963 resultados para D. João III
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A new kind of luminescent organic-inorganic hybrid material (denoted Hybrid I) consisting of europium 1,10-phenanthroline complexes covalently attached to a silica-based network was prepared by a sol-gel process. 1,10-Phenanthroline grafted to 3-(triethoxysilyl)propyl isocyanate was used as one of the precursors for the preparation of an organic-inorganic hybrid materials. For comparison purposes, the hybrid material (denoted Hybrid II) in which phenanthroline was not grafted onto the silica backbone of the frameworks was also prepared. Elemental analysis; NMR, FT-IR, UV/vis absorption, and luminescence spectroscopies, and luminescence decay analysis were used to characterize the obtained hybrid materials. It is shown that the homogeneity of Hybrid I is superior to that of Hybrid II, and a higher concentration europium can be incorporated into Hybrid I than Hybrid II. Excitation at the ligand absorption wavelength (283 nm) resulted in the strong emission of the Eu3+ D-5(0)-F-7(J) (J = 0-4) transition lines as a result of the efficient energy transfer from the ligands to the EU3+ in Hybrid I. The number of water molecules coordinated to the europium ion was estimated, and the structure of the as-synthesized Hybrid I was predicted on the basis of the experimental results.
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A novel terbium complex, Tb(acac)(3)AAP (acac: acetylacetone, AAP: 4-amino-antipyrine), was synthesized and its luminescent properties were studied. When it was used as an emitting center, triple-layer-type device with a structure of glass substrate/ITO (indium-tin oxide)/TPD (N,N'-diphenyl-N,N'-bis(3-methylphenyl)-1,1'-biphenyl-4,4'-diamine)./Tb(acac)(3)AAP/PBD (2-(4-biphenyl)-5-(4-t-butylphenyl)-1,3,4-oxadiazole) or Alq(3) (tris(8-hydroxyquinolinato) aluminum)/Al (aluminum) exhibited bright characteristic emission of terbium ion upon applying d.c. voltage. The maximum luminance of the device is 56 cd/m(2) at 19 V and the maximum luminance efficiency is 0.357 lm/W.
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Crystallization and melting behavior of short ethylene sequence of metallocene ethylene/alpha -olefin copolymer with high comonomer content have been studied by standard DSC and modulated-temperature differential scanning calorimetry (M-TDSC) technique. In addition to high temperature endotherm around 120 degreesC, a low temperature endotherm is observed at lower temperatures (40-80 degreesC), depending on time and temperature of isothermal crystallization. The peak position of the low temperature endotherm T-m(low) varies linearly with the logarithm of crystallization time and the slope, D, decreases with increasing crystallization temperature T-c. The T-m(low) also depends on the thermal history before the crystallization at T-c, and an extrapolation of T-m(low) (30.6 degreesC) to a few seconds has been obtained after two step isothermal crystallization before the crystallization at 30 degreesC. The T-m(low) is nearly equal to T-c, and it indicates that the initial crystallization at low temperature is nearly reversible. Direct evidence of conformational. entropy change of secondary crystallization has been obtained by using M-TDSC technique. Both the M-TDSC result and the activation energy analysis of temperature dependence suggest that crystal perfection process and conformational entropy decreasing in residual amorphous co-exist during secondary crystallization.
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Fluorescence of terbium(III) was sensitized when excited in the presence of sparfloxacin (SPFX) in the aqueous solution because a Tb(III)-SPFX complex was formed. The sensitized fluorescence was further enhanced when this system was exposed to 365 nm ultraviolet light. By the spectral properties and contrast experiments, it is proved that irradiation makes this system undergo photochemical reactions and a new terbium complex which is more favorable to the intramolecular energy transfer is formed. The mechanism of photochemical fluorescence enhancement of the Tb(III)-SPFX system is discussed and a new sensitive and selective photochemical fluorimetry for the determination of SPFX is established. Under the optimum conditions, the linear range is 1.0-50 x 10(-7) M for SPFX, the detection limit is 3.0 x 10(-9) M and the R.S.D. for 5.0 x 10(-7) M SPFX is 1.3% (n = 9). Without any pretreatment the recovery of SPFX in human urine was determined with satisfaction. (C) 1999 Elsevier Science B.V. All rights reserved.
