species 0.000 claims description 8
229930024421 Adenine Natural products 0.000 claims 1
GFFGJBXGBJISGV-UHFFFAOYSA-N Adenine Chemical compound NC1=NC=NC2=C1N=CN2 GFFGJBXGBJISGV-UHFFFAOYSA-N 0.000 claims 1
DFPAKSUCGFBDDF-ZQBYOMGUSA-N [14c]-nicotinamide Chemical compound N[14C](=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-ZQBYOMGUSA-N 0.000 claims 1
229960000643 adenine Drugs 0.000 claims 1
BOPGDPNILDQYTO-NNYOXOHSSA-N nicotinamide-adenine dinucleotide Chemical compound C1=CCC(C(=O)N)=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OC[C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC=NC(N)=C3N=C2)O)O1 BOPGDPNILDQYTO-NNYOXOHSSA-N 0.000 description 24
238000006243 chemical reaction Methods 0.000 description 16
210000004027 cell Anatomy 0.000 description 8
230000001580 bacterial effect Effects 0.000 description 6
239000008363 phosphate buffer Substances 0.000 description 6
238000006911 enzymatic reaction Methods 0.000 description 5
239000000126 substance Substances 0.000 description 5
239000005515 coenzyme Substances 0.000 description 3
238000006479 redox reaction Methods 0.000 description 3
230000008929 regeneration Effects 0.000 description 3
238000011069 regeneration method Methods 0.000 description 3
229920001817 Agar Polymers 0.000 description 2
241000193401 Clostridium acetobutylicum Species 0.000 description 2
239000008272 agar Substances 0.000 description 2
235000010419 agar Nutrition 0.000 description 2
239000000872 buffer Substances 0.000 description 2
238000002848 electrochemical method Methods 0.000 description 2
102000007698 Alcohol dehydrogenase Human genes 0.000 description 1
108010021809 Alcohol dehydrogenase Proteins 0.000 description 1
241000193171 Clostridium butyricum Species 0.000 description 1
108020005199 Dehydrogenases Proteins 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
239000001888 Peptone Substances 0.000 description 1
108010080698 Peptones Proteins 0.000 description 1
239000007997 Tricine buffer Substances 0.000 description 1
239000007983 Tris buffer Substances 0.000 description 1
238000002835 absorbance Methods 0.000 description 1
229940023476 agar Drugs 0.000 description 1
239000000783 alginic acid Substances 0.000 description 1
235000010443 alginic acid Nutrition 0.000 description 1
229920000615 alginic acid Polymers 0.000 description 1
229960001126 alginic acid Drugs 0.000 description 1
150000004781 alginic acids Chemical class 0.000 description 1
230000004888 barrier function Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
229940041514 candida albicans extract Drugs 0.000 description 1
239000000679 carrageenan Substances 0.000 description 1
235000010418 carrageenan Nutrition 0.000 description 1
229920001525 carrageenan Polymers 0.000 description 1
229940113118 carrageenan Drugs 0.000 description 1
239000007979 citrate buffer Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
210000004748 cultured cell Anatomy 0.000 description 1
ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
229910000396 dipotassium phosphate Inorganic materials 0.000 description 1
235000019797 dipotassium phosphate Nutrition 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000002255 enzymatic effect Effects 0.000 description 1
239000000284 extract Substances 0.000 description 1
239000011790 ferrous sulphate Substances 0.000 description 1
235000003891 ferrous sulphate Nutrition 0.000 description 1
239000000499 gel Substances 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
229940014259 gelatin Drugs 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
239000008103 glucose Substances 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
230000007774 longterm Effects 0.000 description 1
235000013372 meat Nutrition 0.000 description 1
229930014626 natural product Natural products 0.000 description 1
235000019319 peptone Nutrition 0.000 description 1
239000002504 physiological saline solution Substances 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
239000000047 product Substances 0.000 description 1
238000000746 purification Methods 0.000 description 1
239000002994 raw material Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
239000012138 yeast extract Substances 0.000 description 1
UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1

