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Improving salt stress tolerance in Zea mays L. by modulating osmolytes accumulation and antioxidant capacity with Rutin

Year 2024, Volume: 8 Issue: 1, 21 - 29, 15.05.2024
https://doi.org/10.30616/ajb.1387695

Abstract

The growth and productivity of maize are severely affected by stress factors. Maize seedlings under salt stress were grown hydroponically to study the effect of rutin (Rut), a flavonoid, on changes in the stress parameters (thiobarbituric acid reactive substances (TBARS), hydrogen peroxide (H2O2), total chlorophyll), water status (leaf relative water content (RWC), osmolytes; proline, total soluble sugar), and activities of the main antioxidant enzymes (superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX), and peroxidase (POD)). After 21 days of growth, plants were applied with Rut as foliar spray. After 24 hours, seedlings were exposed to osmotic stress by 100 and 200 mM NaCI in the Hoagland’s Solution for 72 hours. Six groups were designed including a control (without NaCl or Rut), 150 mM NaCl, 200 mM NaCl, Rut, Rut+150 mM NaCl, and Rut+200 mM NaCl. Plant leaves were harvested 25 days after treatments. Exogenous significantly decreased TBARS and H2O2 contents in leaves of salt-stressed seedlings compared to salt stresses, enhanced the level of osmolytes, leaf RWC, activities of SOD, CAT, APX, and POD, and relative expression levels of SOD, CAT1, and APX1. As a result, findings from the study present reveal the effect of Rut on salt stress tolerance in maize seedlings under different osmotic stress. Here, it was clear that Rut played an active role in stress-alleviating. This application under salt stress can be useful in developing salt stress tolerance in crops for the agriculture sector.

