Institute of Biochemistry, Heinrich-Heine-University, Duesseldorf, Germany.
Center for Structural Studies, Heinrich-Heine-University, Duesseldorf, Germany.
FEBS Lett. 2020 Dec;594(23):3920-3942. doi: 10.1002/1873-3468.13953. Epub 2020 Oct 22.
Bacteria produce under certain stress conditions bacteriocins and microcins that display antibacterial activity against closely related species for survival. Bacteriocins and microcins exert their antibacterial activity by either disrupting the membrane or inhibiting essential intracellular processes of the bacterial target. To this end, they can lyse bacterial membranes and cause subsequent loss of their integrity or nutrients, or hijack membrane receptors for internalisation. Both bacteriocins and microcins are ribosomally synthesised and several are posttranslationally modified, whereas others are not. Such peptides are also toxic to the producer bacteria, which utilise immunity proteins or/and dedicated ATP-binding cassette (ABC) transporters to achieve self-immunity and peptide export. In this review, we discuss the structure and mechanism of self-protection that is conferred by these ABC transporters.
在某些应激条件下,细菌会产生具有抗细菌活性的细菌素和微菌素,以在生存竞争中击败亲缘关系较近的物种。细菌素和微菌素通过破坏细胞膜或抑制细菌靶标的重要细胞内过程来发挥其抗菌活性。为此,它们可以裂解细菌膜并导致随后的完整性丧失或营养物质流失,或者劫持细胞膜受体进行内化。细菌素和微菌素都是核糖体合成的,其中一些经过翻译后修饰,而另一些则没有。这些肽对产生它们的细菌也是有毒的,细菌会利用免疫蛋白和/或专门的 ATP 结合盒 (ABC) 转运蛋白来实现自我免疫和肽的输出。在这篇综述中,我们讨论了这些 ABC 转运蛋白赋予的自我保护的结构和机制。