Loss of nitrogen (N) from dairy manure during storage is an issue of economic, environmental, and social concern for farming communities. The lost N 1) decreases the value of manure as a fertilizer and is an economic loss because supplemental inorganic N fertilizer is purchased to meet N needs on farms; 2) produces the potential pollution for water and air systems, thereby damaging the associated ecosystems; 3) causes challenges to human health. Thus, it is vital to manage and use N in an efficient and eco-friendly manner. N mineralization is a pathway in the N cycle, which converts organic N to inorganic N that is more susceptible to loss. The objective of this study was to conduct lab-scale experiments to assess the effects of temperature, manure solids content, using manure seed and autoclave sterilization operation at the start of storage, and storage time on the N mineralization and the associated microbial community during the storage of liquid dairy manure. Manure scrapped from the barn floor of a commercial dairy farm and diluted to make experimental stocks with high (46 to 78 g/L) and low (19 to 36 g/L) total solids (TS), to simulate what is typically transported to the manure storage pit was used. The manure was incubated in the laboratory at three temperatures (10, 20, and 30°C) for two storage periods (60 and 180 days). Manure samples were taken at different storage time for analyses. The results showed that temperature and using sterilization operation at the start of storage had significant effects on N mineralization for both storage periods (p < 0.05). The highest N mineralization rate occurred at 30℃, which rate constant (k) was 0.096 week-1. While, the lowest N mineralization occurred at 10℃, and its corresponding k was 0.013 week-1. The concentrations of mineralized N (Nm) with non-sterilized (R) manure were significantly higher than that with sterilized (R0) manure (p < 0.05). Compared to that with high TS (H) manure, the concentrations of Nm were significantly higher with low TS (L) manure after 180-d storage (p < 0.05). Raw manure augmented with manure seed (MS) had significantly higher Nm than the manure seed only (SO) (p < 0.05). In order to investigate the changes of microbial community in manure, samples were collected on days 0, 30, 90, and 180 for the 180-d storage experiment, and days 0, 30, and 60 for the 60-d storage experiment, and then manure DNA under different condition was successfully extracted from collected samples and used for 16S rRNA sequencing. This study provided a more comprehensive understanding of the impact factors for manure storage, and was expected to clarify the relationship between N mineralization and the associated microbial community. / Master of Science / Loss of nitrogen (N) from dairy manure during storage is rooted in the process of degradation via microbial activities. During storage of dairy manure, up to 60% of N can be lost to the environment (the air, rivers, groundwater, etc.), causing damages such as global warming and water pollution. However, it is challenging to manage and reduce the N lost during manure storage because of lack of comprehensive knowledge of the complex microbial activities in manure storage structures. Thus, the long-term goal of this study is to discern the interactions of the physical, chemical, and microbial processes that affect the N transformation. The generated information will help to mitigate/minimize the loss of nitrogenous gases during storage of dairy manure. The specific objectives included: 1) to evaluate the effects of selected factors (including storage time, temperature, manure solids content, using manure seed and sterilization operation at the beginning of storage) on N mineralization during storage of liquid dairy manure and determine the associated N mineralization rate; 2) to reveal the microbial communities in stored liquid dairy manure under different conditions (listed above). The outcome of this study could be used to refine N mineralization input parameter of manure storage submodules of the process-based models such as Manure DeNitrification-DeComposition model (Manure-DNDC) and Integrated Farm System Model (IFSM) with the goal to improve their accuracy of estimating or accounting for the fate or cycling of N in dairy manure during storage.

