Cianobactérias são micro-organismos que realizam fotossíntese oxigênica e têm uma distribuição cosmopolita. Algumas cianobactérias são capazes de realizar fotossíntese e fixação biológica de nitrogênio (FBN), dois dos mais importantes processos na natureza, simultaneamente. As cianobactérias da ordem Nostocales são capazes realizar uma separação espacial destes dois processos por meio da formação de células especializadas, os heterócitos, onde acontece a fixação de nitrogênio, restringindo a fotossíntese às células vegetativas. Embora tenham importância ecológica, econômica e social, as cianobactérias foram muito pouco estudas com enfoque genômico. Este trabalho teve como objetivo a caracterização dos agrupamentos gênicos envolvidos na fixação biológica de nitrogênio e na diferenciação de heterócitos de três isolados brasileiros de cianobactérias da ordem Nostocales. Para este fim, culturas das linhagens Sphaerospermopsis torquesreginae ITEP-024, Nostoc sp. CENA67 e Fischerella sp. CENA161 foram sequenciadas com a plataforma MiSeq e então foi realizada a montagem ab initio do genoma com as leituras obtidas. Além desses três isolados, os genomas de outras 31 linhagens disponíveis no banco de dados GenBank foram recuperados e utilizados para comparação. A anotação dos genes foi realizada por meio do alinhamento de sequências nucleotídicas já conhecidas de outras linhagens contra os genomas dessas linhagens, utilizando a ferramenta BLASTn, e por meio do servidor antiSMASH. Além disso, análises filogenéticas foram realizadas a partir dos genes anotados. O sequenciamento dos genomas das três linhagens apresentou altos valores de qualidade de bases e elevada cobertura genômica. A anotação dos agrupamentos envolvidos na FBN revelou a presença de um total de 22 genes envolvidos na síntese da Mo-nitrogenase, sendo 19 presentes em todas as linhagens. Os isolados brasileiros apresentaram sintenia com outras linhagens próximas filogeneticamente, apresentando variação apenas na presença de regiões de excisão e do gene glbN. A linhagem CENA161 apresentou um agrupamento gênico completo para síntese da V-nitrogenase, assim como apenas outras 5 linhagens em toda a ordem. Foram encontradas nas três linhagens sequenciadas os genes devACB, relacionados à formação da camada polissacarídica do heterócito. Os genes hglEGDCA e hetM, que estão relacionados à formação da camada glicolipídica de heterócitos, foram encontrados completos nas linhagens ITEP-024 e CENA67, mas apenas parcialmente na CENA161. Genes reguladores do processo de diferenciação também foram acessados nas três linhagens brasileiras, entretanto apenas os reguladores globais do processo formam encontrados em CENA161. As análises filogenéticas mostraram que o gene nifH não reflete a filogenia do táxon e não é um bom marcador filogenético. Entretanto, a análise de todo o agrupamento refletiu o padrão filogenético de acordo com a taxonomia. Os resultados contribuem para a melhor compreensão dos aspectos genéticos e evolutivos do processo de FBN em cianobactérias. / Cyanobacteria are oxygenic photosynthetic microorganisms that have a worldwide distribution. Some cyanobacteria are capable of photosynthesis and biological nitrogen fixation (BNF), two of the most important processes in nature, simultaneously. Cyanobacteria from the Nostocales order perform a spatial separation of these processes through the formation of specialized cells, heterocytes, where nitrogen fixation is carried out, while photosynthesis is limited to vegetative cells. Although cyanobacterial have ecological, economic and social importance, they have been understudied with genomic approaches. This study aimed to characterize gene clusters involved in nitrogen fixation and heterocytes differentiation from three Brazilian strains of cyanobacteria from Nostocales order. For this purpose, nonaxenic cultures of the strains Sphaerospermopsis torque-reginae ITEP-024, Nostoc sp. CENA67 and Fischerella sp. CENA161 were sequenced with the Illumina MiSeq platform and ab initio genome assembly was performed. In addition to these strains, genomes from 31 strains available in the GenBank database were retrieved and used for comparison. Gene annotation was performed through alignments between known genes present in other cyanobacteria and the strains genomes, using the BLASTn tool, and through the antiSMASH server. Furthermore, phylogenetic analyses were performed on the annotated genes. The genome sequencing showed high bases quality values and genomic coverage. The annotation of clusters involved in the BNF revealed the presence of a total of 22 genes involved in the synthesis of Mo-nitrogenase, among 19 were present in all strains. Brazilian isolates showed synteny with phylogenetically related strains, with variations only in the presence of excision regions and glbN gene. The CENA161 strain showed a complete gene cluster for synthesis of V-nitrogenase, present in only 5 other strains in this order. devACB genes, related to the heterocyte polysaccharide layer formation, were found in the three strains sequenced. The hglEGDCA and hetM genes, related to the formation of heterocyte glycolipid layer, were complete in ITEP-024 and CENA67 strains, but only partial in CENA161. Gene regulation of the heterocyte differentiation process have also been accessed in the three Brazilian strains, but only the general process regulatory genes were found in CENA161. Phylogenetic analysis showed that the gene nifH does not reflect the phylogeny of this group and should not be considered a good phylogenetic marker. However, the complete genes cluster analysis reflected the patterns of phylogenetic grouping according to taxonomy. The results contribute to a better understanding of the genetic and evolutionary aspects of the BNF process in cyanobacteria.

