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GIBERELINAS FUNCIONES PDF

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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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Chloroplasts affect the leaf response to cytokinin. Journal of Experimental Botany 59, Resultados similares se encontraron en soya Glycine max en lo que se refiere a los tratamientos con AG 3pero el efecto de las citoquininas en esta especie es distinto.

Photos were taken 10 days after infection.

Reactive oxygen species in plant cell death. The experiment followed a completely randomized design with seven treatments consisting in 5, giberellnas and 15 mg L -1 solutions of both gibberellic acid GA3 and 6-benzylaminopurine 6BAPplus a hormone-free control.

Disease resistance against Pseudomonas syringae pv. Gibberellic acid influence on vegetative growth, nodulation and yield of cowpea Vigna unguiculata L. Las soluciones se realizaron en agua destilada y desionizada con el fin de garantizar la pureza de la mezcla. Trends in Plant Science The next question is obvious, which ROS is the most suitable to be messenger?

Transgenic lines overexpressing both cytsod and cytapx lines 35 and 39can cope with ROS accumulation and avoid tissue necrotization. They also establish a link to the adaptation of immune system through white blood cells recruitment. Mutual interaction of auxin and cytokinins in regulating correlative dominance. The observed resistance of transgenic lines to bacterial wild fire seemed to be independent of tissue necrosis, as observed in other plant-pathogens interactions Kiraly et al.

Even a decrease in DHA in relation to control plants occurred, and accordingly, an increase in the redox state of ascorbate Table 1. A synergistic effect on lipid peroxidation was observed in salt-treated plantlets grown in the presence of MGBG Fig.

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Transport of exogenous auxin in twobranched dwarf pea seedlings Pisum sativum L. At 6 dpi, the necrotic areas extended to the border of the leaves and finally the necrotic area appeared surrounded by a chlorotic yellow area.

Plant Physiology The indirect role of 2,4-D in the maintenance of apical dominance in decapitated sunflower seedlings Helianthus annuus L. The assembly of the CAAT-box binding complex at a photosynthesis gene promoter is regulated by light, cytokinin, and the stage of the plastids.

Reproducido de Venkatesh y Park Plants have an enormous variety of defense mechanisms, including enzymatic and funcionds defense mechanisms, in order to giberrlinas with the over-production of ROS. Lamb C, Dixon RA, Some foods rich in beta-carotene are carrot, red paprika, tomato, pumpkin, sweet potatoes, peach, apricots, melon, mango and papaya. The effect of over-expression of cytosolic Cu,Zn-superoxide dismutase cyt sod and ascorbate peroxidase cyt apx alone, or in combination, in tobacco plants, increased the resistance to bacterial wild fire, caused by Pseudomonas syringae pv.

In contrast to vitamin C, we can produce our own GSH, as long as we have the amino acids which compose it: Las dosis menores no fueron efectivas Sansberro et al. Singlet oxygen 1O2 is formed by transferring energy from excited chlorophyll to oxygen in chloroplasts.

Influence of seed treatment with 2-chloroethylphosphonic acid, gibberellic acid, ascorbic acid, and simazine on growth and nutrient composition of pea Pisum sativum L.

Therefore, the function of ROS in metabolism is dual; they are toxic for cells when they accumulate in excess, but at low levels it has been proved that they can function as bio-signalling molecules. Biochem Soc Trans Noctor G, Foyer CH.

Functional Plant Biology Effect of cytokinin on the physiological activity of chloroplasts. For this reason, the present work takes on the massive production of high yielding scions, which, notwithstanding, have shown grafting problems, specifically regarding bud initiation and further growth.

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Correlative inhibition of lateral bud growth in Phaseolus vulgaris L. Miller G et al. Therefore, the oxidative stress should not necessarily be viewed as a harmful event needed to be avoided or alleviated, but could also be viewed as a perquisite for the plant to adequately respond and induce proper acclimation mechanisms.

El radical O 2.

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Salinity induced a water deficit as well as an ionic toxicity in the plants resulting in an alteration in the ionic homeostasis. Efecto de cuatro fitoreguladores comerciales en el desarrollo y rendimiento del girasol. Por lo anterior, las auxinas en el tallo pueden influir en el crecimiento de las yemas, a una determinada distancia Bennett et al.

Salt treatment affected the PA contents in grapevine plantlets, especially the free and conjugate forms of agmatine Agm and Put. Sinauer Associates, Sunderland, MA.

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Nowadays, we know that damages produced in plants under stress conditions are mediated, partly, by an increased production of ROS at subcellular level. Gene expression in cytokinin – and light-mediated plastogenesis of Cucurbita cotyledons: Si el ciclo no fuese activo, tanto O 2. Changes in the branching pattern of Pinus radiata derived from grafting are supported by variations in the hormonal content. Nataima, Corpoica, El Espinal, Colombia.

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. Regarding scion number of leaves, foliar area and fresh and dry mass, the highest counts were reached due to the GA 3 treatments.