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diacetyl + NADH + H+ = (S)-acetoin + NAD+
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(2S,3S)-butane-2,3-diol + NAD+ = (2S)-acetoin + NADH + H+
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diacetyl + NADH + H+ = (3S)-acetoin + NAD+
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(2S,3S)-butane-2,3-diol + NAD+ = (2S)-acetoin + NADH + H+
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(2S,3S)-butane-2,3-diol + NAD+ = (S)-acetoin + NADH + H+
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(2R,3S)-butane-2,3-diol + NAD+ = (3S)-acetoin + NADH + H+
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(2S,3S)-butane-2,3-diol + NAD+ = (S)-acetoin + NADH + H+
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(3S)-acetoin + NADH + H+ = (2S,3S)-2,3-butanediol + NAD+
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(2S)-acetoin + NADH + H+ = (2S,3S)-butane-2,3-diol + NAD+
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(3S)-acetoin + NADH + H+ = (2R,3S)-butane-2,3-diol + NAD+
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(2S)-acetoin + NADH + H+ = (2S,3S)-butane-2,3-diol + NAD+
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(3S)-acetoin + NADH + H+ = (2S,3S)-2,3-butanediol + NAD+
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(S)-acetoin + NADH + H+ = meso-2,3-butanediol + NAD+
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diacetyl + NADPH + H+ = (3S)-acetoin + NADP+
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(2S,3S)-2,3-butanediol + NADP+ = (S)-2-acetoin + NADPH + H+
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meso-2,3-butanediol + NADP+ = (S)-2-acetoin + NADPH + H+
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(2S,3S)-2,3-butanediol + NAD+ = (3S)-acetoin + NADH + H+
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diacetyl + NADH + H+ = (3S)-acetoin + NAD+
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diacetyl + beta-NADH + H+ = (S)-acetoin + beta-NAD+
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diacetyl + NADH + H+ = (S)-acetoin + NAD+
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diacetyl + NADPH + H+ = (S)-acetoin + NADP+
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(2S,3S)-butane-2,3-diol + NAD+ = (2S)-acetoin + NADH + H+
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diacetyl + NADH + H+ = (2S)-acetoin + NAD+
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diacetyl + NADH + H+ = (3S)-acetoin + NAD+
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meso-butane-2,3-diol + NAD+ = (3S)-acetoin + NADH + H+
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meso-2,3-butanediol + NAD+ = (3S)-acetoin + NADH
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(2S,3S)-butane-2,3-diol + NAD+ = (2S)-acetoin + NADH + H+
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diacetyl + NADH + H+ = (2S)-acetoin + NAD+
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(2S,3S)-2,3-butanediol + NAD+ = (3S)-acetoin + NADH + H+
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2 diacetyl + 2 NADH + 2 H+ = (3S)-acetoin + (2S,3S)-butane-2,3-diol + NAD+
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(2S,3S)-butane-2,3-diol + NAD+ = (S)-acetoin + NADH + H+
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(2R,3S)-butane-2,3-diol + NAD+ = (3S)-acetoin + NADH + H+
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(2S,3S)-2,3-butanediol + NAD+ = (3S)-acetoin + NADH
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(2S,3S)-2,3-butanediol + NAD+ = (3S)-acetoin + NADH + H+
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diacetyl + NADH + H+ = (3S)-acetoin + NAD+
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(2S,3S)-butane-2,3-diol + NAD+ = (S)-acetoin + NADH + H+
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pyruvate + acetylphosphinate + NAD+ = (S)-acetoin + ? + NADH
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2 pyruvate = (S)-acetoin + 2 CO2
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methylpyruvate + benzaldehyde = (S)-acetoin + CO2
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acetaldehyde + acetaldehyde = (S)-acetoin + ?
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D-(-)-Acetoin = L-(+)-Acetoin
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Reduction of acetoin to 2,3-butanediol in Klebsiella pneumoniae: a new model
1983
Voloch, M.; Ladisch, M.R.; Rodwell, V.W.; Tsao, G.T.
Biotechnol. Bioeng.
25
173-183
Stereoisomeric specificities of 2,3-butanediol dehydrogenase
1960
Taylor, M.B.; Juni, E.
Biochim. Biophys. Acta
39
448-457
Engineering of 2,3-butanediol dehydrogenase to reduce acetoin formation by glycerol-overproducing, low-alcohol Saccharomyces cerevisiae
2009
Ehsani, M.; Fernandez, M.R.; Biosca, J.A.; Julien, A.; Dequin, S.
Appl. Environ. Microbiol.
75
3196-3205
A new NAD(H)-dependent meso-2,3-butanediol dehydrogenase from an industrially potential strain Serratia marcescens H30
2014
Zhang, L.; Xu, Q.; Zhan, S.; Li, Y.; Lin, H.; Sun, S.; Sha, L.; Hu, K.; Guan, X.; Shen, Y.
Appl. Microbiol. Biotechnol.
98
1175-1184
Cloning, expression, and characterization of budC gene encoding meso-2,3-butanediol dehydrogenase from Bacillus licheniformis
2016
Xu, G.C.; Bian, Y.Q.; Han, R.Z.; Dong, J.J.; Ni, Y.
Appl. Biochem. Biotechnol.
178
604-617
Stereospecificity of Corynebacterium glutamicum 2,3-butanediol dehydrogenase and implications for the stereochemical purity of bioproduced 2,3-butanediol
2016
Rados, D.; Turner, D.L.; Catarino, T.; Hoffart, E.; Neves, A.R.; Eikmanns, B.J.; Blombach, B.; Santos, H.
Appl. Microbiol. Biotechnol.
100
10573-10583
Promiscuous activity of (S,S)-butanediol dehydrogenase is responsible for glycerol production from 1,3-dihydroxyacetone in Corynebacterium glutamicum under oxygen-deprived conditions
2015
Jojima, T.; Igari, T.; Moteki, Y.; Suda, M.; Yukawa, H.; Inui, M.
Appl. Microbiol. Biotechnol.
99
1427-1433
Engineering of cofactor regeneration enhances (2S,3S)-2,3-butanediol production from diacetyl
2013
Wang, Y.; Li, L.; Ma, C.; Gao, C.; Tao, F.; Xu, P.
Sci. Rep.
3
2643
Stereospecificity of Corynebacterium glutamicum 2,3-butanediol dehydrogenase and implications for the stereochemical purity of bioproduced 2,3-butanediol
2016
Rados, D.; Turner, D.L.; Catarino, T.; Hoffart, E.; Neves, A.R.; Eikmanns, B.J.; Blombach, B.; Santos, H.
Appl. Microbiol. Biotechnol.
100
10573-10583
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