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2013 | 35 | 08 |

Tytuł artykułu

Glutathione regulates enzymatic antioxidant defence with differential thiol content in perennial pepperweed and helps adapting to extreme environment

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Perennial pepperweed (Lepidium latifolium Linn.) is a preferred ‘phytofood’ that is available for the longest period of a year in Ladakh. Present study was undertaken to identify the mechanism of redox homeostasis and understand factors responsible for its biochemical superiority during low temperatures. Results reveal that despite the stressful environment at higher altitude, the cellular conditions are more reducing for this plant. The reducing environment is maintained by significant induction of GSH rather than changes in its oxidation state, which changes the redox potential by 12 mV. Lower ratio of NADP+/NADPH and induction of new antioxidative isozymes at Leh (3,505 m) suggest crucial role of redox regulation in adaptation. These new proteins have higher thiol content and could provide an efficient redox sensing mechanism in Lepidium latifolium that respond through GSH/NADPH redox buffers. In vitro feeding experiment suggested that GSH plays an important role in induction of antioxidant enzymes, which may not be the direct consequence of H2O2 accumulation. It needs to be further investigated whether its responsive redox metabolism has some role in its invasive growth in riparian plains of America.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

35

Numer

08

Opis fizyczny

p.2501-2511,fig.,ref.

Twórcy

autor
  • Academy of Scientific and Innovative Research, Indian Institute of Integrative Medicine (CSIR), Canal Road, Jammu, Jammu and Kashmir 180001, India
  • Biodiversity and Applied Botany Division, Indian Institute of Integrative Medicine (CSIR), Canal Road, Jammu, Jammu and Kashmir 180001, India
autor
  • Biodiversity and Applied Botany Division, Indian Institute of Integrative Medicine (CSIR), Canal Road, Jammu, Jammu and Kashmir 180001, India
autor
  • Biodiversity and Applied Botany Division, Indian Institute of Integrative Medicine (CSIR), Canal Road, Jammu, Jammu and Kashmir 180001, India
autor
  • Biodiversity and Applied Botany Division, Indian Institute of Integrative Medicine (CSIR), Canal Road, Jammu, Jammu and Kashmir 180001, India
autor
  • Academy of Scientific and Innovative Research, Indian Institute of Integrative Medicine (CSIR), Canal Road, Jammu, Jammu and Kashmir 180001, India
  • Biodiversity and Applied Botany Division, Indian Institute of Integrative Medicine (CSIR), Canal Road, Jammu, Jammu and Kashmir 180001, India

