Simarouba amara Aubl., a native of tropical regions of South and Central America was introduced in India for wasteland reclamation purposes. Present study was conducted to evaluate its ability to grow under salt stress conditions. S. amara seedlings were exposed to different concentrations of sodium chloride (50 mM, 100 mM, 150 mM, and 200 mM). Morphologically, at higher salt concentrations (150 and 200 mM NaCl), S. amara seedlings showed symptoms of leaf chlorosis, wilting, and drooping. A significant reduction in leaf relative water content, photosynthetic pigments and increase in lipid peroxidation was observed under high salt stress conditions. Under salt stress, levels of both enzymatic as well as non-enzymatic antioxidants increased majorly. At 200 mM NaCl, proline and cysteine content increased by 116% and 166% respectively. Among antioxidant enzymes, maximum increase in activity was observed in glutathione reductase (320%) followed by superoxide dismutase (129%), ascorbate peroxidase (80%), guaiacol peroxidase (80%) and catalase (59%) at 200 mM NaCl. A significant increase in the activities of both enzymatic and non-enzymatic antioxidants reveals that S. amara has better defensive mechanism against salt stress, but up to 100 mM concentration. At 150 and 200 mM NaCl, salt toxicity hampered growth of the plants.
<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.2d1 20170631//EN" "JATS-journalpublishing1.dtd">
<article xlink="http://www.w3.org/1999/xlink" dtd-version="1.0" article-type="plant-biotechnology" lang="en">
<front>
<journal-meta>
<journal-id journal-id-type="publisher">JIAR</journal-id>
<journal-id journal-id-type="nlm-ta">Journ of innovation in applied research</journal-id>
<journal-title-group>
<journal-title>Journal of Innovation in Applied Research</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Journ of innovation in applied research</abbrev-journal-title>
</journal-title-group>
<issn pub-type="ppub">2231-2196</issn>
<issn pub-type="opub">0975-5241</issn>
<publisher>
<publisher-name>Radiance Research Academy</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">71</article-id>
<article-id pub-id-type="doi">10.51323/JIAR.5.1.2022.39-51</article-id>
<article-id pub-id-type="doi-url"/>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Plant Biotechnology</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Biochemical and physiological tolerance evaluation of the oil-yielding paradise tree (Simarouba amara Aubl.) under salt stress
</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Das</surname>
<given-names>Amit K</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Rai</surname>
<given-names>Amit Kumar</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kumar</surname>
<given-names>Kaushal Bhargava and Jatin</given-names>
</name>
</contrib>
</contrib-group>
<pub-date pub-type="ppub">
<day>1</day>
<month>01</month>
<year>1970</year>
</pub-date>
<volume>5</volume>
<issue/>
<fpage>39</fpage>
<lpage>51</lpage>
<permissions>
<license license-type="open-access" href="http://creativecommons.org/licenses/by/4.0/">
<license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) Licence. You may share and adapt the material, but must give appropriate credit to the source, provide a link to the licence, and indicate if changes were made.</license-p>
</license>
</permissions>
<abstract>
<p>Simarouba amara Aubl., a native of tropical regions of South and Central America was introduced in India for wasteland reclamation purposes. Present study was conducted to evaluate its ability to grow under salt stress conditions. S. amara seedlings were exposed to different concentrations of sodium chloride (50 mM, 100 mM, 150 mM, and 200 mM). Morphologically, at higher salt concentrations (150 and 200 mM NaCl), S. amara seedlings showed symptoms of leaf chlorosis, wilting, and drooping. A significant reduction in leaf relative water content, photosynthetic pigments and increase in lipid peroxidation was observed under high salt stress conditions. Under salt stress, levels of both enzymatic as well as non-enzymatic antioxidants increased majorly. At 200 mM NaCl, proline and cysteine content increased by 116% and 166% respectively. Among antioxidant enzymes, maximum increase in activity was observed in glutathione reductase (320%) followed by superoxide dismutase (129%), ascorbate peroxidase (80%), guaiacol peroxidase (80%) and catalase (59%) at 200 mM NaCl. A significant increase in the activities of both enzymatic and non-enzymatic antioxidants reveals that S. amara has better defensive mechanism against salt stress, but up to 100 mM concentration. At 150 and 200 mM NaCl, salt toxicity hampered growth of the plants.
</p>
</abstract>
<kwd-group>
<kwd>Simarouba amara</kwd>
<kwd> antioxidants</kwd>
<kwd> lipid peroxidation</kwd>
<kwd> salt stress</kwd>
</kwd-group>
</article-meta>
</front>
</article>
- Yasin Ashraf, M., Awan, A.R., Anwar, S., Khaliq, B., Malik, A., & Ozturk, M. (2020). Economic utilization of salt-affected wasteland for plant production: A case study from Pakistan. Handbook of Halophytes: From Molecules to Ecosystems towards Biosaline Agriculture, 1-24.