Cianobactérias são micro-organismos que realizam fotossíntese oxigênica e têm uma distribuição cosmopolita. Algumas cianobactérias são capazes de realizar fotossíntese e fixação biológica de nitrogênio (FBN), dois dos mais importantes processos na natureza, simultaneamente. As cianobactérias da ordem Nostocales são capazes realizar uma separação espacial destes dois processos por meio da formação de células especializadas, os heterócitos, onde acontece a fixação de nitrogênio, restringindo a fotossíntese às células vegetativas. Embora tenham importância ecológica, econômica e social, as cianobactérias foram muito pouco estudas com enfoque genômico. Este trabalho teve como objetivo a caracterização dos agrupamentos gênicos envolvidos na fixação biológica de nitrogênio e na diferenciação de heterócitos de três isolados brasileiros de cianobactérias da ordem Nostocales. Para este fim, culturas das linhagens Sphaerospermopsis torquesreginae ITEP-024, Nostoc sp. CENA67 e Fischerella sp. CENA161 foram sequenciadas com a plataforma MiSeq e então foi realizada a montagem ab initio do genoma com as leituras obtidas. Além desses três isolados, os genomas de outras 31 linhagens disponíveis no banco de dados GenBank foram recuperados e utilizados para comparação. A anotação dos genes foi realizada por meio do alinhamento de sequências nucleotídicas já conhecidas de outras linhagens contra os genomas dessas linhagens, utilizando a ferramenta BLASTn, e por meio do servidor antiSMASH. Além disso, análises filogenéticas foram realizadas a partir dos genes anotados. O sequenciamento dos genomas das três linhagens apresentou altos valores de qualidade de bases e elevada cobertura genômica. A anotação dos agrupamentos envolvidos na FBN revelou a presença de um total de 22 genes envolvidos na síntese da Mo-nitrogenase, sendo 19 presentes em todas as linhagens. Os isolados brasileiros apresentaram sintenia com outras linhagens próximas filogeneticamente, apresentando variação apenas na presença de regiões de excisão e do gene glbN. A linhagem CENA161 apresentou um agrupamento gênico completo para síntese da V-nitrogenase, assim como apenas outras 5 linhagens em toda a ordem. Foram encontradas nas três linhagens sequenciadas os genes devACB, relacionados à formação da camada polissacarídica do heterócito. Os genes hglEGDCA e hetM, que estão relacionados à formação da camada glicolipídica de heterócitos, foram encontrados completos nas linhagens ITEP-024 e CENA67, mas apenas parcialmente na CENA161. Genes reguladores do processo de diferenciação também foram acessados nas três linhagens brasileiras, entretanto apenas os reguladores globais do processo formam encontrados em CENA161. As análises filogenéticas mostraram que o gene nifH não reflete a filogenia do táxon e não é um bom marcador filogenético. Entretanto, a análise de todo o agrupamento refletiu o padrão filogenético de acordo com a taxonomia. Os resultados contribuem para a melhor compreensão dos aspectos genéticos e evolutivos do processo de FBN em cianobactérias. / Cyanobacteria are oxygenic photosynthetic microorganisms that have a worldwide distribution. Some cyanobacteria are capable of photosynthesis and biological nitrogen fixation (BNF), two of the most important processes in nature, simultaneously. Cyanobacteria from the Nostocales order perform a spatial separation of these processes through the formation of specialized cells, heterocytes, where nitrogen fixation is carried out, while photosynthesis is limited to vegetative cells. Although cyanobacterial have ecological, economic and social importance, they have been understudied with genomic approaches. This study aimed to characterize gene clusters involved in nitrogen fixation and heterocytes differentiation from three Brazilian strains of cyanobacteria from Nostocales order. For this purpose, nonaxenic cultures of the strains Sphaerospermopsis torque-reginae ITEP-024, Nostoc sp. CENA67 and Fischerella sp. CENA161 were sequenced with the Illumina MiSeq platform and ab initio genome assembly was performed. In addition to these strains, genomes from 31 strains available in the GenBank database were retrieved and used for comparison. Gene annotation was performed through alignments between known genes present in other cyanobacteria and the strains genomes, using the BLASTn tool, and through the antiSMASH server. Furthermore, phylogenetic analyses were performed on the annotated genes. The genome sequencing showed high bases quality values and genomic coverage. The annotation of clusters involved in the BNF revealed the presence of a total of 22 genes involved in the synthesis of Mo-nitrogenase, among 19 were present in all strains. Brazilian isolates showed synteny with phylogenetically related strains, with variations only in the presence of excision regions and glbN gene. The