Garcia M E, Dyke K G
Department of Biochemistry, University of Oxford, UK.
Gene. 1993 Feb 14;124(1):87-92. doi: 10.1016/0378-1119(93)90765-u.
The restriction map of the 5.1-kb colicinogenic plasmid ColS8 is reported. Transposon-insertion mutagenesis has been carried out to investigate the location of the various functional regions of this plasmid. Twenty-six independent ColS8::Tn1 insertions and six different deletion mutant plasmids were isolated, and the locations of the insertions and deletions were determined. The mapping of the transposon-insertion sites, together with characterization of the phenotypes of these mutants, permitted the localization of the regions of DNA involved in colicin production, colicin S8 immunity and mobilization by other plasmids. There is a polar effect in some mutants in which single insertions result in the non-expression of all three functions. In minicell preparations, the ColS8 plasmid directed the synthesis of colicin S8 (60 kDa) and a 14-kDa immunity protein. One deletion mutant with a colicin-less phenotype can synthesize colicin S8 in minicells, which placed the DNA region involved in colicin release between the colicin production and immunity regions. Both the 60-kDa and 14-kDa proteins are expressed from pColS8 in maxicell preparations.
报道了5.1kb产大肠杆菌素质粒ColS8的限制酶图谱。已进行转座子插入诱变以研究该质粒各个功能区域的位置。分离出26个独立的ColS8::Tn1插入突变体和6种不同的缺失突变体质粒,并确定了插入和缺失的位置。转座子插入位点的图谱绘制以及这些突变体表型的特征分析,使得能够定位参与大肠杆菌素产生、大肠杆菌素S8免疫和被其他质粒转移的DNA区域。在一些突变体中存在极性效应,其中单个插入导致所有三种功能均不表达。在小细胞制备物中,ColS8质粒指导合成大肠杆菌素S8(60kDa)和一种14kDa的免疫蛋白。一个无大肠杆菌素表型的缺失突变体能够在小细胞中合成大肠杆菌素S8,这表明参与大肠杆菌素释放的DNA区域位于大肠杆菌素产生区域和免疫区域之间。在大细胞制备物中,60kDa和14kDa的蛋白质均由pColS8表达。