Hydrogen peroxide supplementation alleviates the deleterious effects of cadmium on photosynthetic pigments and oxidative stress and improves growth, yield and pods quality of pea (Pisum sativum L.) plants

• Autorzy: Sayed S. , Gadallah M.
• Języki publikacji: EN

Abstrakty

EN

The effects of foliar applied H₂O₂ on chlorophyll, carotenoids, the non-enzymatic defense system (ascorbic acid), malondialdehyde (MDA) hydrogen peroxide (H₂O₂) and growth were assessed in roots and shoots of pea (Pisum sativum L.) plants exposed to excess cadmium. In addition, we evaluated the influences of H₂O₂ spraying on proline, soluble sugars and soluble proteins contents. Excessive cadmium treatment caused reduction in the growth parameters (dry mass, pods and seeds dry weights), chlorophyll and carotenoids contents, roots total free amino acids, roots soluble sugars as well as shoots and roots soluble proteins levels but increased total free amino acids and soluble sugars contents in shoots. Concentrations of hydrogen peroxide and MDA was enhanced under Cd treatment. The foliar treatment of H₂O₂ alleviated the detrimental effects generated under Cd treatment that represented as increment in pea growth. H₂O₂ spraying increased photosynthetic pigments, growth characteristics, soluble proteins, and ascorbic acid contents comparing to the control sets not receiving H₂O₂. Similarly, a higher up-regulation was detected in proline contents of Cd + H₂O₂ set than Cd group ones at 0.25 mM Cd. Contrarily, malondialdehyde (MDA), soluble sugars and total free amino acids contents of Cd + H₂O₂ set revealed a lower decrease than Cd group ones especially in roots. The results demonstrated that H₂O₂ treatment could inverse the harmful effects of cadmium on growth, through inducing the non-enzymatic defense system (ascorbate), proline accumulation, maintenance of chlorophyll in pea leaves and lowering the intensity of H₂O₂ and lipid peroxidation (MDA).

• Wydawca: -
• Czasopismo: Acta Physiologiae Plantarum
• Rocznik: 2019
• Tom: 41
• Numer: 07
• Opis fizyczny: Article 113 [12p.], ref.

Twórcy

autor

Sayed S.

• Botany and Microbiology Department, Faculty of Science, Assiut University, Assiut 71516, Egypt

autor

Gadallah M.

• Botany and Microbiology Department, Faculty of Science, Assiut University, Assiut 71516, Egypt

