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2014 | 36 | 08 |

Tytuł artykułu

Comaparative effects of NaCl and NaHCO3 stresses on respiratory metabolism, antioxidant system, nutritional status, and oragnic acid metabolism in tomato roots

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Physiological responses of tomato roots to NaCl and NaHCO₃ stresses were investigated in a hydroponic setting. The relative growth rate of tomato plants was significantly reduced in both NaCl and NaHCO₃ treatments, especially under NaHCO₃ stress. Tomato root respiration increased under low concentrations of NaCl and NaHCO₃ stresses. However, high concentrations of both NaCl and NaHCO₃ significantly inhibited respiration, especially in the NaHCO₃ treatment. With increasing concentration of NaCl and NaHCO₃ treatment, root Na accumulation increased, while accumulation of N, P, K, Fe, and Mg was significantly lower. Compared to NaCl, NaHCO₃ treatment resulted in more dramatic changes in these nutrients. All organic acids investigated were increased by NaHCO₃ after 5 days of treatment, but only oxalate, tartrate and malate were induced by NaCl. This implies that global regulation of organic acids might play an important role in tomato’s alkali stress tolerance. Compared to NaCl treatments, NaHCO₃ treatments induced much higher levels of reactive oxygen species (ROS) and lipid peroxidation after 5 days of treatment, which was accompanied by higher activities of antioxidant enzymes and higher concentrations of ascorbate–glutathione. However, after 10 days of treatment, 100 mM NaHCO₃ stress led to lower accumulation of ROS, antioxidant enzyme activities, and ascorbate–glutathione content. This may have been because root metabolism had almost completely stopped, as indicated by lower root respiration and activity.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

36

Numer

08

Opis fizyczny

p.2167-2181,fig.,ref.

Twórcy

autor
  • State Key Laboratory of Crop Biology, Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (Huanghuai Region, Ministry of Agriculture), College of Horticulture Science and Engineering, Shandong Agricultural University, 271018 Taian, People's Republic of China
autor
  • State Key Laboratory of Crop Biology, Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (Huanghuai Region, Ministry of Agriculture), College of Horticulture Science and Engineering, Shandong Agricultural University, 271018 Taian, People's Republic of China
autor
  • Department of Plant Pathology, North Carolina State University, Raleigh, NC 27695-7616, USA
autor
  • State Key Laboratory of Crop Biology, Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (Huanghuai Region, Ministry of Agriculture), College of Horticulture Science and Engineering, Shandong Agricultural University, 271018 Taian, People's Republic of China
autor
  • State Key Laboratory of Crop Biology, Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (Huanghuai Region, Ministry of Agriculture), College of Horticulture Science and Engineering, Shandong Agricultural University, 271018 Taian, People's Republic of China
autor
  • State Key Laboratory of Crop Biology, Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (Huanghuai Region, Ministry of Agriculture), College of Horticulture Science and Engineering, Shandong Agricultural University, 271018 Taian, People's Republic of China
autor
  • State Key Laboratory of Crop Biology, Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (Huanghuai Region, Ministry of Agriculture), College of Horticulture Science and Engineering, Shandong Agricultural University, 271018 Taian, People's Republic of China
autor
  • State Key Laboratory of Crop Biology, Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (Huanghuai Region, Ministry of Agriculture), College of Horticulture Science and Engineering, Shandong Agricultural University, 271018 Taian, People's Republic of China

