9 resultados para dupla inoculação

em SAPIENTIA - Universidade do Algarve - Portugal


Relevância:

10.00% 10.00%

Publicador:

Resumo:

Dissertação de Mestrado, Ciências da Educação, Área de Especialização de Educação e Formação de Adultos, Faculdade de Ciências Humanas e Sociais, Universidade do Algarve, 2007

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Dissertação de mest.Ciências Biomédicas. Departamento de Ciências Biomédicas e Medicina, Univ. do Algarve, 2011

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Dissertação de mest., Engenharia Biológica, Faculdade de Ciências e Tecnologia, Univ. do Algarve, 2011

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Dissertação de mest., Engenharia Biológica, Faculdade de Ciências e Tecnologia, Univ. do Algarve, 2011

Relevância:

10.00% 10.00%

Publicador:

Resumo:

The present work has the merit of exploring an insight into the activation of defence genes of Quercus suber during response to infection by Phytophthora cinnamomi. Thus, cDNA-AFLP methodology was used to identify gene fragments differentially present in the mRNA profiles of host cells of micropropagated Q. suber plantlets roots infected with zoospores of P. cinnamomi at different post challenge time points. Six candidate genes were selected based on their interesting cDNA-AFLP expression patterns and homology to genes known to play a role in defence. These six genes encode a cinnamyl alcohol dehydrogenase 2 (QsCAD2), a protein disulphide isomerase (QsPDI), a CC-NBS-LRR resistance protein (QsRPc), thaumatin-like protein (QsTLP), chitinase (QsCHI) and a 1,3-beta glucanase (QsGLU). The current work has been successful in evaluation of the expression of these genes by qRT-PCR. Data analysis revealed that transcript levels of QsRPc, QsCHI, QsCAD2 and QsPDI increased during the early hours of inoculation, while transcript profiles of thaumatin-like protein showed decreasing. No expression was detected for 1,3-beta-glucanase (QsGLU). Furthermore, the choice of suitable reference genes in any new experimental system is absolutely crucial in qRT-PCR; for this reason in this study and for the first time a set of potential reference genes were analyzed and validated for qRT-PCR normalization in the patho-system Phytophthora-Q. suber. Four candidate reference genes polimerase II (QsRPII), eukaryotic translation initiation factor 5A(QsEIF-5A), b-tubulin (QsTUB) and a medium subunit family protein of Clathrin adaptor complexes (QsCACs) were evaluated to determine the most stable internal references in Q. suber. Analysis of stability of genes was carried out using Genex software. Results indicated all these four potential reference genes assumed stable expression. Data analysis revealed that QsRPII and QsCACs were the two most stable genes, while genes QsTUB and QsEIF-5A were the third and the fourth most stable gene, respectively. In this study, a plasmid-based quantitative PCR method was developed to measure P. cinnamomi colonization during infection process of Q. suber. Plasmid-based detection of P. cinnamomi showed a gradual accumulation of the pathogen DNA in cork oak root tips up to 24 h post infection. The higher increase in P. cinnamomi/plasmid DNA ratio occurred between 18 and 24 h. One of the primary objectives of this research was to study the effect of cinnamomins (elicitins secreted by P. cinnamomin) on inducing defence mechanism against the pathogen, as recent histological and ultra-structural studies showed that P. cinnamomi was restricted to the outer cortex root fragments pre-treated with capsicien and cryptogein, suggesting that elicitins can stimulate plant defence reactions against P. cinnamomi. To complement these studies and to have a clear view of the nature of the interaction, the role of cinnamomins in the production of the oxidative burst [ROS and ROS scavenging enzymes such as superoxide dismutase (SOD), catalase (CAT) and peroxidase (POD)] and in the defence responses was evaluated. Cork oak seedlings were pretreated with alpha-cinnamomin and then inoculated with P. cinnamomi mycelia. Results showed a significant higher production of reactive oxygen species (ROS) (H2O2 and O2•-) in elicitin and non-elicitin treated roots in interaction with P. cinnamomi in comparison to the corresponding control. The plant group inoculated with the pathogen after cinnamomin treatment showed an earlier increase in H2O2 production but this was lower as compared with that group inoculated with P. cinnamomi alone. Also, in elicitin pre-treated group generally, a lower level of O2•− production during infection was observed as compared with inoculated roots with P. cinnamomi alone without elicitin treatment. Furthermore, in this study, we evaluated activities of antioxidant enzymes upon challenge with P. cinnamomi, with and without pretreatment with alpha cinnamomin. Results indicated that the activities of defense enzymes POD, SOD and CAT increased after P. cinnamomi inoculation when compared with those in the control group. Also, in the group treated with alpha-cinnamomin followed by P. cinnamomi inoculation, a higher level of enzymatic activities was detected as compared with elicitin non-treated group, which suggest the protective effect of alpha-cinnamomin against the pathogen due to higher elevated levels of defense enzymes POD, SOD and CAT during the infection period. Furthermore, a sensitive qPCR method was applied to measure the pathogen biomass in elicited and non-elicited Q. suber roots challenged with P. cinnamomi to elucidate the effect of cinnamomins on the colonization of P. cinnamomi. Plasmid-based quantification of P. cinnamomi showed a significant decrease in accumulation of the pathogen DNA in cork oak roots after treatment with alpha and beta-cinnamomins which attest the role of cinnamomins in promoting defense responses in cork oak against P. cinnamomi invasion.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

