Foi estudada a degradação do pentaclorofenol (PCP) em reator aneróbio horizontal de leito fixo (RAHLF) de volume de 2000 mL. O reator foi inoculado com microrganismos oriundos de reatores aneróbios não previamente adaptados a PCP. Atividade microbiana foi monitorada através de técnicas clássicas na presença do organoclorado na faixa de 2,0 a 13 mg/L de PCP. O reator apresentou eficiência de 97% na remoção de DQO e completo desaparecimento do composto de PCP em todas as concentrações testadas. A fração orgânica foi consumida totalmente na primeira terça parte do reator de acordo com os valores determinados de ácidos voláteis, DQD e PCP. Não foi verificada inibição da atividade de culturas microbianas. Os exames microscópicos, fluorescência e varredura, permitiram verificar o predomínio de microrganismos pertencentes ao Domínio Archea. As técnicas moleculares PCR, ARDRA e hibridação slot-blot confirmaram o predomínio do Domínio Archaea e possibilitaram a verificação de alterações na diversidade das populações após adição de 2 mg PCP/L. Conclui-se que o reator sem prévia adaptação do inóculo foi eficiente para o tratamento do PCP, e os microrganismos relacionados às Archaea metanogênicas acetocláticas podem estar envolvidas na degradação deste composto. / The degradation of pentachlorophenol (PCP) was studied in a 2000 mL. Horizontal Anaerobic Immobilized System (HAIS). The reactor was inoculated with microorganisms obtained from an anaerobic reactor without previous adaptation to the PCP. The microbial activity was evaluated by using classic techniques in order to . monitor its behavior during the HAIS fed with a range of PCP between 2.0 to 13 mg/L. The reactor presented 97% of efficiency in the removal of COD and complete decrease of PCP in alI concentrations tested. The total consumption of organic fraction took place mainly in the first third part of the reactor according the values of volatile fatty acids, COD and PCP obtained. Microbial inhibition was not verified in during HAIS operation. Microscopic examinations allowed certifying the Archaea Domain predominance according the morphologies observed. The molecular techniques polimerase chain reaction (PCR), ARDRA and slot-blot hibridation confirmed the predominance of Archaea Domain and alIowed verifying some changes in the population\'s diversity under additions of 2mg PCP/L. The efficiency of PCP decreased in the anaerobic reactor was related to the presence of Archaea Domain, especially the acetoclastic methanogens, whose where probably involved with the organochlorine compound degradation.

Foi estudada a degradação do pentaclorofenol (PCP) em reator aneróbio horizontal de leito fixo (RAHLF) de volume de 2000 mL. O reator foi inoculado com microrganismos oriundos de reatores aneróbios não previamente adaptados a PCP. Atividade microbiana foi monitorada através de técnicas clássicas na presença do organoclorado na faixa de 2,0 a 13 mg/L de PCP. O reator apresentou eficiência de 97% na remoção de DQO e completo desaparecimento do composto de PCP em todas as concentrações testadas. A fração orgânica foi consumida totalmente na primeira terça parte do reator de acordo com os valores determinados de ácidos voláteis, DQD e PCP. Não foi verificada inibição da atividade de culturas microbianas. Os exames microscópicos, fluorescência e varredura, permitiram verificar o predomínio de microrganismos pertencentes ao Domínio Archea. As técnicas moleculares PCR, ARDRA e hibridação slot-blot confirmaram o predomínio do Domínio Archaea e possibilitaram a verificação de alterações na diversidade das populações após adição de 2 mg PCP/L. Conclui-se que o reator sem prévia adaptação do inóculo foi eficiente para o tratamento do PCP, e os microrganismos relacionados às Archaea metanogênicas acetocláticas podem estar envolvidas na degradação deste composto. / The degradation of pentachlorophenol (PCP) was studied in a 2000 mL. Horizontal Anaerobic Immobilized System (HAIS). The reactor was inoculated with microorganisms obtained from an anaerobic reactor without previous adaptation to the PCP. The microbial activity was evaluated by using classic techniques in order to . monitor its behavior during the HAIS fed with a range of PCP between 2.0 to 13 mg/L. The reactor presented 97% of efficiency in the removal of COD and complete decrease of PCP in alI concentrations tested. The total consumption of organic fraction took place mainly in the first third part of the reactor according the values of volatile fatty acids, COD and PCP obtained. Microbial inhibition was not verified in during HAIS operation. Microscopic examinations allowed certifying the Archaea Domain predominance according the morphologies observed. The molecular techniques polimerase chain reaction (PCR), ARDRA and slot-blot hibridation confirmed the predominance of Archaea Domain and alIowed verifying some changes in the population\'s diversity under additions of 2mg PCP/L. The efficiency of PCP decreased in the anaerobic reactor was related to the presence of Archaea Domain, especially the acetoclastic methanogens, whose where probably involved with the organochlorine compound degradation.

