dc.creatorSalgado I.
dc.creatorCarmen Martinez M.
dc.creatorOliveira H.C.
dc.creatorFrungillo L.
dc.date2013
dc.date2015-06-25T19:14:53Z
dc.date2015-11-26T14:57:47Z
dc.date2015-06-25T19:14:53Z
dc.date2015-11-26T14:57:47Z
dc.date.accessioned2018-03-28T22:09:34Z
dc.date.available2018-03-28T22:09:34Z
dc.identifier
dc.identifierRevista Brasileira De Botanica. , v. 36, n. 2, p. 89 - 98, 2013.
dc.identifier1008404
dc.identifier10.1007/s40415-013-0013-6
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-84881560705&partnerID=40&md5=8974d3ee58c4d5f3e060736a165ce649
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/89158
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/89158
dc.identifier2-s2.0-84881560705
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1255722
dc.descriptionStudies in the last two decades have firmly established that the gaseous free radical nitric oxide (NO) is an intracellular and intercellular mediator of signal transduction pathways controlling plant growth and development, as well as plant responses to biotic and abiotic stresses. The underlying mechanisms of NO action may rely on its reactivity with different kinds of biomolecules, leading to modulation of enzymatic activities, and of gene transcription, with profound impact on metabolism and signal transduction pathways. NO homeostasis depends on the appropriate coordination of NO synthesis and degradation under different physiological conditions. The mechanisms by which NO is synthesized de novo in plants are still a matter of controversy, although in the last years, the key role of the enzyme nitrate reductase (NR) in plants NO production has been widely accepted. In addition, S-nitrosoglutathione (GSNO), which forms by spontaneous reaction of NO with glutathione, is likely a major NO reservoir and NO donor in plant cells. GSNO levels are controlled by the enzyme GSNO reductase that has emerged as the main enzyme responsible for the modulation of S-nitrosothiol pools. The number of plant processes influenced/modulated by NO has dramatically increased in the last years. This review particularly emphasizes the roles of NR and GSNOR enzymes in NO homeostasis and NO-mediated plant responses to environmental challenges. © 2013 Botanical Society of Sao Paulo.
dc.description36
dc.description2
dc.description89
dc.description98
dc.descriptionAlderton, W.K., Cooper, C.E., Knowles, R.G., Nitric oxide synthases: structure, function and inhibition (2001) Biochem J, 357, pp. 593-615
dc.descriptionBai, X., Yang, L., Tian, M., Chen, J., Shi, J., Yang, Y., Hu, X., Nitric oxide enhances desiccation tolerance of recalcitrant Antiaris toxicaria seeds via protein S-nitrosylation and carbonylation (2011) PLoS ONE, 6, pp. e20714
dc.descriptionBarroso, J.B., Corpas, F.J., Carreras, A., Rodríguez-Serrano, M., Esteban, F.J., Fernández-Ocaña, A., Chaki, M., del Rio, L.A., Localization of S-nitrosoglutathione and expression of S-nitrosoglutathione reductase in pea plants under cadmium stress (2006) J Exp Bot, 57, pp. 1785-1793
dc.descriptionBaudouin, E., The language of nitric oxide signaling (2011) Plant Biol, 13, pp. 233-242
dc.descriptionBesson-Bard, A., Pugin, A., Wendehenne, D., New insights into nitric oxide signaling in plants (2008) Annu Rev Plant Biol, 59, pp. 21-39
dc.descriptionBesson-Bard, A., Astier, J., Rasul, S., Wawer, I., Dubreuil-Maurizi, C., Jeandroz, S., Wendehenne, D., Current view of nitric oxide-responsive genes in plants (2009) Plant Sci, 177, pp. 302-309
