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1-butanol + acceptor
butanal + reduced acceptor
3-methylbenzaldehyde + ferricyanide
3-methylbenzoic acid + ferrocyanide + H+
acetaldehyde + 2 ferricyanide + H2O
acetate + 2 ferrocyanide + 2 H+
acetaldehyde + 2,6-dichlorophenol indophenol
acetate + reduced 2,6-dichlorophenol indophenol
acetaldehyde + 2,6-dichlorophenolindophenol
acetate + reduced 2,6-dichlorophenolindophenol
acetaldehyde + a quinone + H2O
acetate + a quinol
acetaldehyde + acceptor + H2O
acetic acid + reduced acceptor
-
potassium ferricyanide, 2,6-dichlorophenolindophenol, phenazine methosulfate, Wurster's blue and nitroblue tetrazolium are utilized as electron acceptors in aldehyde oxidation
-
-
?
acetaldehyde + ferricyanide
acetic acid + ferrocyanide + H+
acetaldehyde + oxidized 2,6-dichlorophenolindophenol
acetate + reduced 2,6-dichlorophenolindophenol
acetaldehyde + oxidized phenazine methosulfate
acetic acid + reduced phenazine methosulfate
acetaldehyde + oxidized tetramethylphenylenediamine
acetate + reduced tetramethylphenylenediamine
acetaldehyde + phenazine methosulfate
acetate + reduced phenazine methosulfate
acetaldehyde + ubiquinone
acetate + ubiquinol
-
electrons removed from substrate by alcohol dehydrogenase complex are initially transferred to the pyrroloquinoline quinone centre and further tunnelled across four cytochromes c to the membrane ubiquinone
-
-
?
benzaldehyde + a quinone + H2O
benzoate + a quinol
butanal + 2 ferricyanide + H2O
butanoate + 2 ferrocyanide + 2 H+
butanal + a quinone + H2O
butanoate + a quinone
butanal + acceptor + H2O
butanoate + reduced acceptor
-
potassium ferricyanide, 2,6-dichlorophenolindophenol, phenazine methosulfate, Wurster's blue and nitroblue tetrazolium are utilized as electron acceptors in aldehyde oxidation
-
-
?
butanal + ferricyanide
butanoic acid + ferrocyanide + H+
butyraldehyde + 2,6-dichlorophenol indophenol
butanoate + reduced 2,6-dichlorophenol indophenol
butyraldehyde + 2,6-dichlorophenolindophenol
butanoate + reduced 2,6-dichlorophenolindophenol
butyraldehyde + oxidized tetramethylphenylenediamine
butanoate + reduced tetramethylphenylenediamine
-
-
-
-
?
decanal + a quinone + H2O
decanoate + a quinol
-
15% of acetaldehyde oxidation
-
?
dodecanal + a quinone + H2O
dodecanoate + a quinol
-
15% of acetaldehyde oxidation
-
?
formaldehyde + 2 ferricyanide + H2O
formate + 2 ferrocyanide + 2 H+
formaldehyde + oxidized 2,6-dichlorophenolindophenol
formate + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
formaldehyde + oxidized tetramethylphenylenediamine
formate + reduced tetramethylphenylenediamine
furfural + 2 ferricyanide + H2O
2-furoic acid + 2 ferrocyanide + 2 H+
-
-
-
-
?
glutaraldehyde + 2 ferricyanide + H2O
glutarate + 2 ferrocyanide + 2 H+
-
26.4% compared to the activity with acetaldehyde
-
-
?
glutaraldehyde + 4 ferricyanide + 2 H2O
glutarate + 4 ferrocyanide + 4 H+
glutaraldehyde + oxidized phenazine methosulfate
glutaric acid + reduced phenazine methosulfate
-
26.5% of the activity with acetaldehyde
-
-
?
glycolaldehyde + ferricyanide
hydroxyacetic acid + ferrocyanide + H+
glyoxal + ferricyanide
oxoacetic acid + ferrocyanide + H+
heptanal + a quinone + H2O
heptanoate + a quinol
-
46% of acetaldehyde oxidation
-
?
heptanal + oxidized 2,6-dichlorophenolindophenol
heptanoate + reduced 2,6-dichlorophenolindophenol
heptanal + oxidized tetramethylphenylenediamine
heptanoate + reduced tetramethylphenylenediamine
-
-
-
-
?
