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Roles of 2-oxoglutarate oxygenases and isopenicillin N synthase in ß-lactam biosynthesis.
Rabe, Patrick; Kamps, Jos J A G; Schofield, Christopher J; Lohans, Christopher T.
Afiliación
  • Rabe P; Department of Chemistry, Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford, OX1 3TA, UK. christopher.schofield@chem.ox.ac.uk christopher.lohans@chem.ox.ac.uk.
  • Kamps JJAG; Department of Chemistry, Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford, OX1 3TA, UK. christopher.schofield@chem.ox.ac.uk christopher.lohans@chem.ox.ac.uk.
  • Schofield CJ; Department of Chemistry, Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford, OX1 3TA, UK. christopher.schofield@chem.ox.ac.uk christopher.lohans@chem.ox.ac.uk.
  • Lohans CT; Department of Chemistry, Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford, OX1 3TA, UK. christopher.schofield@chem.ox.ac.uk christopher.lohans@chem.ox.ac.uk.
Nat Prod Rep ; 35(8): 735-756, 2018 08 15.
Article en En | MEDLINE | ID: mdl-29808887
ABSTRACT
Covering up to 2017 2-Oxoglutarate (2OG) dependent oxygenases and the homologous oxidase isopenicillin N synthase (IPNS) play crucial roles in the biosynthesis of ß-lactam ring containing natural products. IPNS catalyses formation of the bicyclic penicillin nucleus from a tripeptide. 2OG oxygenases catalyse reactions that diversify the chemistry of ß-lactams formed by both IPNS and non-oxidative enzymes. Reactions catalysed by the 2OG oxygenases of ß-lactam biosynthesis not only involve their typical hydroxylation reactions, but also desaturation, epimerisation, rearrangement, and ring-forming reactions. Some of the enzymes involved in ß-lactam biosynthesis exhibit remarkable substrate and product selectivities. We review the roles of 2OG oxygenases and IPNS in ß-lactam biosynthesis, highlighting opportunities for application of knowledge of their roles, structures, and mechanisms.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oxidorreductasas / Beta-Lactamas / Oxigenasas de Función Mixta Idioma: En Revista: Nat Prod Rep Asunto de la revista: QUIMICA Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oxidorreductasas / Beta-Lactamas / Oxigenasas de Función Mixta Idioma: En Revista: Nat Prod Rep Asunto de la revista: QUIMICA Año: 2018 Tipo del documento: Article