Halogenated heterocycles are common in pharmaceutical and natural products and there is a need to develop a better understanding of processes used to synthesize them. Although the halogenation of simple aromatic molecules is well understood, the mechanisms behind the halogenation of aromatic heterocycles have been more problematic to elucidate because multiple pathways are possible. Recently, new, radical-based mechanisms have been proposed for heterocycle halogenation. In this study, we examine and test the viability of possible nucleophilic substitution, SN2@X, mechanisms in the halogenation of anions derived from the deprotonation of aromatic heterocycles. All the experiments were done in a modified Thermo LCQ Plus equipped with ESI. The modifications allow a neutral reagent to be added to the helium buffer gas in the 3D ion trap. In this system, it is possible to monitor ion/molecule reactions over time periods up to 10 seconds. A variety of aromatic heterocyclic nucleophiles were chosen based on their inclusion of nitrogen and or sulfur as the heteroatoms. In addition to this, the halogenating molecules chosen included traditional halobenzenes and a new class of perfluorinated alkyl iodides. It was found that, experimentally, the SN2@X path is the likely mechanism in the halogenation of deprotonated heterocycles. With computational modeling, we have additional support for this substitution mechanism. From this original study, two more studies were developed to look at the competing nucleophilic aromatic substitution reaction, SNAr. In the first of these studies, the focus was to look at how electron withdrawing substituents about an aromatic ring affect the ratio of SN2@X verses SNAr. As nucleophiles, 2-thiophenide and 5-thiazolide were used. The neutral reagents focus on trifluorobromobenzene derivatives along with pentafluorobromo- and -iodobenzene, and a two trifluoroiodobenzenes. What was found was that the ratio of the reactions depends on where the fluorines, or electron withdrawing substituents are in relation to the bromine or iodine on the ring. If the fluorines are in a close location to stabilize the resulting ionic product, SN2@X proceeds easily. However, the fluorines directly adjacent to the bromine or iodine also provide steric hinderance in the SNAr reaction. In the final project, arylation and benzylation of bromopyridines was examined. The nucleophiles used were benzyl and phenyl anions as well as 5-thiazolide, and the neutral reagents were bromopyridines, with fluorines used as an electron withdrawing groups to help stabilize the transition state. In these experiments, steric hinderance highly affected the results between the phenyl and benzyl nucleophiles. With benzylic anions, the nucleophile is able to reach the aromatic ring with less steric interference and therefore can proceed with an SNAr reaction. In addition to this, with mono and difluorinated pyridine substrates, the nitrogen in the ring activated the ring yielding nucleophilic aromatic substitution losing fluoride rather than bromide in many cases.

Halogenated organic compounds have had widespread and massive applications in industry, agriculture, and private households, for example, as degreasing solvents, flame retardants and in polymer production. They are released to the environment through both anthropogenic and natural sources. The most common chlorinated solvents present as contaminants include tetrachloroethene (PCE, perchloroethene) and trichloroethene (TCE). These chlorinated solvents are problematic because of their health hazards and persistence in the environment, threatening human and environmental health. Microbial reductive dechlorination is emerging as a promising approach for the remediation of chlorinated solvents in aquifers. In microbial reductive dechlorination, specialized bacteria obtain energy for growth from metabolic dechlorination reactions that convert PCE to TCE, cis-1,2-dichloroethene (cDCE), vinyl chloride (VC), and finally to benign ethene. Field studies show incomplete dechlorination of PCE to ethene due to lack of electron donors or other populations competing for the electron donor. Mathematical models are good tools to integrate the processes affecting the fate and transport of chlorinated solvents in the subsurface. This thesis explores the use of modeling to provide a better understanding of the reductive dehalogenation process of chlorinated solvents and their competition with other microorganisms for available electron donors in continuous flow systems such as a continuous stirred tank reactor (CSTR) and a continuous flow column. The model is a coupled thermodynamic and kinetic model that includes inhibition kinetics for the dechlorination reactions, thermodynamic constraints on organic acids fermentation and has incorporated hydrogen competition among microorganisms such as homoacetogenesis, sulfate reducers and ferric iron reducers. The set of equations are coupled to those required for modeling a CSTR. The system of model equations was solved numerically using COMSOL 3.5 a, which employs finite-element methods. The kinetic model was verified by simulation results compared to previously published models and by electron balances. The simulation process progressed by simulating the anaerobic reductive dechlorination, coupled with thermodynamic limitation of electron donor fermentation in batch systems to the modeling of CSTR, and finally to simulate anaerobic reductive dechlorination in continuous flow column, aquifer column including the processes of advection, dispersion and sorption along with the microbial processes of dehalogenation, fermentation, iron and sulfate reduction. The simulations using the developed model captured the general trends of the chemical species, and a good job predicting the dynamics of microbial population responses either the CSTRs or continuous flow column. Although, the kinetic of anaerobic dechlorination processes of chlorinated solvents in those systems have been researched in the past, little progress has been made towards understanding the combined effects of the dechlorination and thermodynamic constraints in continuous flow systems. This work provides a rigorous mathematical model for describing the coupled effects of these processes. / Graduation date: 2012

This master thesis is focused on groundwater remediation of chlorinated ethylenes and methanes in the area of chemical factory Spolchemie in the Czech Republic, Ústí nad Labem city. For these purposes nano zero valent iron particles were used. For the remediation two separate applications of different types of particles together in suspension with tracer (lithium chloride), were carried out. The results from the first application were evaluated by the supervisor of this thesis and are briefly summarized and discussed together with the second application which was evaluated by the author of this thesis. Second application of particles was carried out in October 2015 and observed for 424 days. Observation consisted of monitoring of groundwater level, physical-chemical parameters and collection of water samples for the analysis of concentrations of chlorinated hydrocarbons, their degradation products and several chosen ions. Nanoiron particles had the assumed effect onto the physical-chemical parameters and reduction of contamination. The application of tracer had proven the expected groundwater flow and made a possibility to distinguish between the process of reductive dehalogenation and dilution caused by the injected water, the dilution did not exceeded 5 % in most monitored points. Other...

