Jones C J, Aizawa S
ERATO, Research Development Corporation of Japan, Ibaraki.
Adv Microb Physiol. 1991;32:109-72. doi: 10.1016/s0065-2911(08)60007-7.
The bacterial flagellum is a complex multicomponent structure which serves as the propulsive organelle for many species of bacteria. Rotation of the helical flagellar filament, driven by a proton-powered motor embedded in the cell wall, enables the flagellum to function as a screw propeller. It seems likely that almost all of the genes required for flagellar formation and function have been identified. Continuing analysis of the portions of the genome containing these genes may reveal the existence of a few more. Transcription of the flagellar genes is under the control of the products of a single operon, and so these genes constitute a regulon. Other controls, both transcriptional and post-transcriptional, have been identified. Many of these genes have been sequenced, and the information obtained will aid in the design of experiments to clarify the various regulatory mechanisms of the flagellar regulon. The flagellum is composed of several substructures. The long helical filament is connected via the flexible hook to the complex basal body which is located in the cell wall. The filament is composed of many copies of a single protein, and can adopt a number of distinct helical forms. Structural analyses of the filament are adding to our understanding of this dynamic polymer. The component proteins of the hook and filament have all been identified. Continuing studies on the structure of the basal body have revealed the presence of several hitherto unknown basal-body proteins, whose identities and functions have yet to be elucidated. The proteins essential for energizing the motor, the Mot and switch proteins, are thought to exist as multisubunit complexes peripheral to the basal body. These complexes have yet to be identified biochemically or morphologically. Not surprisingly, flagellar assembly is a complex process, occurring in several stages. Assembly occurs in a proximal-to-distal fashion; the basal body is assembled before the hook, and the hook before the filament. This pattern is also maintained within the filament, with monomers added at the distal end of the polymer; the same is presumably true of the other axial components. An exception to this general pattern is assembly of the Mot proteins into the motor, which appears to be possible at any time during flagellar assembly. With the identification of the genes encoding many of the flagellar proteins, the roles of these proteins in assembly is understood, but the function of a number of gene products in flagellar formation remains unknown.(ABSTRACT TRUNCATED AT 400 WORDS)
细菌鞭毛是一种复杂的多组分结构,是许多细菌的推进细胞器。由嵌入细胞壁的质子驱动马达驱动的螺旋状鞭毛丝的旋转,使鞭毛能够像螺旋桨一样发挥作用。几乎所有鞭毛形成和功能所需的基因似乎都已被识别。对包含这些基因的基因组部分的持续分析可能会发现更多基因的存在。鞭毛基因的转录受单个操纵子产物的控制,因此这些基因构成一个调节子。还发现了其他转录和转录后控制。许多这些基因已经被测序,所获得的信息将有助于设计实验以阐明鞭毛调节子的各种调节机制。鞭毛由几个亚结构组成。长螺旋状的鞭毛丝通过柔性钩连接到位于细胞壁中的复杂基体。鞭毛丝由单一蛋白质的多个拷贝组成,可以呈现多种不同的螺旋形式。对鞭毛丝的结构分析加深了我们对这种动态聚合物的理解。钩和鞭毛丝的组成蛋白都已被识别。对基体结构的持续研究揭示了几种迄今未知的基体蛋白的存在,其身份和功能尚待阐明。为马达提供能量所必需的Mot蛋白和开关蛋白,被认为以多亚基复合物的形式存在于基体周围。这些复合物尚未通过生化或形态学方法鉴定。毫不奇怪,鞭毛组装是一个复杂的过程,分几个阶段进行。组装以近端到远端的方式进行;基体在钩之前组装,钩在鞭毛丝之前组装。这种模式在鞭毛丝内也得以维持,单体在聚合物的远端添加;其他轴向组件可能也是如此。这种一般模式的一个例外是Mot蛋白组装到马达中,这似乎在鞭毛组装的任何时候都有可能。随着许多鞭毛蛋白编码基因的识别,这些蛋白在组装中的作用已为人所知,但一些基因产物在鞭毛形成中的功能仍然未知。(摘要截断于400字)