Skip to main content

Hydrogen Peroxide: Regulator of Plant Development and Abiotic Stress Response

  • Chapter
  • First Online:
Reactive Oxygen Species

Abstract

Due to their immobility both in vitro and in vivo, crop plants are constantly exposed to abiotic and biotic factors. As a result, they have more sophisticated immune defences than animals. They might experience the mixture of these stressors concurrently or successively. The study of hydrogen peroxide (H2O2) is becoming more popular in the realm of molecular biology. It is a significant redox (reduction-oxidation reaction) metabolite that causes oxidative injury to biomolecules at high quantities, which can lead to cell death. Conversely, at low concentrations, H2O2 functions as a signalling molecule and mimics plant hormones in several ways. The hazardous nature of hydrogen peroxide was first understood to result in cell viability losses due to injury at several levels of cell organisation. It is now well-known that H2O2 has a positive role as a major hub integrating signalling network in response to abiotic stress and during developmental processes. In this chapter, the production, scavenging and the dual role of hydrogen peroxide from the point of view of its role in plant growth and developmental process and in abiotic stress tolerance have been presented.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 169.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 139.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Free shipping worldwide - see info
Hardcover Book
USD 219.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Similar content being viewed by others

References

  • Al-Saikhan MS, Shalaby TA (2019) Effect of hydrogen peroxide (H2O2) treatment on physicochemical characteristics of tomato fruits during post-harvest storage. Aust J Crop Sci 13:798–802

    Article  CAS  Google Scholar 

  • An Y, Feng X, Liu L, Xiong L, Wang L (2016) ALA-induced flavonols accumulation in guard cells is involved in scavenging H2O2 and inhibiting stomatal closure in Arabidopsis cotyledons. Front Plant Sci 7:1713

    PubMed  PubMed Central  Google Scholar 

  • Antunes WC, de Menezes DD, Pinheiro DP, Williams TCR, Loureiro ME (2017) Guard cell-specific down-regulation of the sucrose transporter SUT1 leads to improved water use efficiency and reveals the interplay between carbohydrate metabolism and Kþ accumulation in the regulation of stomatal opening. Environ Exp Bot 135:73–85

    Article  CAS  Google Scholar 

  • Asada K (2006) Production and scavenging of reactive oxygen species in chloroplasts and their functions. Plant Physiol 141:391–396

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Ashfaque F, Khan MI, 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 105e:20

    Google Scholar 

  • Azevedo-Neto AD, Prisco JT, Eneas-Filho J, Medeiros JVR, Filho E (2005) Hydrogen peroxide pre-treatment induces salt stress acclimation in maize plants. J Plant Physiol 162:1114–1122

    Article  PubMed  Google Scholar 

  • Bagheri M, Gholami M, Baninasab B (2019) Hydrogen peroxide-induced salt tolerance in relation to antioxidant systems in pistachio seedlings. Sci Hort 243:207e213

    Article  Google Scholar 

  • Banerjee A, Roychoudhury A (2018) Abiotic stress, generation of reactive oxygen species, and their consequences: An overview. In: Singh VP, Singh S, Tripathi DK, Prasad SM, Chauhan DK (eds) Reactive oxygen species in plants: boon or bane-revisiting the role of ROS, 1st edn. Wiley, pp 23–50

    Google Scholar 

  • Begara-Morales JC, Sánchez-Calvo B, Chaki M, Valderrama R, Mata-Pérez C, López-Jaramillo J, Padilla MN, Carreras A, Corpas FJ, Barroso BJ (2013) Dual regulation of cytosolic ascorbate peroxidase (APX)by tyrosine nitration and S-nitrosylation. J Exp Bot 65:527–538

    Article  PubMed  PubMed Central  Google Scholar 

  • Ben Rejeb K, Lefebvre-De Vos D, Le Disquet I, Leprince AS, Bordenave M, Maldiney R, Jdey A, Abdelly C, Savouré A (2015) Hydrogen peroxide produced by NADPH oxidases increases proline accumulation during salt or mannitols tress in Arabidopsis thaliana. New Phytol 208:1138–1148

