Newland J W, Strockbine N A, Neill R J
Walter Reed Army Institute of Research, Walter Reed Army Medical Center, Washington, D.C. 20307.
Infect Immun. 1987 Nov;55(11):2675-80. doi: 10.1128/iai.55.11.2675-2680.1987.
Genes controlling production of Shiga-like toxin type II (SLT-II) in Escherichia coli were cloned from the SLT-II-converting bacteriophage 933W and compared with the Shiga-like toxin type I (SLT-I) genes previously isolated and described from phage 933J. Subcloning analysis identified a region within the 4.9-kilobase EcoRI fragment of phage 933W that was associated with SLT-II production. Experiments with E. coli minicells containing these subclones demonstrated that the 4.9-kilobase EcoRI fragment encodes the structural genes for SLT-II. These experiments additionally showed the genetic organization of the SLT-II genes to be the same as that of the SLT-I genes, with the coding sequence for the large A subunit adjacent to that for the smaller B subunit. The mobilities of the SLT-II subunits in sodium dodecyl sulfate-polyacrylamide gels were slightly greater than those determined for the SLT-I subunits. Although apparent processing of the SLT-I subunits was observed with polymyxin B treatment of the labeled minicells, no processing of the SLT-II subunits was detected. Southern blot hybridization studies suggested that the DNA fragment carrying the SLT-II structural genes shares approximately 50 to 60% homology with the DNA of the SLT-I structural genes.
从产志贺样毒素II型(SLT-II)的大肠杆菌中克隆出控制该毒素产生的基因,这些基因来自噬菌体933W,并与之前从噬菌体933J中分离和描述的志贺样毒素I型(SLT-I)基因进行了比较。亚克隆分析确定了噬菌体933W的4.9千碱基EcoRI片段内与SLT-II产生相关的一个区域。对含有这些亚克隆的大肠杆菌小细胞进行的实验表明,4.9千碱基的EcoRI片段编码SLT-II的结构基因。这些实验还表明,SLT-II基因的遗传组织与SLT-I基因相同,大A亚基的编码序列与较小的B亚基的编码序列相邻。SLT-II亚基在十二烷基硫酸钠-聚丙烯酰胺凝胶中的迁移率略大于SLT-I亚基的迁移率。尽管用多粘菌素B处理标记的小细胞时观察到了SLT-I亚基的明显加工,但未检测到SLT-II亚基的加工。Southern印迹杂交研究表明,携带SLT-II结构基因的DNA片段与SLT-I结构基因的DNA具有约50%至60%的同源性。