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聚苯胺的抗菌作用涉及氧化应激的产生,而聚苯胺的功能化引入了其他机制。

The antimicrobial action of polyaniline involves production of oxidative stress while functionalisation of polyaniline introduces additional mechanisms.

作者信息

Robertson Julia, Gizdavic-Nikolaidis Marija, Nieuwoudt Michel K, Swift Simon

机构信息

Department of Molecular Medicine and Pathology, University of Auckland, Auckland, New Zealand.

School of Chemistry, University of Auckland, Auckland, New Zealand.

出版信息

PeerJ. 2018 Jun 27;6:e5135. doi: 10.7717/peerj.5135. eCollection 2018.

Abstract

Polyaniline (PANI) and functionalised polyanilines (fPANI) are novel antimicrobial agents whose mechanism of action was investigated. single gene deletion mutants revealed that the antimicrobial mechanism of PANI likely involves production of hydrogen peroxide while homopolymer poly(3-aminobenzoic acid), P3ABA, used as an example of a fPANI, disrupts metabolic and respiratory machinery, by targeting ATP synthase and causes acid stress. PANI was more active against in aerobic, compared to anaerobic, conditions, while this was apparent for P3ABA only in rich media. Greater activity in aerobic conditions suggests involvement of reactive oxygen species. P3ABA treatment causes an increase in intracellular free iron, which is linked to perturbation of metabolic enzymes and could promote reactive oxygen species production. Addition of exogenous catalase protected from PANI antimicrobial action; however, this was not apparent for P3ABA treated cells. The results presented suggest that PANI induces production of hydrogen peroxide, which can promote formation of hydroxyl radicals causing biomolecule damage and potentially cell death. P3ABA is thought to act as an uncoupler by targeting ATP synthase resulting in a futile cycle, which precipitates dysregulation of iron homeostasis, oxidative stress, acid stress, and potentially the fatal loss of proton motive force.

摘要

聚苯胺(PANI)和功能化聚苯胺(fPANI)是新型抗菌剂,其作用机制已得到研究。单基因缺失突变体表明,PANI的抗菌机制可能涉及过氧化氢的产生,而作为fPANI示例的均聚物聚(3-氨基苯甲酸)P3ABA通过靶向ATP合酶破坏代谢和呼吸机制,并导致酸胁迫。与厌氧条件相比,PANI在有氧条件下对[具体对象未提及]更具活性,而这仅在丰富培养基中对P3ABA才明显。有氧条件下更高的活性表明活性氧的参与。P3ABA处理会导致细胞内游离铁增加,这与代谢酶的扰动有关,并可能促进活性氧的产生。添加外源过氧化氢酶可保护[具体对象未提及]免受PANI的抗菌作用;然而,这在P3ABA处理的细胞中并不明显。所呈现的结果表明,PANI诱导过氧化氢的产生,过氧化氢可促进羟基自由基的形成,导致生物分子损伤并可能导致细胞死亡。P3ABA被认为通过靶向ATP合酶作为解偶联剂,导致无效循环,从而引发铁稳态失调、氧化应激、酸胁迫,并可能导致质子动力势的致命丧失。

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