Aluminum (A1)-induced damage to leaves and roots of two Al-resistant (cv. Atlas 66, experimental line PT741) and two Al-sensitive (cv. Scout 66, cv. Katepwa) lines of Triticum aestivum L. was estimated using the deposition of (1, 3)-/3-glucans (callose) as a marker for injury. Two-day-old seedlings were grown for forty hours in nutrient solutions with or without added A1, and callose deposition was quantified by spectrofluorometry (0-1000 #M A1) and localized by fluorescence microscopy (0 and 400 #M A1). Results suggested that A1 caused little damage to leaves. No callose was observed in leaves with up to 400 #M A1 treatment. In contrast, root callose concentration increased with A1 treatment, especially in the Al-sensitive lines. At 400 #M A1, root callose concentration of Al-sensitive Scout 66 was nearly four-fold that of Al-resistant Atlas 66. After A1 treatment, large callose deposits were observed in the root cap, epidermis and outer cortex of root tips of Scout 66, but not Atlas 66. The identity of callose was confirmed by a reduced fluorescence in Al-treated roots: firstly, after adding an inhibitor of callose synthesis (2-deoxy-D-glucose) to the nutrient solution, and secondly, after incubating root sections with the callosedegrading enzyme/3-D-glucoside glucohydrolase [EC 3.2.1.21]. Root callose deposition may be a good marker for Al-induced injury due to its early detection by spectrofluorometry and its close association with stress perception.
Abbreviations: DDG-2-deoxy-D-glucose, PAS-periodic acid-Schiffs reagent, PE-pachyman equivalents