Cygler_1995_Can.J.Microbiol_41 Suppl 1_289

Reference

Title : Structural determinants defining common stereoselectivity of lipases toward secondary alcohols - Cygler_1995_Can.J.Microbiol_41 Suppl 1_289
Author(s) : Cygler M , Grochulski P , Schrag JD
Ref : Can J Microbiol , 41 Suppl 1 :289 , 1995
Abstract :

In this review we summarize some aspects of the enantiopreference of the lipase from Candida rugosa following structural analysis of complexes of this lipase with two enantiomers of an analog of a tetrahedral intermediate in the hydrolysis of simple esters. The analysis of the molecular basis of the enantiomeric differentiation suggests that these results can be generalized to a large class of lipases and esterases. We also summarize our experiments on identification of the key regions in the lipases from Geotrichum candidum lipase responsible for differentiation between fatty acyl chains.

PubMedSearch : Cygler_1995_Can.J.Microbiol_41 Suppl 1_289
PubMedID: 7606666

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Citations formats

Cygler M, Grochulski P, Schrag JD (1995)
Structural determinants defining common stereoselectivity of lipases toward secondary alcohols
Can J Microbiol 41 Suppl 1 :289

Cygler M, Grochulski P, Schrag JD (1995)
Can J Microbiol 41 Suppl 1 :289