1.1.99.36: alcohol dehydrogenase (nicotinoprotein)
This is an abbreviated version!
For detailed information about alcohol dehydrogenase (nicotinoprotein), go to the full flat file.
Word Map on EC 1.1.99.36
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1.1.99.36
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nicotinoproteins
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erythropolis
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rhodococcus
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dehydrogenases
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methanolica
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formaldehyde
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amycolatopsis
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nadp
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n,n-dimethyl-4-nitrosoaniline
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dismutase
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methanol
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synthesis
- 1.1.99.36
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nicotinoproteins
- erythropolis
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rhodococcus
- dehydrogenases
- methanolica
- formaldehyde
- amycolatopsis
- nadp
- n,n-dimethyl-4-nitrosoaniline
- dismutase
- methanol
- synthesis
Reaction
Synonyms
4-nitroso-N, N-dimethylaniline-dependent alcohol dehydrogenase, NDMA-ADH, NDMA-dependent alcohol dehydrogenase, np-ADH
ECTree
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Substrates Products
Substrates Products on EC 1.1.99.36 - alcohol dehydrogenase (nicotinoprotein)
for references in articles please use BRENDA:EC1.1.99.36
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REACTION DIAGRAM
1-butanol + N,N-dimethyl-4-nitrosoaniline
butanaldehyde + 4-(hydroxylamino)-N,N-dimethylaniline
Substrates: -
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1-hexanol + N,N-dimethyl-4-nitrosoaniline
hexanal + 4-(hydroxylamino)-N,N-dimethylaniline
Substrates: -
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1-propanol + N,N-dimethyl-4-nitrosoaniline
propanaldehyde + 4-(hydroxylamino)-N,N-dimethylaniline
Substrates: -
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2-butanol + N,N-dimethyl-4-nitrosoaniline
butanone + 4-(hydroxylamino)-N,N-dimethylaniline
Substrates: -
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2-propanol + N,N-dimethyl-4-nitrosoaniline
acetone + 4-(hydroxylamino)-N,N-dimethylaniline
Substrates: -
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acetate + N,N-dimethyl-4-nitrosoaniline
? + 4-(hydroxylamino)-N,N-dimethylaniline
Substrates: -
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acetophenone + 1-propanol
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Substrates: 4.3% yield, enantiomeric excess of 0.99 for (S)-product chiral secondary alcohol
Products: 3.8% yield, enantiomeric excess of 0.99 for (S)-product
Products: 3.8% yield, enantiomeric excess of 0.99 for (S)-product
r
acetophenone + cyclohexanol
?
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Substrates: 2.8-3.7% yield, depending on the ratio of substrates, enantiomeric excess of 0.95-0.99 for (S)-product chiral secondary alcohol
Products: 3.8% yield, enantiomeric excess of 0.99 for (S)-product
Products: 3.8% yield, enantiomeric excess of 0.99 for (S)-product
r
acetophenone + ethanol
?
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Substrates: 3.8% yield, enantiomeric excess of 0.99 for (S)-product chiral secondary alcohol
Products: 3.8% yield, enantiomeric excess of 0.99 for (S)-product
Products: 3.8% yield, enantiomeric excess of 0.99 for (S)-product
r
ethanol + N,N-dimethyl-4-nitrosoaniline
acetaldehyde + 4-(hydroxylamino)-N,N-dimethylaniline
methanol + N,N-dimethyl-4-nitrosoaniline
formaldehyde + 4-(hydroxylamino)-N,N-dimethylaniline
butanal + 4-(hydroxylamino)-N,N-dimethylaniline
Substrates: -
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1-butanol + N,N-dimethyl-4-nitrosoaniline
butanal + 4-(hydroxylamino)-N,N-dimethylaniline
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Substrates: -
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?
acetaldehyde + 4-(hydroxylamino)-N,N-dimethylaniline
Substrates: -
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ethanol + N,N-dimethyl-4-nitrosoaniline
acetaldehyde + 4-(hydroxylamino)-N,N-dimethylaniline
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Substrates: -
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formaldehyde + 4-(hydroxylamino)-N,N-dimethylaniline
Substrates: -
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methanol + N,N-dimethyl-4-nitrosoaniline
formaldehyde + 4-(hydroxylamino)-N,N-dimethylaniline
Substrates: best substrate
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methanol + N,N-dimethyl-4-nitrosoaniline
formaldehyde + 4-(hydroxylamino)-N,N-dimethylaniline
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Substrates: -
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methanol + N,N-dimethyl-4-nitrosoaniline
formaldehyde + 4-(hydroxylamino)-N,N-dimethylaniline
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Substrates: best substrate
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?
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Substrates: enzyme shows formaldehyde dismutase activity producing methylformate when incubated with formaldehyde and methanol
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additional information
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Substrates: enzyme shows formaldehyde dismutase activity producing methylformate when incubated with formaldehyde and methanol
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additional information
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Substrates: no activity with electron acceptors NAD+, NADP+, 3-acetylpyridine adenine dinucleotide, thionicotinamide adenine dinucleotide, phenazine methosulfate, Wurster's Blue, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliurn bromide, or cytochrome c
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additional information
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Substrates: no activity with electron acceptors NAD+, NADP+, 3-acetylpyridine adenine dinucleotide, thionicotinamide adenine dinucleotide, phenazine methosulfate, Wurster's Blue, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliurn bromide, or cytochrome c
Products: -
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additional information
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Substrates: no activity with electron acceptors NAD+, NADP+, 3-acetylpyridine adenine dinucleotide, thionicotinamide adenine dinucleotide, phenazine methosulfate, Wurster's Blue, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliurn bromide, or cytochrome c
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additional information
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Substrates: catalyzes the asymmetric reduction of ketones using cheap reductants, such as ethanol, with high stereoselectivity, but the reaction is too slow to obtain good yields
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