PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2011 | 33 | 1 |

Tytuł artykułu

The responses of the enzymes related with ascorbate–glutathione cycle during drought stress in apple leaves

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
To explore the significance of the ascorbate–glutathione cycle under drought stress, the leaves of 2-yearold potted apple (Malus domestica Borkh.) plants were used to investigate the changes of each component of the ascorbate–glutathione cycle as well as the gene expression of dehydroascorbate reductase (DHAR, EC 1.8.5.1), ascorbate peroxidase (APX, EC 1.11.1.11) and glutathione reductase (GR, EC 1.6.4.2) under drought stress. The results showed that the malondialdehyde (MDA) and H₂O₂ concentrations in apple leaves increased during drought stress and began to decrease after re-watering. The contents of total ascorbate, reduced ascorbic acid (AsA), total glutathione and glutathione (GSH) were obviously upregulated in apple leaves when the soil water content was 40–45%. With further increase of the drought level, the contents of the antioxidants and especially redox state of AsA and GSH declined. However, levels of them increased again after re-watering. Moreover, drought stress induced significant increase of the activities of enzymes such as APX, scavenging H₂O₂, and also of monodehydroascorbate reductase (MDHAR, EC 1.6.5.4), DHAR and GR used to regenerate AsA and GSH, especially when the soil water content was above 40–45%. During severe drought stress, activities of the enzymes were decreased and after rewatering increased again. Gene expression of cytoplasmic DHAR, cytoplasmic APX and cytoplasmic GR showed similar changes as the enzyme activities, respectively. The results suggest that the ascorbate–glutathione cycle is upregulated in response to drought stress, but cannot be regulated at severe drought stress conditions.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

33

Numer

1

Opis fizyczny

p.173-180,fig.,ref.

Twórcy

autor
  • College of Horticulture, Northwest A and F University, Yangling 712100, Shaanxi, China
  • Guizhou Horticulture Institute, Guiyang 550006, Guizhou, China
autor
  • College of Horticulture, Northwest A and F University, Yangling 712100, Shaanxi, China
autor
  • Guizhou Institute of Environmental Science and Desiging, Guiyang 550002, Guizhou, China
autor
  • College of Horticulture, Northwest A and F University, Yangling 712100, Shaanxi, China

