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Tools and Approaches for Dissecting Protein Bacteriocin Import in Gram-Negative Bacteria

机译:剖析革兰氏阴性细菌中蛋白质细菌素导入的工具和方法

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摘要

Bacteriocins of Gram-negative bacteria are typically multi-domain proteins that target and kill bacteria of the same or closely related species. There is increasing interest in protein bacteriocin import; from a fundamental perspective to understand how folded proteins are imported into bacteria and from an applications perspective as species-specific antibiotics to combat multidrug resistant bacteria. In order to translocate across the cell envelope and cause cell death, protein bacteriocins hijack nutrient uptake pathways. Their import is energized by parasitizing intermembrane protein complexes coupled to the proton motive force, which delivers a toxic domain into the cell. A plethora of genetic, structural, biochemical, and biophysical methods have been applied to find cell envelope components involved in bacteriocin import since their discovery almost a century ago. Here, we review the various approaches that now exist for investigating how protein bacteriocins translocate into Gram-negative bacteria and highlight areas of research that will need methodological innovations to fully understand this process. We also highlight recent studies demonstrating how bacteriocins can be used to probe organization and architecture of the Gram-negative cell envelope itself.
机译:革兰氏阴性细菌的细菌素通常是多域蛋白,其靶向并杀死相同或紧密相关物种的细菌。人们对蛋白质细菌素的进口越来越感兴趣。从基本的角度了解折叠蛋白如何导入细菌,并从应用的角度作为对抗多种药物耐药细菌的物种特异性抗生素。为了跨细胞膜转运并引起细胞死亡,蛋白质细菌素劫持了养分吸收途径。通过寄生化与质子动力耦合的膜蛋白复合物来激发它们的输入,质子动力将毒性结构域传递到细胞中。自将近一个世纪以来,已经发现了许多遗传,结构,生化和生物物理方法,用于发现参与细菌素导入的细胞包膜成分。在这里,我们回顾了目前用于研究蛋白质细菌素如何转移到革兰氏阴性细菌中的各种方法,并重点介绍了需要进行方法学创新以充分理解这一过程的研究领域。我们还将重点介绍最近的研究,这些研究表明如何使用细菌素来探测革兰氏阴性细胞包膜本身的组织和结构。

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