Tuning of Redox Regulatory Mechanisms, Reactive Oxygen Species and Redox Homeostasis under Salinity Stress

Mechanisms of Salinity Tolerance

Munns, R., & Tester, M. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092911 · Cited by 13,792

Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants

Gill, S. S., & Tuteja, N. (2010) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2010.08.016 · Cited by 11,663

Oxidative stress, antioxidants and stress tolerance

Mittler, R. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(02)02312-9 · Cited by 10,764

Reactive oxygen gene network of plants

Mittler, R., Vanderauwera, S., Gollery, M., & Van Breusegem, F. (2004) · Trends in Plant Science · doi:10.1016/j.tplants.2004.08.009 · Cited by 5,579

Reactive Oxygen Species, Oxidative Damage, and Antioxidative Defense Mechanism in Plants under Stressful Conditions

Sharma, P., Jha, A. B., Dubey, R. S., & Pessarakli, M. (2012) · Journal of Botany · doi:10.1155/2012/217037 · Cited by 5,473

Roles of glycine betaine and proline in improving plant abiotic stress resistance

Ashraf, M., & Foolad, M. R. (2007) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2005.12.006 · Cited by 4,776

Reactive oxygen species homeostasis and signalling during drought and salinity stresses

MILLER, G., SUZUKI, N., CIFTCI‐YILMAZ, S., & MITTLER, R. (2010) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2009.02041.x · Cited by 3,945

Plant salt tolerance

Zhu, J.-K. (2001) · Trends in Plant Science · doi:10.1016/s1360-1385(00)01838-0 · Cited by 3,511

NOX enzymes and the biology of reactive oxygen

Lambeth, J. D. (2004) · Nature Reviews Immunology · doi:10.1038/nri1312 · Cited by 3,125

Salinity tolerance in halophytes*

Flowers, T. J., & Colmer, T. D. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02531.x · Cited by 2,789

Oxidative Modifications to Cellular Components in Plants

Møller, I. M., Jensen, P. E., & Hansson, A. (2007) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.58.032806.103946 · Cited by 1,943

ROS as key players in plant stress signalling

Baxter, A., Mittler, R., & Suzuki, N. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/ert375 · Cited by 1,933

NADPH oxidase AtrbohD and AtrbohF genes function in ROS-dependent ABA signaling in Arabidopsis

Kwak, J. M. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg277 · Cited by 1,736

Methods and concepts in quantifying resistance to drought, salt and freezing, abiotic stresses that affect plant water status

Verslues, P. E., Agarwal, M., Katiyar‐Agarwal, S., Zhu, J., & Zhu, J. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2005.02593.x · Cited by 1,719

Arabidopsis gp91 phox homologues AtrbohD and AtrbohF are required for accumulation of reactive oxygen intermediates in the plant defense response

Torres, M. A., Dangl, J. L., & Jones, J. D. G. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.012452499 · Cited by 1,703

ROS and redox signalling in the response of plants to abiotic stress

SUZUKI, N., KOUSSEVITZKY, S., MITTLER, R., & MILLER, G. (2012) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2011.02336.x · Cited by 1,694

World salinization with emphasis on Australia

Rengasamy, P. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erj108 · Cited by 1,686

Ascorbate peroxidase - a hydrogen peroxide-scavenging enzyme in plants

Asada, K. (1992) · Physiologia Plantarum · doi:10.1034/j.1399-3054.1992.850216.x · Cited by 1,550

Metabolic implications of stress-induced proline accumulation in plants

Hare, P. D., & Cress, W. A. (1997) · Plant Growth Regulation · doi:10.1023/a:1005703923347 · Cited by 1,397

Mitochondrial metabolism of reactive oxygen species

Andreyev, A. Y., Kushnareva, Y. E., & Starkov, A. A. (2005) · Biochemistry (Moscow) · doi:10.1007/s10541-005-0102-7 · Cited by 1,336

Oxidative burst: an early plant response to pathogen infection

WOJTASZEK, P. (1997) · Biochemical Journal · doi:10.1042/bj3220681 · Cited by 1,300

The Plant NADPH Oxidase RBOHD Mediates Rapid Systemic Signaling in Response to Diverse Stimuli

Miller, G., Schlauch, K., Tam, R., Cortes, D., Torres, M. A., Shulaev, V., Dangl, J. L., & Mittler, R. (2009) · Science Signaling · doi:10.1126/scisignal.2000448 · Cited by 1,141

PHYSIOLOGY AND MOLECULAR BIOLOGY OF SALINITY STRESS TOLERANCE IN PLANTS

Sairam, R. K., & Tyagi, A. (2004) · Cited by 1,029

Respiratory burst oxidases: the engines of ROS signaling

Suzuki, N., Miller, G., Morales, J., Shulaev, V., Torres, M. A., & Mittler, R. (2011) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2011.07.014 · Cited by 995

