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1.
J Appl Microbiol ; 93(4): 656-67, 2002.
Article in English | MEDLINE | ID: mdl-12234349

ABSTRACT

AIMS: To select an autotrophic arsenic(III)-oxidizing population, named CASO1, and to evaluate the performance of the selected bacteria in reactors. METHODS AND RESULTS: An As(III)-containing medium without organic substrate was used to select CASO1 from a mining environment. As(III) oxidation was studied under batch and continuous conditions. The main organisms present in CASO1 were identified with molecular biology tools. CASO1 exhibited significant As(III)-oxidizing activity between pH 3 and 8. The optimum temperature was 25 degrees C. As(III) oxidation was still observed in the presence of 1000 mg l(-1) As(III). In continuous culture mode, the As(III) oxidation rate reached 160 mg l(-1) h(-1). The CASO1 consortium contains at least two organisms - strain b3, which is phylogenetically close to Ralstonia picketii, and strain b6, which is related to the genus Thiomonas. The divergence in 16S rDNA sequences between b6 and the closest related organism was 5.9%, suggesting that b6 may be a new species. CONCLUSIONS: High As(III)-oxidizing activity can be obtained without organic nutrient supply, using a bacterial population from a mining environment. SIGNIFICANCE AND IMPACT OF THE STUDY: The biological oxidation of arsenite by the CASO1 population is of particular interest for decontamination of arsenic-contaminated waste or groundwater.


Subject(s)
Arsenic/metabolism , Betaproteobacteria/classification , Betaproteobacteria/growth & development , Bioreactors , Ecosystem , Betaproteobacteria/isolation & purification , Betaproteobacteria/metabolism , Culture Media , DNA, Ribosomal/analysis , Gold , Industrial Microbiology/methods , Mining , Molecular Sequence Data , Oxidation-Reduction , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Soil Microbiology
2.
Can J Microbiol ; 43(12): 1133-46, 1997 Dec.
Article in English | MEDLINE | ID: mdl-9476350

ABSTRACT

A full-scale nuclear fuel waste disposal container experiment was carried out 240 m below ground in an underground granitic rock research laboratory in Canada. An electric heater was surrounded by buffer material composed of sand and bentonite clay and provided heat equivalent to what is anticipated in a Canadian nuclear fuel waste repository. During the experiment, the heat caused a mass transport of water and moisture content gradients developed in the buffer ranging from 13% closest to the heater to 23% at the rock wall of the deposition hole. Upon decommissioning after 2.5 years, microorganisms could be cultured from all samples having a moisture content above 15% but not from samples with a moisture content below 15%. Heterotrophic aerobic and anaerobic bacteria were found in numbers ranging from 10(1) to 10(6) cells/g dry weight buffer. Approximately 10(2), or less, sulphate-reducing bacteria and methanogens per gram of dry weight buffer were also found. Identification of buffer population members was performed using Analytical Profile Index (API) strips for isolated bacteria and 16S rRNA gene sequencing for in situ samples. A total of 79 isolates from five buffer layers were identified with API strips as representing the beta, gamma and delta groups of Proteobacteria and Gram-positive bacteria. Sixty-seven 16S rRNA clones that were obtained from three buffer layers were classified into 21 clone groups representing alpha and gamma groups of Proteobacteria, Gram-positive bacteria, and a yeast. Approximately 20% of the population comprised Gram-positive bacteria. Members of the genera Amycolatopsis, Bacillus, and Nocardia predominated. Among Gram-negative bacteria, the genera Acinetobacter and Pseudomonas predominated. Analysis of lipid biomarker signatures and in situ leucine uptake demonstrated that the buffer population was viable. The results suggest that a nuclear fuel waste buffer will be populated by active microorganisms only if the moisture content is above a value where free water is available for active life.


Subject(s)
Bacteria, Aerobic/isolation & purification , Bacteria, Anaerobic/isolation & purification , Radioactive Waste , Refuse Disposal , Soil Microbiology , Aluminum Silicates , Analysis of Variance , Bacteria, Aerobic/classification , Bacteria, Anaerobic/classification , Bacterial Typing Techniques , Bentonite , Clay , Cloning, Molecular , Colony Count, Microbial , DNA, Ribosomal/genetics , Fatty Acids/analysis , Hot Temperature , Nuclear Energy , RNA, Ribosomal/genetics , Sequence Analysis, DNA , Silicon Dioxide
3.
Am J Gastroenterol ; 84(9): 1079-83, 1989 Sep.
Article in English | MEDLINE | ID: mdl-2570525

ABSTRACT

A prospective study was conducted in 224 patients to determine the clinical significance of esophageal colonization with yeasts under different conditions. In accordance with the results of direct smear microscopic examination and culture of esophageal brushings, patients were divided into three groups: positive, negative, and the patients, in whom saprophytic forms were detected. A higher prevalence of positive findings was noted in patients with predisposing factors for yeast invasion than in patients free of underlying disease. Eleven percent of patients with an endoscopically normal appearing esophagus were positive. We have the impression that this situation may represent a preclinical condition of fungal esophagitis. Patients treated with H2-blocking agents showed a significantly higher incidence of positive findings, than did those without such treatment. Whether patients suffering from a refluxesophagitis resistant to long-term treatment with H2 blockers, but with a significant colonization by yeasts, could benefit by an additional treatment with antimycotics remains a controversial issue and should be studied in a controlled way.


Subject(s)
Esophagitis/microbiology , Mycoses/microbiology , Adult , Aged , Aged, 80 and over , Esophagitis/epidemiology , Esophagitis/etiology , Esophagoscopy , Female , Histamine H2 Antagonists/adverse effects , Humans , Male , Middle Aged , Mycoses/epidemiology , Mycoses/etiology , Prospective Studies , Risk Factors
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