Issue 22, 1983
From the journal:

Journal of the Chemical Society, Chemical Communications

Penicillin biosynthesis. Dual pathways from a modified substrate

Jack E. Baldwin,   Edward P. Abraham,   Robert M. Adlington,   Bulbul Chakravarti,   Andrew E. Derome,   John A. Murphy,   Leslie D. Field,   Nicholas B. Green,   Hong-Hoi Ting  and  John J. Usher  

Abstract

Preparations of the enzyme isopenicillin N synthetase from Cephalosporium acremonium convert the modified substrate (L-α-amino-δ-adipyl)-L-cysteinyl-D-(α-aminobutyrate) into both penam and cepham products, which have been isolated and their structures established.

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Article information

DOI
https://doi.org/10.1039/C39830001317
Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 1317-1319

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Penicillin biosynthesis. Dual pathways from a modified substrate

J. E. Baldwin, E. P. Abraham, R. M. Adlington, B. Chakravarti, A. E. Derome, J. A. Murphy, L. D. Field, N. B. Green, H. Ting and J. J. Usher, J. Chem. Soc., Chem. Commun., 1983, 1317 DOI: 10.1039/C39830001317

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