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Enzymatic dimerization of penicillin X.
- Source :
-
The Journal of antibiotics [J Antibiot (Tokyo)] 1993 Jan; Vol. 46 (1), pp. 141-8. - Publication Year :
- 1993
-
Abstract
- Penicillin X methyl ester was transformed into three types of dimer by laccase from Coriolus versicolor. The dimers are considered to be formed by free-radical addition of phenoxy radicals produced by laccase. The enzyme reaction with the ester as substrate was more suitable for forming dimers than that with the sodium salt as substrate. Penicillin X pivaloyloxymethyl ester was also transformed into a dimer, which had antibacterial activity in the presence of esterase.
- Subjects :
- Anti-Bacterial Agents pharmacology
Bacteria drug effects
Chromatography, High Pressure Liquid
Esters
Free Radicals chemistry
Laccase
Magnetic Resonance Spectroscopy
Microbial Sensitivity Tests
Penicillin G chemistry
Penicillin G pharmacology
Penicillins chemistry
Penicillins pharmacology
Substrate Specificity
Anti-Bacterial Agents chemistry
Oxidoreductases chemistry
Penicillin G analogs & derivatives
Subjects
Details
- Language :
- English
- ISSN :
- 0021-8820
- Volume :
- 46
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- The Journal of antibiotics
- Publication Type :
- Academic Journal
- Accession number :
- 8436547
- Full Text :
- https://doi.org/10.7164/antibiotics.46.141