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Acta Agron Sin ›› 2009, Vol. 35 ›› Issue (4): 695-703.doi: 10.3724/SP.J.1006.2009.00695

• TILLAGE & CULTIVATION · PHYSIOLOGY & BIOCHEMISTRY • Previous Articles     Next Articles

Distribution of Al3+ in Subcellular Structure of Root Tips Cells and Aluminum Tolerance in soybean

YU Hui-Na,LIU Peng*,XU Gen-Di,CAI Miao-Zhen   

  1. Key laboratory of Botany,Zhejiang Normal University,Jinhua321004,China
  • Received:2008-06-07 Revised:2008-12-15 Online:2009-04-12 Published:2009-02-16
  • Contact: LIU Peng E-mail:sky79@zjnu.cn E-mail:sky79@zjnu.cn

Abstract:

Aluminum(Al) toxicity is a major limiting factor for yield and quality in crop production in acid soil. Micromolar concentrations of Al3+ may inhibit root elongation and consequently influence water and nutrient uptake, resulting in poor plant growth. The microanalysis of the elements was conducted on Zhechun 3 by using Transmission Electron Microscope (TEM) and Energy Dispersive X-ray (EDS) to examine the distribution of Al3+ in root tips and Al resistance of soybean. We found that Al3+ stresses resulted in irregularly thickened cell wall, increased number of mitochondria, expanded nuclear membrane, and densified precipitates of vacuole. Under the highest Al3+ concentration, the mitochondria and other organelles disappeared but cell wall. We detected Al in cell wall, mitochondria and electron-dense precipitates of vacuole of root tip cell under the 10 mg L-1Al3+ stresses by EDS. With the increase of external Al3+ concentration treated, the weight and atomic percentage of Al in the organelles increased. The Al3+ was found in nuclei when the external Al3+ was over 60 mg L-1. And there was no Al3+ in mitochondrion under 60 mg L-1 and 90 mg L-1Al3+ treatments and electron-dense precipitates of vacuole under the 90 mg L-1 Al3+ stresses. The 14 days Al3+ stresses significantly inhibited the growth of root system. The content of Al3+ in cell wall was most significantly impacted by the external Al3+ concentration. The atomic number of P / Al in cell wall and mitochondria decreased with increased Al3+ content. EDS can be used to determine the subcellular location of Al3+. As the treatment concentrations of Al3+ increased, Al3+ primarily accumulated in the cell wall, gradually gathered in part of the organelles and nuclei. The Al3+ concentrations also decreased from out layer to insider in the cell.

Key words: Al3+ stresses, Soybean, Root tip cell, Transmission Electron Microscope-Energy Dispersive X-ray Analysis, Root growth

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