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dc.contributor.author | Gisbert Domenech, Maria Carmen | es_ES |
dc.contributor.author | Timoneda, Alfonso | es_ES |
dc.contributor.author | Porcel, R | es_ES |
dc.contributor.author | Ros, Roc | es_ES |
dc.contributor.author | Mulet, José Miguel | es_ES |
dc.date.accessioned | 2021-06-01T03:31:27Z | |
dc.date.available | 2021-06-01T03:31:27Z | |
dc.date.issued | 2020-11 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/166995 | |
dc.description.abstract | [EN] Drought stress is one of the major threats to agriculture and concomitantly to food production. Tomato is one of the most important industrial crops, but its tolerance to water scarcity is very low. Traditional plant breeding has a limited margin to minimize this water requirement. In order to design novel biotechnological approaches to cope with this problem, we have screened a plant cDNA library from the halotolerant crop sugar beet (Beta vulgaris L.) for genes able to confer drought/osmotic stress tolerance to the yeast model system upon overexpression. We have identified the gene that encodes BvHb2, a class 2 non-symbiotic hemoglobin, which is present as a single copy in the sugar beet genome, expressed mainly in leaves and regulated by light and abiotic stress. We have evaluated its biotechnological potential in the model plant Arabidopsis thaliana and found that BvHb2 is able to confer drought and osmotic stress tolerance. We also generated transgenic lines of tomato (Solanum lycopersicum) overexpressing BvHb2 and found that the resulting plants are more resistant to drought-induce withering. In addition, transgenic lines overexpressing BvHb2 exhibit increased levels of iron content in leaves. Here, we show that class 2 non-symbiotic plant hemoglobins are targets to generate novel biotechnological crops tolerant to abiotic stress. The fact that these proteins are conserved in plants opens the possibility for using Non-GMO approaches, such as classical breeding, molecular breeding, or novel breeding techniques to increase drought tolerance using this protein as a target. | es_ES |
dc.description.sponsorship | This project was funded by the project PAID-00-10 "Introduccion De Genes Relacionados Con La Tolerancia A Estres Hidrico Y Oxidativo En Distintos Materiales Que Presentan Caracteristicas Utiles Para Su Uso Como Patrones De Plantas Horticolas De Interes Agronomico". (Ref. 2726) from the Universitat Politecnica de Valencia. | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | MDPI | es_ES |
dc.relation.ispartof | Agronomy | es_ES |
dc.rights | Reconocimiento (by) | es_ES |
dc.subject | Plant hemoglobin | es_ES |
dc.subject | Non-symbiotic | es_ES |
dc.subject | Sugar beet | es_ES |
dc.subject | Tomato | es_ES |
dc.subject | Drought stress | es_ES |
dc.subject | Iron | es_ES |
dc.subject | Overexpression | es_ES |
dc.subject | Beta vulgaris | es_ES |
dc.subject | Solanum lycopersicum | es_ES |
dc.subject | Water deprivation | es_ES |
dc.subject.classification | GENETICA | es_ES |
dc.subject.classification | BIOQUIMICA Y BIOLOGIA MOLECULAR | es_ES |
dc.title | Overexpression of BvHb2, a Class 2 Non-Symbiotic Hemoglobin from Sugar Beet, Confers Drought-Induced Withering Resistance and Alters Iron Content in Tomato | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.3390/agronomy10111754 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/UPV//PAID-00-10/ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Biotecnología - Departament de Biotecnologia | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Instituto Universitario Mixto de Biología Molecular y Celular de Plantas - Institut Universitari Mixt de Biologia Molecular i Cel·lular de Plantes | es_ES |
