Bramley Helen, Turner Neil C, Turner David W, Tyerman Stephen D
School of Agriculture, Food and Wine, The University of Adelaide (Waite Campus), Plant Research Centre, Glen Osmond SA 5064, Australia.
Plant Cell Environ. 2007 Jul;30(7):861-74. doi: 10.1111/j.1365-3040.2007.01678.x.
Hydrostatic pressure relaxations with the root pressure probe are commonly used for measuring the hydraulic conductivity (Lp(r)) of roots. We compared the Lp(r) of roots from species with different root hydraulic properties (Lupinus angustifolius L. 'Merrit', Lupinus luteus L. 'Wodjil', Triticum aestivum L. 'Kulin' and Zea mays L. 'Pacific DK 477') using pressure relaxations, a pressure clamp and osmotic gradients to induce water flow across the root. Only the pressure clamp measures water flow under steady-state conditions. Lp(r) determined by pressure relaxations was two- to threefold greater than Lp(r) from pressure clamps and was independent of the direction of water flow. Lp(r) (pressure clamp) was two- to fourfold higher than for Lp(r) (osmotic) for all species except Triticum aestivum where Lp(r) (pressure clamp) and Lp(r) (osmotic) were not significantly different. A novel technique was developed to measure the propagation of pressure through roots to investigate the cause of the differences in Lp(r). Root segments were connected between two pressure probes so that when root pressure (P(r)) was manipulated by one probe, the other probe recorded changes in P(r). Pressure relaxations did not induce the expected kinetics in pressure in the probe at the other end of the root when axial hydraulic conductance, and probe and root capacitances were accounted for. An electric circuit model of the root was constructed that included an additional capacitance in the root loaded by a series of resistances. This accounted for the double exponential kinetics for intact roots in pressure relaxation experiments as well as the reduced response observed with the double probe experiments. Although there were potential errors with all the techniques, we considered that the measurement of Lp(r) using the pressure clamp was the most unambiguous for small pressure changes, and provided that sufficient time was allowed for pressure propagation through the root. The differences in Lp(r) from different methods of measurement have implications for the models describing water transport through roots and the potential role of aquaporins.
使用根压探针进行静水压力松弛常用于测量根的水力传导率(Lp(r))。我们使用压力松弛、压力钳和渗透梯度来诱导水流过根,比较了具有不同根水力特性的物种(羽扇豆‘美利特’、白羽扇豆‘沃吉尔’、小麦‘库林’和玉米‘太平洋DK 477’)根的Lp(r)。只有压力钳能测量稳态条件下的水流。通过压力松弛测定的Lp(r)比压力钳测定的Lp(r)大两到三倍,且与水流方向无关。除小麦外,所有物种的Lp(r)(压力钳)比Lp(r)(渗透法)高两到四倍,而小麦的Lp(r)(压力钳)和Lp(r)(渗透法)无显著差异。我们开发了一种新技术来测量压力在根中的传播,以研究Lp(r)差异的原因。将根段连接在两个压力探针之间,这样当一个探针操纵根压(P(r))时,另一个探针记录P(r)的变化。当考虑轴向水力传导率以及探针和根的电容时,压力松弛并未在根另一端的探针中诱导出预期的压力动力学。构建了一个根的电路模型,该模型在根中包含一个由一系列电阻加载的附加电容。这解释了压力松弛实验中完整根的双指数动力学以及双探针实验中观察到的响应降低。尽管所有技术都存在潜在误差,但我们认为对于小压力变化,使用压力钳测量Lp(r)是最明确的,前提是允许有足够的时间让压力在根中传播。不同测量方法得到的Lp(r)差异对描述水分通过根运输的模型以及水通道蛋白的潜在作用具有影响。