Biosynthesis of (-)-Vinigrol

Angew Chem Int Ed Engl. 2025 Jan 21;64(4):e202416795. doi: 10.1002/anie.202416795. Epub 2024 Nov 16.

Abstract

(-)-Vinigrol is one of the most complex and challenging molecules in total synthesis; however, the parallel biosynthetic strategy employed by nature for the synthesis of this compound has not yet been identified. In this study, we identified a minimal gene cluster encoding a diterpene cyclase (VniA) and a cytochrome P450 (VniB) which enables the synthesis of (-)-vinigrol through three steps. VniA first cyclizes geranylgeranyl diphosphate to generate an unusual vinigrol-type diterpene skeleton, and then VniB catalyzes the allylic C(sp3)-H iterative oxidation. Further genome mining investigation provides new fungal sources for this rare and valuable vinigrol-type diterpene skeleton.

Keywords: Biosynthesis; Cytochrome P450; Diterpene Cyclase; Genome Mining; Vinigrol-type skeleton.

MeSH terms

  • Cytochrome P-450 Enzyme System / genetics
  • Cytochrome P-450 Enzyme System / metabolism
  • Diterpenes* / chemistry
  • Diterpenes* / metabolism
  • Molecular Structure
  • Multigene Family
  • Stereoisomerism

Substances

  • Diterpenes
  • Cytochrome P-450 Enzyme System