1932

Abstract

Rising CO concentrations and their effects on plant productivity present challenging issues. Effects on the photosynthesis/photorespiration balance and changes in primary metabolism are known, caused by the competitive interaction of CO and O at the active site of ribulose-1,5-bisphosphate carboxylase/oxygenase. However, impacts on stress resistance are less clear. Reactive oxygen species are key players in biotic and abiotic stress responses, but there is no consensus on whether elevated CO constitutes a stress. Although high CO increases yield in C plants, it can also increase cellular oxidation and activate phytohormone defense pathways. Reduction-oxidation processes play key roles in acclimation to high CO, with specific enzymes acting in compartment-specific signaling. Traditionally, acclimation to high CO has been considered in terms of altered carbon gain, but emerging evidence suggests that CO is a signal as well as a substrate. Some CO effects on defense are likely mediated independently of primary metabolism. Nonetheless, primary photosynthetic metabolism is highly integrated with defense and stress signaling pathways, meaning that plants will be able to acclimate to the changing environment over the coming decades.

Loading

Article metrics loading...

/content/journals/10.1146/annurev-arplant-050718-095955
2020-04-29
2024-03-29
Loading full text...

Full text loading...

/deliver/fulltext/arplant/71/1/annurev-arplant-050718-095955.html?itemId=/content/journals/10.1146/annurev-arplant-050718-095955&mimeType=html&fmt=ahah

Literature Cited

  1. 1. 
    AbdElgawad H, Zinta G, Beemster GT, Janssens IA, Asard H 2016. Future climate CO2 levels mitigate stress impact on plants: increased defense or decreased challenge. Front. Plant Sci. 7:55
    [Google Scholar]
  2. 2. 
    Apanasets O, Grou CP, Van Veldhoven PP, Brees C, Wang B et al. 2014. PEX5, the shuttling import receptor for peroxisomal matrix proteins, is a redox-sensitive protein. Traffic 15:94–103
    [Google Scholar]
  3. 3. 
    Asensio JS, Rachmilevitch S, Bloom AJ 2015. Responses of Arabidopsis and wheat to rising CO2 depend on nitrogen source and nighttime CO2 levels. Plant Physiol 168:156–63
    [Google Scholar]
  4. 4. 
    Astier J, Gross I, Durner J 2017. Nitric oxide production in plants: an update. J. Exp. Bot. 69:3401–11
    [Google Scholar]
  5. 5. 
    Attacha S, Solbach D, Bela K, Moseler A, Wagner S et al. 2017. Glutathione peroxidase–like enzymes cover five distinct cell compartments and membrane surfaces in Arabidopsis thaliana. Plant Cell Environ 40:1281–95
    [Google Scholar]
  6. 6. 
    Backhausen JE, Scheibe R. 1999. Adaptation of tobacco plants to elevated CO2: influence of leaf age on changes in physiology, redox states and NADP-malate dehydrogenase activity. J. Exp. Bot. 50:665–75
    [Google Scholar]
  7. 7. 
    Batelli G, Verslues PE, Agius F, Qiu Q, Fujii H et al. 2007. SOS2 promotes salt tolerance in part by interacting with the vacuolar H+-ATPase and upregulating its transport activity. Mol. Cell Biol. 27:7781–90
    [Google Scholar]
  8. 8. 
    Begara-Morales JC. 2016. Nitric oxide signaling in a CO2-enriched environment. J. Exp. Bot. 67:560–61
    [Google Scholar]
  9. 9. 
    Belin C, Bashandy T, Cela J, Delorme-Hinoux V, Riondet C, Reichheld JP 2015. A comprehensive study of thiol reduction gene expression under stress conditions in Arabidopsis thaliana. Plant Cell Environ 38:299–314
    [Google Scholar]
  10. 10. 
    Bolouri-Moghaddam MR, Le Roy K, Xiang L, Rolland F, Van den Ende W 2010. Sugar signalling and antioxidant network connections in plant cells. FEBS J 277:2022–37
    [Google Scholar]
  11. 11. 
    Botha A-M, Kunert KJ, Maling'a J, Foyer CH 2020. Defining biotechnological solutions for insect control in sub-Saharan Africa. Food Energy Secur 9:e191
    [Google Scholar]
  12. 12. 
    Brodersen P, Petersen M, Bjørn Nielsen H, Zhu S, Newman MA et al. 2006. Arabidopsis MAP kinase 4 regulates salicylic acid– and jasmonic acid/ethylene–dependent responses via EDS1 and PAD4. Plant J 47:532–46
    [Google Scholar]
  13. 13. 
    Camacho-Pereira J, Meyer LE, Machado LB, Oliveira MF, Galina A 2009. Reactive oxygen species production by potato tuber mitochondria is modulated by mitochondrially bound hexokinase activity. Plant Physiol 149:1099–100
    [Google Scholar]
  14. 14. 
    Caplan JL, Kumar AS, Park E, Padmanabhan MS, Hoban K et al. 2015. Chloroplast stromules function during innate immunity. Dev. Cell 34:45–57
    [Google Scholar]
  15. 15. 
    Casteel CL, Segal LM, Niziolek OK, Berenbaum MR, DeLucia EH 2012. Elevated carbon dioxide increases salicylic acid in Glycine max. Environ. Entomol 41:1435–42
    [Google Scholar]
  16. 16. 