dc.description.bibliographicCitation | Gisbert Domenech, MC.; Timoneda, A.; Porcel, R.; Ros, R.; Mulet, JM. (2020). Overexpression of BvHb2, a Class 2 Non-Symbiotic Hemoglobin from Sugar Beet, Confers Drought-Induced Withering Resistance and Alters Iron Content in Tomato. Agronomy. 10(11):1-17. https://doi.org/10.3390/agronomy10111754 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://doi.org/10.3390/agronomy10111754 | es_ES |
dc.description.upvformatpinicio | 1 | es_ES |
dc.description.upvformatpfin | 17 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 10 | es_ES |
dc.description.issue | 11 | es_ES |
dc.identifier.eissn | 2073-4395 | es_ES |
dc.relation.pasarela | S\421582 | es_ES |
dc.contributor.funder | Universitat Politècnica de València | es_ES |
dc.description.references | Mahajan, S., & Tuteja, N. (2005). Cold, salinity and drought stresses: An overview. Archives of Biochemistry and Biophysics, 444(2), 139-158. doi:10.1016/j.abb.2005.10.018 | es_ES |
dc.description.references | Sinclair, T. R. (2011). Challenges in breeding for yield increase for drought. Trends in Plant Science, 16(6), 289-293. doi:10.1016/j.tplants.2011.02.008 | es_ES |
dc.description.references | Burke, M., & Emerick, K. (2016). Adaptation to Climate Change: Evidence from US Agriculture. American Economic Journal: Economic Policy, 8(3), 106-140. doi:10.1257/pol.20130025 | es_ES |
dc.description.references | Zaveri, E., Russ, J., & Damania, R. (2020). Rainfall anomalies are a significant driver of cropland expansion. Proceedings of the National Academy of Sciences, 117(19), 10225-10233. doi:10.1073/pnas.1910719117 | es_ES |
dc.description.references | Gupta, A., Rico-Medina, A., & Caño-Delgado, A. I. (2020). The physiology of plant responses to drought. Science, 368(6488), 266-269. doi:10.1126/science.aaz7614 | es_ES |
dc.description.references | Ashraf, M. (2010). Inducing drought tolerance in plants: Recent advances. Biotechnology Advances, 28(1), 169-183. doi:10.1016/j.biotechadv.2009.11.005 | es_ES |
dc.description.references | Romero, C., Bellés, J. M., Vayá, J. L., Serrano, R., & Culiáñez-Macià, F. A. (1997). Expression of the yeast trehalose-6-phosphate synthase gene in transgenic tobacco plants: pleiotropic phenotypes include drought tolerance. Planta, 201(3), 293-297. doi:10.1007/s004250050069 | es_ES |
dc.description.references | Xiao, B., Huang, Y., Tang, N., & Xiong, L. (2007). Over-expression of a LEA gene in rice improves drought resistance under the field conditions. Theoretical and Applied Genetics, 115(1), 35-46. doi:10.1007/s00122-007-0538-9 | es_ES |
dc.description.references | Van Camp, W. (2005). Yield enhancement genes: seeds for growth. Current Opinion in Biotechnology, 16(2), 147-153. doi:10.1016/j.copbio.2005.03.002 | es_ES |
dc.description.references | Locascio, A., Andrés-Colás, N., Mulet, J. M., & Yenush, L. (2019). Saccharomyces cerevisiae as a Tool to Investigate Plant Potassium and Sodium Transporters. International Journal of Molecular Sciences, 20(9), 2133. doi:10.3390/ijms20092133 | es_ES |
