1.2.5.2: aldehyde dehydrogenase (quinone)
This is an abbreviated version!
For detailed information about aldehyde dehydrogenase (quinone), go to the full flat file.
Word Map on EC 1.2.5.2
-
1.2.5.2
-
dehydrogenases
-
quinoprotein
-
synthesis
-
ferricyanide
-
acetobacter
-
acetaldehyde
-
pqq-adh
- 1.2.5.2
- dehydrogenases
-
quinoprotein
- synthesis
- ferricyanide
- acetobacter
- acetaldehyde
- pqq-adh
Reaction
Synonyms
ADH I, ADH IIB, ADH IIG, aldehyde dehydrogenase (acceptor), ALDH, BOH, dehydrogenase, aldehyde (acceptor), EC 1.2.99.3, FOE, formaldehyde-oxidizing enzyme, glucose sorbosone dehydrogenase, NAD+-independent, PQQ-containing alcohol dehydrogenase, PQQ-AldDH, PQQ-AlDH, pyrroloquinoline quinone-dependent aldehyde dehydrogenase, quinohemoprotein dehydrogenase, Swit_4395, tetrahydrofurfuryl alcohol dehydrogenase
ECTree
1.2.5.2 aldehyde dehydrogenase (quinone)Advanced search results
results (
results (Substrates Products
Substrates Products on EC 1.2.5.2 - aldehyde dehydrogenase (quinone)
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SUBSTRATE 
PRODUCT
REACTION DIAGRAM
ORGANISM
UNIPROT
COMMENTARY
(Substrate)
(Substrate)
LITERATURE
(Substrate)
(Substrate)
COMMENTARY
(Product)
(Product)
LITERATURE
(Product)
(Product)
Reversibility
r=reversible
ir=irreversible
?=not specified
r=reversible
ir=irreversible
?=not specified
acetaldehyde + 2,6-dichlorophenol indophenol
acetate + reduced 2,6-dichlorophenol indophenol
acetaldehyde + 2,6-dichlorophenolindophenol
acetate + reduced 2,6-dichlorophenolindophenol
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 + 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 + 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
-
-
?
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
-
-
?
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 + 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 + oxidized phenazine methosulfate
glutaric acid + reduced phenazine methosulfate
-
26.5% of the activity with acetaldehyde
-
-
?
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
-
-
-
-
?
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 + a quinone + H2O
pentanoate + a quinol
-
58% of acetaldehyde oxidation
-
?
phenylglyoxal + ferricyanide
oxo(phenyl) acetic acid + ferrocyanide + H+
Rhizorhabdus wittichii
A5VEL7
-
-
-
?
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
-
-
-
?
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
Gluconobacter sp. DSM 3504 / ATCC 15163
-
-
-
-
?
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 + 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
Gluconobacter sp. DSM 3504 / ATCC 15163
-
-
-
-
?
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
-
?
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 + 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
-
?
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+
-
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
?
-
-
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
?
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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
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additional information
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ADH I shows no activity with NAD(P), potassium ferricyanide, or molecular oxygen as electron acceptors
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additional information
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ADH I shows no activity with NAD(P), potassium ferricyanide, or molecular oxygen as electron acceptors
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additional information
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ADH I shows no activity with NAD(P), potassium ferricyanide, or molecular oxygen as electron acceptors
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additional information
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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
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additional information
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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
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additional information
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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
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additional information
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isozyme ADH IIG shows no activity with O2
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additional information
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isozyme ADH IIG shows no activity with O2
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additional information
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isozyme ADH IIG shows no activity with O2
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additional information
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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
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additional information
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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
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additional information
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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
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additional information
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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
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additional information
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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
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additional information
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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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additional information
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the NAD+-independent PQQ alcohol dehydrogenase BOH (a quinoprotein) is linked to butane metabolism in conjunction with BDH (a quinohemoprotein)
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additional information
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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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