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(R)-perillyl alcohol + NAD+
(R)-perillaldehyde + NADH
(S)-perillyl alcohol + NAD+
(S)-perillaldehyde + NADH
2,4-dihydroxy-3-(hydroxymethyl)-6-methylbenzoic acid + NAD+
3-formyl-2,4-dihydroxy-6-methylbenzoic acid + NADH
2-aminobenzyl alcohol + NAD+
2-aminobenzaldehyde + NADH
-
-
-
-
r
2-fluorobenzyl alcohol + NAD+
2-fluorobenzaldehyde + NADH
-
-
-
-
r
2-hydroxybenzyl alcohol + NAD+
2-hydroxybenzaldehyde + NADH
2-hydroxymethyl-6-methylnaphthalene + NAD+
2-formyl-6-methylnaphthalene + NADH
low activity
-
-
?
2-hydroxymethylnaphthalene + NAD+
2-formylnaphthalene + NADH
low activity
-
-
?
2-hydroxymethylthiophene + NAD+
2-formylthiophene + NADH
2-methoxybenzyl alcohol + NAD+
2-methoxybenzaldehyde + NADH
-
-
-
-
r
2-methoxybenzyl alcohol + NAD+
2-methoxybenzaldehyde + NADH + H+
-
-
-
?
2-methylbenzyl alcohol + NAD+
2-methylbenzaldehyde + NADH + H+
3,4-dimethoxybenzyl alcohol + NAD+
3,4-dimethoxybenzaldehyde + NADH
-
-
-
-
r
3,4-dimethylbenzyl alcohol + NAD+
3,4-dimethylbenzaldehyde + NADH + H+
-
-
-
-
r
3,5-dichlorobenzyl alcohol + NAD+
3,5-dichlorobenzaldehyde + NADH
-
-
-
-
r
3-aminobenzyl alcohol + NAD+
3-aminobenzaldehyde + NADH
-
-
-
-
r
3-chlorobenzyl alcohol + NAD+
3-chlorobenzaldehyde + NADH
3-hydroxybenzyl alcohol + NAD+
3-hydroxybenzaldehyde + NADH
3-methoxybenzyl alcohol + NAD+
3-methoxybenzaldehyde + NADH
3-methoxybenzyl alcohol + NAD+
3-methoxybenzaldehyde + NADH + H+
-
-
-
?
3-methyl-2-buten-1-ol + NAD+
3-methyl-2-buten-1-al + NADH
3-methylbenzyl alcohol + NAD+
3-methylbenzaldehyde + NADH + H+
3-nitrobenzyl alcohol + NAD+
3-nitrobenzaldehyde + NADH
-
-
-
-
r
4-aminobenzyl alcohol + NAD+
4-aminobenzaldehyde + NADH
4-chlorobenzyl alcohol + NAD+
4-chlorobenzaldehyde + NADH
-
-
-
-
r
4-ethylbenzyl alcohol + NAD+
4-ethylbenzaldehyde + NADH
-
-
-
-
r
4-hydroxy-3-methoxybenzyl alcohol + NAD+
4-hydroxy-3-methoxybenzaldehyde + NADH
-
-
-
-
r
4-hydroxybenzyl alcohol + NAD+
4-hydroxybenzaldehyde + NADH
4-isopropylbenzyl alcohol + NAD+
4-isopropylbenzaldehyde + NADH
-
-
-
-
r
4-methoxybenzyl alcohol + NAD+
4-methoxybenzaldehyde + NADH
-
-
-
-
r
4-methoxybenzyl alcohol + NAD+
4-methoxybenzaldehyde + NADH + H+
-
-
-
?
4-methylbenzyl alcohol + NAD+
4-methylbenzaldehyde + NADH + H+
anisaldehyde + NADH + H+
anisic alcohol + NAD+
-
relative activity: 72.2%
-
-
r
benzaldehyde + NAD(P)H + H+
benzyl alcohol + NAD(P)+
benzaldehyde + NADH + H+
benzyl alcohol + NAD+
-
relative activity: 100%
-
-
r
benzaldehyde + NADPH + H+
benzyl alcohol + NADP+
highest reductive activity with benzaldehyde
-
-
r
benzyl alcohol + NAD(P)+
benzaldehyde + NAD(P)H + H+
benzyl alcohol + NAD+
benzaldehyde + NADH
benzyl alcohol + NADP+
benzaldehyde + NADPH
-
less active in the presence of NADP+ than in the presence of NAD+
-
-
?