References

  • AbdElgawad H, Zinta G, Hegab MM, Pandey R, Asard H, Abuelsoud W (2016). High salinity induces different oxidative stress and antioxidant responses in maize seedlings organs. Front Plant Science 7: 276.
  • Acosta-Motos JR, Diaz-Vivancos P, Álvarez S, Fernández-García N, Sanchez-Blanco MJ, Hernández JA (2015). Physiological and biochemical mechanisms of the ornamental Eugenia myrtifolia L. Plants for coping with NaCl stress and recovery. Planta 42: 829-46.
  • Aebi HE (1983). Catalase. Methods of enzymatic analysis. New York: Akademic press.
  • Ali M, Afzal S, Parveen A, Kamran M, Javed MR, Abbasi GH (2021). Silicon mediated improvement in the growth and ion homeostasis by decreasing Na+ uptake in maize (Zea mays L.) cultivars exposed to salinity stress. Plant Physiology Biochemistry 158: 208-18.
  • Arnao MB, Hernandez RJ (2010). Protective effect of melatonin against chlorophyll degradation during the senescence of barleyleaves. Journal of Pineal Research 46: 58-63
  • Arnon DI (1949). Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant physiology 24(1): 1.
  • Asada K (1999). The water-water cycle in chloroplasts: Scavenging of active oxygens and dissipation of excess photons. Annual Review of Plant Physiology and Plant Molecular Biology 50: 601-639.
  • Ashraf M, Foolad MR (2007). Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environmental and Experimental Botany 59: 206-216.
  • Bates LS, Waldren RP, Teare ID (1973). Rapid determination of free proline for water-stress studies. Plant and soil 39: 205-207.
  • Beauchamp C, Fridovich I (1971). Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Analytical Biochemistry 44: 276-287.
  • Chen S, Wu F, Li Y, Qian Y, Pan X, Li F and Yang A (2019). NtMYB4 and NtCHS1 are critical factors in the regulation of flavonoid biosynthesis and are involved in salinity responsiveness. Frontiers in plant science 10: 178-190.
  • Das K and Roychoudhury A (2014). Reactive oxygen Species, ROS and response of antioxidants as ROS-scavengers during environmental stress in plants. Frontiers in Environmental Science 2: 53.
  • Dubois M, Gilles KA, Hamilton JK, Rebers PT, Smith F (1956). Colorimetric method for determination of sugars and related substances. Analytical Chemistry 28: 350-356.
  • Farooq M, Hussain M, Wakeel A and Siddique KHM (2015). Salt stress in maize: effects, resistance mechanisms, and management. A review. Agronomy for Sustainable Development 35: 461-481.
  • Feng XH, Hussain T, Guo K, An P, Liu XJ (2021). Physiological, morphological and anatomical responses of Hibiscus moscheutos to non-uniform salinity stress. Environmental and Experimental Botany 182: 104301.
  • Gorni PH, Lima GR, Oliveira Pereira LM, Spera KD, Macros LA and Pacheco AC (2022). Increasing plant performance, fruit production and nutritional value of tomato through foliar applied rutin. Scientia Horticulturae 294: 110755.
  • Heath RL, Packer L (1968). Photoperoxidation in isolated chloroplasts: I. Kinetics and stoichiometry of fatty acid peroxidation. Archives of Biochemistry and Biophysics 125: 189-198.
  • Hoagland DR, Arnon DI (1950). The water-culture method for growing plants without soil. Circular. California Agricultural Experiment Station Circular 347: 1-32.
  • Huo LQ, Guo ZJ, Wang P, Zhang ZJ, Jia X, Sun YM (2020). MdATG8i functions positively in apple salt tolerance by maintaining photosynthetic ability and increasing the accumulation of arginine and polyamines. Environmental and Experimental Botany 172: 103989.
  • Isayenkov SV, Maathuis FJM (2019) Plant salinity stress: Many unanswered questions remain. Frontiers of Plant Science 10: 80.
  • Ismail H, Maksimović JD, Maksimović V, Shabala L, Živanović BD, Tian Y and Shabala S (2015). Rutin, a flavonoid with antioxidant activity, improves plant salinity tolerance by regulating K+ retention and Na+ exclusion from leaf mesophyll in quinoa and broad beans. Functional Plant Biology 43(1): 75-86.
  • Jańczak-Pieniążek M, Migut D, Piechowiak T, Buczek J and Balawejder M (2021). The Effect of exogenous application of quercetin derivative solutions on the course of physiological and biochemical processes in wheat seedlings, International Journal of Molecular Sciences 22 (13): 6882.
  • Jiang P, Burczynski F, Campbell C, Pierce, G, Austria JA, Briggs CJ (2007). Rutin and flavonoid contents in three buckwheat species Fagopyrum esculentum, F. tataricum, and F. homotropicum and their protective effects against lipid peroxidation. Food research international 40(3): 356-364.
  • Jiang C, Cui Q, Feng K, Xu D, Li C, Zheng Q (2016). Melatonin improves antioxidant capacity and ion homeostasis and enhances salt tolerance in maize seedlings. Acta Acta Physiologiae Plantarum 38: 82.
  • Joshi S, Nath J, Singh AK, Pareek A, Joshi R (2022). Ion transporters and their regulatory signal transduction mechanisms for salinity tolerance in plants. Physiologia Plantarum 174: 13702.
  • Ju FY, Pang JL, Huo YY, Zhu JJ, Yu K, Sun LY (2021). Potassium application alleviates the negative effects of salt stress on cotton (Gossypium hirsutum L.) yield by improving the ionic homeostasis, photosynthetic capacity and carbohydrate metabolism of the leaf subtending the cotton boll. Field Crop Research 272: 108288.
  • Kang SZ, Su XL, Tong L, Shi PZ, Yang XY, Abe YK (2004). The impacts of human activities on the water-land environment of the Shiyang River basin, an arid region in Northwest China. Hydrological Sciences Journal 49(3): 427.
  • Kumar M, Kumar PM, Kumar N, Bajpai AB and Siddique KHM (2021). Metabolomics and Molecular Approaches Reveal Drought Stress Tolerance in Plants. International Journal of Molecular Sciences 22(17): 9108.
