Emerging Technologies for Enhancing ROS/RNS Homeostasis
Alla I. Yemets
Institute of Food Biotechnology and Genomics, National Academy of Sciences of Ukraine, Kyiv, Ukraine
Search for more papers by this authorYuriy V. Karpets
Dokuchaev Kharkiv National Agrarian University, Kharkiv, Ukraine
Search for more papers by this authorYuriy E. Kolupaev
Dokuchaev Kharkiv National Agrarian University, Kharkiv, Ukraine
Karazin Kharkiv National University, Kharkiv, Ukraine
Search for more papers by this authorYaroslav B. Blume
Institute of Food Biotechnology and Genomics, National Academy of Sciences of Ukraine, Kyiv, Ukraine
Search for more papers by this authorAlla I. Yemets
Institute of Food Biotechnology and Genomics, National Academy of Sciences of Ukraine, Kyiv, Ukraine
Search for more papers by this authorYuriy V. Karpets
Dokuchaev Kharkiv National Agrarian University, Kharkiv, Ukraine
Search for more papers by this authorYuriy E. Kolupaev
Dokuchaev Kharkiv National Agrarian University, Kharkiv, Ukraine
Karazin Kharkiv National University, Kharkiv, Ukraine
Search for more papers by this authorYaroslav B. Blume
Institute of Food Biotechnology and Genomics, National Academy of Sciences of Ukraine, Kyiv, Ukraine
Search for more papers by this authorMirza Hasanuzzaman
Sher-e-Bangla Agricultural University, Dhaka, Bangladesh
Search for more papers by this authorVasileios Fotopoulos
Cyprus University of Technology, Lemesos, Cyprus
Search for more papers by this authorKamrun Nahar
Sher-e-Bangla Agricultural University, Dhaka, Bangladesh
Search for more papers by this authorSummary
Considerable progress has been achieved in our understanding of the complexities of ROS and NO interactions over the last decade. Accumulating literature evidences demonstrates that ROS and RNS play key roles as biological messengers, functioning together to facilitate appropriate responses to biotic and abiotic stresses. ROS/RNS interplay is also important in the regulation of plant development and in the regulation of a wide range of physiological responses to the environment. Such background allows us to summarize our current knowledge about emerging technologies for enhancing ROS/RNS homeostasis. Respectively, in this chapter are considered the possibilities to use nitric oxide donors for abiotic stress tolerance: drought, salt stress, extreme temperatures and heavy metal stress. The perspectives for nitric oxide donors in agriculture are considered in details, especially for controlling seed vigor, dormancy and ripening, their biotechnological applications in wound healing and post harvested shelf life. The ways for improvement of NO donor application are analyzed (co-application of nitric oxide donors with fertilizers and perspectives on the use of nanoparticles releasing nitric oxide in crop industry). Special attention is paid to transgenic approaches for regulation of oxidative stress and antioxidant defense systems and perspectives for regulation of microRNAs and nitric oxide crosstalk in stress tolerance in plants and related challenges dictated by the development of genome editing and synthetic biology.
References
- Abdel-Kader, D.Z.E. (2007). Role of nitric oxide, glutathione and sulfhydryl groups in zinc homeostasis in plants. American Journal of Plant Physiology 2: 59–75.
- Ahmad, P., Latef, A.A.A., Hashem, A. et al. (2016). Nitric oxide mitigates salt stress by regulating levels of osmolytes and antioxidant enzymes in chickpea. Frontiers in Plant Science 7: 347. https://doi.org/10.3389/fpls.2016.00347.
- Ali, Q., Daud, M.K., Haider, M.Z. et al. (2017). Seed priming by sodium nitroprusside improves salt tolerance in wheat (Triticum aestivum L.) by enhancing physiological and biochemical parameters. Plant Physiology and Biochemistry 119: 50–58.
- Alscher, R.G., Erturk, N., and Heath, L.S. (2002). Role of superoxide dismutases (SODs) in controlling oxidative stress in plants. Journal of Experimental Botany 53: 1331–1341.
- Andreev, I.M. (2012). Role of the vacuole in the redox homeostasis of plant cells. Russian Journal of Plant Physiology 59: 611–617.
- Arasimowicz-Jelonek, M., Floryszak-Wieczorek, J., and Kubis, J. (2009). Involvement of nitric oxide in water stress-induced responses of cucumber roots. Plant Science 177: 682–690.
- Arasimowicz-Jelonek, M., Floryszak-Wieczorek, J., and Gwóźdź, E.A. (2011). The message of nitric oxide in cadmium challenged plants. Plant Science 181: 612–620.
- Arasimowicz-Jelonek, M., Floryszak-Wieczorek, J., Deckert, J. et al. (2012). Nitric oxide implication in cadmium-induced programmed cell death in roots and signalling response of yellow lupine plants. Plant Physiology and Biochemistry 58: 124–134.
- Arc, E., Galland, M., Godin, B. et al. (2013a). Nitric oxide implication in the control of seed dormancy and germination. Frontiers in Plant Science 4: 346.
- Arc, E., Sechet, J., Corbineau, F. et al. (2013b). ABA crosstalk with ethylene and nitric oxide in seed dormancy and germination. Frontiers in Plant Science 4: 63.
- Arnaud, N., Murgia, I., Boucherez, J. et al. (2006). An iron-induced nitric oxide burst precedes ubiquitin-dependent protein degradation for Arabidopsis AtFer1 ferritin gene expression. Journal Biological Chemistry 281: 23579–23588.
- Arora, D. and Bhatla, S.C. (2015). Nitric oxide triggers a concentration-dependent differential modulation of superoxide dismutase (FeSOD and Cu/ZnSOD) activity in sunflower seedling roots and cotyledons as an early and long. Plant Signaling and Behavior 10: e1071753.
- Arora, D., Jain, P., Singh, N. et al. (2016). Mechanisms of nitric oxide crosstalk with reactive oxygen species scavenging enzymes during abiotic stress tolerance in plants. Free Radical Research 50: 291–303.
- Astier, J., Gross, I., and Durner, J. (2018). Nitric oxide production in plants: an update. Journal of Experimental Botany 69: 3401–3411.
- Astier, J. and Lindermayr, C. (2012). Nitric oxide-dependent posttranslational modification in plants: an update. International Journal of Molecular Sciences 13: 15193–15208.
- Awasthi, R., Bhandari, K., and Nayyar, H. (2015). Temperature stress and redox homeostasis in agricultural crops. Frontiers in Environmental Science 3: https://doi.org/10.3389/fenvs.2015.00011.
- Axtell, M.J. and Bartel, D.P. (2005). Antiquity of microRNAs and their targets in land plants. The Plant Cell 17: 1658–1673.
- Bai, X., Yang, L., Tian, M. et al. (2011). Nitric oxide enhances desiccation tolerance of recalcitrant Antiaris toxicaria seeds via protein S-nitrosylation and carbonylation. PLoS One e20714.
-
Barand, A., Nasibi, F., and ManouchehriKalantari, K. (2015). The effect of arginine pretreatment in the increase of coldtolerance in Pistacia vera L. in vitro
. Russian Agricultural Sciences 41: 340–346.
10.3103/S1068367415050043 Google Scholar
- Baudouin, E. and Hancock, J.T. (2014). Nitric oxide signaling in plants. Frontiers in Plant Science 4: 553.
-
Baudouin, E. and Jeandroz, S. (2015). Nitric oxide as a mediator of cold stress response: a transcriptional point of view. In: Nitric Oxide Action in Abiotic Stress Responses in Plants (ed. M.N. Khan, M. Mobin, F. Mohammad and F.J. Corpas), 129–139. Switzerland: Springer International Publishing.
10.1007/978-3-319-17804-2_8 Google Scholar
- Baxter, A., Mittler, R., and Suzuki, N. (2014). ROS as key players in plant stress signaling. Journal of Experimental Botany 65: 1229–1240.
- Belousov, V.V., Enikolopov, G.N., and Mishina, N.M. (2013). Compartmentalization of ROS-mediated signal transduction. Russian Journal of Bioorganic Chemistry 39: 341–355.
- Beltran, B., Orsi, A., Clementi, E., and Moncada, S. (2000). Oxidative stress and S-nitrosylation of proteins in cells. British Journal of Pharmacology 129: 953–960.
- Bestwick, C.S., Brown, I.R., Bennett, M.H.R., and Mansfield, J.W. (1997). Localization of hydrogen peroxide accumulation during the hypersensitive reaction of lettuce cells to Pseudomonas syringae pv. Phaseolicola . The Plant Cell 9: 209–221.
- Bethke, P.C., Gubler, F., Jacobsen, J.V., and Jones, R.L. (2004). Dormancy of Arabidopsis seeds and barley grains can be broken by nitric oxide. Planta 219: 847–855.
- Bibi, A., Majid, S.A., Ulfat, A. et al. (2017). Effect of nitric oxide seed priming on chilling inducedwater related physiological attributes in germinating wheat. Journal of Animal and Plant Sciences 27: 186–191.