CENA161 strain showed a complete gene cluster for synthesis of V-nitrogenase, present in only 5 other strains in this order. devACB genes, related to the heterocyte polysaccharide layer formation, were found in the three strains sequenced. The hglEGDCA and hetM genes, related to the formation of heterocyte glycolipid layer, were complete in ITEP-024 and CENA67 strains, but only partial in CENA161. Gene regulation of the heterocyte differentiation process have also been accessed in the three Brazilian strains, but only the general process regulatory genes were found in CENA161. Phylogenetic analysis showed that the gene nifH does not reflect the phylogeny of this group and should not be considered a good phylogenetic marker. However, the complete genes cluster analysis reflected the patterns of phylogenetic grouping according to taxonomy. The results contribute to a better understanding of the genetic and evolutionary aspects of the BNF process in cyanobacteria.

In oligotrophic systems, where primary production is low and nitrogen is in short supply, nitrogen fixation process is intense. Although a few diazotrophs (eg. Trichodesmium) have been widely-studied, the rest of the diazotrophic community is still poorly understood. Furthermore, the global distribution of diazotrophs are yet to be clearly resolved. This dissertation assessed the distribution of diazotrophs in oligotrophic systems, particularly in the tropical and subtropical oceans, using genomics tools including next-generation sequencing. We first tested out a pair of nifH-specific primer that previously performed well in silico, but found that its application on seawater samples was biased towards paralogous, non-functional nitrogenase nifH genes. Instead, we found that the use of a nested PCR method using different primers sets to be more effective in amplifying functional nifH genes. Trichodesmium sp., UCYN-A and Pseudomonas sp. forms the core of the diazotrophic communities in oligotrophic oceans. Temperature is the primary driver of the abundances and distributions of these organisms in the Pacific, Atlantic and Indian Oceans, as well as in the oligotrophic Red Sea. Trichodesmium tends to dominate warm, surface waters, while UCYN-A prefers cooler environments and dwell in sub-surface waters in the Red Sea. Due to the dominance of Pseudomonas in the large-sized fraction samples, they are believed to be part of the Trichodesmium-associated consortia, although this requires further investigations. We also found non-cyanobacterial species of diazotrophs to be dominant previously-described hotspots of nitrogen fixation, and found evidence for the widespread of alternative nitrogenases (Cluster II). Using the Red Sea as an exemplar for future warming ocean, we found patterns of niche partitioning in the Red Sea diazotrophs, based on their distribution along seasons, latitude and depth. Our one-year observation of Red Sea Trichodesmium population witnessed the collapse of the population at temperatures above 32°C. This dissertation not only improve our understanding of the effects of future rising temperature on the natural populations of diazotrophs, but it also helps to establish a baseline understanding of the structure, spatial and temporal dynamics of Red Sea diazotrophs, which has not been discussed elsewhere.

This research investigated the existence of <10 £gm nitrogen-fixing unicellular cyanobacteria in the South China Sea. The surveys covered the period from February 2004 to January 2005 and a total of seven cruises. The unicellular cyanobacteria that express orange-yellow from cellular phycoerythrin were observed under a fluorescence microscope. Their expressions in nitrogen-fixation were confirmed by the results from reverse transcription polymerase chain reaction (RT-PCR) and whole cell fluorescence immunolocalization of nitrogenase. The nifH gene sequences of the unicellular cyanobacteria collected from the South China Sea was with >90% identities of their nucleotides similar to the nifH gene sequences of unicellular diazotrophs from ALOHA (Hawaii) as well as Synechocystis sp. WH 8501, Cyanothece sp. ATCC 51142, Cyanothece sp. WH 8902, Cyanothece sp. WH 8904 and Synechococcus sp. RF-1. Positive reactions of fluorescence immunolocalization of nitrogenase were only observed in some, not all, of <10 £gm unicellular cyanobacteria, suggesting that cell counting alone can not be used to estimate nitrogen fixation rate. There was great seasonal and spatial variation in the unicellular cyanobacteria cell density. There was, however, no significant relationship between cell density and the investigated environmental factors. Cell density was high when temperature was high or where stratification index of water column was high, such as in summer or in basin in contrast to other seasons or the shelf-slope regions.