  • Kurepa, J, Shull T, E and Smalle JA (2016) Quercetin feeding protects plants against oxidative stress. Research 5: 2430.
  • Liang W, Ma X, Wan P, Liu L (2017). Plant salt-tolerance mechanism: a review. Biochemical Biophysical Research Communications 495: 286-291.
  • Linh NT, Cham LTT, Thang VN (2021) Effects of salinity stress on the growth, physiology, and yield of soybean (Glycine max (L.) Merrill). Vietnam Journal of Agricultural Science 4: 1043-1055.
  • Liso R, Calabrese G, Bitonti MB, Arrigoni O (1984). Relationship between ascorbic acid and cell division. Experimental Cell Research 150: 314-320.
  • Meng Q, Chen X, Lobell DL, Cui Z, Zhang Y, Yang H, Zhang F (2016). Growing sensitivity of maize to water scarcity under climate change. Scientific Reports 6: 19605.
  • Mittova V, Guy M, Tal M, Volokita M (2004). Salinity up-regulates the antioxidative system in root mitochondria and peroxisomes of the wild salt-tolerant tomato species Lycopersicon pennellii. Journal Experimental Botany 55: 1105-13.
  • Mukhopadhyay R, Sarkar B, Jat HS, Sharma PC, Bolan NS (2021). Soil salinity under climate change: challenges for sustainable agriculture and food security. Journal of Environmental Management 280: 111736.
  • Nakano Y, Asada K (1981). Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant and Cell Physiology. 22: 867-880.
  • Negrão S, Schmöckel SM, Tester M (2017). Evaluating physiological responses of plants to salinity stress. Annals of Botany 119: 1-11.
  • Ozyigit II, Filiz E, Vatansever R, Kurtoglu KY, Koc I, Öztürk MX and Anjum NA (2016). Identification and comparative analysis of H2O2-scavenging enzymes, ascorbate peroxidase and glutathione peroxidase in selected plants employing bioinformatics approaches. Frontiers in Plant Science 7.
  • Parveen A, Liu W, Hussain S, Asghar J, Perveen S, Xiong Y (2019). Silicon priming regulates morpho-physiological growth and oxidative metabolism in maize under drought stress. Plants 8(10): 431.
  • Parvin K, Hasanuzzaman M, Bhuyan MB, Mohsin SM and Fujita M (2019). Quercetin mediated salt tolerance in tomato through the enhancement of plant antioxidant defense and glyoxalase systems. Plants 8 (8): 247.
  • Ren J, Ye J, Yin L, Li G, Deng X, Wang S (2020). Exogenous melatonin ımproves salt tolerance by mitigating osmotic, ion, and oxidative stresses in maize seedlings. Agronomy 10: 663.
  • Safwat G, Salam HSA (2022). The effect of exogenous proline and glycine betaine on phyto-biochemical responses of salt-stressed basil plants. Egyptian Journal of Botany 62: 537-547.
  • Sánchez-McSweeney A, González-Gordo S, Aranda-Sicilia MN, Rodríguez- Rosales MP, Venema K, Palma JM (2021). Loss of function of the chloroplast membrane K(+)/H(+) antiporters AtKEA1 and AtKEA2 alters the ROS and NO metabolism but promotes drought stress resilience. Plant Physiology and Biochemistry 160: 106-19.
  • Sezgin A, Altuntaş C, Sağlam A, Terzi R, Demiralay M, Kadıoğlu A (2018). Abscisic acid cross-talking with hydrogen peroxide and osmolyte compounds may regulate the leaf rolling mechanism under drought. Acta Physiologiae Plantarum. 40: 1-12.
  • Sharma P, Jha AB, Dubey RS and Pessarakli M (2012). Reactive oxygen species, oxidative damage, and antioxidative defense mechanism in plants under stressful conditions. Journal of Botany 2012: 1-26.
  • Singh A, Gupta R, Pandey R (2017). Exogenous application of rutin and gallic acid regulate antioxidants and alleviate reactive oxygen generation in Oryza sativa L. Physiology and Molecular Biology of Plants. 23: 301-309.
  • Suriya-arunroj D, Supapoj N, Toojinda T, Vanavichit A (2004). Relative leaf water content as an efficient method for evaluating rice cultivars for tolerance to salt stress. Science Asia 30: 411-415.
  • Suzuki T, Honda Y and Mukasa Y (2005). Effects of UV-B radiation, cold and desiccation stress on rutin concentration and rutin glucosidase activity in tartary buckwheat (Fagopyrum tataricum) leaves. Plant Science 168(5): 1303-1307.
  • Suzuki T, Morishita T, KIM SJ, Park SU, Woo SH, Noda T, Takigawa S (2015). Physiological roles of rutin in the buckwheat plant. Japan Agricultural Research Quarterly: JARQ 49(1): 37-43.
  • Taiz L, Zeiger E (2008). Plant Physiology. Ankara: Palme Publishing.
  • Urbanek H, Kuzniak-Gebarowska E, Herka K (1991). Elicitation of defence responses in bean leaves by Botrytis cinerea polygalacturonase. Acta Physiologiae Plantarum 13.
  • Velikova V, Yordanov I, Edreva A (2000). Oxidative stress and some antioxidant systems in acid rain-treated bean plants: protective role of exogenous polyamines. Plant science 151: 59-66.
  • Wei TL, Wang Y, Liu JH (2020). Comparative transcriptome analysis reveals synergistic and disparate defense pathways in the leaves and roots of trifoliate orange (Poncirus trifoliata) autotetraploids with enhanced salt tolerance. Horticulture Research 7: 88.
  • Yang J, Guo J, Yuan J (2008). In vitro antioxidant properties of rutin. Lebensm. Wiss Technology 41: 1060-1066.
  • Yu ZP, Duan XB, Luo L, Dai SJ, Ding ZJ, Xia GM (2020). How plant hormones mediate salt stress responses. Trends in Plant Science 25: 1117-1130.
  • Zelm EV, Zhang YX, Testerink C (2020). Salt tolerance mechanisms of plants. Annual Review Plant Biology 71:403-433.
  • Zhong M, Song R, Wang Y, Shu S, Sun J, Guo SR (2020). TGase regulates salt stress tolerance through enhancing bound polyaminesmediated antioxidant enzymes activity in tomato. Environmental and Experimental Botany 179: 104191.
  • Zhu JK (2016). Abiotic stress signaling and responses in plants. Cell 167: 313-324.

