Miki T, Hiraga S, Nagata T, Yura T
Proc Natl Acad Sci U S A. 1978 Oct;75(10):5099-103. doi: 10.1073/pnas.75.10.5099.
A transducing phage lambdaasn was isolated. The late gene region of its genome was found to have been substituted by an Escherichia coli chromosomal segment containing the genes bgIR, bgIC, glmS, uncA, and asn. Restriction endonuclease cleavage mapping and electron microscopic analysis of the lambdaasn DNA revealed that the size of the bacterial segment is approximately 1.75 X 10(7) daltons, corresponding to about 26.4 kilobases. The circular DNA of lambdaasn was digested with restriction endonuclease EcoRI, diluted, and sealed with DNA ligase. When the reaction mixture was used to transform a recipient E. coli strain, a small plasmid of about 1 X 10(7) daltons (named pMCR115) was obtained. Restriction endonuclease cleavage mapping of pMCR115 and other evidence suggested that it contained the replication origin (oriC) of the E. coli chromosome.
分离出了一种转导噬菌体λasn。发现其基因组的晚期基因区域已被一个含有bgIR、bgIC、glmS、uncA和asn基因的大肠杆菌染色体片段所取代。对λasn DNA进行限制性内切酶切割图谱分析和电子显微镜分析表明,细菌片段的大小约为1.75×10⁷道尔顿,相当于约26.4千碱基。用限制性内切酶EcoRI消化λasn的环状DNA,稀释后用DNA连接酶封闭。当反应混合物用于转化受体大肠杆菌菌株时,获得了一个约1×10⁷道尔顿的小质粒(命名为pMCR115)。pMCR115的限制性内切酶切割图谱分析及其他证据表明,它含有大肠杆菌染色体的复制起点(oriC)。