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1.
Electron. j. biotechnol ; 19(5): 12-20, Sept. 2016. ilus
Article Dans Anglais | LILACS | ID: lil-797332

Résumé

Background: Methyl tert-butyl ether (MTBE) is a pollutant that causes deleterious effects on human and environmental health. Certain microbial cultures have shown the ability to degrade MTBE, suggesting that a novel bacterial species capable of degrading MTBE could be recovered. The goal of this study was to isolate, identify and characterize the members of a bacterial consortium capable of degrading MTBE. Results: The IPN-120526 bacterial consortium was obtained through batch enrichment using MTBE as the sole carbon and energy source. The cultivable fraction of the consortium was identified; of the isolates, only Stenotrophomonas maltophilia IPN-TD and Sphingopyxis sp. IPN-TE were capable of degrading MTBE. To the best of our knowledge, this report is the first demonstrating that S. maltophilia and Sphingopyxis sp. are capable of degrading MTBE. The degradation kinetics of MTBE demonstrated that S. maltophilia IPN-TD had a significantly higher overall MTBE degradation efficiency and rate (48.39 ± 3.18% and 1.56 ± 0.12 mg L-1 h-1, respectively) than the IPN-120526 consortium (38.59 ± 2.17% and 1.25 ± 0.087 mg L-1 respectively). The kinetics of MTBE removal by both cultures fit first-order and pseudo-first-order reaction models. Conclusions: These findings suggest that S. maltophilia IPN-TD in axenic culture has considerable potential for the detoxification of MTBE-contaminated water.


Sujets)
Microbiologie du sol , Stenotrophomonas maltophilia/isolement et purification , Stenotrophomonas maltophilia/métabolisme , Éthers méthyliques/métabolisme , Dépollution biologique de l'environnement , Essence , Cinétique , Réaction de polymérisation en chaîne , Pollution de l'environnement , Consortiums microbiens , Éthers méthyliques/analyse
2.
Braz. j. microbiol ; 43(1): 283-287, Jan.-Mar. 2012. ilus, tab
Article Dans Anglais | LILACS | ID: lil-622815

Résumé

Conventional microbiological culture techniques are frequently insufficient to confirm endophthalmitis clinical cases which could require urgent medical attention because it could lead to permanent vision loss. We are proposing PCR-DGGE and 16S rRNA gene libraries as an alternative to improve the detection and identification rate of bacterial species from endophthalmitis cases.


Sujets)
Humains , Techniques et procédures diagnostiques , Endophtalmie , Techniques in vitro , Infections à staphylocoques , Staphylococcus epidermidis/isolement et purification , Uvéite purulente , Diagnostic , Incidence , Méthodes , Patients
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