Disparador MIDI para batería

La batería acústica es un instrumento de percusión muy complejo que requiere altas dosis de coordinación, interdependencia y musicalidad. Los músicos necesitan nuevas formas de desarrollarse y expresarse. Buscando caminos que mejoren su comprensión. Así también los aprendices requieren herramientas para poder disfrutar del instrumento musical. Construir un disparador MIDI mejora esas prestaciones. Aumenta la cantidad de soni-dos, es adaptable a la forma de tocar y simplifica los conceptos evitando problemas a los principiantes. Actualmente existen escasos disparadores MIDI en el mercado. En su lugar se presen-tan módulos electrónicos con altas características, complejos de utilizar y con alto coste. El proyecto a implementar consiste en un disparador MIDI, un equipo cuyo fin es cap-tar los impactos que efectúa un músico; un percusionista. En el proyecto se estudian y analizan las problemáticas a las que se enfrenta este tipo de dispositivo, se propondrá distintas soluciones de concepto y, finalmente se construirá dicho sistema que será probado en un ordenador personal. Con un ideal en mente, emular una batería acústica y ser un proyecto abierto en el sentido de ser modulable y ampliable. ABSTRACT. Drum set is a very complex percussion instrument that requires a lot of coordination, interdependence and musicality. Musicians need new ways to develop and express themselves, as well as learners re-quire tools to enjoy the musical instrument. Build a MIDI drum trigger improves these benefits. It increases the amount of sounds, is customizable and simplifies problems for drummer beginners. There are currently a few MIDI triggers on the market. Instead, electronic modules with high features, complex to use and they are sold at high cost. The aim of the project is to implement a MIDI drum trigger, a kit to capture the impact that percussionist makes. The project studies and analyzes the problems which this type of device. Different solutions concept will be proposed and finally the system will be built. With an ideal in mind, emulate an acoustic drum.

Optimización de la gasificación de lodos de estaciones depuradoras de aguas residuales urbanas para minimizar la formación de alquitranes

La gasificación de lodos de depuración es una alternativa atractiva para generar gases combustibles como H2 y CO. A su vez, estos gases pueden emplearse como materias primas para la obtención de productos químicos orgánicos y combustibles líquidos. Sin embargo, la gasificación no está exenta de problemas como el ligado a la generación de residuos sólidos y alquitrán. El alquitrán en el gas puede ser un inconveniente para emplear el gas como combustible por las obstrucciones y corrosión en los equipos. Dado que las condiciones de gasificación influyen en la producción de alquitrán, este trabajo de investigación se ha centrado en analizar la influencia de parámetros como la temperatura, la carga de alimentación, el tamaño de partícula, el agente gasificante y la utilización de catalizadores en la gasificación en lecho fluidizado de lodos de depuración. Adicionalmente a la medición del efecto de los anteriores parámetros en la producción y composición del alquitrán, también se ha cuantificado su influencia en la producción y composición del gas y en producción del residuo carbonoso. Los resultados muestran que el incremento de la carga de alimentación (kg/h.m2) provoca el descenso de la producción de gas combustible y el incremento del residuo carbonoso y del alquitrán debido a la reducción del tiempo de residencia del gas lo que supone un menor tiempo disponible para las reacciones gas-gas y gas-sólido ligadas a la conversión del alquitrán y del residuo carbonoso en gases combustibles. También se ha comprobado que, el aumento del tamaño de partícula, al incrementar el tiempo de calentamiento de ésta, tiene un efecto similar en los productos de la gasificación que el derivado del incremento en la carga de alimentación. La utilización de una temperatura de gasificación alta (850 ºC), el empleo de aire-vapor como agente gasificante y/o catalizadores primarios como la dolomía consiguen reducir la producción de alquitrán. ABSTRACT Gasification of sewage sludge is an attractive alternative for generating of fuel gases such as H2 and CO. These gases, in turn, can be used as raw materials for the production of organic chemicals and liquid fuel. However, gasification is not without problems as the linked ones to production of char and tar. The tar in the gas can be an inconvenience for to use it as fuel by the problems of blockage and corrosion in the equipments. Since the gasification conditions affect the production of tar, this research has focused on analysing the influence of parameters such as temperature, throughput, the particle size, the gasifying agent and the use of catalysts in the fluidized bed gasification of sewage sludge. In addition to measuring the effect of the above parameters on the production and composition of the tar, it has also been quantified their influence on the yield and composition of the gas and char production. The results show that higher throughput (kg/h.m2) leads to a reduction of fuel gas production and an increase in the production of char and tar, this owes to a lower of gas residence time or what is the same thing less time available for gas-solid and gas-gas reactions attached to the conversion of tar and char to fuel gases. There has also been proven that the rising in particle size, by the increasing heating time of it, has a similar effect in the products of gasification that the results by the rise in the throughput. The applications a high gasification temperature (850 ° C), the use of air-steam as gasifying agent and/or dolomite as primary catalysts are able to reduce the production of tar.

