Marine Drugs (Jul 2023)

Anthraquinone Derivatives and Other Aromatic Compounds from Marine Fungus <i>Asteromyces cruciatus</i> KMM 4696 and Their Effects against <i>Staphylococcus aureus</i>

  • Olesya I. Zhuravleva,
  • Ekaterina A. Chingizova,
  • Galina K. Oleinikova,
  • Sofya S. Starnovskaya,
  • Alexandr S. Antonov,
  • Natalia N. Kirichuk,
  • Alexander S. Menshov,
  • Roman S. Popov,
  • Natalya Yu. Kim,
  • Dmitrii V. Berdyshev,
  • Artur R. Chingizov,
  • Alexandra S. Kuzmich,
  • Irina V. Guzhova,
  • Anton N. Yurchenko,
  • Ekaterina A. Yurchenko

DOI
https://doi.org/10.3390/md21080431
Journal volume & issue
Vol. 21, no. 8
p. 431

Abstract

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New anthraquinone derivatives acruciquinones A–C (1–3), together with ten known metabolites, were isolated from the obligate marine fungus Asteromyces cruciatus KMM 4696. Acruciquinone C is the first member of anthraquinone derivatives with a 6/6/5 backbone. The structures of isolated compounds were established based on NMR and MS data. The absolute stereoconfigurations of new acruciquinones A–C were determined using ECD and quantum chemical calculations (TDDFT approach). A plausible biosynthetic pathway of the novel acruciquinone C was proposed. Compounds 1–4 and 6–13 showed a significant antimicrobial effects against Staphylococcus aureus growth, and acruciquinone A (1), dendryol B (4), coniothyrinone B (7), and ω-hydroxypachybasin (9) reduced the activity of a key staphylococcal enzyme, sortase A. Moreover, the compounds, excluding 4, inhibited urease activity. We studied the effects of anthraquinones 1, 4, 7, and 9 and coniothyrinone D (6) in an in vitro model of skin infection when HaCaT keratinocytes were cocultivated with S. aureus. Anthraquinones significantly reduce the negative impact of S. aureus on the viability, migration, and proliferation of infected HaCaT keratinocytes, and acruciquinone A (1) revealed the most pronounced effect.

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