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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
121

Structure quaternaire des récepteurs de chimiokines CXCR4 et CCR2 et interaction avec leurs effecteurs

Armando, Sylvain 11 1900 (has links)
Thèse réalisée en cotutelle avec l'université Montpellier2 dans le laboratoire de pharmacologie moléculaire de Jean-Philippe Pin à l'institut de génomique fonctionnelle (IGF), Montpellier, France. / Les récepteurs couplés aux protéines G (RCPG) sont une famille très diversifiée de protéines membranaires capables de répondre à un grand nombre de signaux chimiques tels que des photons, des molécules odorantes, ou des hormones. En plus de cette diversité, l’étude des RCPG montre que des associations protéiques spécifiques multiplient les possibilités de signalisation de chacun de ces récepteurs. En permettant d’atténuer, de potentialiser, ou de générer une nouvelle voie de signalisation, l’association des RCPG en oligomères s’avère une importante source de diversité. L’utilisation du transfert d’énergie de résonance de bioluminescence (BRET) qui permet de détecter les interactions protéiques a révélé de nombreuses associations de RCPG. Durant cette thèse, des outils ont été développés pour combiner efficacement le BRET à des essais de complémentation de protéines (PCA) dans le but de savoir si l’oligomérisation des RCPG pouvait impliquer plus de deux récepteurs. Les résultats présentés montrent que les récepteurs de chimiokines CXCR4 et CCR2 forment des homo et hétéro tétramères, et que l’activation d’un dimère CCR2 peut moduler la conformation d’un dimère CXCR4 par un changement conformationnel trans-récepteur. La coopérativité négative de liaison de ligand qui a été démontrée auparavant entre CXCR4 et CCR2 dans des lymphocytes T CD4+ exprimant les récepteurs de manière endogène confirme la validité biologique de cette interaction. Les données présentées suggèrent également que ces complexes peuvent engager les effecteurs Gαi et β-arrestine2, indiquant qu’ils représentent la forme fonctionnelle de ces récepteurs. Enfin, nous avons pu confirmer que chaque récepteur de l’hétérodimère CXCR4-CCR2 est impliqué dans l’engagement des effecteurs lors de l’activation de CCR2. Un autre niveau de complexité dans la signalisation des RCPG est atteint par leur capacité à coupler de multiples protéines G. La liaison du facteur dérivé des cellules stromales (SDF-1) au récepteur CXCR4 permet la migration des lymphocytes T par une voie de signalisation dépendante de la protéine Gαi. Nous avons pu démontrer en revanche que la migration des cellules de cancer du sein était initiée par un couplage de CXCR4 à la voie Gα13-Rho pour former des métastases dans des organes distants. Enfin, un dernier niveau de régulation des RCPG a été abordé par l’étude de la phosphorylation de CXCR4 suite à son activation, qui permet la désensibilisation du récepteur et l’engagement de voies de signalisation dépendantes de la β-arrestine. Il apparaît que la désensibilisation de la voie du calcium serait médiée par la phosphorylation de CXCR4 par les kinases des RCPG (GRK) GRK2 et GRK6 et le recrutement de β- arrestine2, alors GRK3, GRK6 et la β-arrestine1 potentialiseraient l’activation des kinases régulées par les signaux extracellulaires (ERK1/2). Nous suggérons également que c’est la phosphorylation de l’extrémité C-terminale de CXCR4 qui permettrait son association avec la β-arrestine. / G protein-coupled receptors (GPCRs) are a diverse family of membrane proteins capable of responding to a large number of extracellular stimuli including photons, odorant molecules and hormones. In addition to this diversity, it has been shown that GPCRs form specific protein:protein interactions, multiplying the signalling possibilities of each of these receptors. With the ability to diminish, to potentiate or even generate new signalling pathways, the oligomeric association of GPCRs plays an important role in generating this diversity. The use of bioluminescence resonance energy transfer (BRET), which allows the detection of interactions among proteins, has revealed numerous associations between GPCRs. During this thesis, tools have been developed that effectively combine BRET with protein complementation assays (PCA) with the goal of determining if interactions between GPCRs could involve more than two receptors. The results show that the chemokine receptors CXCR4 and CCR2 form both homo and hetero tetramers, and that the activation of a dimer of CCR2 can modulate the conformation of a CXCR4 dimer through a transreceptor conformational change. Negative cooperativity of ligand binding has previously been demonstrated between CXCR4 and CCR2 in CD4+ T lymphocytes endogenously expressing the receptors, confirming the biological validity of this interaction. The data presented also suggests that these complexes can engage the effector proteins Gαi and β- arrestin 2, indicating that they represent a functional form of the receptors. Furthermore, we have confirmed that each receptor of the CXCR4-CCR2 heterodimer is implicated in the engagement of effectors during the activation of CCR2. An additional level of complexity in GPCR-promoted signaling exists in their capacity to couple of multiple G proteins. Binding of stromal cell-derived factor-1 (SDF-1) to CXCR4 is known to promote T lymphocyte migration through a Gαi-dependent signalling pathway. In addition to this mechanism, we have demonstrated that breast cancer cell migration can initiated by a coupling of CXCR4 to the Gα13-Rho pathway, leading to the formation of metastases in distant organs. Finally, a novel level of GPCR regulation was revealed through the study of CXCR4 phosphorylation following its activation, which leads to the desensitization of the receptor and the engagement of β-arrestin-dependent signalling pathways. It appears that the desensitization of calcium signalling is mediated through the phosphorylation of CXCR4 by the GPCR kinases (GRKs) GRK2 and GRK6 and the recruitment of β-arrestin 2, whereas GRK3, GRK6 and β-arrestin 1 potentiate the activation of extracellular regulated kinase (ERK1/2). We also propose that the phosphorylation of the far C-terminal tail of CXCR4 is required for the interaction between the receptor and β-arrestin.
122