benzyl alcohol + NADP+
benzaldehyde + NADPH + H+
-
-
-
r
cinnamaldehyde + NADH + H+
cinnamic alcohol + NAD+
-
relative activity: 58.7%
-
-
r
cinnamic aldehyde + NADH + H+
cinnamyl alcohol + NAD+
-
-
-
r
cinnamyl alcohol + NAD(P)+
cinnamyl aldehyde + NAD(P)H + H+
cinnamyl alcohol + NAD+
cinnamic aldehyde + NADH
-
-
-
-
r
cinnamyl alcohol + NAD+
cinnamic aldehyde + NADH + H+
-
-
-
r
cinnamyl alcohol + NAD+
cinnamyl aldehyde + NADH + H+
-
67% of the activity with benzyl alcohol
-
-
?
cis-11-hexadecenal + NADH + H+
cis-11-hexadecenol + NAD+
-
relative activity: 4.9%
-
-
r
citral + NADH + H+
citryl alcohol + NAD+
-
relative activity: 7.8%
-
-
r
citronellal + NADH + H+
citronellol + NAD+
-
relative activity: 21.8%
-
-
r
coniferyl alcohol + NAD(P)+
coniferyl aldehyde + NAD(P)H + H+
coniferyl alcohol + NAD+
coniferyl aldehyde + NADH + H+
coniferyl aldehyde + NADH + H+
coniferyl alcohol + NAD+
-
-
-
r
crotonaldehyde + NADPH + H+
crotonyl alcohol + NADP+
-
-
-
r
crotonyl alcohol + NADP+
crotonaldehyde + NADPH + H+
highest oxidative activity with crotyl alcohol
-
-
r
decanal + NADH + H+
decanol + NAD+
-
relative activity: 19.7%
-
-
r
dodecanal + NADH + H+
dodecanol + NAD+
-
relative activity: 8.9%
-
-
r
furan-2-methanol + NAD+
2-formylfuran + NADH
-
-
-
-
r
furfuryl alcohol + NAD+
furfural + NADH
geranial + NADH + H+
geraniol + NAD+
-
-
-
-
r
geraniol + NAD(P)+
geranial + NAD(P)H + H+
geraniol + NAD+
(2Z)-3,7-dimethylocta-2,6-dienal + NADH + H+
-
105% of the activity with benzyl alcohol
-
-
?
geraniol + NAD+
geranial + NADH + H+
glutaraldehyde + NADH + H+
? + NAD+
-
relative activity: 0.6%
-
-
r
glyoxal + NADH + H+
? + NAD+
-
relative activity: 0.7%
-
-
r
hexanal + NADH + H+
hexanol + NAD+
-
relative activity: 6.4%
-
-
r
nerol + NAD(P)+
(2E)-3,7-dimethylocta-2,6-dienal + NAD(P)H + H+
nerol + NAD+
(2E)-3,7-dimethylocta-2,6-dienal + NADH + H+
-
116% of the activity with benzyl alcohol
-
-
?
nerol + NAD+
neral + NADH + H+
octanal + NADH + H+
octanol + NAD+
-
relative activity: 36.5%
-
-
r
perillyl alcohol + NAD+
perillaldehyde + NADH
-
-
-
-
r
phenethyl alcohol + NAD(P)+
phenylacetaldehyde + NAD(P)H + H+
phenethyl alcohol + NAD+
phenylacetaldehyde + NADH + H+
-
73% of the activity with benzyl alcohol
-
-
?
salicyl aldehyde + NADH + H+
salicyl alcohol + NAD+
-
relative activity: 9%
-
-
r
vanillin + NADH + H+
vanillin alcohol + NAD+
-
relative activity: 4%
-
-
r
vanillyl alcohol + NAD+
vanillyl aldehyde + NADH + H+
-
-
-
?
xylene-2,2'-diol + NAD+
? + NADH
low activity
-
-
?
additional information
?
-
(R)-perillyl alcohol + NAD+
(R)-perillaldehyde + NADH
-
61% activity relative to benzyl alcohol
-
?
(R)-perillyl alcohol + NAD+
(R)-perillaldehyde + NADH
-
49% activity relative to benzyl alcohol
-
?
(S)-perillyl alcohol + NAD+
(S)-perillaldehyde + NADH
-
85% activity relative to benzyl alcohol
-
?
(S)-perillyl alcohol + NAD+
(S)-perillaldehyde + NADH
-
68% activity relative to benzyl alcohol
-
?
