细菌
信号肽酶
化学
生物化学
信号肽
抗菌活性
抗菌剂
抗生素
酶
微生物学
生物
肽序列
基因
遗传学
作者
Natalia Szałaj,Andrea Benediktsdottir,Dominika Rusin,Anders Karlén,Sherry L. Mowbray,Anna Więckowska
标识
DOI:10.1016/j.ejmech.2022.114490
摘要
The ever-increasing number of bacteria resistant to the currently available antibacterial agents is a great medical problem today, and new antibiotics with novel mechanisms of action are urgently needed. Among the validated antibacterial drug targets against which new classes of antibiotics might be directed is bacterial type I signal peptidase (SPase I), an essential part of the Tat and Sec secretory systems. SPase I is responsible for the hydrolysis of the N-terminal signal peptides from proteins secreted across the cytoplasmic membrane and plays a key role in bacterial viability and virulence. This review focuses on the antibacterial activity of natural and synthetic SPase I inhibitors reported to date, namely β-lactams, lipopeptides, and arylomycins, but also an example of SPase I activator was presented.
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