Keystone species are widely distributed across aquatic and terrestrial ecosystems and are fundamental in preserving the structure, diversity, and stability of an ecological community due to its disproportionately large impact on its community relative to its biomass. As biodiversity of ecosystems becomes more threatened with urbanization and habitat destruction, it is imperative to understand a keystone species' role in maintaining ecosystem function. One of the ways to do so is by examining their significance and connection to the ecosystem food web. Within North American freshwater ecosystems is the pebble nest-building minnow, the bluehead chub (Nocomis leptocephalus; "chub"). Chubs provide spawning habitat for not only themselves, but for other minnows, collectively called "nest associates". In this work, I observe the predatory and potential mutualistic interactions between chubs, nest associates, and their predators. In Chapter 1, I observe spawning nests to identify the predators of adult chubs, nest associates, and embryos. I further investigate how nest visibility covariates including minnow activity, minnow abundance, nest size (area), and nest growth affect predator encounter rate to spawning nests. I found a total of 23 diverse taxa to prey on the adult minnows and minnow embryos on chub spawning nests, 14 predators of which had not been reported in literature. One of these predators was the common snapping turtle (Chelydra serpentina; "turtle"). Additionally, I found that activity, abundance, nest size (area), and nest growth had a significant effect on predator encounter rate, attracting predators to seek spawning nests for prey. In Chapter 2, I investigate the effect of ambient temperature on turtle epizoic coverage during the spawning season and provide preliminary evidence of a potential cleaning symbiotic mutualism between the turtle and minnows. I found that epizoic coverage decreases during the duration of a minnow spawning season after an initial increase with early summer warming, and my results also present unique and shared bacterial communities across three sources, the ambient environment, gut contents of minnows, and turtles. The results additionally revealed there to be bacterial communities unique between minnows and turtles that were not identified in the ambient environment. Overall, this study is first to systematically document predators of chub spawning nests and first to provide preliminary evidence of a cleaning symbiotic mutualism between a freshwater turtle and minnow species (or freshwater turtles and fish in general), which, thus far, has not been explored in freshwater ecosystems. This work demonstrates that chub spawning nests are a crucial entity of the freshwater food web structure across Nocomis' distribution range and reveals that chub spawning nests create an interconnection between a diversity of fauna in a freshwater ecosystem. / Master of Science / Ecological communities often include species that are essential in ensuring the overall stability and biodiversity of an ecosystem. These species, otherwise called keystone species, play a crucial role in facilitating interconnections within the ecosystem's food web. The bluehead chub (Nocomis leptocephalus; "chub") is an example of a keystone minnow found in North American freshwater streams. This minnow engages in a complex, distinguished act when it reproduces, making mounded, pebble nests using only its mouth. Chubs are not the only minnow species interested in this engineering complexity. Various minnow species called "nest associates" reproduce on the nests as well, providing an appearance of a mutualism: all species involved benefit from the interaction. While this interaction has been observed, there is limited research identifying predators of chub nests and if there are potential mutualisms with any of these predators. In this work, I identify predatory and mutualistic interactions between chubs, nest associates, and their predators. In Chapter 1, I identify predators of chub nests and observe variables that attract these predators to the nests. In Chapter 2, I explore a potential, mutualistic interaction between these minnows and an identified predator from this research, the common snapping turtle (Chelydra serpentina; "turtle"), whereby minnows feed on potentially harmful growth of algae and bacteria on turtles, while turtles benefit from the cleaning. For Chapter 1, my results revealed that a chub nest is a hotspot for predator diversity, showing 23 diverse taxa as predators, in which 14 of the identified taxa are novel for ecological literature. Additionally, variables that were observed to attract predators to chub nests were minnow activity, minnow abundance, nest size (area), and nest growth. Results for Chapter 2 demonstrated that there are unique bacterial communities between turtles and minnows that are not found in the stream environment, therefore providing preliminary evidence of mutualistic interaction between the coexisting species. Overall, this study is the first to systematically document predators of chub nests. This study is also first to investigate a mutualistic interaction between minnows and turtles in a freshwater ecosystem, an area that has not been previously explored, unlike similar interactions in marine ecosystems. Cohesively, the keystone species, the chub, and their reproductive nests, are important for the aquatic food web structure and the interconnectedness to their overall ecosystem function. This research further stewards scientific knowledge about how important Nocomis are to natural freshwater ecosystems.

Innerhalb der Arthropodensystematik sind die phylogenetischen Beziehungen der höheren Crustaceataxa seit langem von besonderen Interesse. Ziel dieser Arbeit ist die Rekonstruktion der phylogenetischen Verwandtschaftsverhältnisse mit Hilfe molekularer Datensätze für die Phyllopoda, die zusammen mit den Anostraca die Branchiopoda bilden und der Astacoidea (Astacida), einer Teilgruppe der Flusskrebse. Folgende molekulare Marker kamen zum Einsatz: 1) Für die Phyllopoda: Die 3. Domäne der mitochondrial codierten 12S rRNA, unter Berücksichtigung von Sekundärtrukturinformationen, das nukleare Gen EF-1 alpha und die Positionen von Introns im Gen EF-1 alpha. 2) Für die Astacoidea: Die 3. Domäne der 12S rRNA und das mitochondrial codierte Gen cox1. Durch die Wahl der molekularen Marker, die mit unterschiedlichen computerkladistischen Methoden ausgewertet wurden, konnten für die meisten Fragen eine eindeutige und im Fall der Astacoidea überraschende phylogenetische Aussage getroffen werden. Die gewonnenen Hypothesen werden ausführlich im Licht morphologischer Hypothesen diskutiert. / The phylogenetic relationships of the higher arthropod taxa are still of special interest. Especially the interrelationships of the different Crustacea taxa have long been debated. The focus of this investigation is to make a contribution to the phylogenies of two Crustacea taxa using molecular markers: The Phyllopoda which belong together with the Anostraca to the branchiopods, and of the Astacoidea, one of the two higher crayfish taxa (Astacida). The following molecular markers were used: 1) Phyllopoda: the 3rd domain of the mitochondrial encoded 12S rRNA taking into account informations of the secondary structure, the nuclear encoded proteingene EF-1 alpha and the positions of introns found in the coding region of EF-1 alpha. 2) Astacoidea: the 3rd domain of the 12S rRNA and the mitochondrial encoded proteingene cox1. The choice of the mentioned markers in combination with different computercladistical methods allowed to give a satisfying, and in the case of the Astacoidea a more surprising answer to most addressed phylogenetic questions. The gained hypotheses are then discussed in detail in the light of morphological features and hypotheses.

