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Results 1 - 10 of 34 > >>
EC Number
Substrates
Commentary Substrates
Organism
Products
Commentary (Products)
Reversibility
more
the localization of the enzyme on the outer surface of the organism is advantageous to facilitate the oxidative fermentation of the cyclic alcohols. Since cyclic alcohols have some biological toxicity to living cells, according to the mechanism of the oxidative fermentation, there is no need to incorporate such toxic compounds into the cytoplasm to oxidize and pump out the oxidation products across the cytoplasmic membrane by the expense of bioenergy. The enzyme not inducible
?
-
-
more
the enzyme is unable to catalyze the reverse reaction of cyclic ketones or aldehydes to cyclic alcohols. This enzyme oxidizes a wide variety of cyclic alcohols. Some minor enzyme activity is found with aliphatic secondary alcohols and sugar alcohols, but not primary alcohols
?
-
-
more
the localization of the enzyme on the outer surface of the organism is advantageous to facilitate the oxidative fermentation of the cyclic alcohols. Since cyclic alcohols have some biological toxicity to living cells, according to the mechanism of the oxidative fermentation, there is no need to incorporate such toxic compounds into the cytoplasm to oxidize and pump out the oxidation products across the cytoplasmic membrane by the expense of bioenergy. The enzyme not inducible
?
-
-
more
the enzyme is unable to catalyze the reverse reaction of cyclic ketones or aldehydes to cyclic alcohols. This enzyme oxidizes a wide variety of cyclic alcohols. Some minor enzyme activity is found with aliphatic secondary alcohols and sugar alcohols, but not primary alcohols
?
-
-
(1R,2R)-trans-1,2-cyclohexanediol + pyrroloquinoline quinone
74% of the activity compared to cyclopentanol
?
-
ir
(1R,2R)-trans-1,2-cyclohexanediol + pyrroloquinoline quinone
74% of the activity compared to cyclopentanol
?
-
ir
(1S,2S)-trans-1,2-cyclohexanediol + pyrroloquinoline quinone
11% of the activity compared to cyclopentanol
?
-
ir
(1S,2S)-trans-1,2-cyclohexanediol + pyrroloquinoline quinone
11% of the activity compared to cyclopentanol
?
-
ir
(2R,3R)-2,3-butanediol + pyrroloquinoline quinone
41% of the activity compared to cyclopentanol
?
-
ir
1,2-butanediol + pyrroloquinoline quinone
63% of the activity compared to cyclopentanol
?
-
ir
Results 1 - 10 of 34 > >>