Biosynthèse de L'Averufine et de la Versicolorine B: Deux Metabolites de L'Aspergillus Versicolor
- 1 January 1976
- journal article
- research article
- Published by Wiley in Bulletin des Sociétés Chimiques Belges
- Vol. 85 (5), 271-276
- https://doi.org/10.1002/bscb.19760850503
Abstract
The labeling distribution of averufin and versicolorin B produced from (1‐13C) acetate by Aspergillus versicolor was determined by 13C FT NMR. The results support the polyketide hypothesis for averufin and versicolorin B biogenesis. The pattern of versicolorin B indicates a biogenetic relationship with bisfuranoids, sterigmatocystin and aflatoxins.This publication has 8 references indexed in Scilit:
- Synthesis of versicolorin A by a mutant strain of Aspergillus parasiticus deficient in aflatoxin productionJournal of Agricultural and Food Chemistry, 1975
- Biosynthesis of averufin from acetate by Aspergillus parasiticusJournal of Agricultural and Food Chemistry, 1975
- 13C nuclear magnetic resonance spectra of aflatoxin B1 derived from acetateTetrahedron, 1975
- Study of the biosynthesis of sterigmatocystin and reassignment of 13C nuclear magnetic resonance spectrumJournal of the Chemical Society, Chemical Communications, 1975
- Biosynthesis of aflatoxin B1 from [2-13C]- and [1,2-13C]-acetateJournal of the Chemical Society, Chemical Communications, 1975
- Utilization of 13C-13C coupling in structural and biosynthetic studies V. The 13C ft nmr spectrum of sterigmatocystinTetrahedron Letters, 1974
- Conversion of sterigmatocystin to aflatoxin B1 byBiochemical and Biophysical Research Communications, 1973
- Biosynthetic studies with carbon-13: 13C nuclear magnetic resonance spectra of the metabolite sterigmatocystinJournal of the Chemical Society D: Chemical Communications, 1970