2,4-dihydroxy-3-(hydroxymethyl)-6-methylbenzoic acid + NAD+
3-formyl-2,4-dihydroxy-6-methylbenzoic acid + NADH
-
-
-
-
?
2,4-dihydroxy-3-(hydroxymethyl)-6-methylbenzoic acid + NAD+
3-formyl-2,4-dihydroxy-6-methylbenzoic acid + NADH
-
the enzyme plays a role in the atranorin pathway
-
-
?
2-hydroxybenzyl alcohol + NAD+
2-hydroxybenzaldehyde + NADH
-
-
-
-
r
2-hydroxybenzyl alcohol + NAD+
2-hydroxybenzaldehyde + NADH
-
-
-
?
2-hydroxymethylthiophene + NAD+
2-formylthiophene + NADH
-
-
-
-
r
2-hydroxymethylthiophene + NAD+
2-formylthiophene + NADH
-
-
-
-
r
2-methylbenzyl alcohol + NAD+
2-methylbenzaldehyde + NADH + H+
-
-
-
-
?
2-methylbenzyl alcohol + NAD+
2-methylbenzaldehyde + NADH + H+
-
-
-
-
r
2-methylbenzyl alcohol + NAD+
2-methylbenzaldehyde + NADH + H+
-
-
-
-
r
2-methylbenzyl alcohol + NAD+
2-methylbenzaldehyde + NADH + H+
-
-
-
-
?
2-methylbenzyl alcohol + NAD+
2-methylbenzaldehyde + NADH + H+
-
-
-
?
2-methylbenzyl alcohol + NAD+
2-methylbenzaldehyde + NADH + H+
-
-
-
?
3-chlorobenzyl alcohol + NAD+
3-chlorobenzaldehyde + NADH
-
-
-
-
?
3-chlorobenzyl alcohol + NAD+
3-chlorobenzaldehyde + NADH
-
-
-
-
r
3-chlorobenzyl alcohol + NAD+
3-chlorobenzaldehyde + NADH
-
-
-
r
3-chlorobenzyl alcohol + NAD+
3-chlorobenzaldehyde + NADH
low activity
-
-
?
3-hydroxybenzyl alcohol + NAD+
3-hydroxybenzaldehyde + NADH
-
-
-
-
?
3-hydroxybenzyl alcohol + NAD+
3-hydroxybenzaldehyde + NADH
-
-
-
-
r
3-hydroxybenzyl alcohol + NAD+
3-hydroxybenzaldehyde + NADH
-
-
-
?
3-methoxybenzyl alcohol + NAD+
3-methoxybenzaldehyde + NADH
-
-
-
-
?
3-methoxybenzyl alcohol + NAD+
3-methoxybenzaldehyde + NADH
-
-
-
-
r
3-methoxybenzyl alcohol + NAD+
3-methoxybenzaldehyde + NADH
-
-
-
r
3-methyl-2-buten-1-ol + NAD+
3-methyl-2-buten-1-al + NADH
-
210% activity relative to benzyl alcohol
-
-
?
3-methyl-2-buten-1-ol + NAD+
3-methyl-2-buten-1-al + NADH
-
180% activity relative to benzyl alcohol
-
r
3-methylbenzyl alcohol + NAD+
3-methylbenzaldehyde + NADH + H+
-
-
-
-
?
3-methylbenzyl alcohol + NAD+
3-methylbenzaldehyde + NADH + H+
-
-
-
?
3-methylbenzyl alcohol + NAD+
3-methylbenzaldehyde + NADH + H+
-
-
-
-
r
3-methylbenzyl alcohol + NAD+
3-methylbenzaldehyde + NADH + H+
-
-
-
-
?
3-methylbenzyl alcohol + NAD+
3-methylbenzaldehyde + NADH + H+
-
-
-
?
3-methylbenzyl alcohol + NAD+
3-methylbenzaldehyde + NADH + H+
-
-
-
?
4-aminobenzyl alcohol + NAD+
4-aminobenzaldehyde + NADH
-
270% activity relative to benzyl alcohol
-
-
r
4-aminobenzyl alcohol + NAD+
4-aminobenzaldehyde + NADH
-
-
-
-
r
4-aminobenzyl alcohol + NAD+
4-aminobenzaldehyde + NADH
-
280% activity relative to benzyl alcohol
-
-
r
4-hydroxybenzyl alcohol + NAD+
4-hydroxybenzaldehyde + NADH
-
-
-
-
r
4-hydroxybenzyl alcohol + NAD+
4-hydroxybenzaldehyde + NADH
-
-
-
?
