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Resumen
Limitations in our understanding about the mechanisms that underlie source-sink assimilate partitioning are increasingly becoming a major hurdle for crop yield enhancement via metabolic engineering. By means of a comprehensive approach, this work reports the functional characterization of a DnaJ chaperone related-protein (named as SPA; sugar partition-affecting) that is involved in assimilate partitioning in tomato plants. SPA protein was found to be [ver mas...]
dc.contributor.authorBermudez Salazar, Luisa
dc.contributor.authorde Godoy, Fabiana
dc.contributor.authorBaldet, Pierre
dc.contributor.authorDemarco, Diego
dc.contributor.authorOsorio, Sonia
dc.contributor.authorQuadrana, Leandro Daniel
dc.contributor.authorAlmeida de Souza, Juliana Beatriz
dc.contributor.authorAsis, Ramón
dc.contributor.authorGibon, Yves
dc.contributor.authorFernie, Alisdair R.
dc.contributor.authorRossi, Maria Magdalena
dc.contributor.authorCarrari, Fernando
dc.date.accessioned2019-03-26T18:31:28Z
dc.date.available2019-03-26T18:31:28Z
dc.date.issued2014-03
dc.identifier.issn1365-313X
dc.identifier.otherhttps://doi.org/10.1111/tpj.12418
dc.identifier.urihttp://hdl.handle.net/20.500.12123/4750
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/full/10.1111/tpj.12418
dc.description.abstractLimitations in our understanding about the mechanisms that underlie source-sink assimilate partitioning are increasingly becoming a major hurdle for crop yield enhancement via metabolic engineering. By means of a comprehensive approach, this work reports the functional characterization of a DnaJ chaperone related-protein (named as SPA; sugar partition-affecting) that is involved in assimilate partitioning in tomato plants. SPA protein was found to be targeted to the chloroplast thylakoid membranes. SPA-RNAi tomato plants produced more and heavier fruits compared with controls, thus resulting in a considerable increment in harvest index. The transgenic plants also displayed increased pigment levels and reduced sucrose, glucose and fructose contents in leaves. Detailed metabolic and enzymatic activities analyses showed that sugar phosphate intermediates were increased while the activity of phosphoglucomutase, sugar kinases and invertases was reduced in the photosynthetic organs of the silenced plants. These changes would be anticipated to promote carbon export from foliar tissues. The combined results suggested that the tomato SPA protein plays an important role in plastid metabolism and mediates the source-sink relationships by affecting the rate of carbon translocation to fruits.es_AR
dc.formatapplication/pdfeng
dc.language.isoeng
dc.publisherWiley; Society for Experimental Biologyeng
dc.rightsinfo:eu-repo/semantics/restrictedAccesseng
dc.sourcePlant journal 77 (5) : 676-687. (March 2014)eng
dc.subjectTomatees_AR
dc.subjectTomatoeseng
dc.subjectSolanum Lycopersicumes_AR
dc.subjectAzúcares_AR
dc.subjectSugareng
dc.subjectMetabolismoes_AR
dc.subjectMetabolismeng
dc.subjectChloroplastseng
dc.subjectCloroplastoes_AR
dc.subject.otherSmall Plastidial Proteineng
dc.subject.otherSource-sink Partitioningeng
dc.titleSilencing of the tomato Sugar Partitioning Affecting protein (SPA) modifies sink strength through a shift in leaf sugar metabolismeng
dc.typeinfo:ar-repo/semantics/artículoes_AR
dc.typeinfo:eu-repo/semantics/articleeng
dc.typeinfo:eu-repo/semantics/publishedVersioneng
dc.description.origenInstituto de Biotecnologíaes_AR
dc.description.filFil: Bermudez Salazar, Luisa. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Biotecnología; Argentina. Universidade de São Paulo. Departamento de Botânica, Instituto de Biociências; Brasiles_AR
dc.description.filFil: de Godoy, Fabiana. Universidade de São Paulo. Departamento de Botânica, Instituto de Biociências; Brasiles_AR
dc.description.filFil: Baldet, Pierre. Universite de Bordeaux; Francia. Institut National de la Recherche Agronomique. Fruit Biology and Pathology Unit; Franciaes_AR
dc.description.filFil: Demarco, Diego. Universidade de São Paulo. Departamento de Botânica, Instituto de Biociências; Brasiles_AR
dc.description.filFil: Osorio, Sonia. Max Planck Institute of Molecular Plant Physiology; Alemaniaes_AR
dc.description.filFil: Quadrana, Leandro Daniel. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Biotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentinaes_AR
dc.description.filFil: Almeida de Souza, Juliana Beatriz. Universidade de São Paulo. Departamento de Botânica, Instituto de Biociências; Brasiles_AR
dc.description.filFil: Asis, Ramón. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentinaes_AR
dc.description.filFil: Gibon, Yves. Universite de Bordeaux; Francia. Institut National de la Recherche Agronomique. Fruit Biology and Pathology Unit; Franciaes_AR
dc.description.filFil: Fernie, Alisdair R. Max-Planck-Institute of Molecular Plant Physiology; Alemania. Center of Plant System Biology and Biotechnology; Bulgariaes_AR
dc.description.filFil: Rossi, Maria Magdalena. Universidade de São Paulo. Departamento de Botânica, Instituto de Biociências; Brasiles_AR
dc.description.filFil: Carrari, Fernando. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Biotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentinaes_AR
dc.subtypecientifico


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