As cianobactérias caracterizam-se como o grupo de micro-organismos fotoautotrófico mais abundante encontrado nas regiões polares. Representantes deste grupo realizam a fotossíntese oxigênica e também podem fixar o nitrogênio atmosférico. A maioria dos levantamentos da comunidade de cianobactérias na Antártica tem sido realizada apenas por meio de observações microscópicas de amostras ambientais. O isolamento de linhagens e consequentes estudos fisiológicos, bem como, análises independentes de cultivo ainda são escassos. Neste estudo a comunidade de cianobactérias de duas ilhas oceânicas da Antártica foi investigada utilizando abordagens moleculares dependentes e independentes de cultivo. O papel ecológico das cianobactérias como fornecedoras de formas assimiláveis de nitrogênio e o potencial genético para biossíntese de produtos naturais também foi avaliado. Sessenta e oito linhagens de cianobactérias foram isoladas a partir de diferentes substratos coletados. Elas pertencem às ordens Chroococcales, Pseudanabaenales, Oscillatoriales e Nostocales, famílias Xenococcaceae, Dermocarpellaceae, Pseudanabaenaceae, Oscillatoriaceae, Nostocaceae, Microchaetaceae e Rivulariaceae. Análises filogenéticas baseadas nas sequências de RNAr 16S dessas cianobactérias revelou a existência de agrupamentos: formado exclusivamente por sequência de linhagem isolada nesse trabalho; composto por sequências antárticas oriundas desse e de outros trabalhos desenvolvidos em outras regiões antárticas; e por sequências originárias de diversas regiões do mundo. Quarenta e uma linhagens apresentaram fragmento do gene nifH, responsável pela codificação do complexo enzimático da nitrogenase, o qual está envolvido na fixação biológica do nitrogênio (FBN). Formas unicelulares (Chroococcales), homocitadas (Pseudanabaenales e Oscillatoriales) e heterocitadas (Nostocales) apresentaram potencial genético para realização da FBN, e 18 delas foram submetidas aos testes de redução de acetileno (ARA) com alta sensibilidade de detecção. Todas as linhagens testadas exibiram alguma atividade em resposta a diferentes concentrações de oxigênio e/ou a luminosidade em diferentes condições de temperatura. Filogeneticamente, as sequências do gene nifH apresentaram três padrões distintos de agrupamento, o que pode estar relacionado aos eventos evolutivos envolvidos na distribuição e ou manutenção deste gene. A presença de genes e ou regiões intergênicas evidenciaram o elevado potencial genético dessas linhagens para sintetizar produtos naturais com interesse biotecnológico. A abundância no número de cópias do gene nifH relacionado às cianobactérias nas amostras de biofilme reforça a importância desse grupo de microorganismos como fornecedor de formas reduzidas de N para o ambiente antártico. A análise da comunidade de cianobactérias por meio do sequenciamento do RNAr 16S de DNA metagenômico evidenciou predominância de UTOs relacionadas às ordens Nostocales, Oscillatoriales e Pseudanabaenales, famílias Pseudanabaenaceae, Phormidiaceae, Nostocaceae e Rivulariaceae. A árvore filogenética contendo as sequências de cianobactérias cultivadas e não-cultivadas mostrou que somente parte da comunidade presente em biofilmes foi acessada por isolamento, indicando a complementariedade entre as duas abordagens utilizadas na análise da comunidade de cianobactérias / Cyanobacteria are characterized as the most abundant group of photoautotrophic microorganisms found in the polar regions. Members of this group perform oxygenic photosynthesis and many of them can also fix atmospheric nitrogen. Investigations on the cyanobacterial community have been made mainly applying microscopic observations of environmental samples. Cyanobacterial isolation, physiological studies and cultureindependent analyses are scarce. In this study the cyanobacterial community from two oceanic islands in Antarctica was investigated using culture-dependent and independent approaches. Also, the ecological role of this group of microorganisms as nitrogen-fixing organisms and the genetic potential for biosynthesis of natural products were evaluated. Sixty-eight cyanobacterial strains were isolated from different environmental samples. They belong to the orders Chroococcales, Pseudanabaenales, Oscillatoriales and Nostocales, families Xenococcaceae, Dermocarpellaceae, Pseudanabaenaceae, Oscillatoriaceae, Nostocaceae, Microchaetaceae and Rivulariaceae. Phylogenetic analyses based on 16S rRNA sequences of these cyanobacteria revealed the existence of groups: exclusively formed by sequence of strain isolated in this work; intermixed sequences from this and other studies developed in other Antarctic regions; and sequences originated from different regions of the world. Fortyone cultured strains possess the nifH gene fragment encoding the nitrogenase enzyme complex, which is related to the biological nitrogen fixation (BNF). Unicellular (Chroococcales), homocytous (Pseudanabaenales and Oscillatoriales) and heterocytous forms (Nostocales) showed genetic potential for BNF, and 18 of them were subjected to acetylene reduction assay (ARA) coupled with a sensitive laser photoacoustic ethylene detector. All strains tested exhibited some nitrogenase activity in response to different concentrations of oxygen and or irradiance under different temperature conditions. Phylogenetically, the nifH gene sequences showed three distinct grouping patterns that may be related to the evolutionary events involved in the distribution and or maintenance of this gene. The presence of genes and or intergenic regions in these cyanobacterial strains underscores the genetic potential of them to synthesize natural products with biotechnological interest.The abundance of nifH gene copies related to cyanobacteria in biofilm samples highlights the importance of this group of microorganisms as suppliers of N reduced forms for Antarctic environment. The analysis of the cyanobacteria community revealed by 16S rRNA sequencing of metagenomic DNA showed a predominance of OTUs related to orders Nostocales, Oscillatoriales and Pseudanabaenales, families Pseudanabaenaceae, Phormidiaceae, Nostocaceae and Rivulariaceae. The phylogenetic tree containing Antarctic sequences from cultivated and uncultivated cyanobacteria showed that only part of this community in biofilms has been accessed by isolation, indicating the complementarity between the two approaches used in the analysis of cyanobacterial community

