Assessment of in vitro growth of apical stem sections and adventitious organogenesis to evaluate salinity tolerance in cultivated tomato

dc.centroFacultad de Cienciases_ES
dc.contributor.authorMercado-Carmona, José Ángel
dc.contributor.authorSancho-Carrascosa, María A.
dc.contributor.authorJiménez-Bermúdez, Silvia
dc.contributor.authorPerán-Quesada, Rosa Amelia
dc.contributor.authorPliego-Alfaro, Fernando
dc.contributor.authorQuesada-Felice, Miguel Ángel
dc.date.accessioned2025-01-29T18:51:43Z
dc.date.available2025-01-29T18:51:43Z
dc.date.created2025
dc.date.issued2000-08-22
dc.departamentoBotánica y Fisiología Vegetal
dc.descriptionSegún se especifica en la web de la editorial Springer Nature : https://www.springer.com/gp/editorial-policies/preprint-sharing. Springer Nature journals encourage posting of preprints of primary research manuscripts on preprint servers of the authors’ choice, authors’ or institutional websites, and open communications between researchers whether on community preprint servers or preprint commenting platforms.es_ES
dc.description.abstractThe possible use of in vitro shoot morphogenesis and shoot apex culture to evaluate salt tolerance in cultivated tomato (Lycopersicon esculentum Mill.) has been analyzed, using two cultivars with similar salt tolerance, Pera and Hellfrucht frühstamm (HF). The effect of salt on shoot regeneration was studied by culturing leaf explants on media supplemented with 0, 43, 86, 129 and 172 mM NaCl. The presence of NaCl in the regeneration media at 86 mM strongly inhibited shoot regeneration in the cultivar HF, but not in Pera. However, the substitution of NaCl by mannitol, maintaining the same water potential in the culture media, decreased the regeneration percentage in Pera but did not affect HF. Shoot apices of both cultivars were also subcultured at 6-week intervals, for 4 subcultures, at the same NaCl concentrations as used in the previous experiment, and the shoot growth, leaf and root number, rooted shoot and shoot necrosis were recorded at the end of each subculture. Root formation was the parameter most affected by salt in both cultivars, Pera being more sensitive than HF. The substitution of NaCl by mannitol significantly increased the percentage of rooted shoots in Pera after four subcultures, and slightly decreased this percentage in HF. Shoot necrosis was only observed in the last subculture at NaCl higher than 86 mM, the percentage of necrotic shoots being higher in Pera than in HF (75% and 45%, respectively). The lack of agreement between the results obtained with the in vitro tests, e.g., adventitious shoot formation and growth of apical stem sections, suggests that this approach may not be a reliable tool to evaluate salt tolerance in cultivated tomato.es_ES
dc.identifier.citationMercado, J.A., Sancho-Carrascosa, M.A., Jiménez-Bermúdez, S. et al. Assessment of in vitro growth of apical stem sections and adventitious organogenesis to evaluate salinity tolerance in cultivated tomato. Plant Cell, Tissue and Organ Culture 62, 101–106 (2000). https://doi.org/10.1023/A:1026503603399es_ES
dc.identifier.doi10.1023/A:1026503603399
dc.identifier.urihttps://hdl.handle.net/10630/37333
dc.language.isoenges_ES
dc.publisherSpringer Naturees_ES
dc.rightsAtribución-NoComercial-CompartirIgual 4.0 Internacional*
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.subjectTomateses_ES
dc.subject.otheradventitious organ formationes_ES
dc.subject.otherin vitro culturees_ES
dc.subject.otherLycopersicon esculentumes_ES
dc.subject.othermannitoles_ES
dc.subject.othersodium chloridees_ES
dc.titleAssessment of in vitro growth of apical stem sections and adventitious organogenesis to evaluate salinity tolerance in cultivated tomatoes_ES
dc.title.alternativeEvaluación del crecimiento in vitro de ápices caulinares y de la organogénesis adventicia para determinar la tolerancia a la salinidad en plantas de tomate cultivadoes_ES
dc.typejournal articlees_ES
dc.type.hasVersionSMURes_ES
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscoverya17cd143-3a4b-4846-9f11-7f5cf2e9391b

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