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dc.contributorEscuela de Ingeniería Agraria y Forestales_ES
dc.contributor.authorGarcía Ulloa, Alba
dc.contributor.authorSanjurjo, Laura
dc.contributor.authorCimini, Sara
dc.contributor.authorEncina García, Antonio Esteban 
dc.contributor.authorMartínez Rubio, Romina
dc.contributor.authorBouza, Rebeca
dc.contributor.authorBarral, Luis
dc.contributor.authorEstévez Pérez, Graciela
dc.contributor.authorNovo Uzal
dc.contributor.authorGara de, Laura
dc.contributor.authorPomar, Federico
dc.contributor.otherFisiologia Vegetales_ES
dc.date2020
dc.date.accessioned2024-06-05T10:58:10Z
dc.date.available2024-06-05T10:58:10Z
dc.identifier.citationGarcía-Ulloa, A., Sanjurjo, L., Cimini, S., Encina, A., Martínez-Rubio, R., Bouza, R., Barral, L., Estévez-Pérez, G., Novo-Uzal, E., De Gara, L., & Pomar, F. (2020). Overexpression of ZePrx in Nicotiana tabacum Affects Lignin Biosynthesis Without Altering Redox Homeostasis. Frontiers in Plant Science, 11. https://doi.org/10.3389/FPLS.2020.00900es_ES
dc.identifier.urihttps://hdl.handle.net/10612/21195
dc.description.abstract[EN] Class III plant peroxidases (Prxs) are involved in the oxidative polymerization of lignins. Zinnia elegans Jacq. Basic peroxidase (ZePrx) has been previously characterized as capable of catalyzing this reaction in vitro and the role in lignin biosynthesis of several of its Arabidopsis thaliana homologous has been previously confirmed. In the present work, ZePrx was overexpressed in Nicotiana tabacum to further characterize its function in planta with particular attention to its involvement in lignin biosynthesis. Since Prxs are known to alter ROS levels by using them as electron acceptor or producing them in their catalytic activity, the impact of this overexpression in redox homeostasis was studied by analyzing the metabolites and enzymes of the ascorbate-glutathione cycle. In relation to the modification induced by ZePrx overexpression in lignin composition and cellular metabolism, the carbohydrate composition of the cell wall as well as overall gene expression through RNA-Seq were analyzed. The obtained results indicate that the overexpression of ZePrx caused an increase in syringyl lignin in cell wall stems, suggesting that ZePrx is relevant for the oxidation of sinapyl alcohol during lignin biosynthesis, coherently with its S-peroxidase nature. The increase in the glucose content of the cell wall and the reduction of the expression of several genes involved in secondary cell wall biosynthesis suggests the occurrence of a possible compensatory response to maintain cell wall properties. The perturbation of cellular redox homeostasis occurring as a consequence of ZePrx overexpression was kept under control by an increase in APX activity and a reduction in ascorbate redox state. In conclusion, our results confirm the role of ZePrx in lignin biosynthesis and highlight that its activity alters cellular pathways putatively aimed at maintaining redox homeostasis.es_ES
dc.languageenges_ES
dc.publisherFrontiers Mediaes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectIngeniería agrícolaes_ES
dc.subject.otherClass Iii Peroxidaseses_ES
dc.subject.otherLigninses_ES
dc.subject.otherSyringyles_ES
dc.subject.otherSecondary Cell Walles_ES
dc.subject.otherRedox Homeostasises_ES
dc.subject.otherRna-seqes_ES
dc.titleOverexpression of ZePrx in Nicotiana tabacum Affects Lignin Biosynthesis Without Altering Redox Homeostasises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doi10.3389/FPLS.2020.00900
dc.description.peerreviewedSIes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MECD/ Programa Estatal de Promoción del Talento y su Empleabilidad/ FPU13/04835/ESes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn1664-462X
dc.journal.titleFrontiers in Plant Sciencees_ES
dc.volume.number11es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.unesco2417.19 Fisiología Vegetales_ES
dc.description.projectXunta de Galicia (Spain) (ED431C 2018/57)es_ES


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