- Blume, Y.B., Krasylenko, Y.A., Demchuk, O.M., and Yemets, A.I. (2013). Tubulin tyrosine nitration regulates microtubule organization in plant cells. Frontiers in Plant Science 4: 530. https://doi.org/10.3389/fpls.2013.00530.
- Boogar, R.A., Salehi, H., and Jowkar, A. (2014). Exogenous nitric oxide alleviates oxidative damage in turfgrasses under drought stress. South African Journal of Botany 92: 78–82.
- Bouchard, J.N. and Yamasaki, H. (2008). Heat stress stimulates nitric oxide production in Symbiodinium microadriaticum: a possible linkage between nitric oxide and the coral bleaching phenomenon. Plant and Cell Physiology 49: 641–652.
- Brown, G.C. (1995). Nitric oxide regulates mitochondrial respiration and cell functions by inhibiting cytochrome oxidase. FEBS Letters 369: 136–139.
- Brunelli, L., Yermilov, V., and Beckman, J.S. (2001). Modulation of catalase peroxidatic and catalatic activity by nitric oxide. Free Radical Biology and Medicine 30: 709–714.
- Buet, A., Moriconi, J.I., Santa-María, G.E., and Simontacchi, M. (2014). An exogenous source of nitric oxide modulates zinc nutritional status in wheat plants. Plant Physiology and Biochemistry 83: 337–345.
-
Burlaka, O.M., Pirko, Y.V., Yemets, A.I., and Blume, Y.B. (2015). Application of carbon nanotubes for plant genetic transformation. In: Nanocomposites, Nanophotonics, Nanobiotechnology, and Applications, vol. 156 (ed. O. Fesenko and L. Yatsenko), 233–255. Springer-Verlag Springer Proceedings in Physics.
10.1007/978-3-319-06611-0_20 Google Scholar
-
Burlaka, O.M., Yemets, A.I., Pirko, Y.V., and Blume, Y.B. (2016). Non-covalent functionalization of carbon nanotubes for efficient gene delivery. In: Nanophysics, Nanophotonics, Surface Studies, and Applications, vol. 183 (ed. O. Fesenko and L. Yatsenko), 355–370. Springer-Verlag Springer Proceedings in Physics.
10.1007/978-3-319-30737-4_30 Google Scholar
- Cai, W., Liu, W., Wang, W.S. et al. (2015). Overexpression of rat neurons nitric oxide synthase in rice enhances drought and salt tolerance. PLoS One 10: e0131599.
- Cantrel, C., Vazquez, T., Puyaubert, J. et al. (2011). Nitric oxide participates in cold-responsive phosphosphingolipid formation and gene expression in Arabidopsis thaliana . New Phytologist 189: 415–427.
- Chaki, M., Valderrama, R., Fernández-Ocaña, A.M. et al. (2011a). Mechanical wounding induces a nitrosative stress by downregulation of GSNO reductase and a rise of Snitrosothiols in sunflower (Helianthus annuus) seedlings. Journal of Experimental Botany 62: 1803–1813.
- Chaki, M., Valderrama, R., Fernández-Ocaña, A.M. et al. (2011b). High temperature triggers the metabolism of S-nitrosothiols in sunflower mediating a process of nitrosative stress which provokes the inhibition of ferredoxin–NADP reductase by tyrosine nitration. Plant, Cell & Environment 34: 1803–1818.
- Christou, A., Filippou, P., Manganaris, G.A., and Fotopoulos, V. (2014). Sodium hydrosulfide induces systemic thermotolerance to strawberry plants through transcriptional regulation of heat shock proteins and aquaporin. BMC Plant Biology 14: 42. https://doi.org/10.1186/1471-2229-14-42.
- Chun, H.J., Park, H.C., Koo, S.C. et al. (2012). Constitutive expression of mammalian nitric oxide synthase in tobacco plants triggers disease resistance to pathogens. Molecules and Cells 34: 463–471.
- Clark, D., Dunar, J., Navarre, D.A., and Klessig, D.F. (2000). Nitric oxide inhibition of tobacco catalase and ascorbate peroxidase. Molecular Plant-Microbe Interactions 14: 1380–1384.
- Cooper, C.E. (1999). Nitric oxide and iron proteins. Biochimica et Biophysica Acta 1411: 290–309.
- Corpas, F.J. and Barroso, J.B. (2017). Nitric oxide synthase-like activity in higher plants. Nitric Oxide 68: 5–6.
- Corpas, F.J., del Rio, L.A., and Barroso, J.B. (2008). Post-translational modifications mediated by reactive nitrogen species. Nitrosative stress responses of components of signal transduction pathways. Plant Signaling & Behavior 3: 301–303.
- Corpas, F.J., Sandalio, L.M., Del Rio, L.A., and Trelease, R.N. (1998). Copper-zinc superoxide dismutase is a constituent enzyme of the matrix of peroxisomes in the cotyledons of oilseed plants. New Phytologist 138: 307–314.
- Correa-Aragunde, N., Graziano, M., and Lamattina, L. (2004). Nitric oxide plays a central role in determining lateral root development in tomato. Planta 218: 900–917.
- Correa-Aragunde, N., Lombardo, C., and Lamattina, L. (2008). Nitric oxide: an active nitrogen molecule that modulates cellulose synthesis in tomato roots. New Phytologist 79: 386–396.
- Crawford, N.M. (2005). Mechanisms for nitric oxide synthesis in plants. Journal of Experimental Botany 57: 471–478.
- Cui, X.M., Zhang, Y.K., Wu, X.B., and Liu, C.S. (2010). The investigation of the alleviated effect of copper toxicity by exogenous nitric oxide in tomato plants. Plant Soil Environmental 56: 274–281.
- Cvetkovska, M. and Vanlerberghe, G.C. (2013). Alternative oxidase impacts the plant response to biotic stress by influencing the mitochondrial generation of reactive oxygen species. Plant Cell & Environment 36: 721–732.
- Daudi, A., Cheng, Z., O'Brien, J.A. et al. (2012). The apoplastic oxidative burst peroxidase in Arabidopsis is a major component of pattern-triggered immunity. The Plant Cell 24: 275–287.
- De Michele, R., Vurro, E., Rigo, C. et al. (2009). Nitric oxide is involved in cadmium-induced programmed cell death in Arabidopsis suspension cultures. Plant Physiology 150: 217–228.
- del Giudice, J., Cam, Y., Damiani, I. et al. (2011). Nitric oxide is required for an optimal establishment of the Medicago truncatula – Sinorhizobium meliloti symbiosis. New Phytologist 191: 405–417.
- del Rio, L.A. (2015). ROS and RNS in plant physiology: an overview. Journal of Experimental Botany 66: 2827–2837.
- del Rio, L.A., Sandalio, L.M., Corpas, F.J. et al. (2006). Reactive oxygen species and reactive nitrogen species in peroxisomes. Production, scavenging, and role in cell signaling. Plant Physiology 141: 330–335.
-
Demidchik, V. (2012). Reactive oxygen species and oxidative stress in plants. In: Plant Stress Physiology (ed. S. Shabala), 24–58. CAB International.
10.1079/9781845939953.0024 Google Scholar
- Demirci, Y., Zhang, B., and Unver, T. (2018). CRISPR/Cas9: an RNA-guided highly precise synthetic tool for plant genome editing. Journal of Cellular Physiology 233: 1844–1859.
- Desikan, R., Griffiths, R., Hancock, J., and Neill, S. (2002). A new role for an old enzyme: nitrate reductase-mediated nitric oxide generation is required for abscisic acid-induced stomatal closure in Arabidopsis thaliana . Proceedings of the National Academy of Sciences of the United States of America 99: 16314–16318.
- Diniz, M.C., Olivon, V.C., Tavares, L.D. et al. (2017). Mechanisms underlying sodium nitroprusside-induced tolerance in the mouse aorta: role of ROS and cyclooxygenase-derived prostanoids. Life Science 176: 26–34.
- Dong, T., Tong, J., Xiao, L. et al. (2012). Nitrate, abscisic acid and gibberellin interactions on the thermoinhibition of lettuce seed germination. Plant Growth Regulation 66: 191–202.
- Dong, Y., Xu, L., Wang, Q. et al. (2014). Effects of exogenous nitric oxide on photosynthesis, antioxidative ability, and mineral element contents of perennial ryegrass under copper stress. International Journal of Plant Sciences 9: 402–411.
- Du, S.T., Liu, Y., Zhang, P. et al. (2015). Atmospheric application of trace amounts of nitric oxide enhances tolerance to salt stress and improves nutritional quality in spinach (Spinacia oleracea L.). Food Chemistry 173: 905–1011.
- Duan, X., Li, X., Ding, F. et al. (2015). Interaction of nitric oxide and reactive oxygen species and associated regulation of root growth in wheat seedlings under zinc stress. Ecotoxicology and Environmental Safety 113: 95–102.
- Dubovskaya, L.V., Kolesneva, E.V., Knyazev, D.M., and Volotovskii, I.D. (2007). Protective role of nitric oxide during hydrogen peroxide-induced oxidative stress in tobacco plants. Russian Journal of Plant Physiology 54: 755–761.