Bibliografia

  • Abrol E, Vyas D, Koul S (2012) Metabolic shift from secondary metabolite production to induction of anti-oxidative enzymes during NaCl stress in Swertia chirata Buch-Ham. Acta Physiol Plant 34:541–546
  • Anderson MD, Prasad TK, Stewart CR (1995) Changes in isozyme profiles of catalase, peroxidase, and glutathione reductase during acclimation to chilling in mesocotyls of maize seedlings. Plant Physiol 109:1247–1257
  • Aravind P, Prasad MN (2005) Modulation of cadmium-induced oxidative stress in Ceratophyllum demersum by zinc involves ascorbate-glutathione cycle and glutathione metabolism. Plant Physiol Biochem 43:107–116
  • Aslam M, Sinha VB, Singh RK, Anandhan S, Ahmed Z, Pande V (2010) Isolation of cold stress-responsive genes from Lepidium latifolium by suppressive subtraction hybridization. Acta Physiol Plant 32:205–210
  • Bartoli CG, Tambussi EA, Diego F, Foyer CH (2009) Control of ascorbic acid synthesis and accumulation and glutathione by the incident light red/far red ratio in Phaseolus vulgaris leaves. FEBS Lett 583:118–122
  • Buchanan BB, Balmer Y (2005) Redox regulation: a broadening horizon. Ann Rev Plant Bio 56:187–220
  • Chen H, Qualls RG, Miller GC (2002) Adaptive responses of Lepidium latifolium to soil flooding: biomass allocation, adventitious rooting, aerenchyma formation and ethylene production. Environ Exp Bot 48:119–128
  • Chronopoulou E, Madesis P, Asimakopoulou B, Dimitrios P, Tsaftaris A, Labrou NE (2012) Catalytic and structural diversity of the fluazifop-inducible glutathione transferases from Phaseolus vulgaris. Planta 235(6):1253–1269
  • Colville L, Smirnoff N (2008) Antioxidant status, peroxidase activity, and PR protein transcript levels in ascorbate-deficient Arabidopsis thaliana vtc mutants. J Exp Bot 59:3857–3868
  • Eskling M, Arvidsson PO, Akerlund H-K (1997) The xanthophyll cycle, its regulation and components. Physiol Plant 100:806–816
  • Fendt SM, Buescher JM, Rudroff F, Picotti P, Zamboni N, Sauer U (2010) Trade off between enzyme and metabolite efficiency maintains metabolic homeostasis upon perturbations in enzyme capacity. Mol Sys Biol 6:356
  • Foyer CH, Noctor G (2009) Redox regulation in photosynthetic organisms: signaling, acclimation, and practical implications. Antioxid Redox Signal 11:861–905
  • Foyer CH, Noctor G (2011) Ascorbate and glutathione: the heart of the redox hub. Plant Physiol 155:2–18
  • Golding AJ, Finazzi G, Johnson GN (2004) Reduction of the thylakoid electron transport chain by stromal reductants: evidence for activation of cyclic electron transport upon dark adaptation or under drought. Planta 220:356–363
  • Gomez LD, Noctor G, Knight M, Foyer CH (2004) Regulation of calcium signaling and gene expression by glutathione. J Exp Bot 55:1851–1859
  • Grace SC, Logan BA (1996) Acclimation of foliar antioxidant systems to growth irradiance in three broad-leaved evergreen species. Plant Physiol 112:1631–1640
  • Guleria S, Tiku AK, Singh G, Vyas D, Bhardwaj A (2011) Antioxidant activity and protective effect against plasmid DNA strand scission of leaf, bark, and Heartwood Extracts from Acacia catechu. J Food Sci 76:959–964
  • Hancock JT, Desikan R, Neill SJ, Cross AR (2004) New equations for redox and nano-signal transduction. J Theor Biol 226(1):65–68
  • Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 12:189–198
  • Hultén E, Fries M (eds) (1986) Atlas of North European vascular plants, part I-III, maps and commentaries. Koeltz Scientific books, Germany
  • Jubany-Mari T, Alegre-Batlle L, Jiang K, Feldman LJ (2010) Use of a redox-sensitive GFP (c-roGFP1) for real-time monitoring of cytosol redox status in Arabidopsis thaliana water-stressed plants. FEBS Lett 584:889–897
  • Karpinski S, Escobar C, Karpinska B, Creissen G, Mullineaux PM (1997) Photosynthetic electron transport regulate the expression of cytosolic ascorbate peroxidase genes in Arabidopsis during excess light stress. Plant Cell 9:627–640
  • Kornas A, Kuźniak E, Slesak I, Miszalski Z (2010) The key role of the redox status in regulation of metabolism in photosynthesizing organisms. Acta Biochem Pol 57:143–151
  • Kramer DM, Evans JR (2011) The importance of energy balance in improving photosynthetic productivity. Plant Physiol 155:70–78
  • Kranner I, Birtić S, Anderson KM, Pritchard HW (2006) Glutathione half-cell reduction potential: a universal stress marker and modulator of programmed cell death? Free Rad Biol Med 40:2155–2165
  • Levitt J (1962) A sulphydryl-disulfide hypothesis of frost injury and resistance in plants. J Theor Biol 3:355–391
  • Lowry OH, Rosebrough NJ, Farr AL, Randall RL (1951) Protein measurement with the folin-phenol reagent. J Biol Chem 193:265–275
  • Mehler AH (1951) Studies on reactions of illuminated chloroplasts I mechanisms of the reduction of oxygen and other hill reagents. Arch Biochem Biophys 33:65–77