    Chamizo-Ampudia A, Sans-Luque E, Llamas A, Galvan A, Fernandez E 2017. Nitrate reductase regulates plant nitric oxide homeostasis. Trends Plant Sci 22:163–73
    [Google Scholar]
  17. 17. 
    Chaouch S, Queval G, Vanderauwera S, Mhamdi A, Vandorpe M et al. 2010. Peroxisomal hydrogen peroxide is coupled to biotic defense responses by ISOCHORISMATIC SYNTHASE1 in a daylength-related manner. Plant Physiol 153:1692–705
    [Google Scholar]
  18. 18. 
    Chaouch S, Queval G, Noctor G 2012. AtRbohF is a crucial modulator of defence-associated metabolism and a key actor in the interplay between intracellular oxidative stress and pathogenesis responses in Arabidopsis. Plant J 69:613–27
    [Google Scholar]
  19. 19. 
    Cheeseman JM. 2006. Hydrogen peroxide concentrations in leaves under natural conditions. J. Exp. Bot. 57:2435–44
    [Google Scholar]
  20. 20. 
    Chioti V, Zervoudakis G. 2017. Is root catalase a bifunctional catalase-peroxidase. Antioxidants 6:39
    [Google Scholar]
  21. 21. 
    Cosio C, Dunand C. 2009. Specific functions of individual class III peroxidase genes. J. Exp. Bot. 60:391–408
    [Google Scholar]
  22. 22. 
    Couée I, Sulmon C, Gouesbet G, El Amrani A 2006. Involvement of soluble sugars in reactive oxygen species balance and responses to oxidative stress in plants. J. Exp. Bot. 57:449–59
    [Google Scholar]
  23. 23. 
    Davison AJ, Kettle AJ, Fatur DJ 1986. Mechanism of the inhibition of catalase by ascorbate. Roles of active oxygen species, copper and semidehydroascorbate. J. Biol. Chem. 261:1193–200
    [Google Scholar]
  24. 24. 
    Diaz Vivancos P, Wolff T, Markovic J, Pallardo FV, Foyer CH 2010. A nuclear glutathione cycle within the cell cycle. Biochem. J. 431:169–78
    [Google Scholar]
  25. 25. 
    Dietz KJ. 2011. Peroxiredoxins in plants and cyanobacteria. Antioxid. Redox Signal. 15:1129–59
    [Google Scholar]
  26. 26. 
    Dietz KJ, Turkan I, Krieger-Liszkay A 2016. Redox- and reactive oxygen species–dependent signaling in and from the photosynthesizing chloroplast. Plant Physiol 171:1541–60
    [Google Scholar]
  27. 27. 
    Dietzel L, Gläßer C, Liebers M, Hiekel S, Courtois F et al. 2015. Identification of early nuclear target genes of plastidial redox signals that trigger the long-term response of Arabidopsis to light quality shifts. Mol. Plant 8:1237–52
    [Google Scholar]
  28. 28. 
    Dixon DP, Hawkins T, Hussey PJ, Edwards R 2009. Enzyme activities and subcellular localization of members of the Arabidopsis glutathione transferase superfamily. J. Exp. Bot. 60:1207–18
    [Google Scholar]
  29. 29. 
    Du S, Zhang R, Zhang P, Liu H, Yan M et al. 2016. Elevated CO2-induced production of nitric oxide (NO) by NO synthase differentially affects nitrate reductase activity in Arabidopsis plants under different nitrate supplies. J. Exp. Bot. 67:893–904
    [Google Scholar]
  30. 30. 
    Engineer CB, Hashimoto-Sugimoto M, Negi J, Israelsson-Nordström M, Azoulay-Shemer T et al. 2016. CO2 sensing and CO2 regulation of stomatal conductance: advances and open questions. Trends Plant Sci 21:16–30
    [Google Scholar]
  31. 31. 
    Feechan A, Kwon E, Yun BW, Wang Y, Pallas JA, Loake GJ 2005. A central role for S-nitrosothiols in plant disease resistance. PNAS 102:8054–59
    [Google Scholar]
  32. 32. 
    Finkemeier I, König AC, Heard W, Nunes-Nesi A, Pham PA et al. 2013. Transcriptomic analysis of the role of carboxylic acids in metabolite signaling in Arabidopsis leaves. Plant Physiol 162:239–53
    [Google Scholar]
  33. 33. 
    Fischer BB, Hideg E, Krieger-Liszkay A 2013. Production, detection and signaling of singlet oxygen in photosynthetic organisms. Antioxid. Redox Signal. 18:2145–62
    [Google Scholar]
  34. 34. 
    Flugel F, Timm S, Arrivault S, Florian A, Stitt M et al. 2017. The photorespiratory metabolite 2-phosphoglycolate regulates photosynthesis and starch accumulation in Arabidopsis. Plant Cell 29:2537–51
    [Google Scholar]
  35. 35. 
    Foyer CH, Noctor G. 2003. Redox sensing and signalling associated with reactive oxygen produced in chloroplasts, peroxisomes, and mitochondria. Physiol. Plant 119:355–64
    [Google Scholar]
  36. 36. 
    Foyer CH, Noctor G. 2016. Stress-triggered redox signalling: What's in pROSpect. Plant Cell Environ 39:951–64
    [Google Scholar]
  37. 37. 
    Foyer CH, Bloom AJ, Queval G, Noctor G 2009. Photorespiratory metabolism: genes, mutants, energetics, and redox signaling. Annu. Rev. Plant Biol. 60:455–84
    [Google Scholar]
  38. 38. 
