Efficient phenol degradation by a newly characterized Pseudomonas sp. SA01 isolated from pharmaceutical wastewaters

Desalination

Volumn 246, Issue 1-3, 2009, Pages 577-594

  Shourian, Mitra ^a   Noghabi, Kambiz Akbari ^a   Zahiri, Hossein Shahbani ^a   Bagheri, Tayebe ^a   Karballaei, Gholamreza ^a   Mollaei, Monir ^a   Rad, Iman ^a   Ahadi, Solmaz ^a   Raheb, Jamshid ^a   Abbasi, Habib ^a  

^a NATIONAL INSTITUTE OF GENETIC ENGINEERING AND BIOTECHNOLOGY   (Iran)

Author keywords

Catechol; Catechol 2,3 dioxygenase; Degradation; Meta pathway; Phenol; Pseudomonas sp. SA01

Indexed keywords

16S RRNA SEQUENCES; BACTERIAL GROWTH; BACTERIAL STRAINS; BIOCHEMICAL CHARACTERISTICS; CARBON AND NITROGEN; CATECHOL; CATECHOL 2,3-DIOXYGENASE; INHIBITORY EFFECT; ISOLATED STRAINS; LAG PHASE; META-CLEAVAGE PATHWAY; META-PATHWAY; PH VALUE; PHARMACEUTICAL WASTEWATER; PHENOL CONCENTRATION; PHENOL DECOMPOSITION; PHENOL DEGRADATION; PHENOL REMOVAL; PHENOL-DEGRADING BACTERIA; PSEUDOMONAS SP; PSEUDOMONAS SP. SA01; SOLE CARBON SOURCE;

BACTERIOLOGY; DEGRADATION; NITROGEN REMOVAL; PHENOLS; PHOTODEGRADATION; STRAIN; WASTEWATER; WASTEWATER DISPOSAL; WASTEWATER TREATMENT;

BIODEGRADATION;

BIOCHEMISTRY; CONCENTRATION (COMPOSITION); EFFICIENCY MEASUREMENT; INDUSTRIAL WASTE; INHIBITOR; METABOLISM; MICROBIAL ACTIVITY; PH; PHARMACEUTICAL INDUSTRY; PHENOL; RNA; WASTEWATER;

BACTERIA (MICROORGANISMS); PSEUDOMONAS; PSEUDOMONAS SP.;

EID: 68449103787     PISSN: 00119164     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.desal.2008.07.015     Document Type: Article

References (56)