AS BRIGAS DIVINAS DE INANA: Reconstrução feminista de repressão e resistência em torno de uma deusa suméria

As análises desta tese, baseadas numa hermenêutica feminista libertadora, têm como centro a figura de Inana, a deusa mais importante e mais popular da Suméria, que predominou, sob o nome de I tar, também nos panteões mesopotâmicos posteriores. O Capítulo 1 oferece uma reconstrução da vida na Suméria, desde os tempos neolíticos até os inícios do Período Babilônico Antigo (aproximadamente de 5000 a 2000 aEC), com especial atenção para dados sobre mulheres e para aspectos de gênero. O Capítulo 2 apresenta documentos pré-sargônicos, iconográficos e filológicos, relacionados com a figura e o culto de Inana, oferecendo as primeiras reflexões sobre aspectos particulares e conflitos que mostram sua posição especial na religião na Suméria e na sua crescente patriarcalização. No Capítulo 3, esses aspectos e conflitos são discutidos enfocando tradições de Inana como Senhora da Eana, dos Me e de Kur, com especial atenção para os mitos Inana e a Eana , Inana e os Me e Inana e o Inframundo (ETCSL 1.3.5; 1.3.1; 1.4.1). É mostrado que o mito Inana e a Eana é o resultado de manipulações para legitimar o culto de An nesse templo de Inana, que Inana e os Me reflete atitudes de resistência contra tentativas de seu desapoderamento, e que Inana e o Inframundo é composto de mitos diferentes que evidenciam vários conflitos relacionados com funções e poderes de Inana. Desse modo mostra-se que os conflitos em torno de Inana refletem repressões e resistências humanas no âmbito de uma sociedade quiriarcal e da crescente patriarcalização de sua religião. Embora a atuação política e religiosa de mulheres em sociedades de hoje não necessite de legitimações a partir de exemplos provenientes de religiões antigas, a reconstrução e memória feministas de tais exemplos podem servir de estímulo para tal atuação quando busca construir uma outra imagem do divino e quando luta por um mundo de igualdade em direitos e dignidade para todas as pessoas.(AU)

AS BRIGAS DIVINAS DE INANA: Reconstrução feminista de repressão e resistência em torno de uma deusa suméria

