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ColE7质粒的克隆与特性分析

Cloning and characterization of the ColE7 plasmid.

作者信息

Chak K F, Kuo W S, Lu F M, James R

机构信息

Department of Biochemistry, National Yang-Ming Medical College, Taipei, Taiwan, ROC.

出版信息

J Gen Microbiol. 1991 Jan;137(1):91-100. doi: 10.1099/00221287-137-1-91.

Abstract

The 6.2 kb ColE7-K317 plasmid was mapped and the DNA fragments of the colicin E7 operon subcloned into pUC18 and pUC19. The size of the functional colicin E7 operon deduced by subcloning was 2.3 kb. The colicin E7 gene product was purified by carboxymethylcellulose chromatography. Both colicin E7 and E9 were demonstrated to exhibit a non-specific DNAase-type activity by in vitro biological assay. The molecular mass of colicin E7 was 61 kDa, as determined by SDS-PAGE. From DNA sequence data, the estimated sizes of the E7 immunity protein and the E7 lysis protein were 9926 Da and 4847 Da, respectively. Comparison of restriction maps and DNA sequence data suggests that ColE7 and ColE2 are more closely related than other E colicin plasmids.

摘要

对6.2 kb的ColE7 - K317质粒进行了图谱绘制,并将大肠杆菌素E7操纵子的DNA片段亚克隆到pUC18和pUC19中。通过亚克隆推导的功能性大肠杆菌素E7操纵子的大小为2.3 kb。通过羧甲基纤维素色谱法纯化了大肠杆菌素E7基因产物。通过体外生物学测定证明大肠杆菌素E7和E9均表现出非特异性DNA酶型活性。通过SDS - PAGE测定,大肠杆菌素E7的分子量为61 kDa。根据DNA序列数据,E7免疫蛋白和E7裂解蛋白的估计大小分别为9926 Da和4847 Da。限制性图谱和DNA序列数据的比较表明,ColE7和ColE2比其他大肠杆菌素质粒的关系更密切。

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