    Foyer CH, Neukermans J, Queval G, Noctor G, Harbinson J 2012. Photosynthetic control of electron transport and the regulation of gene expression. J. Exp. Bot. 63:1637–61
    [Google Scholar]
  39. 39. 
    Foyer CH, Baker A, Wright M, Sparkes IA, Mhamdi A et al. 2020. On the move: redox-dependent protein relocation in plants. J. Exp. Bot. 71:2620–31
    [Google Scholar]
  40. 40. 
    Gao X, Yuan HM, Hu YQ, Li J, Yu YT 2014. Mutation of Arabidopsis CATALASE2 results in hyponastic leaves by changes of auxin levels. Plant Cell Environ 37:175–88
    [Google Scholar]
  41. 41. 
    Gibbs DJ, Conde JV, Berckhan S, Prasad G, Mendiondo GM, Holdsworth MJ 2015. Group VII ethylene response factors coordinate oxygen and nitric oxide signal transduction and stress responses in plants. Plant Physiol 169:23–31This excellent review describes the role of group VII ethylene response factors in low-oxygen signaling in plants. It describes how these transcription factors function as oxygen- and nitric oxide–dependent substrates of the N-end rule pathway of targeted proteolysis and coordinate plant homeostatic responses to oxygen availability.
    [Google Scholar]
  42. 42. 
    Gomez-Casanovas N, Blanc-Betes E, Gonzalez-Meler MA, Azcon-Bieto J 2007. Changes in respiratory mitochondrial machinery and cytochrome and alternative pathway activities in response to energy demand underlie the acclimation of respiration to elevated CO2 in the invasive Opuntia ficus-indica. Plant Physiol 145:49–61
    [Google Scholar]
  43. 43. 
    Gupta KJ, Fernie AR, Kaiser WM, Van Dongen JT 2010. On the origins of nitric oxide. Trends Plant Sci 16:160–168
    [Google Scholar]
  44. 44. 
    Hackenberg T, Juul T, Auzina A, Gwiżdż S, Małolepszy A et al. 2013. Catalase and NO CATALASE ACTIVITY1 promote autophagy-dependent cell death in Arabidopsis. Plant Cell 25:4616–26
    [Google Scholar]
  45. 45. 
    Han Y, Chaouch S, Mhamdi A, Queval G, Zechmann B, Noctor G 2013. Functional analysis of Arabidopsis mutants points to novel roles for glutathione in coupling H2O2 to activation of salicylic acid accumulation and signaling. Antioxid. Redox Signal. 18:2106–21
    [Google Scholar]
  46. 46. 
    Havir EA, McHale NA. 1989. Regulation of catalase activity in leaves of Nicotiana sylvestris by high CO2. Plant Physiol 89:952–57
    [Google Scholar]
  47. 47. 
    Havir EA, McHale NA. 1989. Enhanced peroxidatic activity in specific catalase isozymes of tobacco, barley, and maize. Plant Physiol 91:812–15
    [Google Scholar]
  48. 48. 
    He H, Van Breusegem F, Mhamdi A 2018. Redox-dependent control of nuclear transcription in plants. J. Exp. Bot. 69:3359–72
    [Google Scholar]
  49. 49. 
    Hebbelmann I, Selinski J, Wehmeyer C, Goss T, Voss I et al. 2012. Multiple strategies to prevent oxidative stress in Arabidopsis plants lacking the malate valve enzyme NADP-malate dehydrogenase. J. Exp. Bot. 63:1445–69
    [Google Scholar]
  50. 50. 
    Heineke D, Riens B, Grosse H, Hoferichter P, Peter U et al. 1991. Redox transfer across the inner chloroplast envelope membrane. Plant Physiol 95:1131–37
    [Google Scholar]
  51. 51. 
    Henkes S, Sonnewald U, Badur R, Flachmann R, Stitt M 2001. A small decrease of plastid transketolase activity in antisense tobacco transformants has dramatic effects on photosynthesis and phenylpropanoid metabolism. Plant Cell 13:535–51
    [Google Scholar]
  52. 52. 
    Henzler T, Steudle E. 2000. Transport and metabolic degradation of hydrogen peroxide in Chara corallina: model calculations and measurements with the pressure probe suggest transport of H2O2 across water channels. J. Exp. Bot. 51:2053–66
    [Google Scholar]
  53. 53. 
    Hõrak H, Sierla M, Tõldsepp K, Wang C, Wang YS et al. 2016. A dominant mutation in the HT1 kinase uncovers roles of MAP kinases and GHR1 in CO2-induced stomatal closure. Plant Cell 28:2493–509
    [Google Scholar]
  54. 54. 
    Hu H, Boisson-Dernier A, Israelsson-Nordström M, Böhmer M, Xue S et al. 2010. Carbonic anhydrases are upstream regulators of CO2-controlled stomatal movements in guard cells. Nat. Cell Biol. 12:87–93
    [Google Scholar]
  55. 55. 
    Hu H, Rappel WJ, Occhipinti R, Ries A, Böhmer M et al. 2015. Distinct cellular locations of carbonic anhydrases mediate carbon dioxide control of stomatal movements. Plant Physiol 169:1168–78
    [Google Scholar]
  56. 56. 