Bibliografia

  • Anderson JV, Chevone BI, Hess JL (1992) Seasonal variation in the antioxidant system of eastern white pine needles. Plant Physiol 98:501–508
  • Anoop VM, Basu U, McCammon MT, McAlister-Henn L, Taylor GJ (2003) Modulation of citrate metabolism alters aluminum tolerance in yeast and transgenic canola overexpressing a mitochondrial citrate synthase. Plant Physiol 132:2205–2217
  • Bahr JT, Bonner WDJ (1973) Cyanide-insensitive respiration. II. Control of the alternate pathway. J Biol Chem 248:3446–3450
  • Bouma TJ, Yanai RD, Elkin AD, Hartmond U, Flores-Alva DE, Eissenstat DM (2001) Estimating age-dependent costs and benefits of roots with contrasting life span: comparing apples and oranges. New Phytol 150:685–695
  • Cavalcanti FR, Oliveira JTA, Martins-Miranda AS, Viégas RA, Silveira JAG (2004) Superoxide dismutase, catalase and peroxidase activities do not confer protection against oxidative damage in salt-stressed cowpeas leaves. New Phytol 163:563–571
  • Comas LH, Eissenstat DM, Lakso AN (2000) Assessing root death and root system dynamics in a study of grape canopy pruning. New Phytol 147:171–178
  • Deng Y, Kohlwein SD, Mannella CA (2002) Fasting induces cyanide-resistant respiration and oxidative stress in the amoeba Chaos carolinensis: implications for the cubic structural transition in mitochondrial membranes. Protoplasma 219:160–167
  • De-Azevedo-Neto AD, Prisco JT, Enéas-Filho J, De-Abreu CEB, Gomes-Filho E (2006) Effect of salt stress on antioxidant enzymes and lipid peroxidation in leaves and roots of salt-tolerant and salt-sensitive maize genotypes. Environ Exp Bot 56:87–94
  • Feng HQ, Li X, Duan JG, Li HY, Liang HG (2008) Chilling tolerance of wheat seedlings is related to an enhanced alternative respiratory pathway. Crop Sci 48:2381–2388
  • Foyer CH, Halliwell B (1976) The presence of glutathione and glutathione reductase in chloroplasts: a proposed role in ascorbic acid metabolism. Planta 133:21–25
  • Gao ZX, Wehner TC, Chen H, Lin Y, Wang XF, Wei M, Yang FJ, Shi QH (2013) Deciphering the possible mechanism of exogenous NO alleviating alkali stress on cucumber leaves by transcriptomic analysis. Sci Hortic 150:377–386
  • Ge Y, Li Y, Zhu YM, Bai X, Lv DK, Guo DJ, Ji W, Cai H (2010) Global transcriptome profiling of wild soybean (Glycine soja) roots under NaHCO₃ treatment. BMC Plant Biol 10:153
  • Guo R, Shi L, Yang YF (2009) Germination, growth, osmotic adjustment and ionic balance of wheat in response to saline and alkaline stresses. Soil Sci Plant Nutr 55:667–679
  • Halliwell B, Gutteridge JMC (1989) Protection against oxidants in biological systems: the super oxide theory of oxygen toxicity. Free radicals in biology and medicine. Clarendon Press, Oxford, pp 86–123
  • Hirai M, Ueno I (1977) Development of citrus fruits: fruit development and enzymatic changes in juice vesicle tissue. Plant Cell Physiol 18:791–799
  • Jaspers P, Kangasjärvi J (2010) Reactive oxygen species in abiotic stress signaling. Physiol Plantarum 138:405–413
  • Jin H, Kim HR, Plaha P, Liu SK, Park JY, Piao YZ, Yang ZH, Jiang GB, Kwark SS, An G, Son M, Jin YH, Sohn JH, Lim YP (2008) Expression profiling of the genes induced by Na₂CO₃ and NaCl stresses in leaves and roots of Leymus chinensis. Plant Sci 175:784–792
  • Karaffa L, Sandor E, Kozma J, Kubicek CP, Szentirmai A (1999) The role of the alternative respiratory pathway in the stimulation of cephlosporin C formation by soybean oil in Acremonium chrysogenum. Appl Microbiol Biotechnol 51:633–638
  • Keutgen A, Pawelzik E (2009) Impacts of NaCl stress on plant growth and mineral nutrient assimilation in two cultivars of strawberry. Environ Exp Bot 65:170–176
  • Kingsbury RW, Epstein E, Peary RW (1984) Physiological responses to salinity in selected lines of wheat. Plant Physiol 74:417–423
