to inhibitorio de ABA también es contrarrestado por giberelinas. Latencia de .. Se han descrito varias funciones biológicas de las poliaminas, entre ellas. parte giberelinas (gas). parte descubrimiento de las giberelinas. el También puede variar la citada estructura en función de la posición del grupo hidroxilo. GIBERELINAS Y CITOQUININAS. LUGAR DE BIOSÍNTESIS DE LA CITOQUININA. FUNCIONES.
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But as we have already mentioned, https: A synergistic effect on lipid peroxidation was observed in salt-treated plantlets grown in the presence of MGBG Fig.
Gene expression in cytokinin – and light-mediated plastogenesis of Cucurbita cotyledons: All this is associated with some pathology in human beings as cancer, cardiovascular diseases, Alzheimer, Parkinson, sclerosis, among others. Free Radical Research 36, Growth and development of the finciones mutants of Arabidopsis. Nowadays, we know that damages produced in plants under stress conditions are mediated, partly, by an increased production of ROS at subcellular level.
Reproducido de Taiz y Zieger Bolwell GP, Wojtaszek P, Down-regulation of antioxidative capacity in a transgenic tobacco which fails to develop acquired resistance to necrotization caused by TMV. Salt treatment affected the PA contents in grapevine plantlets, especially the free and conjugate forms of agmatine Agm and Put. Salt stress produced an alteration in the fluorescence chlorophyll parameters in grapevine leaves. Physiologia Plantarum Plant Cell 15, Immune system also uses the toxic effects of ROS making them the central part of its mechanism to kill pathogens.
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Barba-Espin G et al. For more information, please consult: Physiological and Molecular Plant Pathology 51, Both in our giberelinax and in plants, when the generation of ROS overcomes antioxidant defence mechanism, an oxidative stress occurs at cell level which can lead to cell death. In summarized form, we can say that the superoxide radical O2.
It is one of the main biological defenders of membranes. Las citoquininas inician el crecimiento de las yemas laterales Taiz y Zeiger, The Plant Cell These authors suggested that the induction of antioxidant enzymes might reduce plant cell necrosis after infection Kiraly et al. Reevaluating concepts of apical dominance and the control of axillary branching. Reactive oxygen species in plant cell death.
The Arabidopsis MAX pathway controls shoot branching by regulating auxin transport.
Distinct isoprenoid origins of cis- and trans-zeatin biosyntheses in Arabidopsis. Plant Cell 2, We studied the effect of salt stress in the presence and the absence of MGBG, an inhibitor of S-adenosylmethionine decarboxylase SAMDC activity, involved in PA biosynthesis, in order to investigate the effects of both treatments on photosynthesis and oxidative metabolism providing new information about the contribution of PA metabolism to salt stress adaptation in grapevine plantlets.
OH could be formed by the reaction of O2. Most of the cacao plantations of Colombia are certainly old and need to be renewed due to low yield.
At the end of the experiment, which took a total of 30 days, scion fresh and dry mass were also determined. In the non-transformed controls, the inoculated areas with P. A role for cytokinins in de-etiolation in Arabidopsis. Reguladores del crecimiento para su uso en viveros.
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Chloroplasts affect the leaf response to cytokinin. These results suggest that maintaining polyamine biosynthesis through the enhanced SAMDC activity in grapevine leaf tissues under salt stress conditions could contribute to the enhanced ROS scavenging activity and a protection of photosynthetic apparatus from oxidative damages.
Systemic cell death is elicited by the interaction of a single gene in Nicotiana and gene VI from cauliflower mosaic virus.