Bibliografia

  • Almeselmani M, Deshmukh PS, Sairam RK, Kushwaha SR, Singh TP (2006) Protective role of antioxidant enzymes under drought stress. Plant Sci 171:382–388
  • Apel K, Hirt H (2004) Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu Rev Plant Biol 55:373–399
  • Baeka K-H, Skinner DZ (2003) Alteration of antioxidant enzyme gene expression during cold acclimation of near-isogenic wheat lines. Plant Sci 165:1221–1227
  • Buchanan BB, Balmer Y (2005) Redox regulation: a broadening horizon. Annu Rev Plant Biol 56:187–220
  • Chirgwin JM, Przybyla AE, Macdonald RJ, Rutter WJ (1979) Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry 18:5294–5299
  • Conklin PI (2001) Recent advances in the role and biosynthesis of ascorbic acid in plants. Plant Cell Environ 24:383–394
  • Dalton DA, Russell SA, Hanus FJ, Pascoe GA, Evans HJ (1986) Enzymatic reactions of ascorbate and glutathione that prevent peroxide damage in soybean root nodules. Proc Natl Acad Sci USA 83:3811–3815
  • Dat JF, Foyer CH, Scott IM (1998) Changes in salicylic acid and antioxidants during induced thermotolerance in mustard seedlings. Plant Physiol 118:1455–1461
  • Davey MW, Van MM, Sanmatin M, Kanellis A, Smirnoff N, Benzie IJJ, Strain JJ, Favell D, Fletcher J (2000) Plant L-ascorbic acid: chemistry, function, metabolism, bioavailability and effects of processing. J Sci Food Agric 80:825–860
  • Grace SC, Logan BA (1996) Acclimation of foliar antioxidant systems to growth irradiance in three broad-leaved evergreen species. Plant Physiol 112:1631–1640
  • Griffith OW (1980) Determination of glutathione and glutathione disulfide using glutathione reductase and 2-vinylpyridine. Anal Biochem 106:207–212
  • Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198
  • Hodges DM, Andrews CJ, Johnson DA, Hamilton RI (1996) Antioxidant compound responses to chilling stress in differentially sensitive inbred maize lines. Physiol Plantarum 98:685–692
  • Horemans N, Foyer CH, Potters G, Asard H (2000) Ascorbate function and associated transport systems in plants. Plant Physiol Biochem 38:531–540
  • Hsiao CT (1973) Plant responses to water stress. Annu Rev Plant Physiol Plant Mol Biol 24:519–570
  • Kawasaki S, Borchert C, Deyholos M, Wang H, Brazille S, Kawai K, Galbraith D, Bohnert HJ (2001) Gene expression profiles during the initial phase of salt stress in rice. Plant Cell 13:889–905
  • Khanna-Chopra R, Selote DS (2007) Acclimation to drought stress generates oxidative stress tolerance in drought-resistant than-susceptible wheat cultivar under field conditions droughtresistant than -susceptible wheat cultivar under field conditions. Environ Exp Bot 60:276–283
  • Kocsy G, Galiba G, Brunold C (2001) Role of glutathione in adaptation and signaling during chilling and cold acclimation in plants. Plant Physiol 113:158–164
  • Law MY, Charles SA, Halliwell B (1983) Glutathione and ascorbic acid in spinach (Spinacia oleracea) chloroplasts: the effect of hydrogen peroxide and of paraquat. Biochem J 210:899–903
  • Lawlor DW (2002) Limitation to photosynthesis in water stressed leaves: stomata vs. metabolism and the role of ATP. Ann Bot 89:1–15
  • Li HH, Sun Q, Zhao SJ (2000) The principle and technology of plant physiological biochemical experiment. Higher Education Press, Beijing
  • Ma FW, Cheng LL (2003) The sun-exposed peel of apple fruit has higher xanthophyll cycle-dependent thermal dissipation and antioxidants of the ascorbate–glutathione pathway than the shade peel. Plant Sci 165:819–827
  • Ma FW, Cheng LL (2004) Exposure of the shaded side of apple fruit to full sun leads to upregulation of both xanthophyll cycle and the ascorbate–glutathione cycle. Plant Sci 166:1479–1486
  • Mano J (2002) Early events in environmental stresses in plantsinduction mechanisms of oxidative stress. In: Inze D, Montago MV (eds) Oxidative stress in plants. Taylor and Francis Publishers, New York, pp 217–245
  • Meyer AJ (2007) The integration of glutathione homeostasis and redox signaling. J Plant Physiol 31:1–14
  • Miyake C, Asada K (1992) Thylakoid-bound ascorbate peroxidase in spinach chloroplasts and photoreduction of its primary oxidation product monodehydroascorbate radicals in thylakoids. Plant Cell Physiol 33:541–553
  • Moller IM, Jensen PE, Hansson A (2007) Oxidative modifications to cellular components in plants. Annu Rev Plant Biol 58:459–481
  • Munne-Bosch S, Alegre L (2003) Drought-induced changes in the redox state of a-tocopherol, ascorbate and the diterpene cornosic acid in chloroplasts of Labiatae species differing in carnosic acid contents. Plant Physiol 131:1816–1825
  • Nakano Y, Asada K (1981) Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol 22:867–880
  • Nishikawa F, Kato M, Hyodo H, Ikoma Y, Sugiura M, Yano M (2003) Ascorbate metabolism in harvested broccoli. J Exp Bot 54:2439–2448
  • Noctor G, Foyer CH (1998) Ascorbate and glutathione: keeping active oxygen under control. Annu Rev Plant Physiol Plant Mol Biol 49:249–279
  • Patterson BD, Mackae EA, Ferguson IB (1984) Estimation of hydrogen peroxide in plant extracts using titanium (IV). Anal Biochem 139:487–492
  • Ramachandra RA, Chaitanya KV, Vivekanandan M (2004) Droughtinduced responses of photosynthesis and antioxidant metabolism in higher plants. J Plant Physiol 161:1189–1202
  • Ratnayaka H, Molin WT, Sterling TM (2003) Physiological and antioxidant responses of cotton and spurred anoda under interference and mild drought. J Exp Bot 54:2293–2305
  • Sairam RK, Tyagi A (2004) Physiology and molecular biology of salinity stress tolerance in plants. Curr Sci 86:407–421
  • Sgherri CLM, Loggini B, Bochicchio A, Navari-Izzo F (1994) Antioxidant system in Boea hygroscopica: changes in response to desiccation and rehydration. Phytochemistry 37:377–381
  • Shi SG, Liang D, Ma FW, Zhang JK (2007) Cloning and analysis of glutathione reductase cDNA from apple. Acta Agric Borealioccidentalis Sinica 16:97–101
  • Sofo A, Tuzio AC, Dichio B, Xiloyannis C (2005) Influence of water deficit and rewatering on the components of the ascorbate–glutathione cycle in four interspecific Prunus hybrids ascorbate–glutathione cycle in four interspecific Prunus hybrids. Plant Sci 169:403–412
  • Torres-Franklin ML, Contour-Ansel D, Zuily-Fodil Y, Pham-Thi A-T (2008) Molecular cloning of glutathione reductase cDNAs and analysis of GR gene expression in cowpea and common bean leaves during recovery from moderate drought stress. J Plant Physiol 165:514–521
  • Tsai YC, Hong CY, Liu LF, Kao CH (2005) Expression of ascorbate peroxidase and glutathione reductase in roots of rice seedlings in response to NaCl and H₂O₂. J Plant Physiol 162:291–299

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-1acc90e7-fc5c-4714-9467-d52080249eff
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.