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Reduction of hydrogen peroxide at a glassy carbon (GC) electrode modified with sigma-bonded pyrrole iron(III) octaethylporphyrin complex, (OEP)Fe(Pyr), was studied by cyclic voltammetry and a rotating disk electrode. In 0.1N NaOH solution, it is shown that such an (OEP)Fe(Pyr)/GC electrode has a significant catalytic activity towards hydrogen peroxide reduction (E(D) = -0.80 V, k = 0.066 cm s(-1)); however, the electrode stability is low. The deactivation is observed when the reaction charge (Q) is passing through the (OEP)Fe(Pyr)/GC disk electrode. A linear rotation scan method is applied to study the kinetic process by determining the disk electrochemical response (i(D)) to rotation rate (omega) at a definite disk potential (E(D)). Considering that the number of adsorbed electroreduced catalyst molecules (Red) varies according to the disk potential, a factor theta(= Gamma(Red)/(Gamma(Red) + Gamma(Ox))) is introduced to describe the electrode surface area fraction for electroreduced species. The obtained Koutecky-Levich equation is applicable whatever the potential is.
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The crystal structures, electronic spectra, and Cu2p XPS of Cu(III) complexes Na4H[Cu(H2TeO6)(2)]. 17H(2)O and Na4K[Cu(HlO(6))(2)]. 12H(2)O have been described. The characterizations of a Cu(III) atom in a complex are as follows: (i) In a square-planar coordination, the average bond length of Cu-O is 0.183 nm, shorter than the 0.190-0.200 nm found for a Cu(II) complex. (2) The ''blue shift'' occurs for d-d transitions in the electronic spectrum of the Cu(III) complex compared to those of its related Cu(II) complex, resulting from the higher valence state. (3) Cu(III) compounds with CuO4 square-planar coordination are expected to be diamagnetic whereas Cu(II) compounds to be paramagnetic. (4) Comprehensive investigations on Cu2p XPS show that the binding energy of Cu2p(3/2) of a pure Cu(III) compound is about 2.0 eV higher than that of its corresponding Cu(II) compound: the shake-up satellites do not appear in the Cu2p XPS for a pure diamagnetic Cu(III) compound, the same as found for a diamagnetic Ni(II) compound: the FWHM of the signal of Cu2p XPS may become broader for Cu(III) compound because its core hole's lifetime shortens due to the higher valence state of copper. (C) 1995 Academic Press, Inc.
