Obuchowski Pamela L, Jacobs-Wagner Christine
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06520-8103, USA.
J Bacteriol. 2008 Mar;190(5):1718-29. doi: 10.1128/JB.01706-07. Epub 2007 Dec 28.
The bacterial flagellum is important for motility and adaptation to environmental niches. The sequence of events required for the synthesis of the flagellar apparatus has been extensively studied, yet the events that dictate where the flagellum is placed at the onset of flagellar biosynthesis remain largely unknown. We addressed this question for alphaproteobacteria by using the polarly flagellated alphaproteobacterium Caulobacter crescentus as an experimental model system. To identify candidates for a role in flagellar placement, we searched all available alphaproteobacterial genomes for genes of unknown function that cluster with early flagellar genes and that are present in polarly flagellated alphaproteobacteria while being absent in alphaproteobacteria with other flagellation patterns. From this in silico screen, we identified pflI. Loss of PflI function in C. crescentus results in an abnormally high frequency of cells with a randomly placed flagellum, while other aspects of cell polarization remain normal. In a wild-type background, a fusion of green fluorescent protein (GFP) and PflI localizes to the pole where the flagellum develops. This polar localization is independent of the flagellar protein FliF, whose oligomerization into the MS ring is thought to define the site of flagellar synthesis, suggesting that PflI acts before or independently of this event. Overproduction of PflI-GFP often leads to ectopic localization at the wrong, stalked pole. This is accompanied by a high frequency of flagellum formation at this ectopic site, suggesting that the location of PflI is a sufficient marker for a site for flagellar assembly.
细菌鞭毛对于运动性和适应环境生态位很重要。鞭毛装置合成所需的一系列事件已得到广泛研究,但在鞭毛生物合成开始时决定鞭毛位置的事件仍基本未知。我们以极生鞭毛的α-变形菌新月柄杆菌作为实验模型系统,来解决α-变形菌的这个问题。为了确定在鞭毛定位中起作用的候选基因,我们在所有可用的α-变形菌基因组中搜索功能未知的基因,这些基因与早期鞭毛基因聚集在一起,并且存在于极生鞭毛的α-变形菌中,而在具有其他鞭毛模式的α-变形菌中不存在。通过这种计算机筛选,我们鉴定出了pflI。新月柄杆菌中PflI功能的丧失导致鞭毛随机定位的细胞频率异常高,而细胞极化的其他方面仍保持正常。在野生型背景下,绿色荧光蛋白(GFP)与PflI的融合蛋白定位于鞭毛发育的极。这种极性定位独立于鞭毛蛋白FliF,其寡聚形成MS环被认为决定了鞭毛合成的位点,这表明PflI在该事件之前起作用或独立于该事件起作用。PflI-GFP的过量表达常常导致在错误的、有柄的极异位定位。这伴随着在这个异位位点形成鞭毛的频率很高,表明PflI的位置是鞭毛组装位点的一个充分标记。