Antimicrobial Oligophenalenone Dimers from the Soil Fungus Talaromyces stipitatus

J Nat Prod. 2016 Dec 23;79(12):2991-2996. doi: 10.1021/acs.jnatprod.6b00458. Epub 2016 Dec 14.

Abstract

New polyketide-derived oligophenalenone dimers, 9a-epi-bacillisporin E (1) and bacillisporins F-H (2-5), along with the known bacillisporin A (6), were isolated from the fungus Talaromyces stipitatus. Their structures and absolute configurations were determined on the basis of spectroscopic analyses, electronic circular dichroism, and GIAO NMR shift calculation followed by DP4 analysis. The antimicrobial activity of these compounds was evaluated against a panel of human pathogenic bacteria. Among them, bacillisporin H (5) exhibited antimicrobial activity together with modest cytotoxicity against HeLa cells.

MeSH terms

  • Anti-Infective Agents / chemistry
  • Anti-Infective Agents / isolation & purification*
  • Anti-Infective Agents / pharmacology*
  • Bacteria / drug effects
  • Enterococcus faecalis / drug effects
  • Escherichia coli / drug effects
  • HeLa Cells
  • Humans
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Nuclear Magnetic Resonance, Biomolecular
  • Phenalenes / chemistry
  • Phenalenes / isolation & purification*
  • Phenalenes / pharmacology*
  • Soil Microbiology
  • Staphylococcus aureus / drug effects
  • Talaromyces / chemistry*

Substances

  • Anti-Infective Agents
  • Phenalenes
  • bacillisporin E
  • phenalen-1-one