13C‐NMR evidence for the biosynthetic incorporation of acetate into minimycin and compounds related to krebs cycle
- 1 August 1977
- journal article
- Published by Wiley in FEBS Letters
- Vol. 80 (1), 53-56
- https://doi.org/10.1016/0014-5793(77)80405-5
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Biosynthesis of the C-nucleoside, minimycin: Asymmetric incorporation of glutamate and acetate into the oxazine ring.The Journal of Antibiotics, 1977
- N.M.R. with stable isotopes in biosynthetic studiesPublished by Royal Society of Chemistry (RSC) ,1976
- Biosynthesis of the polyoxins, nucleoside peptide antibiotics. Glutamate as an origin of 2-amino-2-deoxy-L-xylonic acid (polyoxamic acid)Biochemistry, 1975
- Use of carbon-13 magnetic resonance spectroscopy for biosynthetic investigationsAccounts of Chemical Research, 1975
- THE BIOSYNTHESIS OF THE NUCLEOSIDE ANTIBIOTICS: MINIMYCIN FORMATION BY STREPTOMYCES HYGROSCOPICUS*Annals of the New York Academy of Sciences, 1975
- Carbon-13 nuclear magnetic resonance in biosynthetic studiesChemical Society Reviews, 1975
- Tautomerism of the nucleoside antibiotic formycin, as studied by carbon-13 nuclear magnetic resonanceJournal of the American Chemical Society, 1973
- Carbon‐13 NMR spectra of C‐nucleosides. Showdomycin and β‐PseudouridineJournal of Heterocyclic Chemistry, 1973
- THE STRUCTURE OF MINIMYCIN, A NOVEL CARBON-LINKED NUCLEOSIDE ANTIBIOTIC RELATED TO β-PSEUDOURIDINEThe Journal of Antibiotics, 1972
- A method of increasing sensitivity in carbon-13 nuclear magnetic resonance spectroscopy via a heteronuclear Overhauser effect without loss of spin–spin coupling informationJournal of the Chemical Society D: Chemical Communications, 1970