4-hydroxybenzyl alcohol + NAD+
4-hydroxybenzaldehyde + NADH
-
125% of benzyl alcohol activity
-
-
r
4-methylbenzyl alcohol + NAD+
4-methylbenzaldehyde + NADH + H+
-
-
-
-
?
4-methylbenzyl alcohol + NAD+
4-methylbenzaldehyde + NADH + H+
-
-
-
-
r
4-methylbenzyl alcohol + NAD+
4-methylbenzaldehyde + NADH + H+
-
-
-
-
?
4-methylbenzyl alcohol + NAD+
4-methylbenzaldehyde + NADH + H+
-
-
-
?
4-methylbenzyl alcohol + NAD+
4-methylbenzaldehyde + NADH + H+
-
-
-
?
benzaldehyde + NAD(P)H + H+
benzyl alcohol + NAD(P)+
-
-
-
-
?
benzaldehyde + NAD(P)H + H+
benzyl alcohol + NAD(P)+
-
-
-
-
?
benzyl alcohol + NAD(P)+
benzaldehyde + NAD(P)H + H+
-
-
-
-
?
benzyl alcohol + NAD(P)+
benzaldehyde + NAD(P)H + H+
-
-
-
-
?
benzyl alcohol + NAD(P)+
benzaldehyde + NAD(P)H + H+
-
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
r
benzyl alcohol + NAD+
benzaldehyde + NADH
-
less active in the presence of NADP+ than in the presence of NAD+
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
r
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
r
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
r
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
a step in methylbenzene conversion
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
a step in methylbenzene conversion
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
r
cinnamyl alcohol + NAD(P)+
cinnamyl aldehyde + NAD(P)H + H+
-
-
-
-
?
cinnamyl alcohol + NAD(P)+
cinnamyl aldehyde + NAD(P)H + H+
-
67% activity compared to activity with benzyl alcohol
-
-
?
cinnamyl alcohol + NAD(P)+
cinnamyl aldehyde + NAD(P)H + H+
-
-
-
-
?
cinnamyl alcohol + NAD(P)+
cinnamyl aldehyde + NAD(P)H + H+
-
67% activity compared to activity with benzyl alcohol
-
-
?
coniferyl alcohol + NAD(P)+
coniferyl aldehyde + NAD(P)H + H+
-
-
-
-
?
coniferyl alcohol + NAD(P)+
coniferyl aldehyde + NAD(P)H + H+
-
59% activity compared to activity with benzyl alcohol
-
-
?
coniferyl alcohol + NAD(P)+
coniferyl aldehyde + NAD(P)H + H+
-
-
-
-
?
coniferyl alcohol + NAD+
coniferyl aldehyde + NADH + H+
-
relative activity: 96%
-
-
r
coniferyl alcohol + NAD+
coniferyl aldehyde + NADH + H+
-
-
-
-
r
coniferyl alcohol + NAD+
coniferyl aldehyde + NADH + H+
-
biotransformation of eugenol to ferulic acid
-
-
?
coniferyl alcohol + NAD+
coniferyl aldehyde + NADH + H+
-
59% of the activity with benzyl alcohol
-
-
?
coniferyl alcohol + NAD+
coniferyl aldehyde + NADH + H+
-
biotransformation of eugenol to ferulic acid
-
-
?
coniferyl alcohol + NAD+
coniferyl aldehyde + NADH + H+
-
-
-
r
coniferyl alcohol + NAD+
coniferyl aldehyde + NADH + H+
CADH requires NAD as a cofactor
-
-
?
furfuryl alcohol + NAD+
furfural + NADH
-
-
-
-
r
furfuryl alcohol + NAD+
furfural + NADH
-
-
-
-
r
geraniol + NAD(P)+
geranial + NAD(P)H + H+
-
-
-
-
?
geraniol + NAD(P)+
geranial + NAD(P)H + H+
-
105% activity compared to activity with benzyl alcohol
-
-
?
geraniol + NAD+
geranial + NADH + H+
-
63% activity relative to benzyl alcohol
-
?
geraniol + NAD+
geranial + NADH + H+
-
68% activity relative to benzyl alcohol
-
?
nerol + NAD(P)+
(2E)-3,7-dimethylocta-2,6-dienal + NAD(P)H + H+
-
-
-
-
?
nerol + NAD(P)+
(2E)-3,7-dimethylocta-2,6-dienal + NAD(P)H + H+
-
116% activity compared to activity with benzyl alcohol
-
-
?
nerol + NAD+
neral + NADH + H+
-
25% activity relative to benzyl alcohol
-
?
nerol + NAD+
neral + NADH + H+
-
77% activity relative to benzyl alcohol
-
?
phenethyl alcohol + NAD(P)+
phenylacetaldehyde + NAD(P)H + H+
-
-
-
-
?
phenethyl alcohol + NAD(P)+
phenylacetaldehyde + NAD(P)H + H+
-
73% activity compared to activity with benzyl alcohol
-
-
?
additional information
?
