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细菌素的多样性、功能、发现及其作为抗菌剂的应用。

Bacteriocin diversity, function, discovery and application as antimicrobials.

机构信息

APC Microbiome Ireland, University College Cork, Cork, Ireland.

School of Microbiology, University College Cork, Cork, Ireland.

出版信息

Nat Rev Microbiol. 2024 Sep;22(9):556-571. doi: 10.1038/s41579-024-01045-x. Epub 2024 May 10.

DOI:10.1038/s41579-024-01045-x
PMID:38730101
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7616364/
Abstract

Bacteriocins are potent antimicrobial peptides that are produced by bacteria. Since their discovery almost a century ago, diverse peptides have been discovered and described, and some are currently used as commercial food preservatives. Many bacteriocins exhibit extensively post-translationally modified structures encoded on complex gene clusters, whereas others have simple linear structures. The molecular structures, mechanisms of action and resistance have been determined for a number of bacteriocins, but most remain incompletely characterized. These gene-encoded peptides are amenable to bioengineering strategies and heterologous expression, enabling metagenomic mining and modification of novel antimicrobials. The ongoing global antimicrobial resistance crisis demands that novel therapeutics be developed to combat infectious pathogens. New compounds that are target-specific and compatible with the resident microbiota would be valuable alternatives to current antimicrobials. As bacteriocins can be broad or narrow spectrum in nature, they are promising tools for this purpose. However, few bacteriocins have gone beyond preclinical trials and none is currently used therapeutically in humans. In this Review, we explore the broad diversity in bacteriocin structure and function, describe identification and optimization methods and discuss the reasons behind the lack of translation beyond the laboratory of these potentially valuable antimicrobials.

摘要

细菌素是由细菌产生的强效抗菌肽。自近一个世纪前发现以来,已经发现并描述了多种肽,其中一些目前被用作商业食品防腐剂。许多细菌素具有广泛的翻译后修饰结构,这些结构编码在复杂的基因簇上,而其他细菌素则具有简单的线性结构。已经确定了许多细菌素的分子结构、作用机制和耐药性,但大多数细菌素仍未完全表征。这些基因编码的肽可通过生物工程策略和异源表达进行修饰,从而实现宏基因组挖掘和新型抗菌药物的修饰。当前的全球抗菌药物耐药性危机要求开发新的治疗方法来对抗感染性病原体。具有特异性靶标且与常驻微生物组兼容的新型化合物将是对抗当前抗菌药物的有价值替代品。由于细菌素在性质上可以是广谱或窄谱的,因此它们是实现这一目标的有前途的工具。然而,很少有细菌素能够超越临床前试验,并且目前没有一种在人类中被用作治疗药物。在这篇综述中,我们探讨了细菌素结构和功能的广泛多样性,描述了鉴定和优化方法,并讨论了这些潜在有价值的抗菌药物在实验室之外缺乏转化的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b337/7616364/1bc2c3268894/EMS196679-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b337/7616364/0c25d11f5f80/EMS196679-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b337/7616364/bc44ec66e693/EMS196679-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b337/7616364/e9f1b21f14cf/EMS196679-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b337/7616364/1bc2c3268894/EMS196679-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b337/7616364/0c25d11f5f80/EMS196679-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b337/7616364/bc44ec66e693/EMS196679-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b337/7616364/e9f1b21f14cf/EMS196679-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b337/7616364/1bc2c3268894/EMS196679-f003.jpg

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