Genome Mining of α-Pyrone Natural Products from Ascidian-Derived Fungus Amphichordafelina SYSU-MS7908

Mar Drugs. 2022 Apr 27;20(5):294. doi: 10.3390/md20050294.

Abstract

Culturing ascidian-derived fungus Amphichorda felina SYSU-MS7908 under standard laboratory conditions mainly yielded meroterpenoid, and nonribosomal peptide-type natural products. We sequenced the genome of Amphichorda felina SYSU-MS7908 and found 56 biosynthetic gene clusters (BGCs) after bioinformatics analysis, suggesting that the majority of those BGCSs are silent. Here we report our genome mining effort on one cryptic BGC by heterologous expression in Aspergillus oryzae NSAR1, and the identification of two new α-pyrone derivatives, amphichopyrone A (1) and B (2), along with a known compound, udagawanone A (3). Anti-inflammatory activities were performed, and amphichopyrone A (1) and B (2) displayed potent anti-inflammatory activity by inhibiting nitric oxide (NO) production in RAW264.7 cells with IC50 values 18.09 ± 4.83 and 7.18 ± 0.93 μM, respectively.

Keywords: Aspergillus oryzae NSAR1; anti-inflammatory activity; genome mining; heterologous expression; α-pyrone natural products.

MeSH terms

  • Animals
  • Beauveria* / metabolism
  • Biological Products* / metabolism
  • Biological Products* / pharmacology
  • Pyrones / pharmacology
  • Urochordata* / genetics
  • Urochordata* / metabolism

Substances

  • Biological Products
  • Pyrones

Supplementary concepts

  • Beauveria felina