So M, Boyer H W, Betlach M, Falkow S
J Bacteriol. 1976 Oct;128(1):463-72. doi: 10.1128/jb.128.1.463-472.1976.
A conjugative plasmid, ESF0041 was isolated from an enterotoxigenic strain of Escherichia coli from calves. ESF0041 was found to be 65 x 10(6) daltons in mass of a member of the F incompatibility complex. Acquisition of ESF0041 by E. coli K-12 was invariably associated with the capacity to produce heat-stable (ST) enterotoxin. ESF0041 and pSC101 deoxyribonucleic acids were cleaved with EcoRI, and the fragments were ligated with polynucleotide ligase. Transformation of E. coli K-12 with the ligation mixture led to the isolation of an ST+ clone. Further analysis of the plasmid deoxyribonucleic acid from this clone showed that a structural gene(s) associated with ST biosynthesis had been isolated as a 5.7 x 10(6)-dalton ESF0041 fragment in pSC101. In turn, 5.7 x 10(6)-dalton fragment was ligated to a multicopy COLE1 derivative, RSF2124, so that toxin synthesis was amplified about threefold.
从一头患肠毒素性大肠杆菌的小牛体内分离出一种接合性质粒ESF0041。发现ESF0041质量为65×10⁶道尔顿,是F不相容性复合体的一个成员。大肠杆菌K-12获得ESF0041后总是具有产生热稳定(ST)肠毒素的能力。用EcoRI切割ESF0041和pSC101脱氧核糖核酸,然后用多核苷酸连接酶连接片段。用连接混合物转化大肠杆菌K-12,得到一个ST⁺克隆。对该克隆的质粒脱氧核糖核酸进行进一步分析表明,与ST生物合成相关的一个或多个结构基因已作为pSC101中一个5.7×10⁶道尔顿的ESF0041片段被分离出来。接着,将5.7×10⁶道尔顿的片段连接到多拷贝COLE1衍生物RSF2124上,使毒素合成放大了约三倍。