Kosono S, Ohashi Y, Kawamura F, Kitada M, Kudo T
Microbiology Laboratory, Institute of Physical and Chemical Research (RIKEN), Wako, Saitama 351-0198, Japan.
J Bacteriol. 2000 Feb;182(4):898-904. doi: 10.1128/JB.182.4.898-904.2000.
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, sigma(H)-dependent expression of spo0A (P(S)) and spoVG at an early stage of sporulation was sensitive to external NaCl. The level of sigma(H) protein was reduced by the addition of NaCl, while the expression of spo0H, which encodes sigma(H), was little affected, indicating that posttranscriptional control of sigma(H) 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 sigma(H). Bypassing the phosphorelay by introducing the sof-1 mutation into this mutant did not restore spo0A (P(S)) expression, suggesting that disruption of shaA affects sigma(H) 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.
ShaA(钠/氢反向转运蛋白,以前称为YufT [或NtrA])负责Na(+)/H(+)反向转运蛋白活性,被认为是枯草芽孢杆菌中的主要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基因破坏突变体显示出孢子形成受损,但营养生长正常。在shaA突变体中,孢子形成早期阶段依赖σ(H)的spo0A(P(S))和spoVG表达对外部NaCl敏感。添加NaCl会降低σ(H)蛋白水平,而编码σ(H)的spo0H的表达几乎不受影响,这表明在shaA突变体中,添加NaCl影响的是σ(H)的转录后调控而非spo0H转录。由于该突变体被认为维持低内部Na(+)浓度的能力减弱,内部Na(+)水平的升高可能会影响σ(H)的转录后调控。通过在该突变体中引入sof-1突变绕过磷酸化信号传递并不能恢复spo0A(P(S))表达,这表明shaA的破坏影响σ(H)的积累,但不干扰磷酸化信号传递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,而不仅仅是在营养生长期间。我们的发现增加了一种可能性,即对细胞质离子水平的精细调控,包括对内部Na(+)浓度的控制,可能对孢子形成过程的进展很重要。