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D-galactose + ferrocenium hexafluorophosphate = 2-dehydro-D-galactose + ferrocene
-
D-glucose + ferrocenium hexafluorophosphate = 2-dehydro-D-glucose + ferrocene
-
D-galactose + ferricenium ion = 2-dehydro-D-galactose + ferrocenium ion
-
D-glucose + ferricenium ion = 2-dehydro-D-glucose + ferrocenium ion
-
D-glucose + ferricenium ion = D-glucono-1,5-lactone + ferrocenium ion
-
D-xylose + ferricenium ion = D-xylono-1,5-lactone + ferrocenium ion
-
cellobiose + ferricenium ion = ? + ferrocene
-
cellobiose + ferrocenium ion = 2-dehydro-cellobiose + ferrocene
-
D-allose + ferricenium ion = ? + ferrocene
-
D-fructose + ferricenium ion = ? + ferrocene
-
D-galactose + ferricenium ion = ? + ferrocene
-
D-galactose + ferrocenium ion = 2-dehydro-D-galactose + ferrocene
-
D-glucose + ferricenium ion = 2-dehydro-D-glucose + ferrocene
-
D-glucose + ferricenium ion = 3-dehydro-D-glucose + ferrocene
-
D-glucose + ferrocenium ion = 2-dehydro-D-glucose + ferrocene
-
D-glucose + ferrocenium ion = 3-dehydro-D-glucose + ferrocene
-
D-maltose + ferricenium ion = ? + ferrocene
-
D-mannose + ferricenium ion = ? + ferrocene
-
D-mannose + ferrocenium ion = 2-dehydro-D-mannose + ferrocene
-
D-ribose + ferricenium ion = ? + ferrocene
-
D-talose + ferricenium ion = ? + ferrocene
-
D-xylose + ferricenium ion = ? + ferrocene
-
D-xylose + ferrocenium ion = 2-dehydro-D-xylose + ferrocene
-
D-xylose + ferrocenium ion = ? + ferrocene
-
L-arabinose + ferricenium ion = ? + ferrocene
-
L-arabinose + ferrocenium ion = 2-dehydro-L-arabinose + ferrocene
-
L-arabinose + ferrocenium ion = ? + ferrocene
-
L-sorbose + ferricenium ion = ? + ferrocene
-
lactose + ferricenium ion = ? + ferrocene
-
lactose + ferrocenium ion = 2-dehydro-lactose + ferrocene
-
lactose + ferrocenium ion = ? + ferrocene
-
maltose + ferricenium ion = ? + ferrocene
-
maltose + ferrocenium ion = 2-dehydro-maltose + ferrocene
-
maltotriose + ferricenium ion = ? + ferrocene
-
methyl-alpha-D-glucopyranoside + ferricenium ion = ? + ferrocene
-
xylobiose + ferricenium ion = ? + ferrocene
-
a [histone H3]-N6,N6-dimethyl-L-lysine4 + ferricenium + H2O = a [histone H3]-N6-methyl-L-lysine4 + formaldehyde + ferrocene
-
4-cresol + ferricenium + H2O = 4-hydroxybenzyl alcohol + ferrocenium
-
(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 + ferricenium = (S)-1-(4-ethylphenyl)ethanol + ferrocene
-
1,4-diethylbenzene + H2O + ferricenium = 1-(4-ethylphenyl)ethanol + 1,1'-(1,4-phenylene)diethanol + ferrocene
-
1-ethyl-2-methylbenzene + H2O + ferricenium = (S)-1-(2-methylphenyl)ethanol + ferrocene
-
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 + 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 + ferricenium = (S)-1-(1H-pyrrol-2-yl)ethanol + ferrocene
-
2-ethylaniline + H2O + ferricenium = ? + ferrocene
-
2-ethylfuran + H2O + ferricenium = (S)-1-(furan-2-yl)ethanol + ferrocene
-
2-ethylfuran + H2O + ferricenium = 1-(2-furyl)ethanol + ferrocene
-
2-ethylnaphthalene + H2O + ferricenium = (S)-1-(naphthalen-2-yl)ethanol + ferrocene
-
2-ethylnaphthalene + H2O + ferricenium = ? + ferrocene
-
2-ethylphenol + H2O + ferricenium = 2-(1-hydroxyethyl)phenol + ferrocene
-
2-ethylpyrrole + H2O + ferricenium = ? + ferrocene
-