dc.description.references | Mulet, J. M., Alemany, B., Ros, R., Calvete, J. J., & Serrano, R. (2004). Expression of a plant serine O-acetyltransferase inSaccharomyces cerevisiae confers osmotic tolerance and creates an alternative pathway for cysteine biosynthesis. Yeast, 21(4), 303-312. doi:10.1002/yea.1076 | es_ES |
dc.description.references | Porcel, R., Bustamante, A., Ros, R., Serrano, R., & Mulet Salort, J. M. (2018). BvCOLD1: A novel aquaporin from sugar beet (Beta vulgarisL.) involved in boron homeostasis and abiotic stress. Plant, Cell & Environment, 41(12), 2844-2857. doi:10.1111/pce.13416 | es_ES |
dc.description.references | Smagghe, B. J., Hoy, J. A., Percifield, R., Kundu, S., Hargrove, M. S., Sarath, G., … Appleby, C. A. (2009). Review: Correlations between oxygen affinity and sequence classifications of plant hemoglobins. Biopolymers, 91(12), 1083-1096. doi:10.1002/bip.21256 | es_ES |
dc.description.references | Bogusz, D., Appleby, C. A., Landsmann, J., Dennis, E. S., Trinick, M. J., & Peacock, W. J. (1988). Functioning haemoglobin genes in non-nodulating plants. Nature, 331(6152), 178-180. doi:10.1038/331178a0 | es_ES |
dc.description.references | Taylor, E. R., Nie, X. Z., MacGregor, A. W., & Hill, R. D. (1994). A cereal haemoglobin gene is expressed in seed and root tissues under anaerobic conditions. Plant Molecular Biology, 24(6), 853-862. doi:10.1007/bf00014440 | es_ES |
dc.description.references | Spyrakis, F., Bruno, S., Bidon-Chanal, A., Luque, F. J., Abbruzzetti, S., Viappiani, C., … Mozzarelli, A. (2011). Oxygen binding to Arabidopsis thaliana AHb2 nonsymbiotic hemoglobin: evidence for a role in oxygen transport. IUBMB Life, 63(5), 355-362. doi:10.1002/iub.470 | es_ES |
dc.description.references | Gupta, K. J., Hebelstrup, K. H., Mur, L. A. J., & Igamberdiev, A. U. (2011). Plant hemoglobins: Important players at the crossroads between oxygen and nitric oxide. FEBS Letters, 585(24), 3843-3849. doi:10.1016/j.febslet.2011.10.036 | es_ES |
dc.description.references | Trevaskis, B., Watts, R. A., Andersson, C. R., Llewellyn, D. J., Hargrove, M. S., Olson, J. S., … Peacock, W. J. (1997). Two hemoglobin genes in Arabidopsis thaliana: The evolutionary origins of leghemoglobins. Proceedings of the National Academy of Sciences, 94(22), 12230-12234. doi:10.1073/pnas.94.22.12230 | es_ES |
dc.description.references | Hill, R. D. (2012). Non-symbiotic haemoglobins—What’s happening beyond nitric oxide scavenging? AoB PLANTS, 2012. doi:10.1093/aobpla/pls004 | es_ES |
dc.description.references | Hunt, P. W., Klok, E. J., Trevaskis, B., Watts, R. A., Ellis, M. H., Peacock, W. J., & Dennis, E. S. (2002). Increased level of hemoglobin 1 enhances survival of hypoxic stress and promotes early growth in Arabidopsis thaliana. Proceedings of the National Academy of Sciences, 99(26), 17197-17202. doi:10.1073/pnas.212648799 | es_ES |
dc.description.references | Yang, L.-X., Wang, R.-Y., Ren, F., Liu, J., Cheng, J., & Lu, Y.-T. (2005). AtGLB1 Enhances the Tolerance of Arabidopsis to Hydrogen Peroxide Stress. Plant and Cell Physiology, 46(8), 1309-1316. doi:10.1093/pcp/pci140 | es_ES |
dc.description.references | Hebelstrup, K. H., & Jensen, E. Ø. (2007). Expression of NO scavenging hemoglobin is involved in the timing of bolting in Arabidopsis thaliana. Planta, 227(4), 917-927. doi:10.1007/s00425-007-0667-z | es_ES |
dc.description.references | Wang, Y., Elhiti, M., Hebelstrup, K. H., Hill, R. D., & Stasolla, C. (2011). Manipulation of hemoglobin expression affects Arabidopsis shoot organogenesis. Plant Physiology and Biochemistry, 49(10), 1108-1116. doi:10.1016/j.plaphy.2011.06.005 | es_ES |
