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首页> 外文期刊>Journal of Virology >Relationship of Bacillus subtilis DNA polymerase III to bacteriophage PBS2-induced DNA polymerase and to the replication of uracil-containing DNA.
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Relationship of Bacillus subtilis DNA polymerase III to bacteriophage PBS2-induced DNA polymerase and to the replication of uracil-containing DNA.

机译:枯草芽孢杆菌DNA聚合酶III与噬菌体PBS2诱导的DNA聚合酶的关系和含尿嘧啶DNA的复制。

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摘要

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.
机译:体内研究PBS2噬菌体枯草芽孢杆菌DNA聚合酶III(POL III)突变体和该突变体的耐温抗逆剂表明POL III在PBS2 DNA合成中的可能累及。以前的结果,6-(p-羟基苯齐氮)-Uuracil(HPura),Pol III的特异性抑制剂和未感染的细胞中的DNA复制,表明POL III由于其对该药物的抗性而不是噬菌体DNA复制。实验旨在审查这种明显矛盾的可能解释。首先,提取物中宿主POL III和噬菌体诱导的DNA聚合酶的测定表明,不稳定的POL III不会导致不稳定的噬菌体诱导的酶,表明该新聚合酶不是POL的改性HPURA抗性形式III。实际上,在所有测定条件下,纯化的噬菌体诱导的酶对活性,减少的HPURA形式抗性。由于体外PolI III能够复制在该噬菌体中发现的含尿嘧啶的DNA,因此使用噬菌体DNA作为模板引物和DUTP作为基质检查纯化酶对降低HPURA的敏感性。这些新的基材没有影响宿主酶对药物的敏感性。

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