O presente trabalho incide sobre o meu percurso profissional com especial relevância na função que desempenho na Caixa Geral de Depósitos1 como Coordenadora de um Gabinete Empresas2. Em 1994, após um período de estágio, ingressei nos quadros da Caixa, maior banco português, no qual desenvolvi todo o meu currículo profissional. Com efeito, passei por diversas unidades de negócio – agência, direção e gabinete – nas quais experienciei e adquiri conhecimentos que consolidei ao longo dos anos, num processo contínuo de aprendizagem do negócio bancário, percurso que descrevo exaustivamente no Curriculum Vitae integrado no presente relatório. A par das competências adquiridas na Caixa em ambiente de trabalho, a formação académica no âmbito da gestão empresarial, na qual se enquadra o presente curso de mestrado, revelou-se essencial no meu crescimento profissional, munindo-me de competências técnicas/científicas relevantes e de aplicabilidade diária. Este facto é particularmente evidente na função que desempenho como Coordenadora de um Gabinete Empresas, unidade bancária totalmente focada no negócio empresarial, destacando a relevância das áreas curriculares de recursos humanos, avaliação de empresas e estratégia. Com efeito, poderá considerar-se que a gestão empresarial na minha atividade profissional é aplicada numa dupla vertente: a de gerir uma unidade de negócio bancário, neste caso um Gabinete Empresas, e; na análise dos variados negócios/projetos dos clientes empresa que constam da carteira do Gabinete, área que inerente tem uma vertente de consultoria. Assim, inerente à minha função, e em alinhamento com as estratégias globais e objetivos definidos na Caixa e respetivas direções, e cumprindo com o normativo existente e delegação de competências atribuída, coordeno o Gabinete nas várias vertentes: financeira, operacional, comercial e recursos humanos. Na sequência, defino objetivos ao nível do Gabinete, analiso, formulo e implemento estratégias que visem a sua prossecução, defino planos de atuação e controlo os desvios. A gestão de uma unidade de negócio exige-me ainda um acompanhamento contínuo dos indicadores de negócio e financeiros através das demonstrações financeiras disponibilizadas numa ótica de potenciar a rendibilidade e solidez. Na vertente de recursos humanos, procuro desenvolver competências que permitam aos colaboradores elevar o desempenho das suas funções, defino objetivos individuais de melhoria que, a par com os outros critérios de avaliação definidos na Caixa, contribuem para a avaliação de desempenho, processo que asseguro no Gabinete. No que respeita à vertente comercial participo na negociação com os clientes, acompanho, analiso e emito pareceres técnico/comerciais e decido sobre crédito e demais produtos que constituem a oferta bancária da Caixa. E é inerente ao crédito, maior ativo de um banco, identificado também como de elevada exigência em termos de análise de risco, que desenvolvo no presente relatório de atividade profissional a temática da gestão de sinais de alerta. Esta matéria é de relevância na função que desempenho e consiste na identificação e validação de sinais de alerta, tomando-se decisões face ao risco de crédito percecionado com vista a potenciar a rentabilidade do banco. Pretendo assim identificar de que forma a gestão dos alertas influi na solidez financeira do banco e a sua importância no atual contexto económico.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Phosphatidylcholine (PC), sphingomyelin (SM) and cholesterol (CHOL) are major constituents of mammalian cell membranes. DPPC/CHOL and DPPC/DMPC are well-known binary mixtures. POPC/CHOL, DOPC/CHOL, egg-SM/CHOL, egg-SM/POPC and egg-SM/DOPC are less studied, but also important for the comprehension of the POPC/egg-SM/CHOL mixtures. These provide complex media for which polarity is hard to access. It is mainly determined by the water penetrating the bilayer (unevenly distributed creating a polarity gradient), though the influence of the dipoles from phospholipids (e.g. –PO, –CO, –OH) and the double bond in the steroid ring of CHOL cannot be neglected. CHOL derivatives are an interesting tool to verify the influence of the double bonds in the polarization of its