    Huang S, Van Aken O, Schwarzländer M, Belt K, Millar AH 2016. The roles of mitochondrial reactive oxygen species in cellular signaling and stress response in plants. Plant Physiol 171:1551–59
    [Google Scholar]
  57. 57. 
    Igamberdiev AU, Bykova NV, Gardeström P 1997. Involvement of cyanide-resistant and rotenone-insensitive pathways of mitochondrial electron transport during oxidation of glycine in higher plants. FEBS Lett 412:265–69
    [Google Scholar]
  58. 58. 
    Johnston EJ, Rylott EL, Beynon E, Lorenz A, Chechik V, Bruce NC 2015. Monodehydroascorbate reductase mediates TNT toxicity in plants. Science 349:1072–75Reported a novel prooxidant function for a classical antioxidative enzyme, underscoring the complexity of ROS-related redox regulation and signaling in plants.
    [Google Scholar]
  59. 59. 
    Juul T, Malolepszy A, Dybkaer K, Kidmose R, Rasmussen JT et al. 2010. The in vivo toxicity of hydroxyurea depends on its direct target catalase. J. Biol. Chem. 285:21411–15
    [Google Scholar]
  60. 60. 
    Kadotani N, Akagi A, Takatsuji H, Miwa T, Igarashi D 2016. Exogenous proteinogenic amino acids induce systemic resistance in rice. BMC Plant Biol 16:60
    [Google Scholar]
  61. 61. 
    Kangasjärvi S, Neukermans J, Li S, Aro EM, Noctor G 2012. Photosynthesis, photorespiration, and light signalling in defence responses. J. Exp. Bot. 63:1619–36
    [Google Scholar]
  62. 62. 
    Karpinska B, Rasool B, Zhang K, Pastok D, Morris J et al. 2018. The redox state of the apoplast influences the acclimation of photosynthesis and leaf metabolism to changing irradiance. Plant Cell Environ 41:1083–97
    [Google Scholar]
  63. 63. 
    Karpinska B, Alomrani SO, Foyer CH 2017. Inhibitor-induced oxidation of the nucleus and cytosol in Arabidopsis thaliana: implications for organelle to nucleus retrograde signalling. Philos. Trans. R. Soc. Lond. B 372:20160392
    [Google Scholar]
  64. 64. 
    Keys AJ. 1999. Biochemistry of photorespiration and the consequences for plant performance. Plant Carbohydrate Biochemistry JA Bryant, MM Burrell, NJ Kruger 147–61 Oxford, UK: BIOS Sci.
    [Google Scholar]
  65. 65. 
    Kneeshaw S, Keyani R, Delorme-Hinoux V, Imrie L, Loake GJ et al. 2017. Nucleoredoxin guards against oxidative stress by protecting antioxidant enzymes. PNAS 114:8414–19
    [Google Scholar]
  66. 66. 
    Krömer S. 1995. Respiration during photosynthesis. Annu. Rev. Plant Physiol. Plant Mol. Biol. 46:45–70
    [Google Scholar]
  67. 67. 
    Kwak JM, Mori IC, Pei ZM, Leonhardt N, Torres MA et al. 2003. NADPH oxidase AtrbohD and AtrbohF genes function in ROS-dependent ABA signaling in Arabidopsis. EMBO J 22:2623–33
    [Google Scholar]
  68. 68. 
    Laloi C, Mestres-Ortega D, Marco Y, Meyer Y, Reichheld JP 2004. The Arabidopsis cytosolic thioredoxin h5 gene induction by oxidative stress and its W-box-mediated response to pathogen elicitor. Plant Physiol 134:1006–16
    [Google Scholar]
  69. 69. 
    Legakis JE, Koepke JI, Jedeszko C, Barlaskar F, Terlecky LJ et al. 2002. Peroxisome senescence in human fibroblasts. Mol. Biol. Cell 13:4243–55
    [Google Scholar]
  70. 70. 
    Li F, Wang J, Ma C, Zhao Y, Wang Y et al. 2013. Glutamate receptor–like channel3.3 is involved in mediating glutathione‐triggered cytosolic Ca2+ transients, transcriptional changes and innate immunity responses in Arabidopsis. Plant Physiol 162:1497–509
    [Google Scholar]
  71. 71. 
    Li Y, Chen L, Mu J, Zuo J 2013. LESION SIMULATING DISEASE1 interacts with catalases to regulate hypersensitive cell death in Arabidopsis. Plant Physiol 163:1059–70
    [Google Scholar]
  72. 72. 
    Li J, Liu J, Wang G, Cha J-Y, Li G et al. 2015. A chaperone function of NO CATALASE ACTIVITY1 is required to maintain catalase activity and for multiple stress responses in Arabidopsis. Plant Cell 27:908–25
    [Google Scholar]
  73. 73. 
    Lillo C, Lea US, Ruoff P 2008. Nutrient depletion as a key factor for manipulating gene expression and product formation in different branches of the flavonoid pathway. Plant Cell Environ 31:587–601
    [Google Scholar]
  74. 74. 
    Lindermayr C, Sell S, Müller B, Leister D, Durner J 2010. Redox regulation of the NPR1-TGA1 system of Arabidopsis thaliana by nitric oxide. Plant Cell 22:2894–907
    [Google Scholar]
  75. 75. 
    Long SP, Ort DR. 2010. More than taking the heat: crops and global change. Curr. Opin. Plant Biol. 13:241–48
    [Google Scholar]
  76. 76. 
