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Exogenous application of nitric oxide and thiourea regulates on growth and some key physiological processes in maize (Zea mays L.) plants under saline stress.

Year 2015, Special Issue, 61 - 66, 31.01.2015
https://doi.org/10.21657/tsd.36165

Abstract

Effect of exogenously applied nitric oxide (NO) and thiourea (TU) in combination was examined in
maize plants under saline stress. Seedlings of two maize cultivars (DK 5783 and Apex 836) were grown
in pots containing soil salinized with 0 or 100 mM NaCl dissolved in irrigation water. Two levels of NO
+ TU (3 + 400 or 6 + 500 mg/L) were applied as presowing seed treatment or through leaves of 10-day
old maize seedlings. Saline stress significantly suppressed plant fresh biomass, leaf water potential and
chlorophyll content, but increased electrolyte leakage in both cultivars. However, these reductions were
higher in Apex 836 than those in Dk 5783. Both treatments of combined NO and TU as seed soaking
or foliar application were effective in mitigating the adverse effects of saline stress on shoot growth. Seed
treatments of both levels of combined NO and TU were more effective in terms of improvement in fresh
weights of DK 5783 than foliar treatments. Leaf Na+ contents increased whereas those of N and P
decreased in maize plants under saline regime. Application of Both modes of treatment of combined
NO and TU increased the contents of N and P, but decreased that NO and TU through both modes
increased Na+ in salt stressed maize plants. The results of the present study indicate that application of
NO and TU compounds in combination alleviated the detrimental effects of salinity and increased
resistance to salinity in the maize plants by improving plant growth