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O estudo que ora se apresenta integrou o conjunto de pesquisas do sub-projeto - Diversidade de Bactérias Associadas à Degradação de Compostos Recalcitrantes, do projeto temático BIOTA FAPESP - Ecologia Molecular e Taxonomia Polifásica de Bactérias de Interesse Ambiental e Agro-Industrial. Apresenta caráter inovador, na medida em que procurou avaliar o potencial de aplicação biotecnológica de microrganismos anaeróbios de uma área severamente contaminada no Brasil, o estuário de Santos-São Vicente, em degradar o pentaclorofenol (PCP). A pergunta fundamental a ser respondida pelos resultados experimentais realizados foi: são os microrganismos autóctones do estuário capazes de servirem de inóculo para degradar o pentaclorofenol em biorreatores sob condições metanogênicas? Dois grupos de amostras foram avaliados, o primeiro, uma parcela composta por vários sedimentos coletados no estuário e, o segundo, sedimentos coletados na região do Largo de Canéus e na frente da Companhia Siderúrgica Paulista (COSIPA). O estabelecimento da determinação cromatográfica do PCP e congêneres menos clorados para o monitoramento experimental mostrou que na análise da presença dos clorofenóis nos sedimentos, o método de extração por ultrassom com posterior metilação dos analitos foi adequado para concentração mínima de 200 'mü'g clorofenóis/Kg sedimento para 2,3; 2,6 diclorofenóis; 2,4,6 e 2,3,6 triclorofenóis. Contudo, não foi adequado para a determinação do PCP e 2,3,4 triclorofenol. Para o meio de cultivo, o método de extração do PCP por agitação em vórtex e acetilação dos analitos mostrou-se adequado para todos os clorofenóis e com limite de quantificação de 0,1 mg/L. A avaliação do potencial metanogênico foi realizada com as amostras compostas do estuário enriquecidas sob condições halofílicas. O valor estável de metano no biogás de 50% foi obtido nos primeiros 20 dias de incubação. O sedimento nessas condições foi utilizado como inóculo para fins de isolamento de culturas metanogênicas, redutoras do íon sulfato e degradadoras de PCP. Não foram obtidas culturas desalogenadoras; porém foram isoladas arquéias metanogênicas, cultivadas em metanol, acetato e formiato de sódio, bem como bactérias cultivadas em lactato de sódio na presença e ausência de sulfato de sódio. Ensaios fisiológicos aliados aos métodos moleculares FISH e DGGE permitiram identificar arquéias metanogênicas do gênero Methanosarcina sp. e microrganismos do domínio Bacteria. Os sedimentos individualmente estudados foram coletados com maior controle de anaerobiose empregando-se amostrador do tipo corer. O enriquecimento destes sedimentos, inicialmente sob concentração de 2,5 mg PCP/g STV e com adições periódicas de 50% da concentração inicial do clorofenol e 1,25 a 2,5 g/L de glicose por 13 meses a 30 graus Celsius, resultou na obtenção de culturas degradadoras do PCP sob anaerobiose estrita. Nos reatores controles sem PCP, já primeiros 20 dias de incubação 70% de metano foi determinado no biogás. Nos reatores com PCP, a produção do metano (20%) iniciou após 100 dias. A adsorção foi o principal mecanismo de remoção de 50% do PCP nas primeiras 12 horas de incubação dos enriquecimentos. Posteriormente, a redução do PCP no meio de 77% para a amostra de Canéus e 70% para a da COSIPA foi relacionada a mecanismos de biodegradação anaeróbia, como a desalogenação redutiva. Exames microscópicos mostraram a seleção de microrganismos na presença de PCP, com predomínio de bacilos formadores de esporos semelhantes ao gênero Clostridium sp., filamentos diversos e filamentos semelhantes as arquéias metanogênicas acetoclásticas relacionadas ao gênero Methanosaeta sp. O enriquecimento foi realizado sob condições halofílicas, segunda a salinidade de cada amostra estudada no estuário. Não houve perda do clorofenol por volatilização. Os resultados obtidos no enriquecimento anterior viabilizaram o estudo seguro do potencial anaeróbio dos microrganismos oriundos do sedimento da COSIPA em metabolizar o PCP em reator contínuo do tipo RAHLF. Assim, sedimento enriquecido sob condições metanogênicas e halofílicas foi inoculado no RAHLF, controlando-se rigorosamente a anaerobiose. O reator preenchido com cubos de espuma de poliuretana foi operado por 126 dias e tempo de detenção hidráulica de 18 horas, com meio de cultura salino contendo glicose (1 g/L) como principal fonte de carbono e PCP-Na nas concentrações de 5, 13, 15 e 21 mg/L. O desempenho do RAHLF foi estável com boa eficiência durante toda a operação. A redução dos níveis de matéria orgânica medida em DQO variou de 70 a 100% e a de PCP foi de 99%, com detecção de intermediários menos clorados e sob teores de metano no biogás de 20%. Da massa de 1111,73 mg de PCP aplicada no reator, 286,9 mg ficou retida no sistema pelo processo de adsorção nas biopartículas e 824,83 mg foi biodegradada. As análises morfológicas dos tipos celulares, em conjunto com as técnicas moleculares DGGE e FISH, revelaram a presença de grupos microbianos do domínio Archaea pertencente à família Methanosarcinacea e grupos do domínio Bacteria. A participação de grupos de domínio Bacteria, cuja estrutura dos tipos microbianos na comunidade variou ao longo do RAHLF e das concentrações de PCP, e dos organismos metanogênicos da família Methanosarcinacea, possibilitou responder a questão inicialmente formulada, uma vez que se pode afirmar que os microrganismos autóctones foram capazes de degradar o PCP sob condições metanogênicas e halofílicas, com eficiência adequada. A prática para a seleção dos microrganismos retirados do ambiente estuarino, de interesse para biotecnologia anaeróbia aplicada ao saneamento ambiental, que empregou o reator do tipo RAHLF, parece promissora para avanços da engenharia na remediação biológica de uma área cuja relevância é indiscutível para o estado de São Paulo / This study has an innovative character, once aimed to evaluate the biotechnological application of anaerobic microorganisms degrading pentachlorophenol (PCP) at a severely polluted area in Brazil, estuary of Santos-São Vicente, São Paulo state. This study integrated a group of researches of the sub-project - Diversity of Bacteria Associated to the Degradation of Recalcitrant Compounds, supported by major project BIOTA FAPESP which theme is Molecular Ecology and Polyphasic Taxonomy of Bacteria of Environmental and Agriculture-Industrial Interest. The fundamental question to be answered by the accomplished experimental results was: are the autochthonus microorganisms of the estuary capable of serving as inoculum to degrade the PCP in bioreactors under methanogenic conditions? In order to evaluate this hypothesis, two groups of samples were collected: sediments taken from several sites of the estuary and sediments taken from two sites, one severely contaminated with organochlorine compounds, in front of the São Paulo Metallurgical Company (COSIPA) and other, less contaminated, in the area of Canéus. The establishment of protocol for the PCP and less chlorinated compounds chromatographic determination showed that the extraction method by ultrosonication