Mickel S, Bauer W
J Bacteriol. 1976 Jul;127(1):644-55. doi: 10.1128/jb.127.1.644-655.1976.
The examination, by agarose gel electrophoresis, of tetracycline-resistant colonies of Escherichia coli K-12 carrying R-factor R12 reveals the presence of smaller plasmid deoxyribonucleic acids (DNAs), incompatible with R12, in many of the clones. These plasmids are demonstrated to be homologous with R12 DNA by electron microscope heteroduplex experiments and by the production of consistent fragment patterns upon digestion with various restriction endonucleases. These autonomously replicating plasmids form a related series of covalently closed circular DNA molecules ranging in size from 3.6 X 10(6) to 61 X 10(6) daltons. Plasmids of molecular weight between 3.6 X 10(6) and 37 X 10(6) confer no antibiotic resistances, but when jointly present with R12 by nonetheless enhance the expression of the tetracycline resistance associated with this latter molecule.
通过琼脂糖凝胶电泳对携带R因子R12的大肠杆菌K - 12的四环素抗性菌落进行检测,结果显示许多克隆中存在与R12不相容的较小质粒脱氧核糖核酸(DNA)。通过电子显微镜异源双链实验以及用各种限制性内切酶消化后产生一致的片段模式,证明这些质粒与R12 DNA同源。这些自主复制的质粒形成了一系列相关的共价闭合环状DNA分子,大小从3.6×10⁶到61×10⁶道尔顿不等。分子量在3.6×10⁶至37×10⁶之间的质粒不赋予抗生素抗性,但当与R12共同存在时,仍能增强与后一种分子相关的四环素抗性的表达。