    Google Scholar 

  • Bose J, Rodrigo-Moreno A, Shabala S (2014) ROS homeostasis in halophytes in the context of salinity stress tolerance. J Exp Bot 65(5):1241–1257

    Article  CAS  PubMed  Google Scholar 

  • Brewer TF, Garcia FJ, Onak CS, Carroll KS, Chang CJ (2015) Chemical approaches to discovery and study of source sand targets of hydrogen peroxide redox signalling through NAPDH oxidase proteins. Annu Rev Biochem 84:765–790

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Brychkova G, Yarmolinsky D, Fluhr R, Sagi M (2012) The determination of sulphite levels and its oxidation in plant leaves. Plant Sci 190:123–130

    Article  CAS  PubMed  Google Scholar 

  • Cerny M, Habanova H, Berka M, Luklova M, Brzobohaty B (2018) Hydrogen peroxide, its role in plant biology and crosstalk with signalling networks. Int J Mol Sci 19:2812

    Article  PubMed  PubMed Central  Google Scholar 

  • Chang Q, Tang H (2014) Optical determination of glucose and hydrogen peroxide using a nanocomposite prepared from glucose oxidase and magnetite nanoparticles immobilized on graphene oxide. Microchim Acta 181:527–534

    Article  CAS  Google Scholar 

  • Chao Y-Y, 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 318:37–45

    Article  CAS  Google Scholar 

  • Chawla S, Goyal SC, Angrish R, Rani C, Arora V, Datta KS, Madaan S, Devi S (2010) Acclimatory response to hydrogen peroxide and glutathione under salt boron stress through their impact on mineral nutrition and antioxidant defense system in pigeonpea (Cajanus cajan L.). Physiol Mol Biol Plants 16:295e304

    Article  Google Scholar 

  • Cona A, Rea G, Botta M, Corelli F, Federico R, Angelini R (2006) Flavin-containing polyamine oxidase is a hydrogen peroxide source in the oxidative response to the protein phosphatase inhibitor cantharidin in Zea mays L. J Exp Bot 57:2277–2289

    Article  CAS  PubMed  Google Scholar 

  • Das K, Roychoudhury A (2014) Reactive oxygen species (ROS) and response of antioxidants as ROS-scavengers during environmental stress in plants. Front Environ Sci 2:53

    Article  Google Scholar 

  • Dat J, Vandenabeele S, Vranová E, Van Montagu M, Inzé D, Van Breusegem F (2000) Dual action of the active oxygen species during plant stress responses. Cell Mol Life Sci 57:779–795

    Article  CAS  PubMed  Google Scholar 

  • De Carvalho MHC (2013) Drought stress and reactive oxygen species. Production, scavenging and signalling. Plant Signal Behav 3:156–165

    Article  Google Scholar 

  • Deng XP, Cheng YJ, Wu XB, Kwak SS, Chen W, Eneji AE (2012) Exogenous hydrogen peroxide positively influences root growth and exogenous hydrogen peroxide positively influences root growth and metabolism in leaves of sweet potato seedlings. Aust J Crop Sci 6:1572

    CAS  Google Scholar 

  • Dickinson BC, Chang CJ (2011) Chemistry and bbiology of reactive oxygen species in signalling or stress responses. Nat Chem Biol 7:504–511

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Dietz KJ, Mittler R, Noctor G (2016) Recent progress in understanding the role of reactive oxygen species in plant cell signaling. Plant Physiol 171:1535–1539

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Dikilitas M, Karakas S, Ahmad P (2018) Predisposition of crop plants to stress is directly related to their DNA health. In: Egamberdieva D, Ahmad P (eds) Plant microbiome: stress response. Springer, Singapore, pp 233–254

    Chapter  Google Scholar 

  • Fan Y, Huang Y (2012) The effective peroxidase-like activity of chitosan-functionalized CoFe2O4 nanoparticles for chemiluminescence sensing of hydrogen peroxide and glucose. Analyst 137(5):1225–1231

    Article  CAS  PubMed  Google Scholar 

  • Fariduddin Q, Khan TA, Yusuf M (2014) Hydrogen peroxide mediated tolerance to copper stress in the presence of 28-homobrassinolide in Vigna radiata. Acta Physiol Plant 36(10):2767–2778

