Hitzeman R A, Price A R
J Virol. 1978 Dec;28(3):697-709. doi: 10.1128/JVI.28.3.697-709.1978.
In vivo studies of PBS2 phage replication in a temperature-sensitive Bacillus subtilis DNA polymerase III (Pol III) mutant and a temperature-resistant revertant of this mutant have suggested the possible involvement of Pol III in PBS2 DNA synthesis. Previous results with 6-(p-hydroxyphenylazo)-uracil (HPUra), a specific inhibitor of Pol III and DNA replication in uninfected cells, suggest that Pol III is not involved in phage DNA replication, due to its resistance to this drug. Experiments were designed to examine possible explanations for this apparent contradiction. First, assays of the host Pol III and the phage-induced DNA polymerase activities in extracts indicated that a labile Pol III did not result in a labile phage-induced enzyme, suggesting that this new polymerase is not a modified HPUra-resistant form of Pol III. Indeed the purified phage-induced enzyme was resistant to the active, reduced form of HPUra under all assay conditions tested. Since in vitro Pol III was capable of replicating the uracil-containing DNA found in this phage, the sensitivity of the purified enzyme to reduced HPUra was examined using phage DNA as template-primer and dUTP as substrate; these new substrates did not affect the sensitivity of the host enzyme to the drug.
在对温度敏感的枯草芽孢杆菌DNA聚合酶III(Pol III)突变体及其温度抗性回复突变体中PBS2噬菌体复制的体内研究表明,Pol III可能参与PBS2 DNA合成。先前使用6-(对羟基苯偶氮)尿嘧啶(HPUra)(一种Pol III和未感染细胞中DNA复制的特异性抑制剂)的研究结果表明,由于其对该药物具有抗性,Pol III不参与噬菌体DNA复制。设计实验以检验对这一明显矛盾的可能解释。首先,对提取物中宿主Pol III和噬菌体诱导的DNA聚合酶活性的测定表明,不稳定的Pol III不会导致不稳定的噬菌体诱导酶,这表明这种新的聚合酶不是修饰的抗HPUra形式的Pol III。实际上,在所有测试的测定条件下,纯化的噬菌体诱导酶对活性还原形式的HPUra具有抗性。由于体外Pol III能够复制该噬菌体中含尿嘧啶的DNA,因此使用噬菌体DNA作为模板引物和dUTP作为底物,检测了纯化酶对还原型HPUra的敏感性;这些新底物不影响宿主酶对该药物的敏感性。