    Manzoor H, Kelloniemi J, Chiltz A, Wendehenne D, Pugin A et al. 2013. Involvement of the glutamate receptor AtGLR33 in plant defense signaling and resistance to Hyaloperonospora arabidopsidis. Plant J 76:466–80
    [Google Scholar]
  77. 77. 
    Marchal C, Delorme-Hinoux V, Bariat L, Siala W, Belin C et al. 2014. NTR/NRX define a new thioredoxin system in the nucleus of Arabidopsis thaliana cells. Mol. Plant 7:30–44
    [Google Scholar]
  78. 78. 
    Marquez-Garcia B, Njo M, Beeckman T, Goormachtig S, Foyer CH 2013. A new role for glutathione in the regulation of root architecture linked to strigolactones. Plant Cell Environ 37:488–98
    [Google Scholar]
  79. 79. 
    Mathioudakis MM, Veiga RS, Canto T, Medina V, Mossialos D et al. 2013. Pepino mosaic virus triple gene block protein 1 (TGBp1) interacts with and increases tomato catalase 1 activity to enhance virus accumulation. Mol. Plant Pathol. 14:589–601
    [Google Scholar]
  80. 80. 
    Matros A, Amme S, Kettig B, Buck-Sorlin GH, Sonnewald U, Mock HP 2006. Growth at elevated CO2 concentrations leads to modified profiles of secondary metabolites in tobacco cv. SamsunNN and to increased resistance against infection with potato virus Y. Plant Cell Environ 29:126–37
    [Google Scholar]
  81. 81. 
    Meyer Y, Belin C, Delorme-Hinoux V, Reichheld JP, Riondet C 2012. Thioredoxin and glutaredoxin systems in plants: molecular mechanisms, crosstalks, and functional significance. Antioxid. Redox Signal. 17:1124–60
    [Google Scholar]
  82. 82. 
    Mhamdi A, Hager J, Chaouch S, Queval G, Han Y et al. 2010. Arabidopsis GLUTATHIONE REDUCTASE 1 is essential for the metabolism of intracellular H2O2 and to enable appropriate gene expression through both salicylic acid and jasmonic acid signaling pathways. Plant Physiol 153:1144–60
    [Google Scholar]
  83. 83. 
    Mhamdi A, Mauve C, Gouia H, Saindrenan P, Hodges M, Noctor G 2010. Cytosolic NADP-dependent isocitrate dehydrogenase contributes to redox homeostasis and the regulation of pathogen responses in Arabidopsis leaves. Plant Cell Environ 33:1112–23
    [Google Scholar]
  84. 84. 
    Mhamdi A, Noctor G. 2016. High CO2 primes plant biotic stress defences through redox-linked pathways. Plant Physiol 172:929–42Reported that marked activation of salicylic acid signaling was caused by high CO2 in a redox-dependent manner.
    [Google Scholar]
  85. 85. 
    Mhamdi A, Noctor G, Baker A 2012. Plant catalases: peroxisomal redox guardians. Arch. Biochem. Biophys. 525:181–94
    [Google Scholar]
  86. 86. 
    Mhamdi A, Queval G, Chaouch S, Vanderauwera S, Van Breusegem F, Noctor G 2010. Catalases in plants: a focus on Arabidopsis mutants as stress-mimic models. J. Exp. Bot. 61:4197–220
    [Google Scholar]
  87. 87. 
    Miller G, Schlauch K, Tam R, Cortes D, Torres MA et al. 2009. The plant NADPH oxidase RBOHD mediates rapid systemic signaling in response to diverse stimuli. Sci. Signal. 2:ra45This study was one of the first to report systemic cell-to-cell signaling via reactive oxygen species.
    [Google Scholar]
  88. 88. 
    Moore M, Gossmann N, Dietz KJ 2016. Redox regulation of cytosolic translation in plants. Trends Plant Sci 21:388–97
    [Google Scholar]
  89. 89. 
    Murota K, Shimura H, Takeshita M, Masuta C 2017. Interaction between Cucumber mosaic virus 2b protein and plant catalase induces a specific necrosis in association with proteasome activity. Plant Cell Rep 36:37–47
    [Google Scholar]
  90. 90. 
    Munné-Bosch S, Queval G, Foyer CH 2013. The impact of global change factors on redox signaling underpinning stress tolerance. Plant Physiol 161:5–19
    [Google Scholar]
  91. 91. 
    Noctor G. 2015. Lighting the fuse on toxic TNT. Science 349:1052–53
    [Google Scholar]
  92. 92. 
    Noctor G, Foyer CH. 1998. A re-evaluation of the ATP: NADPH budget during C3 photosynthesis: a contribution from nitrate assimilation and its associated respiratory activity. J. Exp. Bot. 49:1895–908
    [Google Scholar]
  93. 93. 
    Noctor G, Foyer CH. 1998. Ascorbate and glutathione: keeping active oxygen under control. Annu. Rev. Plant Physiol. Plant Mol. Biol. 49:249–79
    [Google Scholar]
  94. 94. 
    Noctor G, Foyer CH. 2016. Intracellular redox compartmentation and ROS-related communication in regulation and signaling. Plant Physiol 171:1581–92
    [Google Scholar]
  95. 95. 
    Noctor G, Mhamdi A. 2017. Climate change, CO2, and defense: the metabolic, redox, and signaling perspectives. Trends Plant Sci 22:857–70
    [Google Scholar]
  96. 96. 
