Insights into removal of sulfonamides in anaerobic activated sludge system: Mechanisms, degradation pathways and stress responses
Abstract
The fate of antibiotics in activated sludge has attracted increasing interests. However, the focus needs to shift from concerning removal efficiencies to understanding mechanisms and sludge responding to antibiotic toxicity. Herein, we operated two anaerobic sequencing batch reactors (ASBRs) for 200 days with sulfadiazine (SDZ) and sulfamethoxazole (SMX) added. The removal efficiency of SMX was higher than that of SDZ. SDZ was removed via adsorption (9.91–21.18%) and biodegradation (10.20–16.00%), while biodegradation (65.44–86.26%) was dominant for SMX removal. The mechanisms involved in adsorption and biodegradation were investigated, including adsorption strength, adsorption sites and the roles of enzymes. Protein-like substance (tryptophan) functioned vitally in adsorption by forming complexes with sulfonamides. P450 enzymes may catalyze sulfonamides degradation via hydroxylation and desulfurization. Activated sludge showed distinct responses to different sulfonamides, reflected in the changes of microbial communities and functions. These responses were related to sulfonamides removal, corresponding to the stronger adsorption capacity of activated sludge in ASBR-SDZ and degradation capacity in ASBR-SMX. Furthermore, the reasons for different removal efficiencies of sulfonamides were analyzed according to steric and electronic effects. These findings propose insights into antibiotic removal and broaden the knowledge for self-protection mechanisms of activated sludge under chronic toxicities of antibiotics.
- Publication:
-
Journal of Hazardous Materials
- Pub Date:
- February 2022
- DOI:
- Bibcode:
- 2022JHzM..42327248Z
- Keywords:
-
- SMs;
- sulfonamide antibiotics;
- SDZ;
- sulfadiazine;
- SMX;
- sulfamethoxazole;
- ASBR;
- anaerobic sequencing batch reactor;
- ASBR-SDZ;
- the ASBR exposed to SDZ;
- ASBR-SMX;
- the ASBR exposed to SMX;
- EPS;
- extracellular polymeric substance;
- BES;
- 2-bromoethanesulfonate;
- K<SUB loc="post">bio</SUB>;
- rate constant of antibiotic biodegradation;
- PN;
- proteins;
- PS;
- polysaccharides;
- COD;
- chemical oxygen demand;
- EEM;
- three-dimensional excitation-emission matrix;
- FTIR;
- Fourier transform infrared;
- log K<SUB loc="post">ow</SUB>;
- n-octanol-water distribution coefficients;
- PARAFAC;
- parallel factor analysis;
- K<SUB loc="post">q</SUB>;
- biomolecular quenching rate constants;
- K<SUB loc="post">b</SUB>;
- binding constant;
- n;
- the number of binding sites;
- LDA;
- linear discriminant analysis;
- ω;
- electrophilicity index;
- f<SUB loc="post">A</SUB><SUP loc="post">(2)</SUP> (r);
- condensed dual descriptor;
- Antibiotics;
- Stress responses;
- Biodegradation;
- Enzymes;
- Biotransformation products