Radler F, Herzberger S, Schönig I, Schwarz P
Institut für Mikrobiologie und Weinforschung, Johannes Gutenberg-Universität, Mainz, Germany.
J Gen Microbiol. 1993 Mar;139(3):495-500. doi: 10.1099/00221287-139-3-495.
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.
发现巴氏接合酵母412菌株可释放一种对酿酒酵母和光滑念珠菌的敏感菌株具有致死性的杀伤毒素(KT412)。通过超滤浓缩杀伤菌株的培养上清液,并通过凝胶过滤和离子交换色谱法纯化细胞外蛋白。对电泳均一的杀伤蛋白进行凝胶过滤和SDS-PAGE分析,结果表明其表观分子量为10 kDa。杀伤毒素KT412可能未进行糖基化,因为未检测到任何碳水化合物结构。KT412与敏感酵母细胞结合,但不与抗性酵母细胞结合。敏感酵母细胞壁的甘露聚糖部分而非葡聚糖部分是杀伤毒素结合的主要靶点。杀伤菌株巴氏接合酵母412含有三个双链RNA质粒,大小分别为1.9 kb、2.9 kb和4.0 kb。用环己酰亚胺进行消除导致杀伤活性和1.9 kb双链RNA种类同时丧失,因此该双链RNA被认为等同于酿酒酵母的杀伤毒素编码M质粒。