As análises desta tese, baseadas numa hermenêutica feminista libertadora, têm como centro a figura de Inana, a deusa mais importante e mais popular da Suméria, que predominou, sob o nome de I tar, também nos panteões mesopotâmicos posteriores. O Capítulo 1 oferece uma reconstrução da vida na Suméria, desde os tempos neolíticos até os inícios do Período Babilônico Antigo (aproximadamente de 5000 a 2000 aEC), com especial atenção para dados sobre mulheres e para aspectos de gênero. O Capítulo 2 apresenta documentos pré-sargônicos, iconográficos e filológicos, relacionados com a figura e o culto de Inana, oferecendo as primeiras reflexões sobre aspectos particulares e conflitos que mostram sua posição especial na religião na Suméria e na sua crescente patriarcalização. No Capítulo 3, esses aspectos e conflitos são discutidos enfocando tradições de Inana como Senhora da Eana, dos Me e de Kur, com especial atenção para os mitos Inana e a Eana , Inana e os Me e Inana e o Inframundo (ETCSL 1.3.5; 1.3.1; 1.4.1). É mostrado que o mito Inana e a Eana é o resultado de manipulações para legitimar o culto de An nesse templo de Inana, que Inana e os Me reflete atitudes de resistência contra tentativas de seu desapoderamento, e que Inana e o Inframundo é composto de mitos diferentes que evidenciam vários conflitos relacionados com funções e poderes de Inana. Desse modo mostra-se que os conflitos em torno de Inana refletem repressões e resistências humanas no âmbito de uma sociedade quiriarcal e da crescente patriarcalização de sua religião. Embora a atuação política e religiosa de mulheres em sociedades de hoje não necessite de legitimações a partir de exemplos provenientes de religiões antigas, a reconstrução e memória feministas de tais exemplos podem servir de estímulo para tal atuação quando busca construir uma outra imagem do divino e quando luta por um mundo de igualdade em direitos e dignidade para todas as pessoas.(AU)

Functional copies of a human gene can be directly isolated by transformation-associated recombination cloning with a small 3′ end target sequence

Unique, small sequences (sequence tag sites) have been identified at the 3′ ends of most human genes that serve as landmarks in genome mapping. We investigated whether a single copy gene could be isolated directly from total human DNA by transformation-associated recombination (TAR) cloning in yeast using a short, 3′ unique target. A TAR cloning vector was constructed that, when linearized, contained a small amount (381 bp) of 3′ hypoxanthine phosphoribosyltransferase (HPRT) sequence at one end and an 189-bp Alu repeat at the other end. Transformation with this vector along with human DNA led to selective isolations of the entire HPRT gene as yeast artificial chromosomes (YACs) that extended from the 3′ end sequence to various Alu positions as much as 600 kb upstream. These YACs were retrofitted with a NeoR and a bacterial artificial chromosome (BAC) sequence to transfer the YACs to bacteria and subsequently the BACs to mouse cells by using a Neo selection. Most of the HPRT isolates were functional, demonstrating that TAR cloning retains the functional integrity of the isolated material. Thus, this modified version of TAR cloning, which we refer to as radial TAR cloning, can be used to isolate large segments of the human genome accurately and directly with only a small amount of sequence information.

Inhibition of gene expression in human cells through small molecule-RNA interactions

Small molecules that bind their biological receptors with high affinity and selectivity can be isolated from randomized pools of combinatorial libraries. RNA-protein interactions are important in many cellular functions, including transcription, RNA splicing, and translation. One example of such interactions is the mechanism of trans-activation of HIV-1 gene expression that requires the interaction of Tat protein with the trans-activation responsive region (TAR) RNA, a 59-base stem-loop structure located at the 5′ end of all nascent HIV-1 transcripts. Here we demonstrate the isolation of small TAR RNA-binding molecules from an encoded combinatorial library. We have made an encoded combinatorial tripeptide library of 24,389 possible members from d-and l-alpha amino acids on TentaGel resin. Using on-bead screening we have identified a small family of mostly heterochiral tripeptides capable of structure-specific binding to the bulge loop of TAR RNA. In vitro binding studies reveal stereospecific discrimination when the best tripeptide ligand is compared with diastereomeric peptide sequences. In addition, the most strongly binding tripeptide was shown to suppress transcriptional activation by Tat protein in human cells with an IC50 of ≈50 nM. Our results indicate that tripeptide RNA ligands are cell permeable, nontoxic to cells, and capable of inhibiting expression of specific genes by interfering with RNA-protein interactions.

Behavioral responses of Escherichia coli to changes in redox potential.