Rutin ile osmolit birikimi ve antioksidan kapasite modüle edilerek Zea mays L.'de tuz stresi toleransının geliştirilmesi

Year 2024, Volume: 8 Issue: 1, 21 - 29, 15.05.2024
https://doi.org/10.30616/ajb.1387695

Abstract

Mısırın büyümesi ve verimliliği stres faktörlerinden ciddi şekilde etkilenir. Tuz stresi altındaki mısır fideleri, bir flavonoid olan rutinin (Rut) stres parametrelerindeki (tiyobarbitürik asit reaktif maddeleri (TBARS), hidrojen peroksit (H2O2), toplam klorofil), su durumu (yaprak nisbi su içeriği(NSİ), osmolitler; prolin, toplam çözünebilir şeker) ve ana antioksidan enzimlerin (süperoksit dismutaz (SOD), katalaz (CAT), askorbat peroksidaz (APX) ve peroksidaz (POD)) aktiviteleri üzerine etkisini incelemek için hidroponik olarak büyütüldü. 21 günlük büyümenin ardından yapraklara rutin sprey olarak gerçekleştirildi 24 saatin ardından fideler, 72 saat boyunca Hoagland Solüsyonunda 100 ve 200 mM NaCl'nin indüklediği ozmotik strese maruz bırakıldı. Deney grupları, Bir kontrol (NaCl veya Rut içermeyen), 150 mM NaCl, 200 mM NaCI, Rut, Rut+150 mM NaCl ve Rut+200 mM NaCl dahil olmak üzere üç tekrarlı altı grup şeklinde dizayn edildi. Bitki yaprakları uygulamalardan 25 gün sonra hasat edildi. Eksojen Rut, tuz stresine kıyasla tuz stresi altındaki fidelerin yapraklarındaki TBARS ve H2O2 içeriğini önemli ölçüde azalttı, osmolit seviyesini, yaprak NSİ’ni, SOD, CAT, APX ve POD aktivitelerini ve SOD, CAT1 ve APX1’in nisbi ekspresyon seviyelerini artırdı. Sonuç olarak, mevcut çalışmadan elde edilen bulgular, farklı ozmotik stres altındaki mısır fidelerinde Rut'un tuz stresi toleransı üzerindeki etkisini ortaya koymaktadır. Burada Rut'un stresi azaltmada aktif rol oynadığı açıktı. Tuz stresi altında yapılan bu uygulama, tarım sektörü için bitkilerde tuz stresine toleransın geliştirilmesinde faydalı olabilir.

