Gruwel M L.H., Rauw V L., Loewen M, Abrams S R.
National Research Council, Plant Biotechnology Institute, 110 Gymnasium Place, S7N 0W9, Saskatoon, SK, Canada
Plant Sci. 2001 Apr;160(5):785-794. doi: 10.1016/s0168-9452(00)00424-6.
In plant cells, the Na(+)/H(+) antiport at the tonoplast provides a biochemical pathway to transport cytoplasmic Na(+) into the vacuole. Recently it was shown that overexpression of a vacuolar Na(+)/H(+) promotes sustained plant growth at high NaCl levels (Apse et al. Science 285, 1256, 1999). The sequestration of Na(+) ions into the vacuole can be followed using 31P and 23Na NMR spectroscopy. Suspension cell cultures are very suitable for this purpose and allow rapid and accurate assessment of the activity of the Na(+)/H(+) antiport and therefore potentially of salt tolerance. Perfusion experiments with maize cells that are not particularly salt (NaCl) tolerant showed that during salt stress the cytoplasmic pH remains unchanged while the vacuolar pH significantly increased. During Na(+) sequestration into the vacuole, the cytoplasmic pH equilibrates faster than that of the vacuole. Both vacuolar pH and the cellular Na(+) uptake rate were dependent on extracellular Na(+) for concentrations up to approximately 300 mM. For Na(+) concentrations >/=300 mM, both vacuolar pH and cellular Na(+) uptake became independent of the extracellular concentration. This indicates either a saturation of Na(+) uptake at the cell surface or a saturation of the Na(+)/H(+) transporter at the tonoplast. Na(+) uptake into the cell is accompanied by a rapid increase in vacuolar PO(4)(3-), broadening of the 31P resonances and a reduction in glucose monophosphate and UDPG.
在植物细胞中,液泡膜上的Na(+)/H(+)逆向转运蛋白提供了一条将细胞质中的Na(+)转运到液泡中的生化途径。最近有研究表明,液泡Na(+)/H(+)的过表达能促进植物在高NaCl水平下持续生长(阿普斯等人,《科学》285卷,第1256页,1999年)。利用31P和23Na核磁共振光谱可以追踪Na(+)离子在液泡中的隔离情况。悬浮细胞培养非常适合用于此目的,能够快速准确地评估Na(+)/H(+)逆向转运蛋白的活性,进而潜在地评估植物的耐盐性。对耐盐性不强的玉米细胞进行灌注实验表明,在盐胁迫期间,细胞质pH保持不变,而液泡pH显著升高。在Na(+)隔离到液泡的过程中,细胞质pH比液泡pH更快达到平衡。对于浓度高达约300 mM的细胞外Na(+),液泡pH和细胞Na(+)摄取率均与之相关。对于Na(+)浓度≥300 mM,液泡pH和细胞Na(+)摄取均不再依赖于细胞外浓度。这表明要么是细胞表面的Na(+)摄取达到饱和,要么是液泡膜上的Na(+)/H(+)转运蛋白达到饱和。Na(+)进入细胞伴随着液泡PO(4)(3-)的快速增加、31P共振峰变宽以及葡萄糖单磷酸和UDPG的减少。