Skip to main content
Log in

The involvement of hydrogen peroxide in abscisic acid-induced activities of ascorbate peroxidase and glutathione reductase in rice roots

  • Published:
Plant Growth Regulation Aims and scope Submit manuscript

Abstract

We have monitored the changes in antioxidant enzyme activities and H2O2 concentrations in roots of rice (Oryza sativa L., cv. Taichung Native 1) seedlings treated with exogenous abscisic acid(ABA). Decrease in superoxide dismutase (SOD) and catalase (CAT) activities was observed in rice roots in the presence of ABA. However, ascorbate peroxide (APX) and glutathione reductase (GR) activities were increased after the ABA treatment. ABA treatment resulted in an increase in H2O2 concentrations in rice roots. Pre-treatment with dimethylthiourea, a chemical trap for H2O2, and diphenyleneiodonium chloride (DPI), a well known inhibitor of NADPH oxidase, inhibited ABA-induced accumulation of H2O2 and ABA-induced activities of APX and GR. ABA-induced accumulation of H2O2 was found to be prior to ABA-induced activities of APX and GR. Our results suggest that H2O2 is involved in ABA-induced APX and GR activities in rice roots.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Anderson M.D., Prasad T.K., Martin B.A.and Stewart C.R. 1994.differential gene expression in chilling-acclimated maize seedlings and evidence for the involvement of abscisic acid in chilling tolerance.Plant Physiol.105:331–339.

    Google Scholar 

  • Bolwell G.P., Davies D.R., Gerrish C., Auh C.K.and Murphy T.M.1998.Comparative biochemistry of the oxidative burst produced by rose and French bean cells reveals two distinct mechanisms.Plant Physiol.116:1374–1385.

    Google Scholar 

  • Bueno P., Piqueras A., Kurepa J., SavouréA., Verbruggen N. and Van Montagu M.and Inzé D.1998.Expression of antioxidant enzymes in response to abscisic acid and high osmoticum in tobacco BY-2 cell cultures.Plant Sci.138:27–34.

    Google Scholar 

  • Casano L.M., Martin M.and Sabater B.2001.Hydrogen peroxide mediates the induction of the chloroplastic Ndh complex under photooxidative stress in barley.Plant Physiol. 125:1450–1458.

    Google Scholar 

  • Creelman R.A.1989.Abscisic acid physiology and biosynthesis in higher plants.Physiol.Plant.75:131–136.

    Google Scholar 

  • Foster J.S.and Hess J.L.1980.Responses of superoxide dismutase and glutathione reductase activities in cotton leaf tissue exposed to an atmosphere enriched in oxygen.Plant Physiol.66:482–487.

    Google Scholar 

  • Foyer C.H., Lopez-Delgado H., Dat J.F.and Scott I.M.1997. Hydrogen peroxide-and glutathione-associated mechanisms of acclimatory stress tolerance and signalling.Physiol.Plant. 100:241–254.

    Google Scholar 

  • Gong M., Li Y.J.and Chen S.Z.1998.Abscisic acid-induced the tolerance in maize seedlings is mediated by calcium and associated with antioxidant systems.J.Plant Physiol.153: 488–496.

    Google Scholar 

  • Guan L., Zhao J.and Scandalios J.G.2000.Cis-elements and transfactors that regulate expression of the maize Cat1 antioxidant gene in response to ABA and osmotic stress: H2 O2 is the likely intermediary signaling molecule for the response.Plant J.22:87–95.

    Google Scholar 

  • Hung K.T.and Kao C.H.2003.Nitric oxide counteracts the senescence of rice leaves induced by abscisic acid.J.Plant Physiol.160:871–879.

    Google Scholar 

  • Jana S.and Choudhuri M.1981.Glycolate metabolism of three submerged aquatic angiosperms during aging.Aquat.Bot. 12:345–354.

    Google Scholar 

  • Jiang M.and Zhang J.2001.Effect of abscisic acid on active oxygen species,antioxidative defence system and oxidative damage in leaves of maize seedlings.Plant Cell Physiol.42: 1265–1273.

