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Function of a Principal Na+/H+ Antiporter, ShaA, Is Required for Initiation of Sporulation in Bacillus subtilis

机译:主要的Na + / H +反向转运蛋白ShaA的功能是启动枯草芽孢杆菌中的孢子形成所必需的

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摘要

ShaA (sodium/hydrogen antiporter, previously termed YufT [or NtrA]), which is responsible for Na+/H+ antiporter activity, is considered to be the major Na+ excretion system in Bacillus subtilis. We found that a shaA-disrupted mutant of B. subtilis shows impaired sporulation but normal vegetative growth when the external Na+ concentration was increased in a low range. In the shaA mutant, ςH-dependent expression of spo0A (PS) and spoVG at an early stage of sporulation was sensitive to external NaCl. The level of ςH protein was reduced by the addition of NaCl, while the expression of spo0H, which encodes ςH, was little affected, indicating that posttranscriptional control of ςH rather than spo0H transcription is affected by the addition of NaCl in the shaA mutant. Since this mutant is considered to have a diminished ability to maintain a low internal Na+ concentration, an increased level of internal Na+ may affect posttranscriptional control of ςH. Bypassing the phosphorelay by introducing the sof-1 mutation into this mutant did not restore spo0A (PS) expression, suggesting that disruption of shaA affects ςH accumulation, but does not interfere with the phosphorylation and phosphotransfer reactions of the phosphorelay. These results suggest that ShaA plays a significant role at an early stage of sporulation and not only during vegetative growth. Our findings raise the possibility that fine control of cytoplasmic ion levels, including control of the internal Na+ concentration, may be important for the progression of the sporulation process.
机译:负责Na + / H +反向转运活性的ShaA(钠/氢反向转运蛋白,以前称为YufT [或NtrA])被认为是枯草芽孢杆菌中主要的Na +排泄系统。我们发现,当外部Na +浓度在低范围内增加时,枯草芽孢杆菌的shaA破坏突变体显示孢子形成受损,但营养生长正常。在shaA突变体中,孢子形成早期阶段spo0A(PS)和spoVG的ςH依赖性表达对外部NaCl敏感。通过添加NaCl可以降低ςH蛋白的水平,而编码ςH的spo0H的表达几乎没有受到影响,这表明在shaA突变体中添加NaCl会影响ςH而不是spo0H转录的转录后控制。由于该突变体维持内部低Na +浓度的能力降低,因此内部Na +水平的升高可能会影响ςH的转录后控制。通过将sof-1突变引入该突变体来绕过磷光体,不会恢复spo0A(PS)的表达,这表明shaA的破坏会影响ςH的积累,但不会干扰磷光体的磷酸化和磷酸转移反应。这些结果表明,ShaA在孢子形成的早期阶段发挥重要作用,而不仅在营养生长期间。我们的发现增加了对细胞质离子水平进行精细控制(包括控制内部Na +浓度)对孢子形成过程的重要作用的可能性。

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