References

  • AbdElgawad H, Zinta G, Hegab MM, Pandey R, Asard H, Abuelsoud W (2016). High salinity induces different oxidative stress and antioxidant responses in maize seedlings organs. Front Plant Science 7: 276.
  • Acosta-Motos JR, Diaz-Vivancos P, Álvarez S, Fernández-García N, Sanchez-Blanco MJ, Hernández JA (2015). Physiological and biochemical mechanisms of the ornamental Eugenia myrtifolia L. Plants for coping with NaCl stress and recovery. Planta 42: 829-46.
  • Aebi HE (1983). Catalase. Methods of enzymatic analysis. New York: Akademic press.
  • Ali M, Afzal S, Parveen A, Kamran M, Javed MR, Abbasi GH (2021). Silicon mediated improvement in the growth and ion homeostasis by decreasing Na+ uptake in maize (Zea mays L.) cultivars exposed to salinity stress. Plant Physiology Biochemistry 158: 208-18.
  • Arnao MB, Hernandez RJ (2010). Protective effect of melatonin against chlorophyll degradation during the senescence of barleyleaves. Journal of Pineal Research 46: 58-63
  • Arnon DI (1949). Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant physiology 24(1): 1.
  • Asada K (1999). The water-water cycle in chloroplasts: Scavenging of active oxygens and dissipation of excess photons. Annual Review of Plant Physiology and Plant Molecular Biology 50: 601-639.
  • Ashraf M, Foolad MR (2007). Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environmental and Experimental Botany 59: 206-216.
  • Bates LS, Waldren RP, Teare ID (1973). Rapid determination of free proline for water-stress studies. Plant and soil 39: 205-207.
  • Beauchamp C, Fridovich I (1971). Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Analytical Biochemistry 44: 276-287.
  • Chen S, Wu F, Li Y, Qian Y, Pan X, Li F and Yang A (2019). NtMYB4 and NtCHS1 are critical factors in the regulation of flavonoid biosynthesis and are involved in salinity responsiveness. Frontiers in plant science 10: 178-190.
  • Das K and Roychoudhury A (2014). Reactive oxygen Species, ROS and response of antioxidants as ROS-scavengers during environmental stress in plants. Frontiers in Environmental Science 2: 53.
  • Dubois M, Gilles KA, Hamilton JK, Rebers PT, Smith F (1956). Colorimetric method for determination of sugars and related substances. Analytical Chemistry 28: 350-356.
  • Farooq M, Hussain M, Wakeel A and Siddique KHM (2015). Salt stress in maize: effects, resistance mechanisms, and management. A review. Agronomy for Sustainable Development 35: 461-481.
  • Feng XH, Hussain T, Guo K, An P, Liu XJ (2021). Physiological, morphological and anatomical responses of Hibiscus moscheutos to non-uniform salinity stress. Environmental and Experimental Botany 182: 104301.
  • Gorni PH, Lima GR, Oliveira Pereira LM, Spera KD, Macros LA and Pacheco AC (2022). Increasing plant performance, fruit production and nutritional value of tomato through foliar applied rutin. Scientia Horticulturae 294: 110755.
  • Heath RL, Packer L (1968). Photoperoxidation in isolated chloroplasts: I. Kinetics and stoichiometry of fatty acid peroxidation. Archives of Biochemistry and Biophysics 125: 189-198.
  • Hoagland DR, Arnon DI (1950). The water-culture method for growing plants without soil. Circular. California Agricultural Experiment Station Circular 347: 1-32.
  • Huo LQ, Guo ZJ, Wang P, Zhang ZJ, Jia X, Sun YM (2020). MdATG8i functions positively in apple salt tolerance by maintaining photosynthetic ability and increasing the accumulation of arginine and polyamines. Environmental and Experimental Botany 172: 103989.
  • Isayenkov SV, Maathuis FJM (2019) Plant salinity stress: Many unanswered questions remain. Frontiers of Plant Science 10: 80.
