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(1S)-1-(4-ethylphenyl)ethanol + H2O + ferricenium
(1S,1'S)-1,1'-(benzene-1,4-diyl)diethanol + ferrocene
-
-
-
-
?
1,2,3,4-tetrahydronaphthalene + H2O + ferricenium
(S)-1,2,3,4-tetrahydronaphthalen-1-ol + ferrocene
-
-
-
-
?
1,2-diethylbenzene + H2O + ferricenium
(S)-1-(2-ethylphenyl)ethanol + ferrocene
-
-
-
-
?
1,4-diethylbenzene + H2O + acceptor
1-(4-ethylphenyl)ethanol + 1,1'-(1,4-phenylene)diethanol + acceptor
1,4-diethylbenzene + H2O + acceptor
? + reduced acceptor
-
35% of the activity with ethylbenzene
-
-
?
1,4-diethylbenzene + H2O + ferricenium
(S)-1-(4-ethylphenyl)ethanol + ferrocene
-
-
-
-
?
1,4-diethylbenzene + H2O + ferricenium
1-(4-ethylphenyl)ethanol + 1,1'-(1,4-phenylene)diethanol + ferrocene
1,4-diethylbenzene + H2O + ferricenium
1-(4-ethylphenyl)ethanol + 1,1'-(1,4-phenylene)diethanol + ferrocenium
1-ethyl-2-methylbenzene + H2O + acceptor
? + reduced acceptor
-
3.8% of the activity with ethylbenzene
-
-
?
1-ethyl-2-methylbenzene + H2O + ferricenium
(S)-1-(2-methylphenyl)ethanol + ferrocene
-
-
-
-
?
1-ethyl-3-fluorobenzene + H2O + acceptor
? + reduced acceptor
-
15% of the activity with ethylbenzene
-
-
?
1-ethyl-3-methylbenzene + H2O + acceptor
? + reduced acceptor
-
10% of the activity with ethylbenzene
-
-
?
1-ethyl-3-methylbenzene + H2O + ferricenium
(S)-1-(3-methylphenyl)ethanol + ferrocene
-
-
-
-
?
1-ethyl-4-fluorobenzene + H2O + ferricenium
(S)-1-(4-fluorophenyl)ethanol + ferrocene
-
-
-
-
?
1-ethyl-4-methoxybenzene + H2O + ferricenium
(S)-1-(4-methoxyphenyl)ethanol + ferrocene
-
-
-
-
?
1-ethyl-4-methylbenzene + H2O + acceptor
? + reduced acceptor
-
28% of the activity with ethylbenzene
-
-
?
1-ethyl-4-methylbenzene + H2O + ferricenium
(S)-1-(4-methylphenyl)ethanol + ferrocene
-
-
-
-
?
1H-indene + H2O + ferricenium
(S)-1H-inden-1-ol + ferrocene
-
-
-
-
?
2,3-dihydro-1H-indene + H2O + ferricenium
(S)-2,3-dihydro-1H-inden-1-ol + ferrocene
-
-
-
-
?
2-ethyl-1H-pyrrole + H2O + acceptor
? + reduced acceptor
-
234.5% of the activity with ethylbenzene
-
-
?
2-ethyl-1H-pyrrole + H2O + ferricenium
(S)-1-(1H-pyrrol-2-yl)ethanol + ferrocene
-
-
-
-
?
2-ethyl-aniline + H2O + acceptor
? + reduced acceptor
-
94.5% of the activity with ethylbenzene
-
-
?
2-ethylaniline + H2O + acceptor
?
2-ethylaniline + H2O + ferricenium
?
2-ethylaniline + H2O + ferricenium
? + ferrocene
2-ethylfuran + H2O + acceptor
?
2-ethylfuran + H2O + acceptor
? + reduced acceptor
-
133.9% of the activity with ethylbenzene
-
-
?
2-ethylfuran + H2O + ferricenium
(S)-1-(furan-2-yl)ethanol + ferrocene
-
-
-
-
?
2-ethylfuran + H2O + ferricenium
1-(2-furyl)ethanol + ferrocene
2-ethylfuran + H2O + ferricenium
1-(2-furyl)ethanol + ferrocenium
-
-
-
-
?
2-ethylfuran + H2O + ferricenium
?
-
-
-
-
?
2-ethylnaphthalene + H2O + acceptor
?
-
-
-
-
?