    Article  CAS  Google Scholar 

  • Foyer CH, Noctor G (2003) Redox sensing and signalling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondria. Physiol Plant 119: 355–364

    Google Scholar 

  • Francoz E, Ranocha P, Nguyen-Kim H, Jamet E, Burlat V, Dunand C (2015) Roles of cell wall peroxidases in plant development. Phytochemistry 112:15–21

    Article  CAS  PubMed  Google Scholar 

  • Geros H, Chaves M, Delrot S (2012) The biochemistry of the grape fruit: USA: Bentham Science Publishers. ISBN 9781608053605, 304

    Google Scholar 

  • Gondim FA, Gomes-Filho E, Costa JH, Mendes Alencar NLM, Prisco JT (2012) Catalase plays a key role in salt stress acclimation induced by hydrogen peroxide pretreatment in maize. Plant Physiol Biochem 56:62–71

    Article  CAS  PubMed  Google Scholar 

  • 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 25:251–260

    Article  Google Scholar 

  • Gong M, Chen B, Li ZG, Guo LH (2001) Heat-shock-induced cross adaptation to heat, chilling, drought and salt stress in maize seedlings and involvement of H2O2. J Plant Physiol 158:112–1130-00327

    Google Scholar 

  • Grivennikova VG, Vinogradov AD (2013) Partitioning of superoxide and hydrogen peroxide production by mitochondrial respiratory complex I. Biochim Biophys Acta 1827:446–454

    Article  CAS  PubMed  Google Scholar 

  • 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

    Article  PubMed  PubMed Central  Google Scholar 

  • Hameed AM, Farooq SH, Iqbal NA, Arshad RU (2004) Influence of exogenous application of hydrogen peroxide on root and seedling growth on wheat (Triticum aestivum L.). Int J Agric Biol 6:366.e369

    Google Scholar 

  • 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 8:8.e115

    Google Scholar 

  • He JM, Liu ZH, Xu H, She XP, Huang C (2006) The involvement of hydrogen peroxide in UV-B-inhibited pollen germination and tube growth of Paeonia suffruticosa and Paulownia tomentosa in vitro. Plant Growth Regul 49:199–208

    Article  CAS  Google Scholar 

  • Hossain MA, Fujita M (2013) Hydrogen peroxide priming stimulates drought tolerance in mustard (Brassica juncea L.). Plant Gene & Trait 4:109–123

    Google Scholar 

  • Hossain MA, Hossain AZ, Kihara T, Koyama H, Hara T (2005) Aluminum induced lipid peroxidation and lignin deposition are associated with an increase in H2O2 generation in wheat seedlings. Soil Sci Plant Nutr 51:223.e230

    Article  Google Scholar 

  • Hossain MA, Hasanuzzaman M, Fujita M (2010) Up-regulation of antioxidant and glyoxalase systems by exogenous glycine betaine and proline in mungbean confer tolerance to cadmium stress. Physiol Mol Biol Plants 16:259–272

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Hossain MA, Mostofa MG, Fujita M (2013a) Cross protection by cold-shock to salinity and drought stress-induced oxidative stress in mustard (Brassica campestris L.) seedlings. Mol Plant Breed 4:50–70

    Google Scholar 

  • Hossain MA, Mostofa MG, Fujita M (2013b) Heat-shock positively modulates oxidative protection of salt and drought-stressed mustard (Brassica campestris L.) seedlings. J Plant Sci Mol Breed 2:1–14

    Google Scholar 

  • Hu X, Bidney DL, Yalpani N, Duvick JP, Crasta O, Folkerts O, Lu G (2003) Overexpression of a gene encoding hydrogen peroxide-generating oxalate oxidase evokes defense responses in sunflower. Plant Physiol 133:170–181

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • 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 35:1905–1913-1228-7

    Google Scholar 

  • Ishibashi Y, Yamaguchi H, Yuasa T, Iwaya-Inoue M, Arima S, Zheng SH (2011) Hydrogen peroxide spraying alleviates drought stress in soybean plants. J Plant Physiol 168:1562–1567