- Evelin, H., Devi, T.S., Gupta, S., & Kapoor, R. (2019). Mitigation of salinity stress in plants by arbuscular mycorrhizal symbiosis: current understanding and new challenges. Frontiers in Plant Science, 10, 470.
- Shrivastava, P. & Kumar, R. (2015) Soil salinity: A serious environmental issue and plant growth promoting bacteria as one of the tools for its alleviation. Saudi journal of biological sciences, 22, 123-131.
- Tanveer, M. & Yousaf, U. (2020). Plant single-cell biology and abiotic stress tolerance. In: Plant Life under Changing Environment, pp. 611-626. Academic Press.
- Acosta-Motos, J.R., Ortuño, M.F., Bernal-Vicente, A., Diaz-Vivancos, P., Sanchez-Blanco, M.J. & Hernandez, J.A. (2017). Plant responses to salt stress: adaptive mechanisms. Agronomy, 7, 18.
- El-Taher, A.M., Abd El-Raouf, H.S., Osman, N.A., Azoz, S.N., Omar, M.A., Elkelish, A., & Abd El-Hady, M.A. (2021). Effect of salt stress and foliar application of salicylic acid on morphological, biochemical, anatomical, and productivity characteristics of Cowpea (Vigna unguiculata L.) plants. Plants, 11 (1), 115.
- Bre?, W., Kleiber, T., Markiewicz, B., Mieloszyk, E., & Mieloch, M. (2022). The effect of NaCl stress on the response of Lettuce (Lactuca sativa L.). Agronomy, 12 (2), 244.
- Al-huraby, A. I., & Bafeel, S. O. (2022). The effect of salinity stress on the Phaseolus vulgaris L. plant. African Journal of Biological Sciences, 4 (1), 94-107.
- Yan, S., Chong, P., & Zhao, M. (2022). Effect of salt stress on the photosynthetic characteristics and endogenous hormones, and: A comprehensive evaluation of salt tolerance in Reaumuria soongorica seedlings. Plant Signaling & Behavior, 2031782.
- Sarwar, M., Anjum, S., Alam, M.W., Ali, Q., Ayyub, C.M., Haider, M.S., Ashraf, M.I. & Mahboob, W. (2022). Triacontanol regulates morphological traits and enzymatic activities of salinity affected hot pepper plants. Scientific Reports, 12(1), 1-8.
- Zhang, M., Liu, Y., Han, G., Zhang, Y., Wang, B., & Chen, M. (2021). Salt tolerance mechanisms in trees: research progress. Trees, 35(3), 717-730.
- Joshi, S. & Joshi, S. 2008. SIMAROUBA GLAUCA DC (Paradise Tree)(brochure) (No. 1524-2016-131821), pp. 1-18.
- Awate, P.D. & Gaikwad, D.K. (2014). Influence of growth regulators on secondary metabolites of medicinally important oil yielding plant Simarouba glauca DC. under water stress conditions. Journal of Stress Physiology and Biochemistry, 10, 222-229.
- Cuartero, J., Bolarin, M.C., Asins, M.J. & Moreno, V. (2006). Increasing salt tolerance in the tomato. Journal of Experimental Botany, 57, 1045-1058.
- Turner, N.C. & Kramer, P.J. (1980). Adaptation of plants to water and high temperature stress. N.C. Turner and P.J. Kramer (eds.). Wiley Interscience, New York, pp. 9-10.
- Heath, R.L. & Packer, L. (1968). Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Archives of Biochemistry and Biophysics, 125, 189-198.
- Arnon, D.I. (1949). Copper enzymes isolated chloroplasts, polyphenoloxidase in Beta vulgaris. Plant Physiology, 24, 1-15.
- Lichtenthaler, H.K. & Wellburn, A.R. (1983). Determination of total carotenoids and chlorophyll a and b of leaf extract in different solvents. Biochemical Society Transactions, 11, 591-592.
- Weimberg, R. (1987). Solute adjustments in leaves of two species of wheat at two different stages of growth in response to salinity. Physiologia Plantarum, 78: 381-388.
- Bates, L.S., Waldron, R.P. & Teare, I.D. (1973). Rapid determination of free proline for water stress studies. Plant and Soil, 39, 205-207.
- Gaitonde, M.K. (1967). A spectrophotometric method for the direct determination of cysteine in the presence of other naturally occurring amino acids. Biochemical Journal, 104, 627-633.
- Bradford, M.M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72, 248-254.
