Dichlorinated and Brominated Rugulovasines, Ergot Alkaloids Produced by Talaromyces wortmannii

Molecules. 2015 Sep 23;20(9):17627-44. doi: 10.3390/molecules200917627.

Abstract

UHPLC-DAD-HRMS based dereplication guided the detection of new halogenated alkaloids co-produced by Talaromyces wortmannii. From the fungal growth in large scale, the epimers 2,8-dichlororugulovasines A and B were purified and further identified by means of a HPLC-SPE/NMR hyphenated system. Brominated rugulovasines were also detected when the microbial incubation medium was supplemented with bromine sources. Studies from 1D/2D NMR and HRMS spectroscopy data allowed the structural elucidation of the dichlorinated compounds, while tandem MS/HRMS data analysis supported the rationalization of brominated congeners. Preliminary genetic studies revealed evidence that FADH₂ dependent halogenase can be involved in the biosynthesis of the produced halocompounds.

Keywords: Talaromyces; dereplication; halogenation; rugulovasine; tryptophan.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Products / chemistry
  • Biological Products / isolation & purification
  • Chromatography, High Pressure Liquid
  • Ergot Alkaloids / biosynthesis
  • Flavin-Adenine Dinucleotide / analogs & derivatives
  • Flavin-Adenine Dinucleotide / metabolism
  • Fungal Proteins / metabolism
  • Halogenation
  • Indoles / chemistry
  • Indoles / isolation & purification*
  • Molecular Structure
  • Talaromyces / chemistry*
  • Talaromyces / enzymology
  • Talaromyces / growth & development*

Substances

  • Biological Products
  • Ergot Alkaloids
  • Fungal Proteins
  • Indoles
  • rugulovasine B
  • Flavin-Adenine Dinucleotide
  • 1,5-dihydro-FAD
  • rugulovasine A