Meroterpenoids from Penicillium citreo-viride B. IFO 4692 and 6200 hybrid

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

Twenty metabolites, citreohybridones, have been isolated from the mycelium of the hybrid strain KO 0031, prepared by cell fusion technique using Penicillium citreo-viride B. IFO 6200 and 4692. Their stereostructures have been elucidated on the basis of their spectral data and some chemical evidence, and their absolute configurations have been also elucidated by the modified Mosher's methods. Incorporation of 13C-labelled acetate, formate and ethyl 3,5-dimethylorsellinate into citreohybridones has established that their biosynthesis proceeds via a mixed polyketide-terpenoid (meroterpenoid) pathway.

Original languageEnglish
Pages (from-to)5055-5072
Number of pages18
JournalTetrahedron
Volume59
Issue number27
DOIs
Publication statusPublished - 2003 Jun 30

Fingerprint

Polyketides
Cell Fusion
Penicillium
Mycelium
Biosynthesis
Terpenes
Metabolites
Acetates
Fusion reactions
ethyl formate
ethyl acetate

Keywords

  • Absolute configuration
  • Antifeedant
  • Biosynthesis
  • Citreohybridone
  • Hybrid strain
  • Meroterpenoid
  • Penicillium citreo-viride B

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Meroterpenoids from Penicillium citreo-viride B. IFO 4692 and 6200 hybrid. / Kosemura, Seiji.

In: Tetrahedron, Vol. 59, No. 27, 30.06.2003, p. 5055-5072.

Research output: Contribution to journalArticle

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