Ligand-gated ion channels couple intra- and extracellular chemical signals to cellular excitability. In response to a specific ligand, these channels change their permeability to certain ions by opening or closing their ion conductive pathway, a controlling mechanism known as channel gating. Although recent studies with X-ray crystallography and site-directed mutagenesis have revealed several structures potentially important for channel gating, the gating mechanism is still elusive. Ligand-dependent channel gating involves a series of transient events and asymmetric movements of individual subunits. Understanding of these events appears to be a challenge to current approaches in gating studies by using the homomeric wild-type or mutant channels. I therefore took an alternative approach by constructing heteromeric channels. Subunit stoichiometric studies of the Kir1.1 channel showed that a minimum of one functional subunit was required for the pH-dependent gating of the channel. Four subunits in this channel were coordinated as dynamic functional dimers. In Kir6.2 channel, stoichiometry for proton-binding was almost identical to that for channel gating in the M2 helix, suggesting a one-to-one direct coupling of proton binding in C-terminus to channel gating in M2 helix. Positive cooperativity was suggested among subunits in both the proton binding and channel gating. Ligand binding can be differentiated from channel gating by studying the ATP-dependent gating of Kir6.2 channel. Disruptions in ATP binding were found to change both the potency and efficacy of the concentration-dependent curves, while the baseline activity instead of maximum inhibition was affected by disruptions of channel gating. Four subunits in the Kir6.2 channel undergo negative cooperativity in ATP binding and positive cooperativity in channel gating. The ligand binding was coupled to the gating mechanism in the same subunit and neighboring subunits, although the intrasubunit coupling was more effective. These results are well described with the operational model which we have applied to ion channel studies for the first time. By manipulating the relative distance and the interaction of two transmembrane helices, the inner helix bundle of crossing was found to not only serve as a gate but also determine the consequence of ligand binding.

The major objectives of this study were to investigate the antioxidant properties of flaxseed lignans secoisolariciresinol (SECO 2) and secoisolariciresinol diglycoside (SDG 1) and their major oxidative compounds using 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH 47) in an in vitro model of lipid peroxidation. This investigation was facilitated by the structural elucidation of the major oxidative compounds and the ability of flaxseed lignans to delay the onset of oxidation in two model systems. <p>This study showed that SECO 2 oxidation occurs at the aromatic (4-OH) and aliphatic (9-OH) hydroxyl groups. Conversely for SDG 1, only compounds derived from the oxidation of aromatic hydroxyl groups were obtained because the 9-OH position is glucosylated. <p>SECO 2 oxidation with AAPH 47 showed that the intermediate 2a is most likely involved in the generation of early-forming (48 and 52) and 2c for the formation of late-forming (49, 50 and 51) oxidation compounds. Compound 48 is formed from dimerization of 2a that is converted to 52 and then to 51. Compound 50 was formed by the addition of a carbon-centre free radical of AAPH (AP radical) to 2c. Compounds 50 and 51 trap carbon-centered AP radicals supporting SECO 2 as a chain-breaking antioxidant and AAPH 47 as a proper model for study of SECO 2 oxidation in vitro. <p>SDG 1 oxidation with AAPH 47 indicated that intermediates 1b and 1c are most likely involved for the formation of early forming compounds (55 and 58) and 1a leads to the late forming compounds (56 and 57). Compound 55 is a result of dimerization. Compound 56 may be directly formed via intermediate radical 1a by adding AP free radicals. Compound 56 was a stable non-radical compound that could trap AP free radicals, thereby supporting SDG 1 as a chain-breaking antioxidant. Hydrogen abstraction from 4-hydroxyl yielded the radical 1a and hydroxyl radical addition to 1a yielded 57. Compound 58 formed from the addition of OH or H2O to 1c. <p>This study demonstrated that AAPH 47 produces carbon-centred AP radicals upon thermal decomposition and mimics the formation of lipid peroxyl radicals. Interaction of carbon-centred AP radicals with SECO 2 and SDG 1 provides a good model to study the antioxidant reactions of SECO 2 in vitro. p*The relative antioxidant capacity of the flaxseed lignans versus BHT 17, in two model systems, was determined. The stoichiometric ratio for SECO 2 and SDG 1 were 1.5 and 1.1-1.2, respectively, compared to BHT 17 (2.0). The induction time by Rancimat analyzer measured inhibition of autoxidation mediated by flaxseed lignans SECO, SDG and SDG polymer in comparison with BHT 17. The induction time data demonstrated that SECO 2 protected canola oil better than either SDG 1 or SDG polymer 3. <p>These results are important for better understanding about the chemistry behind flaxseed lignan antioxidant activities. This study provided useful evidence that flaxseed lignans can be used as natural antioxidants.