References

  • Agastian, P., Kingsley, S.J., Vivekanandan, M., 2000. Effect of salinity on photosynthesis and biochemical characteristics in mulberry genotypes. Photosynthetica 38, 287–290.
  • Arshadullah, M., Rasheed, M., Zaidi, S.A.R., 2011. Salt tolerance of different rice cultivars for their salt tolerance under salt-affected soils. Int. Res. J. Agri. Sci. Soil Sci. 1, 183- 184
  • Bashir, F., Ali, M., Hussain, K., Majeed, A., Nawaz, K,. 2011. Morphological variations in sorghum (Sorghum bicolor L.) under different levels of Na2SO4 salinity. Bot. Res. Int. 4, 1-3
  • Beligni, M.V., Lamattina, L., 2001. Nitric oxide: A non- traditional regulator of plant growth. Trends Plant Sci. 6, 508–509.
  • Crawford, N.M., Guo, F.Q., 2005. New insights into nitric oxide metabolism and regulatory functions. Trends Plant Sci. 10, 195–200.
  • Delledonne, M., 2005. NO news is good news for plants, Curr. Opin. Plant Biol. 8, 1–7
  • Beligni, M.V., Lamattina, L., 2000. Nitric oxide stimulates seed germination and de-etiolation, and inhibits hypocotyl elongation, three light-inducible responses in plants. Planta 210,215–221.
  • Chapman, H.D., Pratt, P.F., 1982. Methods of Plant Analysis. I. Methods of analysis for soils, plants and water. Riverside, CA: Chapman Publishers.
  • Chen, C.T., Li, C.C., Kao, C.H., 1991. Senescence of rice leaves XXXI. Changes of chlorophyll, protein and polyamine contents and ethylene production during senescence of a chlorophyll-deficient mutant. J. Plant Growth Reg. 10, 201- 205
  • Delledonne, M., 2005. NO news is good news for plants. Curr. Opin. Plant Biol. 8, 1–7.
  • Dhindsa, R.S., Plumb-Dhindsa, P., Thorpe, T.A., 1981. Leaf senescence correlated with increased levels of membrane permeability and lipid peroxidation, and decreased levels of superoxide dismutase and catalase. J. Exp. Bot. 32, 93-101
  • Dionisio-Sese, M.L., Tobita, S., 1998. Antioxidant responses of rice seedlings to salinity stress. Plant Sci. 135, 1- 9
  • Durner, J., Klessig, D.F., 1999. Nitric oxide as a signal in plants, Curr. Opin. Plant Biol. 2, 369–374
  • Farooq, M., Basra, S.M.A., Wahid, A., Rehman, H., 2009. Exogenously applied nitric oxide enhances the drought tolerance in fine grain aromatic rice (Oryza sativa L.). J. Agron. Crop Sci. 14, 220-225
  • Gadallah, M.A.A., 1999. Effects of proline and glycinebetaine on Vicia faba response to salt stress. Biol. Plant. 42, 249–257.
  • Garc´ıa-Mata, C., Lamattina, L., 2001. Nitric oxide induces stomatal closure and enhances the adaptive plant responses against drought stress. Plant Physiol. 126, 1196– 1204
  • Hernandez, J.A., Olmos, E., Corpas, F.J., Sevilla, F., del Rio, L.A., 1995. Salt-induced oxidative stress in chloroplasts of pea plants. Plant Sci. 105, 151–167.
  • Hu, X.S., Neill, J., Tang, Z., Cai, W., 2005. Nitric oxide mediates gravitropic bending in soybean roots. Plant Physiol. 137, 663-670.
  • Hussain, K., Ashraf, M., Ashraf, M.Y., 2008. Relationship between growth and ion relation in pearl millet (Pennisetum glaucum L.) at different growth stages under salt stress. Afr. J. Plant Sci. 2, 23-27
  • Kausar F., Shahbaz, M. 2013. Interactive effect of foliar application of nitric oxide and salinity on wheat (Triticum aestivum). Pak. J. Bot. 45, 67-73
  • Kaya, C., Kirnak, H., Higgs, D., 2001. Enhancement of growth and normal growth parameters by foliar application of potassium and phosphorus in tomato cultivars grown at high (NaCl) salinity. J. Plant Nutr. 24, 357-367
  • Munns, R, Tester, M., 2008. Mechanisms of salinity
  • tolerance. Annu. Rev. Plant Biol. 59, 651-681
  • Naidu, B.P., Williams, R., 2004. Seed treatment and foliar application of osmoprotectants to increase crop establishment and cold tolerance at flowering in rice. A Report of the Rural Industries Research and Development Corporation Project No. CST-2A. CSIRO Tropical Agriculture, Brisbane
  • Pagnussat, G.C., Lanteri, M.L., Lamattina, L., 2003. Nitric oxide and cyclic GMP are messengers in the indole acetic acid-induced adventitious rooting process. Plant Physiol. 132, 1241–1248.
  • Perveen, S., Shahbaz, M., Ashraf, M., 2011. Modulation in activities of antioxidant enzymes in salt stressed and nonstressed wheat (Tritcum aestivum L.) plants raised from seed treated with tricontanol. Pak. J. Bot. 43, 2463-2468.
  • Perveen, S., Shahbaz, M., Ashraf, M., 2012. Changes in mineral composition, uptake and use efficiency of salt stressed wheat (Triticum aestivum L.) plants raised from seed treated with triacontanol. Pak. J. Bot. 44, 27-35
  • Quan, R., Shang, M., Zhang, H., Zhao, Y., Zhang, J., 2004. Engineering of enhanced glycine betaine synthesis improves drought tolerance in maize. Plant Biotech J 2, 477–486
  • Sabater, B., Rodriguez, M.T., 1978. Control of chlorophyll degradation in detached leaves of barley and oat through effect of kinetin on chlorophyllase. Physiol. Plant. 43, 274-276.
  • Sahu, M.P., Singh, D., 1995. Role of thiourea in improving productivity of wheat (Triticum aestivum L.). Plant Growth Regul. 14, 169-173
  • Sahu, M.P., Solanki, N.S., Dashora, L.N., 1993. Effects of thiourea, thiamine and ascorbic acid on growth and yield of maize (Zea mays L.). J. Agron. Crop Sci. 171, 65-69
  • Sahu, M.P., Solanki, N.S., 1991. Role of sulphydryl compounds in improving dry matter partitioning and grain production of maize (Zea mays L.). J. Agron. Crop Sci. 167, 356-359.
  • Shi, S.Y., Wang, G., Wang, Y.D., Zhang, L.A., Zhang, L.X., 2005. Protective effect of nitric oxide against oxidative stress under ultraviolet-B radiation, Nitric Oxide, 13, 1–9.
  • Srivastava, A.K., Ramaswamy, N.K., Suprasanna, P., D'Souza, S. F., 2010. Genome-wide analysis of thiourea- modulated salinity stress responsive transcripts in seeds of Brassica juncea: identification of signalling and effector components of stress tolerance. Ann. Bot.106, 663-674
  • Strain, H.H., Svec, W.A., 1966. In: The chlorophylls, Vernon, L.P. and Seely, S.R. (eds), Acad. Press, New York. pp. 21.
  • Wu, X., Zhu, W., Zhang, H., Ding, H., Zhang, H.J., 2011. Exogenous nitric oxide protects against salt-induced oxidative stress in the leaves from two genotypes of tomato (Lycopersicon esculentum Mill.). Acta Physiol. Plant. 33, 1199-1209.
  • Yasseen, B.T., 1983. An analysis of the effects of salinity on leaf growth in Mexican wheats. UK, The University of Leeds. Ph. D. thesis.
  • Zhang, Y.Y., Liu, J., Liu, Y.L., 2004. Nitric oxide alleviates growth inhibition of maize seedlings under salt stress. J.Plant Physiol. Mol. Biol. 30, 455-459

