Epoxide hydrolases from microbial sources are highly versatile biocatalysts
for the asymmetric hydrolysis of epoxides on a preparative scale. Besides
kinetic resolution, which furnishes the corresponding vicinal diol and rema
ining non-hydrolysed epoxide in nonracemic form, enantioconvergent processe
s are possible: these are highly attractive as they lead to the formation o
f a single enantiomeric diol from a racemic oxirane. The data accumulated o
ver recent years reveal a common picture of the substrate structure selecti
vity pattern of microbial epoxide hydrolases and indicate that substrates o
f various structural types can be selectively hydrolysed with enzymes from
certain microbial sources.