-
-
alcohols that are not oxidized
-
-
?
additional information
?
-
-
no activity with tyrosol, tryptophol, pyrogallol, catechol, phloroglucinol, ethanol, p-coumaric acid, and caffeic acid
-
-
?
additional information
?
-
-
no activity with tyrosol, tryptophol, pyrogallol, catechol, phloroglucinol, ethanol, p-coumaric acid, and caffeic acid
-
-
?
additional information
?
-
-
the enzyme is involved in the toluene metabolic pathway, overview
-
-
?
additional information
?
-
-
the enzyme is involved in the toluene metabolic pathway, overview
-
-
?
additional information
?
-
-
the enzyme plays a role in vanillin and aromatic compound metabolism, application of vanillin to the mycelium leads to up-regulation of enzymes involved in vanillin metabolism and also in glycolysis, the tricarboxylic acid cycle, the pentose-phosphate cycle, and heme biosynthesis, overview
-
-
?
additional information
?
-
-
not: 4-nitrophenyl acetate
-
-
?
additional information
?
-
-
a group of enzymes with broad specificity towards alcohols with an aromatic or cyclohex-1-ene ring, but with low or no activity towards short chain aliphatic alcohols
-
-
?
additional information
?
-
-
not: 4-nitrophenyl acetate
-
-
?
additional information
?
-
-
a group of enzymes with broad specificity towards alcohols with an aromatic or cyclohex-1-ene ring, but with low or no activity towards short chain aliphatic alcohols
-
-
?
additional information
?
-
-
enzyme from Rhodopseudomonas acidophila has broad specificity for aromatic alcohols and is also capable of oxidizing aliphatic alcohols with NAD+
-
-
?
additional information
?
-
-
enzyme also capable of oxidizing aliphatic primary alcohols with NAD+
-
-
?
additional information
?
-
the enzyme may play important role in the fungal conversion of 4-methyldibenzothiophene-5-oxide or its metabolic products
-
-
?
additional information
?
-
-
the enzyme may play important role in the fungal conversion of 4-methyldibenzothiophene-5-oxide or its metabolic products
-
-
?
additional information
?
-
no activity with NADH or NAD+
-
-
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
2,4-dihydroxy-3-(hydroxymethyl)-6-methylbenzoic acid + NAD+
3-formyl-2,4-dihydroxy-6-methylbenzoic acid + NADH
-
the enzyme plays a role in the atranorin pathway
-
-
?
2-hydroxybenzyl alcohol + NAD+
2-hydroxybenzaldehyde + NADH
-
-
-
?
2-hydroxymethyl-6-methylnaphthalene + NAD+
2-formyl-6-methylnaphthalene + NADH
low activity
-
-
?
2-hydroxymethylnaphthalene + NAD+
2-formylnaphthalene + NADH
low activity
-
-
?
2-methoxybenzyl alcohol + NAD+
2-methoxybenzaldehyde + NADH + H+
-
-
-
?
2-methylbenzyl alcohol + NAD+
2-methylbenzaldehyde + NADH + H+
3-chlorobenzyl alcohol + NAD+
3-chlorobenzaldehyde + NADH
low activity
-
-
?
3-hydroxybenzyl alcohol + NAD+
3-hydroxybenzaldehyde + NADH
-
-
-
?
3-methoxybenzyl alcohol + NAD+
3-methoxybenzaldehyde + NADH + H+
-
-
-
?
3-methylbenzyl alcohol + NAD+
3-methylbenzaldehyde + NADH + H+
4-hydroxybenzyl alcohol + NAD+
4-hydroxybenzaldehyde + NADH
-
-
-
?
4-methoxybenzyl alcohol + NAD+
4-methoxybenzaldehyde + NADH + H+
-
-
-
?
