Exogenously applied nitric oxide confers tolerance to salinity-induced oxidativestress in two maize (Zea mays L.) cultivars differing in salinity tolerance

Abstract: A glasshouse study was conducted to examine the ameliorative effects of exogenously applied nitric oxide (NO) on salinity-induced oxidative defense mechanisms and some vital metabolic attributes in two maize cultivars differing in salinity tolerance. It also aimed to compare the effects of two different modes of NO application on different parameters of plants grown under a saline regime. Two maize cultivars, namely DK 5783 (salt-tolerant) and Apex 836 (salt-sensitive), were subjected to saline stress, and two levels of NO were applied as presowing or foliage spray. Saline stress caused significant suppression in total fresh and dry biomass, maximum fluorescence yield (Fv/Fm), leaf water potential, and total chlorophylls (a + b) in the plants of both maize cultivars. On the other hand, it increased leaf osmotic pressure, proline accumulation, hydrogen peroxide (H2O2) and malondialdehyde (MDA) concentrations, membrane permeability, and the activities of some key antioxidant enzymes, peroxidase (POD), superoxide dismutase (SOD), and catalase (CAT). Exogenously applied NO in both modes partly alleviated the adverse effects of salinity on plants of both maize cultivars. In most cases there seemed to be no difference between seed and foliar application of NO in alleviating the adverse effects of salt stress on maize plants. NO partially improved salt tolerance of maize plants; it reduced Na+ but increased N, K+, Ca2+, and P in the maize plants under saline regimes. The NO treatment conferred enhanced tolerance to salinity by reducing MDA and H2O2 levels and antioxidant enzymes such as SOD, CAT, and POD, as well as enhancing photosynthetic pigments under salinity stress.

Exogenously applied nitric oxide confers tolerance to salinity-induced oxidativestress in two maize (Zea mays L.) cultivars differing in salinity tolerance

Abstract: A glasshouse study was conducted to examine the ameliorative effects of exogenously applied nitric oxide (NO) on salinity-induced oxidative defense mechanisms and some vital metabolic attributes in two maize cultivars differing in salinity tolerance. It also aimed to compare the effects of two different modes of NO application on different parameters of plants grown under a saline regime. Two maize cultivars, namely DK 5783 (salt-tolerant) and Apex 836 (salt-sensitive), were subjected to saline stress, and two levels of NO were applied as presowing or foliage spray. Saline stress caused significant suppression in total fresh and dry biomass, maximum fluorescence yield (Fv/Fm), leaf water potential, and total chlorophylls (a + b) in the plants of both maize cultivars. On the other hand, it increased leaf osmotic pressure, proline accumulation, hydrogen peroxide (H2O2) and malondialdehyde (MDA) concentrations, membrane permeability, and the activities of some key antioxidant enzymes, peroxidase (POD), superoxide dismutase (SOD), and catalase (CAT). Exogenously applied NO in both modes partly alleviated the adverse effects of salinity on plants of both maize cultivars. In most cases there seemed to be no difference between seed and foliar application of NO in alleviating the adverse effects of salt stress on maize plants. NO partially improved salt tolerance of maize plants; it reduced Na+ but increased N, K+, Ca2+, and P in the maize plants under saline regimes. The NO treatment conferred enhanced tolerance to salinity by reducing MDA and H2O2 levels and antioxidant enzymes such as SOD, CAT, and POD, as well as enhancing photosynthetic pigments under salinity stress.

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  • Akram MS, Ashraf M, Akram NA (2009). Effectiveness of potassium sulfate in mitigating salt-induced adverse effects on different physio-biochemical attributes in sunflower (Helianthus annuus L.). Flora 204: 471–483.
  • Akram NA, Ashraf M (2013). Regulation in plant stress tolerance by a potential plant growth regulator, 5-aminolevulinic acid. J Plant Growth Regul 32: 663–679.
