Exchange of the valine 2-H in the biosynthesis of L-δ-(α-aminoadipoyl)-L-Cysteinyl-D-valine
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Cell-free synthesis of δ-(L-α-aminoadipyl)-L-cysteine, the first intermediate of penicillin and cephalosporin biosynthesis
2. Biosynthesis of peptides containing α-aminoadipic acid and cysteine in extracts of a Cephalosporium sp
3. [29] δ-(α-Aminoadipyl)cysteinylvaline synthetase
4. Accumulation of tripeptide derivatives by mutants of Cephalosporium acremonium.
5. A study of the biosynthesis of the tripeptide δ-(l-α-aminoadipyl)-l-cysteinyl-d-valine in a β-lactam-negative mutant of Cephalosporium acremonium
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1. l-δ-(α-Aminoadipoyl)-l-cysteine-d-valine Synthetase: Production of Dipeptides Containing Valine Residue at Its C-Terminus;Biochemical and Biophysical Research Communications;2002-04
2. Chemistry of some fluorescamine-amine derivatives with relevance to the biosynthesis of benzylpenicillin by fermentation;Journal of Chemical Technology & Biotechnology;2002
3. Biosynthesis of Sulfur-containing Natural Products;Comprehensive Natural Products Chemistry;1999
4. The Mechanism of ACV Synthetase;Chemical Reviews;1997-11-01
5. l-δ-(α-Aminoadipoyl)-l-cysteinyl-d-valine Synthetase: Thioesterification of Valine Is Not Obligatory for Peptide Bond Formation;Biochemistry;1997-07-01
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