Yasuda S, Sekiguchi M
Proc Natl Acad Sci U S A. 1970 Dec;67(4):1839-45. doi: 10.1073/pnas.67.4.1839.
An enzyme activity, named T4 endonuclease V, was purified from T4-infected Escherichia coli. The enzyme induces single-stranded breaks in ultraviolet-irradiated DNA but does not act on native or heat-denatured DNA. The enzyme activity is dependent on the dose of ultraviolet irradiation, and the number of the breaks formed is approximately equal to the number of pyrimidine dimers present in the DNA. Denatured DNA, which has been exposed to ultraviolet light, is also attacked by the enzyme although the extent of the reaction is greater with irradiated native DNA. The enzyme shows optimal activity at pH 7.5 and does not require added divalent ions. When the enzyme-treated, irradiated DNA is subjected to stepwise degradation by spleen phosphodiesterase, dimers are released more rapidly than thymine into the acid-soluble fraction, suggesting that the enzyme induces a break at the 5'-side of a pyrimidine dimer. The enzyme, whose formation is controlled by the v(+) gene of T4, appears to be responsible for the first step of excision repair.
从感染T4噬菌体的大肠杆菌中纯化出一种名为T4内切核酸酶V的酶活性物质。该酶可在紫外线照射的DNA中诱导单链断裂,但对天然或热变性的DNA不起作用。酶活性取决于紫外线照射剂量,形成的断裂数大约等于DNA中存在的嘧啶二聚体数。已暴露于紫外线下的变性DNA也会受到该酶的攻击,尽管与照射过的天然DNA相比,反应程度更大。该酶在pH 7.5时表现出最佳活性,且不需要添加二价离子。当用脾磷酸二酯酶对经酶处理的照射DNA进行逐步降解时,二聚体比胸腺嘧啶更快地释放到酸溶性部分,这表明该酶在嘧啶二聚体的5'侧诱导断裂。该酶的形成受T4噬菌体v(+)基因控制,似乎负责切除修复的第一步。