    Google Scholar 

  • Jiang M.and Zhang J.2002.Water stress-induced abscisic acid accumulation triggers the increased generation of reactive oxygen species and up-regulates the activites of antioxidant enzymes in maize leaves.J.Exp.Bot.53:2401–2410.

    Google Scholar 

  • Jiang M.and Zhang J.2003.Cross-talk between calcium and reactive oxygen species originated from NADPH oxidase in abscisic acid-induced antioxidant defence in leaves of maize seedlings.Plant Cell Environ.26:929–939.

    Google Scholar 

  • Kato M.and Shimizu S.1987.Chlorophyll metabolism in higher plants.VII.Chlorophyll degradation in senescing tobacco leaves:phenol-dependent peroxidative degradation. Can.J.Bot.65:729–735.

    Google Scholar 

  • Kende H.and Zeevaart A.D.1997.The ve classical plant hormones.Plant Cell 9:1197–1210.

    Google Scholar 

  • Levine A., Tenhaken R., Dixon R.and Lamb C.1994.H2 O2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response.Cell 79:583–593.

    Google Scholar 

  • Lin C.C.and Kao C.H.2001.Abscisic acid induced changes in cell wall peroxidase activity and hydrogen peroxide level in roots of rice seedlings.Plant Sci.160:323–329.

    Google Scholar 

  • Nakano Y.and Asada K.1981.Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts.Plant Cell Physiol.22:867–880.

    Google Scholar 

  • Neill S., Desikan R.and Hancock J.2002.Hydrogen peroxide signaling.Curr.Opin.Plant Biol.5:386–395.

    Google Scholar 

  • Orozco-Cárdenas M.L., Navaez-Vésquez J.and Ryan C.A. 2001.Hydrogen peroxide acts as a second messenger for the induction of genes in tomato plants in response to wounding, systemin,and methyl jasmonate.Plant Cell 13:179–191.

    Google Scholar 

  • Papadakis A.K.and Roubelakis-Angelakis K.A.1999.The generation of active oxygen species differs in tobacco and grapevine mesophyll protoplasts.Plant Physiol.121:197 205.

    Google Scholar 

  • Paoletti F., Aldinucci D., Mocali A.and Capparini A.1986.A sensitive spectrophotometric method for the determination of superoxide dismutase activity in tissue extracts.Anal.Biochem.154:536–541.

    Google Scholar 

  • Pei Z.M., Murata Y., Benning G., Thomine S., Klusener B., Allen G.J., Grill E.and Schroeder J.I.2000.Calcium channels activated by hydrogen peroxide mediated abscisic acid signaling in guard cells.Nature 406:731–734.

    Google Scholar 

  • Rao M.V., Paliyath G., Ormrod D.P., Murr D.P.and Watkins C.B.1997.In.uence of salicylic acid on H2 O2 production, oxidative stress,and H2 O2-metabolizing enzymes.Salicylic acid-mediated oxidative damage requires H2 O2.Plant Physiol.115:137–149.

    Google Scholar 

  • Schopfer P., Plachy C.and Frahry G.2001.Release of reactive oxygen intermediates (superoxide radicals,hydrogen peroxide,and hydroxyl radicals)and peroxidase in germinating radish seeds controlled by light,gibberellin and abscisic acid. Plant Physiol.125:1591–1602.

    Google Scholar 

  • Seo M.and Koshiba T.2002.Complex regulation of ABA biosynthesis.Trends Plant Sci.7:41–48.

    Google Scholar 

  • Zhang X., Zhang L., Dong F., Gao J., Galbraith D.W.and Song C.-P.2001.Hydrogen peroxide is involved in abscisic acid-induced stomatal closure in Vicia faba.Plant Physiol. 126:1438–1448.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tsai, YC., Kao, C.H. The involvement of hydrogen peroxide in abscisic acid-induced activities of ascorbate peroxidase and glutathione reductase in rice roots. Plant Growth Regulation 43, 207–212 (2004). https://doi.org/10.1023/B:GROW.0000046001.24746.df

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/B:GROW.0000046001.24746.df

Navigation