PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2011 | 33 | 4 |

Tytuł artykułu

Modification of chromium (VI) phytotoxicity by exogenous gibberellic acid application in Pisum sativum (L.) seedlings

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Effects of exogenous gibberellic acid (GA; 10 and 100 µM) application on growth, protein and nitrogen contents, ammonium (NH₄⁺) content, enzymes of nitrogen assimilation and antioxidant system in pea seedlings were investigated under chromium (VI) phytotoxicity (Cr VI; 50, 100 and 250 µM). Exposure of pea seedlings to Cr and 100 µM GA resulted in decreased seed germination, fresh and dry weight and length of root and shoot, and protein and nitrogen contents compared to control. Compared to control, Cr and 100 µM GA led to the significant alteration in nitrogen assimilation in pea. These treatments decreased root and shoot nitrate reductase (NR), glutamine synthetase (GS) and glutamine 2-oxoglutarate aminotransferase (GOGAT) activities (except 50 µM Cr alone for GOGAT) while glutamate dehydrogenase (GDH) activity and NH₄⁺ content increased. Compared to control, the root and shoot activities of superoxide dismutase (SOD) and ascorbate peroxidase (APX) increased (except APX activity at 250 µM Cr + 100 µM GA) while catalase (CAT), glutathione reductase (GR) and dehydroascorbate reductase (DHAR) activities were decreased (except GR at 100 µM GA alone) following exposure of Cr and 100 µM GA. Total ascorbate and total glutathione in root and shoot decreased by the treatments of Cr and 100 µM GA while their levels were increased by the application of 10 µMGA compared to Cr treatments alone. It has been reported that application of 10 µM GA together with Cr alleviated inhibited levels of growth, nitrogen assimilation and antioxidant system compared to Cr treatments alone. This study showed that application of 10 µM GA counteracts some of the adverse effects of Cr phytotoxicity with the increased levels of antioxidants and sustained activities of enzymes of nitrogen assimilation; however, 100 µM GA showed apparently reverse effect under Cr phytotoxicity.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

33

Numer

4

Opis fizyczny

p.1385-1397,fig.,ref.

Twórcy

autor
  • Department of Plant Science, MJP Rohilkhand University, Bareilly, 243006, India
autor
  • Ranjan Plant Physiology and Biochemistry Laboratory, Department of Botany, University of Allahabad, Allahabad, 211002, India
  • Ranjan Plant Physiology and Biochemistry Laboratory, Department of Botany, University of Allahabad, Allahabad, 211002, India
autor
  • Department of Plant Science, MJP Rohilkhand University, Bareilly, 243006, India

