Enoate reductase

Chemistry and Biochemistry of Flavoenzymes

Volumn 2, Issue , 2018, Pages 317-328

  Simon, Helmut ^a  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 85063491536     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1201/9781351070584     Document Type: Chapter

References (28)

1. Tischer, W., Bader, J., and Simon, H., Purification and some properties of a hitherto-unknown enzyme reducing the carbon-carbon double bond of a, p-unsaturated carboxylate anions, Eur. J. Biochem., 97, 103, 1979.
2. Giesel, H. and Simon, H., On the occurrence of enoate reductase and 2-oxocarboxylate reductase in clostridia and some observations on the amino acid fermentation by Peptostreptococcus anaerobius, Arch. Microbiol, 135, 51, 1983.
3. Krause, G. and Simon, H., Design and application of sensitive enzyme immuno assays specific for clostridial enoate reductase, Z. Naturforsch., 44C, 345, 1989.
4. Giesel, H. and Simon, H., Immunological relationship of enoate reductase from different clostridia and the classification of Clostridium species La 1, FEMS Lett., 19, 43, 1983.
5. Hashimoto, H., Rambeck, B., Giinther, H., Mannschreck, A., and Simon, H., Uber das Vorkommen einer Reduktase von 2-Carbonsauren in Clostridium kluyveri mit einer von der Butyryl-CoA-Dehydrogenase vershiedenen Stereospezifitat, Hoppe-Seyler’s Z. Physiol. Chem., 356, 1203, 1975.
6. Giesel, H., Machacek, G., Bayerl, J., and Simon, H., On the formation of 3-phenylpropionate and the different stereochemical course of the reduction of cinnamate by Clostridium sporogenes and Peptostreptococcus anaerobius, FEES Lett., 123, 107, 1981.
7. Bartl, K., Cavalar, Ch., Krebs, T., Ripp, E., Retey, J., Hull, W. E., Giinther, H., and Simon, H., Synthesis of stereospecifically deuterated phenylalanines and determination of their configuration, Eur. J. Biochem., 72, 747, 1977.
8. Bader, J., Rauschenbach, P., and Simon, H On a hitherto unknown fermentation path of several amino acids by proteolytic clostridia, FEBS Lett., 140, 67, 1982.
9. Bader, J. and Simon, H., ATP formation is coupled to the hydrogenation of 2-enoates in Clostridium sporogenes, FEMS Lett., 20, 171, 1983.
10. Bader, J. and Simon, H., The activities of hydrogenase and enoate reductase in two Clostridium species, their interrelationship and dependence on growth conditions, Arch. MicrobioL, 127, 279, 1980.
11. Bader, J., Giinther, H., Rambeck, B., and Simon, H., Properties of two clostridia strains acting as catalysts for the preparative stereo specific hydrogenation of 2-enoic acids and 2-alken-l-ols with hydrogen gas, Hoppe-Seyler’sZ. Physiol. Chem., 359, 19, 1978.
12. Kuno, S., Bacher, A., and Simon, H., Structure of enoate reductase from a Clostridium tyrobutyricum (C. spec. La 1), Biol. Chem., Hoppe-Seyler, 366, 463, 1985.
13. Thanos, J., Bader, J., Gunther, H., Neumann, S., Krauss, F., and Simon, H., Electroenzymatic and electromicrobial reduction: preparation of chiral compounds, Methods Enzymol., 136, 302, 1987.
14. Biihler, M. and Simon, H., On the kinetics and mechanism of enoate reductase, Hoppe-Seyler’sZ. Physiol. Chem., 363, 609, 1982.
15. Tischer, W., Biihler, M., Simon, H., and Hemmerich, P., On the mechanism of enoate reductase, Hoppe Seyler’s Z. Physiol. Chem., 361, 339, 1980.
16. Sedlmaier, H., Tischer, W., Rauschenbach, P., and Simon, H., On the mechanism of 2-enoate reductase; elimination of halogen hydracids from 3-halogene-2-enoates during reduction with NADH, FEBS Lett., 100, 129, 1979.
17. Simon, H., Bader, J., Gunther, H., Neumann, S., and Thanos, J., Chiral compounds synthesized by biocatalytic reductions, Angew. Chem. Int. Ed. Engl., 24, 539, 1985.
18. Thanos, I., Deffner, A., and Simon, H, Reductions of 2-enals, dehydrogenation of saturated aldehydes and their racemisation, Biol. Chem., Hoppe-Seyler, 369, 451, 1988.
19. Thanos, I. and Simon, H., Electro-enzymic viologen-mediated stereo specific reduction of 2-enoates with free and immobilized enoate reductase on cellulose filters or modified carbon electrodes, J. Biotechnol, 6, 13, 1987.
20. Bader, J., Kim, M.-A., and Simon, H., The reduction of allylalcohols by Clostridium species is catalyzed by the combined action of alcohol dehydrogenase and enoate reductase, Hoppe Seyler’s Z. Physiol. Chem., 362, 809, 1981.
21. Thanos, J. and Simon, H., Stereospecific reductions with hydrogen gas, modified metal catalysts, methylviologen and enzymes or microorganisms, Angew. Chem. Int. Ed. Engl., 25, 462, 1986.
22. Verhaert, R. M. D., Schaafsma, T. J., Laane, C., Hilhorst, R., and Veeger, C., Optimization of the photo-enzymatic reduction of the carbon-carbon double bond of a-p unsaturated carboxylates in reversed micelles, Photochem, Photobiol, 49, 209, 1989.
23. Verhaert, R. M. D., Tyrakowska, B., Hilhorst, R., Schaafsma, T. J., and Veeger, C., Enzyme kinetics in reversed micelles. II. Behaviour of enoate reductase, Eur. J. Biochem., 187, 73, 1990.
24. Simon, H. and Gunther, H., Microbial and enzymic production of labeled compounds, in Biotechnology, Vol. 6b, VCH D-6940, Rehm, H.-J. and Reed, G., Eds., Weinheim, Deerfield Beach, FL, 1988, 171.
25. Gorgen, G., Boland, W., Preiss, U., and Simon, H., Synthesis of chiral 12-phenyl(2H)dodecanoic acids, Useful metabolic probes for the biosynthesis of 1-alkenes from fatty acids, Helv. Chim. Acta, 72, 917, 1989.
26. Simon, H., Chiral synthons by new oxidoreductases and methodo logics, in Biocatalysis, Abramowicz, D. A., Ed., van Nostrand Reinhold, 1990, 217.
27. Preiss, U., White, H., and Simon, H., Additional enoates and other ot, i-unsaturated carbonyl compounds as substrates for the enoate reductase from Clostridium tyrobutyricum, influence of elevated hydrogen pressure on the reduction rate, in DECHEMA Biotechnology Conferences 3A, Behrens, D., Ed., VCH, Weinheim, Deerfield Beach, FL, 1989, 189.
28. Simon, H., unpublished results.