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Biochemical synthesis of stereospecifically hydrogen labelled compounds on a preparative scale, V1-3. Preparation of (1R) (1-2H)- and (1S) (1-2H)-alcohols by exchange reactions catatyzed by yeast or a coupled enzyme system.

作者信息

Günther H, Alizade M A, Kellner M, Biller F, Simon H

出版信息

Z Naturforsch C. 1973 May-Jun;28(5):241-6.

PMID:4272175
Abstract
摘要

相似文献

1
Biochemical synthesis of stereospecifically hydrogen labelled compounds on a preparative scale, V1-3. Preparation of (1R) (1-2H)- and (1S) (1-2H)-alcohols by exchange reactions catatyzed by yeast or a coupled enzyme system.立体特异性氢标记化合物的制备规模生化合成，V1 - 3。通过酵母或偶联酶系统催化的交换反应制备(1R)(1 - 2H)-和(1S)(1 - 2H)-醇。
Z Naturforsch C. 1973 May-Jun;28(5):241-6.
2
Preparative-scale synthesis of (1R)-and (1S)-monodeuteriopropanol by enzymatic exchange reactions.通过酶促交换反应制备规模合成(1R)-和(1S)-单氘代丙醇。
Angew Chem Int Ed Engl. 1973 Feb;12(2):146-7. doi: 10.1002/anie.197301461.
3
The alcohol dehydrogenase of Clostridium acetobutylicum.丙酮丁醇梭菌的乙醇脱氢酶
Biochem J. 1970 Sep;119(3):19P-20P. doi: 10.1042/bj1190019pb.
4
2H-NMR resolution of the methylenic isotopomers of ethanol applied to the study of stereospecific enzyme-catalysed exchange.
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[On the formation of volatile by-products of fermentation by lactic acid bacteria].[关于乳酸菌发酵挥发性副产物的形成]
Arch Mikrobiol. 1971;76(4):299-307.
6
Biochemical synthesis of stereospecifically hydrogen labeled compounds on a preparative scale, VI1-3 Synthesis of further substrates of NAD(P)-linked dehydrogenases of high specific tritium content.
Z Naturforsch C Biosci. 1975 Mar-Apr;30(2):141-6. doi: 10.1515/znc-1975-3-402.
7
Studies of enzyme-mediated reactions. Part IV. Complementary syntheses of stereospecifically labelled (R)- and (S)-[alpha-3H1]benzyl alcohol derivatives by use of liver alcohol dehydrogenase.酶介导反应的研究。第四部分。利用肝脏乙醇脱氢酶对立体特异性标记的(R)-和(S)-[α-³H₁]苄醇衍生物进行互补合成。
J Chem Soc Perkin 1. 1975(12):1156-61.
8
Biocatalytic deuterium- and hydrogen-transfer using over-expressed ADH-'A': enhanced stereoselectivity and 2H-labeled chiral alcohols.使用过表达的ADH-'A'进行生物催化氘和氢转移：增强的立体选择性和2H标记的手性醇。
Chem Commun (Camb). 2006 Jun 14(22):2402-4. doi: 10.1039/b602487d. Epub 2006 Apr 11.
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Response surface optimization of the critical medium components for carbonyl reductase production by Candida viswanathii MTCC 5158.维斯瓦纳森假丝酵母MTCC 5158产羰基还原酶关键培养基成分的响应面优化
Bioresour Technol. 2007 Mar;98(4):829-33. doi: 10.1016/j.biortech.2006.03.008. Epub 2006 May 11.
10
Analytical application of the stereospecific hydrogen exchange reaction between (R)-carnitine and water, catalyzed by (R)-carnitine dehydrogenase and alpha-lipoamide dehydrogenase (diaphorase).由（R）-肉碱脱氢酶和α-硫辛酸脱氢酶（黄递酶）催化的（R）-肉碱与水之间的立体特异性氢交换反应的分析应用。
Life Sci. 1974 Jun 16;14(12):2447-58. doi: 10.1016/0024-3205(74)90141-6.

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Determination of the absolute configuration of (+)-neopentyl-1-d alcohol by neutron and x-ray diffraction analysis.通过中子和X射线衍射分析确定(+)-新戊基-1-d醇的绝对构型。
Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12872-6. doi: 10.1073/pnas.91.26.12872.
2
Biosynthesis of trans, trans- and cis, trans-farnesols by soluble enzymes from tissue cultures of Andrographis paniculata.穿心莲组织培养物中可溶性酶催化反,反-和顺,反-法尼醇的生物合成。
Biochem J. 1974 Dec;144(3):585-92. doi: 10.1042/bj1440585.
3
Hydrogen transfer between ethanol molecules during oxidoreduction in vivo.
体内氧化还原过程中乙醇分子间的氢转移。
Biochem J. 1985 Jul 15;229(2):315-22. doi: 10.1042/bj2290315.
4
Reduction of acetaldehyde to ethanol by some micro-organisms and its stereospecificity.一些微生物将乙醛还原为乙醇及其立体特异性。
Biochem J. 1988 Mar 15;250(3):929-32. doi: 10.1042/bj2500929.