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Abiotic Stress Tolerance in Plants by Priming and Pretreatment with Hydrogen Peroxide

  • Aditya Banerjee
  • Aryadeep Roychoudhury
Chapter

Abstract

Being a member of the reactive oxygen species, hydrogen peroxide (H2O2) is involved in signaling pathways associated with diverse antioxidant responses during abiotic stress. Thus, priming with H2O2 enables the seeds or seedlings to activate their antioxidant machineries and acclimatize prior to abiotic stress exposures. Hence, H2O2-priming actually hardens the plants to better cope with suboptimal conditions. This chapter discusses on the displayed mechanisms of H2O2-mediated tolerance in plants subjected to diverse abiotic stresses like salinity, drought, heat, cold and heavy metals.

Keywords

Hydrogen peroxide Reactive oxygen species Priming Signaling Antioxidants Abiotic stress Tolerance 

Notes

Acknowledgments

Financial assistance from Council of Scientific and Industrial Research (CSIR), Government of India, through the research grant [38(1387)/14/EMR-II], Science and Engineering Research Board, Government of India, through the grant [EMR/2016/004799] and Department of Higher Education, Science and Technology and Biotechnology, Government of West Bengal, through the grant [264(Sanc.)/ST/P/S&T/1G-80/2017] to Dr. Aryadeep Roychoudhury is gratefully acknowledged. The authors acknowledge University Grants Commission, Government of India, for providing Junior Research Fellowship to Mr. Aditya Banerjee.

