Abstract
Drought stress is a challenging abiotic stress for plants because of global climate change. Drought disrupts the normal transportation of solutes, causes electron leakage, and triggers the production of reactive oxygen species (ROS), which create oxidative injury. These ROS react with different cellular structures such as the nucleus, proteins, and membranes, impairing their integrity. Plants produce various molecular and metabolic changes, which allow the plant to survive under stress conditions. Plants initiate various mechanisms to maintain normal homeostasis of cells, such as enzymatic and nonenzymatic scavenging systems to protect cells from oxidative damage. These enzymatic and nonenzymatic scavenging systems are mediated by plants to detoxify the detrimental effect of drought stress. In this chapter we discuss the oxidative damage caused by water deficit conditions in plant and focus on the production and scavenging system of ROS in plants. We also provide details of ROS production sites and their reactions with different cellular organelles. Moreover, we provide a comprehensive discussion of enzymatic and nonenzymatic ROS-scavenging systems and their modes of action in neutralizing the harmful effects imposed by drought stress. Rapid activation of enzymatic and nonenzymatic ROS-scavenging systems mediates drought tolerance characteristics in plants. Genome-editing technologies should be employed to ensure that genes related to drought tolerance are used as the foremost step in breeding or developing drought-tolerant cultivars. Enzymatic and genetic engineering are two novel strategies to develop tolerant cultivars that can mitigate the effects of oxidative stress.
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References
Ashraf M, Foolad MR (2007) Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environ Exp Bot 59:206–216
Athar HR, Khan A, Ashraf M (2008) Exogenously applied ascorbic acid alleviates salt-induced oxidative stress in wheat. Environ Exp Bot 63:224–231
Berghe VT, Linkermann A, Jouanlanhouet S (2014) Regulated necrosis: the expanding network of non-apoptotic cell death pathways. Nat Rev Mol Cell Biol 15:135–147
Chaves MM, Flexas J, Pinheiro C (2009) Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Ann Bot 103:551–560
Chen C, Dickman MB (2005) Proline suppresses apoptosis in the fungal pathogen Colletotrichum trifolii. Proc Natl Acad Sci 102:3459–3464
Choudhury FK, Rivero RM, Blumwald E, Mittler R (2017) Reactive oxygen species, abiotic stress and stress combination. Plant J 90:856–867
Collins A (2001) Carotenoids and genomic stability. Mutat Res 475:1–28
Conrad M, Angeli JPF, Vandenabeele P, Stockwell BR (2016) Regulated necrosis: disease relevance and therapeutic opportunities. Nat Rev Drug Discov 15:348–366
Creissen G, Firmin J, Fryer M, Kular B, Leyland N, Reynolds H, Pastori G, Wellburn F, Baker N, Wellburn A, Mullineaux P (1999) Elevated glutathione biosynthetic capacity in the chloroplasts of transgenic tobacco plants paradoxically causes increased oxidative stress. Plant Cell 11:1277–1291
Creissen GP, Broadbent P, Kular B, Reynolds H, Wellburn AR, Mullineaux PM (1994) Manipulation of glutathione reductase in transgenic plants: implications for plant responses to environmental stress. Proc R Soc Edinb Biol Sci 102:167–175
De Boeck HJ, Bassin S, Verlinden M, Zeiter M, Hiltbrunner E (2015) Simulated heat waves affected alpine grassland only in combination with drought. New Phytol 209:531–541
