Hörtensteiner S, Martinoia E, Amrhein N
Institute of Plant Sciences, Swiss Federal Institute of Technology, Zürich.
Planta. 1994;192(3):395-403. doi: 10.1007/BF00198576.
The re-formation of vacuoles in miniprotoplasts (evacuolated mesophyll protoplasts) of tobacco was investigated under different conditions. When a constant osmolarity was maintained, increasing the concentration of NaCl in the medium enhanced the regeneration of vacuoles compared to the control (0.5 M mannitol used as osmoticum). An enhanced growth rate of miniprotoplasts could also be observed under low-osmolarity conditions, by substitution of NaCl for KCl or NaNO3, or with different effectors (glycinebetaine and methyljasmonate). Using the polymerase chain reaction, one cDNA fragment of the B-subunit of the vacuolar ATPase and two fragments of the tonoplast-bound pyrophosphatase (PPase) of tobacco were cloned. Southern blot analyses indicates that for both proteins more than one gene is present in tobacco. During the regeneration of vacuoles the transcript level of the PPase increased earlier than that of the B-subunit of the vacuolar ATPase under all conditions tested (0.5 M mannitol, 0.3 M mannitol, and 0.25 M NaCl, respectively). Under salt-stress conditions (0.25 M NaCl used as osmoticum), the expression level of both proton pumps is enhanced compared to the control. This increase is not specifically due to salt stress but generally to an increased growth rate of the vacuole, since under low-osmolarity conditions the expression of the vacuolar pumps is enhanced, too.
在不同条件下,对烟草小原生质体(去核叶肉原生质体)中液泡的重新形成进行了研究。当维持恒定渗透压时,与对照(使用0.5 M甘露醇作为渗透压调节剂)相比,增加培养基中NaCl的浓度可增强液泡的再生。在低渗条件下,通过用NaCl替代KCl或NaNO₃,或使用不同的效应物(甘氨酸甜菜碱和茉莉酸甲酯),也可观察到小原生质体生长速率的提高。利用聚合酶链反应,克隆了烟草液泡ATP酶B亚基的一个cDNA片段和液泡膜结合焦磷酸酶(PPase)的两个片段。Southern印迹分析表明,烟草中这两种蛋白质均存在多个基因。在所有测试条件下(分别为0.5 M甘露醇、0.3 M甘露醇和0.25 M NaCl),液泡再生过程中PPase的转录水平比液泡ATP酶B亚基的转录水平更早升高。在盐胁迫条件下(使用0.25 M NaCl作为渗透压调节剂),与对照相比,两种质子泵的表达水平均增强。这种增加并非特别归因于盐胁迫,而是通常归因于液泡生长速率的提高,因为在低渗条件下液泡泵的表达也会增强。