Response of two tomato cultivars to field-applied proline under irrigation with saline water: Growth, chlorophyll fluorescence and nutritional aspects
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Abstract
The response of tomato (Solanum lycopersicum L.) to abiotic stress has been widely investigated. Recent physiological studies focus on the use of osmoprotectants to ameliorate stress damage, but experiments at a field level are scarce. Two tomato cultivars were used for an experiment with saline water (6.57 dS m−1) and subsurface drip irrigation (SDI) in a silty clay soil. Rio Grande is a salinity-tolerant cultivar, while Heinz-2274 is the salt-sensitive cultivar. Exogenous application of proline was done by foliar spray at two concentrations (10 and 20 mg L−1) during the flowering stage. Control plants were treated with saline water without proline. Proline at the lower concentration (10 mg L−1) increased dry mass of different plant organs (leaves, stems, and roots) and it improved various chlorophyll a fluorescence parameters compared with controls. Regarding mineral nutrition, K+ and P were higher in different organs, while low accumulation of Na+ occurred. However, Mg2+ was very high in all tissues of Rio Grande at the higher concentration of proline applied. Thus, the foliar spray of proline at 10 mg L−1 increased the tolerance of both cultivars. The growth of aboveground biomass of Heinz-2274 was enhanced by 63.5%, while Rio Grande improved only by 38.9%.
Additional key words
chlorophyll fluorescence foliar pulverization proline salt tolerance Solanum lycopersicum TunisiaAbbreviations
- Chl
chlorophyll
- CK
control
- DM
dry mass
- ECw
electrical conductivity of water
- Fm
maximal fluorescence in the dark-adapted leaves
- Fm′
maximal fluorescence in the light-adapted leaves
- F0
minimal fluorescence in the dark-adapted leaves
- Fs
steady-state fluorescence
- Fv
maximal variable fluorescence in the dark-adapted leaves
- Fv′
maximal variable fluorescence in the light-adapted leaves
- Fv/Fm
maximal efficiency of PSII photochemistry
- Fv′/Fm′
efficiency of excitation energy capture by open PSII reaction centers
- NPQ
nonphotochemical quenching
- ϕPSII
the quantum yield of PSII electron transport
- PQ-pool
plastoquinone pool
- Pro
proline
- Pro10
proline concentration of 10 mg L−1
- Pro20
proline concentration of 20 mg L−1
- SAR
sodium adsorption ratio
- ROS
reactive oxygen species
- SC
salt-sensitive cultivar
- SDI
subsurface drip irrigation
- TC
salt-tolerant cultivar
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References
- Alia, A., Kondo, Y., Sakamoto, A. et al.: Enhanced tolerance to light stress of transgenic Arabidopsis plants that express the codA gene for a bacterial choline oxidase. — Plant Mol. Biol. 40: 279–288, 1999.Google Scholar
- Araus, J.L., Amaro, T., Voltas, J. et al.: Chlorophyll fluorescence as a selection criterion for grain yield in durum wheat under Mediterranean conditions. — Field Crop. Res. 55: 209–223, 1998.CrossRefGoogle Scholar
- Ashraf, M., Athar, H.R., Harris, P.J.C., Kwon, T.R.: Some prospective strategies for improving crop salt tolerance. — Adv. Agron. 97: 45–110, 2008.CrossRefGoogle Scholar
- Aziz, A., Martin-Tanguy, J., Larher, F.: Salt stress-induced proline accumulation and changes in tyramine and polyamine levels are linked to ionic adjustment in tomato leaf discs. — Plant Sci. 145: 83–91, 1999.CrossRefGoogle Scholar