dc.description.references | Vigeolas, H., Hühn, D., & Geigenberger, P. (2011). Nonsymbiotic Hemoglobin-2 Leads to an Elevated Energy State and to a Combined Increase in Polyunsaturated Fatty Acids and Total Oil Content When Overexpressed in Developing Seeds of Transgenic Arabidopsis Plants. Plant Physiology, 155(3), 1435-1444. doi:10.1104/pp.110.166462 | es_ES |
dc.description.references | Sainz, M., Pérez-Rontomé, C., Ramos, J., Mulet, J. M., James, E. K., Bhattacharjee, U., … Becana, M. (2013). Plant hemoglobins may be maintained in functional form by reduced flavins in the nuclei, and confer differential tolerance to nitro-oxidative stress. The Plant Journal, 76(5), 875-887. doi:10.1111/tpj.12340 | es_ES |
dc.description.references | FAOSTAThttp://www.fao.org/faostat/es/#home | es_ES |
dc.description.references | Sánchez-Rodríguez, E., Rubio-Wilhelmi, Mªm., Cervilla, L. M., Blasco, B., Rios, J. J., Rosales, M. A., … Ruiz, J. M. (2010). Genotypic differences in some physiological parameters symptomatic for oxidative stress under moderate drought in tomato plants. Plant Science, 178(1), 30-40. doi:10.1016/j.plantsci.2009.10.001 | es_ES |
dc.description.references | Gur, A., & Zamir, D. (2004). Unused Natural Variation Can Lift Yield Barriers in Plant Breeding. PLoS Biology, 2(10), e245. doi:10.1371/journal.pbio.0020245 | es_ES |
dc.description.references | McCormick, S., Niedermeyer, J., Fry, J., Barnason, A., Horsch, R., & Fraley, R. (1986). Leaf disc transformation of cultivated tomato (L. esculentum) using Agrobacterium tumefaciens. Plant Cell Reports, 5(2), 81-84. doi:10.1007/bf00269239 | es_ES |
dc.description.references | Gisbert, C., Rus, A. M., Boları́n, M. C., López-Coronado, J. M., Arrillaga, I., Montesinos, C., … Moreno, V. (2000). The Yeast HAL1 Gene Improves Salt Tolerance of Transgenic Tomato. Plant Physiology, 123(1), 393-402. doi:10.1104/pp.123.1.393 | es_ES |
dc.description.references | Römer, S., Fraser, P. D., Kiano, J. W., Shipton, C. A., Misawa, N., Schuch, W., & Bramley, P. M. (2000). Elevation of the provitamin A content of transgenic tomato plants. Nature Biotechnology, 18(6), 666-669. doi:10.1038/76523 | es_ES |
dc.description.references | Muir, S. R., Collins, G. J., Robinson, S., Hughes, S., Bovy, A., Ric De Vos, C. H., … Verhoeyen, M. E. (2001). Overexpression of petunia chalcone isomerase in tomato results in fruit containing increased levels of flavonols. Nature Biotechnology, 19(5), 470-474. doi:10.1038/88150 | es_ES |
dc.description.references | Schijlen, E., Ric de Vos, C. H., Jonker, H., van den Broeck, H., Molthoff, J., van Tunen, A., … Bovy, A. (2006). Pathway engineering for healthy phytochemicals leading to the production of novel flavonoids in tomato fruit. Plant Biotechnology Journal, 4(4), 433-444. doi:10.1111/j.1467-7652.2006.00192.x | es_ES |
dc.description.references | Fischhoff, D. A., Bowdish, K. S., Perlak, F. J., Marrone, P. G., McCormick, S. M., Niedermeyer, J. G., … Fraley, R. T. (1987). Insect Tolerant Transgenic Tomato Plants. Nature Biotechnology, 5(8), 807-813. doi:10.1038/nbt0887-807 | es_ES |
dc.description.references | KIM, J. W. (1994). Disease Resistance in Tobacco and Tomato Plants Transformed with the Tomato Spotted Wilt Virus Nucleocapsid Gene. Plant Disease, 78(6), 615. doi:10.1094/pd-78-0615 | es_ES |
