Takahashi S, Hours C, Chu A, Denhardt D T
Can J Biochem. 1979 Jun;57(6):855-66. doi: 10.1139/o79-105.
The protein product of the rep gene of Escherichia coli is required for the replication of certain bacteriophage genomes (phi X174, fd, P2) and for the normal replication of E. coli DNA. We have used a specialized transducing phage, lambda p rep+, which complements the defect of rep mutants, to identify the rep protein. The rep protein has been purified from cells infected with lambda p rep+ phage; it has a molecular weight of about 70 000 and appears similar to the protein found in normal cells. Stimulation of phi X174 replicative form DNA synthesis in vitro was observed when highly purified rep protein was supplied to a cell extract derived from phi X-infected E. coli rep cells and supplemented with replicative form DNA. The purified protein has a single-stranded DNA-dependent ATPase activity and is capable of sensitizing duplex DNA to nucleases specific for single-stranded DNA. For this reason we propose the enzyme be called DNA helicase III. We infer that the rep protein uses the energy of hydrolysis of ATP to separate the strands of duplex DNA; the E. coli DNA binding protein need not be present. The rep3 mutant appeared to make a limited amount of active rep protein.
大肠杆菌rep基因的蛋白质产物是某些噬菌体基因组(φX174、fd、P2)复制以及大肠杆菌DNA正常复制所必需的。我们使用了一种特殊的转导噬菌体λp rep +,它能弥补rep突变体的缺陷,来鉴定rep蛋白。rep蛋白已从感染λp rep +噬菌体的细胞中纯化出来;其分子量约为70000,看起来与正常细胞中发现的蛋白质相似。当向来自φX感染的大肠杆菌rep细胞的细胞提取物中提供高度纯化的rep蛋白并补充复制型DNA时,在体外观察到对φX174复制型DNA合成的刺激。纯化的蛋白质具有单链DNA依赖性ATP酶活性,并且能够使双链DNA对单链DNA特异性核酸酶敏感。因此我们提议将该酶称为DNA解旋酶III。我们推断rep蛋白利用ATP水解的能量来分离双链DNA的链;大肠杆菌DNA结合蛋白无需存在。rep3突变体似乎产生了有限量的活性rep蛋白。