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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Effects of 1,10-phenanthroline and hydrogen peroxide in Escherichia coli: lethal interaction.
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Effects of 1,10-phenanthroline and hydrogen peroxide in Escherichia coli: lethal interaction.

机译:1,10-菲咯啉和过氧化氢在大肠杆菌中的作用:致死性相互作用。

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It has been observed that when Escherichia coli cells are treated simultaneously with phenanthroline and H2O2, there is a lethal interaction. In order to analyze the mechanism of this lethal interaction, wild-type and xthA mutant cells of E. coli were treated with 2.5 mM H2O2 and 1 mM phenanthroline. This treatment was preceded by treatments with different metal chelators (dipyridyl for Fe2+, desferal for Fe3+ and neocuproine for Cu2+) or conducted simultaneously to other treatments with chelators and radical scavengers (thiourea, ethanol and sodium benzoate). The lethal interaction was observed in both the E. coli wild-type strain and xthA mutant strain, which is deficient in the exonuclease III repair enzyme. Nevertheless, the mutant strain was much more sensitive than the wild-type one. Dipyridyl pretreatment protected the cells against the lethal interaction, while desferal pretreament was unable to do so. This suggests that the lethal interaction requires Fe2+ and not Fe3+ ions. Ethanol and sodiumbenzoate were incapable of protecting bacterial cells against the lethal interaction. Even a 20-min pretreatment with benzoate did not confer protection. On the other hand, thiourea protected the cells completely. Based on our results, we propose that the lethal interaction may be caused not only by the reaction kinetics of phenanthroline and Fe, but also by the ability of phenanthroline to intercalate in DNA. After forming the mono and bis complexes, phenanthroline would serve as a shuttle and take the Fe2+ ions to the DNA. So, the Fenton reaction would take its course with the consequent generation of OH. radicals near DNA. This proximity to the DNA would protect the OH. radicals against the scavengers' action, thus optimizing the Fenton reaction.
机译:已经观察到,用菲咯啉和H2O2同时处理大肠杆菌细胞时,会产生致命的相互作用。为了分析这种致命相互作用的机理,用2.5 mM H2O2和1 mM菲咯啉处理大肠杆菌的野生型和xthA突变细胞。在此处理之前,先使用不同的金属螯合剂(Fe2 +的联吡啶,Fe3 +的延缓性和Cu2 +的新cuproine)进行处理,或同时进行其他螯合剂和自由基清除剂(硫脲,乙醇和苯甲酸钠)的处理。在大肠杆菌野生型菌株和xthA突变菌株中都观察到了致命的相互作用,这在核酸外切酶III修复酶中是不足的。然而,突变株比野生株敏感得多。双吡啶预处理可以保护细胞免受致命性相互作用的影响,而延缓预处理无法做到这一点。这表明致命的相互作用需要Fe2 +而不是Fe3 +离子。乙醇和苯甲酸钠不能保护细菌细胞免受致命的相互作用。即使使用苯甲酸酯进行20分钟的预处理也无法提供保护。另一方面,硫脲可完全保护细胞。根据我们的结果,我们提出致命相互作用不仅可能是菲咯啉与Fe的反应动力学引起的,而且还可能是菲咯啉插入DNA中的能力引起的。形成单和双配合物后,菲咯啉将作为穿梭物,将Fe2 +离子带入DNA。因此,芬顿反应将随其产生的OH而发展。 DNA附近的自由基。与DNA的这种接近将保护OH。自由基清除剂的作用,从而优化了Fenton反应。

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