La peau, un modèle d'horloge périphérique / The skin as a peripheral clock model

Liu, Taole 03 March 2014 (has links)
Ce travail avait pour objet d’étudier les propriétés d’horloge et de synchronisation de la peau, un modèle potentiel d’horloge périphérique. L’activité rythmique a été analysée par bioluminescence en temps réel, sur des explants de peau abdominale et des fibroblastes dermiques primaires, isolés à partir de rats transgéniques Per1-luciférase. Nous avons montré que des explants de peau présentent une activité rythmique soutenue en culture, indiquant une importante synchronisation interne dans le tissu. Cette synchronisation se manifeste au cours du développement post-natal à partir de 1 mois et augmente jusqu’à 6 mois, avant de décroître, laissant place à des rythmes altérés à l’âge de 2 ans. Nous avons aussi établi que les fibroblastes dermiques présentent la propriété de compensation thermique commune à toutes les horloges circadiennes, et qu’ils sont potentiellement synchronisables par la mélatonine puisque celle-ci augmente leur amplitude en culture. Nous avons aussi préparé un vecteur lentiviral exprimant le gène rapporteur luciférase sous le contrôle du promoteur du gène horloge Bmal1, un nouvel outil pour compléter l’étude des rythmes dans les cellules de la peau. / This work aimed to investigate the skin as a potential model of peripheral clock by characterizing its rhythmic and synchronization properties. Circadian activity was examined in abdominal skin explants and fibroblasts derived from Per1-Luciferase transgenic rats by real-time recording of bioluminescence. First, the skin clock was characterized from early postnatal to old age. Low amplitude oscillations appeared at 1 month only and their robustness increased until 6 months. In 1-2 year-old rats, skin circadian rhythms showed decreasing amplitude and abnormal cycles. Primary fibroblasts derived from the skin at the same ages demonstrated similar pattern of clock activity. Temperature compensation, an intrinsic clock feature, was shown the first time in skin and primary fibroblasts. Secondly, we demonstrated a phase-dependent effect of melatonin to increase the amplitude of oscillations in skin primary fibroblasts, indicating it displays a synchronising role in the circadiansystem. Finally, to facilitate our studies on the multioscillatory skin tissue, we constructed a lentivirus carrying a Bmal1-luciferase reporter, to measure clock genes activities in human skin cells.
123

