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首页> 外文期刊>Journal of bacteriology >Expression of two Rhizobium meliloti flagellin genes and their contribution to the complex filament structure.
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Expression of two Rhizobium meliloti flagellin genes and their contribution to the complex filament structure.

机译:两个根瘤菌鞭毛蛋白基因的表达及其对复杂细丝结构的贡献。

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The complex flagellar filaments of Rhizobium meliloti are composed of two related (87% identical) flagellins that are encoded by closely linked, separately transcribed genes, flaA and flaB (E. Pleier and R. Schmitt, J. Bacteriol. 171:1467-1475, 1989). To elucidate the role of the subunits, A and B, in assembling the complex filament, the wild-type alleles were replaced with defective ones containing a 2,249-bp deletion (accompanied by substitution of a kanamycin resistance cartridge), which eliminates 74% of flaA (3' end) and 85% of flaB (5' end). The resulting nonmotile, filamentless mutant, RU11011, was tested for complementation with wild-type flaA, flaB, and flaA flaB genes provided on the multiple-copy vector pRK290. Whereas flaA alone did not restore motility and filament production, both flaB and flaA flaB restored 20 to 30% of wild-type motility. Apparent causes of this reduced motility were fewer flagella per cell and/or shortened filaments sometimes ending in unusually thin, fragile structures. Tests with enzyme-linked antiflagellin antibodies indicated that flaA is expressed at higher levels than flaB and that multiple copies of flaA lead to reduced flagellin export. We conclude that the proximal portion of the complex filament is assembled from B subunits (not produced sufficiently to form full-length flagella) and that the distal portion is made from A subunits. Multiple copies of the strong flaA promoter may offset transcriptional controls that regulate the synthesis of flagellar structures required for flagellin export.
机译:根瘤菌的复杂鞭毛细丝由两个相关的鞭毛蛋白(87%相同)组成,由紧密连接的,分别转录的基因flaA和flaB编码(E.Pleier和R.Schmitt,J.Bacteriol.171:1467-1475 (1989年)。为了阐明亚基A和B在组装复杂的细丝中的作用,将野生型等位基因替换为含有2249 bp缺失的缺陷等位基因(并伴有卡那霉素抗性盒的替换),从而消除了74%的flaA(3'末端)和flaB(5'末端)的85%。测试所得的非运动性无丝突变体RU11011与多拷贝载体pRK290上提供的野生型flaA,flaB和flaA flaB基因的互补性。单独的flaA不能恢复活力和细丝生成,而flaB和flaA flaB都可以恢复20%至30%的野生型活力。这种运动力降低的明显原因是每个细胞的鞭毛较少和/或花丝缩短,有时以异常细弱的结构结束。酶联抗鞭毛蛋白抗体的测试表明,flaA的表达水平高于flaB,并且flaA的多个拷贝导致鞭毛蛋白输出减少。我们得出的结论是,复杂细丝的近端部分由B个亚基组装而成(未充分生产以形成全长鞭毛),而远端部分由A个亚基制成。强效flaA启动子的多个副本可能抵消调节鞭毛蛋白输出所需鞭毛结构合成的转录控制。

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