Enzymatic Reactions in Aqueous-Organic Media VII. Peptide and Ester Synthesis in Organic Solvents by α-Chymotrypsin Immobilized through Non-Covalent Binding to ... View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

1989-02

AUTHORS

Hidetaka Noritomi, Akira Watanabe, Hideo Kise

ABSTRACT

α-Chymotrypsin (CT) was immobilized to poly(vinyl alcohol) (PVA) by adsorption from its aqueous solutions. The catalytic activity of CT increased markedly by immobilization for peptide or ester synthesis from N-acetyl-l-tyrosine in hydrophilic organic solvents such as acetonitrile or ethanol. The yields of the peptide and ester are strongly dependent on the PVA/CT ratio and water content in the reaction medium. The rate and equilibrium constant of the ester formation reaction are also dependent on water content. These results are discussed in terms of the activation and stabilization of CT in hydrous PVA matrix. The studies on the substrate- and stereo-selectivity for the ester formation reactions suggest that CT maintains its native conformation in PVA matrix. The stability of PVA-immobilized CT is also described. More... »

PAGES

pj198918

Identifiers

URI

http://scigraph.springernature.com/pub.10.1295/polymj.21.147

DOI

http://dx.doi.org/10.1295/polymj.21.147

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1031208461


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