Yasuda S, Sekiguchi M
Biochim Biophys Acta. 1976 Aug 18;442(2):197-207. doi: 10.1016/0005-2787(76)90490-1.
T4 endonuclease V, which is involved in repair of ultraviolet-damaged DNA, has been purified 3600 fold from T4D-infected Escherichia coli. The enzyme shows optimal activity at pH 7.2 and does not require added divalent ions. Endonuclease V attacks both native and heat-denatured DNA provided that the DNA has been irradiated, and the enzyme activity is dependent on the dose of ultraviolet irradiation. The rate and the extent of the reaction are greater with irradiated native DNA although the Km values for the two types of DNA are the same (2.25 - 10(-5) M). The enzyme is readily inactivated by heat and is sensitive to p-chloromercuribenzoate. Endonuclease V-treated irradiated DNA is degraded by spleen phosphodiesterase only when the DNA has been treated with alkaline phosphatase, suggesting that the enzyme produces 5'-phosphoryl termini.
T4 内切核酸酶V参与紫外线损伤DNA的修复,已从感染T4D的大肠杆菌中纯化了3600倍。该酶在pH 7.2时表现出最佳活性,且不需要添加二价离子。内切核酸酶V可攻击天然和热变性的已辐照DNA,酶活性取决于紫外线照射剂量。尽管两种类型DNA的米氏常数相同(2.25×10⁻⁵ M),但辐照天然DNA的反应速率和程度更大。该酶很容易被热灭活,且对对氯汞苯甲酸敏感。只有当DNA用碱性磷酸酶处理后,经内切核酸酶V处理的辐照DNA才会被脾磷酸二酯酶降解,这表明该酶产生5'-磷酸末端。