2-ethylnaphthalene + H2O + acceptor
? + reduced acceptor
-
9.3% of the activity with ethylbenzene
-
-
?
2-ethylnaphthalene + H2O + ferricenium
(S)-1-(naphthalen-2-yl)ethanol + ferrocene
-
-
-
-
?
2-ethylnaphthalene + H2O + ferricenium
? + ferrocene
-
9.3% activity compared to ethylbenzene
-
-
?
2-ethylphenol + H2O + acceptor
2-(1-hydroxyethyl)phenol + reduced acceptor
-
-
-
-
?
2-ethylphenol + H2O + acceptor
? + reduced acceptor
-
56.7% of the activity with ethylbenzene
-
-
?
2-ethylphenol + H2O + ferricenium
2-(1-hydroxyethyl)phenol + ferrocene
-
55% activity compared to ethylbenzene
-
-
?
2-ethylphenol + H2O + ferricenium
2-(1-hydroxyethyl)phenol + ferrocenium
-
-
-
-
?
2-ethylpyrrole + H2O + acceptor
?
-
-
-
-
?
2-ethylpyrrole + H2O + ferricenium
?
-
-
-
-
?
2-ethylpyrrole + H2O + ferricenium
? + ferrocene
-
228% activity compared to ethylbenzene
-
-
?
2-ethylthiophene + ferricyanide
(S)-1-(2-thienyl)-ethanol + ferrocyanide
2-ethylthiophene + H2O + acceptor
?
-
-
-
-
?
2-ethylthiophene + H2O + acceptor
? + reduced acceptor
-
242.9% of the activity with ethylbenzene
-
-
?
2-ethylthiophene + H2O + ferricenium
(S)-1-(thiophen-2-yl)ethanol + ferrocene
-
-
-
-
?
2-ethylthiophene + H2O + ferricenium
1-thien-2-ylethanol + ferrocene
-
236% activity compared to ethylbenzene
-
-
?
2-ethylthiophene + H2O + ferricenium
1-thien-2-ylethanol + ferrocenium
-
-
-
-
?
2-ethylthiophene + H2O + ferricenium
?
-
-
-
-
?
2-ethyltoluene + H2O + acceptor
1-(2-methylphenyl)ethanol + reduced acceptor
-
-
-
-
?
2-ethyltoluene + H2O + ferricenium
? + ferrocene
-
3.8% activity compared to ethylbenzene
-
-
?
3-ethylanisole + H2O + acceptor
1-(3-methoxyphenyl)ethanol + acceptor
-
-
-
-
?
3-ethylphenol + H2O + acceptor
3-(1-hydroxyethyl)phenol + acceptor
-
-
-
-
?
3-ethylphenol + H2O + acceptor
? + reduced acceptor
-
24.3% of the activity with ethylbenzene
-
-
?
3-ethylphenol + H2O + ferricenium
3-(1-hydroxyethyl)phenol + ferrocene
-
19% activity compared to ethylbenzene
-
-
?
3-ethylphenol + H2O + ferricenium
3-(1-hydroxyethyl)phenol + ferrocenium
-
-
-
-
?
3-ethylpyridine + H2O + acceptor
?
-
-
-
-
?
3-ethylpyridine + H2O + acceptor
? + reduced acceptor
-
16.9% of the activity with ethylbenzene
-
-
?
3-ethylpyridine + H2O + ferricenium
?
-
-
-
-
?
3-ethylpyridine + H2O + ferricenium
? + ferrocene
-
16% activity compared to ethylbenzene
-
-
?
3-ethyltoluene + H2O + acceptor
1-(3-methylphenyl)ethanol + acceptor
-
-
-
-
?
3-ethyltoluene + H2O + ferricenium
? + ferrocene
-
10% activity compared to ethylbenzene
-
-
?
3-methyl-2-pentene + molybdopterin
?
3-phenyl-1-propene + H2O + ferricyanide
? + ferrocyanide
3-phenyl-1-propene + H2O + ferrocenium
? + ferrocene
3-phenyl-1-propyne + H2O + ferricyanide
? + ferrocyanide
3-phenyl-1-propyne + H2O + ferrocenium
? + ferrocene
-
-
-
-
?
3-phenylprop-1-ene + H2O + ferricenium
(S)-1-phenylprop-2-en-1-ol + ferrocene
-
-
-
-
?