  • Akram NA, Ashraf M, Al-Qurainy F (2012). Aminolevulinic acid- induced changes in some key physiological attributes and activities of antioxidant enzymes in sunflower (Helianthus annuus L.) plants under saline regimes. Sci Hortic 142: 143– 148.
  • Ali Q, Ashraf M, Shahbaz M, Humera H (2008). Ameliorating effect of foliar applied proline on nutrient uptake in water stressed maize (Zea mays L.) plants. Pak J Bot 40: 211–219.
  • Ashraf M (2009). Biotechnological approach of improving plant salt tolerance using antioxidants as markers. Biotechnol Adv 27: 84–93.
  • Ashraf M, Foolad MR (2005). Pre-sowing seed treatment – a shotgun approach to improve germination, plant growth and crop yield under saline and non-saline conditions. Adv Agron 88: 225– 271.
  • Ashraf M, Foolad MR (2007). Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environ Exp Bot 59: 206–216.
  • Ashraf M, Harris PJC (2013). Photosynthesis under stressful environments: an overview. Photosynthetica 51: 163–190.
  • Athar HUR, Ashraf M, Wahid A, Jamil A (2009). Inducing salt tolerance in canola (Brassica napus L.) by exogenous application of glycinebetaine and proline: response at the initial growth stages. Pak J Bot 41: 1311–1319.
  • Bai XY, Dong YJ, Wang QH, Xu LL, Kong J, Liu S (2015). Effects of lead and nitric oxide on photosynthesis, antioxidative ability, and mineral element content of perennial ryegrass. Biol Plantarum 59: 163–170.
  • Bates LS, Waldren RP, Teare ID (1973). Rapid determination of free proline for water-stress studies. Plant Soil 39: 205–207.
  • Batool N, Shahzad A, Ilyas N, Noor T (2014). Plants and salt stress. Int J Agric Crop Sci 7: 582–589.
  • Beauchamp C, Fridovich I (1971). Superoxide dismutase: Improved assays and an assay applicable to acrylamide gels. Anal Biochem 44: 276–287.
  • Besson-Bard A, Astier J, Rasul S, Wawer I, Dubreuil-Maurizi C, Jeandroz S, Wendehenne D (2009). Current view of nitric oxide-responsive genes in plants. Plant Sci 177: 302–309.
  • Bradford MM (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72: 248–254.
  • Calatayud A, Barreno E (2004). Response to ozone in two lettuce varieties on chlorophyll a fluorescence, photosynthetic pigments and lipid peroxidation. Plant Physiol Bioch 42: 549– 555.
  • Chance B, Maehly C (1955). Assay of catalase and peroxidases. Method Enzymol 2: 764–775.
  • Chapman HD, Pratt PF (1982). Methods of Analysis for Soils, Plants, and Waters. Riverside, CA, USA: Chapman Publishers.
  • Dionisio-Sese ML, Tobita S (1998). Antioxidant responses of rice seedlings to salinity stress. Plant Sci 135: 1–9.
  • Dong YJ, Jinc SS, Liu S, Xu LL, Kong J (2014). Effects of exogenous nitric oxide on growth of cotton seedlings under NaCl stress. J Soil Sci Plant Nutr 14: 1–13.
  • Fayez KA, Bazaid SA (2014). Improving drought and salinity tolerance in barley by application of salicylic acid and potassium nitrate. J Saudi Soc Agric Sci 13: 45–55.
  • Gupta B, Huang B (2014). Mechanism of salinity tolerance in plants: physiological, biochemical, and molecular characterization. Int J Gen 2014: 1–18.
  • Habib N, Ashraf M (2014). Effect of exogenously applied nitric oxide on water relations and ionic composition of rice (Oryza sativa L.) plants under salt stress. Pak J Bot 46: 111–116.
  • Habib N, Ashraf M, Ahmad MSA (2010). Enhancement in seed germinability of rice (Oryza sativa L.) by pre-sowing seed treatment with nitric oxide (NO) under salt stress. Pak J Bot 42: 4071–4078.