dc.description.references | Fillatti, J. J., Kiser, J., Rose, R., & Comai, L. (1987). Efficient Transfer of a Glyphosate Tolerance Gene into Tomato Using a Binary Agrobacterium Tumefaciens Vector. Nature Biotechnology, 5(7), 726-730. doi:10.1038/nbt0787-726 | es_ES |
dc.description.references | Z.-Q., Z., F.-Q., C., Y.-X., L., & G.-X., J. (2002). Transformation of tomato with the BADH gene from Atriplex improves salt tolerance. Plant Cell Reports, 21(2), 141-146. doi:10.1007/s00299-002-0489-1 | es_ES |
dc.description.references | Roy, R., Purty, R. S., Agrawal, V., & Gupta, S. C. (2005). Transformation of tomato cultivar ‘Pusa Ruby’ with bspA gene from Populus tremula for drought tolerance. Plant Cell, Tissue and Organ Culture, 84(1), 56-68. doi:10.1007/s11240-005-9000-3 | es_ES |
dc.description.references | Sheehy, R. E., Kramer, M., & Hiatt, W. R. (1988). Reduction of polygalacturonase activity in tomato fruit by antisense RNA. Proceedings of the National Academy of Sciences, 85(23), 8805-8809. doi:10.1073/pnas.85.23.8805 | es_ES |
dc.description.references | Klee, H. J. (1993). Ripening Physiology of Fruit from Transgenic Tomato (Lycopersicon esculentum) Plants with Reduced Ethylene Synthesis. Plant Physiology, 102(3), 911-916. doi:10.1104/pp.102.3.911 | es_ES |
dc.description.references | Klee, H. J., Hayford, M. B., Kretzmer, K. A., Barry, G. F., & Kishore, G. M. (1991). Control of ethylene synthesis by expression of a bacterial enzyme in transgenic tomato plants. The Plant Cell, 3(11), 1187-1193. doi:10.1105/tpc.3.11.1187 | es_ES |
dc.description.references | Arrillaga, I., Gil-Mascarell, R., Gisbert, C., Sales, E., Montesinos, C., Serrano, R., & Moreno, V. (1998). Expression of the yeast HAL2 gene in tomato increases the in vitro salt tolerance of transgenic progenies. Plant Science, 136(2), 219-226. doi:10.1016/s0168-9452(98)00122-8 | es_ES |
dc.description.references | García-Abellan, J. O., Egea, I., Pineda, B., Sanchez-Bel, P., Belver, A., Garcia-Sogo, B., … Bolarin, M. C. (2014). Heterologous expression of the yeastHAL5gene in tomato enhances salt tolerance by reducing shoot Na+accumulation in the long term. Physiologia Plantarum, 152(4), 700-713. doi:10.1111/ppl.12217 | es_ES |
dc.description.references | Safdar, N., Yasmeen, A., & Mirza, B. (2010). An insight into functional genomics of transgenic lines of tomato cv Rio Grande harbouring yeast halotolerance genes. Plant Biology, 13(4), 620-631. doi:10.1111/j.1438-8677.2010.00412.x | es_ES |
dc.description.references | Sade, N., Vinocur, B. J., Diber, A., Shatil, A., Ronen, G., Nissan, H., … Moshelion, M. (2008). Improving plant stress tolerance and yield production: is the tonoplast aquaporin SlTIP2;2 a key to isohydric to anisohydric conversion? New Phytologist, 181(3), 651-661. doi:10.1111/j.1469-8137.2008.02689.x | es_ES |
dc.description.references | Goel, D., Singh, A. K., Yadav, V., Babbar, S. B., & Bansal, K. C. (2010). Overexpression of osmotin gene confers tolerance to salt and drought stresses in transgenic tomato (Solanum lycopersicum L.). Protoplasma, 245(1-4), 133-141. doi:10.1007/s00709-010-0158-0 | es_ES |
dc.description.references | Goel, D., Singh, A. K., Yadav, V., Babbar, S. B., Murata, N., & Bansal, K. C. (2011). Transformation of tomato with a bacterial codA gene enhances tolerance to salt and water stresses. Journal of Plant Physiology, 168(11), 1286-1294. doi:10.1016/j.jplph.2011.01.010 | es_ES |