3-phenylprop-1-yne + H2O + ferricenium
(S)-1-phenylprop-2-yn-1-ol + ferrocene
-
-
-
-
?
4-bromoethylbenzene + H2O + acceptor
?
-
-
-
-
?
4-chloroethylbenzene + H2O + acceptor
?
-
-
-
-
?
4-cyanoethylbenzene + H2O + acceptor
?
-
-
-
-
?
4-ethyl-1,1'-biphenyl + H2O + ferricenium
(S)-1-([1,1'-biphenyl]-4-yl)ethanol + (R)-1-([1,1'-biphenyl]-4-yl)ethanol + ferrocene
-
-
-
-
?
4-ethyl-N,N-dimethylaniline + H2O + acceptor
?
-
-
-
-
?
4-ethylaniline + H2O + acceptor
?
-
-
-
-
?
4-ethylaniline + H2O + ferricenium
? + ferrocene
-
130% activity compared to ethylbenzene
-
-
?
4-ethylanisole + H2O + acceptor
1-(4-methoxyphenyl)ethanol + acceptor
-
-
-
-
?
4-ethylanisole + H2O + ferricenium
1-(4-methoxyphenyl)ethanol + ferrocene
-
22% activity compared to ethylbenzene
-
-
?
4-ethylanisole + H2O + ferricenium
1-(4-methoxyphenyl)ethanol + ferrocenium
-
-
-
-
?
4-ethylbiphenyl + ferricenium + H2O
1-(1,1'-biphenyl-4-yl)ethanol + ferrocene
4-ethylbiphenyl + H2O + acceptor
1-(1,1'-biphenyl-4-yl)ethanol + reduced acceptor
4-ethylbiphenyl + H2O + ferricenium
1-(1,1'-biphenyl-4-yl)ethanol + reduced ferrocenium
4-ethylbiphenyl + H2O + ferricenium
? + ferrocene
-
30% activity compared to ethylbenzene
-
-
?
4-ethylphenol + ferricenium
?
4-ethylphenol + H2O + acceptor
4-(1-hydroxyethyl)phenol + acceptor
4-ethylphenol + H2O + acceptor
? + reduced acceptor
-
259% of the activity with ethylbenzene
-
-
?
4-ethylphenol + H2O + ferricenium
4-(1-hydroxyethyl)phenol + ferrocene
-
251% activity compared to ethylbenzene
-
-
?
4-ethylphenol + H2O + ferricenium
4-(1-hydroxyethyl)phenol + ferrocenium
-
best substrate
-
-
?
4-ethylpyridine + H2O + acceptor
?
-
substrate shows 50fold decreased activities of hydroxylation, relative specific activity: 2%
-
-
?
4-ethylresorcinol + H2O + acceptor
?
-
-
-
-
?
4-ethyltoluene + H2O + acceptor
1-(4-methylphenyl)ethanol + acceptor
-
-
-
-
?
4-ethyltoluene + H2O + ferricenium
1-(4-methylphenyl)ethanol + ferrocene
-
28% activity compared to ethylbenzene
-
-
?
4-ethyltoluene + H2O + ferricenium
1-(4-methylphenyl)ethanol + ferrocenium
-
-
-
-
?
4-fluoro-ethylbenzene + molybdopterin
?
4-fluoroethylbenzene + H2O + acceptor
?
-
-
-
-
?
4-fluoroethylbenzene + H2O + ferricenium
? + ferrocene
-
15% activity compared to ethylbenzene
-
-
?
4-propylphenol + H2O + acceptor
4-(1-hydroxypropyl)phenol + acceptor
-
-
-
-
?
4-propylphenol + H2O + ferricenium
4-(1-hydroxypropyl)phenol + ferrocene
-
175% activity compared to ethylbenzene
-
-
?
4-propylphenol + H2O + ferricenium
4-(1-hydroxypropyl)phenol + ferrocenium
-
-
-
-
?
5-methoxy-2,3-dihydro-1H-indene + H2O + ferricenium
(S)-5-methoxy-2,3-dihydro-1H-inden-1-ol + (S)-6-methoxy-2,3-dihydro-1H-inden-1-ol + ferrocene
-
-
-
-
?
allylbenzene + ferricenium
?
allylbenzene + H2O + acceptor
?