4-methylbenzyl alcohol + NAD+
4-methylbenzaldehyde + NADH + H+
benzaldehyde + NAD(P)H + H+
benzyl alcohol + NAD(P)+
benzyl alcohol + NAD(P)+
benzaldehyde + NAD(P)H + H+
benzyl alcohol + NAD+
benzaldehyde + NADH
cinnamyl alcohol + NAD(P)+
cinnamyl aldehyde + NAD(P)H + H+
coniferyl alcohol + NAD(P)+
coniferyl aldehyde + NAD(P)H + H+
coniferyl alcohol + NAD+
coniferyl aldehyde + NADH + H+
CADH requires NAD as a cofactor
-
-
?
geraniol + NAD(P)+
geranial + NAD(P)H + H+
-
-
-
-
?
nerol + NAD(P)+
(2E)-3,7-dimethylocta-2,6-dienal + NAD(P)H + H+
-
-
-
-
?
phenethyl alcohol + NAD(P)+
phenylacetaldehyde + NAD(P)H + H+
-
-
-
-
?
vanillyl alcohol + NAD+
vanillyl aldehyde + NADH + H+
-
-
-
?
xylene-2,2'-diol + NAD+
? + NADH
low activity
-
-
?
additional information
?
-
2-methylbenzyl alcohol + NAD+
2-methylbenzaldehyde + NADH + H+
-
-
-
?
2-methylbenzyl alcohol + NAD+
2-methylbenzaldehyde + NADH + H+
-
-
-
?
3-methylbenzyl alcohol + NAD+
3-methylbenzaldehyde + NADH + H+
-
-
-
?
3-methylbenzyl alcohol + NAD+
3-methylbenzaldehyde + NADH + H+
-
-
-
?
4-methylbenzyl alcohol + NAD+
4-methylbenzaldehyde + NADH + H+
-
-
-
?
4-methylbenzyl alcohol + NAD+
4-methylbenzaldehyde + NADH + H+
-
-
-
?
benzaldehyde + NAD(P)H + H+
benzyl alcohol + NAD(P)+
-
-
-
-
?
benzaldehyde + NAD(P)H + H+
benzyl alcohol + NAD(P)+
-
-
-
-
?
benzyl alcohol + NAD(P)+
benzaldehyde + NAD(P)H + H+
-
-
-
-
?
benzyl alcohol + NAD(P)+
benzaldehyde + NAD(P)H + H+
-
-
-
-
?
benzyl alcohol + NAD(P)+
benzaldehyde + NAD(P)H + H+
-
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
r
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
r
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
r
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
r
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
a step in methylbenzene conversion
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
a step in methylbenzene conversion
-
-
?
benzyl alcohol + NAD+
benzaldehyde + NADH
-
-
-
r
cinnamyl alcohol + NAD(P)+
cinnamyl aldehyde + NAD(P)H + H+
-
-
-
-
?
cinnamyl alcohol + NAD(P)+
cinnamyl aldehyde + NAD(P)H + H+
-
-
-
-
?
coniferyl alcohol + NAD(P)+
coniferyl aldehyde + NAD(P)H + H+
-
-
-
-
?
coniferyl alcohol + NAD(P)+
coniferyl aldehyde + NAD(P)H + H+
-
-
-
-
?
additional information
?
-
-
the enzyme is involved in the toluene metabolic pathway, overview
-
-
?
additional information
?
-
-
the enzyme is involved in the toluene metabolic pathway, overview
-
-
?
additional information
?
-
-
the enzyme plays a role in vanillin and aromatic compound metabolism, application of vanillin to the mycelium leads to up-regulation of enzymes involved in vanillin metabolism and also in glycolysis, the tricarboxylic acid cycle, the pentose-phosphate cycle, and heme biosynthesis, overview
-
-
?
additional information
?
-
the enzyme may play important role in the fungal conversion of 4-methyldibenzothiophene-5-oxide or its metabolic products
-
-
?
additional information
?
-
-
the enzyme may play important role in the fungal conversion of 4-methyldibenzothiophene-5-oxide or its metabolic products
-
-
?
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Chalmers, R.M.; Scott, A.J.; Fewson, C.A.
Purification of the benzyl alcohol dehydrogenase and benzaldehyde dehydrogenase encoded by the TOL plasmid pWW53 of Pseudomonas putida MT53 and their preliminary comparison with benzyl alcohol dehydrogenase and benzaldehyde dehydrogenases I and II from Acinetobacter calcoaceticus
J. Gen. Microbiol.
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637-643
1990
Acinetobacter calcoaceticus, Pseudomonas putida
-
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Harayama, S.; Rekik, M.; Wubbolts, M.; Rose, K.; Leppik, R.A.; Timmis, K.N.