dc.description.references | Mishra, K. B., Iannacone, R., Petrozza, A., Mishra, A., Armentano, N., La Vecchia, G., … Nedbal, L. (2012). Engineered drought tolerance in tomato plants is reflected in chlorophyll fluorescence emission. Plant Science, 182, 79-86. doi:10.1016/j.plantsci.2011.03.022 | es_ES |
dc.description.references | Seo, Y. S., Choi, J. Y., Kim, S. J., Kim, E. Y., Shin, J. S., & Kim, W. T. (2012). Constitutive expression of CaRma1H1, a hot pepper ER-localized RING E3 ubiquitin ligase, increases tolerance to drought and salt stresses in transgenic tomato plants. Plant Cell Reports, 31(9), 1659-1665. doi:10.1007/s00299-012-1278-0 | es_ES |
dc.description.references | Muñoz-Mayor, A., Pineda, B., Garcia-Abellán, J. O., Antón, T., Garcia-Sogo, B., Sanchez-Bel, P., … Bolarin, M. C. (2012). Overexpression of dehydrin tas14 gene improves the osmotic stress imposed by drought and salinity in tomato. Journal of Plant Physiology, 169(5), 459-468. doi:10.1016/j.jplph.2011.11.018 | es_ES |
dc.description.references | Zhang, X., Zou, Z., Gong, P., Zhang, J., Ziaf, K., Li, H., … Ye, Z. (2010). Over-expression of microRNA169 confers enhanced drought tolerance to tomato. Biotechnology Letters, 33(2), 403-409. doi:10.1007/s10529-010-0436-0 | es_ES |
dc.description.references | Kanhonou, R., Serrano, R., & Ros Palau, R. (2001). Plant Molecular Biology, 47(5), 571-579. doi:10.1023/a:1012227913356 | es_ES |
dc.description.references | Rosa Téllez, S., Kanhonou, R., Castellote Bellés, C., Serrano, R., Alepuz, P., & Ros, R. (2020). RNA-Binding Proteins as Targets to Improve Salt Stress Tolerance in Crops. Agronomy, 10(2), 250. doi:10.3390/agronomy10020250 | es_ES |
dc.description.references | Brunelli, J. P., & Pall, M. L. (1993). A series of yeast shuttle vectors for expression of cDNAs and other DNA sequences. Yeast, 9(12), 1299-1308. doi:10.1002/yea.320091203 | es_ES |
dc.description.references | Gietz, D., Jean, A. S., Woods, R. A., & Schiestl, R. H. (1992). Improved method for high efficiency transformation of intact yeast cells. Nucleic Acids Research, 20(6), 1425-1425. doi:10.1093/nar/20.6.1425 | es_ES |
dc.description.references | Hoeberichts, F. A., Perez-Valle, J., Montesinos, C., Mulet, J. M., Planes, M. D., Hueso, G., … Serrano, R. (2010). The role of K+ and H+ transport systems during glucose- and H2O2-induced cell death in Saccharomyces cerevisiae. Yeast, 27(9), 713-725. doi:10.1002/yea.1767 | es_ES |
dc.description.references | Sayle, R. (1995). RASMOL: biomolecular graphics for all. Trends in Biochemical Sciences, 20(9), 374-376. doi:10.1016/s0968-0004(00)89080-5 | es_ES |
dc.description.references | Hoy, J. A., & Hargrove, M. S. (2008). The structure and function of plant hemoglobins. Plant Physiology and Biochemistry, 46(3), 371-379. doi:10.1016/j.plaphy.2007.12.016 | es_ES |
dc.description.references | Kay, R., Chan, A., Daly, M., & McPherson, J. (1987). Duplication of CaMV 35 S Promoter Sequences Creates a Strong Enhancer for Plant Genes. Science, 236(4806), 1299-1302. doi:10.1126/science.236.4806.1299 | es_ES |
dc.description.references | Livak, K. J., & Schmittgen, T. D. (2001). Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method. Methods, 25(4), 402-408. doi:10.1006/meth.2001.1262 | es_ES |
dc.description.references | Bissoli, G., Niñoles, R., Fresquet, S., Palombieri, S., Bueso, E., Rubio, L., … Serrano, R. (2012). Peptidyl-prolyl cis-trans isomerase ROF2 modulates intracellular pH homeostasis in Arabidopsis. The Plant Journal, 70(4), 704-716. doi:10.1111/j.1365-313x.2012.04921.x | es_ES |
