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Expression of pGKL killer 28K subunit in Saccharomyces cerevisiae: identification of 28K subunit as a killer protein.

机译:pGKL杀手28K亚基在酿酒酵母中的表达:28K亚基作为杀手蛋白的鉴定。

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摘要

Saccharomyces cerevisiae and other yeast cells harboring the linear double stranded (ds) DNA plasmids pGKL1 and pGKL2 secrete a killer toxin consisting of 97K, 31K and 28K subunits into the culture medium (EMBO J. 5, 1995-2002 (1986), Nucleic Acids Res., 15, 1031-1046 (1987]. The 28K subunit of the killer toxin was successfully expressed in S. cerevisiae when it was cloned on a circular plasmid with its putative promoter region replaced with that of S. cerevisiae chromosomal genes. The expression of the 28K subunit of the killer toxin in killer-sensitive cells resulted in the death of the host cells. This killing activity by the 28K subunit was prevented by the expression of the killer immunity, indicating that the killing activity of the killer toxin complex was carried out by the 28K subunit. Although the 28K subunit was synthesized as a intact precursor protein with its own signal sequence, it was not secreted into the culture medium but remained in the host cells. This indicated that 28K subunit killed host cells from inside of the cells rather than from outside. We further suggested that 28K killer subunit without 97K and 31K subunits did not kill the killer-sensitive cells from outside.
机译:带有线性双链(ds)DNA质粒pGKL1和pGKL2的酿酒酵母和其他酵母细胞向培养基中分泌由97K,31K和28K亚基组成的杀手毒素(EMBO J.5,1995-2002(1986),核酸Res。,15,1031-1046(1987)。当将杀伤毒素的28K亚单位克隆到环状质粒中,推定的启动子区域被啤酒酵母染色体基因替换后,就成功地在啤酒酵母中表达了它。在杀伤敏感细胞中杀伤毒素28K亚基的表达导致宿主细胞的死亡,通过表达杀伤免疫力来阻止28K亚基的这种杀伤活性,这表明杀伤毒素复合物的杀伤活性。尽管28K亚基是作为完整的前体蛋白合成的,具有自己的信号序列,但它并没有分泌到培养基中,而是保留在宿主细胞中。在28K亚单位处,杀死的宿主细胞是从细胞内部而不是外部杀死的。我们进一步建议,没有97K和31K亚基的28K杀手亚基不能从外部杀死对杀手敏感的细胞。

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