Hydroxylation of the triterpenoid nigranoic acid by the fungus Gliocladium roseum YMF1.00133

Chem Biodivers. 2007 Feb;4(2):112-7. doi: 10.1002/cbdv.200790015.

Abstract

The ability of the fungus Gliocladium roseum YMF1.00133 to transform the bioactive nigranoic acid (=(24Z)-9,19-cyclo-3,4-secolanosta-4(28),24-diene-3,26-dioic acid) was investigated. Three new products from the co-cultures of nigranoic acid and G. roseum YMF1.00133 were obtained by employing a combination of Sephadex LH-20 and silica-gel column chromatography. The major metabolite was identified as 15beta-hydroxynigranoic acid, and the minor metabolites as 6alpha,15beta-dihydroxynigranoic acid and 7beta,15beta-dihydroxynigranoic acid by mass spectrometry and NMR spectroscopy. This is the first report of the biotransformation of the A-ring-secocycloartene triterpenoid, nigranoic acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Gliocladium / metabolism*
  • Hydroxylation
  • Mass Spectrometry
  • Triterpenes / chemistry
  • Triterpenes / metabolism*

Substances

  • Triterpenes
  • nigranoic acid