A mutasynthesis approach with a Penicillium chrysogenum ΔroqA strain yields new roquefortine D analogues

Chembiochem. 2015 Apr 13;16(6):915-23. doi: 10.1002/cbic.201402686. Epub 2015 Mar 12.

Abstract

Penicillium chrysogenum, which lacks the roqA gene, processes synthetic, exogenously added histidyltryptophanyldiketopiperazine (HTD) to yield a set of roquefortine-based secondary metabolites also produced by the wild-type strain. Feeding a number of synthetic HTD analogues to the ΔroqA strain gives rise to the biosynthesis of a number of new roquefortine D derivatives, depending on the nature of the synthetic HTD added. Besides delivering semisynthetic roquefortine analogues, the mutasynthesis studies presented here also shed light on the substrate preferences and molecular mechanisms employed by the roquefortine C/D biosynthesis gene cluster, knowledge that may be tapped for the future development of more complex semisynthetic roquefortine-based secondary metabolites.

Keywords: Penicillium; alkaloids; antibiotics; diketopiperazines; mutasynthesis; roquefortines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Fungal Proteins / genetics*
  • Heterocyclic Compounds, 4 or More Rings / chemistry
  • Heterocyclic Compounds, 4 or More Rings / metabolism
  • Indoles / chemistry*
  • Indoles / metabolism*
  • Multigene Family / genetics
  • Mutation*
  • Penicillium chrysogenum / genetics*
  • Penicillium chrysogenum / metabolism*
  • Piperazines / chemistry
  • Piperazines / metabolism

Substances

  • Fungal Proteins
  • Heterocyclic Compounds, 4 or More Rings
  • Indoles
  • Piperazines
  • roquefortine