Synthèse d’analogues de la coelentérazine pour l’imagerie in vivo dynamique des signaux calciques - Synthèse d’analogues du (-)-EGCG comme inhibiteurs de Dyrk1a dans la thérapie symptomatique de la trisomie 21 / Synthesis of coelenterazine analogs for dynamic in vivo imaging of calcium signaling -Synthesis of (-)-EGCG analogs as Dyrk1a inhibitors in the symptomatic therapy of Down syndrome

Gealageas, Ronan 01 December 2011 (has links)
Au cours de cette thèse, deux sujets distincts ont été étudiés : d’une part la synthèse d’analogues de la coelentérazine, substrat de différentes luciférases, pour une application en imagerie in vivo, et d’autre part la synthèse d’analogues du (-)-EGCG, inhibiteur de la kinase Dyrk1a, impliquée notamment dans les troubles cognitifs rencontrés dans la trisomie 21.La problématique du premier sujet consistait à obtenir des analogues de la coelentérazine conservant leur activité sur deux luciférases, la luciférase Renilla et l’aequorine, tout en induisant un déplacement vers le rouge de la bioluminescence produite par ces enzymes. L’aequorine, sensible au calcium, représentait la cible biologique principale du projet.Sept analogues dont six originaux ont été obtenues par des méthodes de synthèse classiques, et leurs activités ont pu être testées sur les deux luciférases choisies, avec des résultats probants : malgré des émissions de lumière moins intenses que celles obtenues avec la coelentérazine native, plusieurs molécules ont entrainé un déplacement vers le rouge de la longueur d’onde d’émission de lumière par bioluminescence allant jusqu’à 27 nm pour l’aequorine et plus de 120 nm pour la luciférase Renilla.Le second sujet, de chimie médicinale classique, a principalement consisté à la synthèse d’analogues du gallate d’épigallocatéchine (EGCG) au squelette simplifié, et au sein desquels le cycle pyranique caractéristique des catéchines a été remplacé par un carbocycle. Plusieurs molécules ont pu être synthétisées, dont deux présentant le motif hexaphénol. Leur activité inhibitrice de Dyrk1a a pu être testée in vitro et l’une d’entre elle s’est déjà révélée plus active que l’EGCG. / During this thesis, two distinct projects were studied: on the one hand, the synthesis of coelenterazine analogs, substrate of several luciferases, in the purpose of using them for in vivo imaging, and on the other, the synthesis of (-)-EGCG analogs, inhibitor of the Dyrk1a kinase, which interests us for the role it plays in the mental retardation existing in the Down Syndrome disease.The problematic of the first project consisted in obtaining coelenterazine analogs that would not only maintain their activity on two luciferases, the Renilla luciferase and aequorine, but they should also induce a red-shift of the bioluminescence produced by these enzymes. Because of its sensitivity to calcium, aequorine was the main biologic target of this project.Seven analogs, of which six had an original structure, were synthesized through usual synthetic methodologies and their activities on both aequorine and Renilla luciferase were tested in vitro, with interesting results: even if the intensities of light emission were weaker than those obtained with native coelenterazine, several molecules produced a red-shift of the emission wavelength of bioluminescence, up to 27nm for aequorine and more than 120nm for the Renilla luciferase. The second project, of classical medicinal chemistry, mainly consisted in the synthesis of epigallocatechin gallate analogs (EGCG) with a simplified backbone and in which the pyranic ring typical of catechins was replaced by a carbocycle. Several molecules were synthesized, two of them possessing the hexaphenol motif. Their inhibiting activity of Dyrk1a was tested in vitro and one already showed a better activity than natural EGCG.
124

Structure quaternaire des récepteurs de chimiokines CXCR4 et CCR2 et interaction avec leurs effecteurs

