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crotonaldehyde + NAD+ + H2O = crotonate + NADH
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crotonaldehyde + NAD+ + H2O = crotonate + NADH
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crotonaldehyde + NAD+ + H2O = crotonate + NADH
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crotonaldehyde + NADP+ + H2O = crotonate + NADPH + H+
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crotonaldehyde + NADP+ = crotonate + NADPH
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crotonaldehyde + NAD+ + H2O = crotonic acid + NADH
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crotonaldehyde + H2O + O2 = crotonate + H2O2
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crotonaldehyde + H2O + O2 = crotonic acid + H2O2
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crotonaldehyde + CoA + 2 oxidized ferredoxin = crotonate + CO2 + 2 reduced ferredoxin + 2 H+
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crotonaldehyde + H2O + 2 NAD+ = crotonate + 2 NADH + 2 H+
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crotonaldehyde + H2O + 2 oxidized benzyl viologen = crotonate + 2 H+ + 2 reduced benzyl viologen
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crotonaldehyde + H2O + oxidized benzyl viologen = crotonate + H+ + reduced benzyl viologen
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crotonaldehyde + H2O + oxidized benzyl viologen = crotonate + reduced benzyl viologen
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crotonaldehyde + H2O + oxidized benzyl viologen = crotonate + reduced benzyl viologen + H+
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crotonaldehyde + H2O + oxidized ferredoxin = crotonate + H+ + reduced ferredoxin
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crotonaldehyde + H2O + oxidized ferredoxin = crotonate + reduced ferredoxin
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crotonaldehyde + H2O + oxidized methyl viologen = crotonate + H+ + reduced methyl viologen
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crotonaldehyde + H2O + oxidized methyl viologen = crotonate + reduced methyl viologen + H+
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crotonaldehyde + H2O + oxidized methyl viologen = crotonate + reduced methyl viologen + H+
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Crotonaldehyde + ES-1 ferredoxin = Crotonate + reduced ES-1 ferredoxin
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Crotonaldehyde + methyl viologen = Crotonate + reduced methyl viologen
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crotonaldehyde + benzyl viologen = crotonic acid + reduced benzyl viologen
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Crotonaldehyde + benzyl viologen = E-2-Butenoate + reduced benzyl viologen
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crotonyl-CoA + H2O = crotonate + CoA
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crotonyl-CoA + acetate = crotonate + acetyl-CoA
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4-methylumbelliferyl (2E)-but-2-enoate + H2O = 4-methylumbelliferone + (2E)-but-2-enoic acid
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crotonylcholine + H2O = crotonate + choline
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crotonyl-CoA = trans-2-butenoate + CoA
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crotonyl-CoA + H2O = CoA + crotonate
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2-butenoyl-CoA + H2O = CoA + 2-butenoate
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crotonyl-CoA + H2O = CoA + crotonate
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crotonitrile + H2O = crotonic acid + NH3
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crotononitrile + 2 H2O = crotonic acid + NH3
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crotononitrile + 2 H2O = crotonic acid + NH3
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2-butenenitrile + H2O = 2-butenic acid + NH3
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2-butenenitrile + H2O = 2-butenoic acid + NH3
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cis-crotononitrile + H2O = crotonic acid + NH3
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crotonitrile + H2O = crotonic acid + NH3
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trans-crotononitrile + H2O = crotonic acid + NH3
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Additional enoates amd other alpha,beta-unsaturated carbonyl compounds as substrates for the enoate reductase from Clostridium tyrobutyricum, influence of elevated hydrogen pressure on the reduction rate
1989
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Design and application of sensitive enzyme immunoassays specific for clostridial enoate reductase
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Enzyme kinetics in reversed micelles. 2. Behaviour of enoate reductase
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Reductions of 2-enals, dehydrogenation of saturated aldehydes and their racemisation
1988
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Electroenzymatic and electromicrobial reduction: preparation of chiral compounds
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Electro-enzymic viologen-mediated stereospecific reduction of 2-enoates with free and immobilized enoate reductase on cellulose filters or modified carbon electrodes
1987
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Structure of enoate reductase from a Clostridium tyrobutyricum (C. spec. La1)
1985
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ATP formation is coupled to the hydrogenation of 2-enoates in Clostridium sporogenes
1983
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20
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On the occurrence of enoate reductase and 2-oxo-carboxylate reductase in clostridia and some observations on the amino acid fermentation by Peptostreptococcus anaerobius
1983
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Immunological relationship of enoate reductases from different clostridia and the classification of Clostridium species La 1
1983
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19
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On the kinetics and mechanism of enoate reductase
1982
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Hoppe-Seyler's Z. Physiol. Chem.
