Study of the mechanism of ε-poly-l-lysine as an antifungal on Candida albicans and Saccharomyces cerevisiae

Biochim Biophys Acta Gen Subj. 2022 Oct;1866(10):130197. doi: 10.1016/j.bbagen.2022.130197. Epub 2022 Jun 19.

Abstract

The antimicrobial activity of ε-poly-l-lysine (EPL) has been documented, but its antifungal activity on yeast is not well defined and its mechanism of action has been vaguely explained. Our studies revealed that on both, Candida albicans and Saccharomyces cerevisiae, the minimum inhibitory concentration (MIC) and the minimum fungicidal concentration (MFC) were 250 μg·mL-1; EPL produced a K+ and Ca2+ efflux, and at higher concentrations also an efflux of material absorbing at 260 nm, small peptides, and phosphate is produced, along with the inhibition of fermentation and extracellular acidification and respiration. Moreover, growth was inhibited, reactive oxygen species (ROS) production increased, and cell viability decreased. The polycation also produced plasma membrane potential hyperpolarization. The effects were dependent both on the cell quantity and polycation concentration, as well as the media used. The plasma membrane disruption was confirmed by TEM and PI staining.

Keywords: Antifungals; Antimicrobial; Candida; Polycations; Saccharomyces; ε-poly-l-lysine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antifungal Agents* / metabolism
  • Antifungal Agents* / pharmacology
  • Candida albicans* / metabolism
  • Microbial Sensitivity Tests
  • Polylysine / metabolism
  • Polylysine / pharmacology
  • Saccharomyces cerevisiae / metabolism

Substances

  • Antifungal Agents
  • Polylysine