Escherichia coli bacteria sensed the redox state in their surroundings and they swam to a niche that had a preferred reduction potential. In a spatial redox gradient of benzoquinone/benzoquinol, E. coli cells migrated to form a sharply defined band. Bacteria swimming out of either face of the band tumbled and returned to the preferred conditions at the site of the band. This behavioral response was named redox taxis. Redox molecules, such as substituted quinones, that elicited redox taxis, interact with the bacterial electron transport system, thereby altering electron transport and the proton motive force. The magnitude of the behavioral response was dependent on the reduction potential of the chemoeffector. The Tsr, Tar, Trg, Tap, and CheR proteins, which have a role in chemotaxis, were not essential for redox taxis. A cheB mutant had inverted responses in redox taxis, as previously demonstrated in aerotaxis. A model is proposed in which a redox effector molecule perturbs the electron transport system, and an unknown sensor in the membrane detects changes in the proton motive force or the redox status of the electron transport system, and transduces this information into a signal that regulates phosphorylation of the CheA protein. A similar mechanism has been proposed for aerotaxis. Redox taxis may play an important role in the distribution of bacterial species in natural environments.

A three-hybrid system to detect RNA-protein interactions in vivo.

RNA-protein interactions are pivotal in fundamental cellular processes such as translation, mRNA processing, early development, and infection by RNA viruses. However, in spite of the central importance of these interactions, few approaches are available to analyze them rapidly in vivo. We describe a yeast genetic method to detect and analyze RNA-protein interactions in which the binding of a bifunctional RNA to each of two hybrid proteins activates transcription of a reporter gene in vivo. We demonstrate that this three-hybrid system enables the rapid, phenotypic detection of specific RNA-protein interactions. As examples, we use the binding of the iron regulatory protein 1 (IRP1) to the iron response element (IRE), and of HIV trans-activator protein (Tat) to the HIV trans-activation response element (TAR) RNA sequence. The three-hybrid assay we describe relies only on the physical properties of the RNA and protein, and not on their natural biological activities; as a result, it may have broad application in the identification of RNA-binding proteins and RNAs, as well as in the detailed analysis of their interactions.

A point mutation in the HIV-1 Tat responsive element is associated with postintegration latency.

Study of the mechanism of HIV-1 postintegration latency in the ACH2 cell line demonstrates that these cells failed to increase HIV-1 production following treatment with exogenous Tat. Reasoning that the defect in ACH2 cells involves the Tat response, we analyzed the sequence of tat cDNA and Tat responsive element (TAR) from the virus integrated in ACH2. Tat cDNA sequence is closely related to that of HIV LAI, and the encoded protein is fully functional in terms of long terminal repeat (LTR) transactivation. Cloning of a region corresponding to the 5'-LTR from ACH2, however, identified a point mutation (C37 -> T) in TAR. This mutation impaired Tat responsiveness of the LTR in transient transfection assays, and the measured defect was complemented in cells that had been treated with tetradecanoyl phorbol acetate or tumor necrosis factor type alpha (TNF-alpha). A compensatory mutation in TAR (G28 -> A), designed to reestablish base pairing in the TAR hairpin, restored wild-type Tat responsiveness. When the (C37 -> T) mutation was introduced in an infectious clone of HIV-1, no viral production was measured in the absence of TNF-alpha, whereas full complementation was observed when the infection was conducted in the presence of TNF-alpha or when a compensatory mutation (G28 -> A) was introduced into TAR. These experiments identify a novel mutation associated with HIV-1 latency and suggest that alterations in the Tat-TAR axis can be a crucial determinant of the latent phenotype in infected individuals.

Human immunodeficiency virus type-1 Tat is an integral component of the activated transcription-elongation complex.

The human immunodeficiency virus type 1 transactivator protein, Tat, stimulates transcriptional elongation from the viral long terminal repeat. To test whether Tat associates directly with activated transcription complexes, we have used the lac repressor protein (LacR) to "trap" elongating RNA polymerases. The arrested transcription complexes were purified by binding biotinylated templates to streptaviridin-coated magnetic beads. Transcription complexes were released from the magnetic beads following cleavage of the templates with restriction enzymes and were immunoblotted with antibodies to Tat, LacR and RNA polymerase II. The Tat protein copurified with RNA polymerase bound to wild-type templates but did not copurify with transcription complexes prepared by using templates carrying mutations in the transactivation response element (TAR) RNA. We conclude that Tat and cellular cofactors become attached to the transcription complex during its transit through TAR.

