Mazaitis A J, Maas R, Maas W K
J Bacteriol. 1981 Jan;145(1):97-105. doi: 10.1128/jb.145.1.97-105.1981.
A physical map of the 117-kilobase conjugative plasmid pCG86 was constructed using electron microscope heteroduplex analysis. This plasmid carries the genes elt, for heat-labile enterotoxin, and estA, for heat-stable enterotoxin, as well as the genes for resistance to tetracycline, streptomycin, sulfonamides, and mercury. These genes were mapped using deletions and Tn5 insertions as physical markers. Analysis of a heteroduplex between pCG86 and a previously described enterotoxin plasmid (EntP307) showed a 48-kilobase region of complete homology which included the genes elt and estA. An 8.8-kilobase BamHI fragment of EntP307 carrying elt, cloned by others, was also shown to be completely homologous with pCG86. The position of elt on the fragment was verified, and it was shown to carry estA as well. A 44-kilobase region of pCG86 showed partial homology with the region of EntP307 previously shown to contain conjugal transfer genes. The gene for tetracycline resistance is carried on a stem-loop structure with the dimensions of Tn10, and the genes for the other drug resistance markers are carried on a 14.6-kilobase segment that forms an insertion loop in heteroduplexes with EntP307. These studies suggest that pCG86 arose either by recombination between an enterotoxin plasmid of incompatibility group FI, like EntP307, and a multiple resistance factor of incompatibility group FII, or by transposition into EntP307 of two transposons.
利用电子显微镜异源双链分析构建了117千碱基的接合质粒pCG86的物理图谱。该质粒携带不耐热肠毒素基因elt、耐热肠毒素基因estA以及对四环素、链霉素、磺胺类药物和汞的抗性基因。这些基因通过缺失和Tn5插入作为物理标记进行定位。对pCG86与先前描述的一种肠毒素质粒(EntP307)之间的异源双链分析表明,存在一个48千碱基的完全同源区域,其中包括elt和estA基因。其他人克隆的携带elt的EntP307的一个8.8千碱基的BamHI片段也显示与pCG86完全同源。验证了elt在该片段上的位置,并且发现它也携带estA。pCG86的一个44千碱基区域与EntP307先前显示含有接合转移基因的区域存在部分同源性。四环素抗性基因位于一个具有Tn10大小的茎环结构上,其他药物抗性标记基因位于一个14.6千碱基的片段上,该片段在与EntP307的异源双链中形成一个插入环。这些研究表明,pCG86要么是由不相容群FI的一种肠毒素质粒(如EntP307)与不相容群FII的一个多重抗性因子之间的重组产生的,要么是由两个转座子转座到EntP307中产生的。