Characterization of five genes in the upper-pathway operon of TOL plasmid pWW0 from Pseudomonas putida and identification of the gene products
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5048-5055
1989
Pseudomonas putida
brenda
Shaw, J.P.; Harayama, S.
Purification and characterisation of TOL plasmid-encoded benzyl alcohol dehydrogenase and benzaldehyde dehydrogenase of Pseudomonas putida
Eur. J. Biochem.
191
705-714
1990
Pseudomonas putida
brenda
Abril, M.A.; Michan, C.; Timmis, K.N.; Ramos, J.L.
Regulator and enzyme specificities of the TOL plasmid-encoded upper pathway for degradation of aromatic hydrocarbons and expansion of the substrate range of the pathway [published erratum appears in J Bacteriol 1990 Jun;172(6):3534]
J. Bacteriol.
171
6782-6790
1989
Pseudomonas putida
brenda
Inouye, S.; Nakazawa, A.; Nakazawa, T.
Molecular cloning of TOL genes xylB and xylE in Escherichia coli
J. Bacteriol.
145
1137-1143
1981
Pseudomonas putida
brenda
MacKintosh, R.W.; Fewson, C.A.
Benzyl alcohol dehydrogenase and benzaldehyde dehydrogenase II from Acinetobacter calcoaceticus. Purification and preliminary characterization
Biochem. J.
250
743-751
1988
Acinetobacter calcoaceticus
brenda
MacKintosh, R.W.; Fewson, C.A.
Benzyl alcohol dehydrogenase and benzaldehyde dehydrogenase II from Acinetobacter calcoaceticus. Substrate specificities and inhibition studies
Biochem. J.
255
653-661
1988
Acinetobacter calcoaceticus
brenda
Poh, C.L.; Bayly, R.C.
Evidence for isofunctional enzymes used in m-cresol and 2,5-xylenol degradation via the gentisate pathway in Pseudomonas alcaligenes
J. Bacteriol.
143
59-69
1980
Pseudomonas alcaligenes
brenda
Keat, M.J.; Hopper, D.J.
The aromatic alcohol dehydrogenases in Pseudomonas putida N.C.I.B. 9869 grown on 3,5-xylenol and p-cresol
Biochem. J.
175
659-667
1978
Pseudomonas putida
brenda
Collins, J.; Hegeman, G.
Benzyl alcohol metabolism by Pseudomonas putida: a paradox resolved
Arch. Microbiol.
138
153-160
1984
Pseudomonas putida
-
brenda
Yamanaka, K.; Minoshima, R.
Identification and characterization of a nicotinamide adenine dinucleotide-dependent p-hydroxybenzyl alcohol dehydrogenase from Rhodopseudomonas acidophila M402
Agric. Biol. Chem.
48
1161-1171
1984
Rhodoblastus acidophilus
-
brenda
Jaaska, V.; Jaaska, V.
Isoenzymes of aromatic alcohol dehydrogenase in rye and triticale
Biochem. Physiol. Pflanz.
179
21-30
1984
Dasypyrum villosum, Elymus repens, Secale cereale, Secale montanum, Secale sylvestre, Triticale turgidocereale, Triticum monococcum subsp. aegilopoides, Triticum turgidum
-
brenda
Curtis, A.J.; Shirk, M.C.; Fall, R.
Allylic or benzylic stabilization is essential for catalysis by bacterial benzyl alcohol dehydrogenases
Biochem. Biophys. Res. Commun.
259
220-223
1999
Acinetobacter calcoaceticus, Pseudomonas putida
brenda
Shaw, J.P.; Rekik, M.; Schwager, F.; Harayama, S.
Kinetic studies on benzyl alcohol dehydrogenase encoded by TOL plasmid pWWO. A member of the zinc-containing long chain alcohol dehydrogenase family
J. Biol. Chem.
268
10842-10850
1993
Pseudomonas putida, Pseudomonas putida (P39849)
brenda
Inoue, J.; Tomioka, N.; Itai, A.; Harayama, S.
Proton transfer in benzyl alcohol dehydrogenase during catalysis: alternate proton-relay routes
Biochemistry
37
3305-3311
1998
Pseudomonas putida
brenda
Biegert, T.; Altenschmidt, U.; Eckerskorn, C.; Fuchs, G.
Purification and properties of benzyl alcohol dehydrogenase from a denitrifying Thauera sp
Arch. Microbiol.
163
418-423
1995
Thauera sp.
brenda
Overhage, J.; Steinbuchel, A.; Priefert, H.
