Cellular impermeability and uptake of biocides and antibiotics in gram-negative bacteria.

S P Denyer, J Y Maillard
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Abstract

The principal targets for antibacterial agents reside at the cytoplasm and cytoplasmic membrane, damage to other structures often arising from initial events at these loci. The gram-negative bacteria offer a complex barrier system to biocides and antibiotics, regulating, and sometimes preventing, their passage to target regions. Routes of entry differ between hydrophobic and hydrophilic agents, often with a structure dependency; specialized uptake mechanisms are exploited and portage transport can occur for pro-drug antibacterials. Uptake isotherms offer insight into the sorption process and can sometimes shed light on biocide mechanisms of action. The multi-component barrier system of gram-negative bacteria offers opportunities for phenotypic resistance development where partitioning or exclusion minimizes the delivery of an antibacterial agent to the target site. Active efflux processes are recognized as increasingly relevant mechanisms for resistance, potentially offering routes to biocide:antibiotic cross-resistance. These mechanisms may be targeted directly in an attempt to compromise their role in microbial survival.

革兰氏阴性菌的细胞不渗透性和杀菌剂和抗生素的吸收。
抗菌剂的主要靶点位于细胞质和细胞质膜,对其他结构的损伤通常是由这些位点的初始事件引起的。革兰氏阴性菌为杀菌剂和抗生素提供了一个复杂的屏障系统,调节并有时阻止它们进入目标区域。疏水剂和亲水剂的进入途径不同,通常具有结构依赖性;利用特殊的摄取机制,前药抗菌素可以发生转运。吸收等温线提供了对吸收过程的洞察,有时可以阐明杀菌剂的作用机制。革兰氏阴性菌的多组分屏障系统为表型耐药的发展提供了机会,其中分区或排除最大限度地减少了抗菌剂对目标部位的递送。主动外排过程被认为是耐药性日益相关的机制,可能为杀菌剂提供途径:抗生素交叉耐药。这些机制可能被直接瞄准,试图破坏它们在微生物生存中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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