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Bacterial flagellar motor PL-ring disassembly subcomplexes are widespread and ancient
- Source :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Year :
- 2020
-
Abstract
- Significance In order to understand the evolution of complex biological machines like the bacterial flagellar motor, it is crucial to know what each component does and when it arose. Here, we show that a subcomplex of the motor thought to act as a bushing for the spinning motor likely also serves another function—it plugs the hole in the outer membrane left when the flagellum disassembles. Moreover, this component and function is ancient, since it appears in diverse phyla without evidence of recent gene transfer.<br />The bacterial flagellum is an amazing nanomachine. Understanding how such complex structures arose is crucial to our understanding of cellular evolution. We and others recently reported that in several Gammaproteobacterial species, a relic subcomplex comprising the decorated P and L rings persists in the outer membrane after flagellum disassembly. Imaging nine additional species with cryo-electron tomography, here, we show that this subcomplex persists after flagellum disassembly in other phyla as well. Bioinformatic analyses fail to show evidence of any recent horizontal transfers of the P- and L-ring genes, suggesting that this subcomplex and its persistence is an ancient and conserved feature of the flagellar motor. We hypothesize that one function of the P and L rings is to seal the outer membrane after motor disassembly.
- Subjects :
- Electron Microscope Tomography
Genetic Speciation
Evolution
macromolecular substances
Biology
Flagellum
Ring (chemistry)
03 medical and health sciences
Bacterial Proteins
Gene
Phylogeny
030304 developmental biology
flagellar motor
0303 health sciences
Multidisciplinary
Evolution of cells
Bacteria
030306 microbiology
Cryoelectron Microscopy
Computational Biology
Biological Sciences
cryo-electron tomography
Cell biology
Bacterial Outer Membrane
Flagella
Genes, Bacterial
Cryo-electron tomography
Bacterial outer membrane
Function (biology)
Bacterial Outer Membrane Proteins
Subjects
Details
- ISSN :
- 10916490
- Volume :
- 117
- Issue :
- 16
- Database :
- OpenAIRE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Accession number :
- edsair.doi.dedup.....d22305a08c891c022c31dc0b6bb5791a