    Noctor G, Mhamdi A, Foyer CH 2016. Oxidative stress and antioxidative systems: recipes for successful data collection and interpretation. Plant Cell Environ 39:1140–60
    [Google Scholar]
  97. 97. 
    Noctor G, Reichheld JP, Foyer CH 2018. ROS-related signaling in plants. Semin. Cell Dev. Biol. 80:3–12
    [Google Scholar]
  98. 98. 
    Noctor G, Veljovic-Jovanovic SD, Driscoll S, Novitskaya L, Foyer CH 2002. Drought and oxidative load in the leaves of C3 plants: a predominant role for photorespiration?. Ann. Bot. 89:841–50
    [Google Scholar]
  99. 99. 
    O'Brien JA, Daudi A, Butt VS, Bolwell GP 2012. Reactive oxygen species and their role in plant defence and cell wall metabolism. Planta 236:765–69
    [Google Scholar]
  100. 100. 
    Oshima Y, Kamigaki A, Nakamori C, Mano S, Hayashi M et al. 2008. Plant catalase is imported into peroxisomes by Pex5p but is distinct from typical PTS1 import. Plant Cell Physiol 49:671–77
    [Google Scholar]
  101. 101. 
    Petersen M, Brodersen P, Naested H, Andreasson E, Lindhart U et al. 2000. Arabidopsis map kinase 4 negatively regulates systemic acquired resistance. Cell 103:1111–20
    [Google Scholar]
  102. 102. 
    Queval G, Foyer CH. 2012. Redox regulation of photosynthetic gene expression. Philos. Trans. R. Soc. Lond. B 367:3475–85
    [Google Scholar]
  103. 103. 
    Queval G, Issakidis-Bourguet E, Hoeberichts FA, Vandorpe M, Gakière B et al. 2007. Conditional oxidative stress responses in the Arabidopsis photorespiratory mutant cat2 demonstrate that redox state is a key modulator of daylength-dependent gene expression and define photoperiod as a crucial factor in the regulation of H2O2-induced cell death. Plant J 52:640–57
    [Google Scholar]
  104. 104. 
    Queval G, Neukermans J, Vanderauwera S, Van Breusegem F, Noctor G 2012. Day length is a key regulator of transcriptomic responses to both CO2 and H2O2 in Arabidopsis. Plant Cell Environ 35:374–87
    [Google Scholar]
  105. 105. 
    Qiu QS, Huber JL, Booker FL, Jain V, Leakey AD et al. 2008. Increased protein carbonylation in leaves of Arabidopsis and soybean in response to elevated [CO2]. Photosynth. Res. 97:155–66
    [Google Scholar]
  106. 106. 
    Rahantaniaina MS, Li S, Chatel-Innocenti G, Tuzet A, Issakidis-Bourguet E et al. 2017. Chloroplastic and cytosolic dehydroascorbate reductases co-operate in oxidative stress-driven activation of the salicylic acid pathway. Plant Physiol 174:956–71
    [Google Scholar]
  107. 107. 
    Rojas CM, Senthil-Kumar M, Wang K, Ryu CM, Kaundal A, Mysore KS 2012. Glycolate oxidase modulates reactive oxygen species–mediated signal transduction during nonhost resistance in Nicotiana benthamiana and Arabidopsis. Plant Cell 24:336–52
    [Google Scholar]
  108. 108. 
    Scheibe R, Backhausen JE, Emmerlich V, Holtgrefe S 2005. Strategies to maintain redox homeostasis during photosynthesis under changing conditions. J. Exp. Bot. 56:1481–89
    [Google Scholar]
  109. 109. 
    Schnaubelt D, Queval G, Dong Y, Diaz-Vivancos P, Makgopa ME et al. 2015. Low glutathione regulates gene expression and the redox potentials of the nucleus and cytosol in Arabidopsis thaliana. Plant Cell Environ 38:266–79
    [Google Scholar]
  110. 110. 
    Seneviratne SI, Rogelj J, Séférian R, Wartenburger R, Allen MR et al. 2018. The many possible climates from the Paris Agreement's aim of 1.5°C warming. Nature 558:41–49
    [Google Scholar]
  111. 111. 
    Sewelam N, Jaspert N, Van Der Kelen K, Tognetti VB, Schmitz J et al. 2014. Spatial H2O2 signaling specificity: H2O2 from chloroplasts and peroxisomes modulates the plant transcriptome differentially. Mol. Plant 7:1191–210
    [Google Scholar]
  112. 112. 
    Shameer S, Ratcliffe RG, Sweetlove LJ 2019. Leaf energy balance requires mitochondrial respiration and export of chloroplast NADPH in the light. Plant Physiol 180:1947–61
    [Google Scholar]
  113. 113. 
    Shi K, Li X, Zhang H, Zhang GQ, Liu YR et al. 2015. Guard cell hydrogen peroxide and nitric oxide mediate elevated CO2-induced stomatal movement in tomato. New Phytol 208:342–53
    [Google Scholar]
  114. 114. 
    Siemens J, González MC, Wolf S, Hofmann C, Greiner S et al. 2011. Extracellular invertase is involved in the regulation of clubroot disease in Arabidopsis thaliana.Mol. Plant Pathol 12:247–62
    [Google Scholar]
  115. 115. 
