Department of Biological Sciences and Technology, National University of Tainan, Tainan 70005, Taiwan, ROC.
Aquat Toxicol. 2013 Nov 15;144-145:265-74. doi: 10.1016/j.aquatox.2013.10.015. Epub 2013 Oct 21.
The calcium-mediated proline accumulation is a critical response under NaCl stress and the function of the induced proline as a glutamine synthetase (GS) protectant in greater duckweed was investigated. The plants were treated with solutions containing 100mM NaCl, 200 mM NaCl, 200 mM NaCl plus 10mM CaCl2, or 10mM CaCl2 alone for 4 days. At the end of the experiment, the fronds of inoculum treated with 200 mM NaCl showed the chlorotic effect, higher glutamate dehydrogenase (NADH-GDH) activity and lower GS activity. At the lower salinity, the activities of GS and NADH-GDH were not altered markedly. A significant accumulation of proline was not found under either low or high salinity. The activity of Δ(1)-pyrroline-5-carboxylate reductase (P5CR) was enhanced only at 200 mM NaCl but remained unchanged at 100mM NaCl. The activity of Δ(1)-pyrroline-5-carboxylate synthetase (P5CS) did not change under salinity-stressed. Addition of CaCl2 to the salt stressed plants not only lowered NaCl injury but also showed an elevated level of proline contents in response to the salinity treatment. In addition, both GS activity and corresponding polypeptides were expressed close to the level of control. Exogenous proline protects GS2 and the 32 kDa protein in photosystem II reaction center (D1) from H2O2-induced redox degradation in the chloroplast lysates of duckweed. The results suggest that calcium-induced proline accumulation may play an important role as a GS protectant under NaCl exposure in S. polyrhiza.
钙介导脯氨酸积累是 NaCl 胁迫下的关键响应,研究了诱导脯氨酸在大浮萍中作为谷氨酰胺合成酶 (GS) 保护剂的功能。将植物用含有 100mM NaCl、200mM NaCl、200mM NaCl 加 10mM CaCl2 或单独 10mM CaCl2 的溶液处理 4 天。实验结束时,用 200mM NaCl 处理的接种叶显示出黄化效应、较高的谷氨酸脱氢酶 (NADH-GDH) 活性和较低的 GS 活性。在较低的盐度下,GS 和 NADH-GDH 的活性没有明显改变。无论是在低盐度还是高盐度下,都没有发现脯氨酸的显著积累。Δ(1)-吡咯啉-5-羧酸还原酶 (P5CR) 的活性仅在 200mM NaCl 下增强,但在 100mM NaCl 下保持不变。在盐胁迫下,Δ(1)-吡咯啉-5-羧酸合成酶 (P5CS) 的活性没有变化。向盐胁迫植物中添加 CaCl2 不仅降低了 NaCl 损伤,而且还表现出对盐处理的脯氨酸含量升高。此外,GS 活性和相应的多肽表达水平接近对照水平。外源脯氨酸可保护浮萍 GS2 和光系统 II 反应中心 (D1) 的 32kDa 蛋白免受叶绿体裂解物中 H2O2 诱导的氧化还原降解。结果表明,钙诱导的脯氨酸积累可能在 S. polyrhiza 暴露于 NaCl 下作为 GS 保护剂发挥重要作用。