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Frontiers in Microbiology, 6, 23. https://doi.org/10.3389/fmicb.2015.00023CrossrefPubMedWeb of Science®Google Scholar
Berry, J. L., & Pelicic, V. (2015). Exceptionally widespread nanomachines composed of type IV pilins: The prokaryotic Swiss Army knives.
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In bacterial pili, an ATPase hexamer rotates at the base of the pilus, which is responsible for pili extension and retraction (Chang et al., 2016; McCallum, Tammam, Khan, Burrows, & Howell, 2017). This rotational property appears to have been adapted in archaella to be used for swimming. It is interesting that the Archaea swimming mode resembles the bacterial flagella swimming mode (Kinosita, Uchida, Nakane, & Nishizaka, 2016), because it likely evolved from pili that display a different mode of motility.
Daum, B., Vonck, J., Bellack, A., Chaudhury, P., Reichelt, R., Albers, S. V., …Kuhlbrandt, W. (2017). Structure and in situ organisation of the Pyrococcus furiosus archaellum machinery. eLife, 6, e27470, https://doi.org/10.7554/eLife.27470CrossrefPubMedWeb of Science®Google Scholar
Holscher, T., & Kovacs, A. T. (2017). Sliding on the surface: Bacterial spreading without an active motor.
Liu, P., Zheng, H., Meng, Q., Terahara, N., Gu, W., Wang, S., … Miyata, M. (2017). Chemotaxis without conventional two-component system, based on cell polarity and aerobic conditions in helicity-switching swimming of Spiroplasma eriocheiris.
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Minamino, T., Terahara, N., Kojima, S., & Namba, K. (2018). Autonomous control mechanism of stator assembly in the bacterial flagellar motor in response to changes in the environment.
Mizutani, M., & Miyata, M. (2019). Behaviors and energy source of Mycoplasma gallisepticum gliding.
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