References

  1. Abass SM, Mohamed HI (2011) Alleviation of adverse effects of drought stress on common bean (Phaseolus vulgaris L.) by exogenous application of hydrogen peroxide. Bangladesh J Bot 41:75–83Google Scholar
  2. Akter S, Huang J, Waszczak C, Jacques S, Gevaert K, Van Breusegem F et al (2015) Cysteines under ROS attack in plants: a proteomics view. J Exp Bot 66:2935–2944PubMedCrossRefPubMedCentralGoogle Scholar
  3. Ashfaque F, Khan MIR, Khan NA (2014) Exogenously applied H2O2 promotes proline accumulation, water relations, photosynthetic efficiency and growth of wheat (Triticum aestivum L.) under salt stress. Annu Res Rev Biol 4:105–120CrossRefGoogle Scholar
  4. Banerjee A, Roychoudhury A (2015) WRKY proteins: signaling and regulation of expression during abiotic stress responses. Sci World J 2015:807560CrossRefGoogle Scholar
  5. Banerjee A, Roychoudhury A (2016a) Group II late embryogenesis abundant (LEA) proteins: structural and functional aspects in plant abiotic stress. Plant Growth Regul 79:1–17CrossRefGoogle Scholar
  6. Banerjee A, Roychoudhury A (2016b) Plant responses to light stress: oxidative damages, photoprotection and role of phytohormones. In: Ahammed GJ, Yu J-Q (eds) Plant hormones under challenging environmental factors. Springer, Dordrecht, pp 181–213Google Scholar
  7. Banerjee A, Roychoudhury A (2017) Abscisic-acid-dependent basic leucine zipper (bZIP) transcription factors in plant abiotic stress. Protoplasma 254:3–16PubMedCrossRefPubMedCentralGoogle Scholar
  8. Banerjee A, Roychoudhury A (2018a) Abiotic stress, generation of reactive oxygen species, and their consequences: an overview. In: Singh VP, Singh S, Tripathi D, Mohan Prasad S, Chauhan DK (eds) Revisiting the role of reactive oxygen species (ROS) in plants: ROS boon or bane for plants? Wiley, Hoboken, pp 23–50Google Scholar
  9. Banerjee A, Roychoudhury A (2018b) Small heat shock proteins: structural assembly and functional responses against heat stress in plants. In: Ahmad P, Ahanger MA, Singh VP, Tripathi DK, Alam P, Alyemeni MN (eds) Plant metabolites and regulation under abiotic stress. Academic/Elsevier, London, pp 367–374CrossRefGoogle Scholar
  10. Banerjee A, Roychoudhury A (2018c) Effect of salinity stress on growth and physiology of medicinal plants. In: Ghorbanpour M et al (eds) Medicinal plants and environmental challenges. Springer, Cham, pp 177–188Google Scholar
  11. Banerjee A, Roychoudhury A (2018d) Interactions of brassinosteroids with major phytohormones: antagonistic effects. J Plant Growth Regul.  https://doi.org/10.1007/s00344-018-9828-5CrossRefGoogle Scholar
  12. Banerjee A, Roychoudhury A (2018e) Strigolactones: multi-level regulation of biosynthesis and diverse responses in plant abiotic stresses. Acta Physiol Plant 40:86CrossRefGoogle Scholar
  13. Banerjee A, Roychoudhury A (2018f) Seed priming technology in the amelioration of salinity stress in plants. In: Rakshit A, Singh HB (eds) Advances in seed priming. Springer Nature, Singapore, pp 81–93CrossRefGoogle Scholar
  14. Banerjee A, Roychoudhury A, Krishnamoorthi S (2016) Emerging techniques to decipher microRNAs (miRNAs) and their regulatory role in conferring abiotic stress tolerance in plants. Plant Biotechnol Rep 10:185–205CrossRefGoogle Scholar
  15. Banerjee A, Wani SH, Roychoudhury A (2017) Epigenetic control of plant cold responses. Front Plant Sci 8:1643PubMedPubMedCentralCrossRefGoogle Scholar
  16. Banerjee A, Tripathi DK, Roychoudhury A (2018a) Hydrogen sulphide trapeze: environmental stress amelioration and phytohormone crosstalk. Plant Physiol Biochem 132:46–53PubMedCrossRefGoogle Scholar
  17. Banerjee A, Tripathi DK, Roychoudhury A (2018b) The karrikin ‘callisthenics’: can compounds derived from smoke help in stress tolerance? Physiol Plant.  https://doi.org/10.1111/ppl.12836PubMedCrossRefGoogle Scholar
  18. Baniwal SK, Bharti K, Chan KY, Fauth M, Ganguli A, Kotak S et al (2004) Heat stress response in plants: a complex game with chaperones and more than twenty heat stress transcription factors. J Biosci 29:471–487PubMedCrossRefGoogle Scholar
  19. Bhattacharjee S (2008) Calcium-dependent signaling pathway in heat-induced oxidative injury in Amaranthus lividus. Biol Plant 52:1137–1140CrossRefGoogle Scholar
  20. Bhattacharjee S (2012) An inductive pulse of hydrogen peroxide pretreatment restores redox-homeostasis and mitigates oxidative membrane damage under extremes of temperature in two rice cultivars (Oryza sativa L., cultivars Ratna and SR26B). Plant Growth Regul 68:395–410CrossRefGoogle Scholar
