ORGANIC-REACTIONS CATALYZED BY INSOLUBILIZED ENZYMES .3. SYNTHESIS OFPEPTIDES CATALYZED BY ALPHA-CHYMOTRYPSIN IMMOBILIZED ON GRAFT-COPOLYMERS

Citation
Ar. Alcantara et al., ORGANIC-REACTIONS CATALYZED BY INSOLUBILIZED ENZYMES .3. SYNTHESIS OFPEPTIDES CATALYZED BY ALPHA-CHYMOTRYPSIN IMMOBILIZED ON GRAFT-COPOLYMERS, Journal of molecular catalysis. A, Chemical, 101(3), 1995, pp. 255-265
Citations number
32
Categorie Soggetti
Chemistry Physical
ISSN journal
13811169
Volume
101
Issue
3
Year of publication
1995
Pages
255 - 265
Database
ISI
SICI code
1381-1169(1995)101:3<255:OCBIE.>2.0.ZU;2-E
Abstract
alpha-Chymotrypsin (alpha-CT) has been covalently immobilized on polye thylene/2-hydroxyethyl methacrylate (PE/HEMA) graft copolymers, with l oadings of 33-87 mg of immobilized protein/g copolymer. These enzymati c derivatives have been used in the kinetically controlled synthesis o f dipeptides. The influence of the enzymatic loading, grafting and hyd rolysis degree of the supports on the synthesis of the model dipeptide Bz-L-Tyr-L-Leu-NH2 is discussed. Organic solvents with different log P values mixed in different proportions with an aqueous buffer have be en used as reaction media The best yields with respect to peptide synt hesis are obtained with ethyl acetate/buffer pH= 9.0 (2/1 v/v)). H-L-L eu-NH2 seems to be a better nucleophile than H-L-Ala-NH2, and Bz-L-Tyr -OEt seems to be a better acyl donor than Ac-L-Phe-OMe under the optim al experimental conditions.