- Ederli, L., Morettini, R., Borgogni, A. et al. (2006). Interaction between nitric oxide and ethylene in the induction of alternative oxidase in ozone-treated tobacco plants. Plant Physiology 142: 595–608.
- Fan, J., Chen, K., Amombo, E. et al. (2015). Physiological and molecular mechanism of nitric oxide (NO) involved in bermudagrass response to cold stress. PLoS One https://doi.org/10.1371/journal.pone.01329910.
- Fan, Q.J. and Liu, J.H. (2012). Nitric oxide is involved in dehydration/drought tolerance in Poncirus trifoliata seedlings through regulation of antioxidant systems and stomatal response. Plant Cell Reports 31: 145–154.
- Fancy, N.N., Bahlmann, A.K., and Loake, G.J. (2017). Nitric oxide function in plant abiotic stress. Plant, Cell & Environment 40: 462–472.
- Farnese, F.S., Menezes-Silva, P.E., Gusman, G.S., and Oliveira, J.A. (2016). When bad guys become good ones: the key role of reactive oxygen species and nitric oxide in the plant responses to abiotic stress. Frontiers in Plant Science 7: 471.
- Farooq, M., Basra, M.A., Wahid, A., and Rehman, H. (2009). Exogenously applied nitric oxide enhances the drought tolerance in fine grain aromatic rice (Oryza sativa L.). Journal of Agronomy and Crop Science 195: 254–261.
- Fitzhugh, A.L. and Keefer, L.K. (2000). Diazeniumdiolates: pro- and antioxidant applications of the “NONOates”. Free Radical Biology and Medicine 28: 1463–1469.
- Floryszak-Wieczorek, J., Arasimowicz, M., Milczarek, G. et al. (2007). Only an early nitric oxide burst and the following wave of secondary nitric oxide generation enhanced effective defence responses of pelargonium to a necrotrophic pathogen. New Phytologist 175: 718–730.
- Ford, P.C. (2010). Reactions of NO and nitrite with heme models and proteins. Inorganic Chemistry 49: 6226–6239.
- Foyer, C.H. and Noctor, G. (2005). Redox homeostasis and antioxidant signaling: a metabolic interface between stress perception and physiological responses. The Plant Cell 17: 1866–1875.
- Foyer, C.H. and Noctor, G. (2009). Redox regulation in photosynthetic organisms: signaling, acclimation, and practical implications. Antioxidants & Redox Signaling 11: 861–906.
- Foyer, C.H. and Shigeoka, S. (2011). Understanding oxidative stress and antioxidant functions to enhance photosynthesis. Plant Physiology 155: 93–100.
- Freschi, L. (2013). Nitric oxide and phytohormone interactions: current status and perspectives. Frontiers in Plant Science 4: 398. https://doi.org/10.3389/fpls.2013.00398.
- Gao, W., Long, L., Tian, X. et al. (2017). Genome editing in cotton with the CRISPR/Cas9 system. Frontiers in Plant Science 8: 1364. https://doi.org/10.3389/fpls.2017.01364.
-
Gautam, V., Kaur, R., Kohli, S.K. et al. (2017). ROS compartmentalization in plant cells under abiotic stress condition. In: Reactive Oxygen Species and Antioxidant Systems in Plants: Role and Regulation Under Abiotic Stress (ed. M.I.R. Khan and N.A. Khan), 89–114. Springer Nature Singapore Pte Ltd.
10.1007/978-981-10-5254-5_4 Google Scholar
- Ghorbani, B., Pakkish, Z., and Khezriss, M. (2017). Nitric oxide increases antioxidant enzyme activity and reduces chilling injury in orange fruit during storage. New Zealand Journal of Crop and Horticultural Science https://doi.org/10.1080/01140671.2017.1345764.
-
Giba, Z., Grubisic, D., and Konjevic, R. (2007). Seeking the role of NO in breaking dormancy. In: Nitric Oxide in Plant Growth, Development and Stress Physiology (ed. L. Lamattina and J.C. Polaacco), 91–111. Berlin: Springer-Verlag.
10.1007/7089_2006_086 Google Scholar
- Gill, S.S., Gill, R., Anjum, N.A., and Tuteja, N. (2013). Transgenic approaches for abiotic stress tolerance in crop plants. In: Stress-Mediated Signaling in Plants (ed. G.K. Pandey), Plant Stress 7 (Special Issue 1), 73–83.
- Gill, S.S. and Tuteja, N. (2010). Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry 48: 909–930.
- Gimalov, F.R., Baymiev, A.K., Matniyazov, R.T. et al. (2004). Initial stages of low-temperature induction of cabbage cold shock protein gene csp5 . Biochemistry (Moscow) 69: 575–579.
- Glyan'ko, A.K., Mitanova, N.B., and Stepanov, A.V. (2012). Influence of environmental factors on the generation of nitric oxide in the roots of etiolated pea seedlings. Applied Biochemistry and Microbiology 48: 83–89. (in Russ.).
- Glyan'ko, A.K. and Vasil'eva, G.G. (2010). Reactive oxygen and nitrogen species in legume-rhizobial symbiosis: a review. Applied Biochemistry and Microbiology 46: 15–22.
- Gniazdowska, A., Krasuska, U., Czajkowska, K., and Bogatek, R. (2010). Nitric oxide, hydrogen cyanide and ethylene are required in the control of germination and undisturbed development of young apple seedlings. Plant Growth Regulation 61: 75–84.
- Go, Y.M. and Jones, D.P. (2013). The redox proteome. Journal of Biological Chemistry 288: 26512–26520.
- Gould, K.S., Lamotte, O., Klinguer, A. et al. (2003). Nitric oxide production in tobacco leaf cells: a generalized stress response? Plant, Cell & Environment 26: 1851–1862.
- Gould, K.S. and Lister, C. (2006). Flavonoid functions in plants. In: Flavonoids: Chemistry, Biochemistry, and Applications (ed. O.M. Andersen and K.R. Markham), 397–442. New York: CRC.
- Guan, L.M. and Scandalios, J.G. (2000). Hydrogen peroxide-mediated catalase gene expression in response to wounding. Free Radical Biology and Medicine 28: 1182–1190.
- Gupta, K.J., Fernie, A.R., Kaiser, W.M., and van Dongen, J.T. (2011). On the origins of nitric oxide. Trends in Plant Science 16: 160–168.
- Gupta, K.J., Shah, J.K., Brotman, Y. et al. (2012). Inhibition of aconitase by nitric oxide leads to induction of the alternative oxidase and to a shift of metabolism towards biosynthesis of amino acids. Journal of Experimental Botany 63: 1773–1784.
- Gupta, K.J. and Kaiser, W.M. (2010). Production and scavenging of nitric oxide by barley root mitochondria. Plant Cell Physiology 51: 576–584.
- Hao, Y., Chen, F., Wu, G., and Gao, W. (2016). Impact of postharvest nitric oxide treatment on lignin biosynthesis-related genes in wax apple (Syzygium samarangense) fruit. Journal of Agricultural and Food Chemistry https://doi.org/10.1021/acs.jafc.6b03281.
- Hasanuzzaman, M., Hossain, M.A., and Fujita, M. (2011). Nitric oxide modulates antioxidant defense and the methylglyoxal detoxification system and reduces salinity-induced damage of wheat seedlings. Plant Biotechnology Reports 5: 353–365.
- Hasanuzzaman, M., Nahar, K., Alam, A., and Fujita, M. (2012). Exogenous nitric oxide alleviates high temperature induced oxidative stress in wheat (Triticum aestivum L.) seedlings by modulating the antioxidant defense and glyoxalase system. Australian Journal of Crop Science 6: 1314–1323.
-
Hasanuzzaman, M., Gill, S.S., and Fujita, M. (2013). Physiological role of nitric oxide in plants grown under adverse environmental conditions. In: Plant Acclimation to Environmental Stress (eds. N. Tuteja and S.S. Gill), 269–322. New York: Springer Science+Business Media.
10.1007/978-1-4614-5001-6_11 Google Scholar
- Hasanuzzaman, M., Oku, H.,·Nahar, K. et al. (2018). Nitric oxide-induced salt stress tolerance in plants: ROS metabolism, signaling, and molecular interactions. Plant Biotechnology Reports. doi:10.1007/s11816-018-0480-0
-
Hayat, S., Yadav, S., Wani, A.S. et al. (2011). Nitric oxide effects on photosynthetic rate, growth, and antioxidant activity in tomato. International Journal of Vegetable Science 17: 333–348.
10.1080/19315260.2011.563275 Google Scholar
- He, J.M., Xu, H., She, X.P. et al. (2005). The role and the interrelationship of hydrogen peroxide and nitric oxide in the UV-B-induced stomatal closure in broad bean. Functional Plant Biology 32: 237–247.
- Hossain, K.K., Itoh, R.D., Yoshimura, G. et al. (2010). Effects of nitric oxide scavengers on thermoinhibition of seed germination in Arabidopsis thaliana . Russian Journal of Plant Physiology 57: 222–232.
- Hsu, Y.T. and Kao, C.H. (2004). Cadmium toxicity is reduced by nitric oxide in rice leaves. Plant Growth Regulation 42: 227–238.
