Khambaty F M, Ely B
Department of Biological Sciences, University of South Carolina, Columbia 29208.
J Bacteriol. 1992 Jun;174(12):4101-9. doi: 10.1128/jb.174.12.4101-4109.1992.
The differentiating bacterium Caulobacter crescentus has been studied extensively to understand how a relatively simple life form can govern the timing of expression of genes needed for the production of stage-specific structures. In this study, a clone containing the 5.3-kb flaP region was shown to contain the flgI, cheL, and flbY genes arranged in an operon with transcription proceeding from flgI to flbY. The predicted flgI polypeptide shows remarkable identity (44%) to the flagellar basal body P-ring protein encoded by the flgI gene of Salmonella typhimurium. flgI mutations case a reduction in the levels of flagellin production and the overproduction of the hook proteins. Therefore, the flgI-encoded P-ring protein is required for normal flagellin and hook protein synthesis, suggesting that basal body assembly may play a role in the regulation of flagellar gene expression. The flbY gene probably is a basal body component as well, since flbY mutants have flagellin and hook protein synthesis patterns similar to those exhibited by other basal body mutants. The smaller cheL gene complements a mutant that is unable to respond to chemotactic signals despite possessing a functional flagellum. This is the first example of an operon containing both flagellar and chemotaxis genes in C. crescentus.
为了理解一种相对简单的生命形式如何控制产生阶段特异性结构所需基因的表达时间,人们对分化细菌新月柄杆菌进行了广泛研究。在本研究中,一个包含5.3 kb flaP区域的克隆被证明含有flgI、cheL和flbY基因,它们排列在一个操纵子中,转录从flgI开始到flbY结束。预测的flgI多肽与鼠伤寒沙门氏菌flgI基因编码的鞭毛基体P环蛋白具有显著的同源性(44%)。flgI突变导致鞭毛蛋白产生水平降低和钩蛋白过量产生。因此,flgI编码的P环蛋白是正常鞭毛蛋白和钩蛋白合成所必需的,这表明基体组装可能在鞭毛基因表达的调控中起作用。flbY基因可能也是一种基体成分,因为flbY突变体的鞭毛蛋白和钩蛋白合成模式与其他基体突变体相似。较小的cheL基因可互补一个尽管具有功能性鞭毛但无法对趋化信号作出反应的突变体。这是新月柄杆菌中一个同时包含鞭毛和趋化基因的操纵子的首个例子。