A role for paxilline in the biosynthesis of indole–diterpenoid penitrem mycotoxins
- 1 January 1989
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 8,p. 1539-1540
- https://doi.org/10.1039/p19890001539
Abstract
[14C] Paxilline was biosynthetically incorporated into penitrem A (3.1–8.7%), and when calculated to include penitrem E to a greater extent (3.3–17%), in submerged fermentations of Penicillium janczewskii; concurrent biotransformation of [14C] paxilline to a hydroxy derivative may indicate another intermediate in penitrem biosynthesis.This publication has 2 references indexed in Scilit:
- Paxilline biosynthesis by Acremonium loliae; a step towards defining the origin of lolitrem neurotoxinsPhytochemistry, 1987
- Paspalum staggers: isolation and identification of tremorgenic metabolites from sclerotia of Claviceps paspaliJournal of Agricultural and Food Chemistry, 1977