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基于细菌素发现新型抗菌剂的方法。

Approaches to the discovery of new antibacterial agents based on bacteriocins.

作者信息

Sit Clarissa S, Vederas John C

机构信息

Department of Chemistry, University of Alberta, 11227 Saskatchewan Drive, Edmonton, AB T6G2G2, Canada.

出版信息

Biochem Cell Biol. 2008 Apr;86(2):116-23. doi: 10.1139/O07-153.

Abstract

The development of antibiotic resistance in pathogenic bacteria has led to a search for novel classes of antimicrobial drugs. Bacteriocins are peptides that are naturally produced by bacteria and have considerable potential to fulfill the need for more effective bacteriocidal agents. In this mini-review, we describe research aimed at generating analogues of bacteriocins from lactic acid bacteria, with the goal of gaining a better understanding of structure-activity relationships in these peptides. In particular, we report recent findings on synthetic analogues of leucocin A, pediocin PA1, and lacticin 3147 A2, as well as on the significance of these results for the design and production of new antibiotics.

摘要

病原菌中抗生素耐药性的发展促使人们寻找新型抗菌药物。细菌素是细菌天然产生的肽,在满足对更有效杀菌剂的需求方面具有巨大潜力。在本综述中,我们描述了旨在生成乳酸菌细菌素类似物的研究,目的是更好地理解这些肽的构效关系。特别是,我们报告了关于亮菌素A、片球菌素PA1和乳酸乳球菌素3147 A2合成类似物的最新发现,以及这些结果对新抗生素设计和生产的意义。

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