-
allylbenzene is hydroxylated 2.8fold faster than ethylbenzene. The introduced CH=CH2 group of the allyl chain may exert both steric and electronic effects on the energetic profile of the reaction. Relative specific activity: 281%
-
-
?
ethylbenzene + H2O + acceptor
(S)-1-phenylethanol + reduced acceptor
ethylbenzene + H2O + ferricenium
(S)-1-phenylethanol + ferrocene
ethylbenzene + H2O + ferricenium
(S)-1-phenylethanol + ferrocenium
-
EBDH catalyzes the oxygen-independent, stereospecific hydroxylation of ethylbenzene to (S)-1-phenylethanol, the direct anaerobic oxidation of a nonactivated hydrocarbon
-
-
?
ethylbenzene + H2O + ferricyanide
(S)-1-phenylethanol + ferrocyanide
-
-
-
-
?
ethylbenzene + H2O + ferrocenium
(S)-1-phenylethanol + ferrocene
-
-
-
-
?
ethylbenzene + H2O + molybdopterin
(S)-1-phenylethanol + molybdopterin (reduced form)
ethylbenzene + H2O + phenazine methosulfate
(S)-1-phenylethanol + reduced phenazine methosulfate
ethylbenzene + H2O + [Fe(III) (C5H5)2]+
(S)-1-phenylethanol + [Fe(II) (C5H5)2]
ethylidenecyclohexane + H2O + ferricenium
?
-
-
-
-
?
ethylidenecyclohexane + molybdopterin
?
n-propylbenzene + H2O + acceptor
?
-
-
-
-
?
n-propylbenzene + H2O + ferricenium
1-phenylpropanol + ferrocene
-
14% activity compared to ethylbenzene
-
-
?
n-propylbenzene + H2O + [Fe(III) (C5H5)2]+
(S)-1-phenylpropanol + [Fe(II) (C5H5)2]
propylbenzene + H2O + acceptor
? + reduced acceptor
-
15% of the activity with ethylbenzene
-
-
?
propylbenzene + H2O + ferricenium
(S)-1-phenylpropan-1-ol + ferrocene
-
-
-
-
?
propylbenzene + H2O + ferricenium
(S)-1-phenylpropanol + ferrocene
propylbenzene + H2O + ferricenium
(S)-1-phenylpropanol + ferrocenium
-
-
-
-
?
rac-1-(4-ethylphenyl)ethanol + H2O + ferricenium
(1S)-1,1'-(benzene-1,4-diyl)diethanol + ferrocene
-
-
-
-
?
additional information
?
-
1,4-diethylbenzene + H2O + acceptor
1-(4-ethylphenyl)ethanol + 1,1'-(1,4-phenylene)diethanol + acceptor
-
-
-
-
?
1,4-diethylbenzene + H2O + acceptor
1-(4-ethylphenyl)ethanol + 1,1'-(1,4-phenylene)diethanol + acceptor
-
-
-
-
?
1,4-diethylbenzene + H2O + ferricenium
1-(4-ethylphenyl)ethanol + 1,1'-(1,4-phenylene)diethanol + ferrocene
-
35% activity compared to ethylbenzene
-
-
?
1,4-diethylbenzene + H2O + ferricenium
1-(4-ethylphenyl)ethanol + 1,1'-(1,4-phenylene)diethanol + ferrocene
-
35% activity compared to ethylbenzene
-
-
?
1,4-diethylbenzene + H2O + ferricenium
1-(4-ethylphenyl)ethanol + 1,1'-(1,4-phenylene)diethanol + ferrocenium
-
-
-
-
?
1,4-diethylbenzene + H2O + ferricenium
1-(4-ethylphenyl)ethanol + 1,1'-(1,4-phenylene)diethanol + ferrocenium
-
-
-
-
?
2-ethylaniline + H2O + acceptor
?
-
-
-
-
?
2-ethylaniline + H2O + acceptor
?
-
-
-
-
?
2-ethylaniline + H2O + ferricenium
?
-
-
-
-
?
2-ethylaniline + H2O + ferricenium
?
-
-
-
-
?
2-ethylaniline + H2O + ferricenium
? + ferrocene
-
92% activity compared to ethylbenzene
-
-
?
2-ethylaniline + H2O + ferricenium
? + ferrocene
-
92% activity compared to ethylbenzene
-
-
?
2-ethylfuran + H2O + acceptor
?
-
-
-
-
?
2-ethylfuran + H2O + acceptor
?
-
-
-
-
?