  21. Brossa R, Lopez-Carbonell M, Jubany-Mari T, Alegre L (2011) Interplay between abscisic acid and jasmonic acid and its role in water-oxidative stress in wild-type, ABA-deficient, JA-deficient, and ascorbate deficient Arabidopsis thaliana plants. J Plant Growth Regul 30:322–333CrossRefGoogle Scholar
  22. Chao YY, Hsu YT, Kao CH (2009) Involvement of glutathione in heat shock-and hydrogen peroxide-induced cadmium tolerance of rice (Oryza sativa L.) seedlings. Plant Soil 318:37–45CrossRefGoogle Scholar
  23. Costa A, Drago I, Behera S, Zottini M, Pizzo P, Schroeder JI et al (2010) H2O2 in plant peroxisomes: an in vivo analysis uncovers a Ca2+-dependent scavenging system. Plant J 62:760–772PubMedPubMedCentralCrossRefGoogle Scholar
  24. Ellouzi H, Sghayar S, Abdelly C (2017) H2O2 seed priming improves tolerance to salinity; drought and their combined effect more than mannitol in Cakile maritima when compared to Eutrema salsugineum. J Plant Physiol 210:38–50PubMedPubMedCentralCrossRefGoogle Scholar
  25. Gondim FA, Miranda RS, 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 25:251–260CrossRefGoogle Scholar
  26. 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 54:26PubMedPubMedCentralCrossRefGoogle Scholar
  27. He JM, Xu H, She XP, Song XG, Zhao WM (2005) The role and the interrelationship of hydrogen peroxide and nitric oxide in the UV-B- induced stomatal closure in broadbean. Funct Plant Biol 32:237–247CrossRefGoogle Scholar
  28. Hossain MA, Fujita M (2013) Hydrogen peroxide priming stimulates drought tolerance in mustard (Brassica juncea L.). Plant Gene Trait 4:109–123Google Scholar
  29. Hossain MA, Bhattacharjee S, Armin S-M, Qian P, Xin W, Li H-Y, 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 6:420PubMedPubMedCentralGoogle Scholar
  30. 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 Regul 59:51–61CrossRefGoogle Scholar
  31. Huang YW, Zhou ZQ, Yang HX, Wei CX, Wan YY, Wang XJ et al (2015) Glucose application protects chloroplast ultrastructure in heat-stressed cucumber leaves through modifying antioxidant enzyme activity. Biol Plant 59:131–138CrossRefGoogle Scholar
  32. Iseri OD, Körpe DA, Sahin FI, Haberal M (2013) Hydrogen peroxide pretreatment of roots enhanced oxidative stress response of tomato under cold stress. Acta Physiol Plant 35:1905–1913CrossRefGoogle Scholar
  33. Ishibashi Y, Yamaguchi H, Yuasa T, Inwaya-Inoue M, Arima S, Zheng S (2011) Hydrogen peroxide spraying alleviates drought stress in soybean plants. J Plant Physiol 168:1562–1567PubMedPubMedCentralCrossRefGoogle Scholar
  34. Jammes F, Song C, Shin D, Muncmasa S, Takeda K (2009) MAP kinases MPK9 and MPK12 are preferentially expressed in guard cells and positively regulate ROS-mediated ABA signaling. Proc Natl Acad Sci U S A 106:20520–20525PubMedPubMedCentralCrossRefGoogle Scholar
  35. Kapoor D, Sharma R, Handa N, Kaur H, Rattan A, Yadav P et al (2015) Redox homeostasis in plants under abiotic stress: role of electron carriers, energy metabolism mediators and proteinaceous thiols. Front Environ Sci 3:13CrossRefGoogle Scholar
  36. Kim TH, Maik B, Hu HH, Noriyuki N, Julian IS (2010) Guard cell signal transduction network advances in understanding abscisic acid, CO2, and Ca2+ signaling. Annu Rev Plant Biol 61:56–91Google Scholar
  37. Li JT, Qiu ZB, Zhang XW, Wang LS (2011) Exogenous hydrogen peroxide can enhance tolerance of wheat seedlings to salt stress. Acta Physiol Plant 33:835–842CrossRefGoogle Scholar
  38. Liu XM, Kim KE, Kim KC, Nguyen XC, Han HJ, Jung MS et al (2010) Cadmium activates Arabidopsis MPK3 and MPK6 via accumulation of reactive oxygen species. Photochemistry 71:614–618CrossRefGoogle Scholar
  39. Mazars C, Bourque S, Mithöfer A, Pugin A, Ranjeva R (2009) Calcium homeostasis in plant cell nuclei. New Phytol 181:261–274PubMedCrossRefGoogle Scholar
  40. Miller G, Mittler R (2006) Could heat shock transcription factors function as hydrogen peroxide sensors in plants? Ann Bot 98:279–288PubMedPubMedCentralCrossRefGoogle Scholar
  41. Miller G, Suzuki N, Ciftci-Yilmaz S, Mittler R (2010) Reactive oxygen species homeostasis and signalling during drought and salinity stresses. Plant Cell Environ 33:453–467PubMedCrossRefGoogle Scholar
  42. Mittler R, Vanderauwera S, Suzuki N, Miller G, Tognetti VB, Vandepoele K et al (2011) ROS signaling: the new wave? Trends Plant Sci 16:300–309PubMedCrossRefGoogle Scholar
  43. Moussa HR, Mohamed MAEFH (2011) Role of nitric acid or H2O2 in antioxidant defense system of Pisum sativum L. under drought stress. Nat Sci 9:211–216Google Scholar
  44. Nahar K, Hasanuzzaman M, Alam MM, Fujita M (2014) Exogenous glutathione confers high temperature stress tolerance in mungbean (Vigna radiata L.) by modulating antioxidant defense and methylglyoxal detoxification system. Environ Exp Bot 112:44–54CrossRefGoogle Scholar