Arabidopsis Mutants Define a Central Role for the Xanthophyll Cycle in the Regulation of Photosynthetic Energy Conversion

Niyogi, K. K., Grossman, A. R., & Björkman, O. (1998) · The Plant Cell · doi:10.1105/tpc.10.7.1121 · Cited by 968

Antioxidant functions of carotenoids

Krinsky, N. I. (1989) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(89)90143-3 · Cited by 926

Production of Reactive Oxygen Species by Plant NADPH Oxidases

Sagi, M., & Fluhr, R. (2006) · Plant Physiology · doi:10.1104/pp.106.078089 · Cited by 843

Evidence for the Presence of the Ascorbate-Glutathione Cycle in Mitochondria and Peroxisomes of Pea Leaves

Jimenez, A., Hernandez, J. A., del Rio, L. A., & Sevilla, F. (1997) · Plant Physiology · doi:10.1104/pp.114.1.275 · Cited by 838

MOLECULAR MECHANISMS OF QUENCHING OF REACTIVE OXYGEN SPECIES BY PROLINE UNDER STRESS IN PLANTS

J.Alia, M., Bhalu, B., & Mohanty, P. S. (2002) · Cited by 832

Studies on reactions of illuminated chloroplasts

Mehler, A. H. (1951) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(51)90082-3 · Cited by 814

Singlet oxygen production in photosynthesis

Krieger-Liszkay, A. (2004) · Journal of Experimental Botany · doi:10.1093/jxb/erh237 · Cited by 800

Photorespiration: metabolic pathways and their role in stress protection

Wingler, A., Lea, P. J., Quick, W. P., & Leegood, R. C. (2000) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2000.0712 · Cited by 768

The role of ABA and MAPK signaling pathways in plant abiotic stress responses

Danquah, A., de Zelicourt, A., Colcombet, J., & Hirt, H. (2014) · Biotechnology Advances · doi:10.1016/j.biotechadv.2013.09.006 · Cited by 755

Antioxidant Systems and O2 .−/H2O2 Production in the Apoplast of Pea Leaves. Its Relation with Salt-Induced Necrotic Lesions in Minor Veins

Hernández, J. A., Ferrer, M. A., Jiménez, A., Barceló, A. R., & Sevilla, F. (2001) · Plant Physiology · doi:10.1104/pp.010188 · Cited by 744

Glycinebetaine protects plants against abiotic stress: mechanisms and biotechnological applications

CHEN, T. H. H., & MURATA, N. (2011) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2010.02232.x · Cited by 735

A burst of plant NADPH oxidases

Marino, D., Dunand, C., Puppo, A., & Pauly, N. (2012) · Trends in Plant Science · doi:10.1016/j.tplants.2011.10.001 · Cited by 726

Duplicated P5CS genes of Arabidopsis play distinct roles in stress regulation and developmental control of proline biosynthesis

Székely, G., Ábrahám, E., Cséplő, Á., Rigó, G., Zsigmond, L., Csiszár, J., Ayaydin, F., Strizhov, N., Jásik, J., Schmelzer, E., et al. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03318.x · Cited by 716

The Roles of Reactive Oxygen Metabolism in Drought: Not So Cut and Dried

Noctor, G., Mhamdi, A., & Foyer, C. H. (2014) · Plant Physiology · doi:10.1104/pp.113.233478 · Cited by 706

Functions of amine oxidases in plant development and defence

Cona, A., Rea, G., Angelini, R., Federico, R., & Tavladoraki, P. (2006) · Trends in Plant Science · doi:10.1016/j.tplants.2005.12.009 · Cited by 662

Drought and Oxidative Load in the Leaves of C3 Plants: a Predominant Role for Photorespiration?

NOCTOR, G. (2002) · Annals of Botany · doi:10.1093/aob/mcf096 · Cited by 644

How reactive oxygen species and proline face stress together

Ben Rejeb, K., Abdelly, C., & Savouré, A. (2014) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2014.04.007 · Cited by 595

Comparative Genomics in Salt Tolerance between Arabidopsis and Arabidopsis-Related Halophyte Salt Cress Using Arabidopsis Microarray

Taji, T., Seki, M., Satou, M., Sakurai, T., Kobayashi, M., Ishiyama, K., Narusaka, Y., Narusaka, M., Zhu, J.-K., & Shinozaki, K. (2004) · Plant Physiology · doi:10.1104/pp.104.039909 · Cited by 594

A Plant Homolog of the Neutrophil NADPH Oxidase gp91phox Subunit Gene Encodes a Plasma Membrane Protein with Ca2+ Binding Motifs

Keller, T., Damude, H. G., Werner, D., Doerner, P., Dixon, R. A., & Lamb, C. (1998) · The Plant Cell · doi:10.1105/tpc.10.2.255 · Cited by 584

Increased resistance to oxidative stress in transgenic plants that overexpress chloroplastic Cu/Zn superoxide dismutase.