  • Ismail H, Maksimović JD, Maksimović V, Shabala L, Živanović BD, Tian Y and Shabala S (2015). Rutin, a flavonoid with antioxidant activity, improves plant salinity tolerance by regulating K+ retention and Na+ exclusion from leaf mesophyll in quinoa and broad beans. Functional Plant Biology 43(1): 75-86.
  • Jańczak-Pieniążek M, Migut D, Piechowiak T, Buczek J and Balawejder M (2021). The Effect of exogenous application of quercetin derivative solutions on the course of physiological and biochemical processes in wheat seedlings, International Journal of Molecular Sciences 22 (13): 6882.
  • Jiang P, Burczynski F, Campbell C, Pierce, G, Austria JA, Briggs CJ (2007). Rutin and flavonoid contents in three buckwheat species Fagopyrum esculentum, F. tataricum, and F. homotropicum and their protective effects against lipid peroxidation. Food research international 40(3): 356-364.
  • Jiang C, Cui Q, Feng K, Xu D, Li C, Zheng Q (2016). Melatonin improves antioxidant capacity and ion homeostasis and enhances salt tolerance in maize seedlings. Acta Acta Physiologiae Plantarum 38: 82.
  • Joshi S, Nath J, Singh AK, Pareek A, Joshi R (2022). Ion transporters and their regulatory signal transduction mechanisms for salinity tolerance in plants. Physiologia Plantarum 174: 13702.
  • Ju FY, Pang JL, Huo YY, Zhu JJ, Yu K, Sun LY (2021). Potassium application alleviates the negative effects of salt stress on cotton (Gossypium hirsutum L.) yield by improving the ionic homeostasis, photosynthetic capacity and carbohydrate metabolism of the leaf subtending the cotton boll. Field Crop Research 272: 108288.
  • Kang SZ, Su XL, Tong L, Shi PZ, Yang XY, Abe YK (2004). The impacts of human activities on the water-land environment of the Shiyang River basin, an arid region in Northwest China. Hydrological Sciences Journal 49(3): 427.
  • Kumar M, Kumar PM, Kumar N, Bajpai AB and Siddique KHM (2021). Metabolomics and Molecular Approaches Reveal Drought Stress Tolerance in Plants. International Journal of Molecular Sciences 22(17): 9108.
  • Kurepa, J, Shull T, E and Smalle JA (2016) Quercetin feeding protects plants against oxidative stress. Research 5: 2430.
  • Liang W, Ma X, Wan P, Liu L (2017). Plant salt-tolerance mechanism: a review. Biochemical Biophysical Research Communications 495: 286-291.
  • Linh NT, Cham LTT, Thang VN (2021) Effects of salinity stress on the growth, physiology, and yield of soybean (Glycine max (L.) Merrill). Vietnam Journal of Agricultural Science 4: 1043-1055.
  • Liso R, Calabrese G, Bitonti MB, Arrigoni O (1984). Relationship between ascorbic acid and cell division. Experimental Cell Research 150: 314-320.
  • Meng Q, Chen X, Lobell DL, Cui Z, Zhang Y, Yang H, Zhang F (2016). Growing sensitivity of maize to water scarcity under climate change. Scientific Reports 6: 19605.
  • Mittova V, Guy M, Tal M, Volokita M (2004). Salinity up-regulates the antioxidative system in root mitochondria and peroxisomes of the wild salt-tolerant tomato species Lycopersicon pennellii. Journal Experimental Botany 55: 1105-13.
  • Mukhopadhyay R, Sarkar B, Jat HS, Sharma PC, Bolan NS (2021). Soil salinity under climate change: challenges for sustainable agriculture and food security. Journal of Environmental Management 280: 111736.
  • Nakano Y, Asada K (1981). Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant and Cell Physiology. 22: 867-880.
  • Negrão S, Schmöckel SM, Tester M (2017). Evaluating physiological responses of plants to salinity stress. Annals of Botany 119: 1-11.
  • Ozyigit II, Filiz E, Vatansever R, Kurtoglu KY, Koc I, Öztürk MX and Anjum NA (2016). Identification and comparative analysis of H2O2-scavenging enzymes, ascorbate peroxidase and glutathione peroxidase in selected plants employing bioinformatics approaches. Frontiers in Plant Science 7.