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迟缓爱德华氏菌(Edwardsiella tarda)是重要的革兰氏阴性致病菌,可以感染包括人类在内的多种动物。由迟缓爱德华氏菌引发的爱德华氏菌病已经在许多水产养殖动物中被发现,每年给淡水和海水水产养殖业带来巨大的损失。目前为止对于迟缓爱德华氏菌病的防治以化学治疗为主,疫苗的研究还在进行中。III型分泌系统(T3SS)是E. tarda重要的致病因子,虽然T3SS基因簇的结构及部分基因的功能得到了初步研究,但其作用机制还未得到阐明。本研究着重开展了迟缓爱德华氏菌T3SS输送器蛋白EseC的分子伴侣的鉴定及功能研究,并对输送器蛋白及其免疫功能进行了初步探讨,希望进一步地了解T3SS在E. tarda致病中的功能及其在疫苗研制中的作用。 一、迟缓爱德华氏菌III型分泌系统(T3SS)输送器蛋白EseC分子伴侣的鉴定和功能研究 以前的工作表明,EseB、EseC和EseD白是E. tarda T3SS输送器蛋白的组成成分,在分泌到细菌细胞外后可以组成输送器装置。分子伴侣对于输送器蛋白的稳定和分泌具有重要的作用,EscC已经被鉴定为EseB和EseD分子伴侣,而EseC的分子伴侣还没有得到鉴定。在本实验中,我们以EseC作为研究对象,主要开展了EseC分子伴侣鉴定的研究。 生物信息学分析表明,在E. tarda T3SS基因簇上的escA基因与eseC相邻,其编码的蛋白形成一个大的螺旋结构,为分子量较小(17.5kD的酸性蛋白(pI 4.79),并与已鉴定的分子伴侣具有序列的同源性,这些符合细菌T3SS分子伴侣的特征。研究发现,EscA蛋白分布在细菌的细胞质和细胞膜上。在escA基因缺失后,大大降低了EseC分泌到细菌细胞外的量,同时EseC蛋白在细菌细胞质中的积聚量也减少,当escA基因缺失突变株得到escA基因互补后,EseC的分泌和在细胞质内的积聚恢复到了野生型菌株水平。氯霉素阻断蛋白质合成的实验发现,当细菌不表达EscA的情况下,EseC蛋白逐渐降解,说明了EscA可以影响EseC在胞质中的稳定。蛋白体外结合试验和免疫共沉淀实验发现,EseC和EscA在体外可以结合,在细菌细胞质中也可以相互结合,表明EseC和EscA可以相互作用。上述结果表明,EscA是EseC的分子伴侣。 在确定了EscA是EseC的分子伴侣之后,我们进一步确定EscA对EseC表达的影响,以及两者相互作用的结构域。通过检测转录水平和翻译水平的EseC-LacZ融合蛋白表达情况,发现在EscA缺失的情况下,EseC的转录水平没有变化,而翻译水平下降,表明EscA对EseC的影响在转录后水平。通过构建含有部分结构域缺失的escA或eseC的体外共表达体系,并进行Western blot分析,确定了EseC的31-137氨基酸序列为与EscA结合的区域,而在EscA中并没有找到与EseC结合的区域。EseC的31-137氨基酸片段缺失后,EseC的分泌和在E. tarda细菌细胞中的积聚下降,其下降幅度与escA突变株相当,进一步表明EseC的31-137氨基酸为与EscA相互作用的区域。最后人工感染实验表明,分子伴侣EscA及其与EseC的相互作用对E. tarda的致病力有影响。 二、迟缓爱德华氏菌T3SS输送器蛋白的研究 一些研究表明,T3SS在细菌与宿主相互作用的过程中表达,在体外诱导的条件下也可表达。为了确定E. tarda T3SS体外诱导表达的条件,我们检测了不同培养温度、pH条件下,E. tarda T3SS输送器蛋白表达的情况。研究表明,37°C条件下,E. tarda生长快,T3SS的输送器蛋白表达较低;28°C条件下,T3SS的输送器蛋白表达最高,而在20°C条件下,没有检测到T3SS输送器蛋白的表达。在28°C和37°C的培养条件下,中性和碱性相对酸性来说适合细菌的生长和T3SS输送器蛋白的表达。我们分析了E. tarda野生型和输送器蛋白突变株中的输送器蛋白的细胞分布,并据此推测输送器形成的机制。单一输送器蛋白的缺失不影响其它两个输送器蛋白的积聚,而输送器蛋白的分泌之间存在一定的相互影响。 通过检测输送器蛋白突变株ΔeseB, ΔeseC, ΔeseD长、泳动、自凝聚和溶血能力的变化,发现在输送器蛋白基因缺失后,体外培养的E. tarda的生长速度变慢,泳动、自凝聚和溶血能力也变弱,说明了输送器蛋白在细菌的生长和功能行使中的重要作用。 为了检测输送器蛋白的免疫保护效果,我们克隆了eseD因,将其在表达菌株BL21(DE3)中进行表达,并将重组表达的EseD白经Ni-NTA树脂进行纯化。以EseD化蛋白作为蛋白抗原对大菱鲆进行注射,EseD白表现出了对鱼类的免疫原性,其抗体效价在第7周达到了最高,为1:5120。攻毒实验表明该蛋白对于保护大菱鲆免疫E. tarda的感染具有帮助作用,在105cfu攻毒浓度下大菱鲆的相对存活率(RPS)为62.5%。结果说明EseD白可以作为蛋白抗原疫苗的候选,并能够在保护鱼类免疫爱德华氏菌病中发挥作用。
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This thesis examines a complete design framework for a real-time, autonomous system with specialized VLSI hardware for computing 3-D camera motion. In the proposed architecture, the first step is to determine point correspondences between two images. Two processors, a CCD array edge detector and a mixed analog/digital binary block correlator, are proposed for this task. The report is divided into three parts. Part I covers the algorithmic analysis; part II describes the design and test of a 32$\time $32 CCD edge detector fabricated through MOSIS; and part III compares the design of the mixed analog/digital correlator to a fully digital implementation.
