Biochemistry

Investigation of a Killer Strain of Zygosaccharomyces Bailii

  • Institut für Mikrobiologie und Weinforschung der Johannes Gutenberg-Universität, Postfach 3980, D-6500 Mainz, Germany
  • *Author for correspondence. Tel. 49 6131 392662; fax 49 6131 392695.
  • Journal of General Microbiology 1993; 139(3):495–500 · https://doi.org/10.1099/00221287-139-3-495

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    Abstract

    Summary: The yeast Zygosaccharomyces bailii strain 412 was found to liberate a killer toxin (KT412) lethal to sensitive strains of Saccharomyces cerevisiae and Candida glabrata. Culture supernatants of the killer strain were concentrated by ultrafiltration and the extracellular protein was purified by gel filtration and ion-exchange chromatography. Gel filtration and SDS-PAGE of the electrophoretically homogeneous killer protein indicated an apparent molecular mass of 10 kDa. The killer toxin KT412 is probably not glycosylated since it did not show any detectable carbohydrate structures. KT412 was bound to sensitive but not to resistant yeast cells. The mannan, and not the glucan, fraction of the cell wall of the sensitive yeast was the primary target for the killer toxin binding. The killer strain Z. bailii 412 contained three double-stranded RNA plasmids of 1·9, 2·9 and 4·0 kb. Curing by cycloheximide resulted in the concomitant loss of killer activity and the 1·9 kb dsRNA species that is therefore regarded as equivalent to the killer-toxin-coding M-plasmids of S. cerevisiae.