followed by metilation of the chlorinated compounds was appropriated to evaluate concentrations of 200 ug chlorophenol/Kg of sediment, 2,3; 2,6 dichlorophenols; 2,4,6 and 2,3,6 trichlorophenols. However, it was not appropriated for evaluation of PCP and 2,3,4 trichlorophenol. For the culture medium, the extraction method by vortex agitation followed by acetilation was appropriated for all of the chlorophenols compounds. The quantification limit was 0,1 mg/L. The evaluation of the methanogenic potential and PCP biodegradation was accomplished with the samples of the estuary enriched under halophylic conditions. In the experiments without PCP was possible to obtain cultures of Methanosarcina sp, identified by FISH technique and cells of domain Bacteria, identified by DGGE. In the experiment with PCP dehalogenated cultures were not obtained. To evaluate PCP anaerobic biodegradation by sediments of COSIPA and Caneus sites, sediments collected under anaerobic conditions by a corer device were enriched in a halophylic brine medium with glucose and PCP at concentration of 2.5 mg PCP/g VTS. Periodic additions of 50% of the initial concentration of PCP and 1.25 to 2.5 g/L of glucose were done. With this strategy was possible to obtain PCP dehalogenated cultures. The adsorption was the main mechanism of 50% of PCP removal in the first 12 hours of incubation. The PCP reduction of 77% for Caneus reactor and 70% for COSIPA reactor was related to anaerobic biodegradation. Microscopic exams showed selection of microorganisms, with predominance of cells related to Clostridium sp., and filaments related to methanogenic acetoclastic archaea Methanosaeta sp. chlorophenols volatilization was not observed. The biotechnological application of HAIB reactor in PCP biodegradation was evaluated using sediment of COSIPA site previously enriched with glucose. The reactor was operated by 126 days and hydraulic detention time of 18 hours, with saline brine medium containing glucose (1 g/L) and NaPCP in concentrations of 5, 13, 15 and 21 mg/L. PCP amendments did not affect the overall performance and functional stability of the process. COD and PCP reduction was close to 80% and 100%, respectively with detection of trichlorophenols and dichlorophenols. Percentage of methane in the biogas closed to 30%. Adsorption analyses demonstrated that 287 mg of PCP was removed by adsorption in the biofilm and 825 mg was removed by biodegradation. Biofilm DGGE-profiling showed the presence of specific bands of Bacteria and Archaea domains when PCP was amended. The appearance of new bands of Bacteria showed that this organisms had a direct influence at PCP dehalogentation. Archaea organisms of Methanosarcinaceae family had an indirect influence in this metabolism. This thesis demonstrated that HAIB reactors, using autochthonous microorganisms under halophylic and methanogenic conditions, are a potential alternative for organochlorines bioremediation

Thyroid hormones, which are secreted by the thyroid gland, are one of the most important halogenated compounds in the body. Thyroid hormones control almost every processes in the body including growth, body temperature, protein synthesis, carbohydrate and fat metabolism, heart rate, and cardiovascular, renal and brain function. Thyroid gland secretes L-thyroxine or 3,3',5,5'-tetraiodothyronine (T4) as a prohormone. While the biologically active hormone 3,3',5-triiodothyronine (T3) is produced by selective phenolic ring deiodination of T4, selective tyrosyl ring deiodination of T4 produces a biologically less active metabolite 3,3',5'-triiodothyronine (rT3). Tyrosyl and phenolic ring deiodination of T3 and rT3, respectively, also produces a biologically inactive metabolite 3,3'-diiodothyronine (3,3'-T2). Regioselective deiodinations of thyroid hormones are catalysed by three isoforms of a selenoenzyme iodothyronine deiodinase (DIO1, DIO2, DIO3). DIO1 can remove iodine from both the tyrosyl and phenolic rings of thyroid hormones, whereas DIO2 and DIO3 are selective towards phenolic and tyrosyl ring, respectively. Although the Figure 1. (A) Deiodination of thyroid hormones by iodothyronine deiodinases (DIOs) (A) and naphthyl-based selenium and/or sulphur compounds (B). mystery behind the origin of regioselectivity of deiodination by DIOs remains unsolved, formation of halogen bonding between selenium in the active site of DIOs and iodine of thyroid hormones has been widely accepted as the mechanism of deiodination. Halogen bonding, a noncovalent interaction between halogen and an electron donor such as nitrogen, oxygen, sulphur, selenium etc., elongates the C-I bond and impart a carbanionic character on the carbon atom that gets protonated after the removal of iodide. Apart from the deiodination, thyroid hormones also undergo decarboxylation, oxidative deamination, sulphate-conjugation to form iodothyronamines, iodothyroaetic acids and sulphated thyroid hormones, respectively. Figure 2. (A) Proposed mechanism of deiodination of thyroid hormones by deiodinase mimics. (B) Halogenation of uracil- and cytosine-containing nucleosides by hypohalous acid (HOX). Recently, naphthyl-based selenium/sulphur-containing compounds, such as compound 1 (Figure 1B), have been reported to mediate the selective tyrosyl ring deiodination of T4 and T3 to form rT3 and 3,3'-T2, respectively. Interestingly, replacement of the selenol moiety in compound 1 with a thiol decreases the activity, whereas replacement of the thiol moiety with another selenol dramatically increases the deiodination activity. Based on the detailed experimental and theoretical investigations, a mechanism involving the Se···I halogen bonding was proposed (Figure 2A). In addition to the halogen bonding between selenium and iodine atom, chalcogen bonding between two nearby chalcogen atoms was also shown to be important for the deiodination activity. Another important class of halogenated compounds in the body are the halogenated nucleosides. Myeloperoxidase and eosinophil peroxidase are heme-containing enzymes, which can convert halide ions (X¯) into a toxic reactive halogen species hypohalous acid (HOX) in presence of hydrogen peroxide (H2O2). Uracil- and cytosine-containing nucleosides are known to undergo halogenation at the 5-position of the nucleobase to form the halogenated nucleosides (Figure 2B). Interestingly, halogenated nucleosides such as 5-halo-2'-deoxyuridine are known to be incorporated in the DNA of dividing cells essentially substituting for thymidine. Incorporation of halogenated nucleosides into the DNA leads to mutagenesis, carcinogenesis and loss of genome integrity. Thymidylate synthase (TSase), the key enzyme involved in the biosynthesis of 2'-deoxythmidine-5'-monophosphate (dTMP) from 2'-deoxyuridine-5'-monophosphate (dUMP), can catalyse the dehalogenation of halogenated nucleotides in presence of external thiols. This thesis consists of five chapters. The first chapter provides a general introduction to halogen bonding, thyroid hormones and halogenated nucleosides. This chapter also briefly describes the halogen bond-mediated biochemical and biomimetic deiodinations of thyroid hormones by iodothyronine deiodinases and naphthyl-based organoselenium compounds. Dehalogenation of halogenated nucleotides by thymidylate synthase and thiol-based small molecules has also been discussed in this chapter. The second chapter of this thesis contains the regioselective deiodination of iodothyronamines (TAMs) by deiodinases mimics. TAMs are the endogenous metabolites produced by the decarboxylation of β-alanine side chain of thyroid hormones (THs). 