Biosynthetic studies of ebelactone A and B by 13C NMR spectrometry.
- 1 January 1982
- journal article
- research article
- Published by Japan Antibiotics Research Association in The Journal of Antibiotics
- Vol. 35 (12) , 1670-1674
- https://doi.org/10.7164/antibiotics.35.1670
Abstract
Biosynthetic pathways [in Streptomyces sp.] of ebelactone A and B were studied by 13C NMR spectroscopy. By using 13C-labeled compounds as precursors, it was determined that ebelactone A was derived from 1 molecule of acetic acid and 6 propionic acids and ebelactone B from 1 molecule of acetic acid, 5 propionic acids and 1 butyric acid.This publication has 4 references indexed in Scilit:
- Structural studies on ebelactone A and B esterase inhibitors produced by Actinomycetes.The Journal of Antibiotics, 1982
- Macrolides. Recent Progress in Chemistry and BiochemistryAngewandte Chemie International Edition in English, 1977
- Biosynthesis of rosamicin.The Journal of Antibiotics, 1976
- The biosynthesis of picromycin using 13C enriched precursors.The Journal of Antibiotics, 1976