Aerobic biodegradation of the sulfonamide antibiotic sulfamethoxazole by activated sludge applied as co-substrate and sole carbon and nitrogen source

被引:266
|
作者
Mueller, Elisabeth [1 ]
Schuessler, Walter [2 ]
Horn, Harald [3 ]
Lemmer, Hilde [2 ]
机构
[1] Tech Univ Munich, Chair Urban Water Syst Engn, D-85748 Garching, Germany
[2] Bavarian Environm Agcy, D-86179 Augsburg, Germany
[3] Karlsruhe Inst Technol, Engler Bunte Inst, D-76131 Karlsruhe, Germany
关键词
Pharmaceutical; Sulfamethoxazole; 3-Amino-5-methyl-isoxazole; 3-Amino-isoxazole; Isoxazole; Hydroxyl-N-(5-methyl-1,2-oxazole-3-yl)benzene-1-sulfonamide; WASTE-WATER TREATMENT; AQUATIC ENVIRONMENT; ORGANIC-COMPOUNDS; TREATMENT PLANTS; PHARMACEUTICALS; RESISTANCE; REMOVAL; SEWAGE; AGENTS; FATE;
D O I
10.1016/j.chemosphere.2013.02.070
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Potential aerobic biodegradation mechanisms of the widely used polar, low-adsorptive sulfonamide antibiotic sulfamethoxazole (SMX) were investigated in activated sludge at bench scale. The study focused on (i) SMX co-metabolism with acetate and ammonium nitrate and (ii) SMX utilization when present as the sole carbon and nitrogen source. With SMX adsorption being negligible, elimination was primarily based on biodegradation. Activated sludge was able to utilize SMX both as a carbon and/or nitrogen source. SMX biodegradation was enhanced when a readily degradable energy supply (acetate) was provided which fostered metabolic activity. Moreover, it was raised under nitrogen deficiency conditions. The mass balance for dissolved organic carbon showed an incomplete SMX mineralization with two scenarios: (i) with SMX as a co-substrate, 3-amino-5-methyl-isoxazole represented the main stable metabolite and (ii) SMX as sole carbon and nitrogen source possibly yielded hydroxyl-N-(5-methyl-1,2-oxazole-3-yl)benzene-1-sulfonamide as a further metabolite. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:969 / 978
页数:10
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