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1.
Microbes Environ ; 30(2): 192-5, 2015.
Article in English | MEDLINE | ID: mdl-25817584

ABSTRACT

Phosphate release from sediments hampers the remediation of aquatic systems from a eutrophic state. Microbial phosphatases in sediments release phosphorus during organic matter degradation. Despite the important role of phosphatase-expressing bacteria, the identity of these bacteria in sediments is largely unknown. We herein presented a culture-independent method to phylogenetically characterize phosphatase-expressing bacteria in sediments. We labeled whole-cell extracts of Baltic Sea sediments with an artificial phosphatase substrate and sorted phosphatase-expressing cells with a flow cytometer. Their phylogenetic affiliation was determined by Denaturing Gradient Gel Electrophoresis. The phosphatase-expressing bacterial community coarsely reflected the whole-cell bacterial community, with a similar dominance of Alphaproteobacteria.


Subject(s)
Bacteria/classification , Bacteria/enzymology , Biodiversity , Geologic Sediments/microbiology , Phosphoric Monoester Hydrolases/metabolism , Phylogeny , Bacteria/genetics , Flow Cytometry , Oceans and Seas
2.
PLoS One ; 9(3): e92401, 2014.
Article in English | MEDLINE | ID: mdl-24667801

ABSTRACT

Phosphorus release from sediments can exacerbate the effect of eutrophication in coastal marine ecosystems. The flux of phosphorus from marine sediments to the overlying water is highly dependent on the redox conditions at the sediment-water interface. Bacteria are key players in the biological processes that release or retain phosphorus in marine sediments. To gain more insight in the role of bacteria in phosphorus release from sediments, we assessed the effect of redox conditions on the structure of bacterial communities. To do so, we incubated surface sediments from four sampling sites in the Baltic Sea under oxic and anoxic conditions and analyzed the fingerprints of the bacterial community structures in these incubations and the original sediments. This paper describes the effects of redox conditions, sampling station, and sample type (DNA, RNA, or whole-cell sample) on bacterial community structure in sediments. Redox conditions explained only 5% of the variance in community structure, and bacterial communities from contrasting redox conditions showed considerable overlap. We conclude that benthic bacterial communities cannot be classified as being typical for oxic or anoxic conditions based on community structure fingerprints. Our results suggest that the overall structure of the benthic bacterial community has only a limited impact on benthic phosphate fluxes in the Baltic Sea.


Subject(s)
Bacteria/classification , Bacteria/isolation & purification , Geologic Sediments/microbiology , Oxidation-Reduction , Phosphorus/metabolism , Bacteria/genetics , Baltic States , DNA, Bacterial/genetics , Oceans and Seas , Oxygen , Phylogeny , RNA, Bacterial/genetics , RNA, Messenger/genetics , Real-Time Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction
3.
ISME J ; 7(11): 2214-28, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23788331

ABSTRACT

Microbes catalyze all major geochemical cycles on earth. However, the role of microbial traits and community composition in biogeochemical cycles is still poorly understood mainly due to the inability to assess the community members that are actually performing biogeochemical conversions in complex environmental samples. Here we applied a polyphasic approach to assess the role of microbial community composition in modulating methane emission from a riparian floodplain. We show that the dynamics and intensity of methane consumption in riparian wetlands coincide with relative abundance and activity of specific subgroups of methane-oxidizing bacteria (MOB), which can be considered as a minor component of the microbial community in this ecosystem. Microarray-based community composition analyses demonstrated linear relationships of MOB diversity parameters and in vitro methane consumption. Incubations using intact cores in combination with stable isotope labeling of lipids and proteins corroborated the correlative evidence from in vitro incubations demonstrating γ-proteobacterial MOB subgroups to be responsible for methane oxidation. The results obtained within the riparian flooding gradient collectively demonstrate that niche partitioning of MOB within a community comprised of a very limited amount of active species modulates methane consumption and emission from this wetland. The implications of the results obtained for biodiversity-ecosystem functioning are discussed with special reference to the role of spatial and temporal heterogeneity and functional redundancy.


Subject(s)
Bacteria/metabolism , Biodiversity , Methane/metabolism , Soil Microbiology , Wetlands , Bacteria/genetics , Carbon Isotopes/analysis , Carbon Isotopes/metabolism , Molecular Sequence Data , Oxidation-Reduction , Soil/chemistry
4.
FEMS Microbiol Ecol ; 71(1): 12-22, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19799630

ABSTRACT

Because methane-oxidizing bacteria (MOB) are the only biological sink for the greenhouse gas methane, knowledge of the functioning of these bacteria in various ecosystems is needed to understand the dynamics observed in global methane emission. The activity of MOB is commonly assessed by methane oxidation assays. The resulting methane depletion curves often follow a biphasic pattern of initial and induced methane oxidation activity, often interpreted as representing the in situ active and total MOB community, respectively. The application of quantitative-PCR on soil incubations, which were stopped before, at and after the transition point in the methane-depletion curve, demonstrated that both pmoA-mRNA was produced as well as substantial cell growth took place already in the initial phase. In addition, type Ia and II MOB displayed markedly different behaviour, which can be interpreted as ecologically different strategies. For the correct interpretation of methane oxidation assays, the use of small time windows is recommended to calculate methane oxidation activities to avoid substantial cell growth.


Subject(s)
Euryarchaeota/physiology , Soil Microbiology , DNA, Bacterial/isolation & purification , Euryarchaeota/genetics , Euryarchaeota/growth & development , Kinetics , Methane/metabolism , Oxidation-Reduction , Polymerase Chain Reaction/methods , RNA, Bacterial/isolation & purification
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