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Merck
CN

Motile ghosts of the halophilic archaeon, Haloferax volcanii.

Proceedings of the National Academy of Sciences of the United States of America (2020-10-15)
Yoshiaki Kinosita, Nagisa Mikami, Zhengqun Li, Frank Braun, Tessa E F Quax, Chris van der Does, Robert Ishmukhametov, Sonja-Verena Albers, Richard M Berry
摘要

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.

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Sigma-Aldrich
腺苷 5′-三磷酸 二钠盐 水合物, Grade I, ≥99%, from microbial
Sigma-Aldrich
腺苷-5′-二磷酸 钠盐, bacterial, ≥95% (HPLC)
Sigma-Aldrich
腺苷5′-[γ-硫代]三磷酸盐 四锂盐, ≥75% (HPLC), powder
Sigma-Aldrich
胆酸钠 水合物, from bovine and/or ovine bile, ≥99%