The nitrogenase enzyme is the biochemical machiner responsible for the conversion of the largely unavailable nitrogen to the easily assimilable ammonia for living organisms by the process termed as biological nitrogen fixation (BNF). This study was focused on understanding the various structural and functional aspects of the nitrogenase enzyme related to maturation and assembly of the FeMo-cofactor (FeMoco) metallocluster of the MoFe protein (the site for final substrate reduction), development of a dimeric MoFe protein and the structural homology of nitrogenase with other metalloenzymes. This research was specifically directed towards the NifHDKX proteins in which the nifHDK genes are the major structural genes that encode the nitrogenase enzyme and nifX is an accessory gene that encodes the NifX protein, indicated to be involved in the formation of the FeMoco. The overall objective of this study was to gain structural and functional information on the nitrogenase enzyme through the study of the NifHDKX proteins. A major part of our study included the detection of protein-protein interactions between the NifD, NifK and a fused NifDK protein. The results of this study could prove to be useful for further studies that are directed towards condensing the nif genes so as to facilitate transfer of nitrogen fixing genes to plants for their improved nutrition. We also determined protein-protein interactions between NifX and other proteins involved in the FeMoco biosynthetic pathway. Based on the results, we were able to describe the role of NifX and propose a modified model for the FeMoco biosynthesis pathway. Apart from this, a comparative structural and evolutionary study was performed on the NifH similar proteins such as ChlL, CompA, MinD and ArsA and the NifDK similar proteins known as ChlBN. Based on the conservation of similar structural domains in NifH and ArsA, NifH was found to complement the function of ArsA1. Also the comparison between NifDK and the homology modeled ChlBN protein structure suggested a potential site for the presence of a FeMoco in ChlN. Thus, these studies helped us to derive meaningful conclusions on the structure and evolution of the nitrogenase enzyme and its homologs in nature.

Mature microbial mats from sandy intertidal beaches of the Texas Gulf coast demonstrated substantial levels of nitrogenase activity. Two species of non-heterocystous cyanobacteria, a Hydrocoleum and a Microcoleus, dominated the upper green layer of mature mats. Subsurface layers of cyanobacteria, but not mature mats, appeared during dry seasons. These "proto-mats" contained almost exclusively Microcoleus and demonstrated neither nitrogenase activity nor detectable nitrogenase reductase (Fe-protein). Hydrocoleum, identified from its morphology and 16s rDNA, was isolated and cultivated as unialgal cultures. Similar diel patterns of nitrogenase activity and Fe-protein expression were found in intact mature mats and in isolated Hydrocoleum cultures. Primers and a probe specific for the Hydrocoleum nifH gene, along with q-rtPCR measurements, demonstrated similar levels, but slightly different patterns, of expression in intact mature mats and cultures of isolated Hydrocoleum. Increased levels of nifH transcripts and Fe-protein in Hydrocoleum cultures appeared before the end of the light period of a diel cycle, and the light period was required for nitrogenase activity in the subsequent dark period. Levels of nifH transcripts stayed very low and nitrogen fixation stopped when cultures were maintained under continuous darkness. The pattern of nitrogenase activity in Hydrocoleum cultures was not affected by elimination of ambient O₂, increasing or decreasing temperature in a range from 20 ˚C to 35 ˚C, or light intensity. However, the level of nitrogenase activity did vary with environmental conditions. Highest nitrogenase activities were observed when assays were conducted in an aerobic rather than an anaerobic environment, at 25 ˚C rather than a higher or lower temperature, and