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在缺失 Pseudomonas putida 中的 Pol I 的情况下,特异性 DNA 聚合酶 Pol II、Pol IV 和 DnaE2 参与 DNA 复制。

Involvement of specialized DNA polymerases Pol II, Pol IV and DnaE2 in DNA replication in the absence of Pol I in Pseudomonas putida.

机构信息

Department of Genetics, Tartu University and Estonian Biocentre, Tartu, Estonia.

出版信息

Mutat Res. 2011 Sep 1;714(1-2):63-77. doi: 10.1016/j.mrfmmm.2011.06.013. Epub 2011 Jul 6.

Abstract

The majority of bacteria possess a different set of specialized DNA polymerases than those identified in the most common model organism Escherichia coli. Here, we have studied the ability of specialized DNA polymerases to substitute Pol I in DNA replication in Pseudomonas putida. Our results revealed that P. putida Pol I-deficient cells have severe growth defects in LB medium, which is accompanied by filamentous cell morphology. However, growth of Pol I-deficient bacteria on solid rich medium can be restored by reduction of reactive oxygen species in cells. Also, mutants with improved growth emerge rapidly. Similarly to the initial Pol I-deficient P. putida, its adapted derivatives express a moderate mutator phenotype, which indicates that DNA replication carried out in the absence of Pol I is erroneous both in the original Pol I-deficient bacteria and the adapted derivatives. Analysis of the spectra of spontaneous Rif(r) mutations in P. putida strains lacking different DNA polymerases revealed that the presence of specialized DNA polymerases Pol II and Pol IV influences the frequency of certain base substitutions in Pol I-proficient and Pol I-deficient backgrounds in opposite ways. Involvement of another specialized DNA polymerase DnaE2 in DNA replication in Pol I-deficient bacteria is stimulated by UV irradiation of bacteria, implying that DnaE2-provided translesion synthesis partially substitutes the absence of Pol I in cells containing heavily damaged DNA.

摘要

大多数细菌拥有与最常见的模式生物大肠杆菌中鉴定出的不同的专门化 DNA 聚合酶。在这里,我们研究了专门化 DNA 聚合酶在假单胞菌属 DNA 复制中替代 Pol I 的能力。我们的结果表明,缺乏 Pol I 的假单胞菌属细胞在 LB 培养基中生长严重缺陷,伴随丝状细胞形态。然而,通过减少细胞中的活性氧,可恢复缺乏 Pol I 的细菌在固体丰富培养基上的生长。此外,具有改善生长能力的突变体迅速出现。与最初缺乏 Pol I 的假单胞菌属相似,其适应的衍生物表现出中度诱变表型,这表明在缺乏 Pol I 的情况下进行的 DNA 复制在原始缺乏 Pol I 的细菌和适应的衍生物中都是错误的。对缺乏不同 DNA 聚合酶的假单胞菌属菌株中自发 Rif(r)突变的谱分析表明,专门化 DNA 聚合酶 Pol II 和 Pol IV 的存在以相反的方式影响 Pol I 有效和缺乏 Pol I 背景下某些碱基替换的频率。另一种专门化 DNA 聚合酶 DnaE2 参与缺乏 Pol I 的细菌中的 DNA 复制,被细菌的 UV 照射刺激,这意味着 DnaE2 提供的跨损伤合成部分替代了含有严重受损 DNA 的细胞中 Pol I 的缺失。

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