首页> 外文OA文献 >Aluminum Activates a Citrate-Permeable Anion Channel in the Aluminum-Sensitive Zone of the Maize Root Apex. A Comparison Between an Aluminum- Sensitive and an Aluminum-Resistant Cultivar1
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Aluminum Activates a Citrate-Permeable Anion Channel in the Aluminum-Sensitive Zone of the Maize Root Apex. A Comparison Between an Aluminum- Sensitive and an Aluminum-Resistant Cultivar1

机译:铝激活了玉米根尖铝敏感区中的柠檬酸盐可渗透的阴离子通道。铝敏感品种和耐铝品种的比较1

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摘要

In search for the cellular and molecular basis for differences in aluminum (Al) resistance between maize (Zea mays) cultivars we applied the patch-clamp technique to protoplasts isolated from the apical root cortex of two maize cultivars differing in Al resistance. Measurements were performed on protoplasts from two apical root zones: The 1- to 2-mm zone (DTZ), described as most Al-sensitive, and the main elongation zone (3–5 mm), the site of Al-induced inhibition of cell elongation. Al stimulated citrate and malate efflux from intact root apices, revealing cultivar differences. In the elongation zone, anion channels were not observed in the absence and presence of Al. Preincubation of intact roots with 90 μm Al for 1 h induced a citrate- and malate-permeable, large conductance anion channel in 80% of the DTZ protoplasts from the resistant cultivar, but only 30% from the sensitive cultivar. When Al was applied to the protoplasts in the whole-cell configuration, anion currents were elicited within 10 min in the resistant cultivar only. La3+ was not able to replace or counteract with Al3+ in the activation of this channel. In the presence of the anion-channel blockers, niflumic acid and 4, 4′-dinitrostilbene-2, 2′disulfonic acid, anion currents as well as exudation rates were strongly inhibited. Application of cycloheximide did not affect the Al response, suggesting that the channel is activated through post-translational modifications. We propose that the Al-activated large anion channel described here contributes to enhanced genotypical Al resistance by facilitating the exudation of organic acid anions from the DTZ of the maize root apex.
机译:为寻找玉米(Zea mays)品种之间铝(Al)抗性差异的细胞和分子基础,我们将膜片钳技术应用于从两个抗铝性不同的玉米品种根尖皮层分离的原生质体。对来自两个根尖区的原生质体进行了测量:1-2毫米区(DTZ)(被描述为对铝最敏感)和主要延伸区(3-5毫米)(铝诱导的铝抑制位点)细胞伸长率。铝刺激柠檬酸和苹果酸从完整的根尖流出,揭示了品种差异。在延伸区中,在不存在和存在Al的情况下未观察到阴离子通道。将完整的根与90μmAl预先孵育1 h,可在抗性品种的80%DTZ原生质体中诱导柠檬酸和苹果酸可渗透的大电导阴离子通道,而敏感品种仅30%。当以全细胞形式将Al应用于原生质体时,仅在抗性品种中在10分钟内引起阴离子电流。在激活此通道中,La3 +无法替换或抵消Al3 +。在阴离子通道阻滞剂尼氟酸和4,4'-二硝基苯乙烯-2,2'二磺酸的存在下,阴离子电流和渗出速率受到强烈抑制。环己酰亚胺的应用未影响Al反应,表明该通道是通过翻译后修饰激活的。我们认为,此处所述的Al活化的大阴离子通道通过促进从玉米根尖的DTZ中渗出有机酸阴离子,有助于增强基因型的Al抗性。

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