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.

Doctor of Philosophy / Department of Entomology / Ming-Shun Chen / John C. Reese / Keeping in view the important roles of bacteria in almost every aspect of insect’s life, the current study is the first systemic and intensive work on microbes associated with Hessian fly, a serious pest of wheat crop. A whole body analysis of Hessian fly larvae, pupae, or adults suggested that a remarkable diversity of bacteria is associated with different stages of the insect life cycle. The overriding detection of genera Acinetobacter and Enterobacter throughout the life cycle of Hessian fly suggested a stable and intimate relationship with the insect host. Adult Hessian flies have the most dissimilar bacterial composition from other stages with Bacillus as the most dominant genus. Analysis of 5778 high quality sequence reads obtained from larval gut estimated 187, 142, and 262 operational taxonomic units at 3% distance level from the 1st, 2nd, and 3rd instar respectively. Pseudomonas was the most dominant genus found in the gut of all three instars. The 3rd instar larval gut had the most diverse bacterial composition including genera Stenotrophomonas, Pantoea, Enterobacter, Ensifer, and Achromobacter. The transovarial transmission of major bacterial groups provided evidence of their intimate relationship with the Hessian fly. The Hessian fly is known to manipulate wheat plants to its own advantage. This study demonstrated that the combination of a decrease in carbon compounds and an increase in nitrogen compounds in the feeding tissues of Hessian fly-infested plants results in a C/N ratio of 17:1, nearly 2.5 times less than the C/N ratio (42:1) observed in control plants. We propose that bacteria associated with Hessian fly perform nitrogen fixation in the infested wheat, which was responsible for shifting the C/N ratio. The following findings made in the current study i.e. the presence of bacteria encoding nitrogenase (nifH) genes both in Hessian fly and infested wheat, exclusive expression of nifH in infested wheat, presence of diverse bacteria (including the nitrogen fixing genera) in the Hessian fly larvae, presence of similar bacterial microbiota in Hessian fly larvae and at the feeding site tissues in the infested wheat, and reduction in survival of Hessian fly larvae due to loss of bacteria are consistent with this hypothesis. The reduction in Hessian fly longevity after the loss of Alphaproteobacteria in first instar larvae, highest proportion of Alphaproteobacteria in insects surviving after the antibiotic treatments and the nitrogen fixation ability of associated Alphaproteobacteria strongly implies that Alphaproteobacteria are critical for the survival of Hessian fly larvae. This study provides a foundation for future studies to elucidate the role of associated microbes on Hessian fly virulence and biology. A better understanding of Hessian fly-microbe interactions may lead to new strategies to control this pest.