- Hu, K.D., Hu, L.Y., Li, Y.H. et al. (2007). Protective roles of nitric oxide on germination and antioxidant metabolism in wheat seeds under copper stress. Plant Growth Regulation 53: 173–183.
- Huang, J., Wei, H., Li, L., and Yu, S. (2018). Transcriptome analysis of nitric oxide-responsive genes in upland cotton (Gossypium hirsutum). PLoS One 13: e0192367.
- Huang, S.L., Kee, P.H., Kim, H. et al. (2009). Nitric oxide-loaded echogenic liposomes for nitric oxide delivery and inhibition of intimal hyperplasia. Journal of the American College of Cardiology 54: 652–659.
- Huang, X., Rad, U., and Durner, J. (2002). Nitric oxide induces transcriptional activation of the nitric oxide-tolerant alternative oxidase in Arabidopsis suspension cells. Planta 215: 914–923.
- Ischiropoulos, H. (2003). Biological selectivity and functional aspects of protein tyrosine nitration. Biochemical and Biophysical Research Communications 305: 776–783.
- Jang, I.C., Oh, S.J., Se, J.S. et al. (2003). Expression of a bifunctional fusion of the Escherichia coli genes for trehalose-6-phosphate synthase and trehalose-6-phosphate phosphatase in transgenic rice plants increases trehalose accumulation and abiotic stress tolerance without stunting growth. Plant Physiology 131: 516–524.
- Jasid, S., Simontacchi, M., Bartoli, C.G., and Puntarulo, S.S. (2006). Chloroplasts as a nitric oxide cellular source. Effect of reactive nitrogen species on chloroplastic lipids and proteins. Plant Physiology 142: 1246–1255.
- Jasid, S., Simontacchi, M., and Puntarulo, S. (2008). Exposure to nitric oxide protects against oxidative damage but increases the labile iron pool in sorghum embryonic axes. Journal of Experimental Botany 59: 3953–3962.
- Kacperska, A. (2004). Sensor types in signal transduction pathways in plant cells responding to abiotic stressors: do they depend on stress intensity? Physiologia Plantarum 122: 159–168.
- Kang, R., Zhang, L., Jiang, L. et al. (2015). Effect of postharvest nitric oxide treatment on the proteome of peach fruit during ripening. Postharvest Biology and Technology https://doi.org/10.1016/j.postharvbio.2015.08.017.
- Karpets, Y.V., Kolupaev, Y.E., and Yastreb, T.O. (2011). Effect of sodium nitroprusside on heat resistance of wheat coleoptiles: dependence on the formation and scavenging of reactive oxygen species. Russian Journal of Plant Physiology 58: 1027–1033.
- Karpets, Y.V., Kolupaev, Y.E., Yastreb, T.O., and Dmitriev, O.P. (2012). Possible pathways of heat resistance induction in plant cells by exogenous nitrogen oxide. Cytology and Genetics 46: 354–359.
- Karpets, Y.V., Kolupaev, Y.E., and Vayner, A.A. (2015a). Functional interaction between nitric oxide and hydrogen peroxide during formation of wheat seedling induced heat resistance. Russian Journal of Plant Physiology 62: 65–70.
- Karpets, Y.V., Kolupaev, Y.E., Yastreb, T.O., and Oboznyi, A.I. (2015b). Effects of NO-status modification, heat hardening, and hydrogen peroxide on the activity of antioxidant enzymes in wheat seedlings. Russian Journal of Plant Physiology 62: 292–298.
- Karpets, Y.V., Kolupaev, Y.E., Yastreb, T.O., and Oboznyi, A.I. (2016). Induction of heat resistance in wheat seedlings by exogenous calcium, hydrogen peroxide, and nitric oxide donor: functional interaction of signal mediators. Russian Journal of Plant Physiology 63: 490–498.
- Karpets, Y.V., Kolupaev, Y.E., Kolomoyets, B.A. et al. (2018a). Influence of sodium nitroprusside as a NO donor on the productivity and resistance of barley to unfavorable factors. Agrochimiya 6: 53–62.
- Karpets, Y.V., Kolupaev, Y.E., Lugovaya, A.A. et al. (2018b). Influence of nitrate and L-arginin on nitric oxide content, activity of antioxidant enzymes in roots of wheat seedlings and their heat resistance. Russian Journal of Plant Physiology 65: 908–915.
- Karpets, Y.V. and Kolupaev, Y.E. (2018). Participation of nitric oxide in 24-epibrassinolide-induced heat resistance of wheat coleoptiles: functional interactions of nitric oxide with reactive oxygen species and Ca ions. Russian Journal of Plant Physiology 65: 177–185.
- Kaye, Y., Golani, Y., Singer, Y. et al. (2011). Inositol polyphosphate 5-phosphatase7 regulates the production of reactive oxygen species and salt tolerance in Arabidopsis. Plant Physiology 157: 229–241.
- Kaur, G., Singh, H.P., Batish, D.R. et al. (2015). Exogenous nitric oxide (NO) interferes with lead (Pb)-induced toxicity by detoxifying reactive oxygen species in hydroponically grown wheat (Triticum aestivum) root. PLoS One 10(9): e0138713. Doi: 10.1371/journal.pone.0138713
- Kausar, F. and Shahbaz, M. (2013). Interactive effect of foliar application of nitric oxide (NO) and salinity on wheat (Triticum aestivum L.). Pakistan Journal of Botany 45: 67–73.
- Kausar, F., Shahbaz, M., and Ashraf, M. (2013). Protective role of foliar-applied nitric oxide in Triticum aestivum under saline stress. Turkish Journal of Botany 37: 1155–1165.
- Kazemi, N., Khavari-Nejad, R.A., Fahimi, H. et al. (2010). Effects of exogenous salicylic acid and nitric oxide on lipid peroxidation and antioxidant enzyme activities in leaves of Brassica napus L. under nickel stress. Scientia Horticulturae 126: 402–407.
- Kepczynski, J., Cembrowska-Lech, D., and Sznigir, P. (2017). Interplay between nitric oxide, ethylene, and gibberellic acid regulating the release of Amaranthus retroflexus seed dormancy. Acta Physiologiae Plantarum 39: 254.
- Kepczynski, J. and Sznigir, P. (2014). Participation of GA3, ethylene, NO and HCN in germination of Amaranthus retroflexus L. seeds with various dormancy levels. Acta Physiologiae Plantarum 36: 1463–1472.
- Khan, M.N., Mobin, M., Abbas, Z.K., and Siddiqui, M.H. (2017). Nitric oxide-induced synthesis of hydrogen sulfide alleviates osmotic stress in wheat seedlings through sustaining antioxidant enzymes, osmolyte accumulation and cysteine homeostasis. Nitric Oxide https://doi.org/10.1016/j.niox.2017.01.001.
-
Khan, M.N., Mohammad, F., Mobin, M., and Ali Saqib, M. (2014). Tolerance of plants to abiotic stress: a role of nitric oxide and calcium. In: Nitric Oxide in Plants: Metabolism and Role in Stress Physiology (ed. M. Khan et al.), 225–242. Switzerland: Springer International Publishing.
10.1007/978-3-319-06710-0_14 Google Scholar
- Klessig, D.F., Durner, J., Noad, R. et al. (2000). Nitric oxide and salicylic acid signalling in plant defense. Proceedings of the National Academy of Sciences of the United States of America 97: 8849–8855.
- Kolbert, Z., Bartha, B., and Erdei, L. (2005). Generation of nitric oxide in roots of Pisum sativum, Triticum aestivum and Petroselinum crispum plants under osmotic and drought stress. Proceedings of the 8th Hungarian congress on plant physiology and the 6th Hungarian conference on photosynthesis. Acta Biologica Szegediensis 49: 13–16.
- Kolupaev, Y.E., Karpets, Y.V., and Dmitriev, A.P. (2015). Signal mediators in plants in response to abiotic stress: calcium, reactive oxygen and nitrogen species. Cytology and Genetics 49: 338–348.
- Kolupaev, Y.E., Karpets, Y.V., Yastreb, T.O., and Lugovaya, A.A. (2018). Combined effect of salicylic acid and nitrogen oxide donor on stress-protective system of wheat plants under drought conditions. Applied Biochemistry and Microbiology 54: 418–424.
- Kolupaev, Y.E., Oboznyi, A.I., and Shvidenko, N.V. (2013). Role of hydrogen peroxide in generation of a signal inducing heat tolerance of wheat seedlings. Russian Journal of Plant Physiology 60: 227–234.
- Kopyra, M., Stachon-Wilk, M., and Gwozdz, E.A. (2006). Effect of exogenous nitric oxide on the antioxidant capacity of cadmium-treated soybean cell suspension. Acta Physiologiae Plantarum 28: 525–536.
- Krasuska, U. and Gniazdowska, A. (2012). Nitric oxide and hydrogen cyanide as regulating factors of enzymatic antioxidant system in germinating apple embryos. Acta Physiologiae Plantarum 34: 683–692.
- Krasylenko, Y.A., Yemets, A.I., and Blume, Y.B. (2010). Functional role of nitric oxide in plants. Russian Journal of Plant Physiology 57: 451–461.