dc.description.references | Witte, C.-P., No�l, L., Gielbert, J., Parker, J., & Romeis, T. (2004). Rapid one-step protein purification from plant material using the eight-amino acid StrepII epitope. Plant Molecular Biology, 55(1), 135-147. doi:10.1007/s11103-004-0501-y | es_ES |
dc.description.references | Saporta, R., Bou, C., Frías, V., & Mulet, J. (2019). A Method for a Fast Evaluation of the Biostimulant Potential of Different Natural Extracts for Promoting Growth or Tolerance against Abiotic Stress. Agronomy, 9(3), 143. doi:10.3390/agronomy9030143 | es_ES |
dc.description.references | Trujillo-Moya, C., & Gisbert, C. (2012). The influence of ethylene and ethylene modulators on shoot organogenesis in tomato. Plant Cell, Tissue and Organ Culture (PCTOC), 111(1), 41-48. doi:10.1007/s11240-012-0168-z | es_ES |
dc.description.references | Koncz, C., & Schell, J. (1986). The promoter of TL-DNA gene 5 controls the tissue-specific expression of chimaeric genes carried by a novel type of Agrobacterium binary vector. Molecular and General Genetics MGG, 204(3), 383-396. doi:10.1007/bf00331014 | es_ES |
dc.description.references | Ríos, G., Cabedo, M., Rull, B., Yenush, L., Serrano, R., & Mulet, J. M. (2013). Role of the yeast multidrug transporter Qdr2 in cation homeostasis and the oxidative stress response. FEMS Yeast Research, 13(1), 97-106. doi:10.1111/1567-1364.12013 | es_ES |
dc.description.references | Citation for the Real Statistics Software or Website. Real Statistics Using Excelhttp://www.real-statistics.com/appendix/citation-real-statistics-software-website/ | es_ES |
dc.description.references | Tukey, J. W. (1949). Comparing Individual Means in the Analysis of Variance. Biometrics, 5(2), 99. doi:10.2307/3001913 | es_ES |
dc.description.references | Forment, J., Naranjo, M. A., Roldan, M., Serrano, R., & Vicente, O. (2002). Expression of Arabidopsis SR-like splicing proteins confers salt tolerance to yeast and transgenic plants. The Plant Journal, 30(5), 511-519. doi:10.1046/j.1365-313x.2002.01311.x | es_ES |
dc.description.references | Hunt, P. W., Watts, R. A., Trevaskis, B., Llewelyn, D. J., Burnell, J., Dennis, E. S., & Peacock, W. J. (2001). Plant Molecular Biology, 47(5), 677-692. doi:10.1023/a:1012440926982 | es_ES |
dc.description.references | Dohm, J. C., Minoche, A. E., Holtgräwe, D., Capella-Gutiérrez, S., Zakrzewski, F., Tafer, H., … Himmelbauer, H. (2013). The genome of the recently domesticated crop plant sugar beet (Beta vulgaris). Nature, 505(7484), 546-549. doi:10.1038/nature12817 | es_ES |
dc.description.references | Hebelstrup, K. H., Igamberdiev, A. U., & Hill, R. D. (2007). Metabolic effects of hemoglobin gene expression in plants. Gene, 398(1-2), 86-93. doi:10.1016/j.gene.2007.01.039 | es_ES |
dc.description.references | Hargrove, M. S., Brucker, E. A., Stec, B., Sarath, G., Arredondo-Peter, R., Klucas, R. V., … Phillips, G. N. (2000). Crystal structure of a nonsymbiotic plant hemoglobin. Structure, 8(9), 1005-1014. doi:10.1016/s0969-2126(00)00194-5 | es_ES |
dc.description.references | Leiva-Eriksson, N., Pin, P. A., Kraft, T., Dohm, J. C., Minoche, A. E., Himmelbauer, H., & Bülow, L. (2014). Differential Expression Patterns of Non-Symbiotic Hemoglobins in Sugar Beet (Beta vulgaris ssp. vulgaris). Plant and Cell Physiology, 55(4), 834-844. doi:10.1093/pcp/pcu027 | es_ES |