Gupta, A. S., Heinen, J. L., Holaday, A. S., Burke, J. J., & Allen, R. D. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.4.1629 · Cited by 558

A tidal wave of signals: calcium and ROS at the forefront of rapid systemic signaling

Gilroy, S., Suzuki, N., Miller, G., Choi, W.-G., Toyota, M., Devireddy, A. R., & Mittler, R. (2014) · Trends in Plant Science · doi:10.1016/j.tplants.2014.06.013 · Cited by 554

C4 photosynthesis and water stress.

Ghannoum, O. (2008) · Annals of Botany · doi:10.1093/aob/mcn093 · Cited by 538

Evidence for a respiratory chain in the chloroplast

Bennoun, P. (1982) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.79.14.4352 · Cited by 481

Overexpression of Glutathione Reductase but Not Glutathione Synthetase Leads to Increases in Antioxidant Capacity and Resistance to Photoinhibition in Poplar Trees

Foyer, C. H., Souriau, N., Perret, S., Lelandais, M., Kunert, K. J., Pruvost, C., & Jouanin, L. (1995) · Plant Physiology · doi:10.1104/pp.109.3.1047 · Cited by 478

Antioxidant defense responses: physiological plasticity in higher plants under abiotic constraints

Jaleel, C. A., Riadh, K., Gopi, R., Manivannan, P., Inès, J., Al-Juburi, H. J., Chang-Xing, Z., Hong-Bo, S., & Panneerselvam, R. (2009) · Acta Physiologiae Plantarum · doi:10.1007/s11738-009-0275-6 · Cited by 478

NADPH oxidase AtrbohD and AtrbohF function in ROS-dependent regulation of Na+/K+ homeostasis in Arabidopsis under salt stress

Ma, L., Zhang, H., Sun, L., Jiao, Y., Zhang, G., Miao, C., & Hao, F. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/err280 · Cited by 471

Overexpression of monodehydroascorbate reductase in transgenic tobacco confers enhanced tolerance to ozone, salt and polyethylene glycol stresses

Eltayeb, A. E., Kawano, N., Badawi, G. H., Kaminaka, H., Sanekata, T., Shibahara, T., Inanaga, S., & Tanaka, K. (2007) · Planta · doi:10.1007/s00425-006-0417-7 · Cited by 456

Response of the cultivated tomato and its wild salt‐tolerant relative Lycopersiconpennellii to salt‐dependent oxidative stress: The root antioxidative system

Shalata, A., Mittova, V., Volokita, M., Guy, M., & Tal, M. (2001) · Physiologia Plantarum · doi:10.1034/j.1399-3054.2001.1120405.x · Cited by 448

Plant Growth-Promoting Rhizobacteria Enhance Salinity Stress Tolerance in Okra through ROS-Scavenging Enzymes

Habib, S. H., Kausar, H., & Saud, H. M. (2016) · BioMed Research International · doi:10.1155/2016/6284547 · Cited by 448

Salt Cress. A Halophyte and Cryophyte Arabidopsis Relative Model System and Its Applicability to Molecular Genetic Analyses of Growth and Development of Extremophiles

Inan, G., Zhang, Q., Li, P., Wang, Z., Cao, Z., Zhang, H., Zhang, C., Quist, T. M., Goodwin, S. M., Zhu, J., et al. (2004) · Plant Physiology · doi:10.1104/pp.104.041723 · Cited by 444

Scavenging of reactive oxygen species in NaCl-stressed rice (Oryza sativa L.)—differential response in salt-tolerant and sensitive varieties

Vaidyanathan, H., Sivakumar, P., Chakrabarty, R., & Thomas, G. (2003) · Plant Science · doi:10.1016/j.plantsci.2003.08.005 · Cited by 443

Contrasting Responses of Photosynthesis to Salt Stress in the Glycophyte Arabidopsis and the Halophyte Thellungiella: Role of the Plastid Terminal Oxidase as an Alternative Electron Sink

Stepien, P., & Johnson, G. N. (2009) · Plant Physiology · doi:10.1104/pp.108.132407 · Cited by 431

Effects of salt on growth, ion accumulation, photosynthesis and leaf anatomy of the mangrove, Bruguiera parviflora

Parida, A. K., Das, A. B., & Mittra, B. (2004) · Trees - Structure and Function · doi:10.1007/s00468-003-0293-8 · Cited by 430

The function of peroxiredoxins in plant organelle redox metabolism

Dietz, K.-J. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erj160 · Cited by 427

Genetic engineering of glycinebetaine synthesis in plants: current status and implications for enhancement of stress tolerance

Sakamoto, A., & Murata, N. (2000) · Journal of Experimental Botany · doi:10.1093/jexbot/51.342.81 · Cited by 402

Ca2+ Regulates Reactive Oxygen Species Production and pH during Mechanosensing in Arabidopsis Roots