hexanal + a quinone + H2O
hexanoate + a quinol
L-sorbosone + ferricyanide
? + ferrocyanide + H+
Rhizorhabdus wittichii
A5VEL7
-
-
-
?
methylglyoxal + ferricyanide
2-oxopropanoic acid + ferrocyanide + H+
Rhizorhabdus wittichii
A5VEL7
-
-
-
?
octanal + a quinone + H2O
octanoate + a quinol
-
48% of acetaldehyde oxidation
-
?
octanal + oxidized tetramethylphenylenediamine
octanoate + reduced tetramethylphenylenediamine
pentanal + 2 ferricyanide + H2O
pentanoate + 2 ferrocyanide + 2 H+
pentanal + a quinone + H2O
pentanoate + a quinol
-
58% of acetaldehyde oxidation
-
?
phenylglyoxal + ferricyanide
oxo(phenyl) acetic acid + ferrocyanide + H+
Rhizorhabdus wittichii
A5VEL7
-
-
-
?
propanal + 2 ferricyanide + H2O
propanoate + 2 ferrocyanide + 2 H+
propanal + a quinone + H2O
propanoate + a quinol
-
-
-
?
propanal + acceptor + H2O
propanoate + reduced acceptor
-
potassium ferricyanide, 2,6-dichlorophenolindophenol, phenazine methosulfate, Wurster's blue and nitroblue tetrazolium are utilized as electron acceptors in aldehyde oxidation
-
-
?
propanal + ferricyanide
propanoic acid + ferrocyanide + H+
Rhizorhabdus wittichii
A5VEL7
-
-
-
?
propanal + oxidized phenazine methosulfate
propanoic acid + reduced phenazine methosulfate
-
72.7% of the activity with acetaldehyde
-
-
?
propanal + oxidized tetramethylphenylenediamine
propionate + reduced tetramethylphenylenediamine
-
-
-
-
?
propionaldehyde + 2 ferricyanide + H2O
propionate + 2 ferrocyanide + 2 H+
-
72.7% compared to the activity with acetaldehyde
-
-
?
propionaldehyde + 2,6-dichlorophenol indophenol
propanoate + reduced 2,6-dichlorophenol indophenol
propionaldehyde + 2,6-dichlorophenolindophenol
propanoate + reduced 2,6-dichlorophenolindophenol
propionaldehyde + oxidized 2,6-dichlorophenolindophenol
propionate + reduced 2,6-dichlorophenolindophenol
valeraldehyde + ferricyanide
pentanoic acid + ferrocyanide + H+
Rhizorhabdus wittichii
A5VEL7
-
-
-
?
additional information
?
-
1-butanol + acceptor
butanal + reduced acceptor
-
the NAD+-independent inducible 1-butanol dehydrogenase, a quinohemoprotein, is responsible for 1-butanol oxidation in the butane metabolism pathway
-
-
?
1-butanol + acceptor
butanal + reduced acceptor
-
the NAD+-independent inducible 1-butanol dehydrogenase, a quinohemoprotein, is responsible for 1-butanol oxidation in the butane metabolism pathway
-
-
?
3-methylbenzaldehyde + ferricyanide
3-methylbenzoic acid + ferrocyanide + H+
Rhizorhabdus wittichii
A5VEL7
-
-
-
?
3-methylbenzaldehyde + ferricyanide
3-methylbenzoic acid + ferrocyanide + H+
Rhizorhabdus wittichii DSM 6014
A5VEL7
-
-
-
?
acetaldehyde + 2 ferricyanide + H2O
acetate + 2 ferrocyanide + 2 H+
-
-
-
-
?
acetaldehyde + 2 ferricyanide + H2O
acetate + 2 ferrocyanide + 2 H+
-
about 30% of the activity with formaldehyde
-
-
?
acetaldehyde + 2 ferricyanide + H2O
acetate + 2 ferrocyanide + 2 H+
-
-
-
-
?
acetaldehyde + 2 ferricyanide + H2O
acetate + 2 ferrocyanide + 2 H+
-
about 30% of the activity with formaldehyde
-
-
?
acetaldehyde + 2 ferricyanide + H2O
acetate + 2 ferrocyanide + 2 H+
-
-
-
-
?