    Article  CAS  PubMed  Google Scholar 

  • Jahan AA, Anis M (2014) Changes in antioxidative enzymatic responses during acclimatization of in vitro raised plantlets of Cardiospermum halicacabum L. against oxidative stress. J Plant Physiol Pathol 4:2

    Google Scholar 

  • Jing LZ, Kui GY, Hang LS, Gang BJ (2009) Effects of exogenous hydrogen peroxide on ultrastructure of chloroplasts and activities of antioxidant enzymes in greenhouse-ecotype cucumber under drought stress. Acta Hortic Sin 36:1140–1146

    Google Scholar 

  • Kang NJ, Kang YI, Kang KH, Jeong BR (2009) Induction of thermotolerance and activation of antioxidant enzymes in H2O2 pre-applied leaves of cucumber and tomato seedlings. J Jpn Soc Hortic Sci 78:320–329

    Article  CAS  Google Scholar 

  • Kapoor D, Sharma R, Handa N, Kaur H, Rattan A, Yadav P, Gautam V, Kaur R, Bhardwaj R (2015) Redox homeostasis in plants under abiotic stress: role of electron carriers, energy metabolism mediators and proteinaceous thiols. Front Environ Sci 3:13

    Article  Google Scholar 

  • Khan MI, Khan NA, Masood A, Per TS, Asgher M (2016) Hydrogen peroxide alleviates nickel-inhibited photosynthetic responses through increase in use efficiency of nitrogen and sulfur, and glutathione production in mustard. Front Plant Sci 7:44

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Khan TA, Yusuf M, Fariduddin Q (2018) Hydrogen peroxide in regulation of plant metabolism: Signalling and its effect under abiotic stress. Photosynthetica 56:1237–1248

    Article  CAS  Google Scholar 

  • Khandaker MM, Boyce AN, Osman N (2012) The influence of hydrogen peroxide on the growth, development and quality of wax apple (Syzygium samarangense, [Blume] Merrill & L.M. Perry var. jambu madu) fruits [Syzygium samarangense [Blume] Merrill & LM Perry var. jambu madu]. Plant Physiol Biochem 53:101–110

    Article  CAS  PubMed  Google Scholar 

  • Kocyigit A, Guler EM, Dikilitas M (2017) Role of antioxidant phytochemicals in prevention, formation and treatment of cancer. In: Cristiana F, Elena A (eds) Reactive oxygen species (ROS) in living cells. Intech Open, pp 21–45

    Google Scholar 

  • Krifka S, Hiller KA, Spagnuolo G, Jewett A, Schmalz G, Schweikl H (2012) The influence of glutathione on redox regulation by antioxidant proteins and apoptosis in macrophages exposed to 2-hydroxyethyl methacrylate (HEMA). Biomaterials 33:5177–5186

    Article  CAS  PubMed  Google Scholar 

  • Kumari S, Verma VK (2019) Hydrogen peroxide mediates suberization, root thickness and stomatal movement in wheats. Int J Curr Microbiol App Sci 8:2448–2454

    Article  CAS  Google Scholar 

  • Li XP, Xu QQ, Liao WB, Ma ZJ, Xu XT, Wang M, Ren PJ, Niu LJ, Jin X, Zhu YC (2016) Hydrogen peroxide is involved in abscisic acid-induced adventitious rooting in cucumber (Cucumis sativus L.) under drought stress. J Plant Biol 59:536–548

    Article  CAS  Google Scholar 

  • Liu ZJ, Guo YK, Bai JG (2010) Exogenous hydrogen peroxide changes antioxidant enzyme activity and protects ultrastructure in leaves of two cucumber ecotypes under osmotic stress. J Plant Growth Regul 29(2):171–183

    Article  Google Scholar 

  • Martinez V, Nieves-Cordones M, Lopez-Delacalle M, Rodenas R, Mestre TC, Garcia-Sanchez F, Rubio F, Nortes PA, Mittler R, Rivero RM (2018) Tolerance to stress combination in tomato plants: new insights in the protective role of melatonin. Molecules 23(3):535