Davletova S, Rizhsky L, Liang H, Shengqiang Z, Oliver DJ, Coutu J, Shulaev V, Schlauch K, Mittler R (2005) Cytosolic ascorbate peroxidase 1 is a central component of the reactive oxygen gene network of Arabidopsis. Plant Cell 17:268–281
Devi R, Kaur N, Gupta AK (2012) Potential of antioxidant enzymes in depicting drought tolerance of wheat (Triticum aestivum L.). Indian J Biochem Biophys 49:257–265
Dias MC, Brüggemann W (2010) Limitations of photosynthesis in Phaseolus vulgaris under drought stress: gas exchange, chlorophyll fluorescence and Calvin cycle enzymes. Photosynthetica 48:96–102
Dixon DP, Skipsey M, Edwards R (2010) Roles for glutathione transferases in plant secondary metabolism. Phytochemistry 71:338–350
Edwards EA, Rawsthorne S, Mullineaux PM (1990) Subcellular distribution of multiple forms of glutathione reductase in leaves of pea (Pisum sativum L.). Planta 180:278–284
Foyer CH, Noctor G (2005) Redox homeostis and antioxidant signaling: a metabolic interface between stress perception and physiological responses. Plant Cell 17:1866–1875
Foyer CH, Noctor G (2013) Redox signaling in plants. Antioxid Redox Signal 18:2087–2090
Garg N, Manchanda G (2009) ROS generation in plants: boon or bane? Plant Biosys 143:8–96
Gill SS, Khan NA, Anjum NA, Tuteja N (2009) Amelioration of cadmium stress in crop plants by nutrients management: morphological, physiological and biochemical aspects. Plant Stress 5:1–23
Halliwell B, Gutteridge JMC (eds) (2007) Free radicals in biology and medicine, 5th edn. Oxford University Press, Oxford
Hollander-Czytko H, Grabowski J, Sandorf I, Weckermann K, Weiler EW (2005) Tocopherol content and activities of tyrosine aminotransferase and cystine lyase in Arabidopsis under stress conditions. J Plant Physiol 162:767–770
Hu X, Wu L, Zhao F, Zhang D, Li N, Zhu G, Li C, Wang W (2015) Phosphoproteomic analysis of the response of maize leaves to drought, heat and their combination stress. Front Plant Sci 6:1–21
Hussein MM, Safinaz SZ (2013) Influence of water stress on photosynthetic pigments of some fenugreek varieties. J Appl Sci Res 9:5238–5245
Jacobsen SE, Jensen CR, Liu F (2012) Improving crop production in the arid Mediterranean climate. Field Crops Res 128:34–47
Jimenez A, Hernandez JA, Pastori G, del Rio LA, Sevilla F (1998) Role of the ascorbate--glutathione cycle of mitochondria and peroxisomes in the senescence of pea leaves. Plant Physiol 118:1327–1335
Kabiri R, Nasibi F, Farahbakhsh H (2014) Effect of exogenous salicylic acid on some physiological parameters and alleviation of drought stress in Nigella sativa plant under hydroponic culture. Plant Prot Sci 50:43–51
Kamal-Eldin A, Appelqvist LA (1996) The chemistry and antioxidant properties of tocopherols and tocotrienols. Lipids 31:671–701
Kaur K, Gupta AK, Kaur N (2007) Effect of water deficit on carbohydrate status and enzymes of carbohydrate metabolism in seedlings of wheat cultivars. Indian J Biochem Biophys 44:223–230
Konig J, Karl-Josef MM, Dietz DJ (2012) Mechanisms and dynamics in the thiol/disulfide redox regulatory network: transmitters, sensors and targets. Curr Opin Plant Biol 15:261–268
Laurindo FR, Araujo TL, Abrahão TB (2014) Nox NADPH oxidases and the endoplasmic reticulum. Antioxid Redox Signal 20:2755–2775
Liu Z, Xin M, Qin J, Peng H, Ni Z, Yao Y, Sun Q (2015) Temporal transcriptome profiling reveals expression partitioning of homeologous genes contributing to heat and drought acclimation in wheat (Triticum aestivum L.). BMC Plant Biol 15:152. https://doi.org/10.1186/s12870-015-0511-8