  • Parveen A, Liu W, Hussain S, Asghar J, Perveen S, Xiong Y (2019). Silicon priming regulates morpho-physiological growth and oxidative metabolism in maize under drought stress. Plants 8(10): 431.
  • Parvin K, Hasanuzzaman M, Bhuyan MB, Mohsin SM and Fujita M (2019). Quercetin mediated salt tolerance in tomato through the enhancement of plant antioxidant defense and glyoxalase systems. Plants 8 (8): 247.
  • Ren J, Ye J, Yin L, Li G, Deng X, Wang S (2020). Exogenous melatonin ımproves salt tolerance by mitigating osmotic, ion, and oxidative stresses in maize seedlings. Agronomy 10: 663.
  • Safwat G, Salam HSA (2022). The effect of exogenous proline and glycine betaine on phyto-biochemical responses of salt-stressed basil plants. Egyptian Journal of Botany 62: 537-547.
  • Sánchez-McSweeney A, González-Gordo S, Aranda-Sicilia MN, Rodríguez- Rosales MP, Venema K, Palma JM (2021). Loss of function of the chloroplast membrane K(+)/H(+) antiporters AtKEA1 and AtKEA2 alters the ROS and NO metabolism but promotes drought stress resilience. Plant Physiology and Biochemistry 160: 106-19.
  • Sezgin A, Altuntaş C, Sağlam A, Terzi R, Demiralay M, Kadıoğlu A (2018). Abscisic acid cross-talking with hydrogen peroxide and osmolyte compounds may regulate the leaf rolling mechanism under drought. Acta Physiologiae Plantarum. 40: 1-12.
  • Sharma P, Jha AB, Dubey RS and Pessarakli M (2012). Reactive oxygen species, oxidative damage, and antioxidative defense mechanism in plants under stressful conditions. Journal of Botany 2012: 1-26.
  • Singh A, Gupta R, Pandey R (2017). Exogenous application of rutin and gallic acid regulate antioxidants and alleviate reactive oxygen generation in Oryza sativa L. Physiology and Molecular Biology of Plants. 23: 301-309.
  • Suriya-arunroj D, Supapoj N, Toojinda T, Vanavichit A (2004). Relative leaf water content as an efficient method for evaluating rice cultivars for tolerance to salt stress. Science Asia 30: 411-415.
  • Suzuki T, Honda Y and Mukasa Y (2005). Effects of UV-B radiation, cold and desiccation stress on rutin concentration and rutin glucosidase activity in tartary buckwheat (Fagopyrum tataricum) leaves. Plant Science 168(5): 1303-1307.
  • Suzuki T, Morishita T, KIM SJ, Park SU, Woo SH, Noda T, Takigawa S (2015). Physiological roles of rutin in the buckwheat plant. Japan Agricultural Research Quarterly: JARQ 49(1): 37-43.
  • Taiz L, Zeiger E (2008). Plant Physiology. Ankara: Palme Publishing.
  • Urbanek H, Kuzniak-Gebarowska E, Herka K (1991). Elicitation of defence responses in bean leaves by Botrytis cinerea polygalacturonase. Acta Physiologiae Plantarum 13.
  • Velikova V, Yordanov I, Edreva A (2000). Oxidative stress and some antioxidant systems in acid rain-treated bean plants: protective role of exogenous polyamines. Plant science 151: 59-66.
  • Wei TL, Wang Y, Liu JH (2020). Comparative transcriptome analysis reveals synergistic and disparate defense pathways in the leaves and roots of trifoliate orange (Poncirus trifoliata) autotetraploids with enhanced salt tolerance. Horticulture Research 7: 88.
  • Yang J, Guo J, Yuan J (2008). In vitro antioxidant properties of rutin. Lebensm. Wiss Technology 41: 1060-1066.
  • Yu ZP, Duan XB, Luo L, Dai SJ, Ding ZJ, Xia GM (2020). How plant hormones mediate salt stress responses. Trends in Plant Science 25: 1117-1130.
  • Zelm EV, Zhang YX, Testerink C (2020). Salt tolerance mechanisms of plants. Annual Review Plant Biology 71:403-433.
  • Zhong M, Song R, Wang Y, Shu S, Sun J, Guo SR (2020). TGase regulates salt stress tolerance through enhancing bound polyaminesmediated antioxidant enzymes activity in tomato. Environmental and Experimental Botany 179: 104191.
  • Zhu JK (2016). Abiotic stress signaling and responses in plants. Cell 167: 313-324.
There are 58 citations in total.