    Article  PubMed  PubMed Central  Google Scholar 

  • Mehler AH (1951) Studies on reactions of illuminated chloroplasts. II. Stimulation and inhibition of the reaction with molecular oxygen. Arch Biochem Biophys 33:339–351 90082–3, 65

    Google Scholar 

  • Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7:405–410

    Article  CAS  PubMed  Google Scholar 

  • Mostofa MG, Fujita M (2013) Salicylic acid alleviates copper toxicity in rice (Oryza sativa L.) seedlings by upregulating antioxidative and glyoxalase systems. Ecotoxicology 22:959–973. https://doi.org/10.1007/s10646-013-1073-x

    Article  CAS  PubMed  Google Scholar 

  • Mostofa MG, Seraj ZI, Fujita M (2014a) Exogenous sodium nitroprusside and glutathione alleviate copper toxicity by reducing copper uptake and oxidative damage in rice (Oryza sativa L.) seedlings. Protoplasma 251:1373–1386

    Article  CAS  PubMed  Google Scholar 

  • Mostofa MG, Yoshida N, Fujita M (2014b) Spermidine pretreatment enhances heat tolerance in rice seedlings through modulating antioxidative and glyoxalase systems. Plant Growth Regul 73:31–44

    Article  CAS  Google Scholar 

  • Munne-Bosch S, Pinto-Marijuan M (2017) Free radicals, oxidative stress and antioxidants. Encycl Appl Plant Sci 2:16–19

    Article  Google Scholar 

  • Navrot N, Rouhier N, Gelhaye E, Jacquot JP (2007) Reactive oxygen species generation and antioxidant systems in plant mitochondria. Physiol Plant 129:185–195

    Article  CAS  Google Scholar 

  • Nazir F, Hussain A, Fariduddin Q (2019) Hydrogen peroxide modulate photosynthesis and antioxidant systems in tomato (Solanum lycopersicum L.) plants under copper stress. Chemosphere 230:544–558

    Article  CAS  PubMed  Google Scholar 

  • Nazir F, Fariduddin Q, Khan TA (2020) Hydrogen peroxide as a signalling molecule in plants and its crosstalk with other plant growth regulators under heavy metal stress. Chemosphere 252:126486

    Article  CAS  PubMed  Google Scholar 

  • Niu L, Liao W (2016) Hydrogen peroxide signaling in plant development and abiotic responses: crosstalk with nitric oxide and calcium. Front Plant Sci 7:230

    Article  PubMed  PubMed Central  Google Scholar 

  • Noctor G, Reichheld JP, Foyer CH (2018) ROS-related redox regulation and signaling in plants. Semin Cell Dev Biol 80:3–12. https://doi.org/10.1016/j.semcdb.2017.07.013

    Article  CAS  PubMed  Google Scholar 

  • Nyathi Y, Baker A (2006) Plant peroxisomes as a source of signalling molecules. Biochim Biophys Acta 1763:1478–1495

    Article  CAS  PubMed  Google Scholar 

  • Petrov VD, Van Breusegem F (2012) Hydrogen peroxide-a central hub for information flow in plant cells. AoB Plants 2012:pls014

    Article  PubMed  PubMed Central  Google Scholar 

  • Prasad TK, Anderson MD, Martin BA, Stewart CR (1994a) Evidence for chilling-induced oxidative stress in maize seedlings and a regulatory role for hydrogen-peroxide. Plant Cell 6:65–74

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Prasad TK, Anderson MD, Stewart CR (1994b) Acclimation, hydrogen peroxide, and abscisic-acid protect mitochondria against irreversible chilling injury in maize seedlings. Plant Physiol 10:619–627

    Article  Google Scholar 

  • Rani V, Deep G, Singh RK, Palle K, Yadav UC (2016) Oxidative stress and metabolic disorders: pathogenesis and therapeutic strategies. Life Sci 148:183–193

    Article  CAS  PubMed  Google Scholar 

  • Remans T, Opdenakker K, Smeets K, Mathijsen D, Vangronsveld J, Cuypers A (2010) Metal-specific and NADPH oxidase dependent changes in lipoxygenase and NADPH oxidase gene expression in Arabidopsis thaliana exposed to cadmium or excess copper. Funct Plant Biol 37:532–544