Bibliografia

• Abdallah EF, Hashem A, Alqarawi AA, Alwathnani HA (2015) Alleviation of adverse impact of cadmium stress in sunflower (Helianthus annuus L.) by arbuscularmycorrhizal fungi. Pak J Bot 47:785–795
• Ahmad P, Sarwat M, Bhat NA, Wani MR, Kazi AG, Tran LP (2015) Alleviation of cadmium toxicity in Brassica juncea L (Czern & Coss) by calcium application involves various physiological and biochemical strategies. PLoS ONE 10(1):e0114571
• Alloway BJ (2013) Trace metals and metalloids in soils and their bioavailability. Environmental pollution, vol 22, 3rd edn. Springer, Dordrecht
• Ashraf M (2009) Biotechnological approach of improving plant salt tolerance using antioxidants as markers. Biotechnol Adv 27:84–93
• AzevedoNeto AD, Prisco JT, Enéas-Filho J, Medeiros JR, Gomes-Filho E (2005) Hydrogen peroxide pre-treatment induces salt-stress acclimation in maize plants. J Plant Physiol l 162:1114–1122
• Bai XJ, Liu LJ, Zhang CH, Ge Y, Cheng WD (2011) Effect of H₂O₂ pretreatment on Cd tolerance of different rice cultivars. Rice Sci 18:29–35
• Bates LS, Waldren RP, Teare ID (1973) Rapid determination of free proline for water stress studies. Plant Soil 39:205–207
• Bienert GP, Schjoerring JK, Jahn TP (2006) Membrane transport of hydrogen peroxide. Biochim Biophys Acta 1758:994–1003
• Blokhina O, Virolainen E, Fagerstedt V (2003) Antioxidants, oxidative damage and oxygen deprivation stress. A review. Ann Bot 91:179–194
• Burzynski M, Migocka M, Klobus G (2005) Cu and Cd transport in cucumber (Cucumis sativus L.) root plasma membranes. Plant Sci 168:1609–1614
• Chakraborty K, Sairam RK, Bhattacharya RC (2012) Differential expression of salt overly sensitive pathway genes determines salinity stress tolerance in Brassica genotypes. Plant Physiol Biochem 51:90–101
• Charest C, Phan CT (1990) Cold acclimation of wheat (Triticum aestivum) properties of enzymes involved in proline metabolism. Physiol Plant 80:159–168
• Clemens S, Aarts MG, Thomine S, Verbruggen N (2013) Plant science: the key to preventing slow cadmium poisoning. Trends Plant Sci 18(2):92–99
• DalCorso G, Farinati S, Maistri S, Furini A (2008) How plants cope with cadmium: staking all on metabolism and gene expression. J Integr Plant Biol 50:1268–1280
• Down RJ, Hellmers H (1975) Environment and experimental control of plant growth. Acad Press, London, New York, San Francisco, p 145
• Dubois M, Gilles KA, Hamilton JK, Rabers PA, Smith F (1956) Colorimetric method for the determination of sugars and related substances. Anal Chem 28:350–356
• Duncan DB (1955) Multiple ranges and multiple F-test. Biometrics 11:1–42
• Gadallah MAA (1995) Effect of cadmium and kinetin on chlorophyll content, saccharides and dry matter accumulation in sunflower plants. Biol Plant 37:233–240
• Gadallah MAA (1999) Effects of proline and glycinebetaine on Vicia faba responses to salt stress. Biol Plant 42:249–257
• Gadallah MAA, Sayed SA (2014) Impacts of different water pollution sources on antioxidant defense ability in three aquatic macrophytes in Assiut Province, Egypt. J Stress Physiol Biochem 10:47–61
• Gill M (2014) Heavy metal stress in plants: a review. Int J Adv Res 2(1043):1055
• Gill SS, Tuteja N (2010) Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem 48:909–930
• Gondim FA, Gomes-Filho E, Lacerda CF, PriscoJ T, André D, AzevedoNetoA D, Marques EC (2010) Pretreatment with H₂O₂ in maize seeds: effects on germination and seedling acclimation to salt stress. Braz J Plant Physiol 22:103–112
• Gondium FA, Miranda RD, Gomes-Filho E, Prisco JT (2013) Enhanced salt tolerance in maize plants induced by H₂O₂ leaf spraying is associated with improved gas exchange rather than with non-enzymatic antioxidant system. Theor Exp Plant Physiol 25(4):251–260