Løvdal T, Olsen KM, Slimestad R, Verheul M, Lillo C (2010) Synergetic effects of nitrogen depletion, temperature, and light on the content of phenolic compounds and gene expression in leaves of tomato. Phytochemistry 71:605–613
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 23:535. https://doi.org/10.3390/molecules23030535
Mattos LM, Moretti CL (2015) Oxidative stress in plants under drought conditions and the role of different enzymes. Enzyme Eng 5:1
Mignolet-Spruyt L, Xu E, Idänheimo N, Hoeberichts FA, Mühlenbock P, Brosché M, Van Breusegem F, Kangasjärvi J (2016) Spreading the news: subcellular and organellar reactive oxygen species production and signalling. J Exp Bot 67:3831–3844
Millar AH, Mittova V, Kiddle G, Heazlewood JL, Bartoli CG, Theodoulou FL, Foyer CH (2003) Control of ascorbate synthesis by respiration and its implication for stress responses. Plant Physiol 133:443–447
Miller G, Suzuki N, Ciftci-Yilmaz S, Mittler R (2010) Reactive oxygen species homeostasis and signalling during drought and salinity stresses. Plant Cell Environ 33:453–467
Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7:405–410
Mittler R (2006) Abiotic stress, the field environment and stress combination. Trends Plant Sci 11:15–19
Mittler R (2017) ROS are good. Trends Plant Sci 22:11–19
Mittler R, Blumwald E (2010) Genetic engineering for modern agriculture: challenges and perspectives. Annu Rev Plant Biol 61:443–462
Mittler R, Vanderauwera S, Suzuki N, Miller G, Tognetti VB, Vandepoele K, Gollery M, Shulaev V, Van Breusegem F (2011) ROS signaling: the new wave? Trends Plant Sci 16:300–309
Mittler R, Zilinskas BA (1992) Molecular cloning and characterization of a gene encoding pea cytosolic ascorbate peroxidase. J Biol Chem 267:21802–21807
Mittler R, Vanderauwera S, Gollery M, Van Breusegem F (2004) Reactive oxygen gene network of plants. Trends Plant Sci 9:490–498
Muller B, Pantin F, Génard M, Turc O, Freixes S, Piques M, Gibon Y (2011) Water deficits uncouple growth from photosynthesis, increase C content, and modify the relationships between C and growth in sink organs. J Exp Bot 62:1715–1729
Nath M, Bhatt D, Prasad R, Gill SS, Anjum NA and Tuteja T (2016) Reactive Oxygen Species Generation-Scavenging and Signaling during Plant-Arbuscular Mycorrhizal and Piriformospora indica Interaction under stress condition. Front. Plant Sci. 7:1574
Niyogi KK, Shih C, Chow WS, Pogson BJ, DellaPenna D, Bjorkman O (2001) Photoprotection in a zeaxanthin-and lutein-deficient double mutant of Arabidopsis. Photosynth Res 67:139–145
Noctor G, Foyer CH (1999) A re-evaluation of the ATP: NADPH budget during C3 photosynthesis. A contribution from nitrate assimilation and its associated respiratory activity? J Exp Bot 49:1895–1908
Noctor G, Gomez L, Vanacker H, Foyer CH (2002) Interactions between biosynthesis, compartmentation, and transport in the control of glutathione homeostasis and signaling. J Exp Bot 53:1283–1304
Olsen KM, Hehn A, Jugde H, Slimestad R, Larbat R, Bourgaud F, Lillo C (2010) Identification and characterisation of CYP75A31, a new flavonoid 3050-hydroxylase, isolated from Solanum lycopersicum. BMC Plant Biol 3:10–21
Polidoros NA, Scandalios JG (1999) Role of hydrogen peroxide and different classes of antioxidants in the regulation of catalase and glutathione S-transferase gene expression in maize (Zea mays L.). Physiol Plant 106:112–120