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2009
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Com o objetivo de prover informações dos recursos de solos da área de expansão do projeto de irrigação do Jaíba (Etapa III, que abrange 12.015 ha), a fim de possibilitar o adequado planejamento e monitoramento das atividades agrossilvipastoris e de preservação ambiental, foi realizado o levantamento de solos em nível de semidetalhe, na escala 1:50.000, conforme as normas preconizadas pela Embrapa. Predomina cobertura sedimentar cenozóica sobre rochas do Grupo Bambuí, dispostas em superfície aplainada, amplamente dominante, pontuada por dolinas e uvalas, além de um trecho de planície fluvial, ao longo do rio Ilha do Retiro. A região é caracterizada por temperaturas médias elevadas, precipitações médias abaixo dos 900 mm anuais e deficiência hídrica anual de 450 mm a 500 mm, evidenciando o curto período favorável ao crescimento das plantas em sequeiro, nas estações de primavera e verão. O ambiente seco também é evidenciado pela vegetação natural, dominada por florestas decíduas e caatingas, ou transição entre essas formações vegetais. A diferenciação de solos na área está bem condicionada ao nível topográfico relativo dos terrenos. Da superfície plana do topo da paisagem em direção às depressões semicirculares dispersas na área têm-se uma topossequência característica, com Latossolos Amarelos de caráter distrófico e textura média leve dominante na ampla área em nível topográfico superior; e solos dessa mesma classe, mas em geral com saturação por bases alta (eutróficos) e teores de argila ligeiramente mais elevados, localizados em depressões suavizadas, ou nas bordas ligeiramente inclinadas das dolinas; seguidos de Cambissolos Háplicos Tb Eutróficos (petroplínticos, endorredxicos ou gleissólicos) de textura argilosa, em nível topográfico intermediário; aos quais se sucedem Planossolos e Gleissolos, que ocorrem associados nos fundos das dolinas e uvalas, mais rebaixadas. O vale do ribeirão Ilha do Retiro, por outro lado, apresenta um padrão de distribuição de solos distinto, com domínio de Neossolos Flúvicos, desenvolvidos de material de textura média ou argilosa de deposição aluvionar, ocorrendo nas partes topográficas inferiores, em associação com Chernossolos Rêndzicos, que tendem a predominar no segmento de nível topográfico um pouco mais alto, limitando-se no topo da encosta com a área de Latossolos Amarelos. A extensa área aplainada apresenta boas condições para agricultura intensiva com irrigação, porém com restrições decorrentes da baixa capacidade de água disponível, elevada taxa de infiltração e baixa fertilidade natural. Em direção aos níveis topográficos mais baixos, há uma tendncia geral de aumentar as limitações à utilização agrícola, sobretudo em decorrência da deficiência de aeração, imposta pela dificuldade de drenagem e escoamento, assim como pela possibilidade de encharcamento por afluxo de água proveniente dos terrenos circundantes.
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O sistema de cultivo em consórcio de fruteiras com outras culturas, sejam anuais, semiperenes ou perenes, constitui uma boa alternativa para propriedades rurais e uma importante forma de recuperação de áreas degradadas. O objetivo deste trabalho foi avaliar o comportamento de bananeira, cv. D'Angola, em monocultivo e consorciada com açaizeiro, Euterpe precatoria, em diferentes espaçamentos, no primeiro ciclo de produção. Para tanto, foi instalado um experimento seguindo um delineamento em blocos casualizados completos com quatro repetições e seis plantas por parcela. Os tratamentos foram: T1 ? bananeira em 3 m x 3 m (1.111 plantas ha-1); T2 ? bananeira em 3 m x 2 m (1.666 plantas ha-1) com açaizeiro em 3 m x 4 m (833 plantas ha-1); T3 ? bananeira em 3 m x 3 m (1.111 plantas ha-1) com açaizeiro em 3 m x 4 m (833 plantas ha-1); T4 ? bananeira em 4 m x 2 m x 2 m (1.666 plantas ha-1) com açaizeiro em 6 m x 3 m (555 plantas ha-1) e T5 ? bananeira em 4 m x 2 m x 2 m (1.666 plantas ha-1) com açaizeiro em 4 m x 2 m x 3 m (1.111 plantas ha-1). O sistema de cultivo da bananeira terra consorciada com açaizeiro em diferentes espaçamentos pode ser considerado como boa alternativa no primeiro ciclo, pois não apresentou interferência nas características de desenvolvimento, de produção e qualidade física dos frutos. Os plantios mais adensados propiciaram maiores produtividades no primeiro ciclo da cultura.
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O espaçamento é um dos principais fatores para aumento de produtividade, sem ocasionar perdas de qualidade de frutos da bananeira, e varia em função das condições de clima e solo da região. Quando a bananeira é cultivada em maiores densidades, aproveita-se melhor a área disponível e o uso da mão de obra é otimizado. Na banana-comprida o espaçamento ideal evita a competição por água, luz e nutrientes, sem comprometer os rendimentos potenciais da cultura.
