Literature summary extracted from

Dong, J.J.; Fernandez-Fueyo, E.; Li, J.; Guo, Z.; Renirie, R.; Wever, R.; Hollmann, F.
Halofunctionalization of alkenes by vanadium chloroperoxidase from Curvularia inaequalis (2017), Chem. Commun. (Camb.), 53, 6207-6210 .

Application

EC Number	Application	Comment	Organism
1.11.1.B2	synthesis	enzyme converts both aromatic and aliphatic alkenes into the corresponding halohydrins. Variation of pH value and addtion of ethanol as solvent leads to variation of product mixtures	Curvularia inaequalis

Organism

EC Number	Organism	UniProt	Comment	Textmining
1.11.1.B2	Curvularia inaequalis	P49053	-	-

Substrates and Products (Substrate)

EC Number	Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
1.11.1.B2	cyclohexene + KBr + H2O2	-	Curvularia inaequalis	2-bromocyclohexan-1-ol + 2 H2O	-	?
1.11.1.B2	hept-1-ene + KBr + H2O2	-	Curvularia inaequalis	1-bromoheptan-2-ol + 2 H2O	-	?
1.11.1.B2	styrene + KBr + H2O2	-	Curvularia inaequalis	2-bromo-1-phenylethan-1-ol + 2-phenyloxirane + 2 H2O	-	?
1.11.1.B2	styrene + KCl + H2O2	-	Curvularia inaequalis	2-chloro-1-phenylethan-1-ol + 2 H2O	-	?
1.11.1.B2	[(1E)-prop-1-en-1-yl]benzene + KBr + H2O2	-	Curvularia inaequalis	(1R,2R)-2-bromo-1-phenylpropan-1-ol + 2 H2O	-	?
1.11.1.B2	[(1Z)-prop-1-en-1-yl]benzene + KBr + H2O2	-	Curvularia inaequalis	(1R,2S)-2-bromo-1-phenylpropan-1-ol + 2 H2O	-	?

Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.

Release 2023.1 (January 2023)