Human immunodeficiency virus type 1 and 2 Tat proteins specifically interact with RNA polymerase II.

The Tat-responsive region (TAR) element is a critical RNA regulatory element in the human immunodeficiency virus (HIV) long terminal repeat, which is required for activation of gene expression by the transactivator protein Tat. Recently, we demonstrated by gel-retardation analysis that RNA polymerase II binds to TAR RNA and that Tat prevents this binding even when Tat does not bind to TAR RNA. These results suggested that direct interactions between Tat and RNA polymerase II may prevent RNA polymerase II pausing and lead to Tat-mediated increases in transcriptional elongation. To test this possibility, we performed protein interaction studies with RNA polymerase II and both the HIV-1 and the closely related HIV-2 Tat protein. These studies indicated that both the HIV-1 and HIV-2 Tat proteins could specifically interact with RNA polymerase II. Mutagenesis of both HIV-1 and HIV-2 Tat demonstrated that the basic domains of both the HIV-1 and HIV-2 Tat proteins were required for this interaction. Furthermore, "far Western" analysis suggested that the largest subunit of RNA polymerase II was the site for interaction with Tat. The interactions between Tat and RNA polymerase II were of similar magnitude to those detected between RNA polymerase II and the cellular transcription factor RAP30, which stably associates with RNA polymerase II during transcriptional elongation. These studies are consistent with the model that RNA polymerase II is a cellular target for Tat resulting in Tat-mediated increases in transcriptional elongation from the HIV long terminal repeat.

Specific cloning of human DNA as yeast artificial chromosomes by transformation-associated recombination.

DNA molecules undergoing transformation into yeast are highly recombinogenic, even when diverged. We reasoned that transformation-associated recombination (TAR) could be employed to clone large DNAs containing repeat sequences, thereby eliminating the need for in vitro enzymatic reactions such as restriction and ligation and reducing the amount of DNA handling. Gently isolated human DNA was transformed directly into yeast spheroplasts along with two genetically marked (M1 and M2) linearized vectors that contained a human Alu sequence at one end and a telomere sequence at the other end (Alu-CEN-M1-TEL and Alu-M2-TEL). Nearly all the M1-selected transformants had yeast artificial chromosomes (YACs) containing human DNA inserts that varied in size from 70 kb to > 600 kb. Approximately half of these had also acquired the unselected M2 marker. The mitotic segregational stability of YACs generated from one (M1) or two (M1 and M2) vector(s) was comparable, suggesting de novo generation of telomeric ends. Since no YACs were isolated when rodent DNAs or a vector lacking an Alu sequence was used, the YACs were most likely the consequence of TAR between the repeat elements on the vector(s) and the human DNA. Using the BLUR13 Alu-containing vector, we demonstrated that human DNA could be efficiently cloned from mouse cells that contained a single human chromosome 16. The distribution of cloned DNAs on chromosome 16 was determined by fluorescence in situ hybridization. We propose that TAR cloning can provide an efficient means for generating YACs from specific chromosomes and subchromosome fragments and that TAR cloning may be useful for isolating families of genes and specific genes from total genome DNA.

Chemotactic signal integration in bacteria.

Chemotactic signaling in Escherichia coli involves transmission of both negative and positive signals. In order to examine mechanisms of signal processing, behavioral responses to dual inputs have been measured by using photoactivable "caged" compounds, computer video analysis, and chemoreceptor deletion mutants. Signaling from Tar and Tsr, two receptors that sense amino acids and pH, was studied. In a Tar deletion mutant the photoactivated release of protons, a Tsr repellent, and of serine, a Tsr attractant, in separate experiments at pH 7.0 resulted in tumbling (negative) or smooth-swimming (positive) responses in ca. 50 and 140 ms, respectively. Simultaneous photorelease of protons and serine resulted in a single tumbling or smooth-swimming response, depending on the relative amounts of the two effectors. In contrast, in wild-type E. coli, proton release at pH 7.0 resulted in a biphasic response that was attributed to Tsr-mediated tumbling followed by Tar-mediated smooth-swimming. In wild-type E. coli at more alkaline pH values the Tar-mediated signal was stronger than the Tsr signal, resulting in a strong smooth-swimming response preceded by a diminished tumbling response. These observations imply that (i) a single receptor time-averages the binding of different chemotactic ligands generating a single response; (ii) ligand binding to different receptors can result in a nonintegrated response with the tumbling response preceding the smooth-swimming response; (iii) however, chemotactic signals of different intensities derived from different receptors can also result in an apparently integrated response; and (iv) the different chemotactic responses to protons at neutral and alkaline pH may contribute to E. coli migration toward neutrality.