- Beyer, W.F. & Fridovich, I. (1987). Assaying for superoxide dismutase activity: some large consequences of minor changes in conditions. Analytical Biochemistry, 161, 559-566.
- Aebi, H. (1984). In: Catalase in Vitro. Methods in Enzymology. Colowick SP, Kaplan NO, editors. Vol. 105. Florida: Acad. Press, pp. 114-121.
- Thimmaiah, S.K. (1999). Standard methods of biochemical analysis, Kalyani Publishers, New Delhi, pp. 248-249.
- Nakano, Y. & Asada, K. (1981). Hydrogen peroxide is scavenged by ascorbate specific peroxidase in spinach chloroplasts. Plant Cell Physiology, 22, 867-880.
- Schaedle, M. & Bassham, A. (1977). Chloroplast glutathione reductase. Plant Physiology, 53, 1011-1012.
- Kumar, J. & Agrawal, V. (2015). Study of some economically important under-utilized crops for cultivation on wastelands and biotechnology approaches for propagation and gene cloning. International Journal of Research in BioSciences, 4, 9-24.
- Mehrizi, M.H., Shariatmadari, H., Khoshgoftarmanesh, A.H. & Dehghani, F. (2012). Copper effects on growth, lipid peroxidation, and total phenolic content of Rosemary leaves under salinity stress. Journal of Agriculture, Science and Technology, 14, 205-212.
- Omami, E.N. & Hammes, P.S. (2006). Interactive effects of salinity and water stress on growth, leaf water relations, and gas exchange in amaranth (Amaranthus spp.). New Zealand Journal of Crop and Horticultural Science, 34, 33-34.
- Kaydan, D. & Yagmur, M. (2008). Germination, seedling growth and relative water content of shoot in different seed sizes of triticale under osmotic stress of water and NaCl. African Journal of Biotechnology, 7, 2862-2868.
- Al Hassan, M., Fuertes, M.M., Sanchezi, F.J.R., Vicente, O. & Boscaiu, M. (2015). Effects of salt and water stress on plant growth and on accumulation of osmolytes and antioxidant compounds in cherry tomato. Notulae Botanicae Horti Agrobotanici Cluj-Napoca, 43, 1-11.
- Kong, W., Liu, F., Zhang, C., Zhang, J. & Feng, H. (2016). Non-destructive determination of Malondialdehyde (MDA) distribution in oilseed rape leaves by laboratory scale NIR hyperspectral imaging. Scientific Reports, 6, 1-8.
- Rakhmankulova, Z.F., Voronin, P.Y.U., Shuyskaya, E.V., Kuznetsova, N.A., Zhukovskaya, N.V. & Toderich, K.N. (2014). Effect of NaCl and isoosmotic polyethylene glycol stress on gas exchange in shoots of the ?4 xerohalophyte Haloxylon aphyllum (Chenopodiaceae). Photosynthetica, 52, 437-443.
- Amirjani, M.R. (2015). Effect of salinity stress on seed germination and antioxidative defense system of Catharanthus roseus. ARPN Journal of Agricultural and Biological Science, 10, 163-171.
- Srivastava, A.K., Srivastava, S., Lokhande, V.H., D Souza, S.F.& Suprasanna, P. (2015). Salt stress reveals differential antioxidant and energetic responses in glycophyte (Brassica juncea L.) and halophyte (Sesuvium portulacastrum L.) Frontiers in Environmental Science, 3, 1-9.
- Mohamed, H.E., Hemeida, A.E. & Mohamed, A.G. (2015). Role of hydrogen peroxide pretreatment on developing antioxidant capacity in the leaves of tomato plant (Lycopersicon esculentum) grown under saline stress. International Journal of Advanced Research, 3, 878-879.
- Farhoudi, R., Modhej, A. & Afrous, A. (2015). Effect of salt stress on physiological and morphological parameters of rapeseed cultivars. Journal of Scientific Research and Development, 2, 111-117.
- Vromman, D., Lefevrea, I., Slejkovecb, Z., Martínezc, J-P, Vanheckea, N., Briceñod, M., Kumare, M. & Lutts, S. (2016). Salinity influences arsenic resistance in the xerohalophyte Atriplex atacamensis Phil. Environmental and Experimental Botany, 126, 32-43.
- Shabani, A., Sepaskhah, A.R. & Kamgar-Haghighi, A.A. (2013). Growth and physiologic response of rapeseed (Brassica napus L.) to deficit irrigation, water salinity and planting method. International Journal of Plant Production, 7, 569-596.
- Eshghizaden, H.R., Mohammad, K.A.F.I. & Nezami, A. (2012). The mechanisms of salinity tolerance in the xero-halophyte Blue Panicgrass (Panicum antidotale Retz). Notulae Scientia Biologicae, 4, 59-64.