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Atomic layer deposition (ALD) is now used in semiconductor fabrication lines to deposit nanometre-thin oxide films, and has thus enabled the introduction of high-permittivity dielectrics into the CMOS gate stack. With interest increasing in transistors based on high mobility substrates, such as GaAs, we are investigating the surface treatments that may improve the interface characteristics. We focus on incubation periods of ALD processes on III-V substrates. We have applied first principles Density Functional Theory (DFT) to investigate detailed chemistry of these early stages of growth, specifically substrate and ALD precursor interaction. We have modelled the ‘clean-up’ effect by which organometallic precursors: trimethylaluminium (TMA) or hafnium and titanium amides clean arsenic oxides off the GaAs surface before ALD growth of dielectric commences and similar effect on Si3N4 substrate. Our simulations show that ‘clean-up’ of an oxide film strongly depends on precursor ligand, its affinity to the oxide and the redox character of the oxide. The predominant pathway for a metalloid oxide such as arsenic oxide is reduction, producing volatile molecules or gettering oxygen from less reducible oxides. An alternative pathway is non-redox ligand exchange, which allows non-reducible oxides (e.g. SiO2) to be cleaned-up. First principles study shows also that alkylamides are more susceptible to decomposition rather than migration on the oxide surface. This improved understanding of the chemical principles underlying ‘clean-up’ allows us to rationalize and predict which precursors will perform the reaction. The comparison is made between selection of metal chlorides, methyls and alkylamides precursors.
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Previously, we and others have shown that MHC class-II deficient humans have greatly reduced numbers of CD4+CD8- peripheral T cells. These type-III Bare Lymphocyte Syndrome patients lack MHC class-II and have an impaired MHC class-I antigen expression. In this study, we analyzed the impact of the MHC class-II deficient environment on the TCR V-gene segment usage in this reduced CD4+CD8- T-cell subset. For these studies, we employed TcR V-region-specific monoclonal antibodies (mAbs) and a semiquantitative PCR technique with V alpha and V beta amplimers, specific for each of the most known V alpha- and V beta-gene region families. The results of our studies demonstrate that some of the V alpha-gene segments are used less frequent in the CD4+CD8- T-cell subset of the patient, whereas the majority of the TCR V alpha- and V beta-gene segments investigated were used with similar frequencies in both subsets in the type-III Bare Lymphocyte Syndrome patient compared to healthy control family members. Interestingly, the frequency of TcR V alpha 12 transcripts was greatly diminished in the patient, both in the CD4+CD8- as well as in the CD4-CD8+ compartment, whereas this gene segment could easily be detected in the healthy family controls. On the basis of the results obtained in this study, it is concluded that within the reduced CD4+CD8- T-cell subset of this patient, most of the TCR V-gene segments tested for are employed. However, a skewing in the usage frequency of some of the V alpha-gene segments toward the CD4-CD8+ T-cell subset was noticeable in the MHC class-II deficient patient that differed from those observed in the healthy family controls.
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The activation parameters and the rate constants of the water-exchange reactions of Mn(III)TE-2-PyP(5+) (meso-tetrakis(N-ethylpyridinium-2-yl)porphyrin) as cationic, Mn(III)TnHex-2-PyP(5+) (meso-tetrakis(N-n-hexylpyridinium-2-yl)porphyrin) as sterically shielded cationic, and Mn(III)TSPP(3-) (meso-tetrakis(4-sulfonatophenyl)porphyrin) as anionic manganese(iii) porphyrins were determined from the temperature dependence of (17)O NMR relaxation rates. The rate constants at 298 K were obtained as 4.12 x 10(6) s(-1), 5.73 x 10(6) s(-1), and 2.74 x 10(7) s(-1), respectively. On the basis of the determined entropies of activation, an interchange-dissociative mechanism (I(d)) was proposed for the cationic complexes (DeltaS(double dagger) = approximately 0 J mol(-1) K(-1)) whereas a limiting dissociative mechanism (D) was proposed for Mn(III)TSPP(3-) complex (DeltaS(double dagger) = +79 J mol(-1) K(-1)). The obtained water exchange rate of Mn(III)TSPP(3-) corresponded well to the previously assumed value used by Koenig et al. (S. H. Koenig, R. D. Brown and M. Spiller, Magn. Reson. Med., 1987, 4, 52-260) to simulate the (1)H NMRD curves, therefore the measured value supports the theory developed for explaining the anomalous relaxivity of Mn(III)TSPP(3-) complex. A magnitude of the obtained water-exchange rate constants further confirms the suggested inner sphere electron transfer mechanism for the reactions of the two positively charged Mn(iii) porphyrins with the various biologically important oxygen and nitrogen reactive species. Due to the high biological and clinical relevance of the reactions that occur at the metal site of the studied Mn(iii) porphyrins, the determination of water exchange rates advanced our insight into their efficacy and mechanism of action, and in turn should impact their further development for both diagnostic (imaging) and therapeutic purposes.