dc.descriptionBethke, P.C., Badger, M.R., Jones, R.L., Apoplastic synthesis of nitric oxide by plant tissues (2004) Plant Cell, 16, pp. 332-341
dc.descriptionBorisjuk, L., Rolletschek, H., The oxygen status of the developing seed (2009) New Phytol, 182, pp. 17-30
dc.descriptionBrown, G.C., Nitric oxide and mitochondria (2007) Frontiers Biosci, 12, pp. 1024-1033
dc.descriptionCastello, P., David, P., McClure, T., Crook, Z., Poyton, R., Mitochondrial cytochrome oxidase produces nitric oxide under hypoxic conditions: implications for oxygen sensing and hypoxia signaling in eukaryotes (2006) Cell Metab, 3, pp. 277-287
dc.descriptionChen, R., Sun, S., Wang, C., Li, Y., Liang, Y., An, F., Li, C., Zuo, J., The ArabidopsisPARAQUAT RESISTANT2 gene encodes an S- nitrosoglutathione reductase that is a key regulator of cell death (2009) Cell Res, 19, pp. 1377-1387
dc.descriptionCooper, C.E., Giulivi, C., Nitric oxide regulation of mitochondrial oxygen consumption II: molecular mechanism and tissue physiology (2007) Am J Physiol-Cell Physiol, 292, pp. 1993-2003
dc.descriptionCorpas, F.J., Chaki, M., Fernández-Ocaña, A., Valderrama, R., Palma, J.M., Carreras, A., Begara-Morales, J.C., Barroso, J.B., Metabolism of reactive nitrogen species in pea plants under abiotic stress conditions (2008) Plant Cell Physiol, 49, pp. 1711-1722
dc.descriptionCorpas, F.J., Chaki, M., Leterrier, M., Barroso, J.B., Protein tyrosine nitration: a new challenge in plants (2009) Plant Signal Behav, 4, pp. 920-923
dc.descriptionCorpas, F.J., Leterrier, M., Valderrama, R., Airaki, M., Chaki, M., Palma, J.M., Barroso, J.B., Nitric oxide imbalance provokes a nitrosative response in plants under abiotic stress (2011) Plant Sci, 181, pp. 604-611
dc.descriptionCourtois, C., Besson, A., Dahan, J., Bourque, S., Dobrowolska, G., Pugin, A., Wendehenne, D., Nitric oxide signalling in plants: interplays with Ca2+ and protein kinases (2008) J Exp Bot, 59, pp. 155-163
dc.descriptionde Oliveira, H.C., Wulff, A., Saviani, E.E., Salgado, I., Nitric oxide degradation by potato tuber mitochondria: evidence for the involvement of external NAD(P)H dehydrogenases (2008) Biochim Biophys Acta, 1777, pp. 470-476
dc.descriptiondel Rio, L.A., Corpas, F.J., Barroso, J.B., Nitric oxide and nitric oxide synthase activity in plants (2004) Phytochemistry, 65, pp. 783-792
dc.descriptionDelledonne, M., Xia, Y., Dixon, R.A., Lamb, C., Nitric oxide functions as a signal in plant disease resistance (1998) Nature, 394, pp. 585-588
dc.descriptionDíaz, M., Achkor, H., Titarenko, E., Martínez, M.C., The gene encoding glutathione-dependent formaldehyde dehydrogenase/GSNO reductase is responsive to wounding, jasmonic acid and salicylic acid (2003) FEBS Lett, 543, pp. 136-139
dc.descriptionDurner, J., Wendehenne, D., Klessing, D.F., Defense gene induction in tobacco by nitric oxide, cyclic GMP, and cyclic ADP-ribose (1998) Proc Natl Acad Sci USA, 95, pp. 10328-10333
dc.descriptionDurrant, W.E., Dong, X., Systemic acquired resistance (2004) Annu Rev Phytopathol, 42, pp. 185-209
dc.descriptionElstner, E.F., Osswald, W., Air pollution: involvement of oxygen radicals (a mini review) (1991) Free Radical Res Commun, 12-13, pp. 795-807
dc.descriptionEspunya, M.C., Michele, R., Gómez-Cadenas, A., Martínez, M.C., S-nitrosoglutathione is a componente of wound- and salicylic acid-induced systemic responses in Arabidopsis thaliana (2012) J Exp Bot, 63, pp. 3219-3227
dc.descriptionFeechan, A., Kwon, E., Yun, B.-W., Wang, Y., Pallas, J.A., Loake, G.J., A central role for S-nitrosothiols in plant disease resistance (2005) Proc Natl Acad Sci USA, 102, pp. 8054-8059
