Penicillin biosynthesis the immediate origin of the sulphur atom
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Incorporation of 3H from δ-(l-α-amino (4,5-3H)adipyl)-l-cysteinyl-d-(4,4-3H)valine into isopenicillin N
2. Cell-free conversion of δ-(l-α-aminoadipyl)-l-cysteinyl-d-valine into an antibiotic with the properties of isopenicillin N in Cephalosporium acremonium
3. Purification of isopenicillin N synthetase
4. Stepwise ring closure in penicillin biosynthesis. Intitial β-lactam formation
5. Inhibition of penicillin biosynthesis by δ-(L-α-amino-δ-adipyl)-L-cysteinylglycine. Evidence for initial β-lactam ring formation
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