Specific binding of RNA polymerase II to the human immunodeficiency virus trans-activating region RNA is regulated by cellular cofactors and Tat.

The regulation of human immunodeficiency virus type 1 (HIV-1) gene expression in response to Tat is dependent on an element downstream of the HIV-1 transcriptional initiation site designated the trans-activating region (TAR). TAR forms a stable stem-loop RNA structure in which a 3-nt bulge structure and a 6-nt loop structure are important for Tat activation. In the absence of Tat, the HIV-1 promoter generates so-called short or nonprocessive transcripts terminating at +60, while in the presence of Tat the synthesis of these short transcripts is markedly decreased and transcripts that extend through the 9.0-kb HIV-1 genome are synthesized. Tat effects on transcriptional elongation are likely due to alterations in the elongation properties of RNA polymerase II. In this study we demonstrated that a set of cellular cofactors that modulate the binding of the cellular protein TRP-185 to the TAR RNA loop sequences also functioned to markedly stimulate the specific binding of hypophosphorylated (IIa) and hyperphosphorylated (IIo) RNA polymerase II to TAR RNA. The concentrations of RNA polymerase II required for this interaction with TAR RNA were similar to those required to initiate in vitro transcription from the HIV-1 long terminal repeat. RNA gel retardation analysis with wild-type and mutant TAR RNAs indicated that the TAR RNA loop and bulge sequences were critical for the binding of RNA polymerase II. The addition of wild-type but not mutant Tat protein to gel retardation analysis with TAR RNA and RNA polymerase II resulted in the loss of binding of RNA polymerase II binding to TAR RNA. These results suggest that Tat may function to alter RNA polymerase II, which is paused due to its binding to HIV-1 TAR RNA with resultant stimulation of its transcriptional elongation properties.

The bend in RNA created by the trans-activation response element bulge of human immunodeficiency virus is straightened by arginine and by Tat-derived peptide.

The trans-activation response element (TAR) found near the 5' end of the viral RNA of the human immunodeficiency virus contains a 3-nt bulge that is recognized by the virally encoded trans-activator protein (Tat), an important mediator of transcriptional activation. Insertion of the TAR bulge into double-stranded RNA is known to result in reduced electrophoretic mobility, suggestive of a bulge-induced bend. Furthermore, NMR studies indicate that Arg causes a change in the structure of the TAR bulge, possibly reducing the bulge angle. However, neither of these effects has been quantified, nor have they been compared with the effects of the TAR-Tat interaction. Recently, an approach for the quantification of bulge-induced bends has been described in which hydrodynamic measurements, employing the method of transient electric birefringence, have yielded precise estimates for the angles of a series of RNA bulges, with the angles ranging from 7 degrees to 93 degrees. In the current study, transient electric birefringence measurements indicate that the TAR bulge introduces a bend of 50 degrees +/- 5 degrees in the absence of Mg2+. Addition of Arg leads to essentially complete straightening of the helix (to < 10 degrees) with a transition midpoint in the 1 mM range. This transition demonstrates specificity for the TAR bulge: no comparable transition was observed for U3 or A3 (control) bulges with differing flanking sequences. An essentially identical structural transition is observed for the Tat-derived peptide, although the transition midpoint for the latter is near 1 microM. Finally, low concentrations of Mg2+ alone reduce the bend angle by approximately 50%, consistent with the effects of Mg2+ on other pyrimidine bulges. This last observation is important in view of the fact that most previous structural/binding studies were performed in the absence of Mg2+.