3,3',5-triiodothyronamine (T3AM) and 3,5-diiodothyronamine (3,5-T2AM) undergoes selective tyrosyl ring deiodination by deiodinase mimics to form 3,3'-diiodothyronamine (3,3'-T2AM) and 3-iodothyronamine (3-T1AM), respectively. Interestingly, when the initial rates of deiodinations of T3 and T3AM were compared, deiodination of T3 was found to be several fold faster than that of T3AM under identical reaction conditions. To understand the ability of the iodine atoms to form Figure 3. (A) HPLC chromatogram of deiodination of T3. (B) Proposed mode of interaction of dimeric T3 and monomeric T3AM with organoselenium compounds. halogen bonding, a model selenolate (MeSe¯) was optimized with the T3 and T3AM. Although both T3 and T3AM forms the expected Se···I halogen bonding with MeSe¯, the strength of halogen bonding was found to be less for T3AM than T3. Furthermore, detailed kinetic and spectroscopic studies indicate that T3 and T3AM exist as dimeric and monomeric species in solution. The dimerization of T3 in solution was shown to have remarkable impact on the activation energy and pre-exponential factor of the deiodination reactions. Single crystal X-Ray crystallography and theoretical calculations indicated that in addition to Se···I halogen bonding, I···I halogen bonding may play an important role in the deodination of thyroid hormones by deiodinase mimics. Furthermore, the presence of heteroatoms such as nitrogen, oxygen and sulphur in the close proximity of one of the selenium atoms of deiodinase mimics was shown to have significant effect on the rate of deiodination reactions. The third chapter of the thesis focusses on the conformational polymorphism and conformation-dependent halogen bonding of L-thyroxine. Synthetic version of L-thyroxine (T4) is a life-saver for millions of people who are suffering from hypothyroidism, a thyroidal disorder recognised by low levels of T4 and elevated levels of TSH in blood plasma. Synthetic version of L-thyroxine is available in the Figure 4. Ball and stick model of the single crystal X-Ray structure of the conformational polymorphs of L-thyroxine. Form I and Form II was exclusively crystallized from methanol and acetonitrile, respectively. Water molecules are omitted for clarity. market with various brand names. However, adverse effects have been observed in the patients when they switch their brand of thyroxine. Based on these observations, the American Thyroid Association (ATA), the Endocrine Society (TES), and the American Association of Clinical Endocrinologists (AACE) declared that the different brands of T4 are not bioequivalent, thus leading to differences in the bioavailability of the drug. We have shown that the commercially available thyroxine exists in at least two stable forms (Form I and Form II) with different three-dimensional structures (Figure 4). These two forms exhibit different intermolecular interactions in crystal packing, spectral behaviours, thermal stabilities, optical activity and very interestingly, different solubility in acidic and basic pH. At pH 4, solubility of Form I is about 42% and 45% greater than that of Form II and bulk T4, respectively, whereas at pH 9, the solubility of Form II is about 38% and 42% higher than that of Form I and bulk T4, respectively. As T4 is a narrow therapeutic index drug, these differences in solubility may have remarkable impact on the bioavailability of the drug. In addition to this, we have shown that the ability of the iodine atoms in the C-I bonds to form halogen bond with donor atoms can be altered by changing the relative orientation of tyrosyl and phenolic rings in T4. In the fourth chapter, the three-dimensional structures and conformations of thyroid hormones (THs) and iodothyronamines (TAMs) are discussed. TAMs, the endogenous decarboxylated metabolites of THs, exhibit different binding affinities to the transport proteins and iodothyronine deiodinases (DIOs) compared to the THs. Figure 5. Change in the structure and conformations of thyroid hormones and iodothyronamines with the decarboxylation of amino acid side chain and deiodination of phenolic and tyrosyl ring. Furthermore, the substrate specificities of DIOs have been found to be dependent on the position of iodine atoms on the phenolic and tyrosyl ring of TAMs and THs. Single crystal X-ray structures of TAMs indicate that decarboxylation of amino acid side chain of THs induces significant changes in the structure and conformation. Furthermore, the positional isomers of THs and TAMs exhibit remarkably different conformations, which may have significant effect on the binding of these metabolites to the active site of DIOs. In addition to the structure and conformations, different categories of the intermolecular halogen···halogen (X···X) interactions in the crystal packing of THs and TAMs have also been discussed. Natural bond orbital (NBO) analysis have been done on the halogen-bonded geometries to understand the electronic nature of these interactions. In the fifth chapter, the dehalogenation of halogenated nucleosides and nucleobases by naphthyl-based sulphur/selenium compounds is discussed. Purine and pyrimidine nucleosides are halogenated at various positions of the aromatic ring by different peroxidases such as myeloperoxidase and eosinophil peroxidase present in the white blood cells. Incorporation of the halogenated nucleosides into the DNA of replicating cells leads to DNA-strand breaks, mutagenesis, carcinogenesis and loss of Figure 6. (A) Dehalogenation of halogenated nucleosides. Effect of base-pairing wih adenine and guanine on the deiodination of IU (B) and debromination of BrU (C) by compound 2. genome integrity. We have shown that the naphthalene-based organoselenium compounds such as compound 2 can mediate the dehalogenation of 5-iodo-2'-deoxyuridine (5-IdUd) and 5-bromo-2'-deoxyuridine (5-BrdUd) to produce 2'-deoxyuridine (dUd) (Figure 6A). The deiodination of 5-IdUd was found to be faster than the debromination of 5-BrdUd by compound 2. The mechanism of dehalogenation of halogenated nucleosides by compound 2 was found to be dependent on the nature of halogen. While the deiodination of 5-IdUd by compound 2 follow halogen bond-mediated pathway like thyroid hormones, debromination of 5-BrdUd follow a Michael addition-elimination pathway. Similar results were obtained when 5-iodo-2'-deoxycytidine (5-IdCd) or 5-bromo-2'-deoxycytidine (5-BrdCd) was used as substrate for dehalogenation reaction. Base-pairing of 5-iodouracil (IU) and 5-bromouracil (5-BrU) with adenine and guanine has a significant effect on the rate of dehalogenations of IU and BrU by compound 2 (Figure 6B and 6C).

