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1.
Environ Microbiol ; 20(2): 755-768, 2018 02.
Artigo em Inglês | MEDLINE | ID: mdl-29194930

RESUMO

The N2 -fixing (diazotrophic) community in marine ecosystems is dominated by non-cyanobacterial microorganisms. Yet, very little is known about their identity, function and ecological relevance due to a lack of cultured representatives. Here we report a novel heterotrophic diazotroph isolated from the oxygen minimum zone (OMZ) off Peru. The new species belongs to the genus Sagittula (Rhodobacteraceae, Alphaproteobacteria) and its capability to fix N2 was confirmed in laboratory experiments. Genome sequencing revealed that it is a strict heterotroph with a high versatility in substrate utilization and energy acquisition mechanisms. Pathways for sulfide oxidation and nitrite reduction to nitrous oxide are encoded in the genome and might explain the presence throughout the Peruvian OMZ. The genome further indicates that this novel organism could be in direct interaction with other microbes or particles. NanoSIMS analyses were used to compare the metabolic potential of S. castanea with single-cell activity in situ; however, N2 fixation by this diazotroph could not be detected at the isolation site. While the biogeochemical impact of S. castanea is yet to be resolved, its abundance and widespread distribution suggests that its potential to contribute to the marine N input could be significant at a larger geographical scale.


Assuntos
Metabolismo Energético/fisiologia , Fixação de Nitrogênio/fisiologia , Rhodobacteraceae/classificação , Rhodobacteraceae/metabolismo , Anaerobiose , Metabolismo Energético/genética , Genoma Bacteriano/genética , Processos Heterotróficos , Nitritos/metabolismo , Fixação de Nitrogênio/genética , Oxirredução , Oxigênio/metabolismo , Peru , Rhodobacteraceae/isolamento & purificação , Água do Mar/microbiologia , Sulfetos/metabolismo
2.
Appl Environ Microbiol ; 80(2): 629-36, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-24212585

RESUMO

Zero-valent sulfur is a key intermediate in the microbial oxidation of sulfide to sulfate. Many sulfide-oxidizing bacteria produce and store large amounts of sulfur intra- or extracellularly. It is still not understood how the stored sulfur is metabolized, as the most stable form of S(0) under standard biological conditions, orthorhombic α-sulfur, is most likely inaccessible to bacterial enzymes. Here we analyzed the speciation of sulfur in single cells of living sulfide-oxidizing bacteria via Raman spectroscopy. Our results showed that under various ecological and physiological conditions, all three investigated Beggiatoa strains stored sulfur as a combination of cyclooctasulfur (S8) and inorganic polysulfides (Sn(2-)). Linear sulfur chains were detected during both the oxidation and reduction of stored sulfur, suggesting that Sn(2-) species represent a universal pool of bioavailable sulfur. Formation of polysulfides due to the cleavage of sulfur rings could occur biologically by thiol-containing enzymes or chemically by the strong nucleophile HS(-) as Beggiatoa migrates vertically between oxic and sulfidic zones in the environment. Most Beggiatoa spp. thus far studied can oxidize sulfur further to sulfate. Our results suggest that the ratio of produced sulfur and sulfate varies depending on the sulfide flux. Almost all of the sulfide was oxidized directly to sulfate under low-sulfide-flux conditions, whereas only 50% was oxidized to sulfate under high-sulfide-flux conditions leading to S(0) deposition. With Raman spectroscopy we could show that sulfate accumulated in Beggiatoa filaments, reaching intracellular concentrations of 0.72 to 1.73 M.


Assuntos
Beggiatoa/metabolismo , Sulfatos/metabolismo , Sulfetos/metabolismo , Água Doce/microbiologia , Oxirredução , Análise Espectral Raman , Sulfatos/química , Sulfetos/química , Enxofre/metabolismo
3.
Environ Microbiol ; 15(7): 2095-113, 2013 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-23601235

RESUMO

The majority of strains belonging to the genus Pseudovibrio have been isolated from marine invertebrates such as tunicates, corals and particularly sponges, but the physiology of these bacteria is poorly understood. In this study, we analyse for the first time the genomes of two Pseudovibrio strains - FO-BEG1 and JE062. The strain FO-BEG1 is a required symbiont of a cultivated Beggiatoa strain, a sulfide-oxidizing, autotrophic bacterium, which was initially isolated from a coral. Strain JE062 was isolated from a sponge. The presented data show that both strains are generalistic bacteria capable of importing and oxidizing a wide range of organic and inorganic compounds to meet their carbon, nitrogen, phosphorous and energy requirements under both, oxic and anoxic conditions. Several physiological traits encoded in the analysed genomes were verified in laboratory experiments with both isolates. Besides the versatile metabolic abilities of both Pseudovibrio strains, our study reveals a number of open reading frames and gene clusters in the genomes that seem to be involved in symbiont-host interactions. Both Pseudovibrio strains have the genomic potential to attach to host cells, interact with the eukaryotic cell machinery, produce secondary metabolites and supply the host with cofactors.