This thesis describes the convenient routes and the preparation conditions (temperature, oxygen partial presssure) which lead to the formation of single phase materials within the quaternary system Cu-Ni-Fe-O. The investigated compositions are the solid solutions CuxNi1-xFe2O4, the ferrites occurring in the phase triangle Cu0.5Ni0.5Fe2O4 -Cu0.9Fe2.1O4 - Cu0.5Fe2.5O4 and some copper-nickel oxide solid solutions. Three synthesis routes have been used, namely (i) the preparation and the thermal decomposition of freeze-dried carboxylate precursors, (ii) the preparation and the oxidation of intermetallic phases and (iii) the preparation and the heat treatment in air of mixed oxide/metallic powders. The thermal decomposition of freeze-dried Cu-Ni-Fe formate has been found as a suitable method for preparing single spinel phases within the Cu-Ni-Fe-O system. In comparison with the conventional solid state reaction, the required temperature is much lower. Concerning the solid solution CuxNi1-xFe2O4 , a single phase spinel is formed at 1000¢XC for x &amp;lt; 0.7; for CuO is identified as second phase. In this latter range the formation of a pure phase required an increase of the iron content in the mixture. The other single spinel phases in the phase triangle Cu0.5Ni0.5Fe2O4 - Cu0.9Fe2.1O4 - Cu0.5Fe2.5O4 have been synthesized under special synthesis p(O2)/T-conditions. For copper ferrites Cu1-xFe2+xO4 with x ?­ 0.1, 0.2, 0.33, 0.4 and 0.5, the change in the conductivity with the temperature is irreversible. The deviation from the linearity of the conductivity ?ã as a function of the temperature occurs due to the thermal history of these samples. The saturation magnetic moment (nB) at 5K, of some synthesized CuxNi1-xFe2O4 compounds has been determined. It has been found that nB increases with the nickel content in the ferrite sample.

What will happen to ecosystems if species continue to go extinct at the high rates seen today? Although ecosystems are often threatened by a myriad of physical or chemical stressors, recent evidence has suggested that the loss of species may have impacts on the functions and services of ecosystems that equal or exceed other major environmental disturbances. The underlying causes that link species diversity to ecosystem functioning include species niche complementarity, facilitative interactions, or selection effects, which cause process rates to be enhanced in more diverse communities. Interference competition, antagonistic interactions, or negative selection effects may otherwise reduce the efficiency or resource processing in diverse communities. While several of these mechanisms have been investigated in controlled experiments, there is an urgent need to understand how species diversity affects ecosystem functioning in nature, where variability of both biotic and abiotic factors is usually high. Species functional traits provide an important conceptual link between the effects of disturbances on community composition and diversity, and their ultimate outcomes for ecosystem functioning. Within this framework, I investigated relationships between the decomposition of leaf litter, a fundamental ecosystem process in stream ecosystems, and the composition and diversity of functional traits within the detritivore feeding guild. These include traits related to species habitat and resource preferences, phenology, and size. I focused on disentangling the biotic and abiotic drivers, including functional diversity, regulating ecosystem functioning in streams in a series of field experiments that captured real-world environmental gradients. Leaf decomposition rates were assessed using litter-bags of 0.5 and 10 mm opening size which allow the quantification of microbial and invertebrate + microbial contributions, respectively, to litter decomposition. I also used PVC chambers where leaf litter and a fixed number of invertebrate detritivores were enclosed in the field for a set time-period. The chemical characterisation of stream detritivores and leaf litter, by means of their nitrogen, phosphorus, and carbon concentration, was used to investigate how stoichiometric imbalance between detritivores and leaf litter may affect consumer growth and resource consumption. I found that the diversity and composition of functional traits within the stream detritivore feeding guild sometimes had effects on ecosystem functioning as strong as those of other major biotic factors (e.g. detritivore density and biomass), and abiotic factors (e.g. habitat complexity and agricultural stressors). However, the occurrence of diversity-functioning relationships was patchy in space and time, highlighting ongoing challenges in predicting the role of diversity a priori. The stoichiometric imbalance between consumers and resource was also identified as an important driver of functioning, affecting consumer growth rates, but not leaf decomposition rates. Overall, these results shed light on the understanding of species functional diversity effect on ecosystems, and indicate that the shifts in the functional diversity and composition of consumer guilds can have important outcomes for the functioning of stream ecosystems.

