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Biotechnol Lett ; 32(4): 513-6, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20013303

ABSTRACT

A newly isolated Bacillus megaterium with epoxide hydrolase activity resolved racemic glycidyl (o, m, p)-methylphenyl ethers to give enantiopure epoxides in 84-99% enantiomeric excess and with 21-73 enantiomeric ratios. The (S)-enantiomer was obtained from rac-glycidyl (o or m)-methylphenyl ether while the (R)-epoxides was obtained from glycidyl p-methylphenyl ether. The observations are explained at the level by enzyme-substrate docking studies.


Subject(s)
Anisoles/isolation & purification , Bacillus megaterium/metabolism , Epoxy Compounds/isolation & purification , Anisoles/chemistry , Anisoles/metabolism , Bacillus megaterium/chemistry , Epoxy Compounds/chemistry , Epoxy Compounds/metabolism , Hydrolysis , Kinetics , Stereoisomerism
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