Efectos de la aplicación de fertilizantes de nueva generación en la dehesa toledana: producción, diversidad y composición florística de pastos herbáceos

Fertilization can be an interesting treatment to improve the different productions of the dehesa and to improve tree vigor. In order to evaluate the effect of different fertilizers of new generation on herbaceous pasture diversity and species composition, in this work we analyzed the effect of three treatments: control (natural pastures), fertization with 36 UF of P2O5 of a complex NPK and low content of N, and natural phosphates. Fertilization was applied in autumn of 2009, 2010 and 2011 and we analized herbaceous pastures composition and yield in springs of 2010, 2011 and 2012 (one control per year). The best results of production were obtained with the NPK application; also, pasture specific richness and diversity improved with the fertilization in years of average regime of precipitation.

Eliminación de nutrientes mediante el empleo de cultivos hidropónicos

La presente investigación se presenta como una alternativa para la reducción de la contaminación por nutrientes que produce el vertido de aguas residuales provenientes de núcleos urbanos que acaban en lagos, lagunas o embalses acelerando los procesos de eutrofización de los mismos. El objetivo de esta tesis es analizar la reducción de nutrientes, fundamentalmente nitrógeno, fósforo y potasio, del agua residual doméstica sometida a tratamiento a través de cultivos hidropónicos en un determinado periodo de tiempo, observando a su vez la evolución del cultivo seleccionado. El sistema se diseñó para funcionar en circuito cerrado con el agua residual circulando por entre las raíces de los vegetales estudiados. El cultivo seleccionado fue el “kenaf”, aunque después de mucho tiempo dedicado a la obtención de semillas de “kenaf “por diferentes proveedores, se decidió comenzar un primer ensayo utilizando plantas de aloe vera durante un periodo de un mes de verano. Se procedió a la colocación de plantas en un tubo conteniendo agua residual de una fosa séptica domiciliaria. La reducción de la DBO5 y la DQO fue notable aunque los resultados de la variación de nitratos y fosfatos no fueron concluyentes. Las altas temperaturas alcanzada en esas fechas por el agua circulante, finalmente imposibilitó la continuación del ensayo. Si bien esta primera puesta en marcha no resultó como se esperaba, aportó numerosa información para modificar el planteo del estudio, la forma de llevarlo a cabo y la puesta a punto de la propia instalación. El segundo ensayo se llevó a cabo en otoño con plantas de kenaf obtenidas del ensayo previo en suelo en una parcela piloto en los llanos de Villamartín, en la provincia de Cádiz. Antes de incorporar el agua al sistema hidropónico se analizaron todos los parámetros requeridos por la normativa española del agua para determinar su clasificación como agua residual doméstica. Luego se le dio seguimiento a la variación de los nutrientes, nitrógeno, fósforo y potasio a lo largo de varias semanas para evaluar la efectividad del tratamiento. Las plantas de kenaf continuaron su desarrollo utilizando las sustancias disueltas en el agua residual como única fuente de nutrientes disponible. This research is presented as an alternative to reduce the pollution that wastewater discharges from towns generate when they end in lakes, ponds and reservoirs, by accelerating the eutrophication processes. The objective of this thesis is to analyze the reduction of nutrients, mainly nitrogen, phosphorus and potassium, of domestic wastewater treated through hydroponics crops in a given period of time, noting at the same time the evolution of the selected crop. The system was designed to operate in closed circuit with the wastewater circulating through the roots of the studied plants. The selected crop was "kenaf", although after much time spent in obtaining seeds of "kenaf"by different vendors and the impossibility of achieving its germination; it was decided to start a first test using Aloe Vera plants for a period of one month in the summer. The plants were introduced in the holes of a tube containing septic wastewater. The BOD5 and COD reduction was remarkable though the results of the variation in nitrates and phosphates were inconclusive. High temperatures achieved in those dates by circulating water, eventually precluded the continuation of the test. Although this first implementation was not running as expected, it provided information to modify the proposal of the study, the way to carry it out and the development of the installation itself. The second test was conducted in autumn with kenaf plants obtained from the previous test in a pilot plant in the flatness of Villamartín, province of Cádiz. Before adding the water to the hydroponic system all the parameters required by the Spanish water regulations were analyzed to determine their classification as domestic waste water. Then, the variation of nutrients, nitrogen, phosphorus and potassium was tracking over several weeks to evaluate the effectiveness of the treatment. Kenaf plants continued its development using the substances dissolved in wastewater as sole source of nutrients available.