dc.descriptionFerrarini, A., De Stefano, M., Baudouin, E., Pucciariello, C., Polverari, A., Puppo, A., Delledonne, M., Expression of Medicago truncatula genes responsive to nitric oxide in pathogenic and symbiotic conditions (2008) Mol Plant Microbe Interact, 21, pp. 781-790
dc.descriptionFlores, T., Todd, C.D., Tovar-Mendez, A., Dhanoa, P.K., Correa-Aragunde, N., Arginase-negative mutants of Arabidopsis exhibit increased nitric oxide signaling in root development (2008) Plant Physiol, 147, pp. 1936-1946
dc.descriptionFreschi, L., Rodrigues, M.A., Domingues, D.S., Purgatto, E., van Sluys, M.A., Magalhaes, J.R., Kaiser, W.M., Mercier, H., Nitric oxide mediates the hormonal control of crassulacean acid metabolism expression in young pineapple plants (2010) Plant Physiol, 152, pp. 1971-1985
dc.descriptionFriebe, A., Koesling, D., The function of NO-sensitive guanylyl cyclase: what we can learn from genetic mouse models (2009) Nitric Oxide, 21, pp. 149-156
dc.descriptionFrungillo, L., de Oliveira, J.F., Saviani, E.E., Oliveira, H.C., Martínez, M.C., Salgado, I., Modulation of mitochondrial activity by S-nitrosoglutathione reductase in Arabidopsis thaliana transgenic cell lines (2013) Biochim Biophys Acta, 1827, pp. 239-247
dc.descriptionGao, Y., The multiple actions of NO (2010) Pflügers Arch Eur J Physiol, 459, pp. 829-839
dc.descriptionGouvêa, C.M.P.C., Souza, F.J., Magalhães, A.C.N., Martins, I.S., NO releasing substances that induce growth elongation in maize root segments (1997) Plant Growth Regul, 21, pp. 183-187
dc.descriptionGrünn, S., Lindermayr, C., Sell, S., Durner, J., Nitric oxide and gene regulation in plants (2006) J Exp Bot, 57, pp. 507-516
dc.descriptionGupta, K.J., Stoimenova, M., Kaiser, W.M., In higher plants, only root mitochondria, but not leaf mitochondria reduce nitrite to NO, in vitro and in situ (2005) J Exp Bot, 56, pp. 2601-2609
dc.descriptionGupta, K.J., Fernie, A.R., Kaiser, W.M., van Dongen, J.T., On the origins of nitric oxide (2011) Trends Plant Sci, 16, pp. 160-168
dc.descriptionHe, Y., Tang, R.H., Hao, Y., Stevens, R.D., Cook, C.W., Ahn, S.M., Jing, L., Pei, Z.M., Nitric oxide represses the Arabidopsis floral transition (2004) Science, 305, pp. 1968-1971
dc.descriptionHebelstrup, K.H., Jensen, E.O., Expression of NO scavenging hemoglobin is involved in the timing of bolting in Arabidopsis thaliana (2008) Planta, 227, pp. 917-927
dc.descriptionHuang, X., von Rad, U., Durner, J., Nitric oxide induces transcriptional activation of the nitric oxide-tolerant alternative oxidase in Arabidopsis suspension cells (2002) Planta, 215, pp. 914-923
dc.descriptionIgamberdiev, A.U., Baron, K., Manac'h-Little, N., Stoimenova, M., Hill, R.D., The haemoglobin/nitric oxide cycle: involvement in flooding stress and effects on hormone signalling (2005) Ann Bot, 96, pp. 557-564
dc.descriptionJasid, S., Simontacchi, M., Bartoli, C.G., Puntarulo, S., Chloroplasts as a nitric oxide cellular source. Effect of reactive nitrogen species on chloroplastic lipids and proteins (2006) Plant Physiol, 142, pp. 1246-1255
dc.descriptionKlepper, L., Nitric oxide (NO) and nitrogen dioxide (NO2) emissions from herbicide-treated soybean plants (1979) Atmos Environ, 13, pp. 537-542
dc.descriptionLamattina, L., Garcia-Mata, C., Graziano, M., Pagnussat, G., Nitric oxide: the versatility of an extensive signal molecule (2003) Annu Rev Plant Biol, 54, pp. 109-136