- Bates, L.S., Waldren, R.P., Teare, I.D.: Rapid determination of free proline for water-stress studies. — Plant Soil 39: 205–207, 1973.CrossRefGoogle Scholar
- Björkman, O., Demmig, B.: Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77K among vascular plants of diverse origins. — Planta 170: 489–504, 1987.CrossRefPubMedGoogle Scholar
- Conka, L.N., Hanson, A.D.: Prokaryotic osmoregulation: genetics and physiology. — Annu. Rev. Microbiol. 45: 569–606, 1991.CrossRefGoogle Scholar
- Colom, M.R., Vazzana, C.: Photosynthesis and PSII functionality of drought-resistant and drought-sensitive weeping lovegrass plants. — Environ. Exp. Bot. 49: 135–144, 2003.CrossRefGoogle Scholar
- Demetriou, G., Neonaki, C.. Navakoudis., E., Kotzabasis, K.: Salt stress impact on the molecular structure and function of the photosynthetic apparatus -the protective role of polyamines. — Biochim. Biophys. Acta 1767: 272–280, 2007.CrossRefPubMedGoogle Scholar
- Efeoğlu, B., Ekmekçi, Y., Çiçek, N.: Physiological responses of three maize cultivars to drought stress and recovery. — S. Afr. J. Bot. 75: 34–42, 2009.CrossRefGoogle Scholar
- Fernandez, R.T., Perry, R.L., Flore, J.A.: Drought response of young three apple trees on three rootstocks. II. Gas exchange, chlorophyll fluorescence, water relations, and leaf abscisic acid. — J. Am. Soc. Hortic. Sci. 122: 841–848, 1997.Google Scholar
- Fernandes-Rodrigues, C.R., Nascimento Silva, E., Ferreira-Silva, S.L. et al.: High K+ supply avoids Na+ toxicity and improves photosynthesis by allowing favorable K+:Na+ ratios through the inhibition of Na+ uptake and transport to the shoots of Jatrophacurcas plants. — J. Plant Nutr. Soil Sci. 176: 157–164, 2013.CrossRefGoogle Scholar
- Genty, B., Briantais, J.M., Baker, N.R.: The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. — Biochim. Biophys. Acta 990: 87–92, 1989.CrossRefGoogle Scholar
- Gericke, S., Kurmies, B: [Colorimetric phosphoric aciddetermination with ammonuim-vanadate-molybdate for their use in plant analysis.]. — Zeitschr. Pflanz. Dung. Bod. 59: 235–247, 1952. [In German]Google Scholar
- Greenway, H., Munns, R.: Mechanisms of salt-tolerance in nonhalophytes. — Annu. Rev. Plant Phys. 31: 149–190, 1980.CrossRefGoogle Scholar
- Hamilton, E.W., Heckathorn, S.A.: Mitochondrial adaptations to NaCl. Complex I is protected by antioxidants and small heat shock proteins, whereas complex II is protected by proline and betaine. — Plant Physiol. 126: 1266–1274, 2001.PubMedCentralCrossRefPubMedGoogle Scholar
- Harbinson, J., Genty, B., Baker, N.R.: Relationship between the quantum efficiencies of photosystems I and II in pea leaves. — Plant Physiol. 90: 1029–1034, 1989.PubMedCentralCrossRefPubMedGoogle Scholar
- Hellmann, H., Funck, D., Rentsch, D., Frommer, W.B.: Hypersensitivity of an arabidopsis sugar signaling mutant toward exogenous proline application. — Plant Physiol. 122: 357–367, 2000.PubMedCentralCrossRefPubMedGoogle Scholar
- Heuer, B.: Influence of exogenous application of proline and glycinebetaine on growth of salt-stressed tomato plants. — Plant Sci. 165: 693–699, 2003.CrossRefGoogle Scholar
- Holmstrom, K.O., Somersalo, S., Mandal, A. et al.: Improved tolerance to salinity and low temperature in transgenic tobacco producing glycinebetaine. — J. Exp. Bot. 51: 177–185, 2000.CrossRefPubMedGoogle Scholar
