Spormann A M
Departments of Civil and Environmental Engineering and of Biological Sciences, Stanford University, Stanford, California 94305, USA.
Microbiol Mol Biol Rev. 1999 Sep;63(3):621-41. doi: 10.1128/MMBR.63.3.621-641.1999.
Gliding motility is observed in a large variety of phylogenetically unrelated bacteria. Gliding provides a means for microbes to travel in environments with a low water content, such as might be found in biofilms, microbial mats, and soil. Gliding is defined as the movement of a cell on a surface in the direction of the long axis of the cell. Because this definition is operational and not mechanistic, the underlying molecular motor(s) may be quite different in diverse microbes. In fact, studies on the gliding bacterium Myxococcus xanthus suggest that two independent gliding machineries, encoded by two multigene systems, operate in this microorganism. One machinery, which allows individual cells to glide on a surface, independent of whether the cells are moving alone or in groups, requires the function of the genes of the A-motility system. More than 37 A-motility genes are known to be required for this form of movement. Depending on an additional phenotype, these genes are divided into two subclasses, the agl and cgl genes. Videomicroscopic studies on gliding movement, as well as ultrastructural observations of two myxobacteria, suggest that the A-system motor may consist of multiple single motor elements that are arrayed along the entire cell body. Each motor element is proposed to be localized to the periplasmic space and to be anchored to the peptidoglycan layer. The force to glide which may be generated here is coupled to adhesion sites that move freely in the outer membrane. These adhesion sites provide a specific contact with the substratum. Based on single-cell observations, similar models have been proposed to operate in the unrelated gliding bacteria Flavobacterium johnsoniae (formerly Cytophaga johnsonae), Cytophaga strain U67, and Flexibacter polymorphus (a filamentous glider). Although this model has not been verified experimentally, M. xanthus seems to be the ideal organism with which to test it, given the genetic tools available. The second gliding motor in M. xanthus controls cell movement in groups (S-motility system). It is dependent on functional type IV pili and is operative only when cells are in close proximity to each other. Type IV pili are known to be involved in another mode of bacterial surface translocation, called twitching motility. S-motility may well represent a variation of twitching motility in M. xanthus. However, twitching differs from gliding since it involves cell movements that are jerky and abrupt and that lack the organization and smoothness observed in gliding. Components of this motor are encoded by genes of the S-system, which appear to be homologs of genes involved in the biosynthesis, assembly, and function of type IV pili in Pseudomonas aeruginosa and Neisseria gonorrhoeae. How type IV pili generate force in S-motility is currently unknown, but it is to be expected that ongoing physiological, genetic, and biochemical studies in M. xanthus, in conjunction with studies on twitching in P. aeruginosa and N. gonorrhoeae, will provide important insights into this microbial motor. The two motility systems of M. xanthus are affected to different degrees by the MglA protein, which shows similarity to a small GTPase. Bacterial chemotaxis-like sensory transduction systems control gliding motility in M. xanthus. The frz genes appear to regulate gliding movement of individual cells and movement by the S-motility system, suggesting that the two motors found in this bacterium can be regulated to result in coordinated multicellular movements. In contrast, the dif genes affect only S-system-dependent swarming.
在多种系统发育上不相关的细菌中都观察到了滑行运动。滑行运动为微生物在低含水量环境中移动提供了一种方式,比如在生物膜、微生物垫和土壤中可能存在的环境。滑行被定义为细胞在表面上沿细胞长轴方向的移动。由于这个定义是基于操作层面而非机制层面的,不同微生物中潜在的分子马达可能有很大差异。事实上,对滑行细菌黄色黏球菌的研究表明,由两个多基因系统编码的两种独立的滑行机制在这种微生物中发挥作用。一种机制使单个细胞能够在表面滑行,无论细胞是单独移动还是成群移动,这种机制需要A运动系统基因的功能。已知这种运动形式需要超过37个A运动基因。根据另一种表型,这些基因被分为两个亚类,即agl基因和cgl基因。对滑行运动的视频显微镜研究以及对两种黏细菌的超微结构观察表明,A系统马达可能由多个沿整个细胞体排列的单个马达元件组成。每个马达元件被认为定位于周质空间并锚定在肽聚糖层上。在此处可能产生的用于滑行的力与在外膜中自由移动的黏附位点相耦合。这些黏附位点与底物形成特定接触。基于单细胞观察,已提出类似模型在不相关的滑行细菌约翰逊黄杆菌(以前称为约翰逊纤维黏菌)、纤维黏菌菌株U67和多形弯曲杆菌(一种丝状滑行菌)中起作用。尽管这个模型尚未经过实验验证,但鉴于现有的遗传工具,黄色黏球菌似乎是测试它的理想生物体。黄色黏球菌中的第二种滑行马达控制细胞群体运动(S运动系统)。它依赖于功能性IV型菌毛,并且仅在细胞彼此紧邻时起作用。已知IV型菌毛参与细菌表面易位的另一种模式,称为颤动运动。S运动可能很好地代表了黄色黏球菌中颤动运动的一种变体。然而,颤动与滑行不同,因为它涉及细胞的突然且急促的运动,缺乏滑行中观察到的组织性和平滑性。这个马达的组件由S系统的基因编码,这些基因似乎是参与铜绿假单胞菌和淋病奈瑟菌中IV型菌毛生物合成、组装和功能的基因的同源物。IV型菌毛如何在S运动中产生力目前尚不清楚,但可以预期,正在对黄色黏球菌进行的生理、遗传和生化研究,以及对铜绿假单胞菌和淋病奈瑟菌中颤动运动的研究,将为这种微生物马达提供重要见解。黄色黏球菌的两种运动系统受到与小GTP酶相似的MglA蛋白不同程度的影响。细菌趋化样感觉转导系统控制黄色黏球菌的滑行运动。frz基因似乎调节单个细胞的滑行运动以及S运动系统的运动,这表明在这种细菌中发现的两种马达可以被调节以导致协调的多细胞运动。相比之下,dif基因仅影响依赖S系统的群体游动。