Identification of wastewater bacteria involved in the degradation of triclocarban and its non-chlorinated congener

Journal of Hazardous Materials

Volumn 183, Issue 1-3, 2010, Pages 766-772

  Miller, Todd R ^a   Colquhoun, David R ^a   Halden, Rolf U ^a,b  

^a The Johns Hopkins University   (United States)

^b ARIZONA STATE UNIVERSITY   (United States)

Author keywords

Alcaligenes; Antimicrobial; Carbanilide; Phenylurea herbicide; Triclocarban; Wastewater bacteria

Indexed keywords

ALCALIGENES; ANTIMICROBIAL; CARBANILIDE; PHENYLUREA HERBICIDES; TRICLOCARBAN;

ADDITIVES; BACTERIOLOGY; BIOLOGY; BIOREMEDIATION; ELECTROPHORESIS; GELS; GENES; HERBICIDES; MICROORGANISMS; RNA; WASTEWATER; WEED CONTROL;

WASTEWATER TREATMENT;

BACTERIAL RNA; CARBANILIDE; RNA 16S; TRICLOCARBAN;

ACTIVATED SLUDGE; ANTIMICROBIAL ACTIVITY; BACTERIUM; BIOREMEDIATION; DEGRADATION; ELECTROKINESIS; GENOTYPE; HERBICIDE; POLLUTANT REMOVAL; RNA; WASTEWATER; WATER TREATMENT;

ACTIVATED SLUDGE; ALCALIGENACEAE; ALPHAPROTEOBACTERIA; ARTICLE; BACTERIAL GROWTH; BACTERIUM IDENTIFICATION; CARBON SOURCE; CHLORINATION; DENATURING GRADIENT GEL ELECTROPHORESIS; DRUG DEGRADATION; ENRICHMENT CULTURE; GENE SEQUENCE; GENOTYPE; INOCULATION; MARINE BACTERIUM; MOLECULAR CLONING; NONHUMAN; NUCLEOTIDE SEQUENCE; PHYLOGENY; WASTE WATER;

ALCALIGENACEAE; ANTI-INFECTIVE AGENTS, LOCAL; BIODEGRADATION, ENVIRONMENTAL; CARBANILIDES; INDUSTRIAL WASTE; RNA, RIBOSOMAL, 16S; WATER MICROBIOLOGY; WATER POLLUTANTS, CHEMICAL;

ALCALIGENACEAE; ALCALIGENES; ALPHAPROTEOBACTERIA;

EID: 77956434302     PISSN: 03043894     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jhazmat.2010.07.092     Document Type: Article

References (43)