Bibliografia

  • Aebi II (1984) Catalase in vitro. Methods Enzymol 105:121–126
  • Arditti J, Dunn A (1969) Environmental plant physiology—experiments in cellular and plant physiology. Holt, Rinehart and Winston Inc, New York
  • Arrigoni O (1994) Ascorbate system in plant development. J Bioenerg Biomemb 26:407–419
  • Asada K (1999) The water-water cycle in chloroplasts: scavenging of active oxygen and dissipation of excess photons. Annu Rev Plant Physiol Plant Mol Biol 50:601–639
  • Balestrasse KB, Benavides MP, Gallego SM, Tomaro ML (2003) Effect of cadmium stress on nitrogen metabolism in nodules and roots of soybean plants. Funct Plant Biol 30:57–64
  • Balestrasse KB, Gallego SM, Tomaro ML (2006) Oxidation of the enzymes involved in ammonium assimilation plays an important role in the cadmium-induced toxicity in soybean plants. Plant Soil 284:187–194
  • Beevers L, Guernsey FS (1966) Changes in some nitrogenous components during the germination of pea seeds. Plant Physiol 41:1455–1458
  • Brehe JE, Burch HB (1976) Enzymatic assay for glutathione. Anal Biochem 74:189–197
  • Celik I, Tuluce Y, Isik I (2007) Evaluation of toxicity of abscisic acid and gibberellic acid in rats: 50 days drinking water study. J Enzym Inhib Med Chem 22:219–226
  • 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
  • Cordoba-Pedregosa MC, Gonzalez-Reyes JA, Sanadillas MS, Navas P, Cordoba F (1996) Role of apoplastic and cell-wall peroxidases on the stimulation of root elongation by ascorbate. Plant Physiol 112:1119–1125
  • Corpas F, Palma JM, Sandalio LM, Lopez-Huertas E, Romero-Puertas MC, Barroso JB (1999) Purification of catalase from pea leaf peroxisomes: identification of five different isoforms. Free Rad Res 31:235–241
  • Debouba M, Gouia H, Suzuki A, Ghorbel MH (2006) NaCl stress effects on enzymes involved in nitrogen assimilation pathway in tomato ‘‘Lycopersicon esculentum’’ seedlings. J Plant Physiol 163:1247–1258
  • Fuchs Y, Lieberman M (1968) Effects of kinetin, IAA and gibberellin on ethylene production and their interactions in growth of seedlings. Plant Physiol 43:2029–2036
  • Gajewska E, Sklodowska M (2009) Nickel-induced changes in nitrogen metabolism in wheat shoots. J Plant Physiol 166:1034–1044
  • Giannopolitis CN, Reis SK (1977) Superoxide dismutase. I. occurrence in higher plants. Plant Physiol 59:309–314
  • Gossett DR, Millhollon EP, Cran LM (1994) Antioxidant response to NaCl stress in salt-sensitive cultivars of cotton. Crop Sci 34:706–714
  • Hansen H, Grossmann K (2000) Auxin-induced ethylene triggers abscisic acid biosynthesis and growth inhibition. Plant Physiol 124:1437–1448
  • Hernández JA, Escobar C, Creissen G, Mullineaux PM (2004) Role of hydrogen peroxide and the redox state of ascorbate in the induction of antioxidant enzymes in pea leaves under excess light stress. Funct Plant Biol 31:359–368
  • Hooley R (1994) Gibberellins: perception, transduction responses. Plant Mol Biol 26:1529–1555
  • Hossain MA, Asada K (1984) Purification of dehydroascorbate reductase from spinach and its characterization as thiol enzyme. Plant Cell Physiol 25:85–92
  • Kerk NM, Feldman LJ (1995) A biochemical model for initiation and maintenance of the quiescent center: implications for organization of root meristems. Plant Dev 121:2825–2833
  • Kotas J, Stasicka Z (2000) Chromium occurrence in the environment and methods of its speciation. Environ Pollut 107:263–283
  • Kumar S, Joshi UN (2008) Nitrogen metabolism as affected by hexavalent chromium in sorghum (Sorghum bicolor L.). Environ Exp Bot 64:135–144
  • Lang CA (1958) Simple microdetermination of Kjeldahl nitrogen in biological materials. Anal Chem 30:1692–1694
  • Lappartient AG, Touraine B (1996) Demand-driven control of root ATP sulfurylase activity and sulphate uptake in intact Canola. Plant Physiol 111:147–157
  • Lillo C (1984) Diurnal variations of nitrite reductase, glutamine synthetase, glutamate synthase, alanine amino transferase and aspartate amino transferase in barley leaves. Physiol Plant 61:214–218
  • Loulakakis KA, Roubelakis-Angelakis KA, Kanellis AK (1994) Regulation of glutamate dehydrogenase and glutamine synthetase in avocado fruit during development and ripening. Plant Physiol 106:217–222
  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the folin phenol reagent. J Biol Chem 193:265–275
  • Masclaux-Daubresse C, Reisdorf-Cren M, Pageau K, Lelandias M, Grandjean J, Valadier MH, Feraud M, Jouglet T, Suzuki A (2006) Glutamine synthetase-glutamate synthase pathway and glutamate dehydrogenase play distinct roles in the sink source nitrogen cycle in tobacco. Plant Physiol 140:444–456
  • Matsuoka M (2003) Gibberellin signaling: how do plant cells respond to GA signals? J Plant Growth Regul 22:123–125
  • Molins-Legua C, Meseguer-Lloret S, Moliner-Martinez Y, Campíns-Falcó P (2006) A guide for selecting the most appropriate method for ammonium determination in water analysis. Trends Anal Chem 25:282–290
