Biodegradation of sulfamethoxazole and other sulfonamides by Achromobacter denitrificans PR1

Journal of Hazardous Materials

Volumn 280, Issue , 2014, Pages 741-749

  Reis, Patrícia J M ^a,b   Reis, Ana C ^a   Ricken, Benjamin ^c   Kolvenbach, Boris A ^c   Manaia, Célia M ^b   Corvini, Philippe F X ^c   Nunes, Olga C ^a  

^a UNIVERSITY OF PORTO   (Portugal)

^b UNIVERSIDADE CATÓLICA PORTUGUESA   (Portugal)

^c UNIVERSITY OF APPLIED SCIENCES AND ARTS NORTHWESTERN SWITZERLAND   (Switzerland)

Author keywords

3 Amino 5 methylisoxazole; Achromobacter; Antibiotic resistance; Pharmaceutical; Xenobiotics

Indexed keywords

3-AMINO-5-METHYLISOXAZOLE; ACHROMOBACTER; ANTIBIOTIC RESISTANCE; SULFAMETHOXAZOLE; XENOBIOTICS;

DRUG PRODUCTS;

AMINO ACID; FUROSEMIDE; GLIBENCLAMIDE; GLICLAZIDE; GLIMEPIRIDE; ISOXAZOLE DERIVATIVE; RNA 16S; SULFACETAMIDE; SULFADIAZINE; SULFADIMETHOXINE; SULFADIMIDINE; SULFAMETHOXAZOLE; SULFAMETHOXYPYRIDAZINE; SULFATHIAZOLE; SULFONAMIDE; SEWAGE;

ANTIBIOTIC RESISTANCE; BACTERIUM; BIODEGRADATION; BIOREMEDIATION; DENITRIFICATION; DRUG; POLLUTANT REMOVAL; XENOBIOTICS;

ACHROMOBACTER; ACHROMOBACTER DENITRIFICANS; ACTIVATED SLUDGE; ARTICLE; BACTERIAL CELL; BACTERIAL GENE; BACTERIAL GROWTH; BACTERIAL STRAIN; BACTERIUM CULTURE; BACTERIUM ISOLATE; BIOCHEMICAL COMPOSITION; BIOMASS; CONTROLLED STUDY; DRUG DEGRADATION; DRY WEIGHT; ENRICHMENT CULTURE; GENUS; MICROBIAL ACTIVITY; MICROBIAL DEGRADATION; MIXED CELL CULTURE; NONHUMAN; NUCLEOTIDE SEQUENCE; STOICHIOMETRY; WASTE WATER; BIOREMEDIATION; ISOLATION AND PURIFICATION; METABOLISM; MICROBIOLOGY; SEWAGE;

ACHROMOBACTER; ACHROMOBACTER DENITRIFICANS;

ACHROMOBACTER DENITRIFICANS; BIODEGRADATION, ENVIRONMENTAL; SEWAGE; SULFAMETHOXAZOLE; SULFONAMIDES;

EID: 84907984539     PISSN: 03043894     EISSN: 18733336     Source Type: Journal    
DOI: 10.1016/j.jhazmat.2014.08.039     Document Type: Article

References (36)