Armando, Sylvain 11 1900 (has links)
Les récepteurs couplés aux protéines G (RCPG) sont une famille très diversifiée de protéines membranaires capables de répondre à un grand nombre de signaux chimiques tels que des photons, des molécules odorantes, ou des hormones. En plus de cette diversité, l’étude des RCPG montre que des associations protéiques spécifiques multiplient les possibilités de signalisation de chacun de ces récepteurs. En permettant d’atténuer, de potentialiser, ou de générer une nouvelle voie de signalisation, l’association des RCPG en oligomères s’avère une importante source de diversité. L’utilisation du transfert d’énergie de résonance de bioluminescence (BRET) qui permet de détecter les interactions protéiques a révélé de nombreuses associations de RCPG. Durant cette thèse, des outils ont été développés pour combiner efficacement le BRET à des essais de complémentation de protéines (PCA) dans le but de savoir si l’oligomérisation des RCPG pouvait impliquer plus de deux récepteurs. Les résultats présentés montrent que les récepteurs de chimiokines CXCR4 et CCR2 forment des homo et hétéro tétramères, et que l’activation d’un dimère CCR2 peut moduler la conformation d’un dimère CXCR4 par un changement conformationnel trans-récepteur. La coopérativité négative de liaison de ligand qui a été démontrée auparavant entre CXCR4 et CCR2 dans des lymphocytes T CD4+ exprimant les récepteurs de manière endogène confirme la validité biologique de cette interaction. Les données présentées suggèrent également que ces complexes peuvent engager les effecteurs Gαi et β-arrestine2, indiquant qu’ils représentent la forme fonctionnelle de ces récepteurs. Enfin, nous avons pu confirmer que chaque récepteur de l’hétérodimère CXCR4-CCR2 est impliqué dans l’engagement des effecteurs lors de l’activation de CCR2. Un autre niveau de complexité dans la signalisation des RCPG est atteint par leur capacité à coupler de multiples protéines G. La liaison du facteur dérivé des cellules stromales (SDF-1) au récepteur CXCR4 permet la migration des lymphocytes T par une voie de signalisation dépendante de la protéine Gαi. Nous avons pu démontrer en revanche que la migration des cellules de cancer du sein était initiée par un couplage de CXCR4 à la voie Gα13-Rho pour former des métastases dans des organes distants. Enfin, un dernier niveau de régulation des RCPG a été abordé par l’étude de la phosphorylation de CXCR4 suite à son activation, qui permet la désensibilisation du récepteur et l’engagement de voies de signalisation dépendantes de la β-arrestine. Il apparaît que la désensibilisation de la voie du calcium serait médiée par la phosphorylation de CXCR4 par les kinases des RCPG (GRK) GRK2 et GRK6 et le recrutement de β- arrestine2, alors GRK3, GRK6 et la β-arrestine1 potentialiseraient l’activation des kinases régulées par les signaux extracellulaires (ERK1/2). Nous suggérons également que c’est la phosphorylation de l’extrémité C-terminale de CXCR4 qui permettrait son association avec la β-arrestine. / G protein-coupled receptors (GPCRs) are a diverse family of membrane proteins capable of responding to a large number of extracellular stimuli including photons, odorant molecules and hormones. In addition to this diversity, it has been shown that GPCRs form specific protein:protein interactions, multiplying the signalling possibilities of each of these receptors. With the ability to diminish, to potentiate or even generate new signalling pathways, the oligomeric association of GPCRs plays an important role in generating this diversity. The use of bioluminescence resonance energy transfer (BRET), which allows the detection of interactions among proteins, has revealed numerous associations between GPCRs. During this thesis, tools have been developed that effectively combine BRET with protein complementation assays (PCA) with the goal of determining if interactions between GPCRs could involve more than two receptors. The results show that the chemokine receptors CXCR4 and CCR2 form both homo and hetero tetramers, and that the activation of a dimer of CCR2 can modulate the conformation of a CXCR4 dimer through a transreceptor conformational change. Negative cooperativity of ligand binding has previously been demonstrated between CXCR4 and CCR2 in CD4+ T lymphocytes endogenously expressing the receptors, confirming the biological validity of this interaction. The data presented also suggests that these complexes can engage the effector proteins Gαi and β- arrestin 2, indicating that they represent a functional form of the receptors. Furthermore, we have confirmed that each receptor of the CXCR4-CCR2 heterodimer is implicated in the engagement of effectors during the activation of CCR2. An additional level of complexity in GPCR-promoted signaling exists in their capacity to couple of multiple G proteins. Binding of stromal cell-derived factor-1 (SDF-1) to CXCR4 is known to promote T lymphocyte migration through a Gαi-dependent signalling pathway. In addition to this mechanism, we have demonstrated that breast cancer cell migration can initiated by a coupling of CXCR4 to the Gα13-Rho pathway, leading to the formation of metastases in distant organs. Finally, a novel level of GPCR regulation was revealed through the study of CXCR4 phosphorylation following its activation, which leads to the desensitization of the receptor and the engagement of β-arrestin-dependent signalling pathways. It appears that the desensitization of calcium signalling is mediated through the phosphorylation of CXCR4 by the GPCR kinases (GRKs) GRK2 and GRK6 and the recruitment of β-arrestin 2, whereas GRK3, GRK6 and β-arrestin 1 potentiate the activation of extracellular regulated kinase (ERK1/2). We also propose that the phosphorylation of the far C-terminal tail of CXCR4 is required for the interaction between the receptor and β-arrestin. / Thèse réalisée en cotutelle avec l'université Montpellier2 dans le laboratoire de pharmacologie moléculaire de Jean-Philippe Pin à l'institut de génomique fonctionnelle (IGF), Montpellier, France.
125