dc.descriptionLamb, C., Dixon, R.A., The oxidative burst in plant disease resistance (1997) Annu Rev Plant Physiol Plant Mol Biol, 48, pp. 251-275
dc.descriptionLea, P.J., Nitrogen Metabolism (1993) Plant Biochemistry and Molecular Biology, pp. 155-180. , P. J. Lea and R. C. Leegood (Eds.), New York: Wiley
dc.descriptionLee, U., Wie, C., Fernandez, B.O., Feelish, M., Vierling, E., Modulation of nitrosative stress by S-nitrosoglutathione reductase is critical for thermotolerance and plant growth in Arabidopsis (2008) Plant Cell, 20, pp. 786-802
dc.descriptionLeitner, M., Vandelle, E., Gaupels, F., Bellin, D., Delledonne, M., NO signals in the haze: nitric oxide signaling in plant defence (2009) Curr Opin Plant Biol, 12, pp. 451-458
dc.descriptionLeterrier, M., Chaki, M., Airaki, M., Valderrama, R., Palma, J.M., Barroso, J.B., Corpas, F.J., Function of S-nitrosoglutathione reductase (GSNOR) in plant development and under biotic/abiotic stress (2011) Plant Signal Behav, 6, pp. 789-793
dc.descriptionLindermayr, C., Saalbach, G., Durner, J., Proteomic identification of S-nitrosylated proteins in Arabidopsis (2005) Plant Physiol, 137, pp. 921-930
dc.descriptionLindermayr, C., Sell, S., Müller, B., Leister, D., Durner, J., Redox regulation of the NPR1-TGA1 system of Arabidopsis thaliana by nitric oxide (2010) Plant Cell, 22, pp. 2894-2907
dc.descriptionLiu, L., Hausladen, A., Zeng, M., Que, L., Heitman, J., Stamler, J.S., A metabolic enzyme for S-nitrosothiol conserved from bacteria to humans (2001) Nature, 410, pp. 490-494
dc.descriptionLiu, W.Z., Kong, D.D., Gu, X.X., Gao, H.B., Wang, J.Z., Xia, M., Gao, Q., He, Y.K., Cytokinins can act as suppressors of nitric oxide in Arabidopsis (2013) Proc Natl Acad Sci USA, 110, pp. 1548-1553
dc.descriptionLozano-Juste, J., Colom-Moreno, R., León, J., In vivo protein tyrosine nitration in Arabidopsis thaliana (2011) J Exp Bot, 62, pp. 3501-3517
dc.descriptionMelo, P.M., Silva, L.S., Ribeiro, I., Seabra, A.R., Carvalho, H.G., Glutamine synthetase is a molecular target of nitric oxide in root nodules of Medicago truncatula and is regulated by tyrosine nitration (2011) Plant Physiol, 157, pp. 1505-1517
dc.descriptionMillar, A.H., Day, D.A., Nitric oxide inhibits the cytochrome oxidase but not the alternative oxidase of plant mitochondria (1996) FEBS Lett, 398, pp. 155-158
dc.descriptionModolo, L.V., Augusto, O., Almeida, I.M.G., Magalhaes, J.R., Salgado, I., Nitrite as the major source of nitric oxide production by Arabidopsis thaliana in response to Pseudomonas syringae (2005) FEBS Lett, 579, pp. 3814-3820
dc.descriptionModolo, L.V., Augusto, O., Almeida, I.M.G., Pinto-Maglio, C.A.F., Oliveira, H.C., Seligman, K., Salgado, I., Decreased arginine and nitrite levels in nitrate reductase-deficient Arabidopsis thaliana plants impair nitric oxide synthesis and the hypersensitive response to Pseudomonas syringae (2006) Plant Sci, 171, pp. 34-40
dc.descriptionMoreau, M., Lindermayr, C., Durner, J., Klessig, D.F., NO synthesis and signaling in plants-where do we stand? (2010) Physiol Plant, 138, pp. 372-383
dc.descriptionMou, Z., Fan, W., Dong, X., Inducers of plant systemic acquired resistance regulate NPR1 function through redox changes (2003) Cell, 113, pp. 935-944
dc.descriptionNeill, S.J., Desikan, R., Hancock, J.T., Nitric oxide signaling in plants (2003) New Phytol, 159, pp. 11-35
dc.descriptionOliveira, H.C., Justino, G.C., Sodek, L., Salgado, I., Amino acid recovery does not prevent susceptibility to Pseudomonas syringae in nitrate reductase double-deficient Arabidopsis thaliana plants (2009) Plant Sci, 176, pp. 105-111
