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1,2-propanediol + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
-
9.1% activity compared to 1-propanol
-
-
r
1,3-butandiol + ubiquinone
? + ubiquinol
-
very low activity, 0.94% of the activity with ethanol
-
-
?
1,3-propandiol + ubiquinone
? + ubiquinol
-
15% of the activity with ethanol
-
-
?
1,3-propanediol + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
-
12.2% activity compared to 1-propanol
-
-
r
1,4-butanediol + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
-
16.2% activity compared to 1-propanol
-
-
r
1-butanol + 2,6-dichlorophenolindophenol
butyraldehyde + reduced 2,6-dichlorophenolindophenol
1-butanol + ubiquinone
butanal + ubiquinol
-
88% of the activity with ethanol
-
-
?
1-heptanol + 2,6-dichlorophenolindophenol
heptanal + reduced 2,6-dichlorophenolindophenol
1-hexanol + 2,6-dichlorophenolindophenol
hexanal + reduced 2,6-dichlorophenolindophenol
1-hexanol + ubiquinone
hexanal + ubiquinol
-
93% of the activity with ethanol
-
-
?
1-octanol + ubiquinone
octanal + ubiquinol
-
66% of the activity with ethanol
-
-
?
1-pentanol + 2,6-dichlorophenolindophenol
pentanaldehyde + reduced 2,6-dichlorophenolindophenol
-
85.5% activity compared to 1-propanol
-
-
r
1-pentanol + ubiquinone
pentanal + ubiquinol
-
97% of the activity with ethanol
-
-
?
1-propanol + 2,6-dichlorophenolindophenol
propionaldehyde + reduced 2,6-dichlorophenolindophenol
1-propanol + phenazine methosulfate
propionaldehyde + reduced phenazine methosulfate
-
100% activity
-
-
r
1-propanol + ubiquinone
propanal + ubiquinol
-
90% of the activity with ethanol
-
-
?
2,3-butanediol + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
-
4.1% activity compared to 1-propanol
-
-
r
2-(S)-butanol + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
-
43.3% activity compared to 1-propanol
-
-
r
2-butanol + ubiquinone
2-butanone + ubiquinol
-
64% of the activity with ethanol
-
-
?
2-propanol + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
-
31.9% activity compared to 1-propanol
-
-
r
2-propanol + ubiquinone
acetone + ubiquinol
-
51% of the activity with ethanol
-
-
?
3-methyl-1-butanol + ubiquinone
3-methyl-1-butanal + ubiquinol
-
48% of the activity with ethanol
-
-
?
5-(hydroxymethyl)furfural + phenazine methosulfate
? + reduced phenazine methosulfate
-
-
-
?
5-(hydroxymethyl)furoic acid + phenazine methosulfate
? + reduced phenazine methosulfate
wild-type enzyme shows no activity, mutant enzymes F412V/W561A, F412I/W561Q and F412I/W561S are active
-
-
?
5-formylfurfural + phenazine methosulfate
? + reduced phenazine methosulfate
-
-
-
?
acetaldehyde + 2,6-dichlorophenolindophenol
?
-
42% activity compared to n-butanol. The enzyme also oxidizes aldehydes, however the affinity for alcohols is at least twice as high
-
-
?
acetaldehyde + ferricyanide
?
-
13% activity compared to n-butanol. The enzyme also oxidizes aldehydes, however the affinity for alcohols is at least twice as high
-
-
?
acetaldehyde + reduced 2,6-dichlorophenolindophenol
ethanol + 2,6-dichlorophenolindophenol
-
-
-
-
r
acetaldehyde + reduced phenazine methosulfate
ethanol + phenazine methosulfate
-
55.6% activity compared to 1-propanol
-
-
r
acetaldehyde + ubiquinol
ethanol + ubiquinone
allyl alcohol + ferricyanide
acrolein + ferricyanide
-
the best substrate
-
-
?
allylic alcohol + 2,6-dichlorophenolindophenol
?
-
91% activity compared to n-butanol
-
-
?
allylic alcohol + ferricyanide
?
