Piñeros Miguel A, Magalhaes Jurandir V, Carvalho Alves Vera M, Kochian Leon V
United States Plant, Soil, and Nutrition Laboratory, United States Department of Agriculture-Agricultural Research Service, Cornell University, Ithaca, New York 14853.
Plant Physiol. 2002 Jul;129(3):1194-206. doi: 10.1104/pp.002295.
Al-induced release of Al-chelating ligands (primarily organic acids) into the rhizosphere from the root apex has been identified as a major Al tolerance mechanism in a number of plant species. In the present study, we conducted physiological investigations to study the spatial and temporal characteristics of Al-activated root organic acid exudation, as well as changes in root organic acid content and Al accumulation, in an Al-tolerant maize (Zea mays) single cross (SLP 181/71 x Cateto Colombia 96/71). These investigations were integrated with biophysical studies using the patch-clamp technique to examine Al-activated anion channel activity in protoplasts isolated from different regions of the maize root. Exposure to Al nearly instantaneously activated a concentration-dependent citrate release, which saturated at rates close to 0.5 nmol citrate h(-1) root(-1), with the half-maximal rates of citrate release occurring at about 20 microM Al(3+) activity. Comparison of citrate exudation rates between decapped and capped roots indicated the root cap does not play a major role in perceiving the Al signal or in the exudation process. Spatial analysis indicated that the predominant citrate exudation is not confined to the root apex, but could be found as far as 5 cm beyond the root cap, involving cortex and stelar cells. Patch clamp recordings obtained in whole-cell and outside-out patches confirmed the presence of an Al-inducible plasma membrane anion channel in protoplasts isolated from stelar or cortical tissues. The unitary conductance of this channel was 23 to 55 pS. Our results suggest that this transporter mediates the Al-induced citrate release observed in the intact tissue. In addition to the rapid Al activation of citrate release, a slower, Al-inducible increase in root citrate content was also observed. These findings led us to speculate that in addition to the Al exclusion mechanism based on root citrate exudation, a second internal Al tolerance mechanism may be operating based on Al-inducible changes in organic acid synthesis and compartmentation. We discuss our findings in terms of recent genetic studies of Al tolerance in maize, which suggest that Al tolerance in maize is a complex trait.
铝诱导的铝螯合配体(主要是有机酸)从根尖释放到根际已被确定为许多植物物种的主要耐铝机制。在本研究中,我们进行了生理研究,以研究耐铝玉米(Zea mays)单交种(SLP 181/71×Cateto Colombia 96/71)中铝激活的根系有机酸分泌的时空特征,以及根系有机酸含量和铝积累的变化。这些研究与使用膜片钳技术的生物物理研究相结合,以检查从玉米根不同区域分离的原生质体中铝激活的阴离子通道活性。暴露于铝几乎立即激活了浓度依赖性的柠檬酸释放,其饱和速率接近0.5 nmol柠檬酸h(-1)根(-1),柠檬酸释放的半最大速率出现在约20 microM Al(3+)活性时。去帽根和带帽根之间柠檬酸分泌速率的比较表明,根冠在感知铝信号或分泌过程中不起主要作用。空间分析表明,主要的柠檬酸分泌不限于根尖,而是可以在根冠以外5 cm处发现,涉及皮层和中柱细胞。在全细胞和外向膜片上获得的膜片钳记录证实,从皮层或中柱组织分离的原生质体中存在铝诱导的质膜阴离子通道。该通道的单位电导为23至55 pS。我们的结果表明,该转运体介导了在完整组织中观察到的铝诱导的柠檬酸释放。除了铝快速激活柠檬酸释放外,还观察到根系柠檬酸含量有较慢的、铝诱导的增加。这些发现使我们推测,除了基于根系柠檬酸分泌的铝排斥机制外,可能还存在基于铝诱导的有机酸合成和区室化变化的第二种内部耐铝机制。我们根据最近对玉米耐铝性的遗传研究讨论了我们的发现,这些研究表明玉米的耐铝性是一个复杂的性状。