FtmOx1, a non-heme Fe(II) and alpha-ketoglutarate-dependent dioxygenase, catalyses the endoperoxide formation of verruculogen in Aspergillus fumigatus

Org Biomol Chem. 2009 Oct 7;7(19):4082-7. doi: 10.1039/b908392h. Epub 2009 Aug 6.

Abstract

Verruculogen is a tremorgenic mycotoxin and contains an endoperoxide bond. In this study, we describe the cloning, overexpression and purification of a non-heme Fe(ii) and alpha-ketoglutarate-dependent dioxygenase FtmOx1 from Aspergillus fumigatus, which catalyses the conversion of fumitremorgin B to verruculogen by inserting an endoperoxide bond between two prenyl moieties. Incubation with (18)O(2)-enriched atmosphere demonstrated that both oxygen atoms of the endoperoxide bond are derived from one molecule of O(2). FtmOx1 is the first endoperoxide-forming non-heme Fe(ii) and alpha-ketoglutarate-dependent dioxygenase reported so far. A mechanism of FtmOx1-catalysed verruculogen formation is postulated and discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aspergillus fumigatus / enzymology*
  • Biocatalysis*
  • Chromatography, High Pressure Liquid
  • Dioxygenases / chemistry
  • Dioxygenases / metabolism*
  • Heme
  • Indoles / chemistry
  • Indoles / metabolism*
  • Iron / metabolism*
  • Ketoglutaric Acids / metabolism*
  • Peroxides / chemistry*
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Indoles
  • Ketoglutaric Acids
  • Peroxides
  • verruculogen
  • Heme
  • Iron
  • Dioxygenases