2-ethylfuran + H2O + ferricenium
1-(2-furyl)ethanol + ferrocene
-
130% activity compared to ethylbenzene
-
-
?
2-ethylfuran + H2O + ferricenium
1-(2-furyl)ethanol + ferrocene
-
130% activity compared to ethylbenzene
-
-
?
2-ethylthiophene + ferricyanide
(S)-1-(2-thienyl)-ethanol + ferrocyanide
-
-
-
-
?
2-ethylthiophene + ferricyanide
(S)-1-(2-thienyl)-ethanol + ferrocyanide
-
-
-
-
?
3-methyl-2-pentene + molybdopterin
?
-
-
-
-
?
3-methyl-2-pentene + molybdopterin
?
-
-
-
-
?
3-phenyl-1-propene + H2O + ferricyanide
? + ferrocyanide
-
-
-
-
?
3-phenyl-1-propene + H2O + ferricyanide
? + ferrocyanide
-
-
-
-
?
3-phenyl-1-propene + H2O + ferrocenium
? + ferrocene
-
-
-
-
?
3-phenyl-1-propene + H2O + ferrocenium
? + ferrocene
-
-
-
-
?
3-phenyl-1-propyne + H2O + ferricyanide
? + ferrocyanide
-
-
-
-
?
3-phenyl-1-propyne + H2O + ferricyanide
? + ferrocyanide
-
-
-
-
?
4-ethylbiphenyl + ferricenium + H2O
1-(1,1'-biphenyl-4-yl)ethanol + ferrocene
-
-
-
-
?
4-ethylbiphenyl + ferricenium + H2O
1-(1,1'-biphenyl-4-yl)ethanol + ferrocene
-
-
-
-
?
4-ethylbiphenyl + H2O + acceptor
1-(1,1'-biphenyl-4-yl)ethanol + reduced acceptor
-
-
-
-
?
4-ethylbiphenyl + H2O + acceptor
1-(1,1'-biphenyl-4-yl)ethanol + reduced acceptor
-
-
-
-
?
4-ethylbiphenyl + H2O + ferricenium
1-(1,1'-biphenyl-4-yl)ethanol + reduced ferrocenium
-
-
-
-
?
4-ethylbiphenyl + H2O + ferricenium
1-(1,1'-biphenyl-4-yl)ethanol + reduced ferrocenium
-
-
-
-
?
4-ethylphenol + ferricenium
?
-
-
-
-
?
4-ethylphenol + ferricenium
?
-
-
-
-
?
4-ethylphenol + H2O + acceptor
4-(1-hydroxyethyl)phenol + acceptor
-
substrate shows 2.5fold increased activities of hydroxylation, relative specific activity: 251%
-
-
?
4-ethylphenol + H2O + acceptor
4-(1-hydroxyethyl)phenol + acceptor
-
-
-
-
?
4-fluoro-ethylbenzene + molybdopterin
?
-
-
-
-
?
4-fluoro-ethylbenzene + molybdopterin
?
-
-
-
-
?
allylbenzene + ferricenium
?
-
-
-
-
?
allylbenzene + ferricenium
?
-
-
-
-
?
ethylbenzene + H2O + acceptor
(S)-1-phenylethanol + reduced acceptor
-
-
-
-
?
ethylbenzene + H2O + acceptor
(S)-1-phenylethanol + reduced acceptor
-
relative specific activity: 100%
-
-
?
ethylbenzene + H2O + acceptor
(S)-1-phenylethanol + reduced acceptor
-
-
-
-
?
ethylbenzene + H2O + acceptor
(S)-1-phenylethanol + reduced acceptor
-
-
-
-
?
ethylbenzene + H2O + acceptor
(S)-1-phenylethanol + reduced acceptor
-
anaerobic degradation of ethylbenzene in bacteria
-
?
ethylbenzene + H2O + acceptor
(S)-1-phenylethanol + reduced acceptor
-
anaerobic degradation of ethylbenzene in bacteria
-
ir
ethylbenzene + H2O + acceptor
(S)-1-phenylethanol + reduced acceptor
-
EBDH catalyzes the oxygen-independent, stereospecific hydroxylation of ethylbenzene to (S)-1-phenylethanol
-
-
?
ethylbenzene + H2O + acceptor
(S)-1-phenylethanol + reduced acceptor
-
anaerobic degradation of ethylbenzene in bacteria
-
?