Population growth over the past ~50 years accompanied by the changes in dietary habits due to economic growth have markedly increased the demand for fixed nitrogen. Aided by biological nitrogen fixation, the Haber-Bosch process has been able to fulfill these demands. However, due to its high temperature and pressure requirements, Haber-Bosch is an expensive process. Every year, approximately 2% of the total energy expenditure by man is used to manufacture fixed nitrogen. Biological systems, on the other hand, produce ammonia at ambient temperature and pressure with much higher efficiency than the Haber-Bosch process. Research in the field of biological nitrogen fixation could prove valuable in understanding the mechanism of the enzyme responsible, nitrogenase. This could eventually allow researchers to mimic the enzyme and fix nitrogen at standard temperature and pressure, which would lead to greater availability of fixed nitrogen and a better standard of living for mankind. As part of this research, nitrogenase of Azotobacter vinelandii was studied to understand the order of events in reduction of substrates and the conformational changes in the enzyme responsible for its ability to reduce said substrates at room temperature and pressure. This knowledge was used to study variant forms of nitrogenase that could be activated using controlled external reductants. This freedom from the biological reductant of nitrogenase opens the door for further research into the understanding and development of enzyme mimics that can reduce substrates at room temperature and pressure.

Tropical seagrass ecosystems are highly productive and important for sustaining marine life and associated coastal societies. In this study, the diversity and role of nitrogen-fixing cyanobacteria associated with five common seagrass genera in coastal regions of the western Indian Ocean (WIO; Tanzania) were examined, as well as the impact of anthropogenic activities. Cyanobacteria were characterized morphologically and genetically (16S rRNA and nifH gene phylogeny), as were diel variations in nifH gene expression, NifH protein levels and nitrogenase activity. The results revealed that WIO seagrass beds supported rich cyanobacterial diversity and that these represented approx. 83% of total clones obtained (DNA and RNA nifH clone libraries). Non-heterocystous genera, such as Oscillatoria, Lyngbya, Leptolyngbya, Phormidium and Microcoleus dominated, while heterocystous morphotypes such as Calothrix were less frequent and unicellular morphotypes (e.g. Gloeocapsa, Chroococcus and Chroococcidiopsis) were few. Additionally, the phylogenetic analysis revealed several novel uncharacterized cyanobacterial clades. Cyanobacterial composition and nitrogenase activity varied over seasons and between the seagrass species. Day time nitrogenase activity originated primarily from heterocystous phylotypes, while non-heterocystous filamentous phylotypes fixed nitrogen at night. The highest activity in the diel cycle was 358 ± 232 nmol C2H4 g-1 h-1at 09.00 associated with epiphytes of the seagrass Cymodocea. Nitrogenase activity was consistently lower in anthropogenically disturbed (eutrophication) seagrass sites. Such data suggest that diazotrophic cyanobacteria may be a significant source of ‘new’ nitrogen in the often oligotrophic coastal regions of tropical oceans. It is also proposed that the rapid shifts in the cyanobacterial population and function found may also be used as early disturbance indicator in coastal management practices. / At the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 3: Manuscript. Paper 4: Manuscript. / SIDA SAREC Bilateral Marine Sciences Project / The Swedish Foundation for International Cooperation in Research and Higher Education