- Ashraf, M. & Harris, P.J.C. (2013). Photosynthesis under stressful environments: An overview. Photosynthetica, 51, 163-190.
- Qados, A.M.A. (2011). Effect of salt stress on plant growth and metabolism of bean plant Vicia faba (L.). Journal of the Saudi Society of Agricultural Sciences, 10, 7-15.
- Bres, W., Bandurska, H., Kupska, A. & Niedziela, Fraszczak, B. (2016). Responses of pelargonium (Pelargonium x hortorum L.H. Bailey) to long-term salinity stress induced by treatment with different NaCl doses. Acta Physiologiae Plantarum, 38, 1-11.
- Akcin, A. & Yalcin, E. (2016). Effect of salinity stress on chlorophyll, carotenoid content, and proline in Salicornia prostrata Pall. and Suaeda prostrata Pall. subsp. prostrata (Amaranthaceae). Brazilian Journal of Botany, 39, 101-106
- Vijayalakshmi, T., Vijayakumar, A.S., Kiranmai, K., Nareshkumar, A. & Sudhakar, C. (2016). Salt stress induced modulations in growth, compatible solutes and antioxidant enzymes response in two cultivars of safflower (Carthamus tinctorius L. Cultivar TSF1 and Cultivar SM) differing in salt tolerance. American Journal of Plant Sciences, 7, 1802-1819.
- Ghosh, N., Adak, M.K., Ghosh, P.D., Gupta, S., Sen Gupta, D.N. & Mandal, C. (2011). Differential responses of two rice varieties to salt stress. Plant Biotechnology Reports, 5, 89-103.
- Razavizadeh, R. & Ehsanpour, A.A. (2009). Effects of salt stress on proline content, expression of delta-1-pyrroline-5-carboxylate synthetase, and activities of catalase and ascorbate peroxidase in transgenic tobacco plants. Biological Letters, 46, 63-75.
- Romero, L.C., Domínguez-Solís, J.R., Gutierrez-Alcala, G. & Gotor, C. (2001). Salt regulation of O-acetylserine (thiol) lyase in Arabidopsis thaliana and increased tolerance in yeast. Plant Physiology and Biochemistry, 39, 643-647.
- Fediuca, E., Lipsa, S.H. & Erdei, L. (2005). O-acetylserine (thiol) lyase activity in Phragmites and Typha plants under cadmium and NaCl stress conditions and the involvement of ABA in the stress response. Journal of Plant Physiology 162, 865-872.
- Vijendra, P.D., Huchappa, K.M., Lingappa, R., Basappa, G., Jayanna, S.G. & Kumar, V. (2016). Physiological and biochemical changes in Moth Bean (Vigna aconitifolia L.) under cadmium stress. Journal of Botany, 1-13.
- Abbasi, G.H., Ijaz, M., Akhtar, J., Anwar-Ul-Haq, M., Jamil, M., Ali, S., Ahmad, R. & Khan, H.N. (2016). Profiling of anti-oxidative enzymes and lipid peroxidation in leaves of salt tolerant and salt sensitive maize hybrids under NaCl and Cd stress. Sains Malay. 45, 177-184.
- Esfandiari, E., Shekari, F., Shekari, F. & Esfandiari, M. (2007). The effect of salt stress on antioxidant enzymes activity and lipid peroxidation on the wheat seedling. Notulae Botanicae Horti Agrobotanici Cluj-Napoca, 35, 48-56.
- Sairam, R.K., Rao, K.V. & Srivastava, G.C. (2002). Differential response of wheat genotypes to long term salinity stress in relation to oxidative stress, antioxidant activity and osmolyte concentration. Plant Science,163, 1037-1046.
- Heidari, M. (2009). Antioxidant activity and osmolyte concentration of sorghum (Sorghum bicolor) and wheat (Triticum aestivum) genotypes under salinity stress. Asian Journal of Plant Science, 8, 240-244.
- Barakat, N.A. (2011). Oxidative stress markers and antioxidant potential of wheat treated with phytohormones under salinity stress. Journal of Stress Physiology & Biochemistry, 250-267.
- Haddadi, B.S., Hassanpour, H. & Niknam, V. (2016). Effect of salinity and waterlogging on growth, anatomical and antioxidative responses in Mentha aquatica L. Acta Physiologiae Plantarum, 38, 1-11.
- Daneshmand, F., Arvin, M.J. & Kalantari, K.M. (2010). Physiological responses to NaCl stress in three wild species of potato in vitro. Acta Physiologiae Plantarum, 32, 91-101.
Department of Life Sciences, School of Basic Sciences and Research (SBSR), Sharda University, Greater Noida, 201310, Uttar Pradesh, India