Monshausen, G. B., Bibikova, T. N., Weisenseel, M. H., & Gilroy, S. (2009) · The Plant Cell · doi:10.1105/tpc.109.068395 · Cited by 389

The combined effects of gibberellic acid and salinity on some antioxidant enzyme activities, plant growth parameters and nutritional status in maize plants

Tuna, A. L., Kaya, C., Dikilitas, M., & Higgs, D. (2008) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2007.06.007 · Cited by 388

Emerging concept for the role of photorespiration as an important part of abiotic stress response

Voss, I., Sunil, B., Scheibe, R., & Raghavendra, A. S. (2013) · Plant Biology · doi:10.1111/j.1438-8677.2012.00710.x · Cited by 377

C HLORORESPIRATION

Peltier, G., & Cournac, L. (2002) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.53.100301.135242 · Cited by 376

Enhancement of Oxidative Stress Tolerance in Transgenic Tobacco Plants Overproducing Fe-Superoxide Dismutase in Chloroplasts

Van Camp, W., Capiau, K., Van Montagu, M., Inze, D., & Slooten, L. (1996) · Plant Physiology · doi:10.1104/pp.112.4.1703 · Cited by 357

Mutations in the Arabidopsis Gene IMMUTANS Cause a Variegated Phenotype by Inactivating a Chloroplast Terminal Oxidase Associated with Phytoene Desaturation

Carol, P., Stevenson, D., Bisanz, C., Breitenbach, J., Sandmann, G., Mache, R., Coupland, G., & Kuntz, M. (1999) · The Plant Cell · doi:10.1105/tpc.11.1.57 · Cited by 340

Metabolite Exchange Between Chloroplasts and Cytoplasm

Heber, U. (1974) · Annual Review of Plant Physiology · doi:10.1146/annurev.pp.25.060174.002141 · Cited by 340

Exogenous proline and glycinebetaine increase NaCl-induced ascorbate–glutathione cycle enzyme activities, and proline improves salt tolerance more than glycinebetaine in tobacco Bright Yellow-2 suspension-cultured cells

Hoque, M. A., Banu, M. N. A., Okuma, E., Amako, K., Nakamura, Y., Shimoishi, Y., & Murata, Y. (2007) · Journal of Plant Physiology · doi:10.1016/j.jplph.2006.10.004 · Cited by 338

Superoxide dismutase, catalase and peroxidase activities do not confer protection against oxidative damage in salt‐stressed cowpea leaves

Cavalcanti, F. R., Oliveira, J. T. A., Martins‐Miranda, A. S., Viégas, R. A., & Silveira, J. A. G. (2004) · New Phytologist · doi:10.1111/j.1469-8137.2004.01139.x · Cited by 323

Induction of phosphatidylinositol 3‐kinase‐mediated endocytosis by salt stress leads to intracellular production of reactive oxygen species and salt tolerance

Leshem, Y., Seri, L., & Levine, A. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03134.x · Cited by 311

The multiplicity of dehydrogenases in the electron transport chain of plant mitochondria

Rasmusson, A. G., Geisler, D. A., & Møller, I. M. (2008) · Mitochondrion · doi:10.1016/j.mito.2007.10.004 · Cited by 299

Proline and glycinebetaine induce antioxidant defense gene expression and suppress cell death in cultured tobacco cells under salt stress

Banu, M. N. A., Hoque, M. A., Watanabe-Sugimoto, M., Matsuoka, K., Nakamura, Y., Shimoishi, Y., & Murata, Y. (2009) · Journal of Plant Physiology · doi:10.1016/j.jplph.2008.03.002 · Cited by 290

Over expression of cytosolic copper/zinc superoxide dismutase from a mangrove plant Avicennia marina in indica Rice var Pusa Basmati-1 confers abiotic stress tolerance

Prashanth, S. R., Sadhasivam, V., & Parida, A. (2008) · Transgenic Research · doi:10.1007/s11248-007-9099-6 · Cited by 266

Strategies to maintain redox homeostasis during photosynthesis under changing conditions

Scheibe, R., Backhausen, J. E., Emmerlich, V., & Holtgrefe, S. (2005) · Journal of Experimental Botany · doi:10.1093/jxb/eri181 · Cited by 262

Evidence of Arabidopsis salt acclimation induced by up‐regulation of HY1 and the regulatory role of RbohD‐derived reactive oxygen species synthesis

Xie, Y., Xu, S., Han, B., Wu, M., Yuan, X., Han, Y., Gu, Q., Xu, D., Yang, Q., & Shen, W. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04488.x · Cited by 257

Arsenite treatment induces oxidative stress, upregulates antioxidant system, and causes phytochelatin synthesis in rice seedlings

Mishra, S., Jha, A. B., & Dubey, R. S. (2011) · Protoplasma · doi:10.1007/s00709-010-0210-0 · Cited by 253

