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1.
Plant Cell Environ ; 43(6): 1376-1393, 2020 06.
Artículo en Inglés | MEDLINE | ID: mdl-32012308

RESUMEN

The species Deschampsia antarctica (DA) is one of the only two native vascular species that live in Antarctica. We performed ecophysiological, biochemical, and metabolomic studies to investigate the responses of DA to low temperature. In parallel, we assessed the responses in a non-Antarctic reference species (Triticum aestivum [TA]) from the same family (Poaceae). At low temperature (4°C), both species showed lower photosynthetic rates (reductions were 70% and 80% for DA and TA, respectively) and symptoms of oxidative stress but opposite responses of antioxidant enzymes (peroxidases and catalase). We employed fused least absolute shrinkage and selection operator statistical modelling to associate the species-dependent physiological and antioxidant responses to primary metabolism. Model results for DA indicated associations with osmoprotection, cell wall remodelling, membrane stabilization, and antioxidant secondary metabolism (synthesis of flavonols and phenylpropanoids), coordinated with nutrient mobilization from source to sink tissues (confirmed by elemental analysis), which were not observed in TA. The metabolic behaviour of DA, with significant changes in particular metabolites, was compared with a newly compiled multispecies dataset showing a general accumulation of metabolites in response to low temperatures. Altogether, the responses displayed by DA suggest a compromise between catabolism and maintenance of leaf functionality.


Asunto(s)
Adaptación Fisiológica , Frío , Nitrógeno/metabolismo , Fósforo/metabolismo , Poaceae/metabolismo , Regiones Antárticas , Antioxidantes/metabolismo , Ascorbato Peroxidasas/metabolismo , Carbono/metabolismo , Catalasa/metabolismo , Respiración de la Célula , Pared Celular/metabolismo , Glutatión/metabolismo , Metabolómica , Oxidación-Reducción , Fotosíntesis , Solubilidad , Especificidad de la Especie , Azufre/metabolismo
2.
Plant Cell Physiol ; 57(10): 2232-2243, 2016 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-27638927

RESUMEN

Acclimation to low CO2 conditions in cyanobacteria involves the co-ordinated regulation of genes mainly encoding components of the carbon-concentrating mechanism (CCM). Making use of several independent microarray data sets, a core set of CO2-regulated genes was defined for the model strain Synechocystis sp. PCC 6803. On the transcriptional level, the CCM is mainly regulated by the well-characterized transcriptional regulators NdhR (= CcmR) and CmpR. However, the role of an additional regulatory protein, namely cyAbrB2 belonging to the widely distributed AbrB regulator family that was originally characterized in the genus Bacillus, is less defined. Here we present results of transcriptomic and metabolic profiling of the wild type and a ΔcyabrB2 mutant of Synechocystis sp. PCC 6803 after shifts from high CO2 (5% in air, HC) to low CO2 (0.04%, LC). Evaluation of the transcriptomic data revealed that cyAbrB2 is involved in the regulation of several CCM-related genes such as sbtA/B, ndhF3/ndhD3/cupA and cmpABCD under LC conditions, but apparently acts supplementary to NdhR and CmpR. Under HC conditions, cyAbrB2 deletion affects the transcript abundance of PSII subunits, light-harvesting components and Calvin-Benson-Bassham cycle enzymes. These changes are also reflected by down-regulation of primary metabolite pools. The data suggest a role for cyAbrB2 in adjusting primary carbon and nitrogen metabolism to photosynthetic activity under fluctuating environmental conditions. The findings were integrated into the current knowledge about the acquisition of inorganic carbon (Ci), the CCM and parts of its regulation on the transcriptional level.


Asunto(s)
Aclimatación/efectos de los fármacos , Proteínas Bacterianas/metabolismo , Dióxido de Carbono/farmacología , Regulación Bacteriana de la Expresión Génica/efectos de los fármacos , Synechocystis/fisiología , Transcripción Genética/efectos de los fármacos , Proteínas Bacterianas/genética , Regulación hacia Abajo/efectos de los fármacos , Regulación hacia Abajo/genética , Genes Bacterianos , Compuestos Inorgánicos/farmacología , Metaboloma/efectos de los fármacos , Metaboloma/genética , Mutación/genética , Sistemas de Lectura Abierta/genética , Complejo de Proteína del Fotosistema II/metabolismo , Synechocystis/efectos de los fármacos , Synechocystis/genética , Regulación hacia Arriba/efectos de los fármacos , Regulación hacia Arriba/genética
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