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两种苜蓿中华根瘤菌鞭毛蛋白基因的表达及其对复杂丝状结构的贡献。

Expression of two Rhizobium meliloti flagellin genes and their contribution to the complex filament structure.

作者信息

Pleier E, Schmitt R

机构信息

Lehrstuhl für Genetik, Universität Regensburg, Federal Republic of Germany.

出版信息

J Bacteriol. 1991 Mar;173(6):2077-85. doi: 10.1128/jb.173.6.2077-2085.1991.

DOI:10.1128/jb.173.6.2077-2085.1991
PMID:2002009
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC207743/
Abstract

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.

摘要

苜蓿中华根瘤菌复杂的鞭毛丝由两种相关的(87% 相同)鞭毛蛋白组成,它们由紧密连锁、分别转录的基因flaA和flaB编码(E. Pleier和R. Schmitt,《细菌学杂志》171:1467 - 1475,1989年)。为了阐明亚基A和B在组装复杂鞭毛丝中的作用,将野生型等位基因替换为含有2249 bp缺失(伴有卡那霉素抗性盒替换)的缺陷型等位基因,该缺失消除了74% 的flaA(3' 端)和85% 的flaB(5' 端)。对产生的无运动能力、无鞭毛的突变体RU11011进行了与多拷贝载体pRK290上提供的野生型flaA、flaB和flaA flaB基因的互补测试。单独的flaA不能恢复运动能力和鞭毛产生,而flaB和flaA flaB都恢复了20% 至30% 的野生型运动能力。这种运动能力降低的明显原因是每个细胞的鞭毛较少和/或鞭毛丝缩短,有时末端是异常细且脆弱的结构。用酶联抗鞭毛蛋白抗体进行的测试表明,flaA的表达水平高于flaB,并且flaA的多个拷贝会导致鞭毛蛋白输出减少。我们得出结论,复杂鞭毛丝的近端部分由B亚基组装而成(产生量不足以形成全长鞭毛),而远端部分由A亚基制成。强flaA启动子的多个拷贝可能会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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