| Literature DB >> 33051299 |
Yoshiaki Kinosita1,2, Nagisa Mikami2, Zhengqun Li2, Frank Braun2, Tessa E F Quax2, Chris van der Does2, Robert Ishmukhametov3, Sonja-Verena Albers2, Richard M Berry3.
Abstract
Archaea swim using the archaellum (archaeal flagellum), a reversible rotary motor consisting of a torque-generating motor and a helical filament, which acts as a propeller. Unlike the bacterial flagellar motor (BFM), ATP (adenosine-5'-triphosphate) hydrolysis probably drives both motor rotation and filamentous assembly in the archaellum. However, direct evidence is still lacking due to the lack of a versatile model system. Here, we present a membrane-permeabilized ghost system that enables the manipulation of intracellular contents, analogous to the triton model in eukaryotic flagella and gliding Mycoplasma We observed high nucleotide selectivity for ATP driving motor rotation, negative cooperativity in ATP hydrolysis, and the energetic requirement for at least 12 ATP molecules to be hydrolyzed per revolution of the motor. The response regulator CheY increased motor switching from counterclockwise (CCW) to clockwise (CW) rotation. Finally, we constructed the torque-speed curve at various [ATP]s and discuss rotary models in which the archaellum has characteristics of both the BFM and F1-ATPase. Because archaea share similar cell division and chemotaxis machinery with other domains of life, our ghost model will be an important tool for the exploration of the universality, diversity, and evolution of biomolecular machinery.Entities:
Keywords: ATPase; Michaelis–Menten kinetics; archaellum; membrane-permeabilized ghost; rotary motor
Mesh:
Substances:
Year: 2020 PMID: 33051299 PMCID: PMC7604481 DOI: 10.1073/pnas.2009814117
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205