1.3.1.31: 2-enoate reductase

This is an abbreviated version!
For detailed information about 2-enoate reductase, go to the full flat file.

Word Map on EC 1.3.1.31

Reaction

Butanoate
+
NAD+
=
but-2-enoate
+
NADH
+
H+

Synonyms

Achr-OYE3, Achr-OYE4, acylate:NAD+ DELTA2 oxidoreductase, enoate reductase, ERED, ERED xenobiotic reductase B, KYE1, LacER, NADPH dehydrogenase 1, NCR, old yellow enzyme, OPR1, OPR3, reductase, 2-enoate, SYE-4, XenA, XenB, yellow enzyme, Yers-ER, YqjM

ECTree

     1 Oxidoreductases
         1.3 Acting on the CH-CH group of donors
             1.3.1 With NAD+ or NADP+ as acceptor
                1.3.1.31 2-enoate reductase

Reference

Reference on EC 1.3.1.31 - 2-enoate reductase

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REF.
AUTHORS
TITLE
JOURNAL
VOL.
PAGES
YEAR
ORGANISM (UNIPROT)
PUBMED ID
SOURCE
Preiss, U.; White, H.; Simon, H.
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
DECHEMA Biotechnol. Conf.
3
189-192
1989
Clostridium tyrobutyricum
-
Manually annotated by BRENDA team
Krause, G.; Simon, H.
Design and application of sensitive enzyme immunoassays specific for clostridial enoate reductase
Z. Naturforsch. C
44
345-352
1989
Clostridium sporogenes, Moorella thermoacetica, Clostridium tyrobutyricum
Manually annotated by BRENDA team
Verhaert, R.M.D.; Tyrakowska, B.; Hilhorst, R.; Schaafsma, T.J.; Veeger, C.
Enzyme kinetics in reversed micelles. 2. Behaviour of enoate reductase
Eur. J. Biochem.
187
73-79
1990
Clostridium sp.
Manually annotated by BRENDA team
Thanos, I.; Deffner, A.; Simon, H.
Reductions of 2-enals, dehydrogenation of saturated aldehydes and their racemisation
Biol. Chem. Hoppe-Seyler
369
451-460
1988
Clostridium kluyveri, Clostridium tyrobutyricum
Manually annotated by BRENDA team
Thanos, I.; Bader, J.; Guenther, H.; Neumann, S.; Krauss, F.; Simon, H.
Electroenzymatic and electromicrobial reduction: preparation of chiral compounds
Methods Enzymol.
136
302-317
1987
Clostridium tyrobutyricum
-
Manually annotated by BRENDA team
Thanos, I.C.G.; Simon, H.
Electro-enzymic viologen-mediated stereospecific reduction of 2-enoates with free and immobilized enoate reductase on cellulose filters or modified carbon electrodes
J. Biotechnol.
6
13-29
1987
Clostridium tyrobutyricum
-
Manually annotated by BRENDA team
Kuno, S.; Bacher, A.; Simon, H.
Structure of enoate reductase from a Clostridium tyrobutyricum (C. spec. La1)
Biol. Chem. Hoppe-Seyler
366
463-472
1985
Clostridium tyrobutyricum
Manually annotated by BRENDA team
Bader, J.; Simon, H.
ATP formation is coupled to the hydrogenation of 2-enoates in Clostridium sporogenes
FEMS Microbiol. Lett.
20
171-175
1983
Clostridium sporogenes
-
Manually annotated by BRENDA team
Giesel, H.; Simon, H.
On the occurrence of enoate reductase and 2-oxo-carboxylate reductase in clostridia and some observations on the amino acid fermentation by Peptostreptococcus anaerobius
Arch. Microbiol.
135
51-57
1983
Paraclostridium bifermentans, Clostridium botulinum, Clostridioides difficile, Paeniclostridium ghonii, Tissierella praeacuta, Clostridioides mangenotii, Clostridium oceanicum, Paeniclostridium sordellii, Clostridium sporogenes, Acetoanaerobium sticklandii, no activity in Clostridium butyricum, no activity in Clostridium pasteurianum, no activity in Clostridium propionicum, Peptostreptococcus anaerobius
Manually annotated by BRENDA team
Giesel, H.; Simon, H.
Immunological relationship of enoate reductases from different clostridia and the classification of Clostridium species La 1
