Intrinsic effects of solvent polarity on enzymic activation energies

Citation
J. Kim et al., Intrinsic effects of solvent polarity on enzymic activation energies, BIOTECH BIO, 67(1), 2000, pp. 112-116
Citations number
21
Categorie Soggetti
Biotecnology & Applied Microbiology",Microbiology
Journal title
BIOTECHNOLOGY AND BIOENGINEERING
ISSN journal
00063592 → ACNP
Volume
67
Issue
1
Year of publication
2000
Pages
112 - 116
Database
ISI
SICI code
0006-3592(20000105)67:1<112:IEOSPO>2.0.ZU;2-K
Abstract
The effect of organic solvents on sublilisin Carlsberg catalysis has been i nvestigated with the aid of a thermodynamic analysis. Saturation solubility experiments were performed to provide a quantitative measure of substrate desolvation from the reaction medium. This enabled calculation of the intri nsic enzymic activation energy and resulted in a linear free energy relatio nship with respect to solvent polarity. The results indicate that the intri nsic activation energy of subtilisin catalysis is lowest: in polar organic solvents, which may be due to transition state stabilization of the enzyme' s polar transition state for transesterification. (C) 2000 John Wiley & Son s, Inc.