Sekizaki T, Terakado N, Hashimoto K
Am J Vet Res. 1984 Feb;45(2):314-8.
The Ent plasmid encoding Escherichia coli heat-stable enterotoxin (ST) isolated from bovine, porcine, and avian strains were used for the cloning of ST genes. The ST+ DNA regions were finally cloned into pBR322 as the 1.75 kilobases PstI fragment. The electron microscopic analysis of self-annealed molecules indicated that ST+ recombinant plasmid had a stem-loop structure of a size the same as that observed in their wild type Ent plasmids. The stem-loop structures and the restriction enzyme cleavage mappings indicated that 4 kinds of ST genes cloned in this experiment may be identical to Tn1681. The ST production levels of the recombinant plasmids were higher than those of the original plasmids.
从牛、猪和禽类菌株中分离出的编码大肠杆菌热稳定肠毒素(ST)的Ent质粒用于ST基因的克隆。ST + DNA区域最终作为1.75千碱基的PstI片段克隆到pBR322中。对自身退火分子的电子显微镜分析表明,ST +重组质粒具有与野生型Ent质粒中观察到的大小相同的茎环结构。茎环结构和限制性内切酶切割图谱表明,本实验中克隆的4种ST基因可能与Tn1681相同。重组质粒的ST产生水平高于原始质粒。