Levin J D, Johnson A W, Demple B
Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138.
J Biol Chem. 1988 Jun 15;263(17):8066-71.
Agents that act via oxygen-derived free radicals form DNA strand breaks with fragmented sugar residues that block DNA repair synthesis. Using a synthetic DNA substrate with a single type of sugar fragment, 3'-phosphoglycolaldehyde esters, we show that in Escherichia coli extracts the only EDTA-resistant diesterase for these damages depends on the bacterial nfo (endonuclease IV) gene. Endonuclease IV was purified to physical homogeneity (Mr = 31,000) from an E. coli strain carrying the cloned nfo gene and in which the enzyme had been induced with paraquat. Although heat-stable and routinely assayed in the presence of EDTA, endonuclease IV was inactivated in the absence of substrate at 23-50 degrees C by either EDTA or 1,10-phenanthroline, suggesting the presence of an essential metal tightly bound to the protein. Purified endonuclease IV released phosphoglycolaldehyde, phosphate, and intact deoxyribose 5-phosphate from the 3'-end of DNA, all with apparent Km of 5-10 nM. The optimal KCl or NaCl concentration for 3'-phosphoglycolaldehyde release was 50-100 mM. The purified enzyme had endonuclease activity against partially depurinated DNA but lacked significant nonspecific nuclease activities. Endonuclease IV also activated H2O2-damaged DNA for repair synthesis by DNA polymerase I. Thus, endonuclease IV can act on a variety of oxidative damages in DNA, consistent with a role for the enzyme in combating free-radical toxicity.
通过氧衍生自由基起作用的试剂会形成DNA链断裂,并带有阻断DNA修复合成的糖残基片段。使用带有单一类型糖片段(3'-磷酸乙醇醛酯)的合成DNA底物,我们发现,在大肠杆菌提取物中,针对这些损伤的唯一耐EDTA二酯酶依赖于细菌的nfo(核酸内切酶IV)基因。核酸内切酶IV从携带克隆nfo基因且用百草枯诱导过该酶的大肠杆菌菌株中纯化至物理纯(Mr = 31,000)。尽管核酸内切酶IV热稳定且通常在EDTA存在下进行检测,但在23 - 50摄氏度无底物时,它会被EDTA或1,10 - 菲咯啉灭活,这表明存在一种与蛋白质紧密结合的必需金属。纯化的核酸内切酶IV从DNA的3'-末端释放磷酸乙醇醛、磷酸和完整的脱氧核糖5-磷酸,所有这些的表观Km均为5 - 10 nM。释放3'-磷酸乙醇醛的最佳KCl或NaCl浓度为50 - 100 mM。纯化的酶对部分脱嘌呤的DNA具有核酸内切酶活性,但缺乏显著的非特异性核酸酶活性。核酸内切酶IV还能激活H2O2损伤的DNA以进行DNA聚合酶I介导的修复合成。因此,核酸内切酶IV可作用于DNA中的多种氧化损伤,这与该酶在对抗自由基毒性中的作用一致。