1. Shah S.S.A., Rivera G., Ashfaq M. Recent advances in medicinal chemistry of sulfonamides. Rational design as anti-tumoral, anti-bacterial and anti-inflammatory agents. Mini. Rev. Med. Chem. 2013, 13:70-86.
2. Michael I., Rizzo L., McArdell C.S., Manaia C.M., Merlin C., Schwartz T., Dagot C., Fatta-Kassinos D. Urban wastewater treatment plants as hotspots for the release of antibiotics in the environment: a review. Water Res. 2013, 47:957-995.
3. Cribb A.E., Spielberg S.P. Sulfamethoxazole is metabolized to the hydroxylamine in humans. Clin. Pharmacol. Ther. 1992, 51:522-526.
4. Peng X., Wang Z., Kuang W., Tan J., Li K. A preliminary study on the occurrence and behavior of sulfonamides, ofloxacin and chloramphenicol anti-microbials in wastewaters of two sewage treatment plants in Guangzhou, China. Sci. Total Environ. 2006, 371:314-322.
5. Kolpin D.W., Furlong E.T., Meyer M.T., Thurman E.M., Zaugg S.D., Barber L.B., Buxton H.T. Pharmaceuticals, hormones, and other organic wastewater contaminants in U.S. streams, 1999-2000: a national reconnaissance. Environ. Sci. Technol. 2002, 36:1202-1211.
6. Barnes K.K., Kolpin D.W., Furlong E.T., Zaugg S.D., Meyer M.T., Barber L.B. A national reconnaissance of pharmaceuticals and other organic wastewater contaminants in the United States-I) groundwater. Sci. Total Environ. 2008, 402:192-200.
7. Laville N., Aït-Aïssa S., Gomez E., Casellas C., Porcher J.M. Effects of human pharmaceuticals on cytotoxicity, EROD activity and ROS production in fish hepatocytes. Toxicology 2004, 196:41-55.
8. García-Galán M.J., Díaz-Cruz M.S., Barceló D. Occurrence of sulfonamide residues along the Ebro river basin: removal in wastewater treatment plants and environmental impact assessment. Environ. Int. 2011, 37:462-473.
9. Trovó A.G., Nogueira R.F.P., Agüera A., Sirtori C., Fernández-Alba A.R. Photodegradation of sulfamethoxazole in various aqueous media: persistence, toxicity and photoproducts assessment. Chemosphere 2009, 77:1292-1298.
10. Jiang L., Hu X., Xu T., Zhang H., Sheng D., Yin D. Prevalence of antibiotic resistance genes and their relationship with antibiotics in the Huangpu River and the drinking water sources, Shanghai, China. Sci. Total Environ. 2013, 458-460:267-272.
11. Hoa P.T.P., Managaki S., Nakada N., Takada H., Shimizu A., Anh D.H., Viet P.H., Suzuki S. Antibiotic contamination and occurrence of antibiotic-resistant bacteria in aquatic environments of northern Vietnam. Sci. Total Environ. 2011, 409:2894-2901.
12. Manaia C.M., Vaz-Moreira I., Nunes O.C. Antibiotic resistence in waste- and surface waters and human health implications. The Handbook of Environmental Chemistry 2012, 173-212. Springer-Verlag, Berlin Heidelberg. D. Barceló (Ed.).
13. Zhang X.X., Zhang T., Fang H. Antibiotic resistance genes in water environment. Appl. Microbiol. Biotechnol. 2009, 82:397-414.
14. Drillia P., Dokianakis S.N., Fountoulakis M.S., Kornaros M., Stamatelatou K., Lyberatos G. On the occasional biodegradation of pharmaceuticals in the activated sludge process: the example of the antibiotic sulfamethoxazole. J. Hazard. Mater. 2005, 122:259-265.
15. Yu T.H., Lin A.Y.C., Lateef S.K., Lin C.F., Yang P.Y. Removal of antibiotics and non-steroidal anti-inflammatory drugs by extended sludge age biological process. Chemosphere 2009, 77:175-181.
16. Yang S.F., Lin C.F., Wu C.J., Ng K.K., Yu-Chen Lin A., Andy Hong P.K. Fate of sulfonamide antibiotics in contact with activated sludge-sorption and biodegradation. Water Res. 2012, 46:1301-1308.
17. Collado N., Buttiglieri G., Marti E., Ferrando-Climent L., Rodriguez-Mozaz S., Barceló D., Comas J., Rodriguez-Roda I. Effects on activated sludge bacterial community exposed to sulfamethoxazole. Chemosphere 2013, 93:99-106.
18. Müller E., Schüssler W., Horn H., Lemmer H. Aerobic biodegradation of the sulfonamide antibiotic sulfamethoxazole by activated sludge applied as co-substrate and sole carbon and nitrogen source. Chemosphere 2013, 92:969-978.
