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Spontaneous adaptation of ion selectivity in a bacterial flagellar motor

Pietro Ridone, Tsubasa Ishida, View ORCID ProfileYoshiyuki Sowa, View ORCID ProfileMatthew A. B. Baker
doi: https://doi.org/10.1101/2021.01.26.427765
Pietro Ridone
1School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, Australia
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Tsubasa Ishida
2Department of Frontier Bioscience, Hosei University, Tokyo, Japan
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Yoshiyuki Sowa
2Department of Frontier Bioscience, Hosei University, Tokyo, Japan
3Research Center for Micro-Nano Technology, Hosei University, Tokyo, Japan
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  • ORCID record for Yoshiyuki Sowa
Matthew A. B. Baker
1School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, Australia
4CSIRO Synthetic Biology Future Science Platform, Brisbane, Australia
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  • ORCID record for Matthew A. B. Baker
  • For correspondence: matthew.baker@unsw.edu.au
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ABSTRACT

Motility provides a selective advantage to many bacterial species and is often achieved by rotation of flagella that propel the cell towards more favourable conditions. In most species, the rotation of the flagellum, driven by the Bacterial Flagellar Motor (BFM), is powered by H+ or Na+ ion transit through the torque-generating stator subunits of the motor complex. The ionic requirements for motility appear to have adapted to environmental changes throughout history but the molecular basis of this adaptation, and the constraints which govern the evolution of the stator proteins are unknown. Here we use CRISPR-mediated genome engineering to replace the native H+-powered stator genes of Escherichia coli with a compatible sodium-powered stator set from Vibrio alginolyticus and subsequently direct the evolution of the stators to revert to H+-powered motility. Evidence from whole genome sequencing indicates both flagellar- and non-flagellar-associated genes that are involved in longer-term adaptation to new power sources. Overall, transplanted Na+-powered stator genes can spontaneously incorporate novel mutations that allow H+-motility when environmental Na+ is lacking.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • Update to include single-cell tracking data (Supplementary Fig. 9).

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted February 22, 2021.
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Spontaneous adaptation of ion selectivity in a bacterial flagellar motor
Pietro Ridone, Tsubasa Ishida, Yoshiyuki Sowa, Matthew A. B. Baker
bioRxiv 2021.01.26.427765; doi: https://doi.org/10.1101/2021.01.26.427765
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Spontaneous adaptation of ion selectivity in a bacterial flagellar motor
Pietro Ridone, Tsubasa Ishida, Yoshiyuki Sowa, Matthew A. B. Baker
bioRxiv 2021.01.26.427765; doi: https://doi.org/10.1101/2021.01.26.427765

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