Details

Primary Language English
Subjects Plant Physiology
Journal Section Articles
Authors

Asiye Sezgin Muslu 0000-0003-0899-0742

Early Pub Date February 23, 2024
Publication Date May 15, 2024
Submission Date November 8, 2023
Acceptance Date January 3, 2024
Published in Issue Year 2024 Volume: 8 Issue: 1

Cite

APA Sezgin Muslu, A. (2024). Improving salt stress tolerance in Zea mays L. by modulating osmolytes accumulation and antioxidant capacity with Rutin. Anatolian Journal of Botany, 8(1), 21-29. https://doi.org/10.30616/ajb.1387695
AMA Sezgin Muslu A. Improving salt stress tolerance in Zea mays L. by modulating osmolytes accumulation and antioxidant capacity with Rutin. Ant J Bot. May 2024;8(1):21-29. doi:10.30616/ajb.1387695
Chicago Sezgin Muslu, Asiye. “Improving Salt Stress Tolerance in Zea Mays L. By Modulating Osmolytes Accumulation and Antioxidant Capacity With Rutin”. Anatolian Journal of Botany 8, no. 1 (May 2024): 21-29. https://doi.org/10.30616/ajb.1387695.
EndNote Sezgin Muslu A (May 1, 2024) Improving salt stress tolerance in Zea mays L. by modulating osmolytes accumulation and antioxidant capacity with Rutin. Anatolian Journal of Botany 8 1 21–29.
IEEE A. Sezgin Muslu, “Improving salt stress tolerance in Zea mays L. by modulating osmolytes accumulation and antioxidant capacity with Rutin”, Ant J Bot, vol. 8, no. 1, pp. 21–29, 2024, doi: 10.30616/ajb.1387695.
ISNAD Sezgin Muslu, Asiye. “Improving Salt Stress Tolerance in Zea Mays L. By Modulating Osmolytes Accumulation and Antioxidant Capacity With Rutin”. Anatolian Journal of Botany 8/1 (May 2024), 21-29. https://doi.org/10.30616/ajb.1387695.
JAMA Sezgin Muslu A. Improving salt stress tolerance in Zea mays L. by modulating osmolytes accumulation and antioxidant capacity with Rutin. Ant J Bot. 2024;8:21–29.
MLA Sezgin Muslu, Asiye. “Improving Salt Stress Tolerance in Zea Mays L. By Modulating Osmolytes Accumulation and Antioxidant Capacity With Rutin”. Anatolian Journal of Botany, vol. 8, no. 1, 2024, pp. 21-29, doi:10.30616/ajb.1387695.
Vancouver Sezgin Muslu A. Improving salt stress tolerance in Zea mays L. by modulating osmolytes accumulation and antioxidant capacity with Rutin. Ant J Bot. 2024;8(1):21-9.

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