The presence and absence of periplasmic rings in bacterial flagellar motors correlates with stator type.
basic_science · Level V
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- Record sourced from PubMed, PMID 30648971.
- Also identified by DOI 10.7554/eLife.43487 and PMC identifier 6375700.
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Abstract
The bacterial flagellar motor, a cell-envelope-embedded macromolecular machine that functions as a cellular propeller, exhibits significant structural variability between species. Different torque-generating stator modules allow motors to operate in different pH, salt or viscosity levels. How such diversity evolved is unknown. Here, we use electron cryo-tomography to determine the in situ macromolecular structures of three Gammaproteobacteria motors: <i>Legionella pneumophila</i>, <i>Pseudomonas aeruginosa</i>, and <i>Shewanella oneidensis</i>, providing the first views of intact motors with dual stator systems. Complementing our imaging with bioinformatics analysis, we find a correlation between the motor's stator system and its structural elaboration. Motors with a single H<sup>+</sup>-driven stator have only the core periplasmic P- and L-rings; those with dual H<sup>+</sup>-driven stators have an elaborated P-ring; and motors with Na<sup>+</sup> or Na<sup>+</sup>/H<sup>+</sup>-driven stators have both their P- and L-rings embellished. Our results suggest an evolution of structural elaboration that may have enabled pathogenic bacteria to colonize higher-viscosity environments in animal hosts.
Medical subject headings
- Flagella
- Gammaproteobacteria
- Molecular Motor Proteins
- Periplasm