The dehydrogenase‐mediated recycling of NADPH is a key antioxidant system against salt‐induced oxidative stress in olive plants

VALDERRAMA, R., CORPAS, F. J., CARRERAS, A., GÓMEZ‐RODRÍGUEZ, M. V., CHAKI, M., PEDRAJAS, J. R., FERNÁNDEZ‐OCAÑA, A., DEL RÍO, L. A., & BARROSO, J. B. (2006) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2006.01530.x · Cited by 248

Alternative oxidase: a target and regulator of stress responses

Van Aken, O., Giraud, E., Clifton, R., & Whelan, J. (2009) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2009.01240.x · Cited by 247

Enhanced tolerance to oxidative stress in transgenic tobacco plants expressing three antioxidant enzymes in chloroplasts

Lee, Y.-P., Kim, S.-H., Bang, J.-W., Lee, H.-S., Kwak, S.-S., & Kwon, S.-Y. (2007) · Plant Cell Reports · doi:10.1007/s00299-006-0253-z · Cited by 239

Differential responses of antioxidative defense system to prolonged salinity stress in salt-tolerant and salt-sensitive Indica rice (Oryza sativa L.) seedlings

Mishra, P., Bhoomika, K., & Dubey, R. S. (2013) · Protoplasma · doi:10.1007/s00709-011-0365-3 · Cited by 230

The Dynamic Changes of DNA Methylation and Histone Modifications of Salt Responsive Transcription Factor Genes in Soybean

Song, Y., Ji, D., Li, S., Wang, P., Li, Q., & Xiang, F. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041274 · Cited by 223

Dual Roles of Reactive Oxygen Species and NADPH Oxidase RBOHD in an Arabidopsis-Alternaria Pathosystem

Pogány, M., von Rad, U., Grün, S., Dongó, A., Pintye, A., Simoneau, P., Bahnweg, G., Kiss, L., Barna, B., & Durner, J. (2009) · Plant Physiology · doi:10.1104/pp.109.141994 · Cited by 213

Plant signaling networks involving Ca2+ and Rboh/Nox-mediated ROS production under salinity stress

Kurusu, T., Kuchitsu, K., & Tada, Y. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00427 · Cited by 207

Antioxidant defense in the leaves of C3 and C4 plants under salinity stress

Stepien, P., & Klobus, G. (2005) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2005.00534.x · Cited by 206

Manganese-excess induces oxidative stress, lowers the pool of antioxidants and elevates activities of key antioxidative enzymes in rice seedlings

Srivastava, S., & Dubey, R. S. (2011) · Plant Growth Regulation · doi:10.1007/s10725-010-9526-1 · Cited by 205

Clathrin and Membrane Microdomains Cooperatively Regulate RbohD Dynamics and Activity in Arabidopsis

Hao, H., Fan, L., Chen, T., Li, R., Li, X., He, Q., Botella, M. A., & Lin, J. (2014) · The Plant Cell · doi:10.1105/tpc.113.122358 · Cited by 205

Early effects of salt stress on the physiological and oxidative status of Cakile maritima (halophyte) and Arabidopsis thaliana (glycophyte)

Ellouzi, H., Ben Hamed, K., Cela, J., Munné‐Bosch, S., & Abdelly, C. (2011) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2011.01450.x · Cited by 200

ROS‐mediated vascular homeostatic control of root‐to‐shoot soil Na delivery in Arabidopsis

Jiang, C., Belfield, E. J., Mithani, A., Visscher, A., Ragoussis, J., Mott, R., Smith, J. A. C., & Harberd, N. P. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.273 · Cited by 196

Protein phosphorylation is a prerequisite for the Ca2+-dependent activation of Arabidopsis NADPH oxidases and may function as a trigger for the positive feedback regulation of Ca2+ and reactive oxygen species

Kimura, S., Kaya, H., Kawarazaki, T., Hiraoka, G., Senzaki, E., Michikawa, M., & Kuchitsu, K. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2011.09.011 · Cited by 195

Molecular Distinction between Alternative Oxidase from Monocots and Dicots

Considine, M. J., Holtzapffel, R. C., Day, D. A., Whelan, J., & Millar, A. H. (2002) · Plant Physiology · doi:10.1104/pp.004150 · Cited by 194

Two rice cytosolic ascorbate peroxidases differentially improve salt tolerance in transgenic Arabidopsis

Lu, Z., Liu, D., & Liu, S. (2007) · Plant Cell Reports · doi:10.1007/s00299-007-0395-7 · Cited by 191

Salt tolerance of transgenic rice overexpressing yeast mitochondrial Mn-SOD in chloroplasts

Tanaka, Y., Hibino, T., Hayashi, Y., Tanaka, A., Kishitani, S., Takabe, T., Yokota, S., & Takabe, T. (1999) · Plant Science · doi:10.1016/s0168-9452(99)00133-8 · Cited by 191

