Anti-Candida activity of a novel killer toxin from the yeast Williopsis mrakii
Abstract
A screening of putative killer yeast strains showed that spore-forming ascomycetous yeasts of the genera Pichia and Williopsis displayed the broadest range of activity against sensitive strains of Candida spp. and Saccharomyces cerevisiae. Williopsis mrakii(NCYC 500) showed extensive anti-Candida activity against strains isolated from clinical specimens.W. mrakii killer factor was produced in minimal media as a function of growth and its activity reached constant levels as cells entered stationary phase. The proteinaceous killer toxin was found to be unstable outwith a specific range of temperature and pH (above 30 �C and pH 4�0), and further analysis showed that the active toxin molecule was an acidic polypeptide with a relative molecular mass between 1�8-5�0 kDa. At critical concentrations the killer factor exerted a greater effect on stationary phase cells of Candida than cells from an exponential phase of growth. At low concentrations, the killer toxin produced a fungistatic effect on sensitive yeasts but at higher concentrations there was evidence to suggest that membrane damage accounted for the zymocidal effects of the killer factor. The cidal nature of the toxin was reflected in a rapid decrease in sensitive cell viability. Findings presented suggest that W. mrakii killer toxin has potential as a novel antimycotic agent in combatting medically important strains of Candida.
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Cyberlindnera sargentensis (synonym Williopsis sargentensis) belongs to a genus of yeasts that have been shown to promote plant growth, produce volatile sulphur compounds, and kill other fungi or bacteria via killer proteins.
“Cyberlindnera sargentensis (synonym Williopsis sargentensis) belongs to a genus of yeasts that have been shown to promote plant growth, produce volatile sulphur compounds, and kill other fungi or bacteria via killer proteins [83–88].”
From Competition assays and physiological experiments of soil and phyllosphere yeasts identify Candida subhashii as a novel antagonist of filamentous fungi (2017) · cites this paper as [86]
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Al-Qaysi, S. A. S., Al-Haideri, H., Thabit, Z. A., Al-Kubaisy, W. H. A. A.-R., & Ibrahim, J. A. A.-R. (2017) · International Journal of Microbiology · doi:10.1155/2017/2605382 · Cited by 49 · see citing works
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- Authors
- Hodgson, V. J., Button, D., & Walker, G. M.
- Affiliations
- Abertay University (GB)
- Corresponding author
- Walker, Graeme M.
- ORCID
- Walker, Graeme M.
- Venue
- Microbiology
- Publisher
- Microbiology Society
- Published
- 1995-08-01
- Volume
- 141
- Issue
- 8
- Pages
- 2003-2012
- ISSN
- 1350-0872 (ISSN-L)
- 1465-2080
- OpenAlex
- W2104262753
- Cited by
- 73
- References
- 0
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 2 · 2023: 2 · 2022: 2 · 2021: 2 · 2020: 4 · 2019: 1 · 2018: 1 · 2017: 4 · 2016: 6 · 2015: 2 · 2014: 3 · 2013: 1 · 2012: 1
- FWCI
- 0.92
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Microbiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Directorate for Biological Sciences
- Biotechnology and Biological Sciences Research Council
- Topics
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Yeasts and Rust Fungi Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Keywords
- killer toxin, anti-Candida activity, Candida, Pichia, Saccharomyces cerevisiae, acidic polypeptides, stationary phase, membrane damage, fungistatic activity, antifungal agents, clinical isolates
- MeSH terms
- Antifungal Agents, Candida, Cell Membrane Permeability, Chromatography, Gel, Culture Media, Dose-Response Relationship, Drug, Saccharomycetales, Microbial Sensitivity Tests, Time Factors, Toxins, Biological, Yeasts, Colony Count, Microbial
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