- Jain, M., Mathur, G., Koul, S., Sarin, N.B.: Ameliorative effects of proline on salt stress- induced lipid peroxidation in cell lines of groundnut (Arachis hypogea L). — Plant Cell Rep. 20: 463–468, 2001.CrossRefGoogle Scholar
- Kahlaoui, B., Hachicha, M., Rejeb, R. et al.: Effect of saline water on tomato under subsurface drip irrigation: nutritional and foliar aspects. — J. Soil Sci. Plant Nut. 11: 69–86, 2011a.CrossRefGoogle Scholar
- Kahlaoui, B., Hachicha, M., Rejeb, S. et al.: Effect of saline water on tomato under subsurface drip irrigation: yield and fruit quality. — Aust. J. Basic Applied Sci. 5: 517–529, 2011b.Google Scholar
- Kahlaoui, B., Hachicha, M., Rejeb, S., Rejeb, M.N.: Effect of drip irrigation and subsurface drip irrigation on tomato crop. — In: Ashraf, M., Öztürk, M., Ahmad, M.S.A., Aksoy, A. (ed.): Crop Production for Agricultural Improvement. Pp. 705–720. Springer, Dordrecht, New York 2012.CrossRefGoogle Scholar
- Kahlaoui, B., Hachicha, M., Teixeira, J. et al.: Response of two tomato cultivars to field-applied proline and salt stress. — J. Stress Phys. Bioch. 9: 257–265, 2013.Google Scholar
- Khadri, M., Tejera, N.A., Lluch, C.: Sodium chloride-ABA interaction in two common bean (Phaseolus vulgaris) cultivars differing in salinity tolerance. — Environ. Exp. Bot. 60: 211–218, 2007.CrossRefGoogle Scholar
- Kingsbury, R.W., Epstein, E.: Selection for salt resistant spring wheat. — Crop Sci. 24: 310–315, 1984.CrossRefGoogle Scholar
- Kocheva, K., Lambrev, P., Georgiev, G., Goltsev, V., Karabaliev, M.: Evaluation of chlorophyll fluorescence and membrane injury in the leaves of barley cultivars under osmotic stress. — Bioelectrochemistry 63: 121–124, 2004.CrossRefPubMedGoogle Scholar
- Kumar, S.G., Reddy, A.M., Sudhakar, C.: NaCl effects on proline metabolism in two high yielding genotypes of mulberry (Morus alba L.) with contrasting salt tolerance. — Plant Sci. 165: 1245–1251, 2003.CrossRefGoogle Scholar
- Lin, C.C., Hsu, Y.T., Kao, C.H.: The effect of NaCl on proline accumulation in rice leaves. — Plant Growth Regul. 36: 275–285, 2002.CrossRefGoogle Scholar
- Lone, M.I., Kueh, J.S.H., Wyn Jones, R.G.W., Bright, S.W.J.: Influence of proline and glycinebetaine on salt tolerance of cultured barley embryos. — J. Exp. Bot. 38: 479–490, 1987.CrossRefGoogle Scholar
- Loukehaich, R., Elyachioui, M., Belhabib, N., Douira, A.: Identifying multiple physiological responses associated with salinity-tolerance for evaluating three tomato cultivars selected from Moroccan territory. — J. Anim. Plant Sci. 10: 1219–1231, 2011.Google Scholar
- Lutts, S., Majerus, V., Kinet, J.M.: NaCl effects on proline metabolism in rice (Oryza sativa L.) seedlings. — Physiol. Plantarum 105: 450–458, 1999.CrossRefGoogle Scholar
- Ma, Q.Q., Wang, W., Li, Y.H. et al.: Alleviation of photoinhibition in drought-stressed wheat (Triticum aestivum) by foliarapplied glycinebetaine. — J. Plant Physiol. 163: 165–175, 2006.CrossRefPubMedGoogle Scholar
- Mansour, M.M.F.: Protection of plasma membrane of onion epidermal cells by glycinebetaine and proline against NaCl stress. — Plant Physiol. Bioch. 36: 767–772, 1998.CrossRefGoogle Scholar
- Maxwell, K., Johnson, G.N.: Chlorophyll fluorescence — a practical guide. — J. Exp. Bot. 50: 659–668, 2000.CrossRefGoogle Scholar