19. Gauthier H., Yargeau V., Cooper D.G. Biodegradation of pharmaceuticals by Rhodococcus rhodochrous and Aspergillus niger by co-metabolism. Sci. Total Environ. 2010, 408:1701-1706.
20. Larcher S., Yargeau V. Biodegradation of sulfamethoxazole by individual and mixed bacteria. Appl. Microbiol. Biotechnol. 2011, 91:211-218.
21. Bouju H., Ricken B., Beffa T., Corvini P.F.X., Kolvenbach B.A. Isolation of bacterial strains capable of mineralizing sulfamethoxazole from an acclimated membrane bioreactor. Appl. Environ. Microbiol. 2012, 78:277-279.
22. Herzog B., Lemmer H., Horn H., Muller E. Characterization of pure cultures isolated from sulfamethoxazole-acclimated activated sludge with respect to taxonomic identification and sulfamethoxazole biodegradation potential. BMC Microbiol. 2013, 13:276.
23. Jiang B., Li A., Cui D., Cai R., Ma F., Wang Y. Biodegradation and metabolic pathway of sulfamethoxazole by Pseudomonas psychrophila HA-4, a newly isolated cold-adapted sulfamethoxazole-degrading bacterium. Appl. Microbiol. Biotechnol. 2014, 98:4671-4681.
24. Barreiros L., Nogales B., Manaia C.M., Ferreira A.C.S., Pieper D.H., Reis M.A., Nunes O.C. A novel pathway for mineralization of the thiocarbamate herbicide molinate by a defined bacterial mixed culture. Environ. Microbiol. 2003, 5:944-953.
25. Nunes O.C., Donato M.M., da Costa M.S. Isolation and characterization of Rhodothermus strains from S. Miguel, Azores. Syst. Appl. Microbiol. 1992, 15:92-97.
26. Maltseva O., Oriel P. Monitoring of an alkaline 2,4,6-trichlorophenol-degrading enrichment culture by DNA fingerprinting methods and isolation of the responsible organism, haloalkaliphilic Nocardioides sp. strain M6. Appl. Environ. Microbiol. 1997, 63:4145-4149.
27. Barreiros L., Fernandes A., Ferreira A.C.S., Pereira H., Bastos M.M.S.M., Manaia C.M., Nunes O.C. New insights into a bacterial metabolic and detoxifying association responsible for the mineralization of the thiocarbamate herbicide molinate. Microbiology 2008, 154:1038-1046.
28. Ricken B., Corvini P.F.X., Cichocka D., Parisi M., Lenz M., Wyss D., Martínez-Lavanchy P.M., Müller J.A., Shahgaldian P., Tulli L.G., Kohler H.-P.E., Kolvenbach B.A. ipso-Hydroxylation and subsequent fragmentation: a novel microbial strategy to eliminate sulfonamide antibiotics. Appl. Environ. Microbiol. 2013, 79:5550-5558.
29. CLSI. Performance standards for anti-microbial susceptibility testing; twenty-second informational supplement. CLSI document M100-S22 2012, Clinical and Laboratory Standards Institute, Wayne, PA.
30. Huang M., Tian S., Chen D., Zhang W., Wu J., Chen L. Removal of sulfamethazine antibiotics by aerobic sludge and an isolated Achromobacter sp. S-3. J. Environ. Sci. 2012, 24:1594-1599.
31. Halling-Sørensen B., Nors Nielsen S., Lanzky P.F., Ingerslev F., Holten Lützhøft H.C., Jørgensen S.E. Occurrence, fate and effects of pharmaceutical substances in the environment-a review. Chemosphere 1998, 36:357-393.
32. Eibes G., Debernardi G., Feijoo G., Moreira M.T., Lema J. Oxidation of pharmaceutically active compounds by a ligninolytic fungal peroxidase. Biodegradation 2011, 22:539-550.
33. Porter A.W., Hay A.G. Identification of opdA, a gene involved in biodegradation of the endocrine disrupter octylphenol. Appl. Environ. Microbiol. 2007, 73:7373-7379.
34. Porter A.W., Campbell B.R., Kolvenbach B.A., Corvini P.F.X., Benndorf D., Rivera-Cancel G., Hay A.G. Identification of the flavin monooxygenase responsible for ipso substitution of alkyl and alkoxyphenols in Sphingomonas sp. TTNP3 and Sphingobium xenophagum Bayram. Appl. Microbiol. Biotechnol. 2012, 94:261-272.
35. Guengerich F.P. Common and uncommon cytochrome P450 reactions related to metabolism and chemical toxicity. Chem. Res. Toxicol. 2001, 14:611-650.
36. Vaz-Moreira I., Egas C., Nunes O.C., Manaia C.M. Bacterial diversity from the source to the tap: a comparative study based on 16S rRNA gene-DGGE and culture-dependent methods. FEMS Microbiol. Ecol. 2013, 83:361-374.