Hydrogen peroxide produced by NADPH oxidases increases proline accumulation during salt or mannitol stress in Arabidopsis thaliana

Ben Rejeb, K., Lefebvre‐De Vos, D., Le Disquet, I., Leprince, A., Bordenave, M., Maldiney, R., Jdey, A., Abdelly, C., & Savouré, A. (2015) · New Phytologist · doi:10.1111/nph.13550 · Cited by 188

The Plastid Terminal Oxidase: Its Elusive Function Points to Multiple Contributions to Plastid Physiology

Nawrocki, W. J., Tourasse, N. J., Taly, A., Rappaport, F., & Wollman, F.-A. (2015) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-043014-114744 · Cited by 187

Redox signal integration: from stimulus to networks and genes

Dietz, K. (2008) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2008.01120.x · Cited by 179

Cloning of peroxisomal ascorbate peroxidase gene from barley and enhanced thermotolerance by overexpressing in Arabidopsis thaliana

Shi, W. M., Muramoto, Y., Ueda, A., & Takabe, T. (2001) · Gene · doi:10.1016/s0378-1119(01)00566-2 · Cited by 177

The activity of antioxidant enzymes in maize and sunflower seedlings as affected by salinity and different nitrogen sources

Rios-Gonzalez, K., Erdei, L., & Lips, S. H. (2002) · Plant Science · doi:10.1016/s0168-9452(02)00040-7 · Cited by 173

Effect of increased polyamine biosynthesis on stress responses in transgenic tobacco by introduction of human S-adenosylmethionine gene

Waie, B., & Rajam, M. V. (2003) · Plant Science · doi:10.1016/s0168-9452(03)00030-x · Cited by 163

Involvement of a Plastid Terminal Oxidase in Plastoquinone Oxidation as Evidenced by Expression of the Arabidopsis thaliana Enzyme in Tobacco

Joët, T., Genty, B., Josse, E.-M., Kuntz, M., Cournac, L., & Peltier, G. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m203538200 · Cited by 159

Consumption of oxygen by astaxanthin biosynthesis: A protective mechanism against oxidative stress in Haematococcus pluvialis (Chlorophyceae)

Li, Y., Sommerfeld, M., Chen, F., & Hu, Q. (2008) · Journal of Plant Physiology · doi:10.1016/j.jplph.2007.12.007 · Cited by 159

Mechanisms of oxygen activation in different compartments of plant cells

Elstner, E. F. (1991) · Cited by 158

Physiological and biochemical mechanisms of the ornamental Eugenia myrtifolia L. plants for coping with NaCl stress and recovery

Acosta‐Motos, J. R., Díaz‐Vivancos, P., Álvarez, S., Fernández‐García, N., Sánchez-Blanco, M. J., & Hernández, J. A. (2015) · Planta · doi:10.1007/s00425-015-2315-3 · Cited by 155

Multiple strategies to prevent oxidative stress in Arabidopsis plants lacking the malate valve enzyme NADP-malate dehydrogenase

Hebbelmann, I., Selinski, J., Wehmeyer, C., Goss, T., Voß, I., Mulo, P., Kangasjärvi, S., Aro, E., Oelze, M.-L., Dietz, K., et al. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err386 · Cited by 154

Characterization of membrane polypeptides from pea leaf peroxisomes involved in superoxide radical generation

López‐Huertas, E., Corpas, F. J., Sandalio, L. M., & del Río, L. A. (1999) · Biochemical Journal · doi:10.1042/0264-6021:3370531 · Cited by 150

Thiol-Based Peroxidases and Ascorbate Peroxidases: Why Plants Rely on Multiple Peroxidase Systems in the Photosynthesizing Chloroplast?

Dietz, K. (2016) · Molecules and Cells · doi:10.14348/molcells.2016.2324 · Cited by 148

NADPH oxidase-dependent H2O2 production is required for salt-induced antioxidant defense in Arabidopsis thaliana

Rejeb, K. B., Benzarti, M., Debez, A., et al. (2014) · Journal of Plant Physiology · doi:10.1016/j.jplph.2014.08.022 · Cited by 135

Redox-shuttling between chloroplast and cytosol: integration of intra-chloroplast and extra-chloroplast metabolism

Taniguchi, M., & Miyake, H. (2012) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2012.01.014 · Cited by 132

Apoplastic Peroxidase Generates Superoxide Anions in Cells of Cotton Cotyledons Undergoing the Hypersensitive Reaction to Xanthomonas campestris pv. malvacearum Race 18

Martinez, C., Montillet, J., Bresson, E., Agnel, J. P., Dai, G. H., Daniel, J.-F., Geiger, J. P., & Nicole, M. (1998) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.1998.11.11.1038 · Cited by 132

Activation of cyclic electron flow by hydrogen peroxide in vivo

Strand, D. D., Livingston, A. K., Satoh-Cruz, M., Froehlich, J. E., Maurino, V. G., & Kramer, D. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1418223112 · Cited by 130

