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1.
Water Res ; 46(13): 4226-34, 2012 Sep 01.
Article in English | MEDLINE | ID: mdl-22673343

ABSTRACT

Triclosan, a synthetic antimicrobial agent, has been considered as an emerging environmental contaminant. Here we reported a triclosan-degrading wastewater bacterial isolate, Sphingopyxis strain KCY1, capable of dechlorinating triclosan with a stoichiometric release of chloride. The stain can degrade diphenyl ether but not 2,4,4'-tribromodiphenyl ether and 2,2',4,4'-tetrabromodiphenyl ether, despite all these three compounds are structurally similar to triclosan. While strain KCY1 was unable to grow on triclosan and catechol, it could grow with glucose, sodium succinate, sodium acetate, and phenol. When grown with complex nutrient medium containing a trace amount of triclosan (as low as 5 µg/L), the strain could retain its degradation ability toward triclosan. The maximum-specific triclosan degradation rate (q(m)) and the half-velocity constant (K(m)) are 0.13 mg-triclosan/mg-protein/day and 2.8 mg-triclosan/L, respectively. As triclosan degradation progressed, five metabolites were identified and these metabolites continue to transform into non-chlorinated end products, which was supported by a sharp drop in androgenic potential. The activity of catechol 2,3-dioxygenase in the cell extract was detected. No triclosan degradation was observed in the presence of 3-fluorocatechol, an inhibitor of meta-cleavage enzyme, suggesting that triclosan degradation proceed via meta-cleavage pathway. Based on all the observations, a degradation pathway for triclosan by strain KCY1 was proposed.


Subject(s)
Sphingomonadaceae/metabolism , Triclosan/metabolism , Water Microbiology , Water Pollutants, Chemical/metabolism , Biodegradation, Environmental , Catechol 2,3-Dioxygenase/metabolism , Catechols/chemistry , Catechols/metabolism , Chlorides/chemistry , Chlorides/metabolism , Glucose/metabolism , Halogenated Diphenyl Ethers , Kinetics , Models, Chemical , Molecular Structure , Phenol/metabolism , Phenyl Ethers/chemistry , Phenyl Ethers/metabolism , Polybrominated Biphenyls/chemistry , Polybrominated Biphenyls/metabolism , Sodium Acetate/metabolism , Sphingomonadaceae/growth & development , Sphingomonadaceae/isolation & purification , Succinates/metabolism , Triclosan/chemistry , Water Pollutants, Chemical/chemistry
2.
J Hazard Mater ; 174(1-3): 416-23, 2010 Feb 15.
Article in English | MEDLINE | ID: mdl-19819067

ABSTRACT

Heat loss can affect experimental flammability limits, and it becomes indispensable to quantify flammability limits when apparatus quenching effect becomes significant. In this research, the lower flammability limits of binary hydrocarbon mixtures are predicted using calculated flame temperature (CFT) modeling, which is based on the principle of energy conservation. Specifically, the hydrocarbon mixture lower flammability limit is quantitatively correlated to its final flame temperature at non-adiabatic conditions. The modeling predictions are compared with experimental observations to verify the validity of CFT modeling, and the minor deviations between them indicated that CFT modeling can represent experimental measurements very well. Moreover, the CFT modeling results and Le Chatelier's Law predictions are also compared, and the agreement between them indicates that CFT modeling provides a theoretical justification for the Le Chatelier's Law.


Subject(s)
Hydrocarbons , Temperature
3.
Chemosphere ; 77(8): 1084-9, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19772981

ABSTRACT

This study examined the biodegradation potential of three wastewater micropollutants (triclosan, bisphenol A, and ibuprofen) by Nitrosomonas europaea and mixed ammonia-oxidizing bacteria in nitrifying activated sludge. N. europaea could degrade triclosan and bisphenol A, but not ibuprofen. The degradation was observed only in the absence of allylthiourea (an inhibitor for ammonia monooxygenase (AMO)), suggesting that AMO might be responsible for triclosan and bisphenol A degradation. Competitive inhibition among ammonia, triclosan, and bisphenol A was observed. Inactivation of N. europaea was observed after degrading a mixture of triclosan and bisphenol A. The inactivation might be due to product toxicity and/or antimicrobial effect of triclosan; however, the causes of the inactivation were not determined. Regardless of the presence of the AMO inhibitor, three micropollutants were degraded by two different nitrified activated sludge samples. The results suggested that both ammonia-oxidizing bacteria and heterotrophic microorganisms in the activated sludge can degrade triclosan and bisphenol A. On the other hand, ibuprofen was more likely degraded by heterotrophic microorganisms in the activated sludge.


Subject(s)
Ammonia/metabolism , Nitrosomonas europaea/metabolism , Water Pollutants, Chemical/metabolism , Benzhydryl Compounds , Biodegradation, Environmental , Environment , Ibuprofen/isolation & purification , Ibuprofen/metabolism , Ibuprofen/toxicity , Nitrites/metabolism , Nitrosomonas europaea/drug effects , Oxidation-Reduction/drug effects , Oxidoreductases/antagonists & inhibitors , Oxidoreductases/metabolism , Phenols/isolation & purification , Phenols/metabolism , Phenols/toxicity , Sewage , Triclosan/isolation & purification , Triclosan/metabolism , Triclosan/toxicity , Water Pollutants, Chemical/isolation & purification , Water Pollutants, Chemical/toxicity
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