Exogenous application of nitric oxide and thiourea regulates on growth and some key physiological processes in maize (Zea mays L.) plants under saline stress.

Year 2015, Special Issue, 61 - 66, 31.01.2015
https://doi.org/10.21657/tsd.36165

Abstract

Effect of exogenously applied nitric oxide (NO) and thiourea (TU) in combination was examined in
maize plants under saline stress. Seedlings of two maize cultivars (DK 5783 and Apex 836) were grown
in pots containing soil salinized with 0 or 100 mM NaCl dissolved in irrigation water. Two levels of NO
+ TU (3 + 400 or 6 + 500 mg/L) were applied as presowing seed treatment or through leaves of 10-day
old maize seedlings. Saline stress significantly suppressed plant fresh biomass, leaf water potential and
chlorophyll content, but increased electrolyte leakage in both cultivars. However, these reductions were
higher in Apex 836 than those in Dk 5783. Both treatments of combined NO and TU as seed soaking
or foliar application were effective in mitigating the adverse effects of saline stress on shoot growth. Seed
treatments of both levels of combined NO and TU were more effective in terms of improvement in fresh
weights of DK 5783 than foliar treatments. Leaf Na+ contents increased whereas those of N and P
decreased in maize plants under saline regime. Application of Both modes of treatment of combined
NO and TU increased the contents of N and P, but decreased that NO and TU through both modes
increased Na+ in salt stressed maize plants. The results of the present study indicate that application of
NO and TU compounds in combination alleviated the detrimental effects of salinity and increased
resistance to salinity in the maize plants by improving plant growth

