Ferjani Ali, Mustardy Laszlo, Sulpice Ronan, Marin Kay, Suzuki Iwane, Hagemann Martin, Murata Norio
Department of Regulation Biology, National Institute for Basic Biology, Okazaki 444-8585, Japan.
Plant Physiol. 2003 Apr;131(4):1628-37. doi: 10.1104/pp.102.017277.
The cyanobacterium Synechocystis sp. PCC 6803 accumulates the compatible solute glucosylglycerol (GG) and sucrose under salt stress. Although the molecular mechanisms for GG synthesis including regulation of the GG-phosphate synthase (ggpS) gene, which encodes GgpS, has been intensively investigated, the role of GG in protection against salt stress remains poorly understood. In our study of the role of GG in the tolerance to salt stress, we found that salt stress due to 450 mM NaCl inhibited cell division and significantly increased cell size in DeltaggpS mutant cells, whereas the inhibition of cell division and increase in cell size were observed in wild-type cells at high concentrations of NaCl, such as 800 mM. Electron microscopy revealed that, in DeltaggpS cells, separation of daughter cells was incomplete, and aborted division could be recognized by the presence of a structure that resembled a division ring. The addition of GG to the culture medium protected DeltaggpS cells against salt stress and reversed the adverse effects of NaCl on cell division and cell size. These observations suggest that GG is important for salt tolerance and thus for the proper division of cells under salt stress conditions.
集胞藻PCC 6803在盐胁迫下会积累相容性溶质葡萄糖基甘油(GG)和蔗糖。尽管对GG合成的分子机制,包括对编码GgpS的GG-磷酸合酶(ggpS)基因的调控,已经进行了深入研究,但GG在抵御盐胁迫中的作用仍知之甚少。在我们对GG在耐盐胁迫中的作用的研究中,我们发现,450 mM NaCl引起的盐胁迫抑制了DeltaggpS突变体细胞的细胞分裂,并显著增大了细胞大小,而在高浓度NaCl(如800 mM)下,野生型细胞中才观察到细胞分裂受到抑制和细胞大小增加。电子显微镜显示,在DeltaggpS细胞中,子细胞的分离不完全,并且通过类似分裂环结构的存在可以识别出异常分裂。向培养基中添加GG可保护DeltaggpS细胞免受盐胁迫,并逆转NaCl对细胞分裂和细胞大小的不利影响。这些观察结果表明,GG对于耐盐性很重要,因此对于盐胁迫条件下细胞的正常分裂也很重要。