大肠杆菌素
亚克隆
质粒
生物
操纵子
分子生物学
pUC19型
DNA
科尔1
限制地图
分子克隆
克隆(编程)
限制地点
序列分析
基因
大肠杆菌
遗传学
限制性酶
肽序列
计算机科学
程序设计语言
作者
Kin-F. Chak,White-S. Kuo,fong-m Lu,Richard James
出处
期刊:Microbiology
[Microbiology Society]
日期:1991-01-01
卷期号:137 (1): 91-100
被引量:100
标识
DOI:10.1099/00221287-137-1-91
摘要
Summary: The 2·6 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.
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