O estudo que ora se apresenta integrou o conjunto de pesquisas do sub-projeto - Diversidade de Bactérias Associadas à Degradação de Compostos Recalcitrantes, do projeto temático BIOTA FAPESP - Ecologia Molecular e Taxonomia Polifásica de Bactérias de Interesse Ambiental e Agro-Industrial. Apresenta caráter inovador, na medida em que procurou avaliar o potencial de aplicação biotecnológica de microrganismos anaeróbios de uma área severamente contaminada no Brasil, o estuário de Santos-São Vicente, em degradar o pentaclorofenol (PCP). A pergunta fundamental a ser respondida pelos resultados experimentais realizados foi: são os microrganismos autóctones do estuário capazes de servirem de inóculo para degradar o pentaclorofenol em biorreatores sob condições metanogênicas? Dois grupos de amostras foram avaliados, o primeiro, uma parcela composta por vários sedimentos coletados no estuário e, o segundo, sedimentos coletados na região do Largo de Canéus e na frente da Companhia Siderúrgica Paulista (COSIPA). O estabelecimento da determinação cromatográfica do PCP e congêneres menos clorados para o monitoramento experimental mostrou que na análise da presença dos clorofenóis nos sedimentos, o método de extração por ultrassom com posterior metilação dos analitos foi adequado para concentração mínima de 200 'mü'g clorofenóis/Kg sedimento para 2,3; 2,6 diclorofenóis; 2,4,6 e 2,3,6 triclorofenóis. Contudo, não foi adequado para a determinação do PCP e 2,3,4 triclorofenol. Para o meio de cultivo, o método de extração do PCP por agitação em vórtex e acetilação dos analitos mostrou-se adequado para todos os clorofenóis e com limite de quantificação de 0,1 mg/L. A avaliação do potencial metanogênico foi realizada com as amostras compostas do estuário enriquecidas sob condições halofílicas. O valor estável de metano no biogás de 50% foi obtido nos primeiros 20 dias de incubação. O sedimento nessas condições foi utilizado como inóculo para fins de isolamento de culturas metanogênicas, redutoras do íon sulfato e degradadoras de PCP. Não foram obtidas culturas desalogenadoras; porém foram isoladas arquéias metanogênicas, cultivadas em metanol, acetato e formiato de sódio, bem como bactérias cultivadas em lactato de sódio na presença e ausência de sulfato de sódio. Ensaios fisiológicos aliados aos métodos moleculares FISH e DGGE permitiram identificar arquéias metanogênicas do gênero Methanosarcina sp. e microrganismos do domínio Bacteria. Os sedimentos individualmente estudados foram coletados com maior controle de anaerobiose empregando-se amostrador do tipo corer. O enriquecimento destes sedimentos, inicialmente sob concentração de 2,5 mg PCP/g STV e com adições periódicas de 50% da concentração inicial do clorofenol e 1,25 a 2,5 g/L de glicose por 13 meses a 30 graus Celsius, resultou na obtenção de culturas degradadoras do PCP sob anaerobiose estrita. Nos reatores controles sem PCP, já primeiros 20 dias de incubação 70% de metano foi determinado no biogás. Nos reatores com PCP, a produção do metano (20%) iniciou após 100 dias. A adsorção foi o principal mecanismo de remoção de 50% do PCP nas primeiras 12 horas de incubação dos enriquecimentos. Posteriormente, a redução do PCP no meio de 77% para a amostra de Canéus e 70% para a da COSIPA foi relacionada a mecanismos de biodegradação anaeróbia, como a desalogenação redutiva. Exames microscópicos mostraram a seleção de microrganismos na presença de PCP, com predomínio de bacilos formadores de esporos semelhantes ao gênero Clostridium sp., filamentos diversos e filamentos semelhantes as arquéias metanogênicas acetoclásticas relacionadas ao gênero Methanosaeta sp. O enriquecimento foi realizado sob condições halofílicas, segunda a salinidade de cada amostra estudada no estuário. Não houve perda do clorofenol por volatilização. Os resultados obtidos no enriquecimento anterior viabilizaram o estudo seguro do potencial anaeróbio dos microrganismos oriundos do sedimento da COSIPA em metabolizar o PCP em reator contínuo do tipo RAHLF. Assim, sedimento enriquecido sob condições metanogênicas e halofílicas foi inoculado no RAHLF, controlando-se rigorosamente a anaerobiose. O reator preenchido com cubos de espuma de poliuretana foi operado por 126 dias e tempo de detenção hidráulica de 18 horas, com meio de cultura salino contendo glicose (1 g/L) como principal fonte de carbono e PCP-Na nas concentrações de 5, 13, 15 e 21 mg/L. O desempenho do RAHLF foi estável com boa eficiência durante toda a operação. A redução dos níveis de matéria orgânica medida em DQO variou de 70 a 100% e a de PCP foi de 99%, com detecção de intermediários menos clorados e sob teores de metano no biogás de 20%. Da massa de 1111,73 mg de PCP aplicada no reator, 286,9 mg ficou retida no sistema pelo processo de adsorção nas biopartículas e 824,83 mg foi biodegradada. As análises morfológicas dos tipos celulares, em conjunto com as técnicas moleculares DGGE e FISH, revelaram a presença de grupos microbianos do domínio Archaea pertencente à família Methanosarcinacea e grupos do domínio Bacteria. A participação de grupos de domínio Bacteria, cuja estrutura dos tipos microbianos na comunidade variou ao longo do RAHLF e das concentrações de PCP, e dos organismos metanogênicos da família Methanosarcinacea, possibilitou responder a questão inicialmente formulada, uma vez que se pode afirmar que os microrganismos autóctones foram capazes de degradar o PCP sob condições metanogênicas e halofílicas, com eficiência adequada. A prática para a seleção dos microrganismos retirados do ambiente estuarino, de interesse para biotecnologia anaeróbia aplicada ao saneamento ambiental, que empregou o reator do tipo RAHLF, parece promissora para avanços da engenharia na remediação biológica de uma área cuja relevância é indiscutível para o estado de São Paulo / This