Oxygen activation at the plasma membrane: relation between superoxide and hydroxyl radical production by isolated membranes

Heyno, E., Mary, V., Schöpfer, P., & Krieger‐Liszkay, A. (2011) · Planta · doi:10.1007/s00425-011-1379-y · Cited by 126

IMMUTANS Does Not Act as a Stress-Induced Safety Valve in the Protection of the Photosynthetic Apparatus of Arabidopsis during Steady-State Photosynthesis

Rosso, D., Ivanov, A. G., Fu, A., Geisler-Lee, J., Hendrickson, L., Geisler, M. J., Stewart, G., Król, M., Hurry, V., Rodermel, S. R., et al. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.085886 · Cited by 125

Salinity induced behavioural changes in malate dehydrogenase and glutamate dehydrogenase activities in rice seedlings of differing salt tolerance

Kumar, R. G., Shah, K., & Dubey, R. S. (2000) · Plant Science · doi:10.1016/s0168-9452(00)00224-7 · Cited by 122

Implications of alternative electron sinks in increased resistance of PSII and PSI photochemistry to high light stress in cold-acclimated Arabidopsis thaliana

Ivanov, A. G., Rosso, D., Savitch, L. V., Stachula, P., Rosembert, M., Öquist, G., Hurry, V., & Hüner, N. P. A. (2012) · Photosynthesis Research · doi:10.1007/s11120-012-9769-y · Cited by 121

Polyamine oxidase activity contributes to sustain maize leaf elongation under saline stress

Rodríguez, A. A., Maiale, S. J., Menéndez, A. B., & Ruiz, O. A. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp256 · Cited by 112

Manipulation of alternative oxidase can influence salt tolerance in Arabidopsis thaliana

Smith, C. A., Melino, V. J., Sweetman, C., & Soole, K. L. (2009) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2009.01305.x · Cited by 111

Molecular Genetics of Crassulacean Acid Metabolism

Cushman, J. C., & Bohnert, H. J. (1997) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.3.667 · Cited by 109

Expression of ascorbate peroxidase and glutathione reductase in roots of rice seedlings in response to NaCl and H2O2

Tsai, Y.-C., Hong, C., Liu, L., & Kao, C. H. (2004) · Journal of Plant Physiology · doi:10.1016/j.jplph.2004.06.004 · Cited by 108

Effects of salt stress on the expression of antioxidant genes and proteins in the model legume Lotus japonicus

Rubio, M. C., Bustos‐Sanmamed, P., Clemente, M. R., & Becana, M. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2008.02718.x · Cited by 105

Voltammetric detection of superoxide production by photosystem II

Cleland, R. E., & Grace, S. C. (1999) · FEBS Letters · doi:10.1016/s0014-5793(99)01067-4 · Cited by 105

Dissecting the integrative antioxidant and redox systems in plant mitochondria. Effect of stress and S-nitrosylation

Lázaro, J. J., Jiménez, A., Camejo, D. M., Iglesias-Baena, I., Martí, M. C., Lázaro-Payo, A., Barranco-Medina, S., & Sevilla, F. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00460 · Cited by 99

Response of mitochondrial thioredoxin PsTrxo1, antioxidant enzymes, and respiration to salinity in pea (Pisum sativum L.) leaves

Martí, M. C., Florez‐Sarasa, I., Camejo, D. M., Ribas‐Carbó, M., Lázaro, J. J., Sevilla, F., & Jiménez, A. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err076 · Cited by 95

In vitro characterization of a plastid terminal oxidase (PTOX)

Josse, E., Alcaraz, J., Labouré, A., & Kuntz, M. (2003) · European Journal of Biochemistry · doi:10.1046/j.1432-1033.2003.03766.x · Cited by 93

Light intensity affects chlorophyll synthesis during greening process by metabolite signal from mitochondrial alternative oxidase in A rabidopsis

Zhang, D., Yuan, S., Xu, F., Zhu, F., Yuan, M., Ye, H., Guo, H., Lv, X., Yin, Y., & Lin, H. (2014) · Plant Cell & Environment · doi:10.1111/pce.12438 · Cited by 91

Plant mitochondria: Source and target for nitric oxide

Igamberdiev, A. U., Ratcliffe, R. G., & Gupta, K. J. (2014) · Mitochondrion · doi:10.1016/j.mito.2014.02.003 · Cited by 86

The role of respiration during adaptation of the freshwater cyanobacterium Synechococcus 6311 to salinity

Fry, I. V., Huflejt, M. E., Erber, W. W. A., Peschek, G. A., & Packer, L. (1986) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(86)90637-5 · Cited by 84

Unravelling mitochondrial retrograde regulation in the abiotic stress induction of rice ALTERNATIVE OXIDASE 1 genes