dc.descriptionOliveira, H.C., Saviani, E.E., Oliveira, J.F.P., Salgado, I., Nitrate reductase-dependent nitric oxide synthesis in the defense response of Arabidopsis thaliana against Pseudomonas syringae (2010) Tropical Plant Pathol, 35, pp. 104-107
dc.descriptionOliveira, H.C., Salgado, I., Sodek, L., Involvement of nitrite in the nitrate-mediated modulation of fermentative metabolism and nitric oxide production of soybean roots during hypoxia (2013) Planta, 237, pp. 255-264
dc.descriptionPalmer, R.M., Ferrige, A.G., Moncada, S., Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor (1987) Nature, 327, pp. 524-526
dc.descriptionPalmieri, M.C., Sell, S., Huang, X., Scherf, M., Werner, T., Durner, J., Lindermayr, C., Nitric oxide-responsive genes and promoters in Arabidopsis thaliana: a bioinformatics approach (2008) J Exp Bot, 59, pp. 177-186
dc.descriptionPerchepied, L., Balagué, C., Riou, C., Claudel-Renard, C., Rivière, N., Grezes-Besset, B., Roby, D., Nitric oxide participates in the complex interplay of defense-related signaling pathways controlling disease resistance to Sclerotinia sclerotiorum in Arabidopsis thaliana (2010) Mol Plant Microbe Interact, 23, pp. 846-860
dc.descriptionQiao, W., Fan, L.M., Nitric oxide signaling in plant responses to abiotic stresses (2008) J Integr Plant Biol, 50, pp. 1238-1246
dc.descriptionRadi, R., Protein tyrosine nitration: Biochemical mechanisms and structural basis of functional effects (2013) Acc Chem Res, 46, pp. 550-559
dc.descriptionRadi, R., Cassina, A., Hodara, R., Nitric oxide and peroxynitrite interactions with mitochondria (2002) Biol Chem, 383, pp. 401-409
dc.descriptionRasul, S., Dubreuil-Maurizi, C., Lamotte, O., Koen, E., Poinssot, B., Alcaraz, G., Wendehenne, D., Jeandroz, S., Nitric oxide production mediates oligogalacturonide-triggered immunity and resistance to Botrytis cinerea in Arabidopsis thaliana (2012) Plant Cell Environ, 35, pp. 1483-1499
dc.descriptionRockel, P., Strube, F., Rockel, A., Wildt, J., Kaiser, W.M., Regulation of nitric oxide (NO) production by plant nitrate reductase in vivo and in vitro (2002) J Exp Bot, 53, pp. 103-110
dc.descriptionRomero-Puertas, M.C., Perazzolli, M., Zago, E.D., Delledonne, M., Nitric oxide signalling functions in plant-pathogen interactions (2004) Cell Microbiol, 6, pp. 795-803
dc.descriptionRomero-Puertas, M.C., Laxa, M., Mattè, A., Zaninotto, F., Finkemeier, I., Jones, A.M.E., Perazzolli, M., Delledonne, M., S-Nitrosylation of peroxiredoxin II E promotes peroxynitrite-mediated tyrosine nitration (2007) Plant Cell, 19, pp. 4120-4130
dc.descriptionRomero-Puertas, M.C., Campostrini, N., Mattè, A., Righetti, P.G., Perazzolli, M., Zolla, L., Roepstorff, P., Delledonne, M., Proteomic analysis of S-nitrosylated proteins in Arabidopsis thaliana undergoing hypersensitive response (2008) Proteomics, 8, pp. 1459-1469
dc.descriptionRumer, S., Gupta, K.J., Kaiser, W.M., Plant cells oxidize hydroxylamines to NO (2009) J Exp Bot, 60, pp. 2065-2072
dc.descriptionRustérucci, C., Espunya, M.C., Díaz, M., Chabannes, M., Martínez, M.C., S-nitrosoglutathione reductase affords protection against pathogens in Arabidopsis, both locally and systemically (2007) Plant Physiol, 143, pp. 1282-1292
dc.descriptionSánchez, C., Cabrera, J.J., Gates, A.J., Bedmar, E.J., Richardson, D.J., Delgado, M.J., Nitric oxide detoxification in the rhizobia-legume symbiosis (2011) Biochem Soc Trans, 39, pp. 184-188