-
96% activity compared to n-butanol
-
-
?
benzyl alcohol + 2,6-dichlorophenolindophenol
benzaldehyde + reduced 2,6-dichlorophenolindophenol
butyraldehyde + reduced 2,6-dichlorophenolindophenol
1-butanol + 2,6-dichlorophenolindophenol
-
32.1% activity compared to 1-propanol
-
-
r
citral + ubiquinol
? + ubiquinone
-
39% of the activity with ethanol
-
-
?
citronellal + ubiquinol
citronellol + ubiquinone
-
45% of the activity with ethanol
-
-
?
citronellol + ubiquinone
citronellal + ubiquinol
-
74% of the activity with ethanol
-
-
?
cyclohexanol + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
-
5.5% activity compared to 1-propanol
-
-
r
D-galactose + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
85% activity compared to D-glucose
-
-
?
D-glucose + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
D-mannose + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
77% activity compared to D-glucose
-
-
?
D-sorbitol + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
9.0% activity compared to D-glucose
-
-
?
D-xylose + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
130% activity compared to D-glucose
-
-
?
ethanol + 2,6-dichlorophenol indophenol
acetaldehyde + reduced 2,6-dichlorophenol indophenol
ethanol + 2,6-dichlorophenolindophenol
acetaldehyde + reduced 2,6-dichlorophenolindophenol
ethanol + acceptor
acetaldehyde + reduced acceptor
ethanol + ferricyanide
acetaldehyde + ferrocyanide
ethanol + phenazine methosulfate
acetaldehyde + reduced phenazine methosulfate
ethanol + phenazine methosulfate + 2,6-dichlorophenolindophenol
?
ethanol + pyrroloquinoline quinone
acetaldehyde + pyrroloquinoline quinol
ethanol + ubiquinone
acetaldehyde + ubiquinol
ethanol + ubiquinone-1
acetaldehyde + ubiquinol-1
ethyleneglycol + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
109% activity compared to D-glucose
-
-
?
formaldehyde + 2,6-dichlorophenolindophenol
?
-
38% activity compared to n-butanol. The enzyme also oxidizes aldehydes, however the affinity for alcohols is at least twice as high
-
-
?
formaldehyde + ferricyanide
?
-
34% activity compared to n-butanol. The enzyme also oxidizes aldehydes, however the affinity for alcohols is at least twice as high
-
-
?
geraniol + ubiquinone
geranial + ubiquinol
-
37% of the activity with ethanol
-
-
?
glutaraldehyde + 2,6-dichlorophenolindophenol
?
-
18% activity compared to n-butanol. The enzyme also oxidizes aldehydes, however the affinity for alcohols is at least twice as high
-
-
?
glutaraldehyde + ferricyanide
?
iso-propanol + ferricyanide
propan-2-one + ferrocyanide
-
about 10% of the activity with n-butanol
-
-
?
isopropanol + 2,6-dichlorophenolindophenol
propionaldehyde + reduced 2,6-dichlorophenolindophenol
121% activity compared to D-glucose
-
-
?
isopropanol + ferricyanide
propan-2-one + ferrocyanide
-
18% of the activity with allyl alcohol
-
-
?
L-sorbose + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
0.6% activity compared to D-glucose
-
-
?
maltotetraose + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
24% activity compared to D-glucose
-
-
?
maltotriose + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
31% activity compared to D-glucose
-
-
?
methanol + 2,6-dichlorophenolindophenol
formaldehyde + reduced 2,6-dichlorophenolindophenol
methanol + ferricyanide
formaldehyde + ferrocyanide
-
9% of the activity with allyl alcohol
-
-
?
methanol + phenazine methosulfate
formaldehyde + reduced phenazine methosulfate
-
6.3% activity compared to 1-propanol
-
-
r
methyl-alpha-D-glucopyranoside + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
5% activity compared to D-glucose
-
-
?
n-butanol + 2,6-dichlorophenolindophenol
butyraldehyde + reduced 2,6-dichlorophenolindophenol
n-butanol + 2,6-dichlorophenolindophenol
n-butanal + reduced 2,6-dichlorophenolindophenol
-
100% activity
-
-
?
n-butanol + ferricyanide
butyraldehyde + ferrocyanide
-
98% of the activity with allyl alcohol
-
-
?
n-butanol + ferricyanide
n-butanal + ferrocyanide
-
-
-
-
?
n-pentanol + ferricyanide
n-pentanal + ferrocyanide
-
about 45% of the activity with n-butanol
-
-
?