2-ethylthiophene + H2O + ferricenium = (S)-1-(thiophen-2-yl)ethanol + ferrocene
-
2-ethylthiophene + H2O + ferricenium = 1-thien-2-ylethanol + ferrocene
-
2-ethyltoluene + H2O + ferricenium = ? + ferrocene
-
3-ethylphenol + H2O + ferricenium = 3-(1-hydroxyethyl)phenol + ferrocene
-
3-ethylpyridine + H2O + ferricenium = ? + ferrocene
-
3-ethyltoluene + H2O + ferricenium = ? + ferrocene
-
3-phenyl-1-propene + H2O + ferrocenium = ? + ferrocene
-
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-ethyl-1,1'-biphenyl + H2O + ferricenium = (S)-1-([1,1'-biphenyl]-4-yl)ethanol + (R)-1-([1,1'-biphenyl]-4-yl)ethanol + ferrocene
-
4-ethylaniline + H2O + ferricenium = ? + ferrocene
-
4-ethylanisole + H2O + ferricenium = 1-(4-methoxyphenyl)ethanol + ferrocene
-
4-ethylbiphenyl + ferricenium + H2O = 1-(1,1'-biphenyl-4-yl)ethanol + ferrocene
-
4-ethylbiphenyl + H2O + ferricenium = ? + ferrocene
-
4-ethylphenol + H2O + ferricenium = 4-(1-hydroxyethyl)phenol + ferrocene
-
4-ethyltoluene + H2O + ferricenium = 1-(4-methylphenyl)ethanol + ferrocene
-
4-fluoroethylbenzene + H2O + ferricenium = ? + ferrocene
-
4-propylphenol + H2O + ferricenium = 4-(1-hydroxypropyl)phenol + ferrocene
-
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
-
ethylbenzene + H2O + ferricenium = (S)-1-phenylethanol + ferrocene
-
ethylbenzene + H2O + ferrocenium = (S)-1-phenylethanol + ferrocene
-
n-propylbenzene + H2O + ferricenium = 1-phenylpropanol + ferrocene
-
propylbenzene + H2O + ferricenium = (S)-1-phenylpropan-1-ol + ferrocene
-
propylbenzene + H2O + ferricenium = (S)-1-phenylpropanol + ferrocene
-
rac-1-(4-ethylphenyl)ethanol + H2O + ferricenium = (1S)-1,1'-(benzene-1,4-diyl)diethanol + ferrocene
-
1,4-diethylbenzene + H2O + ferricenium = 1-(4-ethylphenyl)ethanol + 1,1'-(1,4-phenylene)diethanol + ferrocenium
-
2-ethylfuran + H2O + ferricenium = 1-(2-furyl)ethanol + ferrocenium
-
2-ethylphenol + H2O + ferricenium = 2-(1-hydroxyethyl)phenol + ferrocenium
-
2-ethylthiophene + H2O + ferricenium = 1-thien-2-ylethanol + ferrocenium
-
3-ethylphenol + H2O + ferricenium = 3-(1-hydroxyethyl)phenol + ferrocenium
-
4-ethylanisole + H2O + ferricenium = 1-(4-methoxyphenyl)ethanol + ferrocenium
-
4-ethylphenol + H2O + ferricenium = 4-(1-hydroxyethyl)phenol + ferrocenium
-
4-ethyltoluene + H2O + ferricenium = 1-(4-methylphenyl)ethanol + ferrocenium
-
4-propylphenol + H2O + ferricenium = 4-(1-hydroxypropyl)phenol + ferrocenium
-
ethylbenzene + H2O + ferricenium = (S)-1-phenylethanol + ferrocenium
-
propylbenzene + H2O + ferricenium = (S)-1-phenylpropanol + ferrocenium
-
ethylbenzene + H2O + [Fe(III) (C5H5)2]+ = (S)-1-phenylethanol + [Fe(II) (C5H5)2]
-
n-propylbenzene + H2O + [Fe(III) (C5H5)2]+ = (S)-1-phenylpropanol + [Fe(II) (C5H5)2]
-
ferrocene + O2 = ferricinium + H2O
-
butyryl-CoA + ferricenium = 2-butenoyl-CoA + ferrocene
-
butyryl-CoA + ferrocenium = 2-butenoyl-CoA + ferrocene
-
hexanoyl-CoA + ferricenium = trans-hex-2-enoyl-CoA + ferrocenium
-
N,N-dimethylglycine + ferricenium + H2O = sarcosine + formaldehyde + ferrocene
-
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39.9
-
using D-glucose as cosubstrate, at 30°C, pH 6.5
19.92
-
with D-glucose as cosubstrate, at pH 8.5 and 30°C
22.07
-
with D-glucose as cosubstrate, at pH 8.5 and 30°C
26
-
