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Results 1 - 10 of 10

EC Number	Substrates	Commentary Substrates	Organism	Products	Commentary (Products)	Reversibility
3.1.1.83	(4R)-4-isopropenyl-7-methyl-2-oxo-oxepanone + H2O	-	Rhodococcus erythropolis	6-hydroxy-3-(1-methylethenyl)heptanoic acid	-	?
3.1.1.83	(4R)-4-isopropenyl-7-methyl-2-oxo-oxepanone + H2O	-	Rhodococcus erythropolis DCL14	6-hydroxy-3-(1-methylethenyl)heptanoic acid	-	?
3.1.1.83	(6R)-6-isopropenyl-3-methyl-2-oxo-oxepanone + H2O	-	Rhodococcus erythropolis	5-(hydroxymethyl)-2,6-dimethylhept-6-enoic acid	-	?
3.1.1.83	(6R)-6-isopropenyl-3-methyl-2-oxo-oxepanone + H2O	-	Rhodococcus erythropolis DCL14	5-(hydroxymethyl)-2,6-dimethylhept-6-enoic acid	-	?
3.1.1.83	epsilon-caprolactone + H2O	-	Rhodococcus erythropolis	?	-	?
3.1.1.83	epsilon-caprolactone + H2O	-	Rhodococcus erythropolis DCL14	?	-	?
3.1.1.83	ethyl caproate + H2O	23% of the activity with epsilon-caprolactone	Rhodococcus erythropolis	?	-	?
3.1.1.83	ethyl caproate + H2O	23% of the activity with epsilon-caprolactone	Rhodococcus erythropolis DCL14	?	-	?
3.1.1.83	more	DCL14, catalyzing the ring opening of lactones which are formed during degradation of several monocyclic monoterpenes, including carvone and menthol	Rhodococcus erythropolis	?	-	?
3.1.1.83	more	DCL14, catalyzing the ring opening of lactones which are formed during degradation of several monocyclic monoterpenes, including carvone and menthol	Rhodococcus erythropolis DCL14	?	-	?

Results 1 - 10 of 10

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Release 2023.1 (January 2023)