Stam J C, Kwakman J, Meijer M, Stuitje A R
Nucleic Acids Res. 1986 Sep 11;14(17):6871-84. doi: 10.1093/nar/14.17.6871.
Differential centrifugation of an osmotic lysate of K. lactis protoplasts showed that the linear DNA killer plasmids of K. lactis, pGKL1 and pGKL2, are almost exclusively present in the cytoplasmic fraction. This fractionation procedure allows the rapid isolation of large amounts of plasmid DNA without contamination by chromosomal and mitochondrial DNA. With these DNA preparations the size of the terminally bound proteins was estimated to be 28 and 36 kDal for pGKL1 and pGKL2, respectively. The entire pGKL1 sequence (except for 21 base pairs at the right terminus) was cloned in a shuttle vector that permits autonomous replication in the nucleus of K. lactis. However, killer gene expression could not be established in transformants. In connection with the observed cytoplasmic localization, this result suggests that gene expression of the killer DNA plasmids is entirely cytoplasmic.
乳酸克鲁维酵母原生质体渗透裂解物的差速离心表明,乳酸克鲁维酵母的线性DNA杀伤质粒pGKL1和pGKL2几乎只存在于细胞质部分。这种分级分离程序能够快速分离大量质粒DNA,而不会受到染色体DNA和线粒体DNA的污染。利用这些DNA制品,估计pGKL1和pGKL2末端结合蛋白的大小分别为28和36 kDa。整个pGKL1序列(右端21个碱基对除外)被克隆到一个穿梭载体中,该载体允许在乳酸克鲁维酵母细胞核中自主复制。然而,在转化体中未能建立杀伤基因表达。结合观察到的细胞质定位,这一结果表明杀伤DNA质粒的基因表达完全在细胞质中。