1.14.19.48: tert-amyl alcohol desaturase
This is an abbreviated version!
For detailed information about tert-amyl alcohol desaturase, go to the full flat file.
Reaction
Synonyms
MdpJ, mdpJK
ECTree
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General Information
General Information on EC 1.14.19.48 - tert-amyl alcohol desaturase
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physiological function
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degradation of tert-amyl alcohol leads to formation of beta and gamma isomers of isoamylene. Both tert-alkyl alcohol degradation and alkene production are strictly oxygen dependent, the relative contribution of the dehydration reaction to total alcohol conversion increased with decreasing oxygen concentrations
physiological function
degradation of tert-amyl alcohol leads to formation of beta and gamma isomers of isoamylene. Both tert-alkyl alcohol degradation and alkene production are strictly oxygen dependent, the relative contribution of the dehydration reaction to total alcohol conversion increased with decreasing oxygen concentrations
physiological function
degradation of tert-amyl alcohol leads to formation of beta and gamma isomers of isoamylene. Both tert-alkyl alcohol degradation and alkene production are strictly oxygen dependent, the relative contribution of the dehydration reaction to total alcohol conversion increased with decreasing oxygen concentrations
physiological function
MdpJ knockout mutants are not able to grow on the tertiary alcohols tert-butanol and tert-amyl alcohol, whereas 2-methylpropan-1,2-diol, the putative product of tert-butanol hydroxylation by MdpJ catalysis can still be used as the sole source of energy and carbon. The postulated 2-methylpropan-1,2-diol intermediate 2-hydroxyisobutanoate is metabolized by wild-type and mutant strains at the same rates. tert-amyl alcohol and hemiterpene degradation are linked with the catabolic route of leucine
physiological function
-
degradation of tert-amyl alcohol leads to formation of beta and gamma isomers of isoamylene. Both tert-alkyl alcohol degradation and alkene production are strictly oxygen dependent, the relative contribution of the dehydration reaction to total alcohol conversion increased with decreasing oxygen concentrations
-
physiological function
-
MdpJ knockout mutants are not able to grow on the tertiary alcohols tert-butanol and tert-amyl alcohol, whereas 2-methylpropan-1,2-diol, the putative product of tert-butanol hydroxylation by MdpJ catalysis can still be used as the sole source of energy and carbon. The postulated 2-methylpropan-1,2-diol intermediate 2-hydroxyisobutanoate is metabolized by wild-type and mutant strains at the same rates. tert-amyl alcohol and hemiterpene degradation are linked with the catabolic route of leucine
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