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1.
Appl Environ Microbiol ; 75(10): 3362-5, 2009 May.
Article in English | MEDLINE | ID: mdl-19304831

ABSTRACT

Novel arsenite [As(III)] oxidase structural genes (aoxAB) were cloned from Hydrogenobaculum bacteria isolated from an acidic geothermal spring. Reverse transcriptase PCR demonstrated expression throughout the outflow channel, and the aoxB cDNA clones exhibited distribution patterns relative to the physicochemical gradients in the spring. Microelectrode analyses provided evidence of quantitative As(III) transformation within the microbial mat.


Subject(s)
Bacteria/genetics , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Hot Springs/microbiology , Oxidoreductases/genetics , Oxidoreductases/metabolism , Bacteria/isolation & purification , Cloning, Molecular , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Gene Expression Profiling , Microelectrodes , Molecular Sequence Data , Phylogeny , Reverse Transcriptase Polymerase Chain Reaction , Sequence Analysis, DNA , Sequence Homology
2.
ISME J ; 2(6): 590-601, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18356823

ABSTRACT

The sulfidic Frasassi cave system affords a unique opportunity to investigate niche relationships among sulfur-oxidizing bacteria, including epsilonproteobacterial clades with no cultivated representatives. Oxygen and sulfide concentrations in the cave waters range over more than two orders of magnitude as a result of seasonally and spatially variable dilution of the sulfidic groundwater. A full-cycle rRNA approach was used to quantify dominant populations in biofilms collected in both diluted and undiluted zones. Sulfide concentration profiles within biofilms were obtained in situ using microelectrode voltammetry. Populations in rock-attached streamers depended on the sulfide/oxygen supply ratio of bulk water (r=0.97; P<0.0001). Filamentous epsilonproteobacteria dominated at high sulfide to oxygen ratios (>150), whereas Thiothrix dominated at low ratios (<75). In contrast, Beggiatoa was the dominant group in biofilms at the sediment-water interface regardless of sulfide and oxygen concentrations or supply ratio. Our results highlight the versatility and ecological success of Beggiatoa in diffusion-controlled niches, and demonstrate that high sulfide/oxygen ratios in turbulent water are important for the growth of filamentous epsilonproteobacteria.


Subject(s)
Epsilonproteobacteria/classification , Epsilonproteobacteria/isolation & purification , Sulfur/metabolism , Water Microbiology , Water/analysis , Biofilms/growth & development , DNA, Bacterial/genetics , DNA, Ribosomal/genetics , Epsilonproteobacteria/genetics , Epsilonproteobacteria/metabolism , Gene Library , Italy , Oxygen/analysis , Oxygen/metabolism , Phylogeny , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Sulfur/analysis
3.
Geochem Trans ; 4: 12, 2003.
Article in English | MEDLINE | ID: mdl-35412784

ABSTRACT

A sampling protocol for the retention, extraction, and analysis of sulfoxyanions in hydrothermal waters has been developed in the laboratory and tested at Yellowstone National Park and Green Lake, NY. Initial laboratory testing of the anion-exchange resin Bio-Rad™ AG1-X8 indicated that the resin was well suited for the sampling, preservation, and extraction of sulfate and thiosulfate. Synthetic solutions containing sulfate and thiosulfate were passed through AG1-X8 resin columns and eluted with 1 and 3 M KCl, respectively. Recovery ranged from 89 to 100%. Comparison of results for water samples collected from five pools in Yellowstone National Park between on-site 1C analysis (U.S. Geological Survey mobile lab) and IC analysis of resin-stored sample at SUNY-Stony Brook indicates 96 to 100% agreement for three pools (Cinder, Cistern, and an unnamed pool near Cistern) and 76 and 63% agreement for two pools (Sulfur Dust and Frying Pan). Attempts to extract polythionates from the AG1-X8 resin were made using HCl solutions, but were unsuccessful. Bio-Rad™ AG2-X8, an anion-exchange resin with weaker binding sites than the AG1-X8 resin, is better suited for polythionate extraction. Sulfate and thiosulfate extraction with this resin has been accomplished with KCl solutions of 0.1 and 0.5 M, respectively. Trithionate and tetrathionate can be extracted with 4 M KCl. Higher polythionates can be extracted with 9 M hydrochloric acid. Polythionate concentrations can then be determined directly using ion chromatographic methods, and laboratory results indicate recovery of up to 90% for synthetic polythionate solutions using AG2-X8 resin columns.

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