- Krasylenko, Y.A., Yemets, A.I., Sheremet, Y.A., and Blume, Y.B. (2012). Nitric oxide as a critical factor for perception of UV-B irradiation by microtubules in Arabidopsis . Physiologia Plantarum 145: 505–515.
- Kreslavski, V.D., Allakhverdiev, S.I., Los, D.A., and Kuznetsov, V.V. (2012). Signaling role of reactive oxygen species in plants under stress. Russian Journal of Plant Physiology 59: 141–154.
- Kuzniak, E. and Sklodowska, M. (2004). The effect of Botrytis cinerea infection on the antioxidant profile of mitochondria from tomato leaves. Journal of Experimental Botany 55: 605–612.
- Kwak, J.M., Nguyen, V., and Schroeder, J.I. (2006). The role of reactive oxygen species in hormonal responses. Plant Physiology 141: 323–329.
- Lai, T., Wang, Y., Li, B. et al. (2011) Defense responses of tomato fruit to exogenous nitric oxide during postharvest storage. Postharvest Biology and Technology 62: 127–132.
- Lamotte, O., Courtois, C., Barnavon, L. et al. (2005). Nitric oxide in plants: the biosynthesis and cell signaling properties of a fascinating molecule. Planta 221: 1–4.
- Lanteri, M.L., Laxalt, A.M., and Lamattina, L. (2008). Nitric oxide triggers phosphatidic acid accumulation via phospholipase D during auxin-induced adventitious root formation in Cucumber. Plant Physiology 147: 188–198.
- Laspina, N.V., Groppa, M.D., Tomaro, M.L., and Benavides, M.P. (2005). Nitric oxide protects sunflower leaves against Cd-induced oxidative stress. Plant Science 169: 323–330.
- Leshem, Y.Y., Wills, R.B.H., and Ku, V.V.V. (1998). Evidence for the function of the free radical gas – nitric oxide (NO•) – as an endogenous maturation and senescence regulating factor in higher plants. Plant Physiology and Biochemistry 36: 825–833.
- Leshem, Y.Y. (2001). Nitric Oxide in Plants. Occurance, Function and Use. Boston, MA: Kulwer Academic Publishers.
- Lian, X. and Lei, Y. (2006). Nitric oxide treatment alleviates drought stress in wheat seedlings. Biologia Plantarum 50: 775–778.
- Liao, W.B., Huang, G.B., Yu, J.H., and Zhang, M.L. (2012). Nitric oxide and hydrogen peroxide alleviate drought stress in marigold explants and promote its adventitious root development. Plant Physiology and Biochemistry 58: 6–15.
- Lin, J.-S., Lin, C.-C., Lin, H.H. et al. (2012a). MicroR828 regulates lignin and H2O2 accumulation in sweet potato on wounding. New Phytologist 196: 427–440.
- Lin, Y., Liu, Z., Shi, Q. et al. (2012b). Exogenous nitric oxide (NO) increased antioxidant capacity of cucumber hypocotyl and radicle under salt stress. Scientia Horticulturae 142: 118–127.
- Liu, H.T., Li, B., Shang, Z.L. et al. (2003). Calmodulin is involved in heat shock signal transduction in wheat. Plant Physiology 132: 1186–1195.
- Liu, Y., Hao, Y., Liu, Y., and Huang, W. (2005). Effects of wounding and exogenous jasmonic acid on the peroxidation of membrane lipid in pea seedlings leaves. Agricultural Sciences in China 4: 614–620.
- Liu, X., Wang, L., Liu, L. et al. (2011). Alleviating effect of exogenous nitric oxide in cucumber seedling against chilling stress. African Journal of Biotechnology 10: 4380–4386.
- Loch, D.S., Adkins, S., Heslehurst, M. et al. (2004). Seed formation, development, and germination. In: Warm-season (C4) Grasses (ed. L.E. Moser, B.L. Burson, and L.E. Sollenberger), 95–144. Agronomy Society of America, Inc., Madison, Wisconsin.
- Lozano-Juste, J., Colom-Moreno, R., and Leon, J. (2011). In vivo protein tyrosine nitration in Arabidopsis thaliana . Journal of Experimental Botany 62: 3501–3517.
- Lozano-Juste, J. and Leon, J. (2010). Enhanced abscisic acid-mediated responses in nia1nia2noa1-2 triple mutant impaired in NIA/NR- and AtNOA1-dependent nitric oxide biosynthesis in Arabidopsis . Plant Physiology 152: 891–903.
- Luo, J., Liu, M., Zhang, C. et al. (2017). Transgenic centipedegrass (Eremochloa ophiuroides [Munro] Hack.) Overexpressing S-adenosylmethionine decarboxylase (SAMDC) gene for improved cold tolerance through involvement of H2O2 and NO signaling. Frontiers in Plant Science 8: 1655. https://doi.org/10.3389/fpls.2017.01655.
- Lv, X., Li, H., Chen, X. et al. (2018). The role of calcium-dependent protein kinase in hydrogen peroxide, nitric oxide and ABA-dependent cold acclimation. Journal of Experimental Botany https://doi.org/10.1093/jxb/ery212.
- Mamaeva, A.S., Fomenkov, A.A., Nosov, A.V. et al. (2015). Regulatory role of nitric oxide in plants. Russian Journal of Plant Physiology 62: 427–440.
- Manai, J., Kalai, T., Gouia, H., and Corpas, F.J. (2014). Exogenous nitric oxide (NO) ameliorates salinity-induced oxidative stress in tomato (Solanum lycopersicum) plants. Journal of Soil Science and Plant Nutrition 14: 433–446.
- Marino, D., Dunand, C., Puppo, A., and Pauly, N. (2012). A burst of plant NADPH oxidases. Trends in Plant Science 17: 9–15.
- Martinoia, E., Maeshima, M., and Neuhaus, H.E. (2007). Vacuolar transporters and their essential role in plant metabolism. Journal of Experimental Botany 58: 83–102.
- Marvasi, M. (2017). Potential use and perspectives of nitric oxide donors in agriculture. Journal of the Science of Food and Agriculture 97: 1065–1072.
-
Mehla, N., Sindhi, V., Josula, D., Bisht, P., and Wani, S.H. (2017). An introduction to antioxidants and their roles in plant stress tolerance. In: Reactive Oxygen Species and Antioxidant Systems in Plants: Role and Regulation under Abiotic Stress (eds. M.I.R. Khan and N.A. Khan), 1–24. Singapore: Springer Nature. Pte Ltd.
10.1007/978-981-10-5254-5_1 Google Scholar
- Mehlhorn, H., Lelandais, M., Korth, H.G., and Foyer, C.H. (1996). Ascorbate is the natural substrate for plant peroxidases. FEBS Letters 378: 203–206.
- Meng, Z., Meng, Z., Zhang, R. et al. (2015). Expression of the rice arginase gene OsARG in cotton influences the morphology and nitrogen transition of seedlings. PLoS One 10: e0141530. https://doi.org/10.1371/journal.pone.0141530.
- Miura, K., Okamoto, H., Okuma, E. et al. (2013). SIZ1 deficiency causes reduced stomatal aperture and enhanced drought tolerance via controlling salicylic acid-induced accumulation of reactive oxygen species in Arabidopsis . The Plant Journal 73: 91–104.
-
Mobin, M., Khan, M.N., and Abbas, Z.K. (2015). Nitric oxide impact on plant adaptation to transition metal stress. In: Nitric Oxide Action in Abiotic Stress Responses in Plants (ed. M.N. Khan et al.), 155–167. Switzerland: Springer International Publishing.
10.1007/978-3-319-17804-2_10 Google Scholar
- Mohanta, T.K., Bashir, T., Hashem, A. et al. (2017). Genome editing tools in plants. Genes 8: 399. https://doi.org/10.3390/genes8120399.
- Moller, I.M. (2001). Plant mitochondria and oxidative stress: electron transport, NADPH turnover, and metabolism of reactive oxygen species. Annual Review of Plant Physiology and Plant Molecular Biology 52: 561–591.
- Montilla-Bascón, G., Rubiales, D., and Hebelstrup, K.H. (2017). Reduced nitric oxide levels during drought stress promote drought tolerance in barley and is associated with elevated polyamine biosynthesis. Scientific Reports 7: 13311. https://doi.org/10.1038/s41598-017-13458-1.
- Mostofa, M.G., Fujita, M., and Tran, L.S.P. (2015). Nitric oxide mediates hydrogen peroxide- and salicylic acid-induced salt tolerance in rice (Oryza sativa L.) seedlings. Plant Growth Regulation 77: 265–277.
- Munemasa, S., Oda, K., Watanabe-Sugimoto, M. et al. (2007). The coronatine-insensitive 1 mutation reveals the hormonal signaling interaction between abscisic acid and methyl jasmonate in Arabidopsis guard cells. Specific impairment of ion channel activation and second messenger production. Plant Physiology 143: 1398–1407.
- Munns, R. (2002). Comparative physiology of salt and water stress. Plant, Cell and Environment 25: 239–250.