acetaldehyde + 2 ferricyanide + H2O
acetate + 2 ferrocyanide + 2 H+
-
-
-
?
acetaldehyde + 2 ferricyanide + H2O
acetate + 2 ferrocyanide + 2 H+
-
-
-
?
acetaldehyde + 2 ferricyanide + H2O
acetate + 2 ferrocyanide + 2 H+
-
-
-
-
?
acetaldehyde + 2 ferricyanide + H2O
acetate + 2 ferrocyanide + 2 H+
-
87% of the activity with allyl alcohol
-
-
?
acetaldehyde + 2 ferricyanide + H2O
acetate + 2 ferrocyanide + 2 H+
-
-
-
-
?
acetaldehyde + 2 ferricyanide + H2O
acetate + 2 ferrocyanide + 2 H+
-
-
-
?
acetaldehyde + 2 ferricyanide + H2O
acetate + 2 ferrocyanide + 2 H+
-
-
-
?
acetaldehyde + 2,6-dichlorophenol indophenol
acetate + reduced 2,6-dichlorophenol indophenol
-
-
-
-
?
acetaldehyde + 2,6-dichlorophenol indophenol
acetate + reduced 2,6-dichlorophenol indophenol
-
-
-
-
?
acetaldehyde + 2,6-dichlorophenol indophenol
acetate + reduced 2,6-dichlorophenol indophenol
-
-
-
-
?
acetaldehyde + 2,6-dichlorophenol indophenol
acetate + reduced 2,6-dichlorophenol indophenol
in presence of phenazine methosulfate
-
-
?
acetaldehyde + 2,6-dichlorophenol indophenol
acetate + reduced 2,6-dichlorophenol indophenol
with phenazine methosulfonate
-
-
?
acetaldehyde + 2,6-dichlorophenol indophenol
acetate + reduced 2,6-dichlorophenol indophenol
in presence of phenazine methosulfate
-
-
?
acetaldehyde + 2,6-dichlorophenol indophenol
acetate + reduced 2,6-dichlorophenol indophenol
with phenazine methosulfonate
-
-
?
acetaldehyde + 2,6-dichlorophenolindophenol
acetate + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
acetaldehyde + 2,6-dichlorophenolindophenol
acetate + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
acetaldehyde + a quinone + H2O
acetate + a quinol
-
potassium ferricyanide, phenazine methosulfate, nitro blue tetrazolium or dichlorophenol-indophenol as artificial electron acceptors
-
?
acetaldehyde + a quinone + H2O
acetate + a quinol
-
-
-
?
acetaldehyde + a quinone + H2O
acetate + a quinol
-
-
-
?
acetaldehyde + ferricyanide
acetic acid + ferrocyanide + H+
-
-
-
-
?
acetaldehyde + ferricyanide
acetic acid + ferrocyanide + H+
-
-
-
-
?
acetaldehyde + oxidized 2,6-dichlorophenolindophenol
acetate + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
acetaldehyde + oxidized 2,6-dichlorophenolindophenol
acetate + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
acetaldehyde + oxidized phenazine methosulfate
acetic acid + reduced phenazine methosulfate
-
-
-
-
?
acetaldehyde + oxidized phenazine methosulfate
acetic acid + reduced phenazine methosulfate
-
-
-
-
?
acetaldehyde + oxidized tetramethylphenylenediamine
acetate + reduced tetramethylphenylenediamine
-
-
-
-
?
acetaldehyde + oxidized tetramethylphenylenediamine
acetate + reduced tetramethylphenylenediamine
-
-
-
-
?
acetaldehyde + phenazine methosulfate
acetate + reduced phenazine methosulfate
-
-
-
-
?
acetaldehyde + phenazine methosulfate
acetate + reduced phenazine methosulfate
-
-
-
-
?
acetaldehyde + phenazine methosulfate
acetate + reduced phenazine methosulfate
-
-
-
-
?
benzaldehyde + a quinone + H2O
benzoate + a quinol
-
potassium ferricyanide, phenazine methosulfate, nitro blue tetrazolium or dichlorophenol-indophenol as artificial electron acceptors, 5% activity of acetaldehyde oxidation
-
?
benzaldehyde + a quinone + H2O
benzoate + a quinol
-
-
-
?
butanal + 2 ferricyanide + H2O
butanoate + 2 ferrocyanide + 2 H+
-
-
-
-
?