Assuntos
Genoma Bacteriano/genética , Rhodobacteraceae/fisiologia , Simbiose , Animais , Carbono/metabolismo , Transferência Genética Horizontal/genética , Nitrogênio/metabolismo , Filogenia , RNA Ribossômico 16S/genética , Rhodobacteraceae/classificação , Rhodobacteraceae/genética , Rhodobacteraceae/metabolismo
4.
Curr Biol ; 17(13): 1116-22, 2007 Jul 03.
Artigo em Inglês | MEDLINE | ID: mdl-17583510

RESUMO

Programmed cell death (PCD) is a common host response to microbial infection [1-3]. In plants, PCD is associated with immunity to biotrophic pathogens, but it can also promote disease upon infection by necrotrophic pathogens [4]. Therefore, plant cell-suicide programs must be strictly controlled. Here we demonstrate that the Arabidopsis thaliana Brassinosteroid Insensitive 1 (BRI1)-associated receptor Kinase 1 (BAK1), which operates as a coreceptor of BRI1 in brassinolide (BL)-dependent plant development, also regulates the containment of microbial infection-induced cell death. BAK1-deficient plants develop spreading necrosis upon infection. This is accompanied by production of reactive oxygen intermediates and results in enhanced susceptibility to necrotrophic fungal pathogens. The exogenous application of BL rescues growth defects of bak1 mutants but fails to restore immunity to fungal infection. Moreover, BL-insensitive and -deficient mutants do not exhibit spreading necrosis or enhanced susceptibility to fungal infections. Together, these findings suggest that plant steroid-hormone signaling is dispensable for the containment of infection-induced PCD. We propose a novel, BL-independent function of BAK1 in plant cell-death control that is distinct from its BL-dependent role in plant development.


Assuntos
Proteínas de Arabidopsis/fisiologia , Arabidopsis/imunologia , Proteínas Serina-Treonina Quinases/fisiologia , Pseudomonas syringae/imunologia , Arabidopsis/microbiologia , Arabidopsis/fisiologia , Brassinosteroides , Morte Celular/fisiologia , Colestanóis/metabolismo , Perfilação da Expressão Gênica , Doenças das Plantas , Reguladores de Crescimento de Plantas/metabolismo , Pseudomonas syringae/fisiologia , Transdução de Sinais/fisiologia , Esteroides Heterocíclicos/metabolismo
5.
Syst Appl Microbiol ; 39(7): 476-483, 2016 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-27638196

RESUMO

Seagrass meadows of Posidonia oceanica represent hotspots of productivity in the oligotrophic Mediterranean Sea. The lack of dissolved inorganic nitrogen (DIN) in the seawater suggests that the N-demand of these meadows might be in part supported by microbial dinitrogen (N2) fixation. However, currently there are no direct N2 fixation measurements available for this productive marine macrophyte. Here we investigated N2 fixation activity associated with P. oceanica leaf, rhizome and root pieces. In 15N2 incubations, the roots exhibited highest rates of N2 fixation. The rates varied considerably between replicates, presumably due to a patchy microbial colonization of the roots. Additions of organic carbon compounds (acetate, glucose, sucrose or algal lysate) did not enhance the N2 fixation rates. Sulfate reduction rates measured alongside were also highest in root incubations. Correspondingly, sequences of the nifH gene (a marker gene for the iron protein of the N2-fixing enzyme nitrogenase) related to known sulfate-reducing bacteria were retrieved from P. oceanica roots. Other nifH sequences clustered with known heterotrophic diazotrophs previously identified in other marine macrophytes. In particular, many sequences obtained from P. oceanica roots were similar (>94%) to a saltmarsh rhizosphere-associated heterotrophic diazotroph, indicating that heterotrophic lifestyle might be common among marine macrophyte-associated diazotrophs.


Assuntos
Alismatales/metabolismo , Alismatales/microbiologia , Processos Heterotróficos/fisiologia , Fixação de Nitrogênio/fisiologia , Raízes de Plantas/metabolismo , Raízes de Plantas/microbiologia , Deltaproteobacteria/metabolismo , Gammaproteobacteria/metabolismo , Região do Mediterrâneo , Nitrogênio/metabolismo , Oxirredutases/genética , Folhas de Planta/metabolismo , Folhas de Planta/microbiologia , Água do Mar/química , Sulfatos/metabolismo
6.
PLoS One ; 10(3): e0121675, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25826215

