Abstract
Original language | English |
---|---|
Pages (from-to) | 224-231 |
Number of pages | 7 |
Journal | Environmental and Experimental Botany |
Volume | 63 |
Issue number | 1-3 |
DOIs | |
Publication status | Published - May 2008 |
Keywords
- Antioxidants
- Catalase
- Ion homeostasis
- K+/Na+ ratio
- Photosynthesis
- Salt tolerance
Fingerprint
Dive into the research topics of 'Exogenously applied ascorbic acid alleviates salt-induced oxidative stress in wheat'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver
}
In: Environmental and Experimental Botany, Vol. 63, No. 1-3, 05.2008, p. 224-231.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Exogenously applied ascorbic acid alleviates salt-induced oxidative stress in wheat
AU - Athar, Habib ur Rehman
AU - Khan, Ameer
AU - Ashraf, Muhammad
N1 - 00988472 (ISSN) Cited By (since 1996): 24 Export Date: 27 March 2012 Source: Scopus CODEN: EEBOD doi: 10.1016/j.envexpbot.2007.10.018 Language of Original Document: English Correspondence Address: Ashraf, M.; Department of Botany, University of Agriculture, Faisalabad, 38040, Pakistan; email: [email protected] References: Agarwal, S., Sairam, K.R., Srivastava, G.C., Aruna, T., Meena, C.R., Role of ABA, salicylic acid, calcium and hydrogen peroxide on antioxidant enzymes induction in wheat seed lings (2005) Plant Sci., 169, pp. 559-570; Al-Hakimi, A.M., Hamada, A.M., Counteraction of salinity stress on wheat plants by grain soaking in ascorbic acid, thiamine or sodium salicylate (2001) Biol. Plant., 44, pp. 253-261; Allen, S.E., Grimshaw, H.M., Rowland, A.P., Chemical analysis (1986) Methods in Plant Ecology. second ed., pp. 285-344. , Moore P.D., and Chapman S.B. (Eds), Blackwell Scientific Publications, Oxford; Asada, K., The water-water cycle in chloroplasts: scavenging of active oxygen and dissipation of excess photons (1999) Annu. Rev. Plant Physiol. Plant Mol. Biol., 50, pp. 601-639; Bor, M., Özdemir, F., Türkan, I., The effect of salt stress on lipid peroxidation and antioxidants in leaves of sugar beet (Beta vulgaris L.) and wild beet (Beta maritime L.) (2003) Plant Sci., 164, pp. 77-84; Bradford, M.M., A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding (1976) Ann. Biochem., 72, pp. 248-254; Buettner, G.R., Schafer, F.Q., Ascorbate as an antioxidant in vitamin C (2004) Functions and Biochemistry in Animals and Plants, pp. 173-188. , Asard H., May J.M., and Smirnoff N. (Eds), Bios Scientific Publishers, Oxford; Cabo, R.C., Gonza-lez-Reyes, J.A., Cordoba, F., Navas, P., Rooting hastened in onions by ascorbate and ascorbate free radical (1996) J. Plant Growth Regul., 15, pp. 53-56; Chance, M., Maehly, A.C., Assay of catalases and peroxidases (1955) Methods Enzymol., 2, pp. 764-817; Chen, W.P., Li, P.H., Chilling induced Ca 2+ overload enhances production of active oxygen species in maize (Zea mays L.) cultured cells: the effect of abscisic acid treatment (2001) Plant Cell Environ., 24, pp. 791-800; Chen, Z., Gallie, D.R., The ascorbic acid redox state controls guard cell signaling and stomatal movement (2004) Plant Cell, 16, pp. 1143-1162; Citterio, S., Sgorbati, S., Scippa, S., Sparvoli, E., Ascorbic acid effect on the onset of cell proliferation in pea root (1994) Physiol. Plant., 92, pp. 601-607; Davey, M., Montagu, W.M.V., Inze, D., Sanmartin, M., Kanellis, A., Smirnoff, N., Benzie, I.J.J., Fletcher, J., Plant l-ascorbic acid: chemistry, function, metabolism, bioavailability and effects of processing (2000) J. Sci. Food Agric., 80, pp. 825-860; Dennison, K.L., Robertson, W.R., Lewis, B.D., Hirsch, R.E., Sussman, M.R., Spalding, E.P., Functions of AKT 1 and AKT 2 potassium channels determined by studies of single and double mutants of Arabidopsis (2001) Plant Physiol., 127, pp. 1012-1019; Foyer, C.H., Noctor, G., Redox sensing and signalling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondria (2003) Physiol. Plant., 119, pp. 355-364; Giannopolitis, C.N., Ries, S.K., Superoxide dismutases occurrence in higher plants (1977) Plant Physiol., 59, pp. 309-314; Golldack, D., Quigley, F., Michalowski, C.B., Kamasani, U.R., Bohnert, H.J., Salinity stress-tolerant and sensitive rice (Oryza sativa L.) regulate AKT1-type potassium channel transcripts differently (2003) Plant Mol. Biol., 