• Gong M, Chen B, Li ZG, Guo LH (2001) Heat-shock-induced cross adaptation to heat, chilling, drought and salt in maize seedlings and involvement of H₂O₂. J Plant Physiol 158:1125–1130
• Groppa MD, Ianuzzo MP, Rosales EP, Vazquez SC, Benavides MP (2012) Cadmium modulates NADPH oxidase activity and expression in sunflower leaves. Biol Plant 56:167–171
• Guzel S, Terzi R (2013) Exogenous hydrogen peroxide increases dry matter production, mineral content and level of osmotic solutes in young maize leaves and alleviates deleterious effects of copper stress. Bot Stud 54:26
• Hasanuzzaman M, Nahar K, Gill SS, Alharby HF, Razafindrabe BHN, Fujita M (2017) Hydrogen peroxide pretreatment mitigates cadmium-induced oxidative stress in Brassica napus L.: an intrinsic study on antioxidant defense and glyoxalase systems. Front Plant Sci 8(115):1–10
• Hooda PS (ed) (2010) Trace elements in soils. Wiley, Chichester
• Hossain MA, Bhattacharjee S, Armin SM, Qian P, Xin W, Li Hong-Yu, Burritt DJ, Fujita M, Tran L-SP (2015) Hydrogen peroxide priming modulates abiotic oxidative stress tolerance: insights from ROS detoxification and scavenging. Front Plant Sci 6:1–19
• Hu Y, Ge Y, Zhang C, Ju T, Cheng W (2009) Cadmium toxicity and translocation in rice seedlings are reduced by hydrogen peroxide pretreatment. Plant Growth Reg 59:51–61
• Hyat S, Hayat Q, Alyemeni MN, Ahmad A (2013) Proline enhances antioxidative enzyme activity, photosynthesis and yield of Cicer arietinum L. exposed to cadmium stress. Acta Bot Croat 72:323–335
• Ismail SZ, Khandaker MM, Mat N, Boyce AN (2015) Effects of hydrogen peroxide on growth, development and quality of fruits: a review. J Agron 14(4):331–336
• Jackson ML (1967) Soil chemical analysis. New Delhi, Prentice-Hall of India, Private limited New Delhi, p 498
• Jali P, Pradhan C, Das AB (2016) Effects of cadmium toxicity in plants: a review article. Sch Acad J Biosci 4(12):1074–1081
• Kabta-Pendias A (2011) Trace elements in soils and plants. CRC Press, Taylor and Francis Group, Boca Raton
• Khan DM, Mei L, Ali B, Chen Y, Cheng X, Zhu SJ (2013) Cadmium-induced up regulation of lipid peroxidation and reactive oxygen species caused physiological, biochemical, and ultrastructural changes in upland cotton seedlings. Bio Med Res Int 2013:10
• Khan A, Anwar Y, Hasan MM, Iqbal A, Ali M, Alharby HF, Hakeem KR, Hasanuzzaman M (2017) Attenuation of drought stress in Brassica seedlings with exogenous application of Ca²⁺ and H₂O₂. Plants 6(2):20
• Khandaker M, Boyce AN, Osman N (2012) The influence of hydrogen peroxide on the growth, development and quality of wax apple (Syzygium samarangense, [Blume] Merrill and L.M. Perry var. jambumadu) fruits. Plant Physiol Biochem 53:101–110
• Lee YP, Takahashi T (1966) An improved colorimetric determination of amino acids with the use of ninhydrin. Anal Biochem 14:71–77
• Lin Q, Chen Y, Wang Z, Wang Y (2004) Study on the possibility of hydrogen peroxide pretreatment and plant system to remediate soil pollution. Chemosphere 57:1439–1447
• Lowry OH, Resbrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the folin–phenol reagent. J Biol Chem 193:265–275
• MadhavaRao KV, Sresty TV (2000) Antioxidative parameters in the seedlings of pigeonpea (Cajanus cajan (L.) Millspaugh) in response to Zn and Ni stresses. Plant Sci 157:113–128
• Mendoza-Cozatl D, Loza-Tavera H, Hernandez-Navarro A, Moreno-Sanchez R (2005) Sulfur assimilation and glutathione metabolism under cadmium stress in yeast, protests and plants. FEMS Micro Biol Rev 29:653–671
• Migocka M, Papierniak A, Kosatka E, Klobus G (2011) Comparative study of the active cadmium efflux systems operating at the plasma membrane and tonoplast of cucumber root cells. J Exp Bot 62(14):4903–4916
