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Solvation of CBZ-amino acid nitrophenyl esters in organic media and the kinetics of their transesterification by subtilisin.

作者信息

Reimann A, Robb D A, Halling P J

机构信息

Department of Bioscience and Biotechnology, University of Strathclyde, Glasgow G1 1XW, United Kingdom.

出版信息

Biotechnol Bioeng. 1994 May;43(11):1081-6. doi: 10.1002/bit.260431111.

DOI:10.1002/bit.260431111
PMID:18615519
Abstract

Subtilisin Carlsberg adsorbed on silica particles has been used to catalyze the transesterification of CBZ-Ala-ONp and CBZ-Leu-ONp with 1-butanol in organic systems preequilibrated to water activity of 0.93. Initial reaction rates are conveniently followed by extraction of the released nitrophenol into an alkaline aqueous phase. Kinetic parameters were determined for varied ester concentrations in toluene, isopropyl ether, and hexane. The effect of solvent on substrate solvation was determined by solubility measurements. Much of the observed effect of solvent on V(m)/K(m) may be accounted for by solvation differences. The residual effect of solvent on K(m), after discounting solvation differences, is completely opposite to the apparent trend. (c) 1994 John Wiley & Sons, Inc.

摘要

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