    Slaymaker DH, Navarre DA, Clark D, del Pozo O, Martin GB, Klessig DF 2002. The tobacco salicylic acid–binding protein 3 (SABP3) is the chloroplast carbonic anhydrase, which exhibits antioxidant activity and plays a role in the hypersensitive defense response. PNAS 99:11640–45The authors reported a link between carbonic anhydrase and biotic stress signaling.
    [Google Scholar]
  116. 116. 
    Sørhagen K, Laxa M, Peterhänsel C, Reumann S 2013. The emerging role of photorespiration and non-photorespiratory peroxisomal metabolism in pathogen defence. Plant Biol 15:723–36
    [Google Scholar]
  117. 117. 
    South PF, Cavanagh AP, Liu HW, Ort DR 2019. Synthetic glycolate metabolism pathways stimulate crop growth and productivity in the field. Science 363:eaat9077This work opened up prospects for crop improvement by metabolic diversion of glycolate produced in photorespiration.
    [Google Scholar]
  118. 118. 
    Strader LC, Culler AH, Cohen JD, Bartel B 2010. Conversion of endogenous indole-3-butyric acid to indole-3-acetic acid drives cell expansion in Arabidopsis seedlings. Plant Physiol 153:1577–86
    [Google Scholar]
  119. 119. 
    Sun Y, Li P, Deng M, Shen D, Dai G et al. 2017. The Ralstonia solanacearum effector RipAK suppresses plant hypersensitive response by inhibiting the activity of host catalases. Cell Microbiol 19:e12736
    [Google Scholar]
  120. 120. 
    Tada Y, Spoel SH, Pajerowska-Mukhtar K, Mou Z, Song J et al. 2008. Plant immunity requires conformational changes of NPR1 via S-nitrosylation and thioredoxins. Science 321:952–56
    [Google Scholar]
  121. 121. 
    Tcherkez G, Mahé A, Gauthier P, Mauve C, Gout E et al. 2009. folio respiratory fluxomics revealed by 13C isotopic labeling and H/D isotope effects highlight the noncyclic nature of the tricarboxylic acid “cycle” in illuminated leaves. Plant Physiol 151:620–30
    [Google Scholar]
  122. 122. 
    Tian W, Hou C, Ren Z, Pan Y, Jia J et al. 2015. A molecular pathway for CO2 response in Arabidopsis guard cells. Nat. Commun. 6:6057This article identified the genetic components required for CO2-induced stomatal closure.
    [Google Scholar]
  123. 123. 
    Tognetti VB, Van Aken O, Morreel K, Vandenbroucke K, van de Cotte B et al. 2010. Perturbation of indole-3-butyric acid homeostasis by the UDP-glucosyltransferase UGT74E2 modulates Arabidopsis architecture and water stress tolerance. Plant Cell 22:2660–79
    [Google Scholar]
  124. 124. 
    Torres MA, Jones JD, Dangl JL 2006. Reactive oxygen species signaling in response to pathogens. Plant Physiol 141:373–78
    [Google Scholar]
  125. 125. 
    Tuzet A, Rahantaniaina MS, Noctor G 2018. Analyzing the function of catalase and the ascorbate-glutathione pathway in H2O2 processing: insights from an experimentally constrained kinetic model. Antioxid. Redox Signal. 30:1238–68
    [Google Scholar]
  126. 126. 
    Vanacker H, Carver TL, Foyer CH 2000. Early H2O2 accumulation in mesophyll cells leads to induction of glutathione during the hyper-sensitive response in the barley–powdery mildew interaction. Plant Physiol 123:1289–300
    [Google Scholar]
  127. 127. 
    Vanderauwera S, Zimmermann P, Rombauts S, Vandenabeele S, Langebartels C et al. 2005. Genome-wide analysis of hydrogen peroxide-regulated gene expression in Arabidopsis reveals a high light-induced transcriptional cluster involved in anthocyanin biosynthesis. Plant Physiol 139:806–21
    [Google Scholar]
  128. 128. 
    Vanderauwera S, Suzuki N, Miller G, van de Cotte B, Morsa S et al. 2011. Extranuclear protection of chromosomal DNA from oxidative stress. PNAS 108:1711–16
    [Google Scholar]
  129. 129. 
    Verslues PE, Batelli G, Grillo S, Agius F, Kim YS et al. 2007. Interaction of SOS2 with nucleoside diphosphate kinase 2 and catalases reveals a point of connection between salt stress and H2O2 signaling in Arabidopsis thaliana. Mol. Cell Biol 27:7771–80
    [Google Scholar]
  130. 130. 
    Vestergaard CL, Flyvbjerg H, Møller IM 2012. Intracellular signaling by diffusion: Can waves of hydrogen peroxide transmit intracellular information in plant cells?. Front. Plant Sci. 3:295
    [Google Scholar]
  131. 131. 
    Vlot AC, Dempsey DA, Klessig DF 2009. Salicylic acid, a multifaceted hormone to combat disease. Annu. Rev. Phytopathol. 47:177–206
    [Google Scholar]
  132. 132. 
    Vogel MO, Moore M, König K, Pecher P, Alsharafa K et al. 2014. Fast retrograde signaling in response to high light involves metabolite export, MITOGEN-ACTIVATED PROTEIN KINASE6, and AP2/ERF transcription factors in Arabidopsis. Plant Cell 26:1151–65
    [Google Scholar]
  133. 133. 
