Rifamycin Biosynthesis Studied with 13C Enriched Precursors and Carbon Magnetic Resonance
- 1 June 1973
- journal article
- Published by Springer Nature in Nature
- Vol. 243 (5405) , 273-277
- https://doi.org/10.1038/243273a0
Abstract
No abstract availableThis publication has 28 references indexed in Scilit:
- Incorporation of [1-13C]butyrate into antibiotic X-537 A: 13C nuclear magnetic resonance studyJournal of the Chemical Society, Chemical Communications, 1972
- Carbon-13 Fourier transform nuclear magnetic resonance spectroscopy. II. Pattern of biosynthetic incorporation of [1-13C]- and [2-13C]acetate into prodigiosinJournal of the American Chemical Society, 1971
- Use of carbon-13 nuclear magnetic resonance (Cmr) spectroscopy in biosynthetic studies. Incorporation of carboxyl and methyl carbon-13 labeled acetates into cephalosporin CJournal of the American Chemical Society, 1971
- Biosynthetic studies with carbon-13. AsperlinJournal of the American Chemical Society, 1971
- Use of 13C in biosynthetic studies. Location of isotope from labelled acetate and formate in the fungal tropolone, sepedonin, by 13C nuclear magnetic resonance spectroscopyJournal of the Chemical Society D: Chemical Communications, 1971
- Biosynthetic studies with carbon-13: mollisinBiochemistry, 1970
- Biosynthetic studies with carbon-13: 13C nuclear magnetic resonance spectra of the metabolite sterigmatocystinJournal of the Chemical Society D: Chemical Communications, 1970
- Carbon-13 magnetic resonance. XIII. Assignment of carbon-13 resonances using the nuclear Overhauser effectJournal of the American Chemical Society, 1969
- Use of carbon-13 in biosynthetic studies. Incorporation of isotopically labelled acetate and formate into the fungal tropolone, sepedoninChemical Communications (London), 1968
- The Use of 13C-Labeled Acetate in Biosynthetic Studies1Journal of the American Chemical Society, 1966