CHARACTERIZATION OF A TRANSIENT INTERMEDIATE FORMED IN THE LIVER ALCOHOL-DEHYDROGENASE CATALYZED REDUCTION OF 3-HYDROXY-4-NITROBENZALDEHYDE

被引：11

作者：

MACGIBBON, AKH ^{[1
]}

KOERBER, SC ^{[1
]}

PEASE, K ^{[1
]}

DUNN, MF ^{[1
]}

机构：

[1] UNIV CALIF RIVERSIDE, DEPT BIOCHEM, RIVERSIDE, CA 92521 USA

来源：

BIOCHEMISTRY | 1987年 / 26卷 / 11期

关键词：

D O I：

10.1021/bi00385a017

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：3058 / 3067

页数：10

共 35 条

[21] 3-BETA-HYDROXY-5-BETA-STEROID DEHYDROGENASE-ACTIVITY OF HUMAN-LIVER ALCOHOL-DEHYDROGENASE (ADH) IS SPECIFIC TO GAMMA-SUBUNITS
MCEVILY, AJ
HOLMQUIST, B
AULD, DS
VALLEE, BL
FASEB JOURNAL, 1988, 2 (04): : A551 - A551
[22] ACTIVE-SITE COBALT(II)-SUBSTITUTED HORSE LIVER ALCOHOL-DEHYDROGENASE - CHARACTERIZATION OF INTERMEDIATES IN THE OXIDATION AND REDUCTION PROCESSES AS A FUNCTION OF PH
SARTORIUS, C
GERBER, M
ZEPPEZAUER, M
DUNN, MF
BIOCHEMISTRY, 1987, 26 (03) : 871 - 882
[23] ENZYMES IN ORGANIC-SYNTHESIS .27. HORSE LIVER ALCOHOL-DEHYDROGENASE CATALYZED OXIDOREDUCTIONS OF 3-ALKYLTHIOPYRAN KETONES AND ALCOHOLS
TAKEMURA, T
JONES, JB
JOURNAL OF ORGANIC CHEMISTRY, 1983, 48 (06): : 791 - 796
[24] FORMATE-DRIVEN, NONENZYMATIC NAD(P)H REGENERATION FOR THE ALCOHOL-DEHYDROGENASE CATALYZED STEREOSELECTIVE REDUCTION OF 4-PHENYL-2-BUTANONE
WESTERHAUSEN, D
HERRMANN, S
HUMMEL, W
STECKHAN, E
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1992, 31 (11) : 1529 - 1531
[25] STUDIES ON MECHANISM OF ENZYME-CATALYZED OXIDATION REDUCTION REACTIONS .4. A PROPOSED MECHANISM FOR OVER-ALL REACTION CATALYZED BY LIVER ALCOHOL DEHYDROGENASE
MAHLER, HR
BAKER, RH
SHINER, VJ
BIOCHEMISTRY, 1962, 1 (01) : 47 - &
[26] ENZYMATIC INVITRO REDUCTION OF KETONES .13. HORSE LIVER ALCOHOL-DEHYDROGENASE (HLAD) AS A TOOL FOR THE SYNTHESIS OF ENANTIOMERICALLY PURE ALKYL 3-OXO-CYCLOHEXANECARBOXYLATES AND 3-HYDROXYCYCLOHEXANECARBOXYLATES
WILLAERT, JJ
LEMIERE, GL
DOMMISSE, RA
LEPOIVRE, JA
ALDERWEIRELDT, FC
JOURNAL OF CHEMICAL RESEARCH-S, 1985, (07): : 222 - 223
[27] PIG-LIVER ALCOHOL-DEHYDROGENASE CATALYZED STEREOSELECTIVE REDUCTION OF CAGE-SHAPED KETONES - PREPARATION OF AXIALLY CHIRAL (-)-(R)-ADAMANTANE-2,6-DIOL WITH HIGH ENANTIOMERIC PURITY
HIROSE, Y
OKUTSU, M
ANZAI, M
NAEMURA, K
CHIKAMATSU, H
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1992, (03): : 317 - 319
[28] THE ACTIVE-SITE OF LIVER ALCOHOL-DEHYDROGENASE - MECHANISTIC INFERENCES FROM THE BINDING AND TURNOVER OF 2-PYRIDYLCARBINOL, 3-PYRIDYLCARBINOL, AND 4-PYRIDYLCARBINOL
POCKER, Y
DEROY, SC
ALCOHOL AND ALCOHOLISM, 1986, 21 (02): : A13 - A13
[29] Stereoselective Synthesis of Three Isomers of tert-Butyl 5-Hydroxy-4-methyl-3-oxohexanoate through Alcohol Dehydrogenase-Catalyzed Dynamic Kinetic Resolution
Luedeke, Steffen
Richter, Michael
Mueller, Michael
ADVANCED SYNTHESIS & CATALYSIS, 2009, 351 (1-2) : 253 - 259
[30] HORSE-LIVER ALCOHOL-DEHYDROGENASE AND PSEUDOMONAS-TESTOSTERONI 3(17)BETA-HYDROXYSTEROID DEHYDROGENASE TRANSFER EPIMERIC HYDROGENS FROM NADH TO 17BETA-HYDROXY-5ALPHA-ANDROSTAN-3-ONE - EXCEPTION TO ONE OF ALWORTH-BENTLYE RULES
GROMAN, EV
SCHULTZ, RM
ENGEL, LL
ORR, JC
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1976, 63 (02): : 427 - 429

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