19 Dec 2004. / Published through the Information Bridge: DOE Scientific and Technical Information. "IS-T 2117" Guodong Du. 12/19/2004. Report is also available in paper and microfiche from NTIS.

Made available in DSpace on 2016-06-02T19:19:55Z (GMT). No. of bitstreams: 1 ABREU_Caio_2013.pdf: 2028939 bytes, checksum: 65ae46e6485e945dd8307afeb9a40953 (MD5) Previous issue date: 2013-02-19 / This work studied ultrathin films of titanium oxide were deposited on two substrates, such as pure Si (100) and glass corning 7059, by using r.f. magnetron sputtering with different oxygen flows and maintaining another parameters constant. For the purpose of this work, while keeping all parameters constant, varying only the oxygen flow (reactive gas), it was expected to identify the flow of transition between films of substoichiometric TiOx and TiO2 films, and analyze whether there forming nanostructured TiO2 films because the literature shows that variation of control parameters important characteristics of the nanoparticles as medium sized fraction of coverage of the substrate crystal structure and stoichiometry. The chemistries of the ultrathin films were analyzed through technique of Rutherford Backscattering Spectroscopy (RBS), the surface morphology by Atomic Force Microscopy (AFM), the crystallinity by X-Ray Diffraction (XRD) and the optical properties by UV-vis Spectroscopy. Were deposited ultrathin films with substoichiometric compositions for depositions with 0.10% O2 and 0.35% O2. For depositions between 0.67% O2 and 6.00% O2, films were obtained with concentrations of [O]/[Ti] of about 1.9, near the chemical composition of titanium dioxide (TiO2). Films with concentrations close to the TiO2 showed amorphous, but with characteristics of formation of anatase phase. The optical properties presented optical gap values between 3.33 eV and 3,78 eV and had no significant variation, as calculated by E03, E04 and ETauc methods. The roughness of the films decreased proportionally with increasing oxygen flow in the depositions. / No presente trabalho foram estudados filmes finos de óxido de titânio, depositados em dois substratos, Si (100) e vidro Corning 7059, por meio da utilização da técnica de pulverização catódica por rádio freqüência - magnetron sputtering r.f. - com diferentes fluxos de oxigênio e os outros parâmetros mantidos constantes. Com isso, esperava-se identificar o fluxo de transição entre os filmes de TiOx subestequiométricos e filmes de TiO2, analisar se haveria formação de filmes de TiO2 nanoestruturados e diferenças entre os gaps ópticos. As composições químicas dos filmes finos foram analisadas por meio da técnica de espectroscopia de retroespalhamento Rutherford (RBS), a morfologia da superfície por Microscopia de Força Atômica (AFM), a cristalinidade por difração de raios-X (XRD) e as propriedades ópticas por espectroscopia UV-Visível. Foram depositados filmes finos com composições subestequiométricas nas deposições com 0,10% de O2 e 0,35% de O2. Para deposições de O2 entre 0,67% e 6,00%, os filmes foram obtidos com concentrações de [O]/[Ti] de aproximadamente 1,9, ou seja, perto da composição química do dióxido de titânio (TiO2). Filmes com concentrações de [O]/[Ti] próximas ao TiO2 apresentaram-se amorfas, mas com características de formação de fase anatase. As propriedades ópticas não apresentaram nenhuma variação significativa nos valores de gap óptico, com valor entre 3,33 eV e 3,78 eV, calculado pelos métodos E03, E04 e ETauc. A rugosidade dos filmes diminuiu proporcionalmente com o aumento do fluxo de oxigênio nas deposições.