Deconstructing bioluminescence: from molecular detail to in vivo imaging.

Adams, Spencer T., Jr. 29 January 2020 (has links)
Bioluminescence is the chemical production of light that results when a luciferase enzyme catalyzes the luminogenic oxidation of a small-molecule luciferin substrate. The numerous luciferases and luciferins nature has evolved can be used to illuminate biological processes, from in vitro assays to imaging processes in live animals. However, we can improve the utility of bioluminescence through modification of these enzymes and substrates. My thesis work focuses on developing reporters that expand the bioluminescent toolkit and improving our understanding of how bioluminescence works on a molecular level. The first part of my thesis focuses on characterizing luciferases and luciferins that improve bioluminescence imaging in vivo. Some of our luciferins can outperform the natural D-luciferin substrate in live mouse imaging, while others are selectively utilized by mutant luciferases in live mouse brain. We also engineered luciferins that can selectively report on endogenous enzymatic activity in live mice. The second part of my thesis focuses on determining the molecular details of how enzymes related to firefly luciferase, long-chain fatty acyl-CoA synthetases (ACSLs), can function as latent luciferases. I have determined the structure for one of these enzymes and improved its bioluminescent activity with synthetic luciferins enough to image in live mouse brain. I also characterized the selectivity in chimerized enzymes that combine firefly luciferase and ACSLs. In summary, my work improves the utility of bioluminescence for in vivo use and informs us about how evolutionarily-related enzymes function as luciferases on a molecular level.
126

Étude de la sensibilité du télescope à neutrinos ANTARES aux photons de très haute énergie — Contribution à l'étalonnage en temps du détecteur

Guillard, Goulven 14 October 2010 (has links) (PDF)
Depuis les fonds méditerranéens, les quelques 900 photomultiplicateurs du télescope à neutrinos ANTARES scrutent les abysses pour tenter de discerner, parmi la bioluminescence et la radioactivité marine, les photons Čerenkov émis par les muons issus de neutrinos astrophysiques, et de distinguer ces muons de ceux générés par les gerbes atmosphériques produites par les rayons cosmiques. ANTARES accumule des données depuis 2006 ; cette prouesse technique permet d'envisager un avenir favorable à l'astronomie neutrino sous-marine : ANTARES devrait être le précurseur d'un instrument de plus grande envergure, KM3NeT. Les performances d'un télescope sont caractérisées, entre autres, par sa résolution angulaire. Dans le cas d'ANTARES, celle-ci est directement liée à la résolution temporelle des éléments du détecteur. La correction de l'une des principales sources de dégradation de cette résolution temporelle, l'effet de walk créé par l'établissement d'un seuil fixe pour le filtrage du signal issu des photomultiplicateurs, est exposée dans ce manuscrit. Cette correction, mise en œuvre dans la chaîne logicielle officielle de la collaboration ANTARES, améliore notamment l'estimateur de qualité de la reconstruction des événements. L'implémentation présentée laisse le champ libre à certaines optimisations. L'auteur tente en outre d'évaluer, à partir d'une simulation Monte-Carlo complète, la possibilité d'utiliser des sources de photons de très haute énergie comme sources de muons calibrées afin d'estimer le pointé absolu et la résolution angulaire du télescope. Bien que la procédure soit intrinsèquement entachée de larges incertitudes, il est démontré que la possibilité de détecter de telles sources est extrêmement faible. Cette étude montre également que les photons de très haute énergie ne constituent pas une source notable de bruit de fond neutrino.
127