dc.descriptionSaviani, E.E., Orsi, C.H., Oliveira, J.F.P., Pinto-Maglio, C.A.F., Salgado, I., Participation of the mitochondrial permeability transition pore in nitric oxide-induced plant cell death (2002) FEBS Lett, 510, pp. 136-140
dc.descriptionSeligman, K., Saviani, E.E., Oliveira, H.C., Pinto-Maglio, C.A.F., Salgado, I., Floral transition and nitric oxide emission during flower development in Arabidopsis thaliana is affected in nitrate reductase-deficient plants (2008) Plant Cell Physiol, 49, pp. 1112-1121
dc.descriptionSiddiqui, M.H., Al-Whaibi, M.H., Basalah, M.O., Role of nitric oxide in tolerance of plants to abiotic stress (2011) Protoplasma, 248, pp. 447-455
dc.descriptionSpoel, S.H., Loake, G.J., Redox-based protein modifications: the missing link in plant immune signalling (2011) Curr Opin Plant Biol, 14, pp. 358-364
dc.descriptionStamler, J.S., Singel, D.J., Loscalzo, J., Biochemistry of nitric oxide and its redox-activated forms (1992) Science, 258, pp. 1898-1902
dc.descriptionStamler, J.S., Lamas, S., Fang, F.C., Nitrosylation: the prototypic redox-based signaling mechanism (2001) Cell, 106, pp. 675-683
dc.descriptionStohr, C., Strube, F., Marx, G., Ullrich, W.R., Rockel, P., A plasma membrane-bound enzyme of tobacco roots catalyses the formation of nitric oxide from nitrite (2001) Planta, 212, pp. 835-841
dc.descriptionTada, Y., Spoel, S.H., Pajerowska-Mukhtar, K., Mou, Z., Song, J., Wang, C., Zuo, J., Dong, X., Plant immunity requires conformational changes [corrected] of NPR1 via S-nitrosylation and thioredoxins (2008) Science, 321, pp. 952-956
dc.descriptionTerrile, M.C., París, R., Calderón-Villalobos, L.I., Iglesias, M.J., Lamattina, L., Estelle, M., Casalongué, C.A., Nitric oxide influences auxin signaling through S-nitrosylation of the Arabidopsis TRANSPORT INHIBITOR RESPONSE 1 auxin receptor (2012) Plant J, 70, pp. 492-500
dc.descriptionTun, N.N., Santa-Catarina, C., Begum, T., Silveira, V., Handro, W., Floh, E.I.S., Scherer, G.F.E., Polyamines induce rapid biosynthesis of nitric oxide (NO) in Arabidopsis thaliana seedlings (2006) Plant Cell Physiol, 47, pp. 346-354
dc.descriptionWang, Y.Q., Feechan, A., Yun, B.W., Shafiei, R., Hofmann, A., Taylor, P., Xue, P., Loake, G.J., S-nitrosylation of AtSABP3 antagonizes the expression of plant immunity (2009) J Biol Chem, 284, pp. 2131-2137
dc.descriptionWendehenne, D., Durner, J., Klessig, D.F., Nitric oxide: a new player in plant signaling and defence responses (2004) Curr Opin Plant Biol, 7, pp. 449-455
dc.descriptionWulff, A., Oliveira, H.C., Saviani, E.E., Salgado, I., Nitrite reduction and superoxide-dependent nitric oxide degradation by Arabidopsis mitochondria: influence of external NAD(P)H dehydrogenases and alternative oxidase in the control of nitric oxide levels (2009) Nitric Oxide, 21, pp. 132-139
dc.descriptionYamasaki, H., Sakihama, Y., Takahashi, S., An alternative pathway for nitric oxide production in plants: new features of an old enzyme (1999) Trends Plant Sci, 4, pp. 128-129
dc.descriptionYun, B.W., Feechan, A., Yin, M.H., Saidi, N.B.B., Le Bihan, T., Yu, M., Moore, J.W., Loake, G.J., S-nitrosylation of NADPH oxidase regulates cell death in plant immunity (2011) Nature, 478, pp. 264-268
dc.languageen
dc.publisher
dc.relationRevista Brasileira de Botanica
dc.rightsfechado
dc.sourceScopus
dc.titleNitric Oxide Signaling And Homeostasis In Plants: A Focus On Nitrate Reductase And S-nitrosoglutathione Reductase In Stress-related Responses
dc.typeArtículos de revistas


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