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Made available in DSpace on 2014-10-09T12:53:18Z (GMT). No. of bitstreams: 0 / Made available in DSpace on 2014-10-09T13:59:02Z (GMT). No. of bitstreams: 0 / O compósito de manganito de lantânio dopado com estrôncio (La1-xSrxMnO3 - LSM) e zircônia estabilizada com ítria (ZrO2/Y2O3 - YSZ), tem sido indicado como catodo das células a combustível de óxido sólido, por apresentar melhor desempenho como eletrodo catódico na região da tripla fase reacional (TRIPLE PHASE BOUNDARY - TPB), formada na interface entre eletrólito e eletrodo. Para as temperaturas superiores a 1100 °C, o LSM e o YSZ podem-se reagir formando-se zirconatos de lantânio (La2Zr2O7 - LZO) e zirconatos de estrôncio (SrZrO3 - SZO). Neste sentido, o presente trabalho pretende contribuir no estudo da formação das fases LZO e SZO, estudando diferentes proporções mássicas entre LSM e YSZ e temperaturas de sinterização variando-se entre 1000 °C e 1400 °C. Para obtenção dos pós precursores foram adotadas as rotas de co-precitação para a obtenção do YSZ e mistura convencional de pós para preparação de LSM. Para a preparação do compósito LSM/YSZ, as composições químicas do LSM sintetizado neste trabalho foram para as duas concentrações 30 e 40 % mol de Sr (LSM7 e LSM6) e para YSZ 10 % mol de ítria. Os resultados obtidos por fluorescência de raios X mostraram que as rotas adotadas para síntese de pós foram eficazes na obtenção das composições LSM6, LSM7 e YSZ, com valores próximos aos estequiométricos. As proporções mássicas estudadas foram: 50 % de LSM e 50 % de YSZ (1:1), 25 % de LSM e 75 % de YSZ (1:3) e 75 % de LSM e 25 % de YSZ (3:1). Tais proporções de misturas foram conformadas e submetidas a diferentes condições de temperaturas e tempos de sinterização: 1000 °C, 1200 °C, 1300 °C, 1350 °C e 1400 °C, por 4 e 8 horas. Tanto os valores de tamanho médio das partículas como os valores da área de superfície específica para a mistura de LSM6/YSZ e LSM7/YSZ, após a mistura em um moinho atritor e em diferentes proporções mássicas, são da mesma ordem de grandeza. Na análise por difração de raios X dos compósitos LSM6/YSZ e LSM7/YSZ preparados na proporção 1:1 submetidos às temperaturas a 1200 ºC e a 1400 ºC por 4 horas, verificou-se que não há formação de fases secundárias tais como LZO e SZO. Para estas amostras sinterizadas nestas duas temperaturas, o valor da porosidade obtida é maior para a amostra sinterizada a 1200 ºC. Para as amostras LSM6/YSZ e LSM7/YSZ, com proporções mássicas de 1:3, 1:1 e 3:1, sinterizadas a 1300 °C e 1350 °C, por 8 horas, observou-se o aparecimento de fases de LZO e SZO. Verificou-se também que as intensidades destas fases são maiores para proporção mássica de 3:1, ou seja, para amostras contendo 75 % em massa de LSM no compósito. Para preparação de filmes finos do compósito LSM/YSZ para células a combustível do tipo SOFC, de acordo com as condições adotadas neste trabalho, a temperatura de sinterização adequada é de 1200 °C por tempo abaixo ou igual a 8 horas, sendo que, em tais condições não há formação de fases secundárias como LZO e SZO. / Dissertação (Mestrado) / IPEN/D / Instituto de Pesquisas Energéticas e Nucleares - IPEN-CNEN/SP