Nishiyama Masayoshi, Arai Yoshiyuki
The Hakubi Center for Advanced Research/Institute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University, Yoshida-Honmachi, Sakyo-ku, Kyoto, 606-8501, Japan.
The Institute of Scientific and Industrial Research, Osaka University, 1-8, Mihogaoka, Ibaraki, 567-0047, Osaka, Japan.
Methods Mol Biol. 2017;1593:175-184. doi: 10.1007/978-1-4939-6927-2_13.
Many bacterial species move toward favorable habitats. The flagellum is one of the most important machines required for the motility in solution and is conserved across a wide range of bacteria. The motility machinery is thought to function efficiently with a similar mechanism in a variety of environmental conditions, as many cells with similar machineries have been isolated from harsh environments. To understand the common mechanism and its diversity, microscopic examination of bacterial movements is a crucial step. Here, we describe a method to characterize the swimming motility of cells in extreme environmental conditions. This microscopy system enables acquisition of high-resolution images under high-pressure conditions. The temperature and oxygen concentration can also be manipulated. In addition, we also describe a method to track the movement of swimming cells using an ImageJ plugin. This enables characterization of the swimming motility of the selected cells.
许多细菌种类会朝着适宜的栖息地移动。鞭毛是在溶液中运动所需的最重要的机制之一,并且在广泛的细菌中都存在。运动机制被认为在各种环境条件下以相似的机制高效运作,因为许多具有相似机制的细胞已从恶劣环境中分离出来。为了理解其共同机制及其多样性,对细菌运动进行显微镜检查是关键一步。在此,我们描述一种在极端环境条件下表征细胞游动运动性的方法。该显微镜系统能够在高压条件下获取高分辨率图像。温度和氧气浓度也可以进行调控。此外,我们还描述一种使用ImageJ插件追踪游动细胞运动的方法。这能够对所选细胞的游动运动性进行表征。