study has an innovative character, once aimed to evaluate the biotechnological application of anaerobic microorganisms degrading pentachlorophenol (PCP) at a severely polluted area in Brazil, estuary of Santos-São Vicente, São Paulo state. This study integrated a group of researches of the sub-project - Diversity of Bacteria Associated to the Degradation of Recalcitrant Compounds, supported by major project BIOTA FAPESP which theme is Molecular Ecology and Polyphasic Taxonomy of Bacteria of Environmental and Agriculture-Industrial Interest. The fundamental question to be answered by the accomplished experimental results was: are the autochthonus microorganisms of the estuary capable of serving as inoculum to degrade the PCP in bioreactors under methanogenic conditions? In order to evaluate this hypothesis, two groups of samples were collected: sediments taken from several sites of the estuary and sediments taken from two sites, one severely contaminated with organochlorine compounds, in front of the São Paulo Metallurgical Company (COSIPA) and other, less contaminated, in the area of Canéus. The establishment of protocol for the PCP and less chlorinated compounds chromatographic determination showed that the extraction method by ultrosonication followed by metilation of the chlorinated compounds was appropriated to evaluate concentrations of 200 ug chlorophenol/Kg of sediment, 2,3; 2,6 dichlorophenols; 2,4,6 and 2,3,6 trichlorophenols. However, it was not appropriated for evaluation of PCP and 2,3,4 trichlorophenol. For the culture medium, the extraction method by vortex agitation followed by acetilation was appropriated for all of the chlorophenols compounds. The quantification limit was 0,1 mg/L. The evaluation of the methanogenic potential and PCP biodegradation was accomplished with the samples of the estuary enriched under halophylic conditions. In the experiments without PCP was possible to obtain cultures of Methanosarcina sp, identified by FISH technique and cells of domain Bacteria, identified by DGGE. In the experiment with PCP dehalogenated cultures were not obtained. To evaluate PCP anaerobic biodegradation by sediments of COSIPA and Caneus sites, sediments collected under anaerobic conditions by a corer device were enriched in a halophylic brine medium with glucose and PCP at concentration of 2.5 mg PCP/g VTS. Periodic additions of 50% of the initial concentration of PCP and 1.25 to 2.5 g/L of glucose were done. With this strategy was possible to obtain PCP dehalogenated cultures. The adsorption was the main mechanism of 50% of PCP removal in the first 12 hours of incubation. The PCP reduction of 77% for Caneus reactor and 70% for COSIPA reactor was related to anaerobic biodegradation. Microscopic exams showed selection of microorganisms, with predominance of cells related to Clostridium sp., and filaments related to methanogenic acetoclastic archaea Methanosaeta sp. chlorophenols volatilization was not observed. The biotechnological application of HAIB reactor in PCP biodegradation was evaluated using sediment of COSIPA site previously enriched with glucose. The reactor was operated by 126 days and hydraulic detention time of 18 hours, with saline brine medium containing glucose (1 g/L) and NaPCP in concentrations of 5, 13, 15 and 21 mg/L. PCP amendments did not affect the overall performance and functional stability of the process. COD and PCP reduction was close to 80% and 100%, respectively with detection of trichlorophenols and dichlorophenols. Percentage of methane in the biogas closed to 30%. Adsorption analyses demonstrated that 287 mg of PCP was removed by adsorption in the biofilm and 825 mg was removed by biodegradation. Biofilm DGGE-profiling showed the presence of specific bands of Bacteria and Archaea domains when PCP was amended. The appearance of new bands of Bacteria showed that this organisms had a direct influence at PCP dehalogentation. Archaea organisms of Methanosarcinaceae family had an indirect influence in this metabolism. This thesis demonstrated that HAIB reactors, using autochthonous microorganisms under halophylic and methanogenic conditions, are a potential alternative for organochlorines bioremediation

A pesquisa que ora se apresenta visou estabelecer as condições nutricionais adequadas para o uso do sedimento do estuário de Santos - São Vicente do Estado de São Paulo, como inóculo no reator anaeróbio horizontal de leito fixo (RAHLF) no processo de degradação anaeróbia do pentaclorofenol (PCP) em busca da aplicação da tecnologia em escala real, assim como identificar grupos microbianos envolvidos no processo. Para tanto, sedimento do estuário de Santos-São Vicente, com características metanogênicas foi utilizado. Os microrganismos provenientes do sedimento estuarino foram enriquecidos sob condições metanogênicas e halofílicas, visando a utilização do sedimento como inoculo nos ensaios nutricionais e na operação dos reatores do tipo RAHLF. O meio de cultivo salino Biota, suplementado com glicose e formiato, foi utilizado para o desenvolvimento da comunidade microbiana metanogênica halofílica. Testes de degradação do PCP foram realizados previamente sob diferentes concentrações de nitrogênio e fósforo, com vistas a uma melhor compreensão da relação N:P adequada para o processo anaeróbio. Os resultados provenientes do acompanhamento da diversidade microbiana do domínio Bacteria nas diferentes relações testadas indicaram a seleção de distintas comunidades microbianas, resultando em diferentes velocidades de degradação do PCP. A relação N:P de 10:1 foi a que apresentou melhores resultados, pois além da rápida degradação do PCP quando comparada com as outras relações, apresentou a maior diversidade de microrganismos. Posteriormente, o sistema RAHLF foi operado com vazão média afluente de aproximadamente 44 mL/hora, com meio mineral salino Biota (DQO:N:P de 1000:130:45) para R1 e com a alteração para relação DQO:N:P de 1000:10:1 para R2. Duas diferentes estratégias foram adotadas para partida dos reatores. Para R1, optou-se por acrescentar PCP na concentração inicial de 10,0 mg/L, durante 110 dias causando desestabilização da metanogênese e acúmulo de PCP, requerendo intervenção para recuperação do reator pelo período de 90 dias. Na partida do RAHLF 2, optou-se pelo aumento gradual de concentração do PCP de 0,5 mg/L a 12,0 mg/L durante 52 dias. Após estabelecimento da metanogêsenese, R1 foi alimentado durante 270 dias com 5,0 mg PCP/L, durante 41 dias com 8,0 mg/L e 59 dias com 12 mg/L. O balanço de massa no reator RAHLF 1 demonstrou que 0,52% do PCP adicionado saiu no efluente e que não ocorreu adsorção no sistema. 