Palfree R G, Bussey H
Eur J Biochem. 1979 Feb 1;93(3):487-93. doi: 10.1111/j.1432-1033.1979.tb12847.x.
Killer toxin from killer strains of Saccharomyces cerevisiae was isolated from concentrates of extracellular medium by precipitation in poly(ethylene glycol) and chromatography through glyceryl-controlled-pore glass. The toxin migrated as a single protein band on sodium dodecyl sulfate/polyacrylamide gel electrophoresis. A molecular weight of 11470 was determined for the toxin protein from its electrophoretic mobility and amino acid composition. Gel filtration of the active toxin indicated that the 11,470-Mr monomer was the active unit. Electrophoretic comparison of extracellular concentrates from a killer strain and an isogenic non-killer showed the presence of the toxin protein only in the killer-derived material. The activity of the toxin was most stable between pH 4.2 and 4.6. At 30 degrees C toxin from a superkiller strain was more stable than that from a normal killer.
从酿酒酵母杀伤菌株中提取的杀伤毒素,是通过聚乙二醇沉淀和甘油控制孔径玻璃柱层析从细胞外培养基浓缩物中分离得到的。该毒素在十二烷基硫酸钠/聚丙烯酰胺凝胶电泳中呈现为单一蛋白条带。根据其电泳迁移率和氨基酸组成,测定该毒素蛋白的分子量为11470。活性毒素的凝胶过滤表明,分子量为11470的单体是活性单位。对杀伤菌株和同基因非杀伤菌株的细胞外浓缩物进行电泳比较,结果显示仅在杀伤菌株来源的物质中存在毒素蛋白。该毒素的活性在pH 4.2至4.6之间最为稳定。在30℃时,超杀伤菌株的毒素比正常杀伤菌株的毒素更稳定。