  45. Noctor G, Mhamdi A, Foyer CH (2014) The roles of reactive oxygen metabolism in drought: not so cut and dried. Plant Physiol 164:1636–1648PubMedPubMedCentralCrossRefGoogle Scholar
  46. Pan J, Zhang M, Kong X, Xing X, Liu Y, Zhou Y et al (2012) ZmMPK17,a novel maize group D MAP kinase gene, is involved in multiple stress responses. Planta 235:661–676PubMedCrossRefPubMedCentralGoogle Scholar
  47. Rao MV, Davis KR (1999) Ozone-induced cell death occurs via two distinct mechanisms in Arabidopsis: the role of salicylic acid. Plant J 17:603–614PubMedCrossRefPubMedCentralGoogle Scholar
  48. Rizhsky L (2004) The zinc finger protein Zat12 is required for cytosolic ascorbate peroxidase 1 expression during oxidative stress in Arabidopsis. J Biol Chem 279:11736–11743PubMedCrossRefPubMedCentralGoogle Scholar
  49. Roychoudhury A, Banerjee A (2015) Transcriptome analysis of abiotic stress response in plants. Transcriptomics 3:2CrossRefGoogle Scholar
  50. Roychoudhury A, Banerjee A (2017) Abscisic acid signaling and involvement of mitogen activated protein kinases and calcium-dependent protein kinases during plant abiotic stress. In: Pandey G (ed) Mechanism of plant hormone signaling under stress, vol 1. Wiley, Hoboken, pp 197–241CrossRefGoogle Scholar
  51. Sathiyaraj G, Srinivasan S, Kim YJ, Lee OR, Balusamy SDR, Khorolaragchaa A et al (2014) Acclimation of hydrogen peroxide enhances salt tolerance by activating defense-related proteins in Panax ginseng CA. Meyer. Mol Biol Rep 41:3761–3771PubMedCrossRefGoogle Scholar
  52. Terzi R, Kadioglu A, Kalaycioglu E, Saglam A (2014) Hydrogen peroxide pretreatment induces osmotic stress tolerance by influencing osmolyte and abscisic acid levels in maize leaves. J Plant Interact 9:559–565CrossRefGoogle Scholar
  53. Vlot AC, Dempsey DMA, Klessig DF (2009) Salicylic acid, a multi- faceted hormone to combat disease. Annu Rev Phytopathol 47:177–206PubMedCrossRefPubMedCentralGoogle Scholar
  54. Wang P, Du Y, Li Y, Ren D, Song CP (2010a) Hydrogen peroxide- mediated activation of map kinase 6 modulates nitric oxide biosynthesis and signal transduction in Arabidopsis. Plant Cell 22:2981–2998PubMedPubMedCentralCrossRefGoogle Scholar
  55. Wang Y, Li J, Wang J, Li Z (2010b) Exogenous H2O2 improves the chilling tolerance of manila grass and mascarene grass by activating the antioxidative system. Plant Growth Regul 61:195–204CrossRefGoogle Scholar
  56. Wang KT, Zheng YH, Tang WC, Li TJ, Zhang Q, Shang HT (2012) Effects of methyl jasmonate treatment on levels of nitric oxide and hydrogen peroxide and phytoalexin synthesis in postharvest grapeberries. Acta Hort Sin 39:1559–1566Google Scholar
  57. Wang Y, Zhang J, Li JL, Ma XR (2014) Exogenous hydrogen peroxide enhanced the thermotolerance of Festuca arundinacea and Lolium perenne by increasing the antioxidative capacity. Acta Physiol Plant 36:2915–2924CrossRefGoogle Scholar
  58. Wei S, Hu W, Deng X, Zhang Y, Liu X, Zhao X et al (2014) A rice calcium-dependent protein kinase OsCPK9 positively regulates drought stress tolerance and spikelet fertility. BMC Plant Biol 14:133PubMedPubMedCentralCrossRefGoogle Scholar
  59. Xu FJ, Jin CW, Liu WJ, Zhang YS, Lin XY (2010) Pretreatment with H2O2 alleviates aluminum-induced oxidative stress in wheat seedlings. J Integr Plant Biol 54:44–53Google Scholar
  60. Yildiz M, Terzi H, Bingül N (2013) Protective role of hydrogen peroxide pretreatment on defense systems and BnMP1 gene expression in Cr(VI)-stressed canola seedlings. Ecotoxicology 22:1303–1312PubMedCrossRefGoogle Scholar
  61. Yuan S, Lin HH (2008) Role of salicylic acid in plant abiotic stress. Z Naturforsch C 63:313–320PubMedCrossRefGoogle Scholar
  62. Zhang X, Zhang L, Dong F, Gao J, Galbraith DW, Song C-P (2001) Hydrogen peroxide is involved in abscisic acid-induced stomatal closure in Vicia faba. Plant Physiol 126:1438–1448PubMedPubMedCentralCrossRefGoogle Scholar
  63. Zhou J, Wang J, Shi K, Xia XJ, Zhou YH, Yu JQ (2012) Hydrogen peroxide is involved in the cold acclimation-induced chilling tolerance of tomato plants. Plant Physiol Biochem 60:141–149PubMedCrossRefGoogle Scholar
  64. Zhou J, Xia XJ, Zhou YH, Shi K, Chen Z, Yu JQ (2014) RBOH1- dependent H2O2 production and subsequent activation of MPK1/2 play an important role in acclimation-induced cross-tolerance in tomato. J Exp Bot 65:595–607PubMedCrossRefGoogle Scholar

Copyright information

© Springer Nature Singapore Pte Ltd. 2019

Authors and Affiliations

  • Aditya Banerjee
    • 1
  • Aryadeep Roychoudhury
    • 1
  1. 1.Post Graduate Department of BiotechnologySt. Xavier’s College (Autonomous)KolkataIndia

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