Soils contain highly diverse consortia of bacteria making them very attractive starting points for both culture-dependent and metagenomic discovery efforts. The present diploma thesis analyses the composition of the microbial community from pharmaceutically polluted soil, with the employment of next-generation Illumina sequencing of 16S rDNA region. This analysis revealed high complexity of the soil microbial environment and confirmed that anthropogenic activity (represented by production of beta- lactam antibiotics) influences the variability and abundance of the species, yet without reducing the microbial diversity. In the second part of the thesis, isolation and heterologous expression of a novel gene encoding alpha-amino acid ester hydrolase (AEH) from a cultivable soil microorganism B. cereus is described. AEHs possess industrial potential for biocatalytic synthesis of semi-synthetic beta-lactam antibiotics, which are presently of great clinical importance. Powered by TCPDF (www.tcpdf.org)

Orientador: Lílian Castiglioni-Ruiz / Banca: Fabiano Gazzi Taddei / Banca: Hermione Elly Melara de Campos Bicudo / Resumo: Os camarões do gênero Macrobrachium pertencem à família Palaemonidae. Habitam as proximidades do litoral e, também, ambientes de água doce. Com mais de cem espécies amplamente distribuídas pelas regiões tropicais e subtropicais do mundo, os palemonídeos possuem hábitos crípticos e noturnos. Particularmente na região noroeste do Estado de São Paulo, podemos encontrar várias espécies com importância econômica e ecológica consideráveis. Entretanto, existem poucos estudos na literatura relacionados ao conhecimento da biologia desses crustáceos. Assim, o presente trabalho objetivou analisar a variabilidade genética intra e interpopulacional, de amostras de duas espécies de camarões palemonídeos do gênero Macrobrachium (M. amazonicum e M. jelskii), coletadas em diferentes localidades, utilizando-se a análise das seqüências dos genes mitocondriais COI e rRNA 16S e, ainda, devido à problemática taxonômica existente entre essas duas espécies, também foi analisada a variabilidade genética interespecífica, utilizando-se os mesmos genes.. O cálculo dos índices de divergência genética intrapopulacionais apresentou valores baixos, refletindo uma provável estruturação genética destas populações. Apenas as populações de MjME e do CAUNESP apresentaram valores de divergência genética mais elevados, sugerindo um desequilíbrio na estruturação genética das mesmas, provavelmente causado por interferência antrópica e situação de cativeiro, respectivamente. Nas comparações interpopulacionais, envolvendo M. amazonicum, as taxas de divergência genética apresentaram uma ampla variação, também com média elevada. Os valores elevados nas comparações envolvendo a população do CAUNESP, permitiram descartar a hipótese da provável origem comum das populações de Macrobrachium, a partir de espécimes trazidos do Pará. Da mesma forma, as comparações... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: The genus Macrobrachium (Bate, 1868) belongs to the Palaemonidae family. Their species are widely distributed in lakes, floodplains and rivers in tropical and subtropical regions of South America, having cryptic and nights habits. This genus presents nearly 210 known species with ecological and economic importance. Particulary in the northwestern state of São Paulo, we can find several species with considerable importance. However, there are few studies related to knowledge of the biology of these crustaceans. The aim this work was to analyze the genetic variability interpopulation, and interspecific of two Macrobrachium species (M. amazonicum and M. jelskii), using the mitochondrial gene sequence COI and 16S rRNA. Also, due to taxonomic problems between these two species we analyzed interspecific genetic variability, using the same genes. The intrapopulation rates of genetic divergence values were low, reflecting a probable genetic structure of these populations. Only populations MjME and CAUNESP showed higher divergence values, suggesting changes in their genetic structure of the same, probably caused by human interference and situation of captivity, respectively. In comparisons inferences involving M. amazonicum, rates of genetic divergence showed a wide range, also with high average. High values in comparisons involving the population of CAUNESP, allowed to reject the hypothesis of a probable common origin of populations the Macrobrachium specimens brought from State of Para. Interpopulation comparisons involving M. jelskii also showed high values of divergence, especially for the population collected from the Mendonça dam, whose genetic alteration in population structure was attributed to the frequent introduction of exotic specimens. The values of interspecific genetic divergence in the samples collected in the same geographic location were low for populations Adolfo (0.3%) ...(Complete abstract click electronic access below) / Mestre