butanal + 2 ferricyanide + H2O
butanoate + 2 ferrocyanide + 2 H+
-
about 30% of the activity with formaldehyde
-
-
?
butanal + 2 ferricyanide + H2O
butanoate + 2 ferrocyanide + 2 H+
-
-
-
-
?
butanal + 2 ferricyanide + H2O
butanoate + 2 ferrocyanide + 2 H+
-
about 30% of the activity with formaldehyde
-
-
?
butanal + 2 ferricyanide + H2O
butanoate + 2 ferrocyanide + 2 H+
-
-
-
-
?
butanal + 2 ferricyanide + H2O
butanoate + 2 ferrocyanide + 2 H+
-
-
-
?
butanal + 2 ferricyanide + H2O
butanoate + 2 ferrocyanide + 2 H+
-
-
-
?
butanal + 2 ferricyanide + H2O
butanoate + 2 ferrocyanide + 2 H+
-
-
-
?
butanal + 2 ferricyanide + H2O
butanoate + 2 ferrocyanide + 2 H+
-
-
-
?
butanal + a quinone + H2O
butanoate + a quinone
-
potassium ferricyanide, phenazine methosulfate, nitro blue tetrazolium or dichlorophenol-indophenol as artificial electron acceptors
-
?
butanal + a quinone + H2O
butanoate + a quinone
-
-
-
?
butanal + a quinone + H2O
butanoate + a quinone
-
-
-
?
butanal + ferricyanide
butanoic acid + ferrocyanide + H+
Rhizorhabdus wittichii
A5VEL7
-
-
-
?
butanal + ferricyanide
butanoic acid + ferrocyanide + H+
Rhizorhabdus wittichii DSM 6014
A5VEL7
-
-
-
?
butyraldehyde + 2,6-dichlorophenol indophenol
butanoate + reduced 2,6-dichlorophenol indophenol
in presence of phenazine methosulfate
-
-
?
butyraldehyde + 2,6-dichlorophenol indophenol
butanoate + reduced 2,6-dichlorophenol indophenol
with phenazine methosulfonate
-
-
?
butyraldehyde + 2,6-dichlorophenol indophenol
butanoate + reduced 2,6-dichlorophenol indophenol
in presence of phenazine methosulfate
-
-
?
butyraldehyde + 2,6-dichlorophenol indophenol
butanoate + reduced 2,6-dichlorophenol indophenol
with phenazine methosulfonate
-
-
?
butyraldehyde + 2,6-dichlorophenolindophenol
butanoate + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
butyraldehyde + 2,6-dichlorophenolindophenol
butanoate + reduced 2,6-dichlorophenolindophenol
-
-
-
?
butyraldehyde + 2,6-dichlorophenolindophenol
butanoate + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
formaldehyde + 2 ferricyanide + H2O
formate + 2 ferrocyanide + 2 H+
-
-
-
-
?
formaldehyde + 2 ferricyanide + H2O
formate + 2 ferrocyanide + 2 H+
-
-
-
-
?
formaldehyde + 2 ferricyanide + H2O
formate + 2 ferrocyanide + 2 H+
-
-
-
?
formaldehyde + 2 ferricyanide + H2O
formate + 2 ferrocyanide + 2 H+
-
-
-
?
formaldehyde + oxidized tetramethylphenylenediamine
formate + reduced tetramethylphenylenediamine
-
-
-
-
?
formaldehyde + oxidized tetramethylphenylenediamine
formate + reduced tetramethylphenylenediamine
-
-
-
-
?
glutaraldehyde + 4 ferricyanide + 2 H2O
glutarate + 4 ferrocyanide + 4 H+
-
-
-
-
?
glutaraldehyde + 4 ferricyanide + 2 H2O
glutarate + 4 ferrocyanide + 4 H+
-
about 40% of the activity with formaldehyde
-
-
?
glutaraldehyde + 4 ferricyanide + 2 H2O
glutarate + 4 ferrocyanide + 4 H+
-
25% of the activity with allyl alcohol
-
-
?
glycolaldehyde + ferricyanide
hydroxyacetic acid + ferrocyanide + H+
Rhizorhabdus wittichii
A5VEL7
-
-
-
?
