The degradation of bisphenol A by the newly isolated bacterium Cupriavidus basilensis JF1 can be enhanced by biostimulation with phenol

International Biodeterioration and Biodegradation

Volumn 64, Issue 4, 2010, Pages 324-330

  Fischer, Janett ^a   Kappelmeyer, Uwe ^a   Kastner, Matthias ^a   Schauer, Frieder ^b   Heipieper, Hermann J ^a  

^a HELMHOLTZ CENTRE FOR ENVIRONMENTAL RESEARCH UFZ   (Germany)

^b UNIVERSITY OF GREIFSWALD   (Germany)

Author keywords

Bisphenol A; Continuous culture; Cupriavidus basilensis; Degradation pathway; Phenol

Indexed keywords

16S RRNA; AEROBIC BACTERIUM; ALIPHATIC COMPOUND; BIOSTIMULATION; BISPHENOL A; CELLULAR DEGRADATION; CONTINUOUS CULTURE; CUPRIAVIDUS BASILENSIS; DEGRADATION PATHWAYS; DEGRADATION RATE; ENERGY SOURCE; FIXED BED REACTOR; ISOPROPYLPHENOL; RALSTONIA; SAND COLUMNS; SHAKE CULTURES; SOLE CARBON; SOLE CARBON SOURCE; SPHINGOMONAS;

ACETONE; AGRICULTURE; CHEMICAL REACTORS; DEGRADATION; ETHANOL; METHANOL; PHENOLS; RNA;

BIODEGRADATION;

ACETONE; ALCOHOL; BACTERIUM; BIODEGRADATION; BIOREACTOR; GENETIC ANALYSIS; HYDROCARBON; METABOLISM; PHENOL; PHENOLIC COMPOUND; RNA;

BACTERIA (MICROORGANISMS); CUPRIAVIDUS; CUPRIAVIDUS BASILENSIS; NEGIBACTERIA; RALSTONIA; SPHINGOMONAS;

EID: 77954865862     PISSN: 09648305     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ibiod.2010.03.007     Document Type: Article

References (28)