  • Kono Y (1978) Generation of superoxide radical during autoxidation of hydroxylamine and an assay for superoxide dismutase. Arch Biochem Biophys 186:189–195
  • Kowaltowski AJ, Vercesi AE (1999) Mitochondrial damage induced by conditions of oxidative stress. Free Radic Bio Med 26:463–471
  • Law MY, Charles SA, Halliwell B (1983) Glutathione and ascorbic acid in spinach (Spinacia oleracea) chloroplasts. Biochem J 210:899–903
  • Li J, Shi DC (2010) Photosynthesis, chlorophyll fluorescence, inorganic ion and organic acid accumulations of sunflower in responses to salt and salt-alkaline mixed stress. Photosynthetica 48:127–134
  • Li RL, Shi FC, Fukuda KJ, Yang YL (2010) Effects of salt and alkali stresses on germination, growth, photosynthesis and ion accumulation in alfalfa (Medicago sativa L.). Soil Sci Plant Nutr 56:725–733
  • Locato V, Gadaleta C, De-Gara L, De-Pinto MC (2008) Production of reactive species and modulation of antioxidant network in response to heat shock: a critical balance for cell fate. Plant Cell Environ 31:16–19
  • McIntosh L (1994) Molecular biology of the alternative oxidase. Plant Physiol 105:781–786
  • Mittova V, Tal M, Volokita M, Guy M (2003) Up-regulation of the leaf mitochondrial and peroxisomal antioxidative systems in response to salt-induced oxidative stress in the wild salt-tolerant tomato species Lycopersicon pennellii. Plant Cell Environ 26:845–856
  • Munns R, Tester M (2008) Mechanisms of salinity tolerance. Annu Rev Plant Biol 59:651–681
  • Møller IM (2001) Plant mitochondria and oxidative stress: electron transport, NADPH turnover, and metabolism of reactive oxygen species. Annu Rev Plant Biol 52:561–591
  • Nakano Y, Asada K (1981) Hydrogen peroxide scanvenged by ascorbate-specific peroxidase in spinach chloroplast. Plant Cell Physiol 22:867–880
  • Nickel RS, Cunningham BA (1969) Improved peroxidase assay method using Ieuco 2,3,6-trichlcroindophenol and application to comparative measurements of peroxidase catalysis. Ann Biochem 27:292–299
  • Paradiso A, Berardino R, De-Pinto MC, Di-Toppi LS, Storelli MM, Tommasi F, De-Gara L (2008) Increase in ascorbate-glutathione metabolism as local and precocious systemic responses induced by cadmium in durum wheat plants. Plant Cell Physiol 49:362–374
  • Parida AK, Das AB (2005) Salt tolerance and salinity effects on plants: a review. Ecotox Environ Safe 60:324–349
  • Patra HL, Kar M, Mishre D (1978) Catalase activity in leaves and cotyledons during plant development and senescence. Biochem Physiol 172:385–390
  • Patterson BD, Macrae EA, Ferguson IB (1984) Estimation of hydrogen peroxide in plants extracts using titanium (IV). Ann Biochem 134:487–492
  • Pellet DM, Grunes DL, Kochian LV (1995) Organic acid exudation as an aluminum-tolerance mechanism in maize (Zea mays L.). Planta 196:788–795
  • Qin SJ, Lv DG, Li ZX, Ma HY, Liu LZ, Liu GC (2011) Effects of water stress on respiration and other physiological metabolisms of Cerasus sachalinensis Kom. Seedlings. Sci Agr 44:201–209
  • Rauckman EJ, Rosen GM, Kitchell BB (1979) Superoxide radical as an intermediate in the oxidation of hydroxylamines by mixed function amine oxidase. Mol Pharmacol 15:131–137
  • Sere PA (1969) Malate dehydrogenase. In: Colowick SP, Kaplan NO (eds) Methods in enzymology. Academic Press Inc, New York, 467 p 3–11
  • Shalata A, Mittova V, Volokita M, Guy M, Tal M (2001) Response of the cultivated tomato and its wild salt-tolerant relative Lycopersicon pennellii to salt-dependent oxidative stress: the root antioxidative system. Physiol Plantarum 112:487–494
  • Shen J, Yuan L, Zhang J, Li H, Bai Z, Chen X, Zhang W, Zhang F (2011) Phosphorus dynamics: from soil to plant. Plant Physiol 156:997–2005
