Itoh T, Horii T
Department of Biology, Faculty of Science, Osaka University, Japan.
Mol Gen Genet. 1989 Oct;219(1-2):249-55. doi: 10.1007/BF00261184.
We developed an in vitro replication system for ColE2 and ColE3 plasmids using cell extracts prepared from bacteria with or without these plasmids. DNA synthesis depended on host DNA polymerase I and was sensitive to rifampicin and chloramphenicol. Preincubation of the extracts with plasmid DNA, however, allowed replication of template DNA added subsequently in a plasmid-specific manner in the presence of rifampicin and chloramphenicol. The plasmid-specified trans-acting factor(s) was detected in cell extracts from bacteria carrying a recombinant plasmid with the region of ColE2 or ColE3 encoding the Rep protein. The plasmid-specified factor(s) consisted at least in part of protein, probably the Rep protein. In vitro replication started within a region of ColE2 or ColE3 containing the smallest cis-acting segment essential for in vivo replication and proceeded in a fixed direction.
我们利用从携带或不携带这些质粒的细菌制备的细胞提取物,开发了一种用于ColE2和ColE3质粒的体外复制系统。DNA合成依赖于宿主DNA聚合酶I,并且对利福平和平氯霉素敏感。然而,提取物与质粒DNA的预温育允许随后以质粒特异性方式在利福平和氯霉素存在的情况下复制添加的模板DNA。在携带具有编码Rep蛋白的ColE2或ColE3区域的重组质粒的细菌的细胞提取物中检测到质粒指定的反式作用因子。质粒指定的因子至少部分由蛋白质组成,可能是Rep蛋白。体外复制在ColE2或ColE3的一个区域内开始,该区域包含体内复制所必需的最小顺式作用片段,并以固定方向进行。