Zimmermann U, Steudle E, Lelkes P I
Institut für Biophysikalische Chemie (ICH/2) der Kernforschungsanlage Jülich, D-5170 Jülich, Postfach 1913, Germany.
Plant Physiol. 1976 Nov;58(5):608-13. doi: 10.1104/pp.58.5.608.
The electrical membrane resistance rho(0) of the marine alga Valonia utricularis shows a marked maximum in dependence on the turgor pressure. The critical pressure, P(c), at which the maximum occurs, as well as its absolute value, rho(0) (max), are strongly volume-dependent. Both P(c) and rho(0) (max), increase with decreasing cell volume. It seems likely, that these relationships reflect the elastic properties of the cell wall, because the volumetric elastic modulus, epsilon, is also volume-dependent, increasing hyperbolically with cell volume. Both P(c) and rho(0) (max) can be affected by external application of indole-3-acetic acid at concentrations of 2.10(-7)m to 2 .10(-5)m. The critical pressure is shifted by 1.2 to 6 bars toward higher pressures and the maximum membrane resistance increased up to 5.6-fold. During the course of the experiments (up to 4 hours), however, IAA had no effect on the volumetric elastic modulus, epsilon.The maximum in membrane resistance is discussed in terms of a pressure-dependent change of potassium fluxes. The volume dependence of P(c) and rho(0) (max) suggests that not only turgor pressure but also epsilon must be considered as a regulating parameter during turgor pressure regulation. On this basis a hypothesis is presented for the transformation of both, a pressure signal and of changes in the elastic properties of the cell wall into alterations of ion fluxes. It is assumed that the combined effects of tension and compression of the membranes as well as the interaction between membrane and cell wall opposingly change the number of transport sites for K(+) providing a turgor-sensing mechanism that regulates ion fluxes. The IAA effects demonstrated are consistent with this view, suggesting that the basic mechanisms for turgor pressure regulation and growth regulation are similar.Any relation connecting growth rate with turgor pressure should be governed by two parameters, i.e. by a yielding pressure, at which cell growth starts, and by the critical pressure, at which it ceases again.
海洋藻类巨藻的电膜电阻rho(0) 显示出明显的最大值,该值取决于膨压。最大值出现时的临界压力P(c) 及其绝对值rho(0) (max) 都强烈依赖于体积。P(c) 和rho(0) (max) 都随细胞体积减小而增加。这些关系似乎反映了细胞壁的弹性特性,因为体积弹性模量epsilon也依赖于体积,随细胞体积呈双曲线增加。P(c) 和rho(0) (max) 都可受到浓度为2×10(-7)m至2×10(-5)m的吲哚-3-乙酸的外部施加的影响。临界压力向更高压力方向移动1.2至6巴,最大膜电阻增加高达5.6倍。然而,在实验过程中(长达4小时),吲哚-3-乙酸对体积弹性模量epsilon没有影响。膜电阻的最大值是根据钾通量的压力依赖性变化来讨论的。P(c) 和rho(0) (max) 对体积的依赖性表明,在膨压调节过程中,不仅膨压,而且epsilon都必须被视为调节参数。在此基础上,提出了一个假设,即压力信号和细胞壁弹性特性的变化如何转化为离子通量的改变。假定膜的拉伸和压缩的联合效应以及膜与细胞壁之间的相互作用以相反的方式改变K(+) 的转运位点数量,从而提供一种调节离子通量的膨压传感机制。所证明的吲哚-3-乙酸效应与这一观点一致,表明膨压调节和生长调节的基本机制是相似的。任何将生长速率与膨压联系起来的关系都应由两个参数决定,即细胞生长开始时的屈服压力和细胞生长再次停止时的临界压力。