Landscapes

Preparation Of Compounds By Using Micro-Organisms (AREA)

JP4619684A 1984-03-09 1984-03-09 ニコチンアミドアデニンジヌクレオチドの還元法 Granted JPS60188091A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP4619684A JPS60188091A (ja)	1984-03-09	1984-03-09	ニコチンアミドアデニンジヌクレオチドの還元法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP4619684A JPS60188091A (ja)	1984-03-09	1984-03-09	ニコチンアミドアデニンジヌクレオチドの還元法

Publications (2)

Publication Number	Publication Date
JPS60188091A JPS60188091A (ja)	1985-09-25
JPH0449399B2 true JPH0449399B2 (fr)	1992-08-11

Family

ID=12740314

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP4619684A Granted JPS60188091A (ja)	1984-03-09	1984-03-09	ニコチンアミドアデニンジヌクレオチドの還元法

Country Status (1)

Country	Link
JP (1)	JPS60188091A (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP5826226B2 (ja) *	2013-08-23	2015-12-02	内山　俊一	水素活性化触媒

1984
- 1984-03-09 JP JP4619684A patent/JPS60188091A/ja active Granted

Also Published As

Publication number	Publication date
JPS60188091A (ja)	1985-09-25

Publication	Publication Date	Title
Tarmy et al.	1968	Kinetics of Escherichia coli B D-lactate dehydrogenase and evidence for pyruvate-controlled change in conformation
US4221869A (en)	1980-09-09	Enzymatic synthesis of L-carnitine
EP0164943B1 (fr)	1991-05-22	Procédé de production de la pyrrolo-quinoléine-quinone
US4352885A (en)	1982-10-05	Preparation of a novel NADP linked alcohol-aldehyde/ketone oxidoreductase from thermophilic anaerobic bacteria for analytical and commercial use
IE63497B1 (en)	1995-05-03	Process for the preparation of hydroxy acids
Chibata et al.	1983	Immobilized living microbial cells
Payen et al.	1983	Use of cytoplasmic hydrogenase from Alcaligenes eutrophus for NADH regeneration
EP0142169B1 (fr)	1991-12-04	Réductase de l'acide 2,5-D-cétogluconique
JPH06217769A (ja)	1994-08-09	糖分解酵素の製造法
Matsunaga et al.	1985	Regeneration of NAD (P) H by immobilized whole cells of Clostridium butyricum under hydrogen high pressure
JPH0449399B2 (fr)	1992-08-11
Wong et al.	1985	Enzymatic synthesis of chiral hydroxy compounds using immobilized glucose dehydrogenase from Bacillus cereus for NAD (P) H regeneration
JP2768473B2 (ja)	1998-06-25	Ｎａｄｈオキシダーゼの製造法
King et al.	1988	[63] Immobilization of a cytochrome P-450 enzyme from Saccharomyces cerevisiae
AU603339B2 (en)	1990-11-15	Process for the production of sorbitol by enzymatic reaction, and microorganisms suitable for the purpose
Bergel et al.	1996	First attempts in bioelectrochemical engineering
JPS6156090A (ja)	1986-03-20	ニコチンアミドアデニンジヌクレオチド燐酸の還元方法
JPH0364107B2 (fr)	1991-10-03
JP2936551B2 (ja)	1999-08-23	（ｒ）−（＋）−３−ハロ乳酸の製造法
JP2005211042A (ja)	2005-08-11	フマル酸の製造方法
JPS6167495A (ja)	1986-04-07	Ｌ−アラニンの製造方法
JPS5943157B2 (ja)	1984-10-19	ピキア属菌によるソルビト−ルの製造法
US20010036660A1 (en)	2001-11-01	Method of producing optically active N-methylamino acids
JPH0157959B2 (fr)	1989-12-08
Andersson et al.	1998	Microbial production of d-(S)-chlorolactic acid by Proteus vulgaris cells