n-propanol + 2,6-dichlorophenolindophenol
propionaldehyde + reduced 2,6-dichlorophenolindophenol
n-propanol + ferricyanide
n-propanal + ferrocyanide
n-propanol + ferricyanide
propionaldehyde + ferrocyanide
-
90% of the activity with allyl alcohol
-
-
?
n-propanol + oxidized 2,6-dichlorophenolindophenol
n-propanal + reduced 2,6-dichlorophenolindophenol
-
96% activity compared to n-butanol
-
-
?
propan-1,2,3-triol + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
25% activity compared to D-glucose
-
-
?
propionaldehyde + 2,6-dichlorophenolindophenol
?
-
33% activity compared to n-butanol. The enzyme also oxidizes aldehydes, however the affinity for alcohols is at least twice as high
-
-
?
propionaldehyde + ferricyanide
?
-
24% activity compared to n-butanol. The enzyme also oxidizes aldehydes, however the affinity for alcohols is at least twice as high
-
-
?
propionaldehyde + reduced 2,6-dichlorophenolindophenol
1-propanol + 2,6-dichlorophenolindophenol
-
-
-
-
r
propionaldehyde + reduced phenazine methosulfate
1-propanol + phenazine methosulfate
-
54.5% activity compared to 1-propanol
-
-
r
rac-1,2-propanediol + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
128% activity compared to D-glucose
-
-
?
rac-2-methyl-2,4-pentanediol + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
164% activity compared to D-glucose
-
-
?
xylitol + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
20% activity compared to D-glucose
-
-
?
additional information
?
-
1-butanol + 2,6-dichlorophenolindophenol
butyraldehyde + reduced 2,6-dichlorophenolindophenol
-
82% activity compared to 1-propanol
-
-
r
1-butanol + 2,6-dichlorophenolindophenol
butyraldehyde + reduced 2,6-dichlorophenolindophenol
-
82% activity compared to 1-propanol
-
-
r
1-heptanol + 2,6-dichlorophenolindophenol
heptanal + reduced 2,6-dichlorophenolindophenol
-
44.1% activity compared to 1-propanol
-
-
r
1-heptanol + 2,6-dichlorophenolindophenol
heptanal + reduced 2,6-dichlorophenolindophenol
-
44.1% activity compared to 1-propanol
-
-
r
1-hexanol + 2,6-dichlorophenolindophenol
hexanal + reduced 2,6-dichlorophenolindophenol
-
62.2% activity compared to 1-propanol
-
-
r
1-hexanol + 2,6-dichlorophenolindophenol
hexanal + reduced 2,6-dichlorophenolindophenol
-
62.2% activity compared to 1-propanol
-
-
r
1-propanol + 2,6-dichlorophenolindophenol
propionaldehyde + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
1-propanol + 2,6-dichlorophenolindophenol
propionaldehyde + reduced 2,6-dichlorophenolindophenol
-
-
-
-
r
1-propanol + 2,6-dichlorophenolindophenol
propionaldehyde + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
acetaldehyde + ubiquinol
ethanol + ubiquinone
-
-
-
-
r
acetaldehyde + ubiquinol
ethanol + ubiquinone
-
-
-
-
r
acetaldehyde + ubiquinol
ethanol + ubiquinone
-
-
-
-
r
benzyl alcohol + 2,6-dichlorophenolindophenol
benzaldehyde + reduced 2,6-dichlorophenolindophenol
-
3.9% activity compared to 1-propanol
-
-
r
benzyl alcohol + 2,6-dichlorophenolindophenol
benzaldehyde + reduced 2,6-dichlorophenolindophenol
-
3.9% activity compared to 1-propanol
-
-
r
D-glucose + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
100% activity
-
-
?
