Welch M M, McHenry C S
J Bacteriol. 1982 Oct;152(1):351-6. doi: 10.1128/jb.152.1.351-356.1982.
We successively subcloned the dnaE gene of Escherichia coli into pBR322, resulting in a plasmid that contains 4.6 kilobases of E. coli DNA. This plasmid can complement a dnaE temperature-sensitive mutation. A restriction map of the dnaE gene and the surrounding 10.7-kilobase region of the E. coli chromosome was determined. A unique HindIII restriction endonuclease site within the cloned segment of DNA was identified as a site required for expression of the dnaE gene. By using the maxicell plasmid-directed protein synthesizing system, we demonstrated that dnaE codes for the alpha subunit of DNA polymerase III.
我们将大肠杆菌的dnaE基因依次亚克隆到pBR322中,得到了一个含有4.6千碱基大肠杆菌DNA的质粒。该质粒能够弥补dnaE温度敏感型突变。确定了dnaE基因以及大肠杆菌染色体周围10.7千碱基区域的限制酶图谱。克隆的DNA片段内一个独特的HindIII限制性内切酶位点被鉴定为dnaE基因表达所需的位点。通过使用大细胞质粒导向的蛋白质合成系统,我们证明dnaE编码DNA聚合酶III的α亚基。