References

  • Agastian, P., Kingsley, S.J., Vivekanandan, M., 2000. Effect of salinity on photosynthesis and biochemical characteristics in mulberry genotypes. Photosynthetica 38, 287–290.
  • Arshadullah, M., Rasheed, M., Zaidi, S.A.R., 2011. Salt tolerance of different rice cultivars for their salt tolerance under salt-affected soils. Int. Res. J. Agri. Sci. Soil Sci. 1, 183- 184
  • Bashir, F., Ali, M., Hussain, K., Majeed, A., Nawaz, K,. 2011. Morphological variations in sorghum (Sorghum bicolor L.) under different levels of Na2SO4 salinity. Bot. Res. Int. 4, 1-3
  • Beligni, M.V., Lamattina, L., 2001. Nitric oxide: A non- traditional regulator of plant growth. Trends Plant Sci. 6, 508–509.
  • Crawford, N.M., Guo, F.Q., 2005. New insights into nitric oxide metabolism and regulatory functions. Trends Plant Sci. 10, 195–200.
  • Delledonne, M., 2005. NO news is good news for plants, Curr. Opin. Plant Biol. 8, 1–7
  • Beligni, M.V., Lamattina, L., 2000. Nitric oxide stimulates seed germination and de-etiolation, and inhibits hypocotyl elongation, three light-inducible responses in plants. Planta 210,215–221.
  • Chapman, H.D., Pratt, P.F., 1982. Methods of Plant Analysis. I. Methods of analysis for soils, plants and water. Riverside, CA: Chapman Publishers.
  • Chen, C.T., Li, C.C., Kao, C.H., 1991. Senescence of rice leaves XXXI. Changes of chlorophyll, protein and polyamine contents and ethylene production during senescence of a chlorophyll-deficient mutant. J. Plant Growth Reg. 10, 201- 205
  • Delledonne, M., 2005. NO news is good news for plants. Curr. Opin. Plant Biol. 8, 1–7.
  • Dhindsa, R.S., Plumb-Dhindsa, P., Thorpe, T.A., 1981. Leaf senescence correlated with increased levels of membrane permeability and lipid peroxidation, and decreased levels of superoxide dismutase and catalase. J. Exp. Bot. 32, 93-101
  • Dionisio-Sese, M.L., Tobita, S., 1998. Antioxidant responses of rice seedlings to salinity stress. Plant Sci. 135, 1- 9
  • Durner, J., Klessig, D.F., 1999. Nitric oxide as a signal in plants, Curr. Opin. Plant Biol. 2, 369–374
  • Farooq, M., Basra, S.M.A., Wahid, A., Rehman, H., 2009. Exogenously applied nitric oxide enhances the drought tolerance in fine grain aromatic rice (Oryza sativa L.). J. Agron. Crop Sci. 14, 220-225
  • Gadallah, M.A.A., 1999. Effects of proline and glycinebetaine on Vicia faba response to salt stress. Biol. Plant. 42, 249–257.
  • Garc´ıa-Mata, C., Lamattina, L., 2001. Nitric oxide induces stomatal closure and enhances the adaptive plant responses against drought stress. Plant Physiol. 126, 1196– 1204
  • Hernandez, J.A., Olmos, E., Corpas, F.J., Sevilla, F., del Rio, L.A., 1995. Salt-induced oxidative stress in chloroplasts of pea plants. Plant Sci. 105, 151–167.
  • Hu, X.S., Neill, J., Tang, Z., Cai, W., 2005. Nitric oxide mediates gravitropic bending in soybean roots. Plant Physiol. 137, 663-670.
  • Hussain, K., Ashraf, M., Ashraf, M.Y., 2008. Relationship between growth and ion relation in pearl millet (Pennisetum glaucum L.) at different growth stages under salt stress. Afr. J. Plant Sci. 2, 23-27
  • Kausar F., Shahbaz, M. 2013. Interactive effect of foliar application of nitric oxide and salinity on wheat (Triticum aestivum). Pak. J. Bot. 45, 67-73
  • Kaya, C., Kirnak, H., Higgs, D., 2001. Enhancement of growth and normal growth parameters by foliar application of potassium and phosphorus in tomato cultivars grown at high (NaCl) salinity. J. Plant Nutr. 24, 357-367
  • Munns, R, Tester, M., 2008. Mechanisms of salinity
  • tolerance. Annu. Rev. Plant Biol. 59, 651-681
  • Naidu, B.P., Williams, R., 2004. Seed treatment and foliar application of osmoprotectants to increase crop establishment and cold tolerance at flowering in rice. A Report of the Rural Industries Research and Development Corporation Project No. CST-2A. CSIRO Tropical Agriculture, Brisbane
  • Pagnussat, G.C., Lanteri, M.L., Lamattina, L., 2003. Nitric oxide and cyclic GMP are messengers in the indole acetic acid-induced adventitious rooting process. Plant Physiol. 132, 1241–1248.
  • Perveen, S., Shahbaz, M., Ashraf, M., 2011. Modulation in activities of antioxidant enzymes in salt stressed and nonstressed wheat (Tritcum aestivum L.) plants raised from seed treated with tricontanol. Pak. J. Bot. 43, 2463-2468.
  • Perveen, S., Shahbaz, M., Ashraf, M., 2012. Changes in mineral composition, uptake and use efficiency of salt stressed wheat (Triticum aestivum L.) plants raised from seed treated with triacontanol. Pak. J. Bot. 44, 27-35
  • Quan, R., Shang, M., Zhang, H., Zhao, Y., Zhang, J., 2004. Engineering of enhanced glycine betaine synthesis improves drought tolerance in maize. Plant Biotech J 2, 477–486
  • Sabater, B., Rodriguez, M.T., 1978. Control of chlorophyll degradation in detached leaves of barley and oat through effect of kinetin on chlorophyllase. Physiol. Plant. 43, 274-276.
  • Sahu, M.P., Singh, D., 1995. Role of thiourea in improving productivity of wheat (Triticum aestivum L.). Plant Growth Regul. 14, 169-173
  • Sahu, M.P., Solanki, N.S., Dashora, L.N., 1993. Effects of thiourea, thiamine and ascorbic acid on growth and yield of maize (Zea mays L.). J. Agron. Crop Sci. 171, 65-69
  • Sahu, M.P., Solanki, N.S., 1991. Role of sulphydryl compounds in improving dry matter partitioning and grain production of maize (Zea mays L.). J. Agron. Crop Sci. 167, 356-359.
  • Shi, S.Y., Wang, G., Wang, Y.D., Zhang, L.A., Zhang, L.X., 2005. Protective effect of nitric oxide against oxidative stress under ultraviolet-B radiation, Nitric Oxide, 13, 1–9.
  • Srivastava, A.K., Ramaswamy, N.K., Suprasanna, P., D'Souza, S. F., 2010. Genome-wide analysis of thiourea- modulated salinity stress responsive transcripts in seeds of Brassica juncea: identification of signalling and effector components of stress tolerance. Ann. Bot.106, 663-674
  • Strain, H.H., Svec, W.A., 1966. In: The chlorophylls, Vernon, L.P. and Seely, S.R. (eds), Acad. Press, New York. pp. 21.
  • Wu, X., Zhu, W., Zhang, H., Ding, H., Zhang, H.J., 2011. Exogenous nitric oxide protects against salt-induced oxidative stress in the leaves from two genotypes of tomato (Lycopersicon esculentum Mill.). Acta Physiol. Plant. 33, 1199-1209.
  • Yasseen, B.T., 1983. An analysis of the effects of salinity on leaf growth in Mexican wheats. UK, The University of Leeds. Ph. D. thesis.
  • Zhang, Y.Y., Liu, J., Liu, Y.L., 2004. Nitric oxide alleviates growth inhibition of maize seedlings under salt stress. J.Plant Physiol. Mol. Biol. 30, 455-459
There are 38 citations in total.