- Müller, P., Li, X.P., Niyogi, K.K.: Nonphotochemical quenching. A response to excess light energy. — Plant Physiol. 125: 1558–1566, 2001.PubMedCentralCrossRefPubMedGoogle Scholar
- Nakayama, H., Horie, T., Yonamine, I. et al.: Improving salt tolerance in plant cells. — Plant Biotechnol. 22: 477–487, 2005.CrossRefGoogle Scholar
- Nounjan, N., Nghia, P.T., Theerakulpisut, P.: Exogenous proline and trehalose promote recovery of rice seedlings from saltstress and differentially modulate antioxidant enzymes and expression of related genes. — J. Plant Physiol. 169: 596–604, 2012.CrossRefPubMedGoogle Scholar
- Petrusa, L.M., Winicov, I.: Proline status in salt tolerant and salt sensitive alfalfa cell lines and plants in response to NaCl. — Plant Physiol. Bioch. 35: 303–310, 1997.Google Scholar
- Poustini, K., Siosemardeh, A., Ranjbar, M.:Proline accumulation as a response to salt stress in wheat (Triticum aestivum L.) cultivars differing in salt tolerance. — Genet. Resour. Crop Ev. 54: 925–934, 2004.CrossRefGoogle Scholar
- Prasad, K.V.S.K., Saradhi, P.P.: Enhanced tolerance to photoinhibition in transgenic plants through targeting of glycinebetaine biosynthesis into the chloroplasts. — Plant Sci. 166: 1197–1212, 2004.CrossRefGoogle Scholar
- Rajasekaran, L.R., Kriedemann, P.E., Aspinall, D., Paleg, L.G.: Physiological significance of proline and glycinebetaine: maintaining photosynthesis during NaCl stress in wheat. — Photosynthetica 34: 357–366, 1997.CrossRefGoogle Scholar
- Ranjbarfordoei, A., Samson, R., Van Damme P.: Chlorophyll fluorescence performance of sweet almond [Prunus dulcis (Miller) D. Webb] in response to salinity stress induced by NaCl. — Photosynthetica 44: 513–522, 2006.CrossRefGoogle Scholar
- Roy, D., Basu, N., Bhunia, A., Banerjee, S.K.: Counteraction of exogenous l-proline with NaCl in saltsensitive cultivar of rice. — Biol. Plantarum 35: 69–72, 1993.CrossRefGoogle Scholar
- Sivakumar, P., Sharmila, P., Saradhi, P.P.: Proline suppresses rubisco activity in higher plants. — Biochem. Biophys. Res. Co. 252: 428–432, 1998.CrossRefGoogle Scholar
- Theerakulpisut, P., Bunnag, S., Kong-Ngern, K.: Genetic diversity, salinity tolerance and physiological responses to NaCl of six rice (Oryza sativa L.) cultivars. — Asian J. Plant Sci. 4: 562–573, 2005.CrossRefGoogle Scholar
- Tiwari, B.S., Bose, A., Ghosh, B.: Photosynthesis in rice under a salt stress. — Photosynthetica 34: 303–306, 1997.CrossRefGoogle Scholar
- Vaidyanathan, H., Sivakumar, P., Chakrabarty, R., Thomas, G.: Scavenging of reactive oxygen species in NaCl-stressed rice (Oryza sativa L.) differential response in salt-tolerant and — sensitive varieties. — Plant Sci. 165: 1411–1418, 2003.CrossRefGoogle Scholar
- Wani, A.S., Irfan, M., Hayat, S., Ahmad, A.: Response of two mustard (Brassica juncea L.) cultivars differing in photosynthetic capacity subjected to proline. — Protoplasma 249: 75–87, 2011.Google Scholar
- Yancey, P.H.: Compatible and counteracting solutes. In: Strange, K. (ed.): Cellular and Molecular Physiology of Cell Volume Regulation. Pp. 81–109. CRC Press, Boca Raton 1994.Google Scholar
- Zhu, B.C, Su, J., Chan, M.C. et al.: Overexpression of a D1-pyrroline-5-carboxylate synthetase gene and analysis of tolerance to water- and salt-stress in transgenic rice. — Plant Sci. 139: 41–48, 1998.CrossRefGoogle Scholar