  • Singer TP, Oestreicher G, Hogue P (1973) Regulation of succinate dehydrogenase in higher plants. I. Some general characteristics of the membrane-bound enzyme. Plant Physiol 52:616–621
  • Sivakumar P, Sharmila P, Saradhi PP (2000) Proline alleviates saltstress-induced enhancement in ribulose-1, 5-bisphosphate oxygenase activity. Biochem Bioph Res Co 279:512–515
  • Sobhanian H, Razavizadeh R, Nanjo Y, Ehsanpour AA, Jazii FR, Motamed N, Komatsu S (2010) Proteome analysis of soybean leaves, hypocotyls and roots under salt stress. Proteome Sci 8:19
  • Sohal RS, Dubey A (1994) Mitochondrial oxidative damage; hydrogen peroxide release; and aging. Free Radic Bio Med 16:621–626
  • Stewart RC, Bewley JD (1980) Lipid peroxidation associated with accelerated aging of soybean axes. Plant Physiol 65:245–248
  • Stepin P, Klobus G (2006) Water relations and photosynthesis in Cucumis sativus L. leaves. Biol Plantarum 50:610–616
  • Van-lerberghe GC, McIntosh L (1992) Lower growth temperature increases alternative pathway capacity and alternative oxidase protein in tobacco. Plant Physiol 100:115–119
  • Veselov DS, Sharipova GV, Akhiyarova GR, Kudoyarova GR (2009) Fast growth responses of barley and durum wheat plants to NaCl- and PEG-treatment: resolving the relative contributions of water deficiency and ion toxicity. Plant Growth Regul 58:125–129
  • Wang BS, Zhao KF (1995) Comparison of extractive methods of Na⁺ and K⁺ in wheat leaves. Plant Physiol 31:50–52
  • Wang D, Shi Q, Wang X, Wei M, Hu J, Liu J, Yang F (2010a) Influence of cow manure vermicompost on the growth, metabolite contents, and antioxidant activities of Chinese cabbage (Brassica campestris ssp. chinensis). Biol Fert Soils 46:689–696
  • Wang H, Liang X, Huang J, Zhang D, Lu H, Liu Z, Bi Y (2010b) Involvement of ethylene and hydrogen peroxide in induction of alternative respiratory pathway in salt-treated Arabidopsis calluses. Plant Cell Physiol 51:1754–1765
  • Wang XP, Geng SJ, Ri YJ, Cao DH, Liu J, Shi DH, Yang CW (2011) Physiological responses and adaptive strategies of tomato plants to salt and alkali stresses. Sci Hortic 130:248–255
  • Wang YC, Ma H, Liu GF, Zhang DW, Ban QY, Zhang GD, Xu CX, Yang CP (2008a) Generation and analysis of expressed sequence tags from a NaHCO₃-treated Limonium bicolor cDNA library. Plant Physiol Biochem 46:977–986
  • Wang YC, Ma H, Liu GF, Xu CX, Zhang DW, Ban QY (2008b) Analysis of gene expression profile of limonium bicolor under NaHCO₃ stress using cDNA microarray. Plant Mol Biol Rep 26:241–254
  • Yang CW, Chong JN, Kim CM, Li CY, Shi DC, Wang DL (2007) Osmotic adjustment and ion balance traits of an alkali resistant halophyte Kochia sieversiana during adaptation to salt and alkali conditions. Plant Soil 294:263–276
  • Yang CW, Jianaer A, Li CY, Shi DC, Wang DL (2008a) Comparison of the effects of salt-stress and alkali-stress on photosynthesis and energy storage of an alkali-resistant halophyte Chloris virgata. Photosynthetica 46:273–278
  • Yang CW, Shi DC, Wang DL (2008b) Comparative effects of salt and alkali stresses on growth, osmotic adjustment and ionic balance of an alkali-resistant halophyte Suaeda glauca (Bge.). Plant Growth Regul 56:179–190
  • Zhang JT, Mu CS (2009) Effects of saline and alkaline stresses on the germination, growth, photosynthesis, ionic balance and antioxidant system in an alkali-tolerant leguminous forage Lathyrus quinquenervius. Soil Sci Plant Nutr 55:685–697
  • Zhao MG, Liu YG, Zhang LX, Zheng L, Bi YR (2007) Effects of enhanced UV-B radiation on the activity and expression of alternative oxidase in red kidney bean leaves. J Integr Plant Biol 49:1320–1326
  • Zhu JK (2003) Regulation of ion homeostasis under salt stress. Curr Opin Cell Biol 6:441–445

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Bibliografia

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