  • Mhamdi A, Hager J, Chaouch S, Queval G, Han Y, Taconnat L, Saindrenan P, Gouia H, Isaakidis-Bourguet E, Renou J-P, Noctor G (2010) Arabidopsis glutathione reductase I plays a crucial role in leaf responses to intracellular hydrogen peroxide and in ensuring appropriate gene expression through both salicylic and jasmonic acid signalling pathways. Plant Physiol 153(1144):1160
  • Muller P, Li XP, Niyogi KK (2001) Non-photochemical quenching: a response to excess light energy. Plant Physiol 125:1558–1566
  • Munekage Y, Hashimoto M, Miyake C, Tomizawa K, Endo T, Tasaka M, Shikanai T (2004) Cyclic electron flow around photosystem I is essential for photosynthesis. Nature 429:579–582
  • Nakano Y, Asada K (1981) Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol 22:867–880
  • Navarro E, Alonso J, Rodriguez R, Trujillo J, Boada J (1994) Diuretic action of an aqueous extract of Lepidium latifolium L. J Ethnopharmacol 41:65–69
  • Noctor G (2006) Metabolic signalling in defence and stress: the central roles of soluble redox couples. Plant Cell Environ 29:409–425
  • Noctor G, Foyer CH (1998) Ascorbate and glutathione: keeping active oxygen under control. Ann Rev Plant Physiol Plant Mol Biol 49:249–279
  • Noctor G, Mhamdi A, Chaouchi S, Han Y, Neukermans J, Marquez–Garcia B, Queval G, Foyer CH (2012) Glutathione in plants: an integrated overview. Plant Cell Environ 35:454–484
  • Pal Murugan M, Raj J, Kumar PG, Gupta S, Singh SB (2010) Phytofoods of Nubra valley, Ladakh-The cold desert. Indian J Trad Knowl 9(2):303–308
  • Pimentel D, Lach L, Zuniga R, Morrison D (2000) Environmental and economic costs of non indigenous species in the United States. BioScience 50:53–65
  • Queval G, Noctor G (2007) A plate reader method for the measurement of NAD, NADP, glutathione, and ascorbate in tissue extracts: application to redox profiling during Arabidopsis rosette development. Anal Biochem 363:58–69
  • Rajagopal S, Bukhov NG, Tajmir-Riahi H, Carpentier R (2003) Control of energy dissipation and photochemical activity in photosystem I by NADP-dependent reversible conformational changes. Biochemistry 42:11839–11845
  • Rao MV, Hale BA, Ormrod DP (1995) Amelioration of Ozonelnduced oxidative damage in wheat plants grown under high carbon dioxide role of antioxidant enzymes. Plant Physiol 109:421–432
  • Rollins RC (1993) The Cruciferae of Continental North America. Stanford University Press, Stanford
  • Sawhney SK, Singh R (eds) (2009) Introductory practical biochemistry, 2nd edn. Narosa Publishing House, New Delhi
  • Schafer FQ, Buettner GR (2001) Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple. Free Rad Biol Med 30(11):1191–1212
  • Scheibe R, Backhausen JE, Emmerlich V, Simone H (2005) Strategies to maintain redox homeostasis during photosynthesis under changing conditions. J Exp Bot 56:1481–1489
  • Schultze-Motel W (ed) ((1986)) Lepidium latifolium. Illustrierte Flora von Mittel-europa, 3rd edn. Verlag Paul Parey, Berlin
  • Smirnoff N (2000) Ascorbate biosynthesis and function in photoprotection. Royal Soc 355:1455–1464
  • Smith IK, Vierheller TL, Thorne CA (1988) Assay of glutathione reductase in crude tissue homogenates using 5, 50-dithiobis( 2nitrobenzoic acid). Anal Biochem 175:408–413
  • Snedecor GW, Cochran WG (1989) Statistical methods, 8th edn. Iowa State University Press, Ames
  • Sonnentag O, Detto M, Runkle BRK, Teh YA, Silver WL, Kelly M, Baldocchi DD (2011) Carbon dioxide exchange of a pepperweed (Lepidium latifolium L.) infestation: How do flowering and mowing affect canopy photosynthesis and autotrophic respiration? J Geophys Res 116:G01021. doi:10.1029/2010JG001522
  • Tabassum N, Ahmad F (2011) Role of natural herbs in the treatment of hypertension. Pharmacogn 9:30–34
  • Tietze F (1969) Enzymic method for quantitative determination of nanogram amounts of total and oxidized glutathione: applications to mammalian blood and other tissues. Anal Biochem 27:502–522
  • Vyas D, Kumar S (2005a) Purification and partial characterization of a low temperature responsive Mn-SOD from tea (Camellia sinensis(L.) O. Kuntze.). Biochem Biophys Res Comm 329:831–838
  • Vyas D, Kumar S (2005b) Tea (Camellia sinensis (L.) O. Kuntze) clone with lower period of winter dormancy exhibits lesser cellular damage in response to low temperature. Plant Physio Biochem 43:383–388
  • Woodbury W, Spencer AK, Stahman MA (1971) An improved procedure using ferricyanide for detecting catalase isozymes. Anal Biochem 44:301–305
  • Yabuta Y, Mieda T, Rapolu M, Nakamura A, Motoki T, Maruta T, Yoshimura K, Ishikawa T, Shigeoka S (2007) Light regulation of ascorbate biosynthesis is dependent on the photosynthetic electron transport chain but independent of sugars in Arabidopsis. J Exp Bot 58:2661–2671
  • Young JA, Turner CE, James LF (1995) Perennial pepperweed. Rangelands 17:121–123

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Bibliografia

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