  • Habib N, Ashraf M, Shahbaz M (2013). Effect of exogenously applied nitric oxide on some key physiological attributes of rice (Oryza sativa L.) plants under salt stress. Pak J Bot 45: 1563–1569.
  • Hung KT, Chang CJ, Kao CH (2002). Paraquat toxicity is reduced by nitric oxide in rice leaves. J Plant Physiol 159: 159–166.
  • Kader MA, Lindberg S (2005). Uptake of sodium in protoplasts of salt-sensitive and salt-tolerant cultivars of rice, Oryza sativa L. determined by the fluorescent dye SBFI. J Exp Bot 56: 3149– 3158.
  • Kanwal H, Ashraf M, Hameed M (2013). Water relations and ionic composition in the seedlings of some newly developed and candidate cultivars of wheat (Triticum aestivum L.) under saline conditions. Pak J Bot 45: 1221–1227.
  • Kausar F, Shahbaz M (2013). Interactive effect of foliar application of nitric oxide (NO) and salinity on wheat (Triticum aestivum L.). Pak J Bot 45: 67–73.
  • Kausar F, Shahbaz M, Ashraf M (2013). Protective role of foliar- applied nitric oxide in Triticum aestivum under saline stress. Turk J Bot 37: 1155–1165.
  • Kaya C, Sonmez O, Aydemir S, Ashraf M, Dikilitas M (2013). Exogenous application of mannitol and thiourea regulates plant growth and oxidative stress responses in salt-stressed maize (Zea mays L.). J Plant Interact 8: 234–241.
  • Ke X, Cheng Z, Ma W, Gong M (2013). Nitric oxide enhances osmoregulation of tobacco (Nicotiana tobacam L.) cultured cells under phenylethanoid glycosides (PEG) 6000 stress by regulating proline metabolism. Afr J Biotechnol 12: 1257–1266.
  • Khan A, Ahmad MSA, Athar HUR, Ashraf M (2006). Interactive effect of foliarly applied ascorbic acid and salt stress on wheat (Triticum aestivum L.) at the seedling stage. Pak J Bot 38: 1407– 1414.
  • Khan MN, Siddiqui MH, Mohammad F, Naeem M (2012). Interactive role of nitric oxide and calcium chloride in enhancing tolerance to salt stress. Nitric Oxide 27: 210–218.
  • Kraus TE, Fletcher RA (1994). Paclobutrazol protects wheat seedlings from heat and paraquat injury. Is detoxification of active oxygen involved? Plant Cell Physiol 35: 45–52.
  • Loreto F, Velikova V (2001). Isoprene produced by leaves protects the photosynthetic apparatus against ozone damage, quenches ozone products, and reduces lipid peroxidation of cellular membranes. Plant Physiol 127: 1781–1787.
  • Liu S, Dong Y, Xu L, Kong J (2014). Effects of foliar applications of nitric oxide and salicylic acid on salt-induced changes in photosynthesis and antioxidative metabolism of cotton seedlings. Plant Growth Regul 73: 67–78.
  • Manai J, Gouia H, Corpas FJ (2014). Redox and nitric oxide homeostasis are affected in tomato (Solanum lycopersicum) roots under salinity-induced oxidative stress. J Plant Physiol 171: 1028–1035.
  • Miller GAD, Suzuki N, Ciftci-Yilmaz S, Mittler R (2010). Reactive oxygen species homeostasis and signalling during drought and salinity stresses. Plant Cell Environ 33: 453–467.
  • Muranaka S, Shimizu K, Kato M (2002). A salt-tolerant cultivar of wheat maintains photosynthetic activity by suppressing sodium uptake. Photosynthetica 40: 505–515.
  • Perveen S, Shahbaz M, Ashraf M (2013). Influence of foliar-applied triacontanol on growth, gas exchange characteristics, and chlorophyll fluorescence at different growth stages in wheat under saline conditions. Photosynthetica 51: 541–551.
  • Plaut Z, Edelstein M, Ben-Hur M (2013). Overcoming salinity barriers to crop production using traditional methods. Crit Rev Plant Sci 32: 250–291.
