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      Flagellar polymorphism-dependent bacterial swimming motility in a structured environment

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          Abstract

          Most motile bacteria use supramolecular motility machinery called bacterial flagellum, which converts the chemical energy gained from ion flux into mechanical rotation. Bacterial cells sense their external environment through a two-component regulatory system consisting of a histidine kinase and response regulator. Combining these systems allows the cells to move toward favorable environments and away from their repellents. A representative example of flagellar motility is run-and-tumble swimming in Escherichia coli, where the counter-clockwise (CCW) rotation of a flagellar bundle propels the cell forward, and the clockwise (CW) rotation undergoes cell re-orientation (tumbling) upon switching the direction of flagellar motor rotation from CCW to CW. In this mini review, we focus on several types of chemotactic behaviors that respond to changes in flagellar shape and direction of rotation. Moreover, our single-cell analysis demonstrated back-and-forth swimming motility of an original E. coli strain. We propose that polymorphic flagellar changes are required to enhance bacterial movement in a structured environment as a colony spread on an agar plate.

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          Most cited references73

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          Bacteria swim by rotating their flagellar filaments.

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            Real-time imaging of fluorescent flagellar filaments.

            Bacteria swim by rotating flagellar filaments that are several micrometers long, but only about 20 nm in diameter. The filaments can exist in different polymorphic forms, having distinct values of curvature and twist. Rotation rates are on the order of 100 Hz. In the past, the motion of individual filaments has been visualized by dark-field or differential-interference-contrast microscopy, methods hampered by intense scattering from the cell body or shallow depth of field, respectively. We have found a simple procedure for fluorescently labeling cells and filaments that allows recording their motion in real time with an inexpensive video camera and an ordinary fluorescence microscope with mercury-arc or strobed laser illumination. We report our initial findings with cells of Escherichia coli. Tumbles (events that enable swimming cells to alter course) are remarkably varied. Not every filament on a cell needs to change its direction of rotation: different filaments can change directions at different times, and a tumble can result from the change in direction of only one. Polymorphic transformations tend to occur in the sequence normal, semicoiled, curly 1, with changes in the direction of movement of the cell body correlated with transformations to the semicoiled form.
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              The surprisingly diverse ways that prokaryotes move.

              Prokaryotic cells move through liquids or over moist surfaces by swimming, swarming, gliding, twitching or floating. An impressive diversity of motility mechanisms has evolved in prokaryotes. Movement can involve surface appendages, such as flagella that spin, pili that pull and Mycoplasma 'legs' that walk. Internal structures, such as the cytoskeleton and gas vesicles, are involved in some types of motility, whereas the mechanisms of some other types of movement remain mysterious. Regardless of the type of motility machinery that is employed, most motile microorganisms use complex sensory systems to control their movements in response to stimuli, which allows them to migrate to optimal environments.
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                Author and article information

                Contributors
                yoshiaki.kinosita@gmail.com
                ysowa@hosei.ac.jp
                Journal
                Biophys Physicobiol
                Biophys Physicobiol
                Biophysics and Physicobiology
                The Biophysical Society of Japan
                2189-4779
                14 June 2023
                30 May 2023
                : 20
                : 2
                : e200024
                Affiliations
                [1 ] CPR, RIKEN , Wako, Saitama 351-0198, Japan
                [2 ] Department of Frontier Bioscience, Hosei University , Tokyo 184-8584, Japan
                [3 ] Research Center for Micro-Nano Technology, Hosei University , Tokyo 184-8584, Japan
                Author notes
                Corresponding authors: Yoshiaki Kinosita, CPR, RIKEN, Wako, Saitama 351-0198, Japan. ORCID iD: https://orcid.org/0000-0003-4521-2800, e-mail: yoshiaki.kinosita@gmail.com; Yoshiyuki Sowa, Department of Frontier Bioscience, Hosei University, 3-7-2 Kajino-cho, Koganei, Tokyo 184-8584, Japan. ORCID iD: https://orcid.org/0000-0002-1691-2018, e-mail: ysowa@hosei.ac.jp

                Edited by Makoto Miyata

                Author information
                https://orcid.org/0000-0003-4521-2800
                https://orcid.org/0000-0002-1691-2018
                Article
                JST.JSTAGE/biophysico/e200024 e200024
                10.2142/biophysico.bppb-v20.0024
                10587448
                37867560
                36b6716f-ead4-4ad6-aa05-f1802425c775
                2023 THE BIOPHYSICAL SOCIETY OF JAPAN

                This article is licensed under the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 Inter­national License. To view a copy of this license, visit 
 https://creativecommons.org/licenses/by-nc-sa/4.0/.

                History
                : 18 April 2023
                : 29 May 2023
                Categories
                Review Article (Invited)

                bacterial flagellum,flagellar polymorphism,chemotaxis,colony spreading,tirfm

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