mutant enzyme H103Y, with D-glucose as cosubstrate, at pH 8.5 and 30°C
44.8
-
mutant enzyme N75G/N175Q, at pH 7.5 and 30°C
50.7
-
mutant enzyme N175Q/N252Q, at pH 7.5 and 30°C
54.2
-
mutant enzyme N75G/N175Q/N252Q, at pH 7.5 and 30°C
54.6
-
mutant enzyme N75G/N252Q, at pH 7.5 and 30°C
65.8
-
mutant enzyme N75G, at pH 7.5 and 30°C
66.3
-
mutant enzyme N252Q, at pH 7.5 and 30°C
87.4
-
wild type enzyme, at pH 7.5 and 30°C
104
-
native enzyme, at pH 8.5 and 30°C
111.1
-
with D-glucose as cosubstrate, in 100 mM sodium acetate pH 4.0, at 30°C
125
-
mutant enzyme N75Q, at pH 7.5 and 30°C
130
-
recombinant enzyme, at pH 8.5 and 30°C
130
-
wild type enzyme, with D-glucose as cosubstrate, at pH 8.5 and 30°C
3.55
-
wild-type, pH 7.8, 25°C
9.07
-
mutant H109R, pH 7.8, 25°C
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0.187
-
using D-glucose as cosubstrate, at 30°C, pH 6.5
0.03
-
with D-glucose as cosubstrate, at pH 8.5 and 30°C
0.1
-
mutant enzyme H103Y, with D-glucose as cosubstrate, at pH 8.5 and 30°C
0.1
-
mutant enzyme N75G/N175Q/N252Q, at pH 7.5 and 30°C
0.11
-
mutant enzyme N75G/N175Q, at pH 7.5 and 30°C
0.13
-
native enzyme, at pH 8.5 and 30°C
0.16
-
recombinant enzyme, at pH 8.5 and 30°C
0.16
-
wild type enzyme, with D-glucose as cosubstrate, at pH 8.5 and 30°C
0.17
-
with D-glucose as cosubstrate, in 100 mM sodium acetate pH 4.0, at 30°C
0.24
-
mutant enzyme N75G, at pH 7.5 and 30°C
0.27
-
wild type enzyme, at pH 7.5 and 30°C
0.29
-
mutant enzyme N75G/N252Q, at pH 7.5 and 30°C
0.3
-
mutant enzyme N252Q, at pH 7.5 and 30°C
0.37
-
mutant enzyme N175Q/N252Q, at pH 7.5 and 30°C
0.39
-
mutant enzyme N75Q, at pH 7.5 and 30°C
1.19
-
with D-glucose as cosubstrate, at pH 8.5 and 30°C
0.0098
-
with ethylbenzene as cosubstrate, at pH 7.5 and 25°C
0.018
-
with 3-phenyl-1-propene as cosubstrate, at pH 7.5 and 25°C
0.035
-
with 3-phenyl-1-propyne as cosubstrate, at pH 7.5 and 25°C
1.4
-
wild-type, pH 7.8, 25°C
32.2
-
mutant H109R, pH 7.8, 25°C
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Ethylbenzene dehydrogenase, a novel hydrocarbon-oxidising molybdenum/iron-sulfur/heme enzyme
2001
Kniemeyer, O.; Heider, J.
J. Biol. Chem.
276
21381-21386
-
Characterization and kinetic studies of a novel dye prepared from the oxidation of a water-soluble 1,1'-dimethylferrocene-2-hydroxypropyl-.beta-cyclodextrin complex using immobilized bilirubin oxidase
1994
Male, K.B.; Luong, J.H.T.
Enzyme Microb. Technol.
16
425-431
Using trimethylamine dehydrogenase in an enzyme linked amperometric electrode. Part 1. Wild-type enzyme redox mediation
2003
Loechel, C.; Basran, A.; Basran, J.; Scrutton, N.S.; Hall, E.A.
Analyst
128
166-172
Purification and properties of a novel broad substrate specific alcohol oxidase from Aspergillus terreus MTCC 6324
2008
Kumar, A.K.; Goswami, P.
Biochim. Biophys. Acta
1784
1552-1559
Coupled ferredoxin and crotonyl coenzyme A (CoA) reduction with NADH catalyzed by the butyryl-CoA dehydrogenase/Etf complex from Clostridium kluyveri
2008
Li, F.; Hinderberger, J.; Seedorf, H.; Zhang, J.; Buckel, W.; Thauer, R.K.
J. Bacteriol.
190
843-850
Gene cloning and characterization of dihydrolipoamide dehydrogenase from Microbacterium luteolum: A useful enzymatic regeneration system of NAD+ from NADH
2010
Kurokawa, J.; Asano, M.; Nomoto, S.; Makino, Y.; Itoh, N.
