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DOI 10.1016/j.jhazmat.2024.133558

Медицинская библиотека · Journal of hazardous materials · 2024

Bio-degraded of sulfamethoxazole by microbial consortia without addition nutrients: Mineralization, nitrogen removal, and proteomic characterization.

He Yuzhe, Liu Lei, Wang Qi, Dong Xiaoqi, Huang Jingfei, Jia Xiaoshan, Peng Xingxing

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Sulfamethoxazole (SMX) is widely employed as an antibiotic, while its residue in environment has become a common public concern. Using 100 mg/L SMX as the sole nutrient source, the acclimated sludge obtained by this study displayed an excellent SMX degradation performance. The addition of SMX resulted in significant microbiological differentiation within the acclimated sludge. Microbacterium (6.6%) was identified as the relatively dominant genera in metabolism group that used SMX as sole carbon source. Highly expressed proteins from this strain strongly suggested its essential role in SMX degradation, while the degradation of SMX by other strains (Thaurea 78%) in co-metabolism group appeared to also rely on this strain. The interactions of differentially expressed proteins were primarily involved in metabolic pathways including TCA cycle and nitrogen metabolism. It is concluded that the sulfonamides might serve not only as the carbon source but also as the nitrogen source in the reactor. A total of 24 intermediates were identified, 13 intermediates were newly reported. The constructed pathway suggested the mineralizing and nitrogen conversion ability towards SMX. Batch experiments also proved that the acclimated sludge displayed ability to biodegrade other sulfonamides, including SM2 and SDZ and SMX-N could be removed completely.

Для цитирования: He Yuzhe, Liu Lei, Wang Qi, Dong Xiaoqi, Huang Jingfei, Jia Xiaoshan, Peng Xingxing. Bio-degraded of sulfamethoxazole by microbial consortia without addition nutrients: Mineralization, nitrogen removal, and proteomic characterization.. Journal of hazardous materials. 2024. DOI: 10.1016/j.jhazmat.2024.133558.

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