McClure P R, Kochian L V, Spanswick R M, Shaff J E
Section of Plant Biology, Cornell University, Ithaca, New York 14853.
Plant Physiol. 1990 May;93(1):290-4. doi: 10.1104/pp.93.1.290.
We report here on an investigation of net nitrate and proton fluxes in root cells of maize (Zea mays L.) seedlings grown without (noninduced) and with (induced) 0.1 millimolar nitrate. A microelectrode system described previously (IA Newman, LV Kochian, MA Grusak, WJ Lucas [1987] Plant Physiol 84: 1177-1184) was utilized to quantify net ionic fluxes from the measurement of electrochemical potential gradients for NO(3) (-) and H(+) within the unstirred layer at the root surface. The nitrate-inducibility, pH dependence, and concentration dependence of net NO(3) (-) uptake correlated quite closely with the electrical response of maize roots to nitrate under the same experimental conditions (as described in PR McClure, LV Kochian, RM Spanswick, JE Shaff [1990] Plant Physiol 93: 281-289). Additionally, it was found that potential inhibitors of the plasmalemma H(+)-ATPase (vandate, diethylstilbestrol), which were shown to abolish the electrical response to NO(3) (-) (in PR McClure, LV Kochian, RM Spanswick, JE Shaff [1990] Plant Physiol 93: 281-289), dramatically inhibited NO(3) (-) absorption. These results strongly indicate that the NO(3) (-) electrical response is due to the operation of a NO(3) (-) transport system in the plasmalemma of maize root cells. Furthermore, the results from the H(+)-ATPase inhibitor studies indicate that the NO(3) (-) transport system is linked to the H(+)-ATPase, presumably as a NO(3) (-)/H(+) symport. This is further supported by the pH response of the NO(3) (-) transport system (inhibition at alkaline pH values) and the change in net H(+) flux from a moderate efflux in the absence of NO(3) (-), to zero net H(+) flux after exposing the maize root to exogenous nitrate. Although these results can be explained by other interpretations, the simplest model that fits both the electrical responses and the NO(3) (-)/H(+) flux data is a NO(3) (-)/H(+) symport with a NO(3) (-):H(+) flux stoichiometry >1, whose operation results in the stimulation of the H(+)-ATPase due to the influx of protons through the cotransport system.
我们在此报告了一项关于玉米(Zea mays L.)幼苗根细胞中净硝酸盐和质子通量的研究。这些幼苗分别在未添加(未诱导)和添加(诱导)0.1毫摩尔硝酸盐的条件下生长。利用先前描述的微电极系统(IA Newman、LV Kochian、MA Grusak、WJ Lucas [1987] Plant Physiol 84: 1177 - 1184),通过测量根表面未搅拌层内NO(3) (-)和H(+)的电化学势梯度来量化净离子通量。在相同实验条件下(如PR McClure、LV Kochian、RM Spanswick、JE Shaff [1990] Plant Physiol 93: 281 - 289中所述),净NO(3) (-)吸收的硝酸盐诱导性、pH依赖性和浓度依赖性与玉米根对硝酸盐的电响应密切相关。此外,发现质膜H(+)-ATPase的潜在抑制剂(钒酸盐、己烯雌酚),已证明其能消除对NO(3) (-)的电响应(见PR McClure、LV Kochian、RM Spanswick、JE Shaff [1990] Plant Physiol 93: 281 - 289),能显著抑制NO(3) (-)的吸收。这些结果有力地表明,NO(3) (-)电响应是由于玉米根细胞质膜中存在NO(3) (-)转运系统。此外,H(+)-ATPase抑制剂研究的结果表明,NO(3) (-)转运系统与H(+)-ATPase相关联,推测为NO(3) (-)/H(+)同向转运体。NO(3) (-)转运系统的pH响应(在碱性pH值下受到抑制)以及净H(+)通量从无NO(3) (-)时的适度外流,到玉米根暴露于外源硝酸盐后净H(+)通量变为零的变化,进一步支持了这一点。尽管这些结果可以用其他解释来阐述,但最能同时符合电响应和NO(3) (-)/H(+)通量数据的最简单模型是一种NO(3) (-)/H(+)同向转运体,其NO(3) (-):H(+)通量化学计量比>1,其运作会因质子通过共转运系统内流而刺激H(+)-ATPase。