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publicationDate 1989-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4847200-A
titleOfInvention Biosynthesis of unnatural cephalosporins
abstract A process for producing unnatural penicillins and cephalosporin derivatives thereof in which peptide analogs of ACV in which the L- alpha -aminodipyl moiety is replaced by L-S-carboxymethyl cysteine or other obvious substituents, are reacted with cyclase, epimerase, ring expansion and hydroxylase enzymes isolated from a cell free extract of a prokaryotic organism such as S. clavuligerus. The product depends upon the presence or absence of co-factors such as ferrous ion, alpha -ketoglutarate, and ascorbate. In an alternative embodiment, a penicillin analog having the formula: <IMAGE> may be reduced with L-cysteine to produce an analog of isopenicillin N which may be reacted with the enzyme reagent to produce the desired penicillin or cephalosporin.
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