Oxidative Ring Contraction by a Multifunctional Dioxygenase Generates the Core Cycloocatadiene in the Biosynthesis of Fungal Dimeric Anhydride Zopfiellin

Org Lett. 2020 Mar 6;22(5):1997-2001. doi: 10.1021/acs.orglett.0c00340. Epub 2020 Feb 17.

Abstract

To elucidate the biosynthesis of a fungicidal dimeric anhydride zopfiellin, the putative biosynthetic gene cluster was identified. We conducted heterologous expression of candidate genes for the synthesis of maleic anhydride and its dimerization and identified the two isomeric dimers with 9-membered rings as products. Notably, α-ketoglutarate-dependent dioxygenase ZopK oxidized one of the dimers, giving the 8-membered ring of zopfiellin. The mechanism of oxidative rearrangement is proposed by analyzing the incorporation of 13C-labeled precursors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anhydrides
  • Cyclooctanes / chemistry*
  • Dimerization
  • Dioxygenases / chemistry
  • Dioxygenases / metabolism*
  • Fungi / chemistry*
  • Fungi / metabolism
  • Fungicides, Industrial
  • Maleic Anhydrides / chemistry*
  • Molecular Structure
  • Multigene Family
  • Oxidative Stress

Substances

  • Anhydrides
  • Cyclooctanes
  • Fungicides, Industrial
  • Maleic Anhydrides
  • zopfiellin
  • Dioxygenases