日本語
 
Help Privacy Policy ポリシー/免責事項
  詳細検索ブラウズ

アイテム詳細


公開

学術論文

Growth patterns of giant deep sea Beggiatoaceae from a Guaymas Basin vent site

MPS-Authors
/persons/resource/persons256787

Schutte,  Charles A.
Permanent Research Group Microsensor, Max Planck Institute for Marine Microbiology, Max Planck Society;

/persons/resource/persons210588

MacGregor,  Barbara J.
Department of Molecular Ecology, Max Planck Institute for Marine Microbiology, Max Planck Society;

/persons/resource/persons210736

Salman-Carvalho,  Verena
HGF MPG Joint Research Group for Deep Sea Ecology & Technology, Max Planck Institute for Marine Microbiology, Max Planck Society;

/persons/resource/persons210568

Lavik,  Gaute
Department of Biogeochemistry, Max Planck Institute for Marine Microbiology, Max Planck Society;

/persons/resource/persons210426

Hach,  Philipp F.
Department of Biogeochemistry, Max Planck Institute for Marine Microbiology, Max Planck Society;

/persons/resource/persons210257

de Beer,  Dirk
Permanent Research Group Microsensor, Max Planck Institute for Marine Microbiology, Max Planck Society;

External Resource
There are no locators available
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
フルテキスト (公開)
公開されているフルテキストはありません
付随資料 (公開)
There is no public supplementary material available
引用

Schutte, C. A., Teske, A., MacGregor, B. J., Salman-Carvalho, V., Lavik, G., Hach, P. F., & de Beer, D. (2018). Growth patterns of giant deep sea Beggiatoaceae from a Guaymas Basin vent site. Applied and Environmental Microbiology.


引用: https://hdl.handle.net/21.11116/0000-0003-B77E-2
要旨
Filamentous large sulfur-oxidizing bacteria (FLSB) of the family Beggiatoaceae are globally distributed aquatic bacteria that can control geochemical fluxes from the sediment to the water column through their metabolic activity. FLSB mats from hydrothermal sediments of Guaymas Basin, Mexico, typically have a “fried-egg” appearance, with orange filaments dominating near the center and wider white filaments at the periphery, likely reflecting areas of higher and lower sulfide fluxes, respectively. These FLSB store large quantities of intracellular nitrate that they use to oxidize sulfide. By applying a combination of 15N-labeling techniques and genome sequence analysis, we demonstrate that the white FLSB filaments were capable of reducing their intracellular nitrate stores to both nitrogen gas and ammonium by denitrification and dissimilatory nitrate reduction to ammonium (DNRA), respectively. On the other hand, our combined results show that the orange filaments were primarily capable of DNRA. Microsensor profiles through a laboratory-incubated white FLSB mat revealed a 2- to 3-mm vertical separation between the oxic and sulfidic zones. Denitrification was most intense just below the oxic zone, as shown by the production of nitrous oxide following exposure to acetylene, which blocks nitrous oxide reduction to nitrogen gas. Below this zone, a local pH maximum coincided with sulfide oxidation, consistent with nitrate reduction by DNRA. The balance between internally and externally available electron acceptors (nitrate) and electron donors (reduced sulfur) likely controlled the end product of nitrate reduction both between orange and white FLSB mats and between different spatial and geochemical niches within the white FLSB mat.

IMPORTANCE Whether large sulfur bacteria of the family Beggiatoaceae reduce NO3− to N2 via denitrification or to NH4+ via DNRA has been debated in the literature for more than 25 years. We resolve this debate by showing that certain members of the Beggiatoaceae use both metabolic pathways. This is important for the ecological role of these bacteria, as N2 production removes bioavailable nitrogen from the ecosystem, whereas NH4+ production retains it. For this reason, the topic of environmental controls on the competition for NO3− between N2-producing and NH4+-producing bacteria is of great scientific interest. Recent experiments on the competition between these two types of microorganisms have demonstrated that the balance between electron donor and electron acceptor availability strongly influences the end product of NO3− reduction. Our results suggest that this is also the case at the even more fundamental level of enzyme system regulation within a single organism.