Os microrganismos representam a forma de vida mais abundante e diversificada do planeta. A atividade agrícola leva a uma redução da biodiversidade do solo e a menor diversidade microbiana pode resultar na diminuição da ciclagem de nutrientes e no crescimento das plantas. Como forma de avaliar alterações na atividade microbiana e na estrutura das comunidades de bactérias do solo, decorrentes do cultivo da cana-de-açúcar, foram conduzidos dois experimentos. O primeiro, no município de Novo Horizonte (SP), com o objetivo de determinar ação da queima da cana-de-açúcar sobre a comunidade de bactérias do solo e o segundo experimento, nos municípios de Pirassununga (SP) e Jaboticabal (SP), com o objetivo de verificar o efeito da adubação nitrogenada sobre a comunidade bacteriana do solo. Amostras de terra foram coletadas nas profundidades 0-10 e 10-20 cm, na linha e entrelinha de plantio. No primeiro experimento foram utilizadas três cultivares de cana-de-açúcar (SP81-3250, SP80-1842 e RB72-454) sob os sistemas de manejo de colheita sem queima (mecanizada) e com queima (manual) prévia a colheita. Nesse experimento foram avaliadas a diversidade metabólica (Biolog) e a estrutura das comunidades bacterianas por meio da PCR-DGGE do gene rRNA 16S. A mudança no manejo de colheita da cana-de-açúcar provocou modificações no metabolismo heterotrófico do solo, alterando a diversidade metabólica. No entanto, não houve mudanças na estrutura das comunidades bacterianas do solo com e sem queima sob a variedade SP801842. Dessa forma, a primeira queima da cana-de-açúcar previamente à colheita alterou a capacidade e a diversidade metabólica microbiana, mas não mudou a estrutura das comunidades de bactérias em relação à área sem queima. No segundo experimento foram avaliadas amostras de terra, de duas áreas experimentais, sob cultivo de cana-de-açúcar (SP813250), com diferentes doses de N (0, 40, 80 e 120 kg de N ha-1) na forma de uréia, aplicadas no sulco de plantio. Para verificar possíveis alterações na comunidade bacteriana desses solos, foram avaliadas a estrutura das comunidades bacterianas por PCR-DGGE e a diversidade de bactérias oxidadoras de amônio (AOB), pelo seqüenciamento de bibliotecas do gene rRNA 16S, utilizando oligonucleotídeos iniciadores específicos. As doses de N alteraram a estrutura das comunidades bacterianas do solo nas duas áreas experimentais, determinadas por PCR-DGGE, entretanto, a adubação nitrogenada não alterou a diversidade de AOB no solo, das duas áreas. A estrutura da comunidade de AOB no solo da USA, sem adubação nitrogenada e com 80 kg de N ha-1 diferiu estatisticamente. Nas duas áreas, as unidades taxonômicas operacionais mais abundantes se relacionam filogeneticamente a Nitrosospira multiformes. / The microorganisms are the most abundant and diverse living creatures on earth. The agricultural practices reduce the soil biodiversity and a lower microbial diversity can result in a nutrient cycling and plant growth reduction. Two sugarcane crops experiments were investigated to evaluate modifications in the microbial activity and soil bacterial communities structure. The first of them was done at municipality of Novo Horizonte, Sao Paulo State (SP), and it has the aim to determine the sugarcane burn effects on soil bacterial community. The second experiment was introduced at municipalities of Pirassununga (SP) and Jaboticabal (SP) with the objective to verify the nitrogen fertilizing effect on soil bacterial community. The soil samples were taken in 0-10 cm and 10-20 cm depth, between and in the planting furrows. We used three sugarcane varieties (SP81-3250, SP80-1842 e RB72-454) in the first experiment under unburned and burned sugarcane pre-harvest. We evaluated metabolic diversity (Biolog) and the bacterial community structure performing PCR-DGGE of 16S rRNA gene in the first experiment. The sugarcane harvest management had modified the soil heterotrophic metabolism by altering its diversity. In spite of that, there is no difference between the burned and unburned soil bacterial communities under the variety SP80-1842. For that reason, the first year pre harvest burn altered the microbial metabolic diversity and capacity but did not change the bacterial community structure when related with unburned area. In the second experiment, soil samples under the SP81-3250 variety were analyzed from two sites. Each site received different levels of urea as nitrogen fertilization (0, 40, 80 e 120 kg de N ha-1) applied at planting furrows. The PCR-DGGE was applied to verify changes in the bacterial communities structure in these soils. The ammonia-oxidizing bacteria (AOB) diversity was evaluated by sequencing of 16S rRNA gene libraries after the amplification with specific primers. The levels of nitrogen fertilization altered the soil bacterial communities structure in both study sites, by PCRDGGE evaluation. However, the nitrogen application did not alter the soil AOB diversity in those two sites. The soil AOB community structure under no nitrogen and 80 kg N ha-1 application was different from the community structure under the other levels of fertilization in one of the two sites. The operational taxonomic unit are phylogenetically related to Nitrosospira multiformes in the two sites.