- Mur, L.A.J., Mandon, J., Persijn, S. et al. (2013). Nitric oxide in plants: an assessment of the current state of knowledge. AoB Plants 5: https://doi.org/10.1093/aobpla/pls052.
- Mur, L.A.J., Santosa, I.E., Laarhoven, L.J. et al. (2003). A new partner in the danse Macabre: the role of nitric oxide in the hypersensitive response. Bulgarian Journal of Plant Physiology (Special Issue): 110–123.
- Murgia, I., Delledonne, M., and Soave, C. (2002). Nitric oxide mediates iron-induced ferritin accumulation in Arabidopsis . The Plant Journal 30: 521–528.
- Nair, R., Varghese, S.H., Nair, B.G. et al. (2010). Nanoparticulate material delivery to plants. Plant Science 179: 154–163.
- Navari-Izzo, F., Quartacci, M.F., Pinzino, C. et al. (1998). Thylakoid-bound and stromal antioxidative enzymes in wheat treated with excess copper. Physiology Plantarum 104: 630–638.
- Negi, S., Santisree, P., Kharshiing, E.V., and Sharma, R. (2010). Inhibition of the ubiquitin – proteasome pathway alters cellular levels of nitric oxide in tomato seedlings. Molecular Plant 3: 854–869.
- Neill, S.J., Desikan, R., Clarke, A. et al. (2002). Hydrogen peroxide and nitric oxide as signalling molecules in plants. Journal of Experimental Botany 53: 1237–1247.
- Neill, S., Barros, R., Bright, J. et al. (2008). Nitric oxide, stomatal closure and abiotic stress. Journal of Experimental Botany 59: 165–176.
- Niu, L. and Liao, W. (2016). Hydrogen peroxide signaling in plant development and abiotic responses: crosstalk with nitric oxide and calcium. Frontiers in Plant Science 7: 230.
- Noman, A., Aqeel, M., and He, S. (2016). CRISPR-Cas9: tool for qualitative and quantitative plant genome editing. Frontiers in Plant Science 7: 1740. https://doi.org/10.3389/fpls.2016.01740.
- Noman, A., Fahad, S., Aqeel, M. et al. (2017). miRNAs: major modulators for crop growth and development under abiotic stresses. Biotechnology Letters 39: 685–700.
- Ogawa, K., Kanematsu, S., Takabe, K., and Asada, K. (1995). Attachment of CuZn-superoxide dismutase to thylakoid membranes at the site of Superoxide generation (PSI) in spinach chloroplasts: detection by immuno-gold labeling after rapid freezing and substitution method.Plant and Cell Physiology 36: 565–573.
- Ogasawara, Y., Kaya, H., Hiraoka, G. et al. (2008). Synergistic activation of the Arabidopsis NADPH oxidase AtrbohD by Ca2+ and phosphorylation. Journal of Biological Chemistry 283: 8885–8892.
- Oliveira, H.C., Gomes, B.C., Pelegrino, M.T., and Seabra, A.B. (2016). Nitric oxide-releasing chitosan nanoparticles alleviate the effects of salt stress in maize plants. Nitric Oxide 61: 10–19.
- Oz, M.T., Eyidogan, F., Yucel, M., and Oktem, H.A. (2015). Functional role of nitric oxide under abiotic stress conditions. In: Nitric Oxide in Plants: Metabolism and Role in Stress Physiology (ed. M. Khan et al.), 21–42. Switzerland: Springer International Publishing.
- Pál, M., Szalai, G., and Janda, T. (2015). Speculation: polyamines are important in abiotic stress signaling. Plant Science 237: 16–23.
- Palma, J.M., Huertas, E.L., Corpas, F.J. et al. (1998). Peroxisomal manganese superoxide dismutase: purification and properties of the isozyme from pea leaves. Physiologia Plantarum 104: 720–726.
- París, R., Lamattina, L., and Casalongué, C.A. (2007). Nitric oxide promotes the wound-healing response of potato leaflets. Plant Physiology and Biochemistry 45: 80–86.
- Pasuphaty, K., Lin, S., Hu, Q. et al. (2008). Direct plant gene delivery with a poly (amidoamine) dendrimer. Biotechnology Journal 3: 1078–1082.
- Peng, S., Huang, J., Sheehy, J.E. et al. (2004). Rice yields decline with higher night temperature from global warming. Proceedings of the National Academy of Sciences of the United States of America 101: 9971–9975.
- Piatek, A., Lenaghan, S., and Stewart, C.N. (2018). Advanced editing of nuclear and plastid genomes in plants. Plant Science 273. https://doi.org/10.1016/j.plantsci.
- Pradedova, E.V., Nimaeva, O.D., and Salyaev, R.K. (2017). Redox processes in biological systems. Russian Journal of Plant Physiology 64: 822–832.
- Procházková, D., Haisel, D., Wilhelmová, N. et al. (2013). Effects of exogenous nitric oxide on photosynthesis. Photosynthetica 51: 483–489.
-
Procházková, D., Wilhelmová, N., and Milan, P. (2015). Reactive nitrogen species and nitric oxide. In: Nitric Oxide Action in Abiotic Stress Responses in Plants (ed. M.N. Khan et al.), 3–20. Switzerland: Springer International Publishing.
10.1007/978-3-319-17804-2_1 Google Scholar
- Prouhdon, D., Wei, J., and Theil, E.C. (1996). Ferritin gene organization: differences between plants and animals suggest possible kingdom-specific selective constraints. Journal of Molecular Evolution 42: 325–336.
- Pucciariello, C., Banti, V., and Perata, P. (2012). ROS signaling as common element in low oxygen and heat stresses. Plant Physiology and Biochemistry 59: 3–10.
- Puyaubert, J. and Baudouin, E. (2014). New clues for a cold case: nitric oxide response to low temperature. Plant, Cell & Environment 37: 2623–2630.
- Radi, R. (2004). Nitric oxide, oxidants, and protein tyrosine nitration. Proceedings of the National Academy of Sciences of the United States of America 101: 4003–4008.
- Rajjou, L., Duval, M., Gallardo, K. et al. (2012). Seed germination and vigor. Annual Review of Plant Biology 63: 507–533.
- Ramirez, L., Zabaleta, E.J., and Lamattina, L. (2010). Nitric oxide and frataxin: two players contributing to maintain cellular iron homeostasis. Annals of Botany 105: 801–810.
- Romero-Puertas, M.C., Corpas, F.J., Sandalio, L.M. et al. (2006). Glutathione reductase from pea leaves: response to abiotic stress and characterization of the peroxisomal isozyme. New Phytologist 170: 432–452.
-
Roszer, T. (2014). Biosynthesis of nitric oxide in plants. In: Nitric Oxide in Plants: Metabolism and Role in Stress Physiology (ed. M.N. Khan et al.), 17–32. Switzerland: Springer International Publishing.
10.1007/978-3-319-06710-0_2 Google Scholar
- Rozentsvet, O.A., Nesterov, V.N., and Bogdanova, E.S. (2017). Structural, physiological, and biochemical aspects of salinity tolerance of halophytes. Russian Journal of Plant Physiology 64: 464–477.
- Rubilar, O., Diez, M.C., Tortella, G.R. et al. (2014). New strategies and challenges for nanobiotechnology in agriculture. Journal of Biobased Materials and Bioenergy 8: 1–12.
- Saba, K. and Moradi, S.M. (2017). Sodium nitroprusside (SNP) spray to maintain fruit quality and alleviate postharvest chilling injury of peach fruit. Scientia Horticulturae 216: 193–199.
- Saidi, Y., Finka, A., Muriset, M. et al. (2009). The heat shock response in moss plants is regulated by specific calcium-permeable channels in the plasma membrane. The Plant Cell 21: 2829–2843.
- Sakihama, Y., Tamaki, R., Shimoji, H. et al. (2003). Enzymatic nitration of phytophenolics: evidence for peroxynitrite-independent nitration of plant secondary metabolites. FEBS Letters 553: 377–380.
- Sami, F., Faizan, M., Faraz, A. et al. (2018). Nitric oxide-mediated integrative alterations in plant metabolism to confer abiotic stress tolerance, NO crosstalk with phytohormones and NO-mediated post translational modifications in modulating diverse plant stress. Nitric Oxide https://doi.org/10.1016/j.niox.2017.12.005.
- Sánchez-Romera, B., Porcel, R., Ruiz-Lozano, J.M., and Aroca, R. (2018). Arbuscular mycorrhizal symbiosis modifies the effects of a nitric oxide donor (sodium nitroprusside; SNP) and a nitric oxide synthesis inhibitor (Nω-nitro-L-arginine methyl ester; L-NAME) on lettuce plants under well watered and drought conditions. Symbiosis 74: 11–20.
- Sang, J., Jiang, M., Lin, F. et al. (2008). Nitric oxide reduces hydrogen peroxide accumulation involved in water stress-induced subcellular antioxidant defense in maize plants. Journal of Integrative Plant Biology 50: 231–243.
- Santisree, P., Adimulam, S.S., Bhatnagar-Mathur, P., and Sharma, K.K. (2017). Nitric oxide (NO) in plant heat stress tolerance: current knowledge and perspectives. Frontiers in Plant Science 8: 1582.
