首页> 美国卫生研究院文献>Antioxidants Redox Signaling >Antimicrobial Activity of the Manganese Photoactivated Carbon Monoxide-Releasing Molecule Mn(CO)3(tpa-κ3N)+ Against a Pathogenic Escherichia coli that Causes Urinary Infections
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Antimicrobial Activity of the Manganese Photoactivated Carbon Monoxide-Releasing Molecule Mn(CO)3(tpa-κ3N)+ Against a Pathogenic Escherichia coli that Causes Urinary Infections

机译:锰光活化一氧化碳释放分子Mn(CO)3(tpa-κ3N) +对引起尿路感染的致病性大肠杆菌的抗菌活性。

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>Aims: We set out to investigate the antibacterial activity of a new Mn-based photoactivated carbon monoxide-releasing molecule (PhotoCORM, [Mn(CO)3(tpa-κ3N)]+) against an antibiotic-resistant uropathogenic strain (EC958) of Escherichia coli. >Results: Activated PhotoCORM inhibits growth and decreases viability of E. coli EC958, but non-illuminated carbon monoxide-releasing molecule (CORM) is without effect. NADH-supported respiration rates are significantly decreased by activated PhotoCORM, mimicking the effect of dissolved CO gas. CO from the PhotoCORM binds to intracellular targets, namely respiratory oxidases in strain EC958 and a bacterial globin heterologously expressed in strain K-12. However, unlike previously characterized CORMs, the PhotoCORM is not significantly accumulated in cells, as deduced from the cellular manganese content. Activated PhotoCORM reacts avidly with hydrogen peroxide producing hydroxyl radicals; the observed peroxide-enhanced toxicity of the PhotoCORM is ameliorated by thiourea. The PhotoCORM also potentiates the effect of the antibiotic, doxycycline. >Innovation: The present work investigates for the first time the antimicrobial activity of a light-activated PhotoCORM against an antibiotic-resistant pathogen. A comprehensive study of the effects of the PhotoCORM and its derivative molecules upon illumination is performed and mechanisms of toxicity of the activated PhotoCORM are investigated. >Conclusion: The PhotoCORM allows a site-specific and time-controlled release of CO in bacterial cultures and has the potential to provide much needed information on the generality of CORM activities in biology. Understanding the mechanism(s) of activated PhotoCORM toxicity will be key in exploring the potential of this and similar compounds as antimicrobial agents, perhaps in combinatorial therapies with other agents. Antioxid. Redox Signal. 24, 765–780.
机译:>目标:我们着手研究一种新型的基于Mn的光活化一氧化碳释放分子(PhotoCORM,[Mn(CO)3(tpa-κ 3 N)] + )对抗大肠埃希菌的抗生素耐药性尿毒原性菌株(EC958)。 >结果:活化的PhotoCORM抑制大肠杆菌EC958的生长并降低其活力,但未照明的一氧化碳释放分子(CORM)无效。通过激活PhotoCORM可以大大降低NADH支持的呼吸速率,从而模拟溶解的CO气体的影响。来自PhotoCORM的CO与细胞内靶标结合,即EC958株中的呼吸氧化酶和K-12株中异源表达的细菌球蛋白。但是,与以前表征的CORM不同,从细胞锰含量推断出,PhotoCORM不会在细胞中显着积累。活化的PhotoCORM与过氧化氢剧烈反应,产生羟基自由基。硫脲可改善观察到的PhotoCORM的过氧化物增强的毒性。 PhotoCORM还增强了抗生素强力霉素的作用。 >创新:本工作首次调查了光激活的PhotoCORM对抗生素抗性病原体的抗菌活性。对PhotoCORM及其衍生物分子对照明的影响进行了全面研究,并研究了活化的PhotoCORM的毒性机理。 >结论:PhotoCORM可以在细菌培养物中实现CO的特定位置释放和时间控制释放,并有潜力提供有关CORM生物学活动一般性的急需信息。了解活化的PhotoCORM毒性的机制将是探索这种化合物和类似化合物作为抗菌剂的潜力的关键,也许是在与其他药物联合治疗时。抗氧化。氧化还原信号。 24,765–780。

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