illuminated with bright (~ 900 [mu]E/m²s¹), rather than less intense light. Average levels of nifH transcripts were positively correlated with levels of nitrogenase activity. Isolated cultures of Hydrocoleum formed mat-like structures in undisturbed flasks, suggesting that Hydrocoleum may be an early colonizer of intertidal sand for mat formation. However, observations of subsurface proto-mats indicate that Microcoleus is more likely to serve as the foundation for cyanobacterial mats, with Hydrocoleum later providing structural integrity and nitrogen availability. A process of successional development of microbial mats from the South Texas Gulf Coast is hypothesized. / text

No presente estudo, a diversidade bacteriana endofítica fixadora de nitrogênio foi pesquisada utilizando métodos microbiológicos e moleculares. Isolaram-se microrganismos de raiz, caule e folha de cana-de-açúcar. Análises por seqüenciamento do 16S rDNA identificaram 150 endófitos. No total, foram identificados 18 gêneros. Destes, apenas 4 estavam presentes em cana-de-açúcar submetida aos 3 tratamentos. A maior diversidade de gêneros foi encontrada em cana sob adubação orgânica: 10 gêneros, em cana sob adubação inorgânica foram 11 gêneros e 8 em cana sem adubação. A maior parte dos gêneros pertence à família Enterobacteriaceae, como Klebsiella, Pantoea e Enterobacter. A enzima endoglicanase foi produzida por 82% dos isolados de cana sob adubação orgânica, (54%) inorgânica e (48%) sem adubação. Quanto à atividade de pectinase: 42%, 60% e 36% foram apresentadas por isolados de cana orgânica, inorgânica e sem adubação, respectivamente. A capacidade de solubilizar fosfatos inorgânicos foi detectada em 76,6% dos isolados, sendo a maior capacidade de solubilização de fosfatos encontrada em bactérias isoladas de cana-de-açúcar sob adubação orgânica (71%), de cana submetida a adubação convencional (78%) e sem adubação (88%). Foram realizados estudos de colonização em plântulas de cana-de-açúcar com 4 endofitos geneticamente modificados (EGMs) capazes de expressar os genes gfp e dsred. A avaliação da colonização na cana pela microscopia de fluorescência, mostrou que os (EGMs) gfp e dsred colonizaram as raízes e caules das plantas inoculadas, sem causar qualquer sintoma de doença. / In the present study, endophytic bacterial diversity has been searched using both microbiologic and molecular methods. Microorganisms were isolated from sugarcane root, shoot and leaf. 150 isolates were identified by 16S rDNA sequencing. 18 genera were found and only 4 were present in sugarcane submitted to the three treatments. The greatest genera diversity was found in sugarcane submited to organic fertlization: 10 genera in sugarcane submitted to inorganic fertilization were found 11 genera and 8 genera in sugarcane without fertilization. Great part of the found genera belongs to the Enterobacteriaceae family: Klebsiella, Pantoea and Enterobacter. Some physiological characteristics were determined in the isolates. Endoglucanase was produced by 82% of the isolates from sugarcane submitted to organic fertilization. Lower activities were found in bacteria isolated from inorganic fertilization and no fertilization, respectively 54% and 48%. As far as pectinase activity is concerned, a percentage of 42%, 60% and 36% was presented by the isolates from organic fertilization, inorganic fertilization and no fertilization, respectively. The hability of phosphate solubilization was detected in 76.6% of the isolates. In sugarcane under organic fertilization a percentage of 71% was found, in bacteria from inorganic fertilization, 78%, and without fertilization, 88%. Plant colonization was determined using sugarcane plantlets inoculated with four genetically modified bactéria (GMEs), able to express the genes gfp and dsred. The colonization was evaluated by fluorescence microscopy, which showed that the endophytic bacteria expressing gfp and dsred genes had invaded roots and shoots from inoculated plants, without causing any disease symptom.