ethylbenzene + H2O + acceptor
(S)-1-phenylethanol + reduced acceptor
-
anaerobic degradation of ethylbenzene in bacteria
-
ir
ethylbenzene + H2O + acceptor
(S)-1-phenylethanol + reduced acceptor
-
-
-
-
?
ethylbenzene + H2O + acceptor
(S)-1-phenylethanol + reduced acceptor
-
EBDH catalyzes the oxygen-independent, stereospecific hydroxylation of ethylbenzene to (S)-1-phenylethanol
-
-
?
ethylbenzene + H2O + acceptor
(S)-1-phenylethanol + reduced acceptor
-
initial step of the degradation pathway from the toxic ethylbenzene to benzoyl-CoA
-
-
?
ethylbenzene + H2O + ferricenium
(S)-1-phenylethanol + ferrocene
-
-
-
-
?
ethylbenzene + H2O + ferricenium
(S)-1-phenylethanol + ferrocene
-
100% activity
-
-
?
ethylbenzene + H2O + ferricenium
(S)-1-phenylethanol + ferrocene
-
-
-
-
?
ethylbenzene + H2O + molybdopterin
(S)-1-phenylethanol + molybdopterin (reduced form)
-
-
-
?
ethylbenzene + H2O + molybdopterin
(S)-1-phenylethanol + molybdopterin (reduced form)
-
-
-
?
ethylbenzene + H2O + phenazine methosulfate
(S)-1-phenylethanol + reduced phenazine methosulfate
-
-
-
-
?
ethylbenzene + H2O + phenazine methosulfate
(S)-1-phenylethanol + reduced phenazine methosulfate
-
-
-
-
?
ethylbenzene + H2O + [Fe(III) (C5H5)2]+
(S)-1-phenylethanol + [Fe(II) (C5H5)2]
-
-
-
ir
ethylbenzene + H2O + [Fe(III) (C5H5)2]+
(S)-1-phenylethanol + [Fe(II) (C5H5)2]
-
-
-
ir
ethylidenecyclohexane + molybdopterin
?
-
-
-
-
?
ethylidenecyclohexane + molybdopterin
?
-
-
-
-
?
n-propylbenzene + H2O + [Fe(III) (C5H5)2]+
(S)-1-phenylpropanol + [Fe(II) (C5H5)2]
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-
-
?
n-propylbenzene + H2O + [Fe(III) (C5H5)2]+
(S)-1-phenylpropanol + [Fe(II) (C5H5)2]
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-
-
?
propylbenzene + H2O + ferricenium
(S)-1-phenylpropanol + ferrocene
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-
-
-
?
propylbenzene + H2O + ferricenium
(S)-1-phenylpropanol + ferrocene
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-
?
additional information
?
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EBDH is a bacterial molybdopterin enzyme capable of stereospecific anaerobic hydroxylation of alkylaromatic compounds to secondary alcohols
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?
additional information
?
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no activity with ethylidenecyclohexane, n-propylbenzene and 2-ethylpyrazine
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?
additional information
?
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no activity with ethylidenecyclohexane, n-propylbenzene and 2-ethylpyrazine
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?
additional information
?
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substrate specificity, product identification by GC- and LC-MS, overview
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?
additional information
?
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substrate specificity, product identification by GC- and LC-MS, overview
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?
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Kniemeyer, O.; Heider, J.
Ethylbenzene dehydrogenase, a novel hydrocarbon-oxidising molybdenum/iron-sulfur/heme enzyme
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Azoarcus sp., Azoarcus sp. EbN1
brenda
Johnson, H.A.; Pelletier, D.A.; Spormann, A.M.
Isolation and characterisation of anaerobic ethylbenzene dehydrogenase, a novel Mo-Fe-S enzyme
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Azoarcus sp., Azoarcus sp. EB1
brenda
Rabus, R.; Kube, M.; Beck, A.; Widdel, F.; Reinhardt, R.
Genes involved in the anaerobic degradation of ethylbenzene in a denitrifying bacterium, strain EbN1
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uncultured bacterium
brenda
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2005
uncultured bacterium
brenda
Szaleniec, M.; Witko, M.; Tadeusiewicz, R.; Goclon, J.
Application of artificial neural networks and DFT-based parameters for prediction of reaction kinetics of ethylbenzene dehydrogenase
J. Comput. Aided Mol. Des.
20
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2006
Azoarcus sp.
brenda
Szaleniec, M.; Hagel, C.; Menke, M.; Nowak, P.; Witko, M.; Heider, J.