D-glucose + 2,6-dichlorophenolindophenol
? + reduced 2,6-dichlorophenolindophenol
100% activity
-
-
?
ethanol + 2,6-dichlorophenol indophenol
acetaldehyde + reduced 2,6-dichlorophenol indophenol
with phenazine methosulfonate
-
-
?
ethanol + 2,6-dichlorophenol indophenol
acetaldehyde + reduced 2,6-dichlorophenol indophenol
with phenazine methosulfonate
-
-
?
ethanol + 2,6-dichlorophenol indophenol
acetaldehyde + reduced 2,6-dichlorophenol indophenol
with phenazine methosulfonate
-
-
?
ethanol + 2,6-dichlorophenol indophenol
acetaldehyde + reduced 2,6-dichlorophenol indophenol
with phenazine methosulfonate
-
-
?
ethanol + 2,6-dichlorophenolindophenol
acetaldehyde + reduced 2,6-dichlorophenolindophenol
-
88% activity compared to n-butanol
-
-
?
ethanol + 2,6-dichlorophenolindophenol
acetaldehyde + reduced 2,6-dichlorophenolindophenol
-
88% activity compared to n-butanol
-
-
?
ethanol + 2,6-dichlorophenolindophenol
acetaldehyde + reduced 2,6-dichlorophenolindophenol
16% activity compared to D-glucose
-
-
?
ethanol + 2,6-dichlorophenolindophenol
acetaldehyde + reduced 2,6-dichlorophenolindophenol
16% activity compared to D-glucose
-
-
?
ethanol + 2,6-dichlorophenolindophenol
acetaldehyde + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
ethanol + 2,6-dichlorophenolindophenol
acetaldehyde + reduced 2,6-dichlorophenolindophenol
-
-
-
-
r
ethanol + 2,6-dichlorophenolindophenol
acetaldehyde + reduced 2,6-dichlorophenolindophenol
-
-
-
-
r
ethanol + 2,6-dichlorophenolindophenol
acetaldehyde + reduced 2,6-dichlorophenolindophenol
-
-
-
-
?
ethanol + acceptor
acetaldehyde + reduced acceptor
-
direct electron-transfer processes between the polypyrrole entrapped quinohemoprotein alcohol dehydrogenase and a platinum electrode take place via the conducting-polymer network, mechanism modelling, overview
-
-
?
ethanol + acceptor
acetaldehyde + reduced acceptor
-
direct electron-transfer processes between the polypyrrole entrapped quinohemoprotein alcohol dehydrogenase and a platinum electrode take place via the conducting-polymer network, mechanism modelling, overview
-
-
?
ethanol + ferricyanide
acetaldehyde + ferrocyanide
-
about 40% of the activity with n-butanol
-
-
?
ethanol + ferricyanide
acetaldehyde + ferrocyanide
-
electrons extracted from ethanol at PQQ site are transferred to ubiquinone via heme c in subunit I and two of the three hemes c in subunit II
-
-
?
ethanol + ferricyanide
acetaldehyde + ferrocyanide
-
electrons extracted from ethanol at PQQ site are transferred to ubiquinone via heme c in subunit I and two of the three hemes c in subunit II
-
-
?
ethanol + ferricyanide
acetaldehyde + ferrocyanide
-
-
-
-
?
ethanol + ferricyanide
acetaldehyde + ferrocyanide
-
95% of the activity with allyl alcohol
-
-
?
ethanol + ferricyanide
acetaldehyde + ferrocyanide
-
-
-
-
?
ethanol + ferricyanide
acetaldehyde + ferrocyanide
-
91% activity compared to n-butanol
-
-
?
ethanol + ferricyanide
acetaldehyde + ferrocyanide
-
91% activity compared to n-butanol
-
-
?
ethanol + phenazine methosulfate
acetaldehyde + reduced phenazine methosulfate
-
-
-
?
ethanol + phenazine methosulfate
acetaldehyde + reduced phenazine methosulfate
-
88.9% activity compared to 1-propanol
-
-
r
ethanol + phenazine methosulfate + 2,6-dichlorophenolindophenol
?
-
-
-
-
?
ethanol + phenazine methosulfate + 2,6-dichlorophenolindophenol
?
-
-
-
-
?
ethanol + phenazine methosulfate + 2,6-dichlorophenolindophenol
?
-
-
-
-
?
ethanol + phenazine methosulfate + 2,6-dichlorophenolindophenol
?
