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Contrasting fates for 6-α-methylpenicillin N upon oxidation by deacetoxycephalosporin C synthase (DAOCS) and deacetoxy/deacetylcephalosporin C synthase (DAOC/DACS)

Authors :
Matthew D. Lloyd
Jack E. Baldwin
Christopher S Hamilton
Akito Yasuhara
Peter J. Rutledge
Source :
Bioorganic & Medicinal Chemistry Letters. 11:2511-2514
Publication Year :
2001
Publisher :
Elsevier BV, 2001.

Abstract

6-alpha-methylpenicillin N was synthesised via known routes from 6-aminopenicillanic acid, and tested as a substrate for recombinant DAOCS and DAOC/DACS. Incubation with DAOCS resulted in conversion of 2-oxoglutarate without oxidation of the penicillin substrate ('uncoupled turnover'). Incubation with DAOC/DACS resulted in oxidation to the cephem aldehyde. This is the first example of substrate-induced 'uncoupled turnover', which has been proposed to be an editing mechanism for these enzymes.

Details

ISSN :
0960894X
Volume :
11
Database :
OpenAIRE
Journal :
Bioorganic & Medicinal Chemistry Letters
Accession number :
edsair.doi.dedup.....a2f2085d7a5733662b5a94f5ad6ecd6e
Full Text :
https://doi.org/10.1016/s0960-894x(01)00470-x