dc.description.references | NARANJO, M. A., FORMENT, J., ROLDAN, M., SERRANO, R., & VICENTE, O. (2006). Overexpression of Arabidopsis thaliana LTL1, a salt-induced gene encoding a GDSL-motif lipase, increases salt tolerance in yeast and transgenic plants. Plant, Cell and Environment, 29(10), 1890-1900. doi:10.1111/j.1365-3040.2006.01565.x | es_ES |
dc.description.references | Rausell, A., Kanhonou, R., Yenush, L., Serrano, R., & Ros, R. (2003). The translation initiation factor eIF1A is an important determinant in the tolerance to NaCl stress in yeast and plants. The Plant Journal, 34(3), 257-267. doi:10.1046/j.1365-313x.2003.01719.x | es_ES |
dc.description.references | Rus, A. M., Estañ, M. T., Gisbert, C., Garcia-Sogo, B., Serrano, R., Caro, M., … Bolarín, M. C. (2001). Expressing the yeast HAL1 gene in tomato increases fruit yield and enhances K+ /Na+ selectivity under salt stress. Plant, Cell & Environment, 24(8), 875-880. doi:10.1046/j.1365-3040.2001.00719.x | es_ES |
dc.description.references | Hoogewijs, D., Dewilde, S., Vierstraete, A., Moens, L., & Vinogradov, S. N. (2012). A Phylogenetic Analysis of the Globins in Fungi. PLoS ONE, 7(2), e31856. doi:10.1371/journal.pone.0031856 | es_ES |
dc.description.references | Bai, X., Long, J., He, X., Yan, J., Chen, X., Tan, Y., … Xu, H. (2016). Overexpression of spinach non-symbiotic hemoglobin in Arabidopsis resulted in decreased NO content and lowered nitrate and other abiotic stresses tolerance. Scientific Reports, 6(1). doi:10.1038/srep26400 | es_ES |
dc.description.references | Evangelou, E., Tsadilas, C., Tserlikakis, N., Tsitouras, A., & Kyritsis, A. (2016). Water Footprint of Industrial Tomato Cultivations in the Pinios River Basin: Soil Properties Interactions. Water, 8(11), 515. doi:10.3390/w8110515 | es_ES |
dc.description.references | (2012). The tomato genome sequence provides insights into fleshy fruit evolution. Nature, 485(7400), 635-641. doi:10.1038/nature11119 | es_ES |
dc.description.references | Chen, Y., & Barak, P. (1982). Iron Nutrition of Plants in Calcareous Soils. Advances in Agronomy Volume 35, 217-240. doi:10.1016/s0065-2113(08)60326-0 | es_ES |
dc.description.references | Dutt, M., Dhekney, S. A., Soriano, L., Kandel, R., & Grosser, J. W. (2014). Temporal and spatial control of gene expression in horticultural crops. Horticulture Research, 1(1). doi:10.1038/hortres.2014.47 | es_ES |
dc.subject.ods | 08.- Fomentar el crecimiento económico sostenido, inclusivo y sostenible, el empleo pleno y productivo, y el trabajo decente para todos | es_ES |
dc.subject.ods | 06.- Garantizar la disponibilidad y la gestión sostenible del agua y el saneamiento para todos | es_ES |
dc.subject.ods | 03.- Garantizar una vida saludable y promover el bienestar para todos y todas en todas las edades | es_ES |
dc.subject.ods | 02.- Poner fin al hambre, conseguir la seguridad alimentaria y una mejor nutrición, y promover la agricultura sostenible | es_ES |
dc.subject.ods | 15.- Proteger, restaurar y promover la utilización sostenible de los ecosistemas terrestres, gestionar de manera sostenible los bosques, combatir la desertificación y detener y revertir la degradación de la tierra, y frenar la pérdida de diversidad biológica | es_ES |
dc.subject.ods | 13.- Tomar medidas urgentes para combatir el cambio climático y sus efectos | es_ES |
dc.subject.ods | 01.- Erradicar la pobreza en todas sus formas en todo el mundo | es_ES |
dc.subject.ods | 12.- Garantizar las pautas de consumo y de producción sostenibles | es_ES |