Design of proteinase-cataiyzed synthesis of oligopeptides in an aqueous-organic biphasic system

Kazuhiro Nakanishi, Yukitaka Kimura, Ryuichi Matsuno

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

Thermolysin-catalyzed condensation of N - (benzylxycarbyl) - glycyl - glycyl - L -phenylalanyl-L-leucine ethyl ester (Z-Gly-GlyPheLeuOEt), the precursor of the des-TyrMeucine enkephalin from N-(benzyl-oxycarbonyl)-glycyl-glycine (Z-GlyGly) and L-phenylalanyl-L-leucine ethyl ester (PheLeuOEt) was elucidated as a model reaction for the enzymatic synthesis of oligopeptides with many side reactions. In buffer solution, the yield of Z-GlyGly-PheLeuOEt was extremely low with considerable by-products. A large increase in both yield and purity became possible in the aqueous-organic biphasic system by the systematic selection of experimental conditions.

Original languageEnglish
Pages (from-to)452-454
Number of pages3
JournalBio/Technology
Volume4
Issue number5
DOIs
Publication statusPublished - 1986
Externally publishedYes

    Fingerprint

ASJC Scopus subject areas

  • Biotechnology

Cite this