  • Mori IC, Schroeder JI (2004) Reactive oxygen species activation of plant Ca²⁺ channels. a signaling mechanism in polar growth, hormone transduction, stress signaling and hypothetically mechanotransduction. Plant Physiol 135:702–708
  • 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 CH (1998) Ascorbate and glutathione: keeping active oxygen under control. Annu Rev Plant Physiol Plant Mol Biol 49:249–279
  • Nouairi I, Ammar WB, Youssef NB, Miled DDB, Ghorbal MB, Zarrouk M (2009) Antioxidant defense system in leaves of Indian mustard (Brassica juncea) and rape (Brassica napus) under cadmium stress. Acta Physiol Plant 31:237–247
  • Ogawa K, Soutome R, Hiroyama K, Hagio T, Ida S, Nakagawa H (2000) Co-regulation of nitrate reductase and nitrite reductase in cultured spinach cells. J Plant Physiol 157:299–306
  • Panda SK (2007) Chromium-mediated oxidative stress and ultrastructural changes in root cells of developing rice seedlings. J Plant Physiol 164:1419–1428
  • Pandey V, Dixit V, Shyam R (2009a) Chromium (VI) induced changes in growth and root plasma membrane redox activities in pea plants. Protoplasma 235:49–55
  • Pandey V, Dixit V, Shyam R (2009b) Chromium effect on ROS generation and detoxification in pea (Pisum sativum) leaf chloroplasts. Protoplasma 236:85–95
  • Romero-Puertas M, Palma JM, Gómez M, del Río LA (2002) Cadmium causes the oxidative modification of proteins in pea plants. Plant Cell Environ 25:677–686
  • Salin ML (1988) Toxic oxygen species and protective systems of the chloroplast. Physiol Plant 72:681–689
  • 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
  • Schaedle M, Bassham JA (1977) Chloroplast glutathione reductase. Plant Physiol 59:1011–1012
  • Scheller HV, Huang B, Hatch E, Goldsbrough PB (1987) Phytochelatin synthesis and glutathione levels in response to heavy metals in tomato cells. Plant Physiol 85:1031–1035
  • Schiavon M, Pilon-Smits EAH, Wirtz M, Hell R, Malagoli M (2008) Interaction between chromium and sulfur metabolism in Brassica juncea. J Environ Qual 37:1536–1545
  • Shan C, Liang Z (2010) Jasmonic acid regulates ascorbate and glutathione metabolism in Agropyron cristatum leaves under water stress. Plant Sci 178:130–139
  • Shanker AK, Djanaguiraman M, Sudhagar R, Chandrashekar CN, Pathmanabhan G (2004) Differential antioxidative response of ascorbate glutathione pathway enzymes and metabolites to chromium speciation stress in green gram (Vigna radiata (L.) R. Wilczek. Cv CO 4) roots. Plant Sci 166:1035–1043
  • Sharma P, Dubey RS (2005) Modulation of nitrate reductase activity in rice seedlings under aluminium toxicity and water stress: role of osmolytes as enzyme protectant. J Plant Physiol 162:854–864
  • Shen Z, Shen Q, Liang Y, Liu Y (1994) Effect of nitrogen on the growth and photosynthetic activity of salt-stressed barley. J Plant Nutr 17:787–789
  • Singh RP, Srivastava HS (1983) Regulation of glutamate dehydrogenase activity by amino acids in maize seedlings. Physiol Plant 57:549–554
  • Singh RP, Srivastava HS (1986) Increase in glutamate synthase (NADH) activity in maize seedlings in response to nitrate and ammonium nitrogen. Physiol Plant 66:413–416
  • Skopelitis DS, Paranychianakis NV, Paschalidis KA (2006) Abiotic stress generates ROS that signal expression of anionic glutamate dehydrogenases to form glutamate for proline synthesis in tobacco and grapevine. Plant Cell 18:2767–2781
  • Solomonson LP, Barber MJ (1990) Assimilatory nitrate reductase; functional properties and regulation. Annu Rev Plant Physiol Plant Mol Biol 41:225–253
  • Srivastava HS, Singh RP (1987) Role and regulation of L-glutamate dehydrogenase during defence response in maize. Phytochemistry 26:597–610
  • Syntichaki KM, Loulakakis KA, Roubelaki-Angelakis KA (1996) The amino acid sequence similarity of plant glutamate dehydrogenase to the extremophilic archaeal enzyme conforms to its stressrelated function. Gene 168:87–92
  • Tuna AL, Kaya C, Dikilitas M, Higgs D (2008) The combined effects of gibberellic acid and salinity on some antioxidant enzyme activities, plant growth parameters and nutritional status in maize plants. Environ Exp Bot 62:1–9
  • Vazques MD, Poschenrieder C, Barcelo J (1987) Chromium VI induced structural and ultrastructural changes in bush bean plants (Phaseolus vulgaris L.). Ann Bot (Lond) 59:427–438
  • Vernay P, Gauthier-Moussard C, Hitmi A (2007) Interaction of bioaccumulation of heavy metal chromium with water relation, mineral nutrition and photosynthesis in developed leaves of Lolium perenne L. Chemosphere 68:1563–1575
  • Wallace A, Soufi SM, Cha JW, Romney EM (1976) Some effects of chromium toxicity on bush bean plants grown in soil. Plant Soil 44:471–473
  • Wen F, Zhang Z, Bai T, Xu Q, Pan Y (2010) Proteomics reveals the effects of gibberellic acid (GA₃) on salt-stressed rice (Oryza sativa L.) shoots. Plant Sci 178:170–175

Uwagi

PL
Rekord w opracowaniu

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-e48452d6-02d2-4b40-a550-8e8e85e2341e
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.