glycolaldehyde + ferricyanide
hydroxyacetic acid + ferrocyanide + H+
Rhizorhabdus wittichii DSM 6014
A5VEL7
-
-
-
?
glyoxal + ferricyanide
oxoacetic acid + ferrocyanide + H+
Rhizorhabdus wittichii
A5VEL7
-
-
-
?
glyoxal + ferricyanide
oxoacetic acid + ferrocyanide + H+
Rhizorhabdus wittichii DSM 6014
A5VEL7
-
-
-
?
heptanal + oxidized 2,6-dichlorophenolindophenol
heptanoate + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
heptanal + oxidized 2,6-dichlorophenolindophenol
heptanoate + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
hexanal + a quinone + H2O
hexanoate + a quinol
-
potassium ferricyanide, phenazine methosulfate, nitro blue tetrazolium or dichlorophenol-indophenol as artificial electron acceptors
-
?
hexanal + a quinone + H2O
hexanoate + a quinol
-
-
-
?
hexanal + a quinone + H2O
hexanoate + a quinol
-
-
-
?
octanal + oxidized tetramethylphenylenediamine
octanoate + reduced tetramethylphenylenediamine
-
-
-
-
?
octanal + oxidized tetramethylphenylenediamine
octanoate + reduced tetramethylphenylenediamine
-
-
-
-
?
pentanal + 2 ferricyanide + H2O
pentanoate + 2 ferrocyanide + 2 H+
-
-
-
-
?
pentanal + 2 ferricyanide + H2O
pentanoate + 2 ferrocyanide + 2 H+
-
-
-
?
pentanal + 2 ferricyanide + H2O
pentanoate + 2 ferrocyanide + 2 H+
-
-
-
?
propanal + 2 ferricyanide + H2O
propanoate + 2 ferrocyanide + 2 H+
-
-
-
-
?
propanal + 2 ferricyanide + H2O
propanoate + 2 ferrocyanide + 2 H+
-
about 40% of the activity with formaldehyde
-
-
?
propanal + 2 ferricyanide + H2O
propanoate + 2 ferrocyanide + 2 H+
-
-
-
?
propanal + 2 ferricyanide + H2O
propanoate + 2 ferrocyanide + 2 H+
-
-
-
?
propanal + 2 ferricyanide + H2O
propanoate + 2 ferrocyanide + 2 H+
-
42% of the activity with allyl alcohol
-
-
?
propanal + 2 ferricyanide + H2O
propanoate + 2 ferrocyanide + 2 H+
-
-
-
?
propanal + 2 ferricyanide + H2O
propanoate + 2 ferrocyanide + 2 H+
-
-
-
?
propionaldehyde + 2,6-dichlorophenol indophenol
propanoate + reduced 2,6-dichlorophenol indophenol
in presence of phenazine methosulfate
-
-
?
propionaldehyde + 2,6-dichlorophenol indophenol
propanoate + reduced 2,6-dichlorophenol indophenol
with phenazine methosulfonate
-
-
?
propionaldehyde + 2,6-dichlorophenol indophenol
propanoate + reduced 2,6-dichlorophenol indophenol
in presence of phenazine methosulfate
-
-
?
propionaldehyde + 2,6-dichlorophenol indophenol
propanoate + reduced 2,6-dichlorophenol indophenol
with phenazine methosulfonate
-
-
?
propionaldehyde + 2,6-dichlorophenolindophenol
propanoate + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
propionaldehyde + 2,6-dichlorophenolindophenol
propanoate + reduced 2,6-dichlorophenolindophenol
30% of the activity with 2-butanol
-
-
?
propionaldehyde + 2,6-dichlorophenolindophenol
propanoate + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
propionaldehyde + oxidized 2,6-dichlorophenolindophenol
propionate + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
propionaldehyde + oxidized 2,6-dichlorophenolindophenol
propionate + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
additional information
?
-
-
no oxidation of formaldehyde
-
-
?
additional information
?
-
-
the substrate specificity of the enzyme is broad toward aldehydes and alcohols
-
-
?
additional information
?
-
-
the substrate specificity of the enzyme is broad toward aldehydes and alcohols
-
-
?
additional information
?
-
-
primary alcohols (except methanol), secondary alcohols and aldehydes are substrates, and a broad range of dyes functions as artificial electron acceptor
-
-
?
additional information
?
