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dc.contributor.author
Saigo, Mariana  
dc.contributor.author
Alvarez, Clarisa Ester  
dc.contributor.author
Andreo, Carlos Santiago  
dc.contributor.author
Drincovich, Maria Fabiana  
dc.date.available
2016-01-07T19:05:18Z  
dc.date.issued
2013-02  
dc.identifier.citation
Saigo, Mariana; Alvarez, Clarisa Ester; Andreo, Carlos Santiago; Drincovich, Maria Fabiana; Plastidial NADP-Malic Enzymes from grasses: unravelling the way to the C4 specific isoforms; Elsevier France-editions Scientifiques Medicales Elsevier; Plant Physiology And Biochemistry; 63; 2-2013; 39-48  
dc.identifier.issn
0981-9428  
dc.identifier.uri
http://hdl.handle.net/11336/3418  
dc.description.abstract
Malic enzyme is present in many plant cell compartments such as plastids, cytosol and mitochondria. Particularly relevant is the plastidial isoform that participates in the C4 cycle providing CO2 to RuBisCO in C4 species. This type of photosynthesis is more frequent among grasses where anatomical preconditioning would have facilitated the evolution of the C4 syndrome. In maize (C4 grass), the photosynthetic NADP dependent Malic enzyme (ZmC4-NADP-ME, L-malate:NADP oxidoreductase, E.C. 1.1.1.40) and the closest related non-photosynthetic isoform (ZmnonC4-NADPME, L-malate:NADP oxidoreductase, E.C. 1.1.1.40) are both plastidial but differ in expression pattern,kinetics and structure. Features like high catalytic efficiency, inhibition by high malate concentration at pH 7.0, redox modulation and tetramerization are characteristic of the photosynthetic NADP-ME. In this work, the proteins encoded by sorghum (C4 grass) and rice (C3 grass) NADP-ME genes,orthologues of the plastidial NADP-MEs from maize, were recombinantly expressed, purified and characterized. In a global comparison, we could identify a small group of residues which may explain the special features of C4 enzymes. Overall, the present work presents biochemical and molecular data that helps to elucidate the changes that took place in the evolution of C4 NADP-ME in grasses.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier France-editions Scientifiques Medicales Elsevier  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/  
dc.subject
C4 Photosynthesis  
dc.subject
Nadp-Malic Enzyme  
dc.subject
Structure And Function Relasionship  
dc.subject
Maize Sorghum Rice  
dc.subject.classification
Bioquímica y Biología Molecular  
dc.subject.classification
Ciencias Biológicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Plastidial NADP-Malic Enzymes from grasses: unravelling the way to the C4 specific isoforms  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2016-03-30 10:35:44.97925-03  
dc.journal.volume
63  
dc.journal.pagination
39-48  
dc.journal.pais
Francia  
dc.journal.ciudad
Paris  
dc.description.fil
Fil: Saigo, Mariana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Centro de Estudios Fotosintéticos y Bioquímicos (i); Argentina. Universidad Nacional de Rosario; Argentina  
dc.description.fil
Fil: Alvarez, Clarisa Ester. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Centro de Estudios Fotosintéticos y Bioquímicos (i); Argentina. Universidad Nacional de Rosario; Argentina  
dc.description.fil
Fil: Andreo, Carlos Santiago. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Centro de Estudios Fotosintéticos y Bioquímicos (i); Argentina. Universidad Nacional de Rosario; Argentina  
dc.description.fil
Fil: Drincovich, Maria Fabiana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Centro de Estudios Fotosintéticos y Bioquímicos (i); Argentina. Universidad Nacional de Rosario; Argentina  
dc.journal.title
Plant Physiology And Biochemistry  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.plaphy.2012.11.009  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.plaphy.2012.11.009