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A new linear peptide, higapeptin, isolated from the mud flat-derived fungus Acremonium persicinum inhibits mitochondrial energy metabolism.

Ahmed H El-DesokyYuki HitoraYoshitomo NishimeYusaku SadahiroTeppei KawaharaSachiko Tsukamoto
Published in: Journal of natural medicines (2024)
A combination of LC-MS/MS and feature-based molecular networking analyses led to the isolation of a new adenopeptin analog, higapeptin (1), and four known peptides, adenopeptin (2), adenopeptins B and C (3 and 4), and acremopeptin (5), from the rice culture of the fungus Acremonium persicinum (18F04103) isolated from a mud flat of the Ariake Sea in Kyushu, Japan. The structure of 1 was determined by NMR and MS/MS fragmentation analyses. The absolute configuration of the constituent amino acids was determined by Marfey's analysis after acid hydrolysis. The C-terminal residue was synthesized, and its absolute configuration was established by Marfey's analysis. Compounds 1 and 2 were found to inhibit mitochondrial energy metabolism, similar to efrapeptin D (6), a known mitochondrial ATPase inhibitor.
Keyphrases
  • oxidative stress
  • amino acid
  • ms ms
  • magnetic resonance
  • mass spectrometry
  • liquid chromatography tandem mass spectrometry
  • simultaneous determination
  • data analysis