-
-
-
-
?
ethanol + pyrroloquinoline quinone
acetaldehyde + pyrroloquinoline quinol
-
-
-
-
r
ethanol + pyrroloquinoline quinone
acetaldehyde + pyrroloquinoline quinol
-
-
-
-
r
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
CCU55317
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
CCU55317
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
the enzyme is required for the non-energy producing, cyanide-insensitive bypass oxidase activity
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
electron transfer mechanism, intramolecular transfer of electrons from pyrroloquinoline quinone to ubiquinone and the quinone binding sites, overview
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
the enzyme is required for the non-energy producing, cyanide-insensitive bypass oxidase activity
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
electron transfer mechanism, intramolecular transfer of electrons from pyrroloquinoline quinone to ubiquinone and the quinone binding sites, overview
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
r
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
r
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
r
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
best substrate
-
-
?
ethanol + ubiquinone
acetaldehyde + ubiquinol
-
-
-
-
?
ethanol + ubiquinone-1
acetaldehyde + ubiquinol-1
-
-
-
-
?
ethanol + ubiquinone-1
acetaldehyde + ubiquinol-1
-
electrons extracted from ethanol at PQQ site are transferred to ubiquinone via heme c in subunit I and two of the three hemes c in subunit II
-
-
?
ethanol + ubiquinone-1
acetaldehyde + ubiquinol-1
-
-
-
-
?
ethanol + ubiquinone-1
acetaldehyde + ubiquinol-1
-
electrons extracted from ethanol at PQQ site are transferred to ubiquinone via heme c in subunit I and two of the three hemes c in subunit II
-
-
?
ethanol + ubiquinone-1
acetaldehyde + ubiquinol-1
-
the ADH complex shows a high affinity for ubiquinone-1 with ethanol as cosubstrate
-
-
?
glutaraldehyde + ferricyanide
?
-
8% activity compared to n-butanol. The enzyme also oxidizes aldehydes, however the affinity for alcohols is at least twice as high
-
-
?
glutaraldehyde + ferricyanide
?
-
8% activity compared to n-butanol. The enzyme also oxidizes aldehydes, however the affinity for alcohols is at least twice as high
-
-
?
methanol + 2,6-dichlorophenolindophenol
formaldehyde + reduced 2,6-dichlorophenolindophenol
3.0% activity compared to D-glucose
-
-
?
methanol + 2,6-dichlorophenolindophenol
formaldehyde + reduced 2,6-dichlorophenolindophenol
3.0% activity compared to D-glucose
-
-
?
n-butanol + 2,6-dichlorophenolindophenol
butyraldehyde + reduced 2,6-dichlorophenolindophenol
241% activity compared to D-glucose
-
-
?
n-butanol + 2,6-dichlorophenolindophenol
butyraldehyde + reduced 2,6-dichlorophenolindophenol
241% activity compared to D-glucose
-
-
?
n-propanol + 2,6-dichlorophenolindophenol
propionaldehyde + reduced 2,6-dichlorophenolindophenol
120% activity compared to D-glucose
-
-
?
n-propanol + 2,6-dichlorophenolindophenol
propionaldehyde + reduced 2,6-dichlorophenolindophenol
120% activity compared to D-glucose
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?
n-propanol + ferricyanide
n-propanal + ferrocyanide
-
about 95% of the activity with n-butanol
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?
n-propanol + ferricyanide
n-propanal + ferrocyanide
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98% activity compared to n-butanol
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?
additional information
?
-
the quinohemoprotein is able to oxidize alcohols, structure-function relationship, overview
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?
additional information
?
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in ADH, electrons pass from PQQH2 to a heme c on the same quinohemoprotein subunit, and then to ubiquinone in the membrane by way of a separate cytochrome c subunit in the three-component membrane complex, ovreview
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?
additional information
?
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in ADH, electrons pass from PQQH2 to a heme c on the same quinohemoprotein subunit, and then to ubiquinone in the membrane by way of a separate cytochrome c subunit in the three-component membrane complex, ovreview
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?
additional information
?
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-
broad substrate specificity of PQQ-ADH
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?
additional information
?
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broad substrate specificity of PQQ-ADH
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?
additional information
?
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the enzyme activity is correlated with resistance to acetic acid, due to lower enzyme activity in the organism, the growth of Acetobacter pasteurianus on high acetic acid concentrations is limited, overview
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?
additional information
?
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the enzyme activity is correlated with resistance to acetic acid, due to lower enzyme activity in the organism, the growth of Acetobacter pasteurianus on high acetic acid concentrations is limited, overview
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-
?
additional information
?