Manguezais são ecossistemas de transição entre ambientes terrestres e marinhos encontrados em regiões tropicais e subtropicais. A ampla faixa de variações de salinidade e teor oxigênio, típica desses ambientes, está entre os principais fatores condicionantes da colonização e desenvolvimento da biota. Apesar disso, são ambientes com elevada produção primária. Entre os nutrientes, o nitrogênio é um dos principais fatores limitantes que afetam o desenvolvimento da vegetação do manguezal e somente baixa disponibilidade de formas reduzidas está presente. Portanto, há a necessidade de determinar os micro-organismos fixadores de nitrogênio que colonizam os ecossistemas de manguezais. Dentre esses, existem as cianobactérias, um grupo bem conhecido de micro-organismos fotossintéticos oxigênicos e fixadores de nitrogênio. Neste estudo, 50 linhagens de cianobactérias foram isoladas de amostras ambientais de solos, água e material perifítico, coletadas nos ecossistemas de manguezais da Ilha do Cardoso e Bertioga, São Paulo. Essas linhagens foram isoladas usando meios específicos de crescimento e análises morfológicas identificaram representantes das ordens Chroococcales (35 linhagens, 70%), Oscillatoriales (9 linhagens, 18%) e Nostocales (6 linhagens, 12%). Dezesseis linhagens distribuídas entre as ordens Chroococcales e Nostocales foram selecionadas para os estudos de filogenia usando o gene rpoC1. A maioria das sequências de rpoC1 geradas pela amplificação por PCR usando o conjunto específico de primer rpoC1-1/rpoC1-T mostraram baixas similaridades (menor que 90%) com seqüências disponíveis no GenBank, indicando que estas linhagens de cianobactérias são únicas. As exceções foram somente duas linhagens (Synechococcus sp. CENA177 and Cyanothece sp. CENA169) que apresentaram altas similaridades com sequências de cianobactérias isoladas de ambientes de água doce do Brasil. A análise filogenética Neighbor-Joining mostrou que várias das novas linhagens cianobactérias dos manguezais se agruparam, sem relação com a descrição taxonômica baseada na caracterização morfotípica. Uma busca pelo gene funcional nifH, o qual codifica para a redutase da nitrogenase, em 27 isolados dos manguezais, revelou a sua presença em 21 linhagens (77%) dispersas entre as ordens Chroococcales, Oscillatoriales e Nostocales. Os 21 fragmentos do gene nifH amplificados foram clonados e seqüenciados e todas as sequências também mostram baixas similaridades (menor que 95%) com seqüências de cianobactérias disponíveis no GenBank. A análise filogenética do gene nifH posicionou as novas linhagens de cianobactérias dos manguezais em vários agrupamentos distribuídos ao longo da árvore, e como também observado para o gene rpoC1, sem correlação com a descrição taxonômica baseada na caracterização morfotípica. Atividade da nitrogenase, avaliada pela técnica de redução de acetileno, foi encontrada em cinco linhagens pertencentes à ordem Nostocales e em uma linhagem pertencente à ordem Chroococcales. A estimativa da fixação biológica de nitrogênio por essas linhagens variaram de 327,01 a 1.954,15 pmol N2.g-1 de biomassa seca.dia-1. / Mangroves are transitional ecosystems between terrestrial and marine environments found in tropical and subtropical regions. The broad range of variations of salinity and oxygen content, typical of these environments, is among the main constraint factors for the establishment and development of biota. Nevertheless, mangroves have high primary production. Among the nutrients, nitrogen is one of the most important limiting factors affecting the development of mangrove vegetation and only low availability of reduced forms is present. Therefore, there is a need to determine the nitrogen fixing microorganisms that colonize mangrove ecosystems. Among those, there are the cyanobacteria, a well known group of oxygenic photosynthetic and nitrogen fixing microorganisms. In this study, 50 cyanobacterial strains were isolated from environmental samples of soil, water and periphytic material collected in the Cardoso Island and Bertioga mangrove ecosystems, São Paulo. These strains were isolated using specific growth media and morphological analyses identified representatives of the orders Chroococcales (35 strains, 70%), Oscillatoriales (9 strains, 18%) and Nostocales (6 strains, 12%). Sixteen strains belong to the orders Chroococcales and Nostocales were selected for phylogeny studies using the gene rpoC1. The majority of rpoC1 sequences generated by PCR amplification using the specific set primer rpoC1-1/rpoC1-T showed low similarities (below 90%) with sequences available in the GenBank, indicating that these cyanobacterial strains are unique. The exceptions were only two strains (Synechococcus sp. CENA177 and Cyanothece sp. CENA169) that had high similarities with cyanobacterial sequences isolated from Brazilian freshwater environments. The Neighbor-Joining phylogenetic analysis showed that several of the new mangrove cyanobacterial strains clustered together, with no relationship with the taxonomical description based on morphotypic characterization. A search for the functional nifH gene, which coding for nitrogenase reductase, on 27 mangrove isolates revealed its presence in 21 strains (77%) dispersed among the orders Chroococcales, Oscillatoriales and Nostocales. The 21 amplified fragments of nifH were cloned and sequenced, and all the sequences also showed low similarities (below 95%) with cyanobacterial sequences available in the GenBank. The phylogenetic analysis of nifH gene positioned the new mangrove cyanobacterial strains in several clusters distributed along the tree, and as also observed for rpoC1 gene, with no correlation with the taxonomical description based on morphotypic characterization. Nitrogenase activity, measured by the acetylene reduction technique, was found in five strains belonging to the order Nostocales and one strain belonging to the order Chroococcales. The estimation of biological nitrogen fixation by these strains ranged from 327.01 to 1954.15 pmol N2.g-1 dry biomass.day-1.