-
-
product determination, overview. The enzyme shows broad substrate specificity converting different primary alcohols, starting from C2 compounds, secondary alcohols, diols, polyethylene glycol 6000, and aldehydes, including formaldehyde, detailed overview
-
-
?
additional information
?
-
-
no activity with glucose, benzaldehyde, formaldehyde, acetone, sorbitol or glycerol
-
-
?
additional information
?
-
-
formaldehyde and benzaldehyde are not oxidized at all. Aliphatic alcohols and sugar aldehydes, are not substrates. The enzyme is specific for aliphatic aldehydes (C2-C6) and is able to use ferricyanide or phenazine methosulfate plus 2,6-dichlorophenolindophenol as electron acceptors having optimal pH values of 3.5 and 7.0, respectively. Ubiquinone-1 is also able to accept electrons from the dithionite-reduced enzyme
-
-
?
additional information
?
-
-
no substrates: formaldehyde, benzaldehyde, aliphatic alcohols, sugar aldehydes
-
-
?
additional information
?
-
-
formaldehyde and benzaldehyde are not oxidized at all. Aliphatic alcohols and sugar aldehydes, are not substrates. The enzyme is specific for aliphatic aldehydes (C2-C6) and is able to use ferricyanide or phenazine methosulfate plus 2,6-dichlorophenolindophenol as electron acceptors having optimal pH values of 3.5 and 7.0, respectively. Ubiquinone-1 is also able to accept electrons from the dithionite-reduced enzyme
-
-
?
additional information
?
-
-
no substrates: formaldehyde, benzaldehyde, aliphatic alcohols, sugar aldehydes
-
-
?
additional information
?
-
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. ADH I is formed most abundantly in the cells grown on ethanol
-
-
?
additional information
?
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. ADH I is formed most abundantly in the cells grown on ethanol
-
-
?
additional information
?
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. ADH I is formed most abundantly in the cells grown on ethanol
-
-
?
additional information
?
-
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. ADH IIB is induced by n-butanol, 1,3-butandiol, and alcohols of medium chain length
-
-
?
additional information
?
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. ADH IIB is induced by n-butanol, 1,3-butandiol, and alcohols of medium chain length
-
-
?
additional information
?
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. ADH IIB is induced by n-butanol, 1,3-butandiol, and alcohols of medium chain length
-
-
?
additional information
?
-
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. Induction of ADH IIG is restricted to 1,2-propanediol or glycerol
-
-
?
additional information
?
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. Induction of ADH IIG is restricted to 1,2-propanediol or glycerol
-
-
?
additional information
?
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. Induction of ADH IIG is restricted to 1,2-propanediol or glycerol
-
-
?
additional information
?
-
-
ADH I shows no activity with NAD(P), potassium ferricyanide, or molecular oxygen as electron acceptors
-
-
?
additional information
?
-
ADH I shows no activity with NAD(P), potassium ferricyanide, or molecular oxygen as electron acceptors
-
-
?
additional information
?
-
ADH I shows no activity with NAD(P), potassium ferricyanide, or molecular oxygen as electron acceptors
-
-
?
additional information
?
-
-
isozyme ADH IIG shows no activity with O2
-
-
?
additional information
?
-
isozyme ADH IIG shows no activity with O2
-
-
?
additional information
?
-
isozyme ADH IIG shows no activity with O2
-
-
?
additional information
?
-
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. ADH I is formed most abundantly in the cells grown on ethanol
-
-
?
additional information
?
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. ADH I is formed most abundantly in the cells grown on ethanol
-
-
?
additional information
?
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. ADH I is formed most abundantly in the cells grown on ethanol
-
-
?
additional information
?
-
-
ADH I shows no activity with NAD(P), potassium ferricyanide, or molecular oxygen as electron acceptors
-
-
?
additional information
?
-
ADH I shows no activity with NAD(P), potassium ferricyanide, or molecular oxygen as electron acceptors
-
-
?
additional information
?
-
ADH I shows no activity with NAD(P), potassium ferricyanide, or molecular oxygen as electron acceptors
-
-
?
additional information
?
-
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. Induction of ADH IIG is restricted to 1,2-propanediol or glycerol
-
-
?
additional information
?
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. Induction of ADH IIG is restricted to 1,2-propanediol or glycerol
-
-
?
additional information
?