-
-
the quinohemoprotein is able to oxidize alcohols, structure-function relationship, overview
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-
?
additional information
?
-
-
by the defect of type III ADH in Acetobacter pasteurianus SKU1108, the strain turns out to grow even better than the wild strain in ethanol containing medium, where two NAD-dependent ADHs, present in only a small amount in the wild-type strain, are dramatically increased in the cytoplasm, concomitant to the increase of the key enzyme activities in TCA and glyoxylate cycles
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?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
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?
additional information
?
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-
PQQ-ADH has a Q-1 reductase activity at acidic pH 4.0-5.0
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-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
PQQ-ADH has a Q-1 reductase activity at acidic pH 4.0-5.0
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
PQQ-ADH has a Q-1 reductase activity at acidic pH 4.0-5.0
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
PQQ-ADH has a Q-1 reductase activity at acidic pH 4.0-5.0
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
PQQ-ADH has a Q-1 reductase activity at acidic pH 4.0-5.0
-
-
?
additional information
?
-
-
the quinohemoprotein is able to oxidize alcohols, structure-function relationship, overview
-
-
?
additional information
?
-
-
by the defect of type III ADH in Acetobacter pasteurianus SKU1108, the strain turns out to grow even better than the wild strain in ethanol containing medium, where two NAD-dependent ADHs, present in only a small amount in the wild-type strain, are dramatically increased in the cytoplasm, concomitant to the increase of the key enzyme activities in TCA and glyoxylate cycles
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
PQQ-ADH has a Q-1 reductase activity at acidic pH 4.0-5.0
-
-
?
additional information
?
-
-
the quinohemoprotein is able to oxidize alcohols, structure-function relationship, overview
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
PQQ-ADH has a Q-1 reductase activity at acidic pH 4.0-5.0
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
PQQ-ADH has a Q-1 reductase activity at acidic pH 4.0-5.0
-
-
?
additional information
?
-
CCU55317
substrate specificity, overview
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-
?
additional information
?
-
-
substrate specificity, overview
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-
?
additional information
?
-
CCU55317
substrate specificity, overview
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-
?
additional information
?
-
-
no activity with glucose, benzaldehyde, formaldehyde, acetone, sorbitol or glycerol
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-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
the quinohemoprotein is able to oxidize alcohols, structure-function relationship, overview
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
the quinohemoprotein is able to oxidize alcohols, structure-function relationship, overview
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH. The organism shows enantiospecific oxidation of alcoholic compounds, e.g. oxidation of prochiral compound 2-methylpropane-1,3-diol to (R)-beta-hydroxyisobutyric acid with 83% enantiomeric excess
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?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH. The organism shows enantiospecific oxidation of alcoholic compounds, e.g. oxidation of prochiral compound 2-methylpropane-1,3-diol to (R)-beta-hydroxyisobutyric acid with 83% enantiomeric excess
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?
additional information
?
-
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the enzyme is involved in the cellular adaptation mechanism to high acetic acid concentrations, overview
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-
?
additional information
?
-
high alcohol dehydrogenase activity in the Gluconacetobacter europaeus cells and high acetic acid stability of the purified enzyme represent two of the unique features that enable this species to grow and stay metabolically active at extremely high concentrations of acetic acid
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-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
the enzyme is involved in the cellular adaptation mechanism to high acetic acid concentrations, overview
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
the enzyme activity is correlated with resistance to acetic acid, due to lower enzyme activity in the organism, the growth of Gluconacetobacter intermedius on high acetic acid concentrations is limited, overview
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
the enzyme activity is correlated with resistance to acetic acid, due to lower enzyme activity in the organism, the growth of Gluconacetobacter intermedius on high acetic acid concentrations is limited, overview
-
-
?
additional information
?
-
-
purified ADH oxidizes primary alcohols (C2-C6) but not methanol
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-
?
additional information
?
-
-
broad substrate specificity of PQQ-ADH
-
-
?
additional information
?
-
-
purified ADH oxidizes primary alcohols (C2-C6) but not methanol
-
-
?
additional information
?
-
-
substrate specificity, assayed with dichlorophenolindophenol and phenazinemethosulfate as electron acceptors, overview
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-
?