A Brachiaria brizantha é considerada uma das forrageiras preferidas entre os agropecuaristas por possuir elevada produção de forragem, tolerância ao calor e ao déficit hídrico, alta resposta à aplicação de fertilizantes, produção em grande massa de raízes e sementes, resistência à cigarrinha das pastagens (exceto as pertencentes ao gênero Mahanarva) e boa competição com plantas invasoras. É considerada a principal fonte de alimento para bovinos, sendo utilizada tanto na cria, recria, como na engorda dos animais. As bactérias fixadoras de nitrogênio ou diazotróficas são procariotos capazes de reduzir o N2 a NH3, forma assimilável pelos organismos, e também podem produzir hormônios vegetais, como ácido-indol-acético, que estimulam o crescimento radicular da planta. Estes micro-organismos apresentam grande importância para a manutenção dos ecossistemas. Sua associação com as raízes de plantas e seu efeito promotor quando associados à Brachiaria brizantha possibilitaria a recuperação de áreas de pastagens que apresentam deficiência de nitrogênio, o que é um mecanismo ainda pouco explorado. Com o objetivo de estudar esta possibilidade, foram escolhidas três áreas (Nova Odessa-SP, São Carlos- SP e Campo Verde-MT), preferencialmente onde o nitrogênio era limitante, constituídas por pastagem de Brachiaria brizantha para a amostragem de solo e raiz. Os três locais demonstraram a ocorrência de diazotróficos, após o isolamento e cultivo das bactérias em meio de cultivo semisólido sem adição de nitrogênio na forma combinada (JNFb). Foram obtidas 110 estirpes bacterianas e, após sorteio aleatório, 72 isolados foram mantidos para realização de testes a fim de se avaliar o potencial biotecnológico das bactérias. Destes, 10 demonstraram atividade da nitrogenase quando submetidos ao método de aumento na concentração de nitrogênio total (Ntotal) em meio de cultura. 57 isolados foram capazes de reduzir o gás acetileno a etileno quando submetidos à técnica de redução de acetileno. As estirpes bacterianas C4 (Pseudomonas sp.) e C7 (Azospirillum sp.), isoladas da rizosfera de Brachiaria brizantha da área de Campo Verde-MT, se destacaram das demais por apresentar atividade da nitrogenase muito superior até a de bactérias diazotróficas que foram incluídas na avaliação como testemunhas positivas. Outros 68 isolados produziram o hormônio vegetal ácido-indol-acético quando cultivados em meio de cultivo LB, na presença de triptofano. A produção variou de 0,39µg/mL a 195 µg/mL de AIA. Todos os 72 isolados foram utilizados em experimento em casa de vegetação para avaliar o efeito de inoculação em B. brizantha quando com eles inoculada. Avaliaram-se a matéria seca da parte aérea e raiz e o teor de nitrogênio total da parte aérea através do método micro-Kjeldhal. Nenhum isolado diferiu significativamente do controle sem inoculação bacteriana que continha a mesma dose de nitrogênio fornecido às plantas. O seqüenciamento parcial do gene 16S rRNA dos 72 isolados permitiu a caracterização de sete grupos genotípicos: Stenotrophomonas sp, Pseudomonas sp., Xanthomonas sp., Bacillus sp., Rhizobium sp, Sphingomonas sp. e Azospirillum sp. O gênero Stenotrophomonas sp. predominou (69%) nas três áreas de estudo. / Brachiaria brizantha is considered one of preferred fodders among farmers for having high forage yield, tolerance to heat and drought, high response to fertilizer application, large production of root mass and seeds, resistance to grassland leafhopper (except those belonging to the genus Mahanarva) and good competition with weeds. It is considered the main source of food for cattle, being used in the raising, breeding, and fattening of animals. The nitrogen fixing bacteria or diazotrophs are prokaryotes able to reduce N2 to NH3, which is assimilated by organisms, and may also produce plant hormones such as indole-acetic acid, which stimulates root growth. These micro-organisms have great importance for the maintenance of ecosystems. Their association with plant roots and their promoting effect when combined with Brachiaria brizantha enable recovery of nitrogen-deficient grazing areas, which is a mechanism still little explored. Therefore, three areas were chosen (Nova Odessa-SP, Sao Carlos-SP and Campo Verde-MT), preferably where nitrogen was limiting, consisting of Brachiaria brizantha from which samples of soil and roots were collected. The three sites showed the occurrence of diazotrophs after the isolation and cultivation of bacteria in semi-solid culture medium with no nitrogen added in the combined form (JNFb). It was obtained 110 bacterial strains and, after the raffle random, 72 were kept isolated for testing in order to assess the biotechnological potential of bacteria. From which, 10 showed nitrogenase activity when subjected to the method of total nitrogen concentration increase (N-total) in the culture medium. 57 isolates were able to reduce acetylene to ethylene when subjected to the acetylene reduction technique. The strains C4 (Pseudomonas sp.) and C7 (Azospirillum sp.), isolated from the rhizosphere of Brachiaria brizantha in the area of Campo Verde-MT, stood out from the others by presenting nitrogenase activity far superior to that of diazotrophs recommended as positive controls. Other 68 isolates produced the plant hormone indole-acetic acid when grown in LB culture medium in the presence of tryptophan. Production ranged from 0.39 g/mL to 195 g/mL of IAA. All 72 isolates were used in an experiment in a greenhouse to evaluate the effect of inoculation on B. brizantha. Evaluations were carried out on dry matter of shoot and root and total nitrogen content of the shoot through the micro-Kjeldahl method. None of the isolates differed significantly from the control without bacterial inoculation which contained the same amount of nitrogen supplied to plants. Partial sequencing of the 16S rRNA of the 72 isolates allowed the characterization of seven genotype groups: Stenotrophomonas sp., Pseudomonas sp., Xanthomonas sp., Bacillus sp., Rhizobium, Sphingomonas sp. and Azospirillum sp. The genus Stenotrophomonas sp. predominated (69%) in the three study areas.