Details

Primary Language English
Journal Section Articles
Authors

Cengiz Kaya

Osman Sönmez This is me

Muhammed Ashraf This is me

Tahir Polat This is me

Levent Tuna This is me

Salih Aydemir This is me

Publication Date January 31, 2015
Published in Issue Year 2015 Special Issue

Cite

APA Kaya, C., Sönmez, O., Ashraf, M., Polat, T., et al. (2015). Exogenous application of nitric oxide and thiourea regulates on growth and some key physiological processes in maize (Zea mays L.) plants under saline stress. Toprak Su Dergisi61-66. https://doi.org/10.21657/tsd.36165
AMA Kaya C, Sönmez O, Ashraf M, Polat T, Tuna L, Aydemir S. Exogenous application of nitric oxide and thiourea regulates on growth and some key physiological processes in maize (Zea mays L.) plants under saline stress. SWJ. Published online January 1, 2015:61-66. doi:10.21657/tsd.36165
Chicago Kaya, Cengiz, Osman Sönmez, Muhammed Ashraf, Tahir Polat, Levent Tuna, and Salih Aydemir. “) Plants under Saline Stress”. Toprak Su Dergisi, January (January 2015), 61-66. https://doi.org/10.21657/tsd.36165.
EndNote Kaya C, Sönmez O, Ashraf M, Polat T, Tuna L, Aydemir S (January 1, 2015) Exogenous application of nitric oxide and thiourea regulates on growth and some key physiological processes in maize (Zea mays L.) plants under saline stress. Toprak Su Dergisi 61–66.
IEEE C. Kaya, O. Sönmez, M. Ashraf, T. Polat, L. Tuna, and S. Aydemir, “) plants under saline stress”., SWJ, pp. 61–66, January 2015, doi: 10.21657/tsd.36165.
ISNAD Kaya, Cengiz et al. “) Plants under Saline Stress”. Toprak Su Dergisi. January 2015. 61-66. https://doi.org/10.21657/tsd.36165.
JAMA Kaya C, Sönmez O, Ashraf M, Polat T, Tuna L, Aydemir S. Exogenous application of nitric oxide and thiourea regulates on growth and some key physiological processes in maize (Zea mays L.) plants under saline stress. SWJ. 2015;:61–66.
MLA Kaya, Cengiz et al. “) Plants under Saline Stress”. Toprak Su Dergisi, 2015, pp. 61-66, doi:10.21657/tsd.36165.
Vancouver Kaya C, Sönmez O, Ashraf M, Polat T, Tuna L, Aydemir S. Exogenous application of nitric oxide and thiourea regulates on growth and some key physiological processes in maize (Zea mays L.) plants under saline stress. SWJ. 2015:61-6.

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Kapak Tasarım : Hüseyin Oğuzhan BEŞEN
Grafik Tasarım : Filiz ERYILMAZ
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