Functional Organization of Central and Peripheral Circadian Oscillators

Ko, Caroline Hee-Jeung 24 September 2009 (has links)
The suprachiasmatic nucleus (SCN) of the anterior hypothalamus has long been considered a master circadian pacemaker that drives rhythms in physiology and behavior in mammals. The recent discovery of self-sustained and cell-autonomous circadian oscillators in peripheral tissues has challenged this position. This dissertation tested the general hypothesis that the SCN has properties that distinguish it from other oscillators, thereby positioning it atop a circadian hierarchy. The general approach was to compare the consequences of altering the molecular circadian clock on tissue-autonomous rhythmicity in mice. In the first experiments, the role of the SCN as a master clock was tested by manipulating the expression of a circadian gene in the brain. Specifically, the expression of the short period tau mutation of casein kinase-1-epsilon (CK1ε) was controlled in an anatomically- and a temporally-specific manner via a tetracycline transactivator regulatory system. This inducible expression of CK1εtau affected the period of activity rhythms when expressed in the SCN, but did not affect the tissue-autonomous rhythmic properties in the peripheral tissues. Second, real-time bioluminescence imaging of tissues from PER2::LUCIFERASE mice revealed that period and phase of different circadian oscillators were tissue specific. Various circadian gene mutations (Cry1-/-, Cry2-/-, Cry1-/-;Cry2-/-, Clock∆19/∆19) produced little difference in rhythmic properties between the SCN and peripheral oscillators, although Cry1-/- SCN had more robust and persistent rhythms compared with the periphery. Third, the loss of Bmal1, which produces behavioral arrhythmicity, eliminated rhythms in the peripheral tissues, but not in the SCN. Bmal1-/- SCN rhythms were highly variable in period and amplitude, fitting a stochastic, but not a deterministic model of rhythm generation. Unlike mutations in other circadian genes, rhythmicity was completely abolished in single SCN neurons in Bmal1-/- mice, indicating that rhythms in Bmal1-/- SCN tissue are a property of the tissue organization rather than an averaging of single-cell autonomous rhythms. The SCN, therefore, has a unique anatomical organization that contributes to long-term stability and temporal organization of the circadian hierarchy.
128

Chronic effects of silica nanoparticles in Vibrio fischeri, Raphidocelis subcaptata, Danio rerio and Allium cepa / Efeitos crônicos das nanopartículas de sílica em Vibrio fischeri, Raphidocelis subcaptata, Danio rerio e Allium cepa