A Terra Preta Antropogênica (TPA) tem essa denominação porque é encontrada em sítios arqueológicos, onde viveram grupos pré-históricos e é considerada um dos solos mais férteis do mundo. Nela é encontrada grande quantidade de material deixado por grupos indígenas como fragmentos cerâmicos, artefatos líticos, e especialmente carvão pirogênico. Estudos realizados com o carvão pirogênico verificaram que ele aumenta a capacidade de trocas catiônicas nesses solos. Por meio de microscopia de fluorencência, foi observada a presença de microrganismos habitando esse carvão, no entanto, não se sabe quais seriam. Devido à falta de informações sobre a diversidade bacteriana nessas estruturas, este trabalho estudou a diversidade bacteriana em amostras de carvão pirogênico de solos TPA coletadas nos sítios Lagoa Balbina (Amazônia Central- Amazonas) e Mina I (Amazônia Oriental - Pará), através de técnicas moleculares independentes de cultivo. O estudo visou também comparar essa diversidade com a encontrada no solo de onde carvão foi isolado. As estruturas de carvão foram separadas fisicamente dos solos e seu DNA genômico total extraído e usado como molde em reação de PCR utilizando oligonucleotídeos do gene 16S rRNA para o Domínio Bacteria. O produto da PCR foi clonado em vetor e os clones foram sequenciados e comparados com o banco de dados de 16S rRNA do RDPX. Com a construção das bibliotecas de clones do gene 16S rRNA a partir das amostras de carvão pirogênico observou-se que existe maior número de bactérias desconhecidas no carvão pirogênico do que no solo onde ele foi isolado. Acidobacteria foi o filo predominante nas bibliotecas de carvão pirogênico das duas localidades de estudo, assim como na biblioteca do solo do sítio Mina I. Já na biblioteca do solo do sítio Lagoa Balbina houve predominância do filo Firmicutes. Por meio do método de rarefação foi possível constatar uma menor riqueza de UTOs nas comunidades bacterianas presentes nas estruturas de carvão pirogênico quando comparado à riqueza de UTOs das comunidades bacterianas cujo habitat é o solo. Mas quando se compara a riqueza de UTOs entre as estruturas de carvão isoladas das duas localidades, observa-se que a riqueza é maior no sítio Mina I. Os valores obtidos com os índices de diversidade revelaram menor diversidade de UTOs nas bibliotecas obtidas para o carvão pirogênico das duas regiões estudadas se comparado dos valores para as bibliotecas obtidas do solo da mesma região. Os valores obtidos com os métodos não paramétricos revelaram maior riqueza de UTOs para as bibliotecas do carvão do sítio Mina I e solo TPA do sítio Balbina. A análise da PCA revelou que as bibliotecas do sítio Balbina mostraram-se altamente similares. Em adição, a análise com S-Libshuff, verificou que todas as bibliotecas comparadas são significativamente diferentes quanto à composição das comunidades bacterianas. O carvão pirogênico não é uma estrutura inerte, pois é capaz de ser habitado por diferentes bactérias e a sua estrutura da comunidade bacteriana é diferente daquela de onde ele foi segregado / Anthropogenic Dark Earth (ADE) has this denomination because it is found at archeological sites, where prehistoric groups lived, and it is considered one of the most fertile soils of the world. In this soil a great amount of material left by indigenous groups was found as ceramic fragments, lithic workmanships, and especially pyrogenic black carbon. Studies accomplished with the pyrogenic black carbon verified that it increases the capacity of cationic changes in soils. Through fluorescence microscopy, the presence of microorganisms was observed inhabiting that black carbon, however, this community is still unknown,due to the lack of information about the bacterial diversity in those structures.This work studied the bacterial diversity in samples of pyrogenic black carbon of ADE soils, collected at the sites Lagoa Balbina (Central Amazon) and Mina I (Oriental Amazon), through molecular techniques independent of cultivation. The study also sought to compare that diversity with the one of the soil where black carbon was isolated. The structures of black carbon were separate physically from the soils and total genomic DNA was extracted and used as template in a PCR reaction, using primers of the 16S rRNA gene for the Bacteria Domain. The PCR product was used for construction of clone libraries and the clones were sequenced and compared with the 16S rRNA of RDPX database. The 16S rRNA gene clone libraries from the samples of pyrogenic black carbon, it shown that is a larger number of unknown bacteria in the black carbon than in the soil where it was isolated. Acidobacteria was the predominant phylum in the pyrogenic black carbon libraries from the both studied places, as well as in the soil library from Mina I site. However in the library Lagoa Balbina site there was predominance of the phylum Firmicutes. Through the rarefaction method it was possible to verify a smaller richness of OTUs in the bacterial communities