- Santisree, P., Bhatnagar-Mathur, P., and Sharma, K.K. (2015). NO to drought-multifunctional role of nitric oxide in plant drought: do we have all the answers? Plant Science 239: 44–55.
- Sanz, L., Albertos, P., Mateos, I. et al. (2015). Nitric oxide (NO) and phytohormones crosstalk during early plant development. Journal of Experimental Botany 66: 2857–2868.
- Scandalios, J.G. (2002). The rise of ROS. Trends in Biochemical Sciences 27: 483–486.
- Schoenfisch, M.H., Hetrick, E.M., Stasko, N.A., and Johnson, C.B. (2009). Use of nitric oxide to enhance the efficacy of silver and other topical wound care agents. PCT Int Appl WO 2 009 049 208
- Seabra, A.B., Rai, M., and Duran, N. (2014). Nano carriers for nitric oxide delivery and its potential applications in plant physiological process: a mini review. Journal of Plant Biochemistry and Biotechnology 23: 1–10.
- Sehrawat, A. and Deswal, R. (2014). S-Nitrosylation analysis in Brassica juncea apoplast highlights the importance of nitric oxide in cold-stress signaling. Journal of Proteome 13: 2599–2619.
- Shan, C., Zhou, Y., and Liu, M. (2015). Nitric oxide participates in the regulation of the ascorbate-glutathione cycle by exogenous jasmonic acid in the leaves of wheat seedlings under drought stress. Protoplasma 252: 1397–1405.
- Sharova, E.I. and Medvedev, S.S. (2017). Redox reactions in apoplast of growing cells. Russian Journal of Plant Physiology 64: 1–14.
- She, X.P., Song, X.G., and He, J.M. (2004). Role and relationship of nitric oxide and hydrogen peroxide in light/dark-regulated stomatal movement in Vicia faba . Acta Botanica Sinica 46: 1292–1300.
- Shi, F.M. and Li, Y.Z. (2008). Verticillium dahliae toxins-induced nitric oxide production in Arabidopsis is major dependent on nitrate reductase. BMB Reports 41: 79–85.
- Shi, H.T., Li, R.J., Cai, W. et al. (2012a). Increasing nitric oxide content in Arabidopsis thaliana by expressing rat neuronal nitric oxide synthase resulted in enhanced stress tolerance. Plant and Cell Physiology 53: 344–357.
- Shi, H.T., Li, R.J., Cai, W. et al. (2012b). In vivo role of nitric oxide in plant response to abiotic and biotic stress. Plant Signaling and Behavior 7: 437–439.
- Shi, H., Ye, T., Zhu, J.-K., and Chan, Z. (2014). Constitutive production of nitric oxide leads to enhanced drought stress resistance and extensive transcriptional reprogramming in Arabidopsis . Journal of Experimental Botany 65: 4119–4131.
- Shin, J.H., Metzger, S.K., and Schoenfisch, M.H. (2007). Synthesis of nitric oxide-releasing silica nanoparticles. Journal of American Chemical Society 129: 4612–4619.
- Shriram, V., Kumar, V., Devarumath, R.M. et al. (2016). MicroRNAs as potential targets for abiotic stress tolerance in plants. Frontiers in Plant Science 7: 817. https://doi.org/10.3389/fpls.2016.00817.
-
Sidana, S., Bose, J., Shabala, L., and Shabala, S. (2015). Nitric oxide in drought stress signalling and tolerance in plants. In: Nitric Oxide Action in Abiotic Stress Responses in Plants (ed. M.N. Khan et al.), 95–114. Switzerland: Springer International Publishing.
10.1007/978-3-319-17804-2_6 Google Scholar
- Siddiqui, M.H., Alamri, S.A., Al-Khaishany, M.Y.Y. et al. (2017). Nitric oxide and calcium induced physiobiochemical changes in tomato (Solanum lycopersicum) plant under heat stress. Fresenius Environmental Bulletin 26 (2a): 1663–11672.
- Siddiqui, M.H., Mohammad, F., and Khan, M.N. (2009). Morphological and physiological and biochemical characterization of Brassica juncea L. Czern. & Coss. Genotypes under salt stress. Journal of Plant Interactions 4: 67–80.
- Siddiqui, M.H., Mohammad, F., Khan, M.N. et al. (2010). Nitrogen in relation to photosynthetic capacity and accumulation of osmoprotectant and nutrients in Brassica genotypes grown under salt stress. Agricultural Sciences in China 9: 671–680.
- Signorelli, S. and Considine, M.J. (2018). Nitric oxide enables germination by a four-pronged attack on ABA-induced seed dormancy. Frontiers in Plant Science 9: 296.
- Silveira, N., Hancock, J.T., Frungillo, L. et al. (2017). Evidence towards the involvement of nitric oxide in drought tolerance of sugarcane. Plant Physiology and Biochemistry 115: 354–359.
- Singh, H.P., Batish, D.R., Kaur, G. et al. (2008). Nitric oxide (as sodium nitroprusside) supplementation ameliorates Cd toxicity in hydroponically grown wheat roots. Environmental and Experimental Botany 63: 158–167.
- Singh, R., Parihar, P., Singh, S. et al. (2017). Micro RNAs and nitric oxide cross talk in stress tolerance in plants. Plant Growth Regulation 83: 199–205.
- Snyder, S.H. (1992). Nitric oxide: first in a new class of neurotransmitters? Science 257: 494–496.
- Song, L., Ding, W., Zhao, M. et al. (2006). Nitric oxide protects against oxidative stress under heat stress in the calluses from two ecotypes of reed. Plant Science 171: 449–458.
- Srivastava, S. and Dubey, R.S. (2012). Nitric oxide alleviates manganese toxicity by preventing oxidative stress in excised rice leaves. Acta Physiologiae Plantarum 34: 819–825.
- Stasko, N.A., Fischer, T.H., and Schoenfisch, M.H. (2008). S-Nitrosothiol-modified dendrimers as nitric oxide delivery vehicles. Biomacromolecules 9: 834–841.
- Sun, C., Liu, L., Lu, L. et al. (2018). Nitric oxide acts downstream of hydrogen peroxide in regulating aluminum-induced antioxidant defense that enhances aluminum resistance in wheat seedlings. Environmental and Experimental Botany 145: 95–103.
- Suzuki, N. and Mittler, R. (2006). Reactive oxygen species and temperature stresses: a delicate balance between signaling and destruction. Physiologia Plantarum 126: 45–51.
- Tan, J., Zhao, H., Hong, J. et al. (2008). Effects of exogenous nitric oxide on photosynthesis, antioxidant capacity and proline accumulation in wheat seedlings subjected to osmotic stress. World Journal of Agricultural Sciences 4: 307–313.
- Tereshina, E.V., Laskavy, V.N., and Ivanenko, S.I. (2015). Four components of the conjugated redox system in organisms: carbon, nitrogen, sulfur, oxygen. Biochemistry (Moscow) 80: 1186–1200.
- Tewari, R.K., Hahn, E.J., and Paek, K.Y. (2008). Function of nitric oxide and superoxide anion in the adventitious root development and antioxidant defence in Panax ginseng . Plant Cell Reports 27: 563–573.
- Tewari, R.K., Prommer, J., and Watanabe, M. (2013). Endogenous nitric oxide generation in protoplast chloroplasts. Plant Cell Reports 32: 31–44.
- Tian, X., He, M., Wang, Z. et al. (2015). Application of nitric oxide and calcium nitrate enhances tolerance of wheat seedlings to salt stress. Plant Growth Regulation 77: 343–356.
- Torney, F., Trewyn, B.G., Lin, V.S.Y., and Wang, K. (2007). Mesoporous silica nanoparticles deliver DNA and chemicals into plants. Nature Nanotechnology l2: 295–300.
- Torres, M.A., Dangl, J.L., and Jones, J.D. (2002). Arabidopsis gp91phox homologues AtrbohD and AtrbohF are required for accumulation of reactive oxygen intermediates in the plant defense response. Proceedings of the National Academy of Sciences ofthe United States of America 99: 517–522.
-
Trchounian, A., Petrosyan, M., and Sahakyan, N. (2016). Plant cell redox homeostasis and reactive oxygen species. In: Redox State as a Central Regulator of Plant-Cell Stress Responses (ed. D.K. Gupta et al.), 25–50. Switzerland: Springer International Publishing.
10.1007/978-3-319-44081-1_2 Google Scholar
- Trentin, A.R., Pivato, M., Mehdi, S.M.M. et al. (2015). Proteome readjustments in the apoplastic space of Arabidopsis thaliana ggt1 mutant leaves exposed to UV-B radiation. Frontiers in Plant Science 6: 128. https://doi.org/10.3389/fpls.2015.00128.
- Uchida, A., Jagendorf, A.T., Hibino, T. et al. (2002). Effects of hydrogen peroxide and nitric oxide on both salt and heat stress tolerance in rice. Plant Science 163: 515–523.
- Ueda, Y., Wu, L., and Frei, M. (2013). A critical comparison of two high-throughput ascorbate analyses methods for plant samples. Plant Physiology and Biochemistry 70: 418–423.
