Sulfamethoxazole is Metabolized and Mineralized at Extremely Low Concentrations
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ISSN: 0013-936X
E-ISSN: 1520-5851
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ACS
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The presence of organic micropollutants in water and sediments motivates investigation of their biotransformation at environmentally low concentrations, usually in the range of μg L–1. Many are biotransformed by cometabolic mechanisms; however, there is scarce information concerning their direct metabolization in this concentration range. Threshold concentrations for microbial assimilation have been reported in both pure and mixed cultures from different origins. The literature suggests a range value for bacterial growth of 1–100 μg L–1 for isolated aerobic heterotrophs in the presence of a single substrate. We aimed to investigate, as a model case, the threshold level for sulfamethoxazole (SMX) metabolization in pure cultures of Microbacterium strain BR1. Previous research with this strain has covered the milligram L–1 range. In this study, acclimated cultures were exposed to concentrations from 0.1 to 25 μg L–1 of 14C-labeled SMX, and the 14C–CO2 produced was trapped and quantified over 24 h. Interestingly, SMX removal was rapid, with 98% removed within 2 h. In contrast, mineralization was slower, with a consistent percentage of 60.0 ± 0.7% found at all concentrations. Mineralization rates increased with rising concentrations. Therefore, this study shows that bacteria are capable of the direct metabolization of organic micropollutants at extremely low concentrations (sub μg L–1)
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Environ. Sci. Technol. 2024, 58, 22, 9723–9730
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https://doi.org/10.1021/acs.est.4c02191Sponsors
This work was funded by the European Union’s Horizon 2020 research and innovation program under the Marie Skłodowska-Curie grant agreement No. 812880 (MSCA-ITN-2018: EJD Nowelties). A.T.-S. acknowledges a Juan de la Cierva-Formación postdoctoral grant (FJC2019-041664-I). A.T.-S. and J.M.L. belong to the Galician Competitive Research Group (GRC)_ ED431C-2021/37
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Atribución 4.0 Internacional
© 2024 The Authors. Published by American Chemical Society. This publication is licensed under CC-BY 4.0
© 2024 The Authors. Published by American Chemical Society. This publication is licensed under CC-BY 4.0








