| Literature DB >> 3873879 |
J E Baldwin, S E Moroney, H H Ting.
Abstract
The development of a coupled enzyme assay for the determination of isopenicillin N synthetase activity in purified extracts from Cephalosporium acremonium was described. Isopenicillin N formed from its precursor, delta-(L-alpha-aminoadipyl)-L-cysteinyl-D-valine (ACV), by the synthetase was hydrolyzed by beta-lactamase I to the corresponding penicilloic acid. Automatic titration of the acid with standard sodium hydroxide delivered by a pH-stat gave a continuous plot of product formed vs time. This assay has been used in kinetic studies and to determine the effects of pH, ionic strength, and temperature on the enzyme's activity.Entities:
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Year: 1985 PMID: 3873879 DOI: 10.1016/0003-2697(85)90345-8
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365