1. Bligh E.G., Dyer W.J. A rapid method of total lipid extraction and purification. Can. J. Biochem. Physiol. 1959, 37:911-917.
2. Cousins I.T., Staples C.A., Klecka G.M., Mackay D. A multimedia assessment of the environmental fate of bisphenol A. Hum. Ecol. Risk Assess. 2002, 8:1107-1135.
3. El Fantroussi S., Agathos S.N. Is bioaugmentation a feasible strategy for pollutant removal and site remediation?. Curr. Opin. Microbiol. 2005, 8:268-275.
4. Hartmans S., Smits J.P., van der Werf M.J., Volkering F., de Bont J.A.M. Metabolism of styrene oxide and 2-phenylethanol in the styrene-degrading Xanthobacter strain 124X. Appl. Environ. Microbiol. 1989, 55:2850-2855.
5. Heipieper H.J., de Bont J.A.M. Adaptation of Pseudomonas putida S12 to ethanol and toluene at the level of the fatty acid composition of membranes. Appl. Environ. Microbiol. 1994, 60:4440-4444.
6. Heipieper H.J., Loffeld B., Keweloh H., de Bont J.A.M. The cis/trans isomerization of unsaturated fatty acids in Pseudomonas putida S12: an indicator for environmental stress due to organic compounds. Chemosphere 1995, 30:1041-1051.
7. Heipieper H.J., Neumann G., Cornelissen S., Meinhardt F. Solvent-tolerant bacteria for biotransformations in two-phase fermentation systems. Appl. Microbiol. Biotechnol. 2007, 74:961-973.
8. Heipieper H.J., Weber F.J., Sikkema J., Keweloh H., de Bont J.A.M. Mechanisms behind resistance of whole cells to toxic organic solvents. Trends Biotechnol. 1994, 12:409-415.
9. Hopper D.J., Cottrell L. Alkylphenol biotransformations catalyzed by 4-ethylphenol methylenehydroxylase. Appl. Environ. Microbiol. 2003, 69:3650-3652.
10. Ike M., Jin C.S., Fujita M. Biodegradation of bisphenol A in the aquatic environment. Water Sci. Technol. 2000, 42:31-38.
11. Kappelmeyer U., Wiessner A., Kuschk M., Kastner M. Planted fixed bed reactor (PFR) - a universal unit for planted bed filters. Chem. Ing. Tech. 2001, 73:1472-1477.
12. Kolvenbach B., Schlaich N., Raoui Z., Prell J., Zuhlke S., Schaffer A., et al. Degradation pathway of bisphenol A: does ipso substitution apply to phenols containing a quaternary alpha-carbon structure in the para position?. Appl. Environ. Microbiol. 2007, 73:4776-4784.
13. Lindholst C., Pedersen S.N., Bjerregaard P. Uptake, metabolism and excretion of bisphenol A in the rainbow trout (Oncorhynchus mykiss). Aquat. Toxicol. 2001, 55:75-84.
14. Lobos J.H., Leib T.K., Su T.M. Biodegradation of bisphenol A and other bisphenols by a gram-negative aerobic bacterium. Appl. Environ. Microbiol. 1992, 58:1823-1831.
15. Masuda M., Yamasaki Y., Ueno S., Inoue A. Isolation of bisphenol A-tolerant/degrading Pseudomonas monteilii strain N-502. Extremophiles 2007, 11:355-362.
16. Matsushima A., Kakuta Y., Teramoto T., Koshiba T., Liu X.H., Okada H., et al. Structural evidence for endocrine disruptor bisphenol A binding to human nuclear receptor ERR gamma. J. Biochem. 2007, 142:517-524.
17. Moonen M.J.H., Kamerbeek N.M., Westphal A.H., Boeren S.A., Janssen D.B., Fraaije M.W., van Berkel W.J.H. Elucidation of the 4-hydroxyacetophenone catabolic pathway in Pseudomonas fluorescens ACB. J. Bacteriol. 2008, 190:5190-5198.
18. Morrison W.R., Smith L.M. Preparation of fatty acid methyl esters and dimethylacetals from lipids with boron fluoride-methanol. J. Lipid Res. 1964, 5:600-608.
19. Owen W.F., Stuckey D.C., Healy J.B., Young L.Y., McCarty P.L. Bioassay for monitoring biochemical methane potential and anaerobic toxicity. Water Res. 1979, 13:485-492.
20. Ronen Z., Abeliovich A. Anaerobic-aerobic process for microbial degradation of tetrabromobisphenol A. Appl. Environ. Microbiol. 2000, 66:2372-2377.
21. Sasaki M., Akahira A., Oshiman K.I., Tsuchido T., Matsumura Y. Purification of cytochrome P450 and ferredoxin, involved in bisphenol A degradation, from Sphingomonas sp. strain AO1. Appl. Environ. Microbiol. 2005, 71:8024-8030.
22. Sasaki M., Maki J., Oshiman K., Matsumura Y., Tsuchido T. Biodegradation of bisphenol A by cells and cell lysate from Sphingomonas sp. strain AO1. Biodegradation 2005, 16:449-459.
23. Spivack J., Leib T.K., Lobos J.H. Novel pathway for bacterial metabolism of bisphenol A. Rearrangements and stilbene cleavage in bisphenol A metabolism. J. Biol. Chem. 1994, 269:7323-7329.
24. Staples C.A., Dorn P.B., Klecka G.M., O'Block S.T., Harris L.R. A review of the environmental fate, effects, and exposures of bisphenol A. Chemosphere 1998, 36:2149-2173.
25. Staples C.A., Woodburn K., Caspers N., Hall A.T., Klecka G.M. A weight of evidence approach to the aquatic hazard assessment of bisphenol A. Hum. Ecol. Risk Assess. 2002, 8:1083-1105.
26. Suzuki T., Nakagawa Y., Takano I., Yaguchi K., Yasuda K. Environmental fate of bisphenol A and its biological metabolites in river water and their xeno-estrogenic activity. Environ. Sci. Technol. 2004, 38:2389-2396.
27. Vandamme P., Coenye T. Taxonomy of the genus Cupriavidus: a tale of lost and found. Int. J. Syst. Evol. Microbiol. 2004, 54:2285-2289.
28. Vaneechoutte M., Kampfer P., De Baere T., Falsen E., Verschraegen G. Wautersia gen. nov., a novel genus accommodating the phylogenetic lineage including Ralstonia eutropha and related species, and proposal of Ralstonia [Pseudomonas] syzygii (Roberts et al. 1990) comb. nov. Int. J. Syst. Evol. Microbiol. 2004, 54:317-327.