FEMS Microbiol. Lett.
19
43-45
1983
Clostridium kluyveri, Clostridium sp., Clostridium sporogenes, Clostridium tyrobutyricum
-
Manually annotated by BRENDA team
Buehler, M.; Simon, H.
On the kinetics and mechanism of enoate reductase
Hoppe-Seyler's Z. Physiol. Chem.
363
609-625
1982
Clostridium kluyveri, Clostridium sp.
Manually annotated by BRENDA team
Egerer, P.; Buehler, M.; Simon, H.
Rhein as an electron acceptor for various flavoproteins and for electron transport particles
Hoppe-Seyler's Z. Physiol. Chem.
363
627-633
1982
Clostridium sp.
Manually annotated by BRENDA team
Bader, J.; Kim, M.A.; Simon, H.
The reduction of allyl alcohols by Clostridium species is catalyzed by the combined action of alcohol dehydrogenase and enoate reductase
Hoppe-Seyler's Z. Physiol. Chem.
362
809-820
1981
Clostridium kluyveri, Clostridium sp.
Manually annotated by BRENDA team
Bader, J.; Simon, H.
The activities of hydrogenase and enoate reductase in two Clostridium species, their interrelationship and dependence on growth conditions
Arch. Microbiol.
127
279-287
1980
Clostridium kluyveri, Clostridium sp.
Manually annotated by BRENDA team
Buehler, M.; Giesel, H.; Tischer, W.; Simon, H.
Occurrence and the possible physiological role of 2-enoate reductases
FEBS Lett.
109
244-246
1980
Clostridium kluyveri, Clostridium sp., Clostridium sporogenes, Peptostreptococcus anaerobius
Manually annotated by BRENDA team
Tischer, W.; Bader, J.; Simon, H.
Purification and some properties of a hitherto-unknown enzyme reducing the carbon-carbon double bond of alpha, beta-unsaturated carboxylate anions
Eur. J. Biochem.
97
103-112
1979
Clostridium kluyveri, Clostridium sp.
Manually annotated by BRENDA team
Caldeira, J.; Feicht, R.; White, H.; Teixeira, M.; Moura, J.J.G.; Simon, H.; Moura, I.
EPR and Moessbauer spectroscopic studies on enoate reductase
J. Biol. Chem.
271
18743-18748
1996
Clostridium tyrobutyricum
Manually annotated by BRENDA team
Rohdich, F.; Wiese, A.; Feicht, R.; Simon, H.; Bacher, A.
Enoate reductases of Clostridia: cloning, sequencing, and expression
J. Biol. Chem.
276
5779-5787
2001
Clostridium tyrobutyricum (O52933), Moorella thermoacetica (O52935)
Manually annotated by BRENDA team
de Kraker, J.W.; Franssen, M.C.R.; Joerink, M.; de Groot, A.; Bouwmeester, H.J.
Biosynthesis of costunolide, dihydrocostunolide, and leucodin. Demostration of cytochrome P450-catalyzed formation of the lactone ring present in sesquiterpene lactones of chicory
Plant Physiol.
129
257-268
2002
Cichorium intybus
Manually annotated by BRENDA team
Chaparro-Riggers, J.F.; Rogers, T.A.; Vazquez-Figueroa, E.; Polizzi, K.M.; Bommarius, A.S.
Comparison of three enoate reductases and their potential use for biotransformations
Adv. Synth. Catal.
349
1521-1531
2007
Yersinia bercovieri, Kluyveromyces lactis (P40952), Pseudomonas putida (Q9R9V9)
-
Manually annotated by BRENDA team
Stuermer, R.; Hauer, B.; Hall, M.; Faber, K.
Asymmetric bioreduction of activated C:C bonds using enoate reductases from the old yellow enzyme family
Curr. Opin. Chem. Biol.
11
203-213
2007
Saccharomyces cerevisiae, Burkholderia sp., Marchantia polymorpha, Rhodotorula sp., Rhodotorula
Manually annotated by BRENDA team
Stueckler, C.; Hall, M.; Ehammer, H.; Pointner, E.; Kroutil, W.; Macheroux, P.; Faber, K.
Stereocomplementary bioreduction of alpha,beta-unsaturated dicarboxylic acids and dimethyl esters using enoate reductases: enzyme- and substrate-based stereocontrol