1. Heidler J., Sapkota A., Halden R.U. Partitioning, persistence, and accumulation in digested sludge of the topical antiseptic triclocarban during wastewater treatment. Environ. Sci. Technol. 2006, 40:3634-3639.
2. Halden R.U., Paull D.H. Analysis of triclocarban in aquatic samples by liquid chromatography electrospray ionization mass spectrometry. Environ. Sci. Technol. 2004, 38:4849-4855.
3. Heidler J., Halden R.U. Meta-analysis of mass balances examining chemical fate during wastewater treatment. Environ. Sci. Technol. 2008, 42:6324-6332.
4. Miller T.R., Heidler J., Chillrud S., Delaquil A., Ritchie J.C., Mihalic J.N., Bopp R., Halden R.U. Fate of triclosan and evidence for reductive dechlorination of triclocarban in estuarine sediments. Environ. Sci. Technol. 2008, 42:4570-4576.
5. Coogan M.A., Edziyie R.E., La Point T.W., Venables B.J. Algal bioaccumulation of triclocarban, triclosan, and methyl-triclosan in a North Texas wastewater treatment plant receiving stream. Chemosphere 2007, 67:1911-1918.
6. Gledhill W.E. Biodegradation of 3,4,4′-trichlorocarbanilide, TCC, in sewage and activated-sludge. Water Res. 1975, 9:649-654.
7. Ying G.-G., Yu X.-Y., Kookana R.S. Biological degradation of triclocarban and triclosan in a soil under aerobic and anaerobic conditions and comparison with environmental fate modelling. Environ. Pollut. 2007, 150:300-305.
8. Sorensen S.R., Arbeli Z., Aamand J., Ronen Z. Metabolism of diphenylurea by a Marinobacter sp. isolated from a contaminated ephemeral stream bed in the Negev Desert. FEMS Microbiol. Lett. 2002, 213:199-204.
9. Dejonghe W., Berteloot E., Goris J., Boon N., Crul K., Maertens S., Hofte M., De Vos P., Verstraete W., Top E.M. Synergistic degradation of linuron by a bacterial consortium and isolation of a single linuron-degrading Variovorax strain. Appl. Environ. Microbiol. 2003, 69:1532-1541.
10. Surovtseva E.G., Vasil'eva G.K., Ivoilov V.S., Karasevich Y.N. Chlorinated anilines as sources of carbon, nitrogen, and energy for Pseudomonas diminuta. Mikrobiologiya 1992, 54:948-952.
11. Surovtseva E.G., Sukhikh A.P., Ivoilov V.S. Isozymes of the pathway for aniline and 4-chloroaniline preparatory metabolism in Alcaligenes sp. Microbiology 1992, 61:99-106.
12. Travkin V.M., Golovleva L.A. The degradation of 3,4-dichloroaniline by Pseudomonas fluorescens strain 26-K. Microbiology 2003, 72:240-243.
13. Keener W.K., Arp D.J. Transformations of aromatic compounds by Nitrosomonas europaea. Appl. Environ. Microbiol. 1994, 60:1914-1920.
14. Heidler J., Halden R.U. Fate of organohalogens in US wastewater treatment plants and estimated chemical releases to soils nationwide from biosolids recycling. J. Environ. Monit. 2009, 11:2207-2215.
15. Sambrook J., Fritsch E.F., Maniatis T. Molecular Cloning: A Laboratory Manual 1989, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY. second ed.
16. Ausubel F.M. Current Protocols in Molecular Biology 2001, J. Wiley, New York.
17. Dong W., Xie G., Miller T.R., Franklin M.P., Oxenberg T.P., Bouwer E.J., Ball W.P., Halden R.U. Sorption and bioreduction of hexavalent uranium at a military facility by the Chesapeake Bay. Environ. Pollut. 2006, 142:132-142.
18. Ewing B., Hillier L., Wendl M.C., Green P. Base-calling of automated sequencer traces using phred. I. Accuracy assessment. Genome Res. 1998, 8:175-185.
19. Huber T., Faulkner G., Hugenholtz P. Bellerophon; a program to detect chimeric sequences in multiple sequence alignments. Bioinformatics 2004, 20:2317-2319.
20. Maidak B.L., Olsen G.J., Larsen N., Overbeek R., McCaughey M.J., Woese C.R. The RDP (Ribosomal Database Project). Nucl. Acids Res. 1997, 25:109-110.
21. Altschul S., Gish W., Miller W., Myers E., Lipman D. Basic local alignment search tool. J. Mol. Biol. 1990, 215:403-410.
22. Ludwig W., Strunk O., Westram R., Richter L., Meier H., Yadhukumar A., Buchner T., Lai S., Steppi G., Jobb W., Forster I., Brettske S., Gerber A.W., Ginhart O., Gross S., Grumann S., Hermann R., Jost A., Konig T., Liss R., Lussmann M., May B., Nonhoff B., Reichel R., Strehlow A., Stamatakis N., Stuckmann A., Vilbig M., Lenke T., Ludwig A., Bode K.H., Schleifer ARB: a software environment for sequence data. Nucl. Acids Res. 2004, 32:1363-1371.
