首页> 美国卫生研究院文献>Journal of Bacteriology >Postdivisional Synthesis of the Sporosarcina ureae DNA Translocase SpoIIIE either in the Mother Cell or in the Prespore Enables Bacillus subtilis To Translocate DNA from the Mother Cell to the Prespore
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Postdivisional Synthesis of the Sporosarcina ureae DNA Translocase SpoIIIE either in the Mother Cell or in the Prespore Enables Bacillus subtilis To Translocate DNA from the Mother Cell to the Prespore

机译:在母细胞或孢子中的孢子菌尿素DNA转移酶SpoIIIE的除后合成使枯草芽孢杆菌能够将DNA从母细胞转移到孢子

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摘要

The differentiation of vegetative cells of Bacillus subtilis into spores involves asymmetric cell division, which precedes complete chromosome partitioning. The DNA translocase SpoIIIE is required to translocate the origin distal 70% of the chromosome from the larger mother cell into the smaller prespore, the two cells that result from the division. We have tested the effect of altering the time and location of SpoIIIE synthesis on spore formation. We have expressed the spoIIIE homologue from Sporosarcina ureae in B. subtilis under the control of different promoters. Expression from either a weak mother cell-specific (σE) promoter or a weak prespore-specific (σF) promoter partly complemented the sporulation defect of a spoIIIE36 mutant; however, expression from a strong prespore-specific (σF) promoter did not. DNA translocation from the mother cell to the prespore was assayed using spoIIQ-lacZ inserted at thrC; transcription of spoIIQ occurs only in the prespore. Translocation of thrC::spoIIQ-lacZ into the prespore occurred efficiently when spoIIIESu was expressed from the weak σE- or σF-controlled promoters but not when it was expressed from the strong σF-controlled promoter. It is speculated that the mechanism directing SpoIIIE insertion into the septum in the correct orientation may accommodate slow postseptational, prespore-specific SpoIIIE synthesis but may be swamped by strong prespore-specific synthesis.
机译:枯草芽孢杆菌营养细胞向孢子的分化涉及不对称细胞分裂,该过程先于染色体完全分区。需要DNA转移酶SpoIIIE才能将染色体起源的远端70%从较大的母细胞转移到较小的芽孢中,这是分裂产生的两个细胞。我们已经测试了改变SpoIIIE合成的时间和位置对孢子形成的影响。我们已经在不同启动子的控制下在枯草芽孢杆菌中表达了来自Sporosarcina脲的spoIIIE同源物。弱的母亲细胞特异性启动子(σ E )启动子或弱的孢子特异性启动子(σ F )启动子的表达部分弥补了spoIIIE36突变体的孢子形成缺陷。然而,从强烈的芽孢前特异性(σ F )启动子表达却没有。使用插入thrC的spoIIQ-lacZ分析了从母细胞到芽孢的DNA易位; spoIIQ的转录仅发生在芽孢前。当从弱的σ E -或σ F 控制的启动子表达spoIIIESu时,thrC :: spoIIQ-lacZ高效地转移到孢子中,而从强σ F 控制的启动子。据推测,以正确的方向引导SpoIIIE插入隔膜的机制可能适应缓慢的分离后,芽孢前特异性SpoIIIE合成,但可能被强烈的芽孢前特异性合成所淹没。

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