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C‐terminal regulatory domain of the ε subunit of FoF1 ATP synthase enhances the ATP‐dependent H+ pumping that is involved in the maintenance of cellular membrane potential in Bacillus subtilis

机译:FoF1 ATP合酶ε亚基的C末端调节域增强了ATP依赖的H +泵送该泵送与维持枯草芽孢杆菌的细胞膜电位有关

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摘要

The ε subunit of FoF1‐ATPase/synthase (FoF1) plays a crucial role in regulating FoF1 activity. To understand the physiological significance of the ε subunit‐mediated regulation of FoF1 in Bacillus subtilis, we constructed and characterized a mutant harboring a deletion in the C‐terminal regulatory domain of the ε subunit (ε∆C). Analyses using inverted membrane vesicles revealed that the ε∆C mutation decreased ATPase activity and the ATP‐dependent H+‐pumping activity of FoF1. To enhance the effects of ε∆C mutation, this mutation was introduced into a ∆rrn8 strain harboring only two of the 10 rrn (rRNA) operons (∆rrn8 ε∆C mutant strain). Interestingly, growth of the ∆rrn8 ε∆C mutant stalled at late‐exponential phase. During the stalled growth phase, the membrane potential of the ∆rrn8 ε∆C mutant cells was significantly reduced, which led to a decrease in the cellular level of 70S ribosomes. The growth stalling was suppressed by adding glucose into the culture medium. Our findings suggest that the C‐terminal region of the ε subunit is important for alleviating the temporal reduction in the membrane potential, by enhancing the ATP‐dependent H+‐pumping activity of FoF1.
机译:FoF1-ATPase /合酶(FoF1)的ε亚基在调节FoF1活性中起关键作用。为了了解枯草芽孢杆菌中ε亚基介导的FoF1调控的生理学意义,我们构建并表征了一个突变体,该突变体在ε亚基的C端调控域中具有一个缺失(ε ∆C ) 。使用倒膜小泡的分析表明,εΔC突变降低了FoF1的ATPase活性和依赖ATP的H + -泵浦活性。为了增强εΔC突变的影响,将此突变引入仅包含10个rrn(rRNA)操纵子中的两个(Δrrn8εΔC突变株)。有趣的是,Δrrn8εΔC突变体的生长停滞在指数后期。在停滞的生长阶段,Δrrn8εΔC突变细胞的膜电位显着降低,导致70S核糖体细胞水平降低。通过将葡萄糖添加到培养基中来抑制生长停滞。我们的发现表明,通过增强FoF1的ATP依赖性H + 泵浦活性,ε亚基的C端区域对于缓解膜电位的暂时降低很重要。

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