Romero-Puertas MC, Corpas FJ, Sandalio LM, Leterrier M, Serrano RM, del Rio LA, Palma JM (2006) Glutathione reductase from pea leaves: response to abiotic stress and characterization of the peroxisomal isozyme. New Phytol 170:43–52
Seki M, Narusaka M, Ishida J, Nanjo T, Fujita M, Oono Y, Kamiya A, Nakajima M, Enju A, Sakurai T (2002) Monitoring the expression profiles of 7000 Arabidopsis genes under drought, cold and high-salinity stresses using a full-length cDNA microarray. Plant J 31:279–292
Sieferman-Harms D (1987) The light harvesting function of carotenoids in photosynthetic membrane. Plant Physiol 69:561–568
Sirokmany G, Donkó Á, Geiszt M (2016) Nox/Duox family of NADPH oxidases: lessons from knockout mouse models. Trends Pharmacol Sci 37:318–327
Smirnoff N (2000) Ascorbic acid: metabolism and functions of a multifacetted molecule. Curr Opin Plant Biol 3:229–235
Smirnoff N (2005) Ascorbate, tocopherol and carotenoids: metabolism, pathway engineering and functions. In: Smirnoff N (ed) Antioxidants and reactive oxygen species in plants. Blackwell, Oxford, pp 53–86
Sumimoto H (2008) Structure, regulation and evolution of Nox family NADPH oxidases that produce reactive oxygen species. FEBS J 275:3249–3277
Suzuki N, Miller G, Morales J, Shulaev V, Torres MA, Mittler R (2011) Respiratory burst oxidases: the engines of ROS signaling. Curr Opin Plant Biol 14:691–669
Suzuki N, Miller G, Salazar C (2013) Temporal--spatial interaction between reactive oxygen species and abscisic acid regulates rapid systemic acclimation in plants. Plant Cell 25:3553–3569
Suzuki N, Rivero RM, Shulaev V, Blumwald E, Mittler R (2014) Abiotic and biotic stress combinations. New Phytol 203:32–43
Vaahtera L, Brosché M, Wrzaczek M, Kangasjärvi J (2014) Specificity in ROS signaling and transcript signatures. Antioxid Redox Signal 21:1422–1441
Verbruggen N, Hermans C (2008) Proline accumulation in plants: a review. Amino Acids 35:753–759
Xiang C, Werner BL, Christensen EM, Oliver DJ (2001) The biological functions of glutathione revisited in Arabidopsis transgenic plants with altered glutathione levels. Plant Physiol 126:564–574
Xie Y, Hou W, Song X, Yu Y, Huang J, Sun X, Kang R, Tang D (2016) Ferroptosis: process and function. Cell Death Differ 23:369–379
Zandalinas SI, Balfagón D, Arbona V, Gómez-Cadenas A (2017) Modulation of antioxidant defense system is associated with combined drought and heat stress tolerance in citrus. Front Plant Sci 8:953–963
Zhang YP, E ZG, Jiang H, Wang L, Zhou J, Zhu DF (2015) A comparative study of stress-related gene expression under single stress and intercross stress in rice. Genet Mol Res 14:3702–3717
Zhou Y, Lam HM, Zhang J (2007) Inhibition of photosynthesis and energy dissipation induced by water and high light stresses in rice. J Exp Bot 58:1207–1217
Zinta G, Abd Elgawad H, Domagalska MA, Vergauwen L, Knapen D, Nijs I, Janssens IA, Beemster GTS, Asard H (2014) Physiological, biochemical, and genome-wide transcriptional analysis reveals that elevated CO2 mitigates the impact of combined heat wave and drought stress in Arabidopsis thaliana at multiple organizational levels. Glob Chang Biol 20:3670–3685
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Hussain, S. et al. (2019). Oxidative Stress and Antioxidant Defense in Plants Under Drought Conditions. In: Hasanuzzaman, M., Hakeem, K., Nahar, K., Alharby, H. (eds) Plant Abiotic Stress Tolerance. Springer, Cham. https://doi.org/10.1007/978-3-030-06118-0_9
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