Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.
Geisel School of Medicine at Dartmouth, Hanover, New Hampshire 03755, USA; email:
Annu Rev Microbiol. 2020 Sep 8;74:607-631. doi: 10.1146/annurev-micro-011520-094214. Epub 2020 Jul 20.
Biofilms are the dominant bacterial lifestyle. The regulation of the formation and dispersal of bacterial biofilms has been the subject of study in many organisms. Over the last two decades, the mechanisms of biofilm formation and regulation have emerged as among the best understood of any bacterial biofilm system. Biofilm formation by occurs through the localization of an adhesin, LapA, to the outer membrane via a variant of the classical type I secretion system. The decision between biofilm formation and dispersal is mediated by LapD, a c-di-GMP receptor, and LapG, a periplasmic protease, which together control whether LapA is retained or released from the cell surface. LapA localization is also controlled by a complex network of c-di-GMP-metabolizing enzymes. This review describes the current understanding of LapA-mediated biofilm formation by and discusses several emerging models for the regulation and function of this adhesin.
生物膜是细菌的主要生存方式。许多生物体的研究都集中在细菌生物膜的形成和分散的调节上。在过去的二十年中,生物膜的形成和调节机制已成为最被理解的细菌生物膜系统之一。 通过一种变体的经典 I 型分泌系统,将一种黏附素 LapA 定位到外膜,从而形成生物膜。生物膜形成和分散的决定是由 c-di-GMP 受体 LapD 和周质蛋白酶 LapG 介导的,它们共同控制 LapA 是保留在细胞表面还是从细胞表面释放。LapA 的定位也受到 c-di-GMP 代谢酶的复杂网络的控制。这篇综述描述了目前对 生物膜形成的理解,并讨论了这个黏附素的几个新兴调节和功能模型。