363
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Rhein as an electron acceptor for various flavoproteins and for electron transport particles
1982
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363
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The reduction of allyl alcohols by Clostridium species is catalyzed by the combined action of alcohol dehydrogenase and enoate reductase
1981
Bader, J.; Kim, M.A.; Simon, H.
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362
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The activities of hydrogenase and enoate reductase in two Clostridium species, their interrelationship and dependence on growth conditions
1980
Bader, J.; Simon, H.
Arch. Microbiol.
127
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Occurrence and the possible physiological role of 2-enoate reductases
1980
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FEBS Lett.
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Purification and some properties of a hitherto-unknown enzyme reducing the carbon-carbon double bond of alpha, beta-unsaturated carboxylate anions
1979
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Eur. J. Biochem.
97
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EPR and Moessbauer spectroscopic studies on enoate reductase
1996
Caldeira, J.; Feicht, R.; White, H.; Teixeira, M.; Moura, J.J.G.; Simon, H.; Moura, I.
J. Biol. Chem.
271
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Enoate reductases of Clostridia: cloning, sequencing, and expression
2001
Rohdich, F.; Wiese, A.; Feicht, R.; Simon, H.; Bacher, A.
J. Biol. Chem.
276
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Specificity and kinetics of Rhodotorula gracilis D-amino acid oxidase
1992
Pollegioni, L.; Falbo, A.; Pilone, M.S.
Biochim. Biophys. Acta
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Inhibition of prostaglandin synthase by some low molecular mass fatty acids
1988
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Purification and properties of Escherichia coli coenzyme A-transferase
1975
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Arch. Biochem. Biophys.
171
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Butyryl-CoA:acetoacetate CoA-transferase from a lysine-fermenting Clostridium
1978
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Glutaconate CoA-transferase from Acidaminococcus fermentans
1981
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Eur. J. Biochem.
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Remaining acetamide in acetonitrile degradation using nitrile hydratase- and amidase-producing microorganisms
2007
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Appl. Microbiol. Biotechnol.
74
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Dihydroorotate dehydrogenase from Saccharomyces cerevisiae: spectroscopic investigations with the recombinant enzyme throw light on catalytic properties and metabolism of fumarate analogues
2007
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FEMS Yeast Res.
7
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Identification of geranic acid, a tyrosinase inhibitor in lemongrass (Cymbopogon citratus)
2008
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J. Agric. Food Chem.
56
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Purification and some properties of an acryloyl-CoA reductase of Clostridium kluyveri
1985
Sedlmeier, H.; Simon, H.
Biol. Chem. Hoppe-Seyler
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Inhibitory effects of fatty acids on the activity of mushroom tyrosinase
2010
Guo, Y.J.; Pan, Z.Z.; Chen, C.Q.; Hu, Y.H.; Liu, F.J.; Shi, Y.; Yan, J.H.; Chen, Q.X.
Appl. Biochem. Biotechnol.
162
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A propionate CoA-transferase of Ralstonia eutropha H16 with broad substrate specificity catalyzing the CoA thioester formation of various carboxylic acids
2012
Lindenkamp, N.; Schuermann, M.; Steinbuechel, A.
Appl. Microbiol. Biotechnol.
97
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Is rat an appropriate animal model to study the involvement of D-serine catabolism in schizophrenia? Insights from characterization of D-amino acid oxidase
2011
Frattini, L.F.; Piubelli, L.; Sacchi, S.; Molla, G.; Pollegioni, L.
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Identification of missing genes and enzymes for autotrophic carbon fixation in crenarchaeota
2011
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J. Bacteriol.
193
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Regulatory and functional diversity of methylmercaptopropionate coenzyme A ligases from the dimethylsulfoniopropionate demethylation pathway in Ruegeria pomeroyi DSS-3 and other proteobacteria
2014
Bullock, H.A.; Reisch, C.R.; Burns, A.S.; Moran, M.A.; Whitman, W.B.
J. Bacteriol.
196
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Characterization of propionate CoA-transferase from Ralstonia eutropha H16
2014
Volodina, E.; Schuermann, M.; Lindenkamp, N.; Steinbuechel, A.
Appl. Microbiol. Biotechnol.
98
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A highly stable d-amino acid oxidase of the thermophilic bacterium Rubrobacter xylanophilus
2014
Takahashi, S.; Furukawara, M.; Omae, K.; Tadokoro, N.; Saito, Y.; Abe, K.; Kera, Y.
Appl. Environ. Microbiol.
80
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