- Venkatachalam, K. (2018). Exogenous nitric oxide treatment impacts antioxidant response and alleviates chilling injuries in longkong pericarp. Scientia Horticulturae 237: 311–317.
- Wang, P.G., Xian, M., Tang, X. et al. (2002). Nitric oxide donors: chemical activities and biological applications. Chemical Reviews 102: 1091–1134.
- Wang, W., Vinocur, B., and Altman, A. (2003). Plant responses to drought, salinity and extreme temperatures: towards genetic engineering for stress tolerance. Planta 218: 1–14.
- Wang, Y., Luo, Z., Khan, Z.U. et al. (2015). Effect of nitric oxide on energy metabolism in postharvest banana fruit in response to chilling stress. Postharvest Biology and Technology 108: 21–27.
- Wang, Y., Meng, Z., Liang, C. et al. (2017). Increased lateral root formation by CRISPR/Cas9-mediated editing of arginase genes in cotton. Science China. Life sciences 60: 524–527.
- Waraich, E.A., Ahmad, R., Halim, A., and Aziz, T. (2012). Alleviation of temperature stress by nutrient management in crop plants: a review. Journal of Soil Science and Plant Nutrition 12: 221–244.
-
Wills, R., McGlasson, W., Graham, D., and Joyce, D. (2007). Postharvest: An Introduction to Postharvest Handling and Physiology of Fruit and Vegetables, 5e. Sydney: New South Wales University Press.
10.1079/9781845932275.0013 Google Scholar
-
Wills, R.B.H., Pristijono, P., and Golding, J.B. (2015). Nitric oxide and postharvest stress of fruits, vegetables and ornamentals. In: Nitric Oxide Action in Abiotic Stress Responses in Plants (ed. M.N. Khan et al.), 221–237. Switzerland: Springer International Publishing.
10.1007/978-3-319-17804-2_14 Google Scholar
- Wilson, I.D., Neill, S.J., and Hancock, J.T. (2008). Nitric oxide synthesis and signaling in plants. Plant, Cell & Environment 31: 622–631.
- Wimalasekera, R., Villar, C., Begum, T., and Scherer, G.F. (2001). Coper amine oxidase1 (CuAO) of Arabidopsis thaliana contributes to abscisic acid- and polyamine-induced nitric oxide biosynthesis and abscisic acid signal transduction. Molecular Plant 4: 663–678.
- Wimalasekera, R., Tebartz, F., and Scherer, G.F.E. (2011). Polyamines, polyamine oxidases and nitric oxide in development, abiotic and biotic stresses. Plant Science 181: 593–603.
- Wink, D.A., Hanbauer, I., Krishna, M.C. et al. (1993). Nitric oxide protects against cellular damage and cytotoxicity from reactive oxygen species. Proceedings of the National Academy of Sciences of the United States of America 90: 9813–9817.
- Wong, H.L., Pinontoan, R., Hayashi, K. et al. (2007). Regulation of rice NADPH oxidase by binding of Rac GTPase to its N-terminal extension. The Plant Cell 19: 4022–4034.
- Wu, B., Guo, Q., Li, Q. et al. (2014). Impact of postharvest nitric oxide treatment on antioxidant enzymes and related genes in banana fruit in response to chilling tolerance. Postharvest Biology and Technology 92: 157–163.
- Xie, F.L., Jones, D.C., Wang, Q.L. et al. (2015). Small RNA sequencing identifies miRNA roles in ovule and fiber development. Plant Biotechnology Journal 13: 355–369.
- Xing, H., Tan, L., An, L. et al. (2004). Evidence for the involvement of nitric ox-ide and reactive oxygen species in osmotic stress tolerance of wheat seed-lings: inverse correlation between leaf abscisic acid accumulation and leaf water loss. Plant Growth Regulation 42: 61–68.
- Xiong, J., An, L., Lu, H., and Zhu, C. (2009). Exogenous nitric oxide enhances cadmium tolerance of rice by increasing pectin and hemicellulose contents in root cell wall. Planta 230: 755–765.
- Xu, J., Yin, H., Li, Y., and Liu, X. (2010). Nitric oxide is associated with long-term zinc tolerance in Solanum nigrum . Plant Physiology 154: 1319–1334.
- Xuan, Y., Zhou, S., Wang, L. et al. (2010). Nitric oxide functions as a signal and acts upstream of atcam3 in thermotolerance in Arabidopsis seedlings. Plant Physiology 153: 1895–1906.
- Yastreb, Т.О., Kolupaev, Y.Е., Kokorev, А.I. et al. (2018). Methyl jasmonate and nitric oxide in regulation of stomatal apparatus of Arabidopsis thaliana . Cytology and Genetics 52: 400–405.
-
Yemets, A.I., Krasylenko, Y.A., and Blume, Y.B. (2015). Nitric oxide and UV-B radiation. In: Nitric Oxide Action in Abiotic Stress Responses in Plants (ed. M.N. Khan et al.), 141–154. Switzerland: Springer International Publishing.
10.1007/978-3-319-17804-2_9 Google Scholar
- Yu, Q., Sun, L., Jin, H. et al. (2012). Lead-induced nitric oxide generation plays a critical role in lead uptake by Pogonatherum crinitum root cells. The Plant Cell Physiology 53: 1728–1736.
- Yu, M., Lamattina, L., Spoel, S.H., and Loake, G.J. (2014). Nitric oxide function in plant biology: a redox cue in deconvolution. New Phytologist 202: 1142–1156.
- Yuan, S., Liu, W.J., Zhang, N.H. et al. (2005). Effects of water stress on major photosystem II gene expression and protein metabolism in barley leaves. Physiologia Plantarum 125: 464–473.
- Yun, B.W., Feechan, A., Yin, M. et al. (2011). S-nitrosylation of NADPH oxidase regulates cell death in plant immunity. Nature 478: 264–268.
- Yurina, N.P. and Odintsova, M.S. (2010). Signal transduction pathways of plant mitochondria: retrograde regulation. Russian Journal of Plant Physiology 57: 7–19.
- Zhang, H., Shen, W.B., and Xu, L.L. (2003). Effects of nitric oxide on the germination of wheat seeds and its reactive oxygen species metabolisms under osmotic stress. Acta Botanica Sinica 45: 901–905.
- Zhang, X.W., Dong, Y.J., Qiu, X.K. et al. (2012). Exogenous nitric oxide alleviates iron-deficiency chlorosis in peanut growing on calcareous soil. Plant Soil Environment 58: 111–120.
- Zhang, Y., Wang, L., Liu, Y. et al. (2006). Nitric oxide enhances salt tolerance in maize seedlings through increasing activities of proton-pump and Na+/H+ antiport in the tonoplast. Planta 224: 545–555.
- Zhang, A., Jiang, M., Zhang, J. et al. (2007). Nitric oxide induced by hydrogen peroxide mediates abscisic acid-induced activation of the mitogen-activated protein kinase cascade involved in antioxidant defense in maize leaves. New Phytologist 175: 36–50.
- Zhang, B. (2015). MicroRNA: a new target for improving plant tolerance to abiotic stress. Journal of Experimental Botany 66: 1749–1761.
- Zhang, B. and Wang, Q. (2015). MicroRNA-based biotechnology for plant improvement. Journal of Cellular Physiology 230: 1–15.
- Zhang, H., Li, Y.H., Hu, L.Y. et al. (2008). Effects of exogenous nitric oxide donor on antioxidant metabolism in wheat leaves under aluminum stress. Russian Journal of Plant Physiology 55: 469–474.
- Zhang, T., Che, F., Zhang, H. et al. (2017a). Effect of nitric oxide treatment on chilling injury, antioxidant enzymes and expression of the CmCBF1 and CmCBF3 genes in cold-stored Ham melon (Cucumis melo L.) fruit. Postharvest Biology and Technology 127: 88–98.
- Zhang, Y., Ma, X., Xie, X., and Liu, Y.G. (2017b). CRISPR/Cas9-based genome editing in plants. Progress in Molecular Biology and Translational Science 149: 133–150.
- Zhao, M.G., Chen, L., Zhang, L.L., and Zhang, W.H. (2009). Nitric reductase-dependent nitric oxide production is involved in cold acclimation and freezing tolerance in Arabidopsis . Plant Physiology 151: 755–767.
- Zhu, T., Deng, X.-G., Tan, W.R. et al. (2016). Nitric oxide is involved in brassinosteroid-induced alternative respiratory pathway in Nicotiana benthamiana seedlings' response to salt stress. Physiologia Plantarum 156: 150–163.
- Ziogas, V., Tanou, G., Filippou, P. et al. (2013). Nitrosative responses in citrus plants exposed to six abiotic stress conditions. Plant Physiology and Biochemistry 68: 118–126.
-
Ziogas, V. and Molassiotis, A. (2015). Nitric oxide action in the improvement of plant tolerance to nutritional stress. In: Nitric Oxide Action in Abiotic Stress Responses in Plants (ed. M.N. Khan et al.), 169–180. Switzerland: Springer International Publishing.
10.1007/978-3-319-17804-2_11 Google Scholar