LI, C., LIANG, D., LI, J., DUAN, Y., Li, H., Yang, Y., Qin, R., Li, L., Wei, P., & YANG, J. (2012) · Plant Cell & Environment · doi:10.1111/pce.12013 · Cited by 84

The Dual Role of the Plastid Terminal Oxidase PTOX: Between a Protective and a Pro-oxidant Function

Krieger‐Liszkay, A., & Feilke, K. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2015.01147 · Cited by 82

Occurrence and environmental stress responses of two plastid terminal oxidases in Haematococcus pluvialis (Chlorophyceae)

Wang, J., Sommerfeld, M. R., & Hu, Q. (2009) · Planta · doi:10.1007/s00425-009-0932-4 · Cited by 78

Fine and coarse regulation of reactive oxygen species in the salt tolerant mutants of barnyard grass and their wild-type parents under salt stress

Abogadallah, G. M., Serag, M. M., & Quick, W. P. (2009) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2009.01297.x · Cited by 77

Alternative oxidase: distribution, induction, properties, structure, regulation, and functions

Rogov, A. G., Sukhanova, E. I., Uralskaya, L. A., Aliverdieva, D. A., & Zvyagilskaya, R. A. (2014) · Biochemistry (Moscow) · doi:10.1134/s0006297914130112 · Cited by 73

Distinct responses of the mitochondrial respiratory chain to long‐ and short‐term high‐light environments in Arabidopsis thaliana

Yoshida, K., WATANABE, C. K., Hachiya, T., Tholen, D., Shibata, M., Terashima, I., & Noguchi, K. (2011) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2010.02267.x · Cited by 73

Thioredoxin-h1 Reduces and Reactivates the Oxidized Cytosolic Malate Dehydrogenase Dimer in Higher Plants

Hara, S., Motohashi, K., Arisaka, F., Romano, P. G. N., Hosoya‐Matsuda, N., Kikuchi, N., Fusada, N., & Hisabori, T. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m605784200 · Cited by 63

Identification of intra‐ and intermolecular disulphide bonding in the plant mitochondrial proteome by diagonal gel electrophoresis

Winger, A. M., Taylor, N. L., Heazlewood, J. L., Day, D. A., & Millar, A. H. (2007) · PROTEOMICS · doi:10.1002/pmic.200700209 · Cited by 61

Changes in Carotenoid Composition and Photosynthesis in Sorghum under High Light and Salt Stresses

Sharma, P. K., & Hall, D. O. (1992) · Journal of Plant Physiology · doi:10.1016/s0176-1617(11)81020-5 · Cited by 57

Molecular cloning and expression of chloroplast NADP-malate dehydrogenase during Crassulacean acid metabolism induction by salt stress

Cushman, J. C. (1993) · Photosynthesis Research · doi:10.1007/bf02185408 · Cited by 54

Knockdown of mitochondrial alternative oxidase induces the ‘stress state’ of signaling molecule pools in Nicotiana tabacum, with implications for stomatal function

Cvetkovska, M., Dahal, K., Alber, N. A., Jin, C., Cheung, M., & Vanlerberghe, G. C. (2014) · New Phytologist · doi:10.1111/nph.12773 · Cited by 54

Strategies of ROS regulation and antioxidant defense during transition from C3 to C4 photosynthesis in the genus Flaveria under PEG-induced osmotic stress

Uzilday, B., Türkan, İ., Ozgur, R., & Sekmen, A. H. (2013) · Journal of Plant Physiology · doi:10.1016/j.jplph.2013.06.016 · Cited by 53

Functional and molecular characterization of plastid terminal oxidase from rice (Oryza sativa)

Yu, Q., Feilke, K., Krieger‐Liszkay, A., & Beyer, P. (2014) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2014.04.007 · Cited by 52

Changes in Properties of Barley Leaf Mitochondria Isolated from NaCl-Treated Plants

Jolivet, Y., Pireaux, J., & Dizengremel, P. (1990) · PLANT PHYSIOLOGY · doi:10.1104/pp.94.2.641 · Cited by 44

Efficacy of ascorbate-glutathione cycle for scavenging H2O2 in two contrasting rice genotypes during salinity stress

Hossain, M., Ismail, M. R., Uddin, K., Islam, M. R., & Ashrafuzzaman, M. (2013) · Australian Journal of Crop Science · Cited by 33

Long term salinity stress in relation to lipid peroxidation, super oxide dismutase activity and proline content of salt-sensitive and salt-tolerant wheat cultivars

Borzouei, A., Kafi, M., Ghogdi, E. A., & Mousavi-Shalmani, M. (2012) · Chilean journal of agricultural research · doi:10.4067/s0718-58392012000400003 · Cited by 30

Induction of alternative oxidase chain under salt stress conditions

Ferreira, A. L. A., Arrabaça, J. D., Vaz-Pinto, V., & Lima‐Costa, M. F. (2008) · Biologia Plantarum · doi:10.1007/s10535-008-0009-4 · Cited by 13