Kinetics and mechanism of oxygen-independent hydrocarbon hydroxylation by ethylbenzene dehydrogenase
Biochemistry
46
7637-7646
2007
Azoarcus sp., Azoarcus sp. EbN1
brenda
Szaleniec, M.; Witko, M.; Heider, J.
Quantum chemical modelling of the C-H cleavage mechanism in oxidation of ethylbenzene and its derivates by ethylbenzene dehydrogenase
J. Mol. Catal. A
286
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2008
Azoarcus sp., Azoarcus sp. EbN1
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brenda
Szaleniec, M.; Borowski, T.; Schuehle, K.; Witko, M.; Heider, J.
Ab initio modeling of ethylbenzene dehydrogenase reaction mechanism
J. Am. Chem. Soc.
132
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2010
Aromatoleum aromaticum
brenda
Knack, D.H.; Marshall, J.L.; Harlow, G.P.; Dudzik, A.; Szaleniec, M.; Liu, S.Y.; Heider, J.
BN/CC isosteric compounds as enzyme inhibitors: N- and B-ethyl-1,2-azaborine inhibit ethylbenzene hydroxylation as nonconvertible substrate analogues
Angew. Chem. Int. Ed. Engl.
52
2599-2601
2013
Aromatoleum aromaticum
brenda
Szaleniec, M.; Salwinski, A.; Borowski, T.; Heider, J.; Witko, M.
Quantum chemical modeling studies of ethylbenzene dehydrogenase activity
Int. J. Quantum Chem.
112
1990-1999
2012
Aromatoleum aromaticum
-
brenda
Muhr, E.; Schuehle, K.; Clermont, L.; Suenwoldt, K.; Kleinsorge, D.; Seyhan, D.; Kahnt, J.; Schall, I.; Cordero, P.R.; Schmitt, G.; Heider, J.
Enzymes of anaerobic ethylbenzene and p-ethylphenol catabolism in Aromatoleum aromaticum differentiation and differential induction
Arch. Microbiol.
197
1051-1062
2015
Aromatoleum aromaticum, Aromatoleum aromaticum EbN1
brenda
Dorer, C.; Vogt, C.; Kleinsteuber, S.; Stams, A.J.; Richnow, H.H.
Compound-specific isotope analysis as a tool to characterize biodegradation of ethylbenzene
Environ. Sci. Technol.
48
9122-9132
2014
Aromatoleum aromaticum, Aromatoleum aromaticum EbN1
brenda
Tataruch, M.; Heider, J.; Bryjak, J.; Nowak, P.; Knack, D.; Czerniak, A.; Liesiene, J.; Szaleniec, M.
Suitability of the hydrocarbon-hydroxylating molybdenum-enzyme ethylbenzene dehydrogenase for industrial chiral alcohol production
J. Biotechnol.
192
400-409
2014
Aromatoleum aromaticum, Aromatoleum aromaticum EbN1
brenda
Szaleniec, M.; Dudzik, A.; Kozik, B.; Borowski, T.; Heider, J.; Witko, M.
Mechanistic basis for the enantioselectivity of the anaerobic hydroxylation of alkylaromatic compounds by ethylbenzene dehydrogenase
J. Inorg. Biochem.
139
9-20
2014
Aromatoleum aromaticum
brenda
Heider, J.; Szaleniec, M.; Suenwoldt, K.; Boll, M.
Ethylbenzene dehydrogenase and related molybdenum enzymes involved in oxygen-independent alkyl chain hydroxylation
J. Mol. Microbiol. Biotechnol.
26
45-62
2016
Aromatoleum aromaticum, Aromatoleum aromaticum EbN1
brenda
Jimenez-Halla, J.; Nazemi, A.; Cundari, T.
DFT study of substituent effects in the hydroxylation of methane and toluene mediated by an ethylbenzene dehydrogenase active site model
J. Organomet. Chem.
864
44-49
2018
Aromatoleum aromaticum
-
brenda
Kalimuthu, P.; Heider, J.; Knack, D.; Bernhardt, P.V.
Electrocatalytic hydrocarbon hydroxylation by ethylbenzene dehydrogenase from Aromatoleum aromaticum
J. Phys. Chem. B
119
3456-3463
2015
Aromatoleum aromaticum, Aromatoleum aromaticum EbN1
brenda