presents in the pyrogenic black carbon structures when compared to the OTUs richness of the bacterial soil communities.But, when the OTUs richness is compared among the isolated structures of pyrogenic black carbon of the two places, it is observed that the richness is higher in the Mina I site. The values from diversity indexes revealed smaller diversity of OTUs in the pyrogenic black carbon libraries when compared with the soil libraries for the two studied areas. The obtained values with the nonparametric methods revealed larger OTUs richness in the black carbon library of Mina I site and in the ADE soil library of the Balbina site. The PCA analysis showed that the libraries of the site Balbina site were highly similar. In addition, the analysis with S-Libshuff verified that all of the compared libraries were significantly different in bacterial communities composition. The pyrogenic black carbon is not an inert structure, once it is capable of being inhabited by different bacteria, and its bacterial community structure is different from that one where is was segregated

O objetivo deste trabalho foi enriquecer consórcio microbiano a partir de mistura de lodo granular de digestor anaeróbio de fluxo ascendente sob condições fototróficas anoxigênicas. Por meio de técnica de biologia molecular foi possível identificar 17 unidades taxonômicas operacionais (UTO) no consórcio microbiano, dentre as quais seqüências similares a Rhodobacter, gênero amplamente citado nos estudos de produção de gás hidrogênio por bactérias fototróficas. Exames microscópicos do consórcio fototrófico indicaram predomínio de bacilos Gram-negativos. Ensaios sob condições fototróficas foram realizados com dois meios de cultivo (RCVB e FANG) e os seguintes substratos orgânicos: ácido acético, butírico, cítrico, lático e málico, empregados como fonte de carbono, tanto para o crescimento celular, como para a produção do gás hidrogênio. A relação C/N inicial foi 30/4 e posteriormente 15/2, com o objetivo de favorecer o crescimento celular e a produção do \'H IND.2\'. A concentração dos substratos foi determinada de forma com que essa relação se mantivesse a mesma. O crescimento celular e consumo dos ácidos orgânicos foram similares para os dois meios de cultivo empregados. Entretanto, a produção do gás hidrogênio foi maior nos ensaios com o meio FANG. Dentre os substratos utilizados o consumo dos ácidos cítrico e málico foram os maiores (~100%), para concentrações iniciais de 3,3 g/L e 2,6 g/L, respectivamente. O menor consumo 25% foi observado em meio RCVB e ácido acético (2,5 g/L). O crescimento da biomassa variou de 0,06 g/L a 1,1 g/L, enquanto que a velocidade máxima específica de crescimento variou de 0,4 a 0,2 g SSV/L.d entre os substratos utilizados. A menor e maior concentração de hidrogênio foram de 8,5 e 22 mmol \'H IND.2\'/L, para os reatores alimentados com ácido lático e málico em meio FANG, respectivamente. Pôde-se concluir que o consórcio fototrófico enriquecido foi capaz de utilizar os ácidos orgânicos para produção do gás hidrogênio. / The aim of this work was enrich a mixture of granular sludge of an up flow anaerobic sludge blanket (UASB) under anoxygenic phototrophic conditions. The techniques of molecular biology identified 17 operational taxonomic units (UTO) in the microbial consortium among the sequences analised, which were similar to Rhodobacter, genus widely cited in studies of hydrogen gas production by phototrophic bacteria. Microscopic examinations of the phototrophic consortium showed predominance of Gram-negative bacilli. Tests were conducted under phototrophic conditions with two culture media (RCVB and FANG) and the following organic substrates: acetic, butyric, citric, lactic and malic acids that were used as carbon source for both cell growth and for the hydrogen gas production. The carbon nitrogen ratio (C/N) in the preliminaries tests was 30/4 and then it was changed to15/2 in order to improve the cell growth and hydrogen production. The concentration of substrates was determined for remain the same carbon/nitrogen ratio among the substrates. The cell growth and consumption of organic acids were similar for the two culture media used. However, the production of hydrogen gas was higher in trials with the medium FANG. Among the substrates used, the consumption of malic and citric acids were the highest (~100%) for initial concentrations of 3.3 g/L and 2.6 g/L, respectively. The shortest consumption (25%) was observed for the cells that grew on acetic acid, 2.5 g/L in RCVB culture medium. The growth of the biomass varied from 0.06 g/L to 1.1 g/L, whereas the maximum specific growth rate ranged from 0.4 to 0.2 g VSS/L.d between the substrates used. The lowest and highest concentrations of hydrogen were 8.5 and 22 mmol \'H IND.2\'/L for the reactor fed with lactic acid and malic acid in FANG\'s medium, respectively. It was concluded that the phototrophic consortium was able to use those organic acids for the production of hydrogen gas.