Manguezais são ecossistemas de transição entre ambientes terrestres e marinhos encontrados em regiões tropicais e subtropicais. A ampla faixa de variações de salinidade e teor oxigênio, típica desses ambientes, está entre os principais fatores condicionantes da colonização e desenvolvimento da biota. Apesar disso, são ambientes com elevada produção primária. Entre os nutrientes, o nitrogênio é um dos principais fatores limitantes que afetam o desenvolvimento da vegetação do manguezal e somente baixa disponibilidade de formas reduzidas está presente. Portanto, há a necessidade de determinar os micro-organismos fixadores de nitrogênio que colonizam os ecossistemas de manguezais. Dentre esses, existem as cianobactérias, um grupo bem conhecido de micro-organismos fotossintéticos oxigênicos e fixadores de nitrogênio. Neste estudo, 50 linhagens de cianobactérias foram isoladas de amostras ambientais de solos, água e material perifítico, coletadas nos ecossistemas de manguezais da Ilha do Cardoso e Bertioga, São Paulo. Essas linhagens foram isoladas usando meios específicos de crescimento e análises morfológicas identificaram representantes das ordens Chroococcales (35 linhagens, 70%), Oscillatoriales (9 linhagens, 18%) e Nostocales (6 linhagens, 12%). Dezesseis linhagens distribuídas entre as ordens Chroococcales e Nostocales foram selecionadas para os estudos de filogenia usando o gene rpoC1. A maioria das sequências de rpoC1 geradas pela amplificação por PCR usando o conjunto específico de primer rpoC1-1/rpoC1-T mostraram baixas similaridades (menor que 90%) com seqüências disponíveis no GenBank, indicando que estas linhagens de cianobactérias são únicas. As exceções foram somente duas linhagens (Synechococcus sp. CENA177 and Cyanothece sp. CENA169) que apresentaram altas similaridades com sequências de cianobactérias isoladas de ambientes de água doce do Brasil. A análise filogenética Neighbor-Joining mostrou que várias das novas linhagens cianobactérias dos manguezais se agruparam, sem relação com a descrição taxonômica baseada na caracterização morfotípica. Uma busca pelo gene funcional nifH, o qual codifica para a redutase da nitrogenase, em 27 isolados dos manguezais, revelou a sua presença em 21 linhagens (77%) dispersas entre as ordens Chroococcales, Oscillatoriales e Nostocales. Os 21 fragmentos do gene nifH amplificados foram clonados e seqüenciados e todas as sequências também mostram baixas similaridades (menor que 95%) com seqüências de cianobactérias disponíveis no GenBank. A análise filogenética do gene nifH posicionou as novas linhagens de cianobactérias dos manguezais em vários agrupamentos distribuídos ao longo da árvore, e como também observado para o gene rpoC1, sem correlação com a descrição taxonômica baseada na caracterização morfotípica. Atividade da nitrogenase, avaliada pela técnica de redução de acetileno, foi encontrada em cinco linhagens pertencentes à ordem Nostocales e em uma linhagem pertencente à ordem Chroococcales. A estimativa da fixação biológica de nitrogênio por essas linhagens variaram de 327,01 a 1.954,15 pmol N2.g-1 de biomassa seca.dia-1. / Mangroves are transitional ecosystems between terrestrial and marine environments found in tropical and subtropical regions. The broad range of variations of salinity and oxygen content, typical of these environments, is among the main constraint factors for the establishment and development of biota. Nevertheless, mangroves have high primary production. Among the nutrients, nitrogen is one of the most important limiting factors affecting the development of mangrove vegetation and only low availability of reduced forms is present. Therefore, there is a need to determine the nitrogen fixing microorganisms that colonize mangrove ecosystems. Among those, there are the cyanobacteria, a well known group of oxygenic photosynthetic and nitrogen fixing microorganisms. In this study, 50 cyanobacterial strains were isolated from environmental samples of soil, water and periphytic material collected in the Cardoso Island and Bertioga mangrove ecosystems, São Paulo. These strains were isolated using specific growth media and morphological analyses identified representatives of the orders Chroococcales (35 strains, 70%), Oscillatoriales (9 strains, 18%) and Nostocales (6 strains, 12%). Sixteen strains belong to the orders Chroococcales and Nostocales were selected for phylogeny studies using the gene rpoC1. The majority of rpoC1 sequences generated by PCR amplification using the specific set primer rpoC1-1/rpoC1-T showed low similarities (below 90%) with sequences available in the GenBank, indicating that these cyanobacterial strains are unique. The exceptions were only two strains (Synechococcus sp. CENA177 and Cyanothece sp. CENA169) that had high similarities with cyanobacterial sequences isolated from Brazilian freshwater environments. The Neighbor-Joining phylogenetic analysis showed that several of the new mangrove cyanobacterial strains clustered together, with no relationship with the taxonomical description based on morphotypic characterization. A search for the functional nifH gene, which coding for nitrogenase reductase, on 27 mangrove isolates revealed its presence in 21 strains (77%) dispersed among the orders Chroococcales, Oscillatoriales and Nostocales. The 21 amplified fragments of nifH were cloned and sequenced, and all the sequences also showed low similarities (below 95%) with cyanobacterial sequences available in the GenBank. The phylogenetic analysis of nifH gene positioned the new mangrove cyanobacterial strains in several clusters distributed along the tree, and as also observed for rpoC1 gene, with no correlation with the taxonomical description based on morphotypic characterization. Nitrogenase activity, measured by the acetylene reduction technique, was found in five strains belonging to the order Nostocales and one strain belonging to the order Chroococcales. The estimation of biological nitrogen fixation by these strains ranged from 327.01 to 1954.15 pmol N2.g-1 dry biomass.day-1.

