State Key Laboratory of Plant Physiology and Biochemistry, College of Life Sciences, Zhejiang University, Hangzhou 310058, China.
Plant Physiol. 2011 Apr;155(4):1885-92. doi: 10.1104/pp.111.172221. Epub 2011 Feb 1.
The cell wall (CW) has been recognized as the major target of aluminum (Al) toxicity. However, the components responsible for Al accumulation and the mechanisms of Al-induced CW function disruption are still elusive. The contribution of different CW components (pectin, hemicellulose 1 [HC1], and HC2) to adsorb Al and the effect of Al on xyloglucan endotransglucosylase/hydrolyase activity were investigated in Arabidopsis (Arabidopsis thaliana) in this study. A fractionation procedure was optimized to effectively extract different CW components, especially to prevent the HC fraction from pectin contamination. When CW materials extracted from Al-treated roots (50 μm Al for 24 h) were fractionated, about 75% of CW Al accumulated in the HC1 fraction. A time-dependent kinetic study showed that only when the HC1 fraction was removed was the amount of Al adsorbed decreased sharply. In vivo localization of xyloglucan endotransglucosylase (XET) activity showed that Al greatly inhibited this enzyme activity within 30 min of exposure, which was concomitant with Al-induced callose deposition in roots. Results from real-time reverse transcription-polymerase chain reaction indicated that three genes may constitute the major contributors to XET activity and that the inhibition of XET activity by Al is caused by transcriptional regulation. These results, to our knowledge for the first time, demonstrate that HC is the major pool for Al accumulation. Furthermore, Al-induced reduction in XET activity could play an important role in Al-induced root growth inhibition.
细胞壁 (CW) 已被认为是铝 (Al) 毒性的主要靶标。然而,负责 Al 积累的成分以及 Al 诱导的 CW 功能障碍的机制仍不清楚。本研究在拟南芥 (Arabidopsis thaliana) 中研究了不同 CW 成分(果胶、半纤维素 1 [HC1] 和 HC2)对 Al 吸附的贡献以及 Al 对木葡聚糖内转糖基酶/水解酶活性的影响。优化了一种分级程序,以有效提取不同的 CW 成分,特别是防止 HC 部分受到果胶污染。当从 Al 处理的根中提取 CW 材料(50 μm Al 处理 24 h)时,约 75%的 CW Al 积累在 HC1 部分。时程动力学研究表明,只有当 HC1 部分被去除时,吸附的 Al 量才会急剧减少。木葡聚糖内转糖基酶 (XET) 活性的体内定位表明,Al 在暴露 30 分钟内极大地抑制了这种酶活性,这与 Al 诱导的根中几丁质沉积同时发生。实时逆转录聚合酶链反应的结果表明,三个基因可能构成 XET 活性的主要贡献者,并且 Al 对 XET 活性的抑制是由转录调控引起的。这些结果,据我们所知,首次表明 HC 是 Al 积累的主要库。此外,Al 诱导的 XET 活性降低可能在 Al 诱导的根生长抑制中起重要作用。