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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)
- 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.
- Subjects :
- Models, Molecular
Magnetic Resonance Spectroscopy
Penicillin binding proteins
Protein Conformation
Stereochemistry
Clinical Biochemistry
Pharmaceutical Science
Penicillins
Biochemistry
Aldehyde
Drug Discovery
Penicillin-Binding Proteins
Intramolecular Transferases
Molecular Biology
chemistry.chemical_classification
Cephem
biology
ATP synthase
Deacetoxycephalosporin-C synthase
Chemistry
Organic Chemistry
Substrate (chemistry)
Active site
Recombinant Proteins
Enzyme
Oxygenases
biology.protein
Molecular Medicine
Oxidation-Reduction
Subjects
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