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Model studies on carboxypeptidase Y catalyzed peptide synthesis in an aqueous-organic two-phase system
Authors:Peter Kuhl  Nina P. Zapevalova  Andreas Könnecke  Hans-Dieter Jakubke
Affiliation:(1) Sektion Biowissenschaften, Bereich Biochemie, Karl-Marx-Universität, DDR-7010 Leipzig, German Democratic Republic;(2) Institute of Protein Research, Academy of Sciences of the USSR, Poustchino, Moscow Region, USSR
Abstract:Carboxypeptidase Y catalyzes in a biphasic system containing carbon tetrachloride and carbonate buffer the reaction ofZ-Phe-OMe and variousZ-andBoc-protected dipeptide methyl esters with Val-NH2 and Leu-NH2, respectively. This method has been applied to the synthesis of the corresponding N-protected tripeptide amides on a preparative scale. Using a substrate—nucleophile ratio of only 1:2 or 1:3 the peptide derivatives are obtained in yields of 56–97%.Abbreviations: IUPAC-IUB rules for peptides are followed, see Eur. J. Biochem.27, 201 (1972).Boc=tert-butyloxycarbonyl,Z=benzyloxycarbonyl,-OMe=methyl ester, HPLC=high performance liquid chromatography, TLC=thin layer chromatography,CPD-Y=carboxypeptidase Y.
Keywords:Carboxypeptidase Y catalyzed peptide bond formation  Enzymic synthesis in biphasic systems  Peptide synthesis
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