The kinetics of aluminum adsorption and desorption by root cell walls of an aluminum resistant wheat (Triticum aestivum L.) cultivar

2004 ◽  
Vol 261 (1/2) ◽  
pp. 85-90 ◽  
Author(s):  
Shao Jian Zheng ◽  
Xianyong Lin ◽  
Jianli Yang ◽  
Qiang Liu ◽  
Caixian Tang
2019 ◽  
Vol 239 ◽  
pp. 10-17 ◽  
Author(s):  
Kristína Šípošová ◽  
Karin Kollárová ◽  
Desana Lišková ◽  
Zuzana Vivodová

1979 ◽  
Vol 6 (2) ◽  
pp. 201 ◽  
Author(s):  
MM Smith ◽  
TP O'brien

In the wheat root, peroxidases and esterases specific for a-naphthyl esters of acetate, propionate and butyrate are concentrated in cell walls, particularly the outer wall of epidermal cells undergoing extension. In contrast esterases specific for β-naphthyl esters of propionate and butyrate were intra- cellular and concentrated in epidermal and outer root-cap cells of the wheat root. Both α-naphthyl and β-naphthyl esters of longer-chain fatty acids proved to be poor substrates. The esterases and peroxidases associated with the outer epidermal wall may well be involved in turnover of phenolic acids cross-linked to polysaccharides. In this regard, ferulic acid and diferulate were shown to be constituents of wheat-root cell walls. The distribution of these substances can also be inferred from autofluorescence. Treatment with a commercial pig-liver esterase was without effect on the auto- fluorescence of the root cell-walls. Culture filtrates from Gaeumannomyces graminis did remove significant amounts of autofluorescent wall material. These preparations contained α-naphthyl acetate esterase as well as many polysaccharide hydrolase activities.


2020 ◽  
Vol 26 (S2) ◽  
pp. 348-351
Author(s):  
Timothy Pegg ◽  
Daniel Gladish ◽  
Richard Edelmann ◽  
Robert Baker

1997 ◽  
Vol 45 (4) ◽  
pp. 285-292 ◽  
Author(s):  
Kay M. Cocker ◽  
Martin J. Hodson ◽  
David E. Evans ◽  
Allan G. Sangster

Seedlings ofTriticum aestivumL. (cv. Celtic) were suspended in plastic tubs containing 500 μmol L−1Ca(NO3)2and 31 μmol L−1KC1 as background solution. A1C13(0 and 100 μmol L−1) and Na2SiO3.5H2O (0 and 2000 μmol; L−1) were added to this basal nutrient medium, and solution pH was set at 4.2 or 4.6. Tubs were aerated and supplied with a continuous flow of pH-adjusted test solution. Plants were grown for 4 d in a growth cabinet at 25 °C with a 16 h photoperiod. At pH 4.2 and 4.6 root length of the seedlings was inhibited at 100 μmol L−1Al. An amelioration of Al-induced toxicity symptoms was observed in the 100 μmol L−1A1/2000 μmol L−1Si treatment at pH 4.6, but not at pH 4.2. Both the shoot (S) and root (R) dry weight of seedlings treated with 100 μmol L−1Al were reduced when compared with controls. Treatment with Al increased S:R ratios, and this effect was ameliorated by Si, but only at pH 4.6.Al content of roots treated with 100 μmol L−1Al or 100 μmol L−1Al/2000 μmol L−1Si increased significantly when compared with controls. More Al accumulated in the roots of seedlings of the 100 μmol L−1Al/2000 μmol L−1Si treatment than in the 100 μmol L−1treatment. Al treatment reduced root and shoot K concentrations under both pH regimes, and Si did not ameliorate this effect. Al treatment had little effect on seedling Ca levels.Three treatments were selected for a microanalytical investigation of the basal third of the root, and the zone 3.5 mm behind the root tip: 2800 μmol L−1Si; 75 μmol Al; and a combination of the two. When plants were grown in 2800 μmol L−1Si the major silica deposition sites in the roots were the endodermal walls. In the 75 μmol L−1Al treatment, Al was mainly located in the epidermal and hypodermal walls. Al treatment caused a leakage of phosphorus into these cell walls. When both 2800 μmol L−1and 75 μmol L−1Al were present in the nutrient solution, only Si was deposited in the endodermal walls, while both elements were present in the epidermal walls. Leakage of phosphorus appeared to be prevented in the presence of Si.


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