Assignment of Absolute Configurations of Two Promising Anti- Helicobacter pylori Agents from the Marine Sponge-Derived Fungus Aspergillus niger L14

Molecules. 2021 Aug 20;26(16):5061. doi: 10.3390/molecules26165061.

Abstract

A chemical investigation into endozoic fungus Aspergillus niger L14 derived from the marine sponge of Reniera japonica collected off Xinghai Bay (China) resulted in the isolation of two dimeric naphtho-γ-pyrones, fonsecinone A (1) and isoaurasperone A (2). Through a combination of ECD spectra and X-ray diffraction analysis, the chiral axes of compounds 1 and 2 were unambiguously determined as Rα-configurations. Bioassay results indicated that these substances exhibited remarkably inhibitory effects on human pathogens Helicobacter pylori G27 and 159 with MIC values of ≤4 μg/mL, which are similar to those of the positive control, ampicillin sodium. To the best of our knowledge, this is the first report on absolute configuration of 1 and crystallographic data of 2, as well as their potent anti-H. pylori activities.

Keywords: Aspergillus niger; anti Helicobacter pylori; aurasperone A; chiral axis; endozoic fungus; fonsecinone A.

MeSH terms

  • Ampicillin / pharmacology
  • Animals
  • Anti-Bacterial Agents / metabolism*
  • Anti-Bacterial Agents / pharmacology*
  • Aspergillus niger / metabolism*
  • Helicobacter pylori / drug effects*
  • Microbial Sensitivity Tests
  • Porifera / metabolism*
  • Pyrones / metabolism
  • Pyrones / pharmacology

Substances

  • Anti-Bacterial Agents
  • Pyrones
  • Ampicillin