Silva, Gabriela Helena da 03 October 2014 (has links)
Scientific research using nanotechnology is a relatively recent development with a variety of potential applications in many fields of science. Within this field of research, many new products, with improved performances, have been developed. Despite increased research on its toxicity to ecosystem, the knowledge about this area is still limited. To evaluate the toxicity and genotoxicity of different sizes silica nanoparticles (SiNP)to the environment, different species, on different trophic levels (Vibrio fisheri, Raphidocelissubcapitata, Daniorerio and Allium cepa) were exposed to TM40 (22 nm), HS30 (12 nm), SM30 (7 nm) with concentrations ranging from0.19 to 163.8 g/L (TM40) and 0.29 to 122.85 g/L (HS30 and SM30), and the following parameters were monitored during exposure: production of bioluminescence (V. fischeri), growth rate (R. subcapitata), embryonic development and DNA damage (D. rerio) and germination rate, growth and DNA damage (A. cepa). Within each test SiNPpresent a size dependent chronic toxicity. The bioluminescence test present a EC50 of 29.11, 32.34 and 4.58 g/L for TM40, HS30 and SM30, respectively. For the growth rate assay the EC50 was 9.32, 9.07 and 7.93 g/L for TM40, HS30 and SM30, respectively. And for the zebra fish embryonic development test for TM40, HS30 and SM30, the EC50 was 5.85, 1.13 and 2.68 g/L respectively. All particles also induce phytotoxicity in A.cepa, growth and germination reduce significatively when expose to SiNP. Futhermoregenotoxic effects were also induced by the particles for both A.cepaand D. rerio. Therefore, SiNP can cause toxicity to the environment and size can strongly influence this toxicity / Com uma variedade de aplicações potenciais, em diversos campos da ciência, as pesquisas científicas utilizando nanotecnologia são de desenvolvimento relativamente recente. Dentro deste campo de pesquisa, vários novos produtos, com desempenhos melhorados têm sido desenvolvidos. Apesar do aumento de pesquisas sobre a toxicidade dessas tecnologias à biota, o conhecimento sobre esta área ainda é limitado. Visando avaliar a toxicidade e genotoxicidade denanopartículasde sílica (SiNP) no meio ambiente diferentes espécies pertencentes a diversos níveis tróficos (Vibriofisheri, Raphidocelissubcapitata, DaniorerioandAllium cepa) foram expostos a Ludox TM40 (22 nm), Ludox HS30 (12 nm) e Ludox SM30 (7 nm). As espécies de teste foram expostas a concentrações de nanopartículas (NP) variando de 0.29 a 163.8 g/L (TM40) e 0.19 a 122.85 g/L (HS30 e SM30) e os seguintes parâmetros monitorizados durante a exposição: a produção de bioluminescência (V. fischeri), o crescimento taxa (R. subcapitata), inibição de alimentação (D. magna), desenvolvimento embrionário e dano ao DNA (D. rerio) e taxa de germinação, crescimento e danos ao DNA (A. cepa). Nos testes feitos com as SiNPfoi observado que a toxicidade é dependente do tamanho da partícula. O ensaio de bioluminescência apresentou um EC50 de 29.11, 32.34 e 4.58 g/L para TM40, HS30 e SM30, respectivamente. Para o ensaio de taxa de crescimento o EC50 foi 9.32, 9.07 e 7.93 g/Lpara TM40, HS30 e SM30, respectivamente. E para o teste de desenvolvimento embrionário com peixe zebra, para o TM40, HS30 e SM30 o EC50 foi de 5.85, 1.13 e 2.68g/L, respectivamente. Todas as partículas também induziram fitotoxicidade em A. cepa, crescimento e germinação reduziram significativamente quando o organismo foi exposto a SiNP. Efeitos genotóxicos também foram induzir pelas partículas, tanto para A. cepa quanto paraD. rerio. Portanto, as SiNP podem causar toxicidade ao ambiente e o tamanho pode influenciar fortemente a essa toxicidade
129

Construção de sistemas bacterianos para a detecção de metais pesados em amostras ambientais. / Construction of bacterial systems for the detection of heavy metals in environmental samples.

