Weiss R B, Duker N J
Nucleic Acids Res. 1986 Aug 26;14(16):6621-31. doi: 10.1093/nar/14.16.6621.
Photoalkylation, the ultraviolet irradiation of DNA with isopropanol and di-tert-butylperoxide, causes a variety of base alterations. These include 8-(2-hydroxy-2-propyl)guanines, 8-(2-hydroxy-2-propyl)adenines and thymine dimers. An E. coli endonuclease against photoalkylated DNA was assayed by conversion of superhelical PM2 phage DNA to the nicked form. Enzyme activities were compared between extracts of strain BW9109 (xth-), lacking exonuclease III activity, and strain BW434 (xth-,nth-), deficient in both exonuclease III and endonuclease III. The endonuclease level in the double mutant against substrate photoalkylated DNA was under 20% of the activity in the mutant lacking only exonuclease III. Irradiation of the DNA substrate in the absence of isopropanol did not affect the activity in either strain. Analysis by polyacrylamide gel electrophoresis identified the sites of DNA cleavage by purified E. coli endonuclease III as cytosines, both in DNA irradiated at biologically significant wavelengths and in photoalkylated DNA. Neither 8-(2-hydroxy-2-propyl)purines, pyrimidine dimers, uracils nor 6-4'-(pyrimidin-2'-one)pyrimidines were substrates for the enzyme.
光烷基化反应,即使用异丙醇和二叔丁基过氧化物对DNA进行紫外线照射,会导致多种碱基改变。这些改变包括8 -(2 - 羟基 - 2 - 丙基)鸟嘌呤、8 -(2 - 羟基 - 2 - 丙基)腺嘌呤和胸腺嘧啶二聚体。通过将超螺旋PM2噬菌体DNA转化为切口形式来检测大肠杆菌中针对光烷基化DNA的内切核酸酶。比较了缺乏外切核酸酶III活性的BW9109菌株(xth -)和同时缺乏外切核酸酶III和内切核酸酶III的BW434菌株(xth -,nth -)提取物中的酶活性。双突变体中针对底物光烷基化DNA的内切核酸酶水平不到仅缺乏外切核酸酶III的突变体活性的20%。在没有异丙醇的情况下对DNA底物进行照射,对两种菌株的活性均无影响。通过聚丙烯酰胺凝胶电泳分析确定,纯化的大肠杆菌内切核酸酶III在生物意义波长照射的DNA以及光烷基化DNA中切割DNA的位点均为胞嘧啶。8 -(2 - 羟基 - 2 - 丙基)嘌呤、嘧啶二聚体、尿嘧啶或6 - 4' -(嘧啶 - 2' - 酮)嘧啶均不是该酶的底物。