• Mukherjee SP, Choudhuri MA (1983) Implications of water stress induced changes in the levels of endogenous ascorbic acid and H₂O₂ in Vigna seedlings. Plant Physiol 58:166–170
• Muradoglu F, Gundogdu M, Ercisli S, EncuT Balta F, Jaafar HZE (2015) Cadmium toxicity affects chlorophyll a and b content, antioxidant enzyme activities and mineral nutrient accumulation in strawberry. Biol Res 48:11
• Nayyar H (2003) Variation in osmoregulation in differentially drought-sensitive wheat genotypes involves calcium. Biologia Plant 47:541–547
• Nazar R, Iqbal N, Masood A, Khan MIR, Syeed S, Khan NF (2012) Cadmium toxicity in plants and role of mineral nutrients in its alleviation. Am J Plant Sci 3:1476–1489
• Neill S, Desikan R, Hancock J (2002) Hydrogen peroxide signaling. Curr Opin Plant Biol 5:388–395
• Noctor G, Foyer CH (1998) Ascorbate and glutathione: keeping active oxygen under control. Ann Rev Plant Physiol 49:249–279
• Peng Q, Chen W, Wu L, Bai L (2017) The uptake, accumulation, and toxic effects of cadmium in barnyard grass (Echinochloa crus–galli). Pol J Environ Stud 26(2):779–784
• Plaza S, Weber J, Pajonk S, Thomas J, Talke IN, Schellenberg M, Pradervand S, Burla B, Geisler M, Martinoia E, Krämer U (2015) Wounding of Arabidopsis halleri leaves enhances cadmium accumulation that acts as a defense against herbivory. Biometals 28(3):521–528
• Shah K, Mankad AU, Reddy MN (2017) Cadmium accumulation and its effects on growth and biochemical parameters in Tagetes erecta L. J Pharmacogn Phytochem 6(3):111–115
• Singh A, Prasad SM (2014) Effect of agro-industrial waste amendment on Cd uptake in Amaranthus caudatus grown under contaminated soil: an oxidative biomarker response. Ecotoxicol Environ Saf 100:105–113
• Ślesak I, Libik M, Karpinska B, Karpinski S, Miszalski Z (2007) The role of hydrogen peroxide in regulation of plant metabolism and cellular signalling in response to environmental stresses. Acta Biochim Pol 54:39–50
• Song Y, Miao Y, Song CP (2014) Behind the scenes: the roles of reactive oxygen species in guard cells. New Phytol 201:1121–1140
• Terzi R, Kadioglua A, Kalaycioglua E, Saglamb A (2014) Hydrogen peroxide pretreatment induces osmotic stress tolerance by influencing osmolyte and abscisic acid levels in maize leaves. J Plant Interact 9:559–565
• Uchida A, Jagendorf AT, Hibino T, Takabe T, Takabe T (2002) Effects of hydrogen peroxide and nitric oxide on both salt and heat stress tolerance in rice. Plant Sci 163:515–523
• Velikova V, Yordanov L, Edreva A (2000) Oxidative stress and some antioxidant systems in acid rain treated bean plants, protective role of exogenous polyamines. Plant Sci 151:59–66
• Verbruggen N, Juraniec M, Baliardini C, Meyer CL (2013) Tolerance to cadmium in plants: the special case of hyperaccumulators. Biometals 26(4):633–638
• Vranová E, Inzé D, Breusegem FV (2002) Signal transduction during oxidative stress. J Exp Bot 53:1227–1236
• Wang Y, Li JL, Wang JZ, Li ZK (2010) Exogenous H₂O₂ improves the chilling tolerance of manila grass and mascarene grass by activating the antioxidative system. Plant Growth Reg 61:195–204
• Wellburn AR (1994) The spectral determination of chlorophyll a and b, as well as total caretenoids, using various solvent with spectrophotometers of different solution. J Plant Physiol 144:307–313
• Xu FJ, Jin CW, Liu W, Zhang YS, LinX Y (2011) Pretreatment with H₂O₂ alleviates aluminum-induced oxidative stress in wheat seedlings. J Integr Plant Biol 54:44–53
• Yang SL, Lan SS, Gong M (2009) Hydrogen peroxide-induced proline and metabolic pathway of its accumulation in maize seedlings. J Plant Physiol 166(15):1694–1699

Identyfikatory

DOI

10.1007/s11738-019-2901-2