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. Induction of ADH IIG is restricted to 1,2-propanediol or glycerol
-
-
?
additional information
?
-
-
isozyme ADH IIG shows no activity with O2
-
-
?
additional information
?
-
isozyme ADH IIG shows no activity with O2
-
-
?
additional information
?
-
isozyme ADH IIG shows no activity with O2
-
-
?
additional information
?
-
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. ADH IIB is induced by n-butanol, 1,3-butandiol, and alcohols of medium chain length
-
-
?
additional information
?
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. ADH IIB is induced by n-butanol, 1,3-butandiol, and alcohols of medium chain length
-
-
?
additional information
?
-
three distinct quinoprotein ADHs (ADHs, ADH IIB and ADH IIG) are synthesized by the bacterium under different growth conditions. ADH IIB is induced by n-butanol, 1,3-butandiol, and alcohols of medium chain length
-
-
?
additional information
?
-
Rhizorhabdus wittichii
A5VEL7
the enzyme can also transfer electrons to the electron acceptor system DCPIP/PMS, but the activity is only 50% of the rate obtained with ferricyanide. Enzyme displays a broad substrate spectrum and oxidizes short- and medium-chain aliphatic aldehydes (C1-C6), ketoaldehydes, dialdehydes; some aromatic aldehydes and hydroxyaldehydes to the corresponding carboxylic acids
-
-
?
additional information
?
-
Rhizorhabdus wittichii DSM 6014
A5VEL7
the enzyme can also transfer electrons to the electron acceptor system DCPIP/PMS, but the activity is only 50% of the rate obtained with ferricyanide. Enzyme displays a broad substrate spectrum and oxidizes short- and medium-chain aliphatic aldehydes (C1-C6), ketoaldehydes, dialdehydes; some aromatic aldehydes and hydroxyaldehydes to the corresponding carboxylic acids
-
-
?
additional information
?
-
-
the enzyme has a broad substrate range, including primary alcohols, secondary alcohols, aldehydes, C4 diols and aromatic alcohols, BDH exhibits a marked preference towards 2-pentanol and the activity gradually decreases with longer-chain secondary alcohols, BDH exhibits ferricyanide-dependent ADH activity
-
-
?
additional information
?
-
the NAD+-independent PQQ alcohol dehydrogenase BOH (a quinoprotein) is linked to butane metabolism in conjunction with BDH (a quinohemoprotein)
-
-
?
additional information
?
-
-
the enzyme has a broad substrate range, including primary alcohols, secondary alcohols, aldehydes, C4 diols and aromatic alcohols, BDH exhibits a marked preference towards 2-pentanol and the activity gradually decreases with longer-chain secondary alcohols, BDH exhibits ferricyanide-dependent ADH activity
-
-
?
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Adachi, O.; Shinagawa, E.; Matsushita, K.; Ameyama, M.
Preparation of cells and cytoplasmic membranes of acetic acid bacteria which exclusively contain quinoprotein aldehyde dehydrogenase
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52
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Acetobacter aceti
-
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Acetobacter aceti, Gluconobacter oxydans
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22
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-
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Acetobacter aceti
-
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Quinoprotein ethanol dehydrogenase from Pseudomonas
Antonie van Leeuwenhoek
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Pseudomonas aeruginosa, Pseudomonas putida
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Quinoprotein alcohol dehydrogenase from ethanol-grown Pseudomonas aeruginosa
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223
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1984
Pseudomonas aeruginosa
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Groen, B.W.; van Kleef, M.A.G.; Duine, J.A.
Quinohaemoprotein alcohol dehydrogenase apoenzyme from Pseudomonas testosteroni
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234
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1986
Comamonas testosteroni
brenda
Zarnt, G.; Schrder, T.; Andreesen, J.R.
Catalytic and molecular properties of the quinohemoprotein tetrahydrofurfuryl alcohol dehydrogenase from Ralstonia eutropha strain Bo
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183
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2001
Cupriavidus necator (Q9KH03), Cupriavidus necator, Cupriavidus necator Bo (Q9KH03)
brenda
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Purification, crystallisation and characterization of quinoprotein ethanol dehydrogenase from Pseudomonas aeruginosa
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369
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1988
Pseudomonas aeruginosa
brenda
Zarnt, G.; Schraeder, T.; Andreesen, J.R.