La biogenèse des ribosomes est un processus complexe et dynamique requérant l’intervention d’une multitude de facteurs d’assemblage et de maturation pour permettre la maturation du pré-ARNr et l’assemblage des protéines ribosomiques. Chez les eucaryotes, la biogenèse de la petite sous-unité ribosomique 40S, débute dans le nucléole par la transcription d’un long précurseur contenant 3 des 4 futurs ARNr matures. Le pré-ARNr 18S est modifié par un ensemble de snoRNP à boîtes C/D et H/ACA et libéré par une série de clivages précoces au niveau des sites A0, A1 et A2. Ces clivages se déroulent au sein d’un macro-complexe, le SSU-processome. Celui-ci s’assemble de manière séquentielle à l’extrémité 5’ du pré-ARNr et est composé d’une multitude de facteurs intervenant dans la maturation, notamment de la snoRNP U3, une snoRNP à boîtes C/D qui joue un rôle de chaperon du pré-ARNr. En effet, le snoARN U3 est impliqué dans la formation de 5 appariements avec le pré-ARNr permettant de positionner correctement les sites de clivages A0, A1 et A2. En plus des 4 protéines cœur retrouvées au sein des snoRNP à boîtes C/D, la snoRNP U3 possède une protéine supplémentaire essentielle à la viabilité cellulaire, Rrp9p. En C-terminal, Rrp9 présente un enchainement de 7 domaines WD40 s’organisant en une structure « beta propeller ». Pour définir le rôle essentiel de cette protéine, nous avons généré des mutants et testé leur fonction. Nous avons ainsi pu montrer que le résidu R289 de Rrp9p est important pour les étapes de clivages précoces du pré-ARNr aux sites A1 et A2. De plus, nous avons identifié de nouveaux partenaires de la protéine Rrp9p au sein du processome et montré que le résidu R289 est impliqué dans une interaction directe avec le facteur Rrp36p. Lorsque ce résidu est muté, certains des défauts de croissance cellulaire liés à la stabilisation des appariements établis entre le pré-ARNr et le snoARN U3 par mutation du snoARN U3 sont fortement renforcés, montrant un lien fonctionnel entre Rrp9p et ces appariements. Nous avons mis en évidence un réseau d’interaction au sein du processome impliquant les protéines Rrp9p, Rrp36p, Sgd1p et Rrp5p : Rrp9p interagit avec Rrp36p et Sgd1p, et ces deux dernières interagissent ensemble, ainsi qu’avec Rrp5p. Les domaines responsables de ces interactions ont été étudiés / Ribosome biogenesis is a complex and dynamic process requiring several assembly and maturation factors needed for processing of the pre-rRNA and assembly of the ribosomal protein. In eukarya, biogenesis of the 40S small subunit starts in the nucleolus with the transcription of a long pre-rRNA, containing 3 out of the 4 future rRNAs. The 18S pre-rRNA is modified by several C/D or H/ACA box snoRNPs and processed by endonucleolytic cleavages at sites A0, A1 and A2 sites. These early cleavages occur within a huge complex termed the SSU-processome. The processome assembles at the 5’ extremity of the pre-rRNA, and contains multiple factors, including the U3 snoRNP, a C/D box snoRNP chaperoning the pre-rRNA. Indeed, the U3 snoRNA is involved in formation of 5 intermolecular helix with the pre-rRNA, which defines the A0, A1 and A2 cleavage sites. In addition to the four C/D box snoRNP core proteins, the U3 snoRNP contains additional protein, Rrp9p, required for cell viability. The Rrp9p C-terminal extremity folds into a beta propeller structure. To try to decipher the Rrp9p role, we mutated several surface residues of the beta propeller protein and the effects of the mutations on cell growth were tested. Through this approach, we found that the R289 residue is important for the maturation events at A1 and A2 sites. Moreover, we identified new protein partners of Rrp9p within the processome and showed that R289 residue is involved in a direct interaction with Rrp36p. We identified a network of protein-protein interactions including Rrp9p, Rrp36p, Sgd1p and Rrp5p : Rrp9p interacts with Rrp36p and Sgd1p, Rrp36p and Sgd1p interact together and with Rrp5p. Some of the protein domains involved in the interactions were identified. In addition, the R289A mutation in Rrp9p has a strong negative effect on growth with mutations in U3 snoRNA that destabilize the U3 snoRNA/pre-rRNA interaction