No presente estudo, a diversidade bacteriana endofítica fixadora de nitrogênio foi pesquisada utilizando métodos microbiológicos e moleculares. Isolaram-se microrganismos de raiz, caule e folha de cana-de-açúcar. Análises por seqüenciamento do 16S rDNA identificaram 150 endófitos. No total, foram identificados 18 gêneros. Destes, apenas 4 estavam presentes em cana-de-açúcar submetida aos 3 tratamentos. A maior diversidade de gêneros foi encontrada em cana sob adubação orgânica: 10 gêneros, em cana sob adubação inorgânica foram 11 gêneros e 8 em cana sem adubação. A maior parte dos gêneros pertence à família Enterobacteriaceae, como Klebsiella, Pantoea e Enterobacter. A enzima endoglicanase foi produzida por 82% dos isolados de cana sob adubação orgânica, (54%) inorgânica e (48%) sem adubação. Quanto à atividade de pectinase: 42%, 60% e 36% foram apresentadas por isolados de cana orgânica, inorgânica e sem adubação, respectivamente. A capacidade de solubilizar fosfatos inorgânicos foi detectada em 76,6% dos isolados, sendo a maior capacidade de solubilização de fosfatos encontrada em bactérias isoladas de cana-de-açúcar sob adubação orgânica (71%), de cana submetida a adubação convencional (78%) e sem adubação (88%). Foram realizados estudos de colonização em plântulas de cana-de-açúcar com 4 endofitos geneticamente modificados (EGMs) capazes de expressar os genes gfp e dsred. A avaliação da colonização na cana pela microscopia de fluorescência, mostrou que os (EGMs) gfp e dsred colonizaram as raízes e caules das plantas inoculadas, sem causar qualquer sintoma de doença. / In the present study, endophytic bacterial diversity has been searched using both microbiologic and molecular methods. Microorganisms were isolated from sugarcane root, shoot and leaf. 150 isolates were identified by 16S rDNA sequencing. 18 genera were found and only 4 were present in sugarcane submitted to the three treatments. The greatest genera diversity was found in sugarcane submited to organic fertlization: 10 genera in sugarcane submitted to inorganic fertilization were found 11 genera and 8 genera in sugarcane without fertilization. Great part of the found genera belongs to the Enterobacteriaceae family: Klebsiella, Pantoea and Enterobacter. Some physiological characteristics were determined in the isolates. Endoglucanase was produced by 82% of the isolates from sugarcane submitted to organic fertilization. Lower activities were found in bacteria isolated from inorganic fertilization and no fertilization, respectively 54% and 48%. As far as pectinase activity is concerned, a percentage of 42%, 60% and 36% was presented by the isolates from organic fertilization, inorganic fertilization and no fertilization, respectively. The hability of phosphate solubilization was detected in 76.6% of the isolates. In sugarcane under organic fertilization a percentage of 71% was found, in bacteria from inorganic fertilization, 78%, and without fertilization, 88%. Plant colonization was determined using sugarcane plantlets inoculated with four genetically modified bactéria (GMEs), able to express the genes gfp and dsred. The colonization was evaluated by fluorescence microscopy, which showed that the endophytic bacteria expressing gfp and dsred genes had invaded roots and shoots from inoculated plants, without causing any disease symptom.