    Article  CAS  Google Scholar 

  • Sun Y, Zhang C, Qi A, Luo W (2009) Effects of hydrogen peroxide on the germination characteristics of cucumber seeds. In: International conference on environmental science and information application technology, pp 272.e275

    Google Scholar 

  • Sun Y, Wang H, Liu S, Peng X (2016) Exogenous application of hydrogen peroxide alleviates drought stress in cucumber seedlings. S Afr J Bot 106:23–28

    Article  CAS  Google Scholar 

  • 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. https://doi.org/10.1016/S0168-9452(02)00159-0

    Article  CAS  Google Scholar 

  • Wahid A, Perveen M, Gelani S, Basra SMA (2007) Pretreatment of seed with H2O2 improves salt tolerance of wheat seedlings by alleviation of oxidative damage and expression of stress proteins. J Plant Physiol 164:283–294

    Article  CAS  PubMed  Google Scholar 

  • 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 22:2981–2998

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • 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 61:195–204

    Article  CAS  Google Scholar 

  • 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 36:2915–2924

    Article  CAS  Google Scholar 

  • Wen JF, Gong M, Liu Y, Hu JL, Deng MH (2013) Effect of hydrogen peroxide on growth and activity of some enzymes involved in proline metabolism of sweet corn seedlings under copper stress. Sci Hortic (Canterb) 164:366e371

    Google Scholar 

  • Willekens H, Chamnongpol S, Davey M, Schraudner M, Langebartels C, Van Montagu M, Inzé D, Van Camp W (1997) Catalase is a sink for H2O2 and is indispensable for stress defence inC3 plants. EMBO J 16:4806–4816

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Wu Z, Zhang C, Yan J, Yue Q, Ge Y (2015) Effects of sulfur supply and hydrogen peroxide pretreatment on the responses by rice under cadmium stress. Plant Growth Regul 77:299–306

    Article  CAS  Google Scholar 

  • Xiong J, Yang Y, Fu G, Tao L (2015) Novel roles of hydrogen peroxide (H2O2) in regulating pectin synthesis and dimethyl esterification in the cell wall of rice (Oryza sativa) root tips. New Phytol 206:118.e126

    Article  Google Scholar 

  • Xu PL, Guo YK, Bai JG, Shang L, Wang XJ (2008) Effects of long-term chilling on ultrastructure and antioxidant activity in leaves of two cucumber cultivar sunder lowlight. Physiol Plant 132:467–478

    Article  CAS  PubMed  Google Scholar 

  • Xu FJ, Jin CW, Liu WJ (2010) Pretreatment with H2O2 alleviates aluminum-induced oxidative stress in wheat seedlings. Plant Biol 54:44–53

    Google Scholar 

  • Yıldız 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 22:1303–1312

    Article  PubMed  Google Scholar 

  • You J, Chan Z (2015) ROS regulation during abiotic stress responses in crop plants. Front Plant Sci 6:1092

    Article  PubMed  PubMed Central  Google Scholar 

  • Zhang YH, She XP (2012) The involvement of nitric oxide and hydrogen peroxide in eATP-inhibited pollen germination and tube growth of Paulownia tomentosa in vitro. Adv Mater Res 343:347.e350

    Google Scholar 

  • Zhang H, Lv S, Xu H, Hou D, Li Y, Wang F (2017) H2O2 is involved in the metallothionein-mediated rice tolerance to copper and cadmium toxicity. Int J Mol Sci 18:2083

    Article  PubMed  PubMed Central  Google Scholar 

  • Zhou J, Xia XJ, Zhou YH, Shi K, Chen Z, Yu JQ (2014) OH1-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.e607

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2023 The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd.

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Jahan, A., Khan, M.M.A., Ahmad, B., Ahmed, K.B.M., Pandey, R.P., Gulfishan, M. (2023). Hydrogen Peroxide: Regulator of Plant Development and Abiotic Stress Response. In: Faizan, M., Hayat, S., Ahmed, S.M. (eds) Reactive Oxygen Species. Springer, Singapore. https://doi.org/10.1007/978-981-19-9794-5_12

Download citation

Publish with us

Policies and ethics