Ridgway H F, Lewin R A
Scripps Institution of Oceanography, University of California, San Diego, La Jolla.
Cell Motil Cytoskeleton. 1988;11(1):46-63. doi: 10.1002/cm.970110106.
Motility of the marine gliding bacterium Flexibacter polymorphus was studied by using microcinematographic techniques. Following adhesion to a glass surface, multicellular filaments and individual cells usually began to glide within a few seconds at a speed of approximately 12 micron per second (at 23 degrees C). Adhesion to the glass surface was evidently mediated by multitudes of extremely fine extracellular fibrils. Gliding velocity was independent of filament length but directly related to electron-transport activity and substratum temperature in the range 3-35 degrees C. The rate of gliding was inversely related to medium viscosity, suggesting that the locomotor apparatus functions at constant torque. Forward motion was occasionally interrupted by direction reversals, somersaults (observed primarily in single cells of short filaments), or spinning of filaments tethered by one pole. The frequency of direction reversal was found to be an inverse function of filament length. Translational motility was invariably accompanied by sinistral revolution about the longitudinal axis of a filament. The sense and pitch of revolution were constant among filaments of different length. Polystyrene microspheres or India ink particles adsorbed to gliding cells were actively displaced in either direction, their movement tracing either a regular zigzag or helical path along the filament surface. Because microspheres were also observed to move on nonmotile filaments, particle translocation was evidently not obligatorily linked to gliding locomotion. Multiple particles adsorbed to a single filament often moved independently. The data are consistent with a motility mechanism involving limited motion in numerous mechanically independent (yet functionally coordinated) domains on the cell surface.
利用显微电影摄影技术研究了海洋滑行细菌多形屈挠杆菌的运动性。在附着于玻璃表面后,多细胞丝状体和单个细胞通常在几秒钟内开始以约每秒12微米的速度滑行(在23摄氏度时)。对玻璃表面的附着显然是由大量极细的细胞外纤丝介导的。滑行速度与丝状体长度无关,但与电子传递活性以及3至35摄氏度范围内的基质温度直接相关。滑行速率与培养基粘度成反比,这表明运动装置以恒定扭矩起作用。向前运动偶尔会因方向反转、翻跟头(主要在短丝状体的单个细胞中观察到)或由一端固定的丝状体旋转而中断。发现方向反转的频率是丝状体长度的反函数。平移运动总是伴随着丝状体围绕其纵轴的左旋旋转。不同长度丝状体的旋转方向和螺距是恒定的。吸附在滑行细胞上的聚苯乙烯微球或印度墨汁颗粒在任一方向上都被主动移动,它们的运动沿着丝状体表面描绘出规则的之字形或螺旋形路径。由于也观察到微球在不运动的丝状体上移动,颗粒移位显然不一定与滑行运动相关联。吸附在单根丝状体上的多个颗粒通常独立移动。这些数据与一种运动机制一致,该机制涉及细胞表面众多机械上独立(但功能上协调)的区域中的有限运动。