Marine Drugs (Nov 2013)

Crambescidin-816 Acts as a Fungicidal with More Potency than Crambescidin-800 and -830, Inducing Cell Cycle Arrest, Increased Cell Size and Apoptosis in Saccharomyces cerevisiae

  • Félix V. Vega,
  • Mercedes R. Vieytes,
  • Luis M. Botana,
  • Olivier P. Thomas,
  • Henar López-Alonso,
  • Juan A. Rubiolo,
  • Eva Ternon

DOI
https://doi.org/10.3390/md11114419
Journal volume & issue
Vol. 11, no. 11
pp. 4419 – 4434

Abstract

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In this paper, we show the effect of crambescidin-816, -800, and -830 on Saccharomyces cerevisiae viability. We determined that, of the three molecules tested, crambescidin-816 was the most potent. Based on this result, we continued by determining the effect of crambescidin-816 on the cell cycle of this yeast. The compound induced cell cycle arrest in G2/M followed by an increase in cell DNA content and size. When the type of cell death was analyzed, we observed that crambescidin-816 induced apoptosis. The antifungal effect indicates that crambescidins, and mostly crambescidin-816, could serve as a lead compound to fight fungal infections.

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