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铝诱导拟南芥中的离子转运:耐铝性与根离子流之间的关系。

Aluminium-induced ion transport in Arabidopsis: the relationship between Al tolerance and root ion flux.

机构信息

School of Earth and Environment, the University of Western Australia, Crawley WA 6009, Australia.

出版信息

J Exp Bot. 2010 Jun;61(11):3163-75. doi: 10.1093/jxb/erq143. Epub 2010 May 23.

DOI:10.1093/jxb/erq143
PMID:20497972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2892157/
Abstract

Aluminium (Al) rhizotoxicity coincides with low pH; however, it is unclear whether plant tolerance to these two factors is controlled by the same mechanism. To address this question, the Al-resistant alr104 mutant, two Al-sensitive mutants (als3 and als5), and wild-type Arabidopsis thaliana were compared in long-term exposure (solution culture) and in short-term exposure experiments (H(+) and K(+) fluxes, rhizosphere pH, and plasma membrane potential, E(m)). Based on biomass accumulation, als5 and alr104 showed tolerance to low pH, whereas alr104 was tolerant to the combined low-pH/Al treatment. The sensitivity of the als5 and als3 mutants to the Al stress was similar. The Al-induced decrease in H(+) influx at the distal elongation zone (DEZ) and Al-induced H(+) efflux at the mature zone (MZ) were higher in the Al-sensitive mutants (als3 and als5) than in the wild type and the alr104 mutant. Under combined low-pH/Al treatment, alr104 and the wild type had depolarized plasma membranes for the entire 30 min measurement period, whereas in the Al-sensitive mutants (als3 and als5), initial depolarization to around -60 mV became hyperpolarization at -110 mV after 20 min. At the DEZ, the E(m) changes corresponded to the changes in K(+) flux: K(+) efflux was higher in alr104 and the wild type than in the als3 and als5 mutants. In conclusion, Al tolerance in the alr104 mutant correlated with E(m) depolarization, higher K(+) efflux, and higher H(+) influx, which led to a more alkaline rhizosphere under the combined low-pH/Al stress. Low-pH tolerance (als5) was linked to higher H(+) uptake under low-pH stress, which was abolished by Al exposure.

摘要

铝(Al)的根系毒性与低 pH 值有关;然而,尚不清楚植物对这两个因素的耐受性是否受同一机制控制。为了解决这个问题,我们比较了耐铝 alr104 突变体、两个铝敏感突变体(als3 和 als5)和野生型拟南芥在长期暴露(溶液培养)和短期暴露实验(H(+)和 K(+)通量、根际 pH 值和质膜电位,E(m))中的表现。基于生物量积累,als5 和 alr104 对低 pH 值表现出耐受性,而 alr104 对低 pH 值/Al 联合处理具有耐受性。als5 和 als3 突变体对 Al 胁迫的敏感性相似。在远端伸长区(DEZ)中,Al 诱导的 H(+)内流减少和在成熟区(MZ)中,Al 诱导的 H(+)外排在铝敏感突变体(als3 和 als5)中比野生型和 alr104 突变体更高。在低 pH 值/Al 联合处理下,alr104 和野生型在整个 30 分钟测量期间质膜去极化,而在铝敏感突变体(als3 和 als5)中,初始去极化至约-60 mV 在 20 分钟后变为超极化。在 DEZ 处,E(m)变化与 K(+)通量变化相对应:在 alr104 和野生型中,K(+)外排高于 als3 和 als5 突变体。总之,alr104 突变体中的 Al 耐受性与 E(m)去极化、更高的 K(+)外排和更高的 H(+)内流相关,这导致在低 pH 值/Al 联合胁迫下根际更碱性。低 pH 值耐受性(als5)与低 pH 值胁迫下更高的 H(+)摄取有关,而 Al 暴露会消除这种摄取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/0f800dc0d875/jexboterq143f09_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/70eb0421e353/jexboterq143f01_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/9a567aa049ea/jexboterq143f02_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/a3d77f32aab5/jexboterq143f03_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/6b42eb04c168/jexboterq143f04_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/6453054f8ff2/jexboterq143f05_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/85c9a2e5c239/jexboterq143f06_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/e885fd0fccf8/jexboterq143f07_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/09ec0ca66b18/jexboterq143f08_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/0f800dc0d875/jexboterq143f09_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/70eb0421e353/jexboterq143f01_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/9a567aa049ea/jexboterq143f02_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/a3d77f32aab5/jexboterq143f03_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/6b42eb04c168/jexboterq143f04_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/6453054f8ff2/jexboterq143f05_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/85c9a2e5c239/jexboterq143f06_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/e885fd0fccf8/jexboterq143f07_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/09ec0ca66b18/jexboterq143f08_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c0f/2892157/0f800dc0d875/jexboterq143f09_lw.jpg

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