23. Pruesse E., Quast C., Knittel K., Fuchs B.M., Ludwig W.G., Peplies J., Glockner F.O. SILVA: a comprehensive online resource for quality checked and aligned ribosomal RNA sequence data compatible with ARB. Nucl. Acids Res. 2007, 35:7188-7196.
24. Retief J.D. Phylogenetic analysis using PHYLIP. Methods Mol. Biol. 2000, 132:243-258.
25. Jukes T.H., Cantor C.R. Evolution of protein molecules. Mammalian Protein Metabolism 1969, 21-132. Academic Press, New York, N.Y. H.N. Munro (Ed.).
26. Stamatakis A., Hoover P., Rougemont J. A rapid bootstrap algorithm for the RAxML web servers. Syst. Biol. 2008, 57:758-771.
27. Swofford D.L. PAUP*. Version 4. Phylogenetic Analysis Using Parsimony (*and Other Methods) 2003, Sinauer Associates, Sunderland, Massachusetts.
28. Ronquist F., Huelsenbeck J.P. MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics 2003, 19:1572-1574.
29. Watanabe K., Teramoto M., Harayama S. An outbreak of nonflocculating catabolic populations caused the breakdown of a phenol-digesting activated-sludge process. Appl. Environ. Microbiol. 1999, 65:2813-2819.
30. Krieger B.U., Schwermer C., Rezakhani N., Horn M.A., Gieseke A., Cytryn E., Minz D., Rijn J.V., Drake H.L., Schramm A. Diversity of nitrate-reducing and denitrifying bacteria in a marine aquaculture biofilter and their response to sulfide. 11th International Symposium on Microbial Ecology, International Society for Microbial Ecology 2006.
31. Friedrich U., Prior K., Altendorf K., Lipski A. High bacterial diversity of a waste gas-degrading community in an industrial biofilter as shown by a 16S rDNA clone library. Environ. Microbiol. 2002, 4:721-734.
32. Vandamme P., Segers P., Ryll3 M., Hommez J., Vancanneyt M., Coopman R., Baere R.D., Peer Y.V.D., Kersters K., Wachter R.D., Hinz K.H. Pelistega europaea gen. nov., sp. nov., a bacterium associated with respiratory disease in pigeons: taxonomic structure and phylogenetic allocation. Int. J. Syst. Evol. Microbiol. 1998, 48:431-440.
33. Stolz A., Burger S., Kuhm A., Kampfer P., Busse H.J. Pusillimonas noertemannii gen. nov., sp. nov., a new member of the family Alcaligenaceae that degrades substituted salicylates. Int. J. Syst. Evol. Microbiol. 2005, 55:1077-1081.
34. Coenye T., Henry D., Speert D.P., Vandamme P. Burkholderia phenoliruptrix sp. nov., to accommodate the 2,4,5-trichlorophenoxyacetic acid and halophenol-degrading strain AC1100. Syst. Appl. Microbiol. 2004, 27:623-627.
35. Willems A., Gilhaus H., Beer W., Mietke H., Gelderblom H.R., Burghardt B., Voigt W., Reissbrodt R. Brackiella oedipodis gen. nov., sp. nov., gram-negative, oxidase-positive rods that cause endocarditis of cotton-topped tamarin (Saguinus oedipus). Int. J. Syst. Evol. Microbiol. 2002, 52:179-186.
36. Snyder E.H., O'Connor G.A., McAvoy D.C. Fate of (14)C-triclocarban in biosolids-amended soils. Sci. Total Environ. 2010.
37. Zeyer J., Kearney P.C. Microbial-degradation of para-chloroaniline as sole carbon and nitrogen source. Pestic. Biochem. Physiol. 1982, 17:215-223.
38. Zeyer J., Wasserfallen A., Timmis K.N. Microbial mineralization of ring-substituted anilines through an ortho-cleavage pathway. Appl. Environ. Microbiol. 1985, 50:447-453.
39. Loidl M., Hinteregger C., Ditzelmuller G., Ferschl A., Streichsbier F. Degradation of aniline and monochlorinated anilines by soil-born Pseudomonas-acidovorans strains. Arch. Microbiol. 1990, 155:56-61.
40. Radianingtyas H., Robinson G.K., Bull A.T. Characterization of a soil-derived bacterial consortium degrading 4-chloroaniline. Microbiology 2003, 149:3279-3287.
41. Travkin V.M., Solyanikova I.P., Rietjens I.M.C.M., Vervoort J., van Berkel W.J.H., Golovleva L.A. Degradation of 3,4-dichloro- and 3,4-difluoroaniline by Pseudomonas fluorescens 26-K. J. Environ. Sci. Health. Part B Pestic. Food Contam. Agric. Wastes 2003, 38:121-132.
42. Balajee S., Mahadevan A. Utilization of aromatic substances by Azotobacter chroococcum. Res. Microbiol. 1990, 141:577-584.
43. Noh S.J., Kim Y., Min K.H., Karegoudar T.B., Kim C.K. Cloning and nucleotide sequence analysis of xylE gene responsible for meta-cleavage of 4-chlorocatechol from Pseudomonas sp. S-47. Mol. Cell. 2000, 10:475-479.