J. Biosci. Bioeng.
109
218-223
Characterisation of recombinant pyranose oxidase from the cultivated mycorrhizal basidiomycete Lyophyllum shimeji (hon-shimeji)
2010
Salaheddin, C.; Takakura, Y.; Tsunashima, M.; Stranzinger, B.; Spadiut, O.; Yamabhai, M.; Peterbauer, C.K.; Haltrich, D.
Microb. Cell Fact.
9
57
Simple and efficient expression of Agaricus meleagris pyranose dehydrogenase in Pichia pastoris
2012
Sygmund, C.; Gutmann, A.; Krondorfer, I.; Kujawa, M.; Glieder, A.; Pscheidt, B.; Haltrich, D.; Peterbauer, C.; Kittl, R.
Appl. Microbiol. Biotechnol.
94
695-704
-
Recombinant pyranose dehydrogenase - A versatile enzyme possessing both mediated and direct electron transfer
2012
Yakovleva, M.; Killyéni, A.; Ortiz, R.; Schulz, C.; MacAodha, D.; Conghaile, P.; Leech, D.; Popescu, I.; Gonaus, C.; Peterbauer, C.; Gorton, L.
Electrochem. Commun.
24
120-122
Further insights into the catalytical properties of deglycosylated pyranose dehydrogenase from Agaricus meleagris recombinantly expressed in Pichia pastoris
2013
Yakovleva, M.E.; Killyeni, A.; Seubert, O.; O Conghaile, P.; Macaodha, D.; Leech, D.; Gonaus, C.; Popescu, I.C.; Peterbauer, C.K.; Kjellstroem, S.; Gorton, L.
Anal. Chem.
85
9852-9858
Agaricus meleagris pyranose dehydrogenase: influence of covalent FAD linkage on catalysis and stability
2014
Krondorfer, I.; Brugger, D.; Paukner, R.; Scheiblbrandner, S.; Pirker, K.F.; Hofbauer, S.; Furtmueller, P.G.; Obinger, C.; Haltrich, D.; Peterbauer, C.K.
Arch. Biochem. Biophys.
558
111-119
Pyranose dehydrogenase from Agaricus campestris and Agaricus xanthoderma: characterization and applications in carbohydrate conversions
2013
Staudigl, P.; Krondorfer, I.; Haltrich, D.; Peterbauer, C.K.
Biomolecules
3
535-552
Analysis of Agaricus meleagris pyranose dehydrogenase N-glycosylation sites and performance of partially non-glycosylated enzymes
2017
Gonaus, C.; Maresch, D.; Schropp, K.; O Conghaile, P.; Leech, D.; Gorton, L.; Peterbauer, C.K.
Enzyme Microb. Technol.
99
57-66
Inter-domain electron transfer in cellobiose dehydrogenase: modulation by pH and divalent cations
2015
Kracher, D.; Zahma, K.; Schulz, C.; Sygmund, C.; Gorton, L.; Ludwig, R.
FEBS J.
282
3136-3148
Reaction of pyranose dehydrogenase from Agaricus meleagris with its carbohydrate substrates
2015
Graf, M.M.; Sucharitakul, J.; Bren, U.; Chu, D.B.; Koellensperger, G.; Hann, S.; Furtmueller, P.G.; Obinger, C.; Peterbauer, C.K.; Oostenbrink, C.; Chaiyen, P.; Haltrich, D.
FEBS J.
282
4218-4241
Engineering of pyranose dehydrogenase for increased oxygen reactivity
2014
Krondorfer, I.; Lipp, K.; Brugger, D.; Staudigl, P.; Sygmund, C.; Haltrich, D.; Peterbauer, C.K.
PLoS ONE
9
e91145
Transcription analysis of pyranose dehydrogenase from the basidiomycete Agaricus bisporus and characterization of the recombinantly expressed enzyme
2016
Gonaus, C.; Kittl, R.; Sygmund, C.; Haltrich, D.; Peterbauer, C.
Protein Expr. Purif.
119
36-44
Specificity of glucose oxidase from Penicillium funiculosum 46.1 towards some redox mediators
2013
Semashko, T.; Mikhailova, R.; Ramanaviciene, A.; Ramanavicius, A.
Appl. Biochem. Biotechnol.
171
1739-1749
Structure and biochemical properties of recombinant human dimethylglycine dehydrogenase and comparison to the disease-related H109R variant
2016
Augustin, P.; Hromic, A.; Pavkov-Keller, T.; Gruber, K.; Macheroux, P.
FEBS J.
283
3587-3603
Suitability of the hydrocarbon-hydroxylating molybdenum-enzyme ethylbenzene dehydrogenase for industrial chiral alcohol production
2014
Tataruch, M.; Heider, J.; Bryjak, J.; Nowak, P.; Knack, D.; Czerniak, A.; Liesiene, J.; Szaleniec, M.
J. Biotechnol.
192
400-409
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