Org. Lett.
9
5409-5411
2007
Bacillus subtilis, Solanum lycopersicum
Manually annotated by BRENDA team
Richter, N.; Groeger, H.; Hummel, W.
Asymmetric reduction of activated alkenes using an enoate reductase from Gluconobacter oxydans
Appl. Microbiol. Biotechnol.
89
79-89
2011
Gluconobacter oxydans
Manually annotated by BRENDA team
Liu, Y.J.; Pei, X.Q.; Lin, H.; Gai, P.; Liu, Y.C.; Wu, Z.L.
Asymmetric bioreduction of activated alkenes by a novel isolate of Achromobacter species producing enoate reductase
Appl. Microbiol. Biotechnol.
95
635-645
2012
Achromobacter sp. (I3V5V5)
Manually annotated by BRENDA team
Wang, H.; Pei, X.; Wu, Z.
An enoate reductase Achr-OYE4 from Achromobacter sp. JA81: characterization and application in asymmetric bioreduction of CC bonds
Appl. Microbiol. Biotechnol.
98
705-15
2013
Achromobacter sp. (I3V5V6), Achromobacter sp. JA81 (I3V5V6)
Manually annotated by BRENDA team
Romagnolo, A.; Spina, F.; Carusetta, D.; Nerva, L.; Cramarossa, M.; Parmeggiani, F.; Forti, L.; Brenna, E.; Varese, G.
Fungal laccases and enoate reductases as biocatalysts of fine chemical transformations
Chem. Eng. Technol.
32
961-966
2013
Absidia glauca, Penicillium citrinum
-
Manually annotated by BRENDA team
Gao, X.; Ren, J.; Wu, Q.; Zhu, D.
Biochemical characterization and substrate profiling of a new NADH-dependent enoate reductase from Lactobacillus casei
Enzyme Microb. Technol.
51
26-34
2012
Lacticaseibacillus casei
Manually annotated by BRENDA team
Iqbal, N.; Rudroff, F.; Brige, A.; Van Beeumen, J.; Mihovilovic, M.D.
Asymmetric bioreduction of activated carbon-carbon double bonds using Shewanella yellow enzyme (SYE-4) as novel enoate reductase
Tetrahedron
68
7619-7623
2012
Shewanella sp.
Manually annotated by BRENDA team
Gall, M.; Thomsen, M.; Peters, C.; Pavlidis, I.V.; Jonczyk, P.; Gruenert, P.P.; Beutel, S.; Scheper, T.; Gross, E.; Backes, M.; Geissler, T.; Ley, J.P.; Hilmer, J.M.; Krammer, G.; Palm, G.J.; Hinrichs, W.; Bornscheuer, U.T.
Enzymatic conversion of flavonoids using bacterial chalcone isomerase and enoate reductase
Angew. Chem. Int. Ed. Engl.
53
1439-1442
2014
Eubacterium ramulus (V9P074), Eubacterium ramulus
Manually annotated by BRENDA team
Skrobiszewski, A.; Ogorek, R.; Plaskowska, E.; Gladkowski, W.
Pleurotus ostreatus as a source of enoate reductase
Biocatal. Agricult. Biotechnol.
2
26-31
2013
Pleurotus ostreatus, Pleurotus ostreatus PO310783
-
Manually annotated by BRENDA team
Peters, C.; Rudroff, F.; Mihovilovic, M.D.; T Bornscheuer, U.
Fusion proteins of an enoate reductase and a Baeyer-Villiger monooxygenase facilitate the synthesis of chiral lactones
Biol. Chem.
398
31-37
2017
Pseudomonas putida
Manually annotated by BRENDA team
Classen, T.; Pietruszka, J.; Schuback, S.
Revisiting the enantioselective sequence patterns in enoate reductases
ChemCatChem
5
711-713
2013
Solanum lycopersicum, Photorhabdus luminescens
-
Manually annotated by BRENDA team
Sun, J.; Lin, Y.; Shen, X.; Jain, R.; Sun, X.; Yuan, Q.; Yan, Y.
Aerobic biosynthesis of hydrocinnamic acids in Escherichia coli with a strictly oxygen-sensitive enoate reductase
Metab. Eng.
35
75-82
2016
Clostridium acetobutylicum
Manually annotated by BRENDA team
Paul, C.; Gargiulo, S.; Opperman, D.; Lavandera, I.; Gotor-Fernandez, V.; Gotor, V.; Taglieber, A.; Arends, I.; Hollmann, F.
Mimicking nature: Synthetic nicotinamide cofactors for C=C bioreduction using enoate reductases
Org. Lett.
15
180-183
2013
Thermus scotoductus
Manually annotated by BRENDA team