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细菌DNA复制基因在噬菌体λ中的克隆

Cloning of bacterial DNA replication genes in bacteriophage lambda.

作者信息

Rowen L, Kobori J A, Scherer S

出版信息

Mol Gen Genet. 1982;187(3):501-9. doi: 10.1007/BF00332635.

Abstract

Recombinant lambda phages containing the genes for dnaZ protein (the gamma subunit of DNA polymerse III holoenzyme), primase (dnaG protein) and dnaC protein from Escherichia coli and Salmonella typhimurium were isolated. Each gene cloned from S. typhimurium has extensive DNA sequence homology to the corresponding E. coli gene. Clones selected by complementation of a dnaA temperature-sensitive mutant appear similar to other isolated suppressors of dnaA (Projan and Wechsler 1981). Derivatives of each cloned fragment suitable for overproduction of the protein were constructed. Of those tested, only the phage containing the E. coli dnaZ gene resulted in significant overproduction.

摘要

分离出了含有来自大肠杆菌和鼠伤寒沙门氏菌的dnaZ蛋白基因(DNA聚合酶III全酶的γ亚基)、引发酶(dnaG蛋白)和dnaC蛋白基因的重组λ噬菌体。从鼠伤寒沙门氏菌克隆的每个基因与相应的大肠杆菌基因都有广泛的DNA序列同源性。通过dnaA温度敏感突变体互补筛选出的克隆与其他已分离的dnaA抑制子相似(Projan和Wechsler,1981)。构建了适合过量表达蛋白质的每个克隆片段的衍生物。在测试的那些衍生物中,只有含有大肠杆菌dnaZ基因的噬菌体导致了显著的过量表达。

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