Biotransformation of eugenol to ferulic acid by a recombinant strain of Ralstonia eutropha H16
Appl. Environ. Microbiol.
68
4315-4321
2002
Cupriavidus necator, Pseudomonas putida
brenda
Ichinose, H.; Wariishi, H.; Tanaka, H.
Molecular analysis of arylalcohol dehydrogenase of Coriolus versicolor expressed against exogenous addition of dibenzothiophene derivatives
J. Basic Microbiol.
42
327-336
2002
Trametes versicolor (Q8X1V7), Trametes versicolor
brenda
Millanes, A.M.; Fontaniella, B.; Legaz, M.E.; Vicente, C.
Histochemical detection of an haematommoyl alcohol dehydrogenase in the lichen Evernia prunastri
Plant Physiol. Biochem.
41
786-791
2003
Evernia prunastri
-
brenda
Garcia-Pena, I.; Hernandez, S.; Auria, R.; Revah, S.
Correlation of biological activity and reactor performance in biofiltration of toluene with the fungus Paecilomyces variotii CBS115145
Appl. Environ. Microbiol.
71
4280-4285
2005
Paecilomyces variotii, Paecilomyces variotii CBS115145
brenda
Peng, X.; Taki, H.; Komukai, S.; Sekine, M.; Kanoh, K.; Kasai, H.; Choi, S.K.; Omata, S.; Tanikawa, S.; Harayama, S.; Misawa, N.
Characterization of four Rhodococcus alcohol dehydrogenase genes responsible for the oxidation of aromatic alcohols
Appl. Microbiol. Biotechnol.
71
824-832
2006
Rhodococcus erythropolis (Q2Z1W3), Rhodococcus erythropolis (Q2Z1W4), Rhodococcus erythropolis (Q2Z1W5), Rhodococcus erythropolis PR4 (Q2Z1W3), Rhodococcus erythropolis PR4 (Q2Z1W4), Rhodococcus erythropolis PR4 (Q2Z1W5)
brenda
Shimizu, M.; Yuda, N.; Nakamura, T.; Tanaka, H.; Wariishi, H.
Metabolic regulation at the tricarboxylic acid and glyoxylate cycles of the lignin-degrading basidiomycete Phanerochaete chrysosporium against exogenous addition of vanillin
Proteomics
5
3919-3931
2005
Phanerodontia chrysosporium
brenda
Landete, J.M.; Rodriguez, H.; de Las Rivas, B.; Munoz, R.
Characterization of a benzyl alcohol dehydrogenase from Lactobacillus plantarum WCFS1
J. Agric. Food Chem.
56
4497-4503
2008
Lactiplantibacillus plantarum, Lactiplantibacillus plantarum WCFS1, Lactiplantibacillus plantarum WCFS1 NCIMB 8826
brenda
Matsuzaki, F.; Shimizu, M.; Wariishi, H.
Proteomic and metabolomic analyses of the white-rot fungus Phanerochaete chrysosporium exposed to exogenous benzoic acid
J. Proteome Res.
7
2342-2350
2008
Phanerodontia chrysosporium
brenda
Uthoff, S.; Steinbuechel, A.
Purification and characterization of an NAD+-dependent XylB-like aryl alcohol dehydrogenase identified in Acinetobacter baylyi ADP1
Appl. Environ. Microbiol.
78
8743-8752
2012
Acinetobacter baylyi
brenda
Nishimura, M.; Kohno, K.; Nishimura, Y.; Inagaki, M.; Davies, J.
Characterization of two isozymes of coniferyl alcohol dehydrogenase from Streptomyces sp. NL15-2K
Biosci. Biotechnol. Biochem.
75
1770-1777
2011
Streptomyces sp. (M5AJW4)
brenda
Ying, X.; Wang, Y.; Xiong, B.; Wu, T.; Xie, L.; Yu, M.; Wang, Z.
Characterization of an allylic/benzyl alcohol dehydrogenase from Yokenella sp. strain WZY002, an organism potentially useful for the synthesis of alpha,beta-unsaturated alcohols from allylic aldehydes and ketones
Appl. Environ. Microbiol.
80
2399-2409
2014
Yokenella sp. WZY002 (W6CX26)
brenda
Nishimura, M.
Molecular cloning and expression of the Streptomyces coniferyl alcohol dehydrogenase gene in Escherichia coli
Protein Expr. Purif.
89
109-115
2013
Streptomyces sp. (M5AJW4)
brenda