22,34 mg de 2,4,6 TCP, intermediário da degradação do PCP, ficaram adsorvidos na biopartícula. Os resultados das análises de diversidade microbiana apontaram para mudança da comunidade microbiana do domínio Bacteria ao longo do período operacional e morfologias de bacilos fluorescentes semelhantes a Methanobacterium sp estiveram presentes no reator. No RAHLF 2, a degradação do PCP foi de 100%, até a concentração de 10,0 mg/L. No final da fase com 12,0 mg PCP/L, a concentração no efluente foi de 1,4 mg PCP/L, com eficiência média de remoção de 93,2 \'+ ou -\' 5,5%. 2,4,6 TCP foi o intermediário principal no efluente do reator. 4,06% do PCP adicionado ao sistema foram encontradas no efluente e 15,94% ficaram adsorvidas nas biopartículas do reator. Portanto, considera-se que 80% do PCP adicionado sofreu degradação anaeróbia microbiana. A presença dos microrganismos Methanocalcullus e Methanosaeta na fase final de operação do RAHLF 2 e determinadas no sedimento coletado foi considerada fundamental para manter estabilidade do reator. Essa descoberta contribui com informações sobre a real diversidade microbiana de ecossistemas tropicais, sobretudo em habitats anaeróbios, bem como sobre as condições nutricionais e os procedimentos necessários para confiná-la em reatores e usá-la em processos de biorremediação. / The research presented here aimed to determine the optimal nutritional conditions for the use of sediment from the Santos-São Vicente estuary in the state of São Paulo, Brazil, as an inoculum for a horizontal-flow anaerobic immobilized biomass reactor (HAIB) applied to the anaerobic degradation of pentachlorophenol (PCP), seeking to apply the technology on the real scale and to identify the microbial groups involved in the process. To this end, sediment with methanogenic characteristics from the Santos-São Vicente estuary was used. The microorganisms from the estuarine sediment were enriched under methanogenic and halophilic conditions, aiming to use the sediment as an inoculum in nutritional assays and in the operation of HAIB reactors. Biota saline culture medium supplemented with glucose and formiate was used to develop the halophilic methanogenic microbial community. PCP degradation tests were carried out previously under different concentrations of nitrogen and phosphorus in order to gain a better understanding of the optimal N:P ratio for the anaerobic process. The findings on the microbial diversity of the domain Bacteria at the various ratios tested here indicated the selection of distinct microbial communities, resulting in different PCP degradation velocities. The N:P ratio utilized was 10:1 since it presented the best results not only in terms of faster PCP degradation than the other ratios but also highest diversity of microorganisms. The HAIB reactor was then operated with a mean inflow of approximately 44 mL/hour, using the biota saline mineral medium with a COD:N:P ratio of 1000:130:45 in R1 (reactor 1) and a COD:N:P ratio of 1000:10:1 in R2. Two distinct strategies were adopted to start up the reactors. In R1 PCP was added at an initial concentration of 10.0 mg/L for 100 days, causing destabilization of the methanogenesis and accumulation of PCP, requiring a 90-day intervention for the reactor\'s recovery. To start up R2, the PCP concentration was increased gradually from 0.5 mg/L to 12.0 mg/L for 52 days. After methanogenesis was established, R1 was fed for 270 days with 5.0 mg of PCP/L, followed by 41 days with 8.0 mg/L and 59 days with 12 mg/L. The mass balance in R1 indicated that 0.52% of the added PCP exited through the reactor\'s outflow and that adsorption of the system did not occur. 22.34 mg of 2,4,6 TCP, an intermediary of PCP degradation, was adsorbed in the bioparticles. The results of the analysis of microbial diversity indicated a change in the microbial community of the domain Bacteria along the operational period, with fluorescent bacilli morphologies resembling Methanobacterium sp present in the reactor. PCP degradation in R2 was 100% up to a concentration of 10.0 mg/L. At the end of the phase with 12.0 mg PCP/L, the effluent concentration was 1.4 mg PCP/L, with a mean removal efficiency of 93.2 \'+ or -\' 5,5%. 2,4,6 TCP was the main intermediary in the reactor\'s effluent. 4.06% of the PCP added to the system was found in the effluent and 15.94% was absorbed in the bioparticles of the reactor. Therefore, it was concluded that 80% of the added PCP underwent microbial anaerobic degradation. The presence of Methanocalcullus and Methanosaeta microorganisms in the final operating phase of R2, which was determined in the collected sediment, was considered fundamental for maintaining the reactor\'s stability. This discovery contributes to the body of information about the real microbial diversity of tropical ecosystems, above all in anaerobic habitats, and about the nutritional conditions and procedures involved in confining these microorganisms in reactors and using them in bioremediation processes.