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2012 | 34 | 2 |

Tytuł artykułu

The decline in potasium concentration is associated with cadmium toxicity of rice seedlings

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Cadmium (Cd) is one of the most dangerous environmental pollutants, among other things, affecting plant mineral composition. Thus, in this study, we investigated the changes in potassium (K) concentration in Cd-treated rice (Oryza sativa L.) seedlings of two cultivars. On treatment with 5 µM CdCl₂, the Cd concentration increased in the shoot and roots of Cd-sensitive cultivar (cv. Taichung Native 1, TN1) but not or slightly in the Cd-tolerant cultivar (cv. Tainung 67, TNG67). The decrease in K concentration in the shoot and roots of TN1 caused by Cd was more pronounced than that of TNG67. Exogenous addition of KCl decreased Cd concentration and reduced Cd toxicity of TN1 seedlings. Evidence presented in this study suggests that the improvement of K status is able to reduce toxicity of rice seedlings to CdCl₂.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

34

Numer

2

Opis fizyczny

p.495-502,fig.,ref.

Twórcy

autor
  • Department of Agronomy, National Taiwan University, Taipei, ROC, Taiwan
autor
  • Department of Agronomy, National Taiwan University, Taipei, ROC, Taiwan
autor
  • Department of Agronomy, National Taiwan University, Taipei, ROC, Taiwan

Bibliografia

  • Amtmann A, Hammond JP, Armengaud P, White PJ (2005) Nutrient sensing and signaling in plants: potassium and phosphorus. Adv Bot Res 43:209–257
  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254
  • Cakmak I (2005) The role of potassium in alleviating detrimental effect of abiotic stresses in plants. J Plant Nutr Soil Sci 168:521–530
  • Carroll MJ, Slaughter LH, Krouse JM (1994) Turgor potential and osmotic constituents of Kentucky bluegrass leaves supplied with four levels of potassium. Agron J 86:1079–1083
  • Chao YY, Hong CY, Kao CH (2010) The decline in ascorbic acid content is associated with cadmium toxicity of rice seedlings. Plant Physiol Biochem 48:374–381
  • Chien H-F, Kao CH (2000) Accumulation of ammonium in rice leaves in response to excess cadmium. Plant Sci 156:111–115
  • Cho U-H, Seo N-H (2005) Oxidative stress in Arabidopsis thaliana exposed to cadmium is due to hydrogen peroxide accumulation. Plant Sci 168:113–120
  • Das P, Samantaray S, Rout GR (1997) Studies on cadmium toxicity in plants: a review. Environ Pollut 98:29–36
  • Dixit V, Pandey V, Shyam R (2001) Differential antioxidative responses to cadmium in roots and leaves of pea (Pisum sativum L. cv. Azad). J Exp Bot 52:1101–1109
  • Foster JG, Hess JL (1980) Response of superoxide dismutase and glutathione reductase activities in cotton leaf tissue exposed to an atmosphere enriched in oxygen. Plant Physiol 66:482–487
  • Goncalves JF, Antes FG, Maldaner J, Pereira LB, Tabaldi LA, Tauber R, Rossato LV, Bisognin DA, Dressler VL, de Moraes Flores EM, Nicoloso FT (2009) Cadmium and mineral nutrient accumulation in potato plantlets grown under cadmium stress in two different experimental culture conditions. Plant Physiol Biochem 47:814–821
  • Gratăo PL, Polle A, Lea PJ, Azevedo RA (2005) Making the life of heavy metal-stressed plants a little easier. Funct Plant Biol 32:481–494
  • Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplasts: I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198
  • Hsu YT, Kao CH (2003) Role of abscisic acid in cadmium tolerance of rice (Oryza sativa L.) seedlings. Plant Cell Environ 26:867–874
  • Hsu YT, Kao CH (2005) Abscisic acid accumulation and cadmium tolerance in rice seedlings. Physiol Plant 124:71–80
  • Hsu YT, Kao CH (2007) Toxicity in leaves of rice exposed to cadmium is due to hydrogen peroxide accumulation. Plant Soil 298:231–241
  • Jalil A, Selles F, Clarke JM (1994) Effect of cadmium on growth and the uptake of cadmium and other elements by durum wheat. J Plant Nutr 17:1839–1858
  • Kato M, Shimizu S (1987) Chlorophyll metabolism in higher plants. VII: chlorophyll degradation in senescing tobacco leaves: phenolic-dependent peroxidative degradation. Can J Bot 65:729–735
  • Kuo MC, Kao CH (2004) Antioxidant enzyme activities are upregulated in response to cadmium in sensitive, but not in tolerant, rice (Oryza sativa L.) seedlings. Bot Bull Acad Sin 45:291–299
  • Leigh RA, Wyn Jones RG (1984) A hypothesis relating critical potassium concentrations for growth to the distribution and functions of this ion in the plant cell. New Phytol 97:1–13
  • Metwally A, Safronova VI, Belimov AA, Dietz K-J (2005) Genotypic variation of the response to cadmium toxicity in Pisum sativum L. J Exp Bot 56:167–178
  • Moral R, Gomez I, Pedreno JN, Mataix J (1994) Effects of cadmium on nutrient distribution, yield, and growth of tomato grown in soilless culture. J Plant Nutr 17:953–962
  • Nakano Y, Asada K (1981) Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol 22:867–880
  • Noctor G, Foyer C (1998) Ascorbate and glutathione: keeping active oxygen under control. Annu Rev Plant Physiol Plant Mol Biol 49:249–279
  • Ouariti O, Gouia H, Ghorbal MH (1997) Responses of bean and tomato plants to cadmium: growth, mineral nutrition, and nitrate reduction. Plant Physiol Biochem 35:347–354
  • Ouzounidou G, Moustakas M, Eleftheriou EP (1997) Physiological and ultrastructural effects of cadmium on wheat (Triticum aestivum L.) leaves. Arch Environ Contam Toxicol 32:154–160
  • Paoletti F, Aldinucci D, Mocali A, Capparrini A (1986) A sensitive spectrophotometric method for the determination of superoxide dismutase activity in tissue extracts. Anal Biochem 154:536–541
  • Sandalio LM, Dalurzo HC, Gómez M, Romero-Puertas MC, del Río LA (2001) Cadmium-induced changes in the growth and oxidative metabolism of pea plants. J Exp Bot 52:2115–2126
  • Smeets K, Ruytinx J, Semane B, Van Belleghem F, Remans T, Van Sanden S, Vangronsveld J, Cuypers A (2008) Cadmium-induced transcriptional and enzymatic alterations related to oxidative stress. Environ Exp Bot 63:1–8
  • Szczerba MW, Britto DT, Kronzucker HJ (2009) K⁺ transport in plants: physiology and molecular biology. J Plant Physiol 166:447–466
  • Tsai Y-C, Hong C-Y, Liu L-F, Kao CH (2004) Relative importance of Na⁺ and Cl⁻ in NaCl-induced antioxidant systems in roots of rice seedlings. Physiol Plant 122:86–94
  • Wintermans JFGM, De Mots A (1965) Spectrophotometric characteristics of chlorophylls a and b and their pheophytin in ethanol. Biochim Biophys Acta 109:448–453
  • Wu FB, Chen F, Wei K, Zhang GP (2004) Effect of cadmium on free amino acid, glutathione and ascorbic acid concentrations in two barley genotype (Hordeum vulgare L.) differing in cadmium tolerance. Chemosphere 57:447–454
  • Yoshida S, Forno DA, Cock JH, Gomez KA (1972) Laboratory manual for physiological studies of rice. The International Rice Research Institute, Los Bańos

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Bibliografia

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