  • Ruan HH, Shen WB, Ye M, Xu L (2002). Protective effects of nitric oxide on salt stress-induced oxidative damages to wheat (Triticum aestivum) leaves. Chinese Sci Bull 47: 677–681.
  • Sabir P, Ashraf M (2007). Screening of local accession Panicum mliaceum for salt tolerance at the seedling stage using biomass production and ion accumulation as selection criteria. Pak J Bot 39: 1655–1661.
  • Saleem M, Ashraf M, Akram NA (2011). Salt (NaCl)-induced modulation in some key physio-biochemical attributes in okra (Abelmoschus esculentus L.). J Agron Crop Sci 197: 202–213.
  • Santos C, Campos A, Azevedo H, Caldeira G (2001). In situ and in vitro senescence induced by KCl stress: nutritional imbalance, lipid peroxidation and antioxidant metabolism. J Exp Bot 52: 351–360.
  • Shaheen S, Naseer S, Ashraf M, Akram NA (2012). Salt stress affects water relations, photosynthesis and oxidative defense mechanisms in Solanum melongena L. J Plant Interact 8: 85–96.
  • Siddiqui MH, Al-Whaibi MH, Basalah MO (2011). Role of nitric oxide in tolerance of plants to abiotic stress. Protoplasma 248: 447–455.
  • Strain HH, Svec WA (1966). Extraction, separation, estimation and isolation of the chlorophylls. In: Vernon LP, Seely GR, editors. The Chlorophylls. New York, NY, USA: Academic Press, pp. 21–65.
  • Sun BT, Jing Y, Chen KM, Song LL, Chen FJ, Zhang LX (2007). Protective effect of nitric oxide on iron deficiency-induced oxidative stress in maize (Zea mays). J Plant Physiol 164: 536– 543.
  • Tanou G, Filippou P, Belghazi M, Job D, Diamantidis G, Fotopoulos V, Molassiotis A (2012). Oxidative and nitrosative-based signaling and associated post-translational modifications orchestrate the acclimation of citrus plants to salinity stress. Plant J 72: 585–599.
  • Wang RG, Chen SL, Zhou XY, Shen X, Deng L, Zhu HJ, Shao J, Shi Y, Dai SX, Fritz E et al. (2008). Ionic homeostasis and reactive oxygen species control in leaves and xylem sap of two poplars subjected to NaCl stress. Tree Physiol 28: 947–957.
  • Weisany W, Sohrabi Y, Heidari G, Siosemardeh A, Ghassemi- Golezani K (2012). Changes in antioxidant enzymes activity and plant performance by salinity stress and zinc application in soybean (Glycine max L.). Plant Omics 5: 60–67.
  • Yan K, Chen P, Shao H, Zhao S, Zhang L, Zhang L, Xu G, Sun J (2012). Responses of photosynthesis and photosystem II to higher temperature and salt stress in sorghum. J Agron Crop Sci 198: 218–226.
  • Yang KY, Liu Y, Zhang S (2001). Activation of a mitogen activated protein kinase pathway is involved in disease resistance in tobacco. P Natl Acad Sci USA 98: 741–746.
  • Yildiztugay E, Ozfidan-Konakci C, Kucukoduk M (2014). Exogenous nitric oxide (as sodium nitroprusside) ameliorates polyethylene glycol-induced osmotic stress in hydroponically grown maize roots. J Plant Growth Regul 33: 683–696.
  • Zhang LP, Mehta SK, Liu ZP, Yang ZM (2008). Copper-induced proline synthesis is associated with nitric oxide generation in Chlamydomonas reinhardtii. Plant Cell Physiol 49: 411–419.
  • Zheng C, Jiang D, Liu F, Dai T, Liu W, Jing Q, Cao W (2009). Exogenous nitric oxide improves seed germination in wheat against mitochondrial oxidative damage induced by high salinity. Environ Exp Bot 67: 222–227.
Turkish Journal of Agriculture and Forestry-Cover
  • ISSN: 1300-011X
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
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