Overexpression of human copper,zinc-superoxide dismutase (SOD1) prevents postischemic injury

Superoxide and superoxide-derived oxidants have been hypothesized to be important mediators of postischemic injury. Whereas copper,zinc-superoxide dismutase, SOD1, efficiently dismutates superoxide, there has been controversy regarding whether increasing intracellular SOD1 expression would protect against or potentiate cellular injury. To determine whether increased SOD1 protects the heart from ischemia and reperfusion, studies were performed in a newly developed transgenic mouse model in which direct measurement of superoxide, contractile function, bioenergetics, and cell death could be performed. Transgenic mice with overexpression of human SOD1 were studied along with matched nontransgenic controls. Immunoblotting and immunohistology demonstrated that total SOD1 expression was increased 10-fold in hearts from transgenic mice compared with nontransgenic controls, with increased expression in both myocytes and endothelial cells. In nontransgenic hearts following 30 min of global ischemia a reperfusion-associated burst of superoxide generation was demonstrated by electron paramagnetic resonance spin trapping. However, in the transgenic hearts with overexpression of SOD1 the burst of superoxide generation was almost totally quenched, and this was accompanied by a 2-fold increase in the recovery of contractile function, a 2.2-fold decrease in infarct size, and a greatly improved recovery of high energy phosphates compared with that in nontransgenic controls. These results demonstrate that superoxide is an important mediator of postischemic injury and that increasing intracellular SOD1 dramatically protects the heart from this injury. Thus, increasing intracellular SOD1 expression may be a highly effective approach to decrease the cellular injury that occurs following reperfusion of ischemic tissues.

Src-induced activation of inducible T cell kinase (ITK) requires phosphatidylinositol 3-kinase activity and the Pleckstrin homology domain of inducible T cell kinase

The Tec family of tyrosine kinases are involved in signals emanating from cytokine receptors, antigen receptors, and other lymphoid cell surface receptors. One family member, ITK (inducible T cell kinase), is involved in T cell activation and can be activated by the T cell receptor and the CD28 cell surface receptor. This stimulation of tyrosine phosphorylation and activation of ITK can be mimicked by the Src family kinase Lck. We have explored the mechanism of this requirement for Src family kinases in the activation of ITK. We found that coexpression of ITK and Src results in increased membrane association, tyrosine phosphorylation and activation of ITK, which could be blocked by inhibitors of the lipid kinase phosphatidylinositol 3-kinase (PI 3-kinase) as well as overexpression of the p85 subunit of PI 3-kinase. Removal of the Pleckstrin homology domain (PH) of ITK resulted in a kinase that could no longer be induced to localize to the membrane or be activated by Src. The PH of ITK was also able to bind inositol phosphates phosphorylated at the D3 position. Membrane targeting of ITK without the PH recovered its ability to be activated by Src. These results suggest that ITK can be activated by a combination of Src and PI 3-kinase.

The first step of aminoacylation at the atomic level in histidyl-tRNA synthetase

The crystal structure of an enzyme–substrate complex with histidyl-tRNA synthetase from Escherichia coli, ATP, and the amino acid analog histidinol is described and compared with the previously obtained enzyme–product complex with histidyl-adenylate. An active site arginine, Arg-259, unique to all histidyl-tRNA synthetases, plays the role of the catalytic magnesium ion seen in seryl-tRNA synthetase. When Arg-259 is substituted with histidine, the apparent second order rate constant (kcat/Km) for the pyrophosphate exchange reaction and the aminoacylation reaction decreases 1,000-fold and 500-fold, respectively. Crystals soaked with MnCl2 reveal the existence of two metal binding sites between β- and γ-phosphates; these sites appear to stabilize the conformation of the pyrophosphate. The use of both conserved metal ions and arginine in phosphoryl transfer provides evidence of significant early functional divergence of class II aminoacyl-tRNA synthetases.