Degradation of tetrahydrofurfuryl alcohol by Ralstonia eutropha is initiated by an inducible pyrroloquinoline quinone-dependent alcohol dehydrogenase
Appl. Environ. Microbiol.
63
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1997
Cupriavidus necator
brenda
Shinagawa, E.; Toyama, H.; Matsushita, K.; Tuitemwong, P.; Theeragool, G.; Adachi, O.
A novel type of formaldehyde-oxidizing enzyme from the membrane of Acetobacter sp. SKU 14
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70
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2006
Acetobacter sp., Acetobacter sp. SKU 14
brenda
Gomez-Manzo, S.; Contreras-Zentella, M.; Gonzalez-Valdez, A.; Sosa-Torres, M.; Arreguin-Espinoza, R.; Escamilla-Marvan, E.
The PQQ-alcohol dehydrogenase of Gluconacetobacter diazotrophicus
Int. J. Food Microbiol.
125
71-78
2008
Gluconacetobacter diazotrophicus
brenda
Toyama, H.; Fujii, A.; Matsushita, K.; Shinagawa, E.; Ameyama, M.; Adachi, O.
Three distinct quinoprotein alcohol dehydrogenases are expressed when Pseudomonas putida is grown on different alcohols
J. Bacteriol.
177
2442-2450
1995
Pseudomonas putida, Pseudomonas putida (Q4W6G0), Pseudomonas putida (Q8GR64), Pseudomonas putida HK5, Pseudomonas putida HK5 (Q4W6G0), Pseudomonas putida HK5 (Q8GR64)
brenda
Vangnai, A.S.; Arp, D.J.; Sayavedra-Soto, L.A.
Two distinct alcohol dehydrogenases participate in butane metabolism by Pseudomonas butanovora
J. Bacteriol.
184
1916-1924
2002
Thauera butanivorans (Q9AGW3)
brenda
Vangnai, A.S.; Arp, D.J.
An inducible 1-butanol dehydrogenase, a quinohaemoprotein, is involved in the oxidation of butane by Pseudomonas butanovora
Microbiology
147
745-756
2001
Thauera butanivorans
brenda
Aquino Neto, S.; Suda, E.; Xu, S.; Meredith, M.; De Andrade, A.; Minteer, S.
Direct electron transfer-based bioanodes for ethanol biofuel cells using PQQ-dependent alcohol and aldehyde dehydrogenases
Electrochim. Acta
87
323-329
2013
Gluconobacter sp., Gluconobacter sp. 33 (DSM Z 3504)
-
brenda
Xu, S.; Minteer, S.
Investigating the impact of multi-heme pyrroloquinoline quinone-aldehyde dehydrogenase orientation on direct bioelectrocatalysis via site specific enzyme immobilization
ACS Catal.
3
1756-1763
2013
Gluconobacter oxydans, Gluconobacter oxydans DSM 3504
-
brenda
Zeiser, J.; Muehlenbeck, L.H.; Schweiger, P.; Deppenmeier, U.
Characterization of a periplasmic quinoprotein from Sphingomonas wittichii that functions as aldehyde dehydrogenase
Appl. Microbiol. Biotechnol.
98
2067-2079
2014
Rhizorhabdus wittichii (A5VEL7), Rhizorhabdus wittichii DSM 6014 (A5VEL7)
brenda
Aquino Neto, S.; Hickey, D.P.; Milton, R.D.; De Andrade, A.R.; Minteer, S.D.
High current density PQQ-dependent alcohol and aldehyde dehydrogenase bioanodes
Biosens. Bioelectron.
72
247-254
2015
Gluconobacter oxydans, Gluconobacter oxydans DSM 3504
brenda
Gomez-Manzo, S.; Chavez-Pacheco, J.L.; Contreras-Zentella, M.; Sosa-Torres, M.E.; Arreguin-Espinosa, R.; Perez de la Mora, M.; Membrillo-Hernandez, J.; Escamilla, J.E.
Molecular and catalytic properties of the aldehyde dehydrogenase of Gluconacetobacter diazotrophicus, a quinoheme protein containing pyrroloquinoline quinone, cytochrome b, and cytochrome c
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192
5718-5724
2010
Gluconacetobacter diazotrophicus, Gluconacetobacter diazotrophicus ATCC 49037
brenda