51, pp. 71-81; Gossett, D.R., Banks, S.W., Millhollon, E.P., Lucas, M.C., Antioxidant response to NaCl stress in a control and a NaCl-tolerant cotton line grown in the presence of paraquat, buthionine sulfoxime and exogenous glutathione (1996) Plant Physiol., 112, pp. 803-809; Gossett, D.R., Millhollon, E.P., Lucas, M.C., Antioxidant response to NaCl stress salt-tolerant and salt-sensitive cultivars of cotton (1994) Crop Sci., 34, pp. 706-714; Hartmann, T.N., Fricker, M.D., Rennenberg, H., Meyer, A.J., Cell specific measurement of cytosolic glutathione in poplar leaves (2003) Plant Cell Environ., 26, pp. 965-975; Iturbe-Ormaetxe, I., Escudero, P.R., Arrese-Igor, C., Becana, M., Oxidative damage in pea plants exposed to water deficit or paraquat (1998) Plant Physiol., 116, pp. 173-181; Loreto, F., Velikova, V., Di Marco, G., Respiration in the light measured by CO 2 emission in CO 2 atmosphere in maize leaves (2001) Aust. J. Plant Physiol., 28, pp. 1103-1108; Mittler, R., Oxidative stress, antioxidants and stress tolerance (2002) Trends Plant Sci., 7, pp. 405-410; Mittova, V., Guy, M., Tal, M., Volokita, M., Response of the cultivated tomato and its wild salt-tolerant relative Lycopersicon pennellii to salt-dependent oxidative stress: increased activities of antioxidant enzymes in root plastids (2002) Free Radical Res., 36, pp. 195-202; Mukherjee, S.P., Choudhuri, M.A., Implication of water stress-induced changes in the levels of endogenous ascorbic acid and hydrogen peroxide in Vigna seedlings (1983) Plant Physiol., 58, pp. 166-170; Müller-Moulé, P., Golan, T., Niyogi, K.K., Ascorbate-deficient mutants of Arabidopsis grow in high light despite chronic photooxidative stress (2004) Plant Physiol., 134, pp. 1163-1172; Müller-Moulé, P., Havaux, M., Niyogi, K.K., Zeaxanthin deficiency enhances the high light sensitivity of an ascorbate-deficient mutant of Arabidopsis (2003) Plant Physiol., 133, pp. 748-760; Noctor, G., Foyer, C.H., Ascorbate and glutathione: keeping active oxygen under control (1998) Annu. Rev. Plant Physiol. Plant Mol. Biol., 49, pp. 249-279; Noctor, G., Veljovic-Jovanovic, S., Driscoll, S., Novitskaya, L., Foyer, C.H., Drought and oxidative load in the leaves of C 3 plants: a predominant role for photorespiration? (2002) Ann. Bot., 89 (7), pp. 841-850; Pardo, J.M., Reddy, M.P., Yang, S., Maggio, A., Huh, G.H., Mutasumoto, T., Coca, M.A., Hasegawa, P.M., Stress signaling through Ca 2+ calmodulin-dependent protein phosphatase calcineurin mediates salt adaptation in plants (1998) Proc. Natl. Acad. Sci. U.S.A., 95, pp. 9681-9686; Pilot, G., Gaymard, F., Mouline, K., Cherel, I., Sentenac, H., Regulated expression of Arabidopsis shaker K + channel genes involved in K + uptake and distribution in the plant (2003) Plant Mol. Biol., 51, pp. 773-787; Raza, S.H., Athar, H.u.R., Ashraf, M., Influence of exogenously applied glycinebetaine on the photosynthetic capacity of two differently adapted wheat cultivars under salt stress (2006) Pak. J. Bot., 38, pp. 341-351; Salama, S., Trivedi, S., Busheva, M., Arafat, A.A., Garab, G., Erdei, L., Effects of NaCl salinity on growth, cation accumulation, chloroplast structure and function in wheat cultivars differing in salt tolerance (1994) J. Plant Physiol., 144, pp. 241-247; Shalata, A., Neumann, P.M., Exogenous ascorbic acid (Vitamin C) increases resistance to salt tolerance and reduced lipid peroxidation (2001) J. Exp. Bot., 364, pp. 2207-2211; Shigeoka, S., Ishikawa, T., Tamoi, M., Miyagawa, Y., Takeda, T., Yabuta, Y., Yoshimura, K., Regulation and function of ascorbate peroxidase isoenzymes (2002) J. Exp. Bot., 53 (372), pp. 1305-1319; Smirnoff, N., Ascorbate biosynthesis and function in photo protection (2000) Biol. Sci., 355, pp. 1455-1465; Smirnoff, N., Ascorbate, tocopherol and carotenoids: metabolism, pathway engineering and functions (2005) Antioxidants and Reactive Oxygen Species in Plants, pp. 53-86. , Smirnoff N. (Ed), Blackwell Publishing Ltd., Oxford, UK; Snedecor, G.W., Cochran, G.W., (1980) Statistical Methods. seventh ed., , The Iowa State University Press, Ames, Iowa; Veljovic-Jovanovic, S.D., Pignocchi, C., Noctor, G., Foyer, C.H., Low ascorbic acid in the vtc-1 mutant of Arabidopsis is associated with decreased growth and intracellular redistribution of the antioxidant system (2001) Plant Physiol., 127, pp. 426-435; Willekens, H., Inze, D., van Montagu, M., van Camp, W., Catalases in plants (1995) Mol. Breed., 1, pp. 207-228