Identification of specific Rp-phosphate oxygens in the tRNA anticodon loop required for ribosomal P-site binding

tRNA binding to the ribosomal P site is dependent not only on correct codon–anticodon interaction but also involves identification of structural elements of tRNA by the ribosome. By using a phosphorothioate substitution–interference approach, we identified specific nonbridging Rp-phosphate oxygens in the anticodon loop of tRNAPhe from Escherichia coli which are required for P-site binding. Stereo-specific involvement of phosphate oxygens at these positions was confirmed by using synthetic anticodon arm analogues at which single Rp- or Sp-phosphorothioates were incorporated. Identical interference results with yeast tRNAPhe and E. coli tRNAfMet indicate a common backbone conformation or common recognition elements in the anticodon loop of tRNAs. N-ethyl-N-nitrosourea modification–interference experiments with natural tRNAs point to the importance of the same phosphates in the loop. Guided by the crystal structure of tRNAPhe, we propose that specific Rp-phosphate oxygens are required for anticodon loop (“U-turn”) stabilization or are involved in interactions with the ribosome on correct tRNA–mRNA complex formation.

Altered peptide ligands act as partial agonists by inhibiting phospholipase C activity induced by myasthenogenic T cell epitopes

Myasthenia gravis (MG) is a T cell-regulated, antibody-mediated autoimmune disease. Two peptides representing sequences of the human acetylcholine receptor α-subunit, p195–212 and p259–271, previously were shown to stimulate the proliferation of peripheral blood lymphocytes of patients with MG and were found to be immunodominant T cell epitopes in SJL and BALB/c mice, respectively. Single amino acid-substituted analogs of p195–212 and p259–271, as well as a dual analog composed of the tandemly arranged two single analogs, were shown to inhibit, in vitro and in vivo, MG-associated autoimmune responses. Stimulation of T cells through the antigen-specific T cell receptor activates tyrosine kinases and phospholipase C (PLC). Therefore, in attempts to understand the mechanism of action of the analogs, we first examined whether the myasthenogenic peptides trigger tyrosine phosphorylation and activation of phospholipase C. For that purpose, we measured generation of inositol phosphates and tyrosine phosphorylation of PLC after stimulation of the p195–212- and p259–271-specific T cell lines with these myasthenogenic peptides. Both myasthenogenic peptides stimulated generation of inositol phosphates as well as tyrosine phosphorylation of PLC. However, the single and dual analogs, although inducing tyrosine phosphorylation of PLC, could not induce PLC activity. Furthermore, the single and dual analogs inhibited the induced PLC activity whereas they could not inhibit tyrosine phosphorylation of PLC that was caused by the myasthenogenic peptides. Thus, the altered peptides and the dual analog act as partial agonists. The down-regulation of PLC activity by the analogs may account for their capacity to inhibit in vitro MG-associated T cell responses.

ER-27319, an acridone-related compound, inhibits release of antigen-induced allergic mediators from mast cells by selective inhibition of Fcɛ receptor I-mediated activation of Syk

Engagement of the mast cell high-affinity receptor for immunoglobulin E (IgE), FcɛRI, induces tyrosine phosphorylation of Syk, a non-receptor tyrosine kinase, that has been demonstrated as critical for degranulation. Herein we describe a synthetic compound, ER-27319, as a potent and selective inhibitor of antigen or anti-IgE-mediated degranulation of rodent and human mast cells. ER-27319 affected neither Lyn kinase activity nor the antigen-induced phosphorylation of the FcɛRI but did effectively inhibit the tyrosine phosphorylation of Syk and thus its activity. As a consequence, tyrosine phosphorylation of phospholipase C-γ1, generation of inositol phosphates, release of arachidonic acid, and secretion of histamine and tumor necrosis factor α were also inhibited. ER-27319 did not inhibit the anti-CD3-induced tyrosine phosphorylation of phospholipase C-γ1 in Jurkat T cells, demonstrating a specificity for Syk-induced signals. In contrast the tyrosine phosphorylation and activation of Syk, induced by in vitro incubation with the phosphorylated immunoreceptor tyrosine-based activation motif (ITAM) of FcɛRI γ subunit or by antigen activation of RBL-2H3 cells, was specifically inhibited by ER-27319. However, when ER-27319 was added to immunoprecipitated Syk, derived from activated cells, no effect was seen on Syk activity. ER-27319 did not inhibit the tyrosine phosphorylation of Syk induced by activation in the presence of Igβ ITAM or the anti-IgM-induced phosphorylation of Syk in human peripheral B cells. Therefore, ER-27319 selectively interferes with the FcɛRI γ phospho-ITAM activation of Syk in vitro and in intact cells. These results confirm the importance of Syk in FcɛRI-mediated responses in mast cells and demonstrate the mast cell selectivity and therapeutic potential of ER-27319 in the treatment of allergic disease.