    Wang J, Cheung M, Rasooli L, Amirsadeghi S, Vanlerberghe GC 2014. Plant respiration in a high CO2 world: How will alternative oxidase respond to future atmospheric and climatic conditions. Can. J. Plant Sci. 94:1091–101
    [Google Scholar]
  134. 134. 
    Wang YQ, Feechan A, Yun BW, Shafiei R, Hofmann A et al. 2009. S-Nitrosylation of AtSABP3 antagonizes the expression of plant immunity. J. Biol. Chem. 284:2131–37
    [Google Scholar]
  135. 135. 
    Wasczcak C, Carmody M, Kangasjärvi J 2018. Reactive oxygen species in plant cell signaling. Annu. Rev. Plant Biol. 69:209–36
    [Google Scholar]
  136. 136. 
    Williams A, Pétriacq P, Schwarzenbacher RE, Beerling DJ, Ton J 2018. Mechanisms of glacial-to-future atmospheric CO2 effects on plant immunity. New Phytol 218:752–61
    [Google Scholar]
  137. 137. 
    Xiang L, Li Y, Roland F, Van Den Ende W 2011. Neutral invertase, hexokinase and mitochondrial ROS homeostasis. Emerging links between sugar metabolism, sugar signaling and ascorbate synthesis. Plant Signal Behav 6:1567–73
    [Google Scholar]
  138. 138. 
    Yang T, Poovaiah BW. 2002. Hydrogen peroxide homeostasis: activation of plant catalase by calcium/calmodulin. PNAS 99:4097–102
    [Google Scholar]
  139. 139. 
    Yang Z, Mhamdi A, Noctor G 2019. Analysis of catalase mutants underscores the essential role of CATALASE2 for plant growth and day length–dependent oxidative signalling. Plant Cell Environ 42:688–700
    [Google Scholar]
  140. 140. 
    Yi C, Yao K, Cai S, Li H, Zhou J et al. 2015. High atmospheric carbon dioxide-dependent alleviation of salt stress is linked to RESPIRATORY BURST OXIDASE 1 (RBOH1)-dependent H2O2 production in tomato (Solanum lycopersicum). J. Exp. Bot. 66:7391–404
    [Google Scholar]
  141. 141. 
    Yuan H-M, Liu W-C, Lu Y-T 2017. CATALASE2 coordinates SA-mediated repression of both auxin accumulation and JA biosynthesis in plant defences. Cell Host Microbe 21:143–55
    [Google Scholar]
  142. 142. 
    Zámock M, Gasselhuber B, Furtmüller PG, Obinger C 2012. Molecular evolution of hydrogen peroxide degrading enzymes. Arch. Biochem. Biophys. 525:131–44
    [Google Scholar]
  143. 143. 
    Zavala JA, Nabity PD, DeLucia EH 2013. An emerging understanding of mechanisms governing insect herbivory under elevated CO2. Annu. Rev. Entomol. 58:79–97
    [Google Scholar]
  144. 144. 
    Zhang M, Li Q, Liu T, Liu L, Shen D et al. 2015. Two cytoplasmic effectors of Phytophthora sojae regulate plant cell death via interactions with plant catalases. Plant Physiol 167:164–75
    [Google Scholar]
  145. 145. 
    Zhang S, Li X, Sun Z, Shao S, Hu L et al. 2015. Antagonism between phytohormone signalling underlies the variation in disease susceptibility of tomato plants under elevated CO2. J. Exp. Bot. 66:1951–63
    [Google Scholar]
  146. 146. 
    Zhang X, Ivanova A, Vandepoele K, Radomiljac J, Van de Velde J et al. 2017. The transcription factor MYB29 is a regulator of ALTERNATIVE OXIDASE1a. Plant Physiol 173:1824–43
    [Google Scholar]
  147. 147. 
    Zhao Y, Luo L, Xu J, Xin P, Guo H et al. 2018. Malate transported from chloroplast to mitochondrion triggers production of ROS and PCD in Arabidopsis thaliana. Cell Res 28:448–61
    [Google Scholar]
  148. 148. 
    Zhou H, Finkemeier I, Guan W, Tossounian M, Wei B et al. 2018. Oxidative stress–triggered interactions between the succinyl- and acetyl-proteomes of rice leaves. Plant Cell Environ 41:1139–53
    [Google Scholar]
  149. 149. 
    Zhou YH, Ge S, Jin L, Yao K, Wang Y et al. 2019. A novel CO2-responsive systemic signaling pathway controlling plant mycorrhizal symbiosis. New Phytol 224:106–16
    [Google Scholar]
  150. 150. 
    Zhou YB, Liu C, Tang DY, Yan L, Wang D et al. 2018. The receptor-like cytoplasmic kinase STRK1 phosphorylates and activates CatC, thereby regulating H2O2 homeostasis and improving salt tolerance in rice. Plant Cell 30:1100–18
    [Google Scholar]
  151. 151. 
    Zou JJ, Li XD, Ratnasekera D, Wang C, Liu WX et al. 2015. Arabidopsis CALCIUM-DEPENDENT PROTEIN KINASE8 and CATALASE3 function in abscisic acid–mediated signaling and H2O2 homeostasis in stomatal guard cells under drought stress. Plant Cell 27:1445–60
    [Google Scholar]
/content/journals/10.1146/annurev-arplant-050718-095955
Loading
/content/journals/10.1146/annurev-arplant-050718-095955
Loading

Data & Media loading...

  • Article Type: Review Article
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error