PY - 2008/5
Y1 - 2008/5
N2 - Although ascorbic acid (AsA) is one of the most important and abundantly occurring water soluble antioxidants in plants, relatively little is known about its role in counteracting the adverse effects of salt stress on plant growth. To address this issue that whether exogenous application of ascorbic acid (AsA) through rooting medium could alleviate the adverse effects of salt stress on wheat plants, a hydroponic experiment was conducted under glasshouse conditions using two wheat cultivars, S-24 (salt tolerant) and MH-97 (moderately salt sensitive). Plants of both cultivars were subjected to 0 or 150 mM NaCl solution supplemented with 0, 50, or 150 mg L-1 AsA for 58 days. Imposition of salt stress reduced the growth of both wheat cultivars by causing reduction in photosynthesis, and endogenous AsA level, and enhancing accumulation of Na+ and Cl- coupled with a decrease in K+ and Ca2+ in the leaves and roots of both cultivars thereby decreasing tissue K+/Na+ ratio. However, root applied AsA counteracted the adverse effects of salt stress on the growth of cv. S-24 only, particularly at 100 mg L-1 AsA level. AsA-induced enhancement in growth of salt-stressed plants of S-24 was associated with enhanced endogenous AsA level and CAT activity, and higher photosynthetic capacity, and accumulation of K+ and Ca2+ in the leaves. Although root applied AsA did not improve the growth of salt-stressed plants of MH-97, it enhanced endogenous level of AsA, CAT activity, photosynthetic capacity, and leaf K+ and Ca2+. These findings led us to conclude that root applied AsA counteracts the adverse effects of salt stress on growth of wheat by improving photosynthetic capacity of wheat plants against salt-induced oxidative stress and maintaining ion homeostasis, however, these effects were cultivar specific. © 2007 Elsevier B.V. All rights reserved.
AB - Although ascorbic acid (AsA) is one of the most important and abundantly occurring water soluble antioxidants in plants, relatively little is known about its role in counteracting the adverse effects of salt stress on plant growth. To address this issue that whether exogenous application of ascorbic acid (AsA) through rooting medium could alleviate the adverse effects of salt stress on wheat plants, a hydroponic experiment was conducted under glasshouse conditions using two wheat cultivars, S-24 (salt tolerant) and MH-97 (moderately salt sensitive). Plants of both cultivars were subjected to 0 or 150 mM NaCl solution supplemented with 0, 50, or 150 mg L-1 AsA for 58 days. Imposition of salt stress reduced the growth of both wheat cultivars by causing reduction in photosynthesis, and endogenous AsA level, and enhancing accumulation of Na+ and Cl- coupled with a decrease in K+ and Ca2+ in the leaves and roots of both cultivars thereby decreasing tissue K+/Na+ ratio. However, root applied AsA counteracted the adverse effects of salt stress on the growth of cv. S-24 only, particularly at 100 mg L-1 AsA level. AsA-induced enhancement in growth of salt-stressed plants of S-24 was associated with enhanced endogenous AsA level and CAT activity, and higher photosynthetic capacity, and accumulation of K+ and Ca2+ in the leaves. Although root applied AsA did not improve the growth of salt-stressed plants of MH-97, it enhanced endogenous level of AsA, CAT activity, photosynthetic capacity, and leaf K+ and Ca2+. These findings led us to conclude that root applied AsA counteracts the adverse effects of salt stress on growth of wheat by improving photosynthetic capacity of wheat plants against salt-induced oxidative stress and maintaining ion homeostasis, however, these effects were cultivar specific. © 2007 Elsevier B.V. All rights reserved.
KW - Antioxidants
KW - Catalase
KW - Ion homeostasis
KW - K+/Na+ ratio
KW - Photosynthesis
KW - Salt tolerance
U2 - 10.1016/j.envexpbot.2007.10.018
DO - 10.1016/j.envexpbot.2007.10.018
M3 - Article
SN - 0098-8472
VL - 63
SP - 224
EP - 231
JO - Environmental and Experimental Botany
JF - Environmental and Experimental Botany
IS - 1-3
ER -