Quadros, Oeber de Freitas 24 January 2012 (has links)
Visando a construção de três biossensores bacterianos para os metais mercúrio, arsênio e chumbo, Cupriavidus metallidurans CH34 foi escolhida para obtenção dos fragmentos de DNA (por PCR) correspondentes aos operons mer, ars e pbr. Os fragmentos foram inseridos à montante do gene EGFP, no plasmídeo pBB-EGFP, obtendo três novos plasmídeos: pGHg, pGAs e pGPb. Estes foram clonados em C. metallidurans CH34 e Escherichia coli DH5<font face=\"Symbol\">&#945;. As linhagens recombinantes foram submetidas a várias situações de cultivo e diferentes intensidades de fluorescência, detectadas em microscopia e quantificadas por citometria de fluxo. As linhagens recombinantes C. metallidurans CH34 / pGHg, E. coli DH5<font face=\"Symbol\">&#945; / pGHg, C. metallidurans CH34 / pGAs e C. metallidurans CH34 / pGPb mostraram-se eficazes e, consequentemente, poderão ser utilizadas em rápidos diagnósticos de amostras contaminadas por mercúrio, arsênio e chumbo. / Aiming at the construction of three bacterial biosensors for metals mercury, arsenic and lead, Cupriavidus metallidurans CH34 was chosen to obtain the DNA fragments (by PCR) corresponding to operons mer, ars and pbr. The fragments were inserted upstream of the EGFP gene, in plasmid pBB-EGFP, getting three new plasmids: pGHg, pGAs and pGPb. They were cloned in C. metallidurans CH34 and Escherichia coli DH5<font face=\"Symbol\">&#945;. The recombinant strains were subjected to various conditions of cultivation. Different intensities of fluorescence were detected microscopy and quantified by flow cytometry. The recombinant strains C. metallidurans CH34 / pGHg, E. coli DH5<font face=\"Symbol\">&#945; / pGHg, C. metallidurans CH34 / pGAs and C. metallidurans CH34 / pGPb were effective and therefore may be used in rapid diagnosis of samples contaminated by mercury, arsenic and lead.
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Purificação e caracterização de enzimas envolvidas na bioluminescência de fungos / Purification and Caracterization of enzymes involved in fungi bioluminescence

Pereira, Tatiana Araujo 13 December 2017 (has links)
Esta tese descreve estudos realizados na tentativa de purificar e caracterizar enzimas envolvidas na BL de fungos, além de trabalhos conduzidos a fim de investigar o mecanismo da bioluminescência de fungos. Inicialmente, tentou-se isolar as duas enzimas supostamente responsáveis pala reação bioluminescente em fungos. Parâmetros de atividade ótima (pH e temperatura) e comportamento cinético foram investigados. Todavia, com a descoberta de que a luciferina fúngica é o derivado hidroxilado da hispidina (3-hidróxihispidina), novas estratégias foram abordadas. Os esforços se concentraram na purificação da luciferase, visto que a hidroxilase não faz parte do sistema bioluminescente de fungos. Avaliação da interação da luciferase fúngica com a luciferina ou derivados dela sugeriram comportamento relativamente promíscuo da enzima. Os resultados indicaram que a reação luciferina-luciferase é favorecida em meio básico (pH ~8), a ~20 &#176;C. Ensaios com 18O2 revelaram que a inserção de oxigênio na molécula de luciferina produz um intermediário cuja descarboxilação gera a oxiluciferina. Paralelamente, a síntese da hispidina in vitro a partir de ácido cafeico na presença de malonil-CoA e de extrato de micélios bioluminescentes resultou na emissão de luz, confirmando que a luciferina é reciclada no processo. / This work describes studies performed to purify and characterize enzymes responsible for the fungal bioluminescence. Also, it shows important data that contributes to understand the mechanism for bioluminescence reaction in fungi. First, we tried to isolate two enzymes suspected of being involved on fungal bioluminescence. Optimum activity parameters (pH and temperature) and kinetic behavior were investigated. However, the discovery that fungal luciferin is the hispidin derivative 3-hydroxyhispidin demanded adaptations in the project. First of all, concentrates efforts to luciferase purification was priority, since hydroxylase is not part of the bioluminescent system of fungi. Studies on the luciferase interaction with different substrates showed some promiscuity for the enzyme. The results indicated higher intensity of light from luciferin-luciferase reaction in alkaline solutions (pH ~ 8) at ~ 20 &#176;C. The reaction in medium with 18O2 revealed that insertion of oxygen into the luciferin structure produces an intermediate whose decarboxylation generates oxyluciferin. In parallel, the in vitro synthesis of hispidin using caffeic acid and malonyl-CoA with the mycelium extract resulted in the emission of light, confirming that luciferin is recycled in the process.

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