RESUMO

Marine planktonic bacteria often live in habitats with extremely low concentrations of dissolved organic matter (DOM). To study the use of trace amounts of DOM by the facultatively oligotrophic Pseudovibrio sp. FO-BEG1, we investigated the composition of artificial and natural seawater before and after growth. We determined the concentrations of dissolved organic carbon (DOC), total dissolved nitrogen (TDN), free and hydrolysable amino acids, and the molecular composition of DOM by electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI FT-ICR-MS). The DOC concentration of the artificial seawater we used for cultivation was 4.4 µmol C L(-1), which was eight times lower compared to the natural oligotrophic seawater we used for parallel experiments (36 µmol C L(-1)). During the three-week duration of the experiment, cell numbers increased from 40 cells mL(-1) to 2x10(4) cells mL(-1) in artificial and to 3x10(5) cells mL(-1) in natural seawater. No nitrogen fixation and minor CO2 fixation (< 1% of cellular carbon) was observed. Our data show that in both media, amino acids were not the main substrate for growth. Instead, FT-ICR-MS analysis revealed usage of a variety of different dissolved organic molecules, belonging to a wide range of chemical compound groups, also containing nitrogen. The present study shows that marine heterotrophic bacteria are able to proliferate with even lower DOC concentrations than available in natural ultra-oligotrophic seawater, using unexpected organic compounds to fuel their energy, carbon and nitrogen requirements.


Assuntos
Rhodobacteraceae/metabolismo , Água do Mar , Contagem de Colônia Microbiana , Meios de Cultura , Ciclotrons , Rhodobacteraceae/crescimento & desenvolvimento , Extração em Fase Sólida , Solubilidade , Espectrometria de Massas por Ionização por Electrospray , Espectroscopia de Infravermelho com Transformada de Fourier
7.
Front Microbiol ; 2: 276, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-22291687

RESUMO

The chemolithoautotrophic strain Beggiatoa sp. 35Flor shows an unusual migration behavior when cultivated in a gradient medium under high sulfide fluxes. As common for Beggiatoa spp., the filaments form a mat at the oxygen-sulfide interface. However, upon prolonged incubation, a subpopulation migrates actively downward into the anoxic and sulfidic section of the medium, where the filaments become gradually depleted in their sulfur and polyhydroxyalkanoates (PHA) inclusions. This depletion is correlated with the production of hydrogen sulfide. The sulfur- and PHA-depleted filaments return to the oxygen-sulfide interface, where they switch back to depositing sulfur and PHA by aerobic sulfide oxidation. Based on these observations we conclude that internally stored elemental sulfur is respired at the expense of stored PHA under anoxic conditions. Until now, nitrate has always been assumed to be the alternative electron acceptor in chemolithoautotrophic Beggiatoa spp. under anoxic conditions. As the medium and the filaments were free of oxidized nitrogen compounds we can exclude this metabolism. Furthermore, sulfur respiration with PHA under anoxic conditions has so far only been described for heterotrophic Beggiatoa spp., but our medium did not contain accessible organic carbon. Hence the PHA inclusions must originate from atmospheric CO(2) fixed by the filaments while at the oxygen-sulfide interface. We propose that the directed migration of filaments into the anoxic section of an oxygen-sulfide gradient system is used as a last resort to preserve cell integrity, which would otherwise be compromised by excessive sulfur deposition occurring in the presence of oxygen and high sulfide fluxes. The regulating mechanism of this migration is still unknown.

8.
Eur J Cell Biol ; 89(2-3): 169-74, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-20018402

RESUMO

Plant receptor-like kinases (RLKs) are transmembrane proteins with putative N-terminal extracellular ligand-binding domains and C-terminal intracellular protein kinase domains. RLKs have been implicated in multiple physiological programs including plant development and immunity to microbial infection. Arabidopsis thaliana gene expression patterns support an important role of this class of proteins in biotic stress adaptation. Here, we provide a comprehensive survey of plant immunity-related RLK gene expression. We further document the role of the Arabidopsis Brassinosteroid Insensitive 1 (BRI1)-associated receptor kinase 1 (BAK1) in seemingly unrelated biological processes, such as plant development and immunity, and propose a role of this protein as an adaptor molecule that is required for proper functionality of numerous RLKs. This view is supported by the identification of an additional RLK, PEPR1, and its closest homolog, PEPR2 as BAK1-interacting RLKs.


Assuntos
Proteínas de Arabidopsis/metabolismo , Arabidopsis , Regulação da Expressão Gênica de Plantas , Sistema Imunitário/fisiologia , Proteínas Serina-Treonina Quinases/metabolismo , Arabidopsis/enzimologia , Arabidopsis/crescimento & desenvolvimento , Arabidopsis/imunologia , Proteínas de Arabidopsis/genética , Análise por Conglomerados , Biologia Computacional , Regulação Enzimológica da Expressão Gênica , Proteínas Serina-Treonina Quinases/genética , Receptores de Superfície Celular/genética , Receptores de Superfície Celular/metabolismo
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