Seasonal dynamics of unicellular diazotrophs were investigated in the upstream Kuroshio and the northern South China Sea (SCS). Unicellular diazotrophs had been postulated as an important N2-fixing contributor for the phenomenon of N* in the SCS where abundances of filamentous Trichodesmium and Richelia were scarced. Samples were collected during four cruises between August 2008 and August 2009 in summer (CR1310 and CR910), winter (CR886), and late spring (CR899), respectively. Sampling stations located between 21¢XN-22¢XN and 116¢XE-122¢XE in the upstream Kuroshio off southeast Taiwan and covering the shelf and basin waters of the northern SCS. The abundance of the unicellular diazotrophs was determined using whole-cell immunocytochemical method in which antibody of nitrogenase was used as the probe. Cells containing nitrogenase can be visualized and counted after the antigen-antibody reaction under microscope. Unicellular diazotrophs were classified to four types according to their sizes and shapes. For diameters of those with 1-3 £gm and in coccoid shape are called 1-3 £gm C, diameters of 1-3 £gm and in rod shape are called 1-3 £gm R, diameters of >3-10 £gm and in coccoid shape are called >3 £gm C, and diameters of >3-10 £gm and in rod shape are called >3 £gm R. Surface abundance of the unicellular diazotrophs was highest in winter in both the Kuroshio and the SCS, followed by summer, and was least in late spring. Among four cell types, 1-3 £gm C usually was the most abundant group, followed by 1-3 £gm R and >3 £gm R, and was least for the group of >3 £gm C. The abundances between groups of 1-3 £gm C and 1-3 £gm R were positively correlated. Likewise, the abundances between >3 £gm C and >3 £gm R were positively correlated. However, the total abundance of small cells (1-3 £gm C+R) was not significantly related to the large cells (>3 £gm C+R). During summer and late spring, the abundance of unicellular diazotrophs in the SCS was 1.3-2 times of that in the Kuroshio. However, in winter the abundance in the Kuroshio was 1.2 times of that in the SCS. Surface water temperature was found negatively correlated to the abundance of 1-3 £gm C, >3 £gm C, >3 £gm R, and large cells (>3 £gm C+R), respectively. Significant correlations among surface water temperature and surface chlorophyll a, [NO2+NO3], SRP and N:P ratio implicated that the dynamics of cell abundances could be attributed to the correlated ecological variables of surface water temperature. The dynamics for the abundances of >3 £gm C, >3 £gm R, and large cells (>3 £gm C+R) were suggested to relate with the fluctuation of SRP concentration. Unicellular diazotrophs accounted for 60-90 % of total unicellular cells in terms of cell number. Vertical distributions of unicellular diazotrophs in the Kuroshio and the SCS were in similar trends, with maximum abundance in deep water during summer and late spring, and on surface water during winter.

Hydrogen has an extensive potential as a clean and renewable energy source. Photosynthetic, non-sulphur, purple bacteria, Rhodobacter sphaeroides O.U.001 produces molecular hydrogen by nitrogenase enzyme. Nitrogenase enzyme is encoded by nifHDK genes and expression of the structural genes, nifHDK, is controlled by NifA which is encoded by nifA gene. The transcription of nifA is under the control of Ntr system and product of prrA gene. Relationship between the genes that have roles in nitrogenase synthesis should be understood well to increase biological hydrogen production. In this work, expression levels of nitrogenase encoding nifH and control genes nifA, prrA were examined at different physiological conditions. In addition to modifications in expression levels, changes in hydrogen production and growth capacity were also investigated in response to different concentrations of ammonium source, oxygen and different light intensities. In this study, it was found that increasing concentrations of ammonium chloride caused decrease in hydrogen production. Glutamate containing medium had the capacity for higher hydrogen production. The expression levels of nifH and nifA genes decreased with the increase in concentrations of ammonium chloride. There was a negative correlation between the expression levels of prrA gene and its target, nifA gene. Hydrogen production was observed even in aerobic conditions of the same media compositions. It was observed that different culture media had changing growth and hydrogen production capabilities at different light intensities. There was no direct proportion between the expression levels of nifH gene and amount of hydrogen at different light intensities.

In this study, Azotobacter vinelandii ATCC13705 (A. vinelandii), which is a free-living, nitrogen-fixing, gram-negative, and aerobic rod bacterium, was need to evaluate its ability to biodegrade tetracyanonickelate (TCN) under different conditions. Results show that A. vinelandii was able to biodegrade various concentrations of TCN (1, 10, and 20 mM) under aerobic conditions. Oxygen consumption and nitrogenase activity were investigated at 1 mM of TCN. Results indicate that the production of ammonia and methane was observed when TCN was consumed. Results suggest that nitrogenase was possibly involved in the enzymatic degradation of TCN. Moreover, higher degradation rate of TCN, higher nitrogenase activity, higher oxygen consumption, and higher specific growth rates were also observed at log growth period. Results suggest that the hypothesis of respiratory protection of nitrogenase is supported. Moreover, the addition of ammonia (1, 5, and 10 mM) would cause the decrease of TCN degradation rate (28%) during a 24-hr incubation period. Inhibition of TCN degradation (degradation rate¡G16% for 24 hrs) was observed when nitrite (5 and 10 mM) was added into the growth medium. Furthermore, the addition of 8% of glucose would significantly enhance the TCN degradation by the resting cells (degradation rate¡G43% for 8 hrs) . Results from this study provide us insight into the characteristics and mechanisms of TCN conversion by A. vinelandii.

Thesis (Ph.D.) -- Mississippi State University. Department of Biological Sciences. / Title from title screen. Includes bibliographical references.

Universiẗat, Diss., 2004--Jena.