surroundings. Pyrene fluorescence was used to access an equivalent polarity (associated to the dielectric constant) near the lipid/water interface of lipid bilayers. POPC/CHOL and DOPC/CHOL have similar thermal behavior and variation with CHOL content, though for lower CHOL content the equivalent polarity is higher for the DOPC/CHOL mixtures. The studies with DPPC and DMPC showed that pyrene does not seem to have a marked preference for either ordered or disordered phases. For DPPC/CHOL and egg-SM/CHOL the highlight goes to the behavior of the mixtures at higher CHOL amounts, where there is a substantial change in the thermal behavior and polarity values especially for the egg-SM/CHOL mixture. Egg-SM/POPC and egg-SM/DOPC show different behavior depending on which phospholipid has a higher molar proportion. The ternary mixtures analyzed do not exhibit significant differences, though there is the indication of the existence of a more ordered environment at lower temperatures and a less ordered environment for higher temperatures. The presence of 7DHC or DCHOL in egg-SM bilayers showed a tendency for the same behavior detected upon mixing higher amounts of CHOL.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Cardiogenesis is a delicate and complex process that requires the coordination of an intricate network of pathways and the different cell types. Therefore, understanding heart development at the morphogenetic level is an essential requirement to uncover the causes of congenital heart disease and to provide insight for disease therapies. Mouse Cerberus like 2 (Cerl2) has been defined as a Nodal antagonist in the node with an important role in the Left-Right (L/R) axis establishment, at the early embryonic development. As expected, Cerl2 knockout mice (Cerl2-/-) showed multiple laterality defects with associated cardiac failure. In order to identify the endogenous role of Cerl2 during heart formation independent of its described functions in the node, we accurately analyzed animals where laterality defects were not present. We thereby unravel the consequences of Cerl2 lossof- function in the heart, namely increased left ventricular thickness due to hyperplasia of cardiomyocytes and de-regulated expression of cardiac genes. Furthermore, the Cerl2 mutant neonates present impaired cardiac function. Once that the cardiac expression of Cerl2 is mostly observed in the left ventricle until around midgestration, this result suggest a specific regulatory role of Cerl2 during the formation of the left ventricular myoarchitecture. Here, we present two possible molecular mechanisms underlying the cardiac Cerl2 function, the regulation of Cerl2 antagonist in activation of the TGFßs/Nodal/Activin/Smad2 signaling identified by increased Smad2 phosphorilation in Cerl2-/- hearts and the negative feedback between Cerl2 and Wnt/ß-catenin signaling in heart formation. In this work and since embryonic stem cells derived from 129 mice strain is extensively used to produce targeted mutants, we also present echocardiographic reference values to progressive use of juveniles and young adult 129/Sv strain in cardiac studies. In addition, we investigate the cardiac physiology of the surviving Cerl2 mutants in 129/Sv background over time through a follow-up study using echocardiographic analysis. Our results revealed that Cerl2-/- mice are able to improve and maintain the diastolic and most of systolic cardiac physiologic parameters as analyzed until young adult age. Since Cerl2 is no longer expressed in the postnatal heart, we suggest that an intrinsic and compensatory mechanism of adaptation may be active for recovering the decreased cardiac function found in Cerl2 mutant neonates. Altogether, these data highlight the role of Cerl2 during embryonic heart development in mice. Furthermore, we also suggest that Cerl2-/- may be an interesting model to uncover the molecular, cellular and physiological mechanisms behind the improvement of the cardiac function, contributing to the development of therapeutic approaches to treat heart failures.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Tese de doutoramento, Ciências Biomédicas, Universidade do Algarve, Departamento de Ciências Biomédicas e Medicina, 2014