1. Saha N.C., Bhunia F., and Kaviraj A. Toxicity of phenol to fish and aquatic ecosystems. Bull. Environ. Contam. Toxicol. 63 (1999) 195
2. Ahn S., Congeevaram S., Choung Y.K., and Park J. Enhanced phenol removal by floating fungal populations in a high concentration phenol-fed membrane bioreactor. Desalination 221 (2008) 494
3. Aksu S., and Yener J. Investigation of biosorption of phenol and monochlorianated phenols on the dried activated sludge. Process Biochem. 33 (1998) 649
4. Manojlovic D., Ostojic D.R., Obradovic B.M., Kuraica M.M., Krsmanovic V.D., and Puric J. Removal of phenol and chlorophenols from water. Desalination 213 (2007) 116
5. Vione D., Minero C., Maurino V., Carlotti M.E., Picatonotto T., and Pelizzetti E. Degradation of phenol and benzoic acid in the presence of a TiO2- based heterogeneous photocatalyst. Appl. Catalysis B: Environ. 58 (2005) 79
6. Zumriye A., Derya A., Elif R., and Burcin K. Simultaneous biosorption of phenol and nickel from binary mixtures onto dried aerobic activated sludge. Process Biochem. 35 (1999) 301
7. Allsop P.J., Chisti Y., Moo-Young M., and Sullivan G.R. Dynamics of phenol degradation by Pseudomonas putida. Biotechnol. Bioeng. 41 (1993) 572
8. Wang S.J., and Loh K.C. Modeling the role of metabolic intermediates in kinetics of phenol biodegradation. Enzyme Microbial. Technol. 25 (1999) 177
9. Bouchez M., Blanchet D., and Vandecasteele J.P. Degradation of polycyclic aromatic hydrocarbons by pure strains and by defined strain associations: Inhibition phenomena and cometabolism. Appl. Microbiol. Biotechnol. 43 (1995) 156
10. Yuan S.Y., Wei S.H., and Chang B.V. Biodegradation of polycyclic aromatic hydrocarbons by a mixed culture. Chemosphere 41 (2000) 1463
11. Sá C.S.A., and Boaventura R.A.R. Biodegradation of phenol by Pseudomonas putida DSM 548 in a trickling bed reactor. Biochem. Eng. J. 9 (2001) 211
12. Leitao A.L., Duarte M.P., and Santos Oliveira J. Degradation of phenol by a halotolerant strain of Penicillium chrysogenum. Int. Biodeterioration Biodegradation 59 (2007) 220
13. Stoilova I.A., Krastanov Stanchev V., Daniel D., Gerginova M., and Alexieva Z. Biodegradation of high amounts of phenol, catechol, 2,4-dichlorophenol and 2,6-dimethoxyphenol by Aspergillus awamori cells. Enzyme Microbial. Technol. 39 (2006) 1036
14. Fialová A., Boschke E., and Bley T. Rapid monitoring of the biodegradation of phenol-like compounds by the yeast Candida maltosa using BOD measurements. Int. Biodeterioration & Biodegradation 54 (2004) 69
15. Monteiro Á.A.M.G., Boaventura R.A.R., and Rodrigues A.E. Phenol biodegradation by Pseudomonas putida DSM 548 in a batch reactor. Biochem. Eng. J. 6 (2000) 45
16. Aleksieva Z., Ivanova D., Godjevargova T., and Atanasov B. Degradation of some phenol derivatives by Trichosporon cutaneum R57. Process Biochem. 37 (2002) 1215
17. Chen K.C., Lin Y.H., Chen W.H., and Liu Y.C. Degradation of phenol by PPA-immobilized Candida tropicalis. Enzyme Microbial. Technol. 31 (2002) 490
18. Karigar C., Mahesh A., Nagenahalli M., and Yun D.J. Phenol degradation by immobilized cells of Arthrobacter citreus. Biodegradation 17 (2006) 47
19. Godjevargova T., Aleksieva Z., and Ivanova D. Cell immobilization of Trichosporon cutaneum strain with phenol degradation ability on new modified polymer carriers. Process Biochem. 35 (2000) 699
20. Fava F., Di Gioia D., and Marchetti L. Dichlorobiphenyl degradation by an uncharacterized Pseudomonas species, strain CPE1, in a fixed film bioreactor. Int. Biodeterioration Biodegradation 37 (1996) 53
21. Gibson J., and Harwood C.S. Metabolic diversity in aromatic compound utilization by anaerobic microbes. Ann. Rev. Microbiol. 56 (2002) 345
22. Caplan J.S. The worldwide bioremediation industry: prospects for profit. Trends Biotechnol. 11 (1993) 320
23. Polymenakou P.N., and Stephanou E.G. Effect of temperature and additional carbon sources on phenol degradation by an indigenous soil Pseudomonad. Biodegradation 16 (2005) 403
24. Loh K.C., and Tar P.P. Effect of additional carbon sources on biodegradation of phenol. Bull. Environ. Contam. Toxicol. 64 (2000) 756
25. Loh K.C., and Wang S.J. Enhancement of biodegradation of phenol and a nongrowth substrate 4-chlorophenol by medium augmentation with conventional carbon sources. Biodegradation 8 (1998) 329
26. Topp E., Crawford R.L., and Hanson R.S. Influence of readily metabolisable carbon on pentachlorophenol-degrading Flavobacterium sp. Appl. Environ. Microbiol. 54 (1988) 2452
27. Alva V.A., and Peyton B.M. Phenol and catechol biodegradation by the haloalkaliphile Halomonas campisalis: influence of pH and salinity. Environ. Sci. Technol. 37 (2003) 4397
28. Leung K.T., Moore M., Lee H., and Trevors J.T. Effect of carbon starvation on p-nitophenol degradation by a Moraxella strain in buffer and river water. FEMS Microbial Ecol. 51 (2005) 237
29. Folsom B.R., Chapman P.J., and Pritchard P.H. Phenol and trichloroethylene degradation by Pseudomonas cepacia G4: kinetics and interactions between substrates. Appl. Environ. Microbiol. 56 (1990) 1279
30. Chakravorty S., Danica H., Burday M., Connell N., and Alland D. A detailed analysis of 16S ribosomal RNA gene segments for the diagnosis of pathogenic bacteria. J. Microbiol. Methods 69 (2007) 330
31. Altschul S.F., Gish W., Mille W., Myer E.W., and Lipman D.J. Basic local alignment search tool. J. Mol. Biol. 219 (1990) 403
32. Tamura K., Dudley J., Nei M., and Kumar S. MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) Software Version 4.0. Mol. Biol. Evol. 24 (2007) 1596
33. Yang R.D., and Humphrey A.E. Dynamic and steady state studies of phenol. biodegradation in pure and mixed cultures. Biotechnol. Bioeng. 17 (1975) 1211
34. Feist C.F., and Hegeman G.D. Phenol and benzoate metabolism by Pseudomonas putida: regulation of tangential pathways. J. Bacteriol. 100 (1969) 869
35. Hegeman G.D. Synthesis of the enzymes of the mandelate pathway by Pseudomonas putida. Isolation and properties of constitutive mutants. J. Bacteriol. 91 (1966) 1161
36. Hilario E., Buckley T.R., and Young J.M. Improved resolution on the phylogenetic relationships among Pseudomonas by the combined analysis of atpD, carA, recA and 16S rDNA. Antonie van Leeuwenhoek 86 (2004) 51
37. E.D. Weinberg, V. Krumphanjyl, B. Sikyta and Z. Vanek, Overproduction of Microbial Production, Academic Press, New York, 1982, p. 181.
38. M. Nozaki, S. Kotani, K. Ono and S. Senoh, Metapyrocatechase III. Substrate specificity and mode of ring fission, Biochemica Biophysica Acta, 220 (1970) 213.
39. Mason J.R., and Cammack R. The electron-transport proteins of hydroxylating bacterial dioxygenases. Ann. Rev. Microbiol. 46 (1992) 277
40. Powlowski J., and Shingler V. In vitro analysis of polypeptide requirements of multicomponent phenol hydroxylase from Pseudomonas sp. strain CF600. J. Bacteriol. 172 (1990) 6834
41. Ampe F., Leonard D., and Lindley N.D. Repression of phenol catabolism by organic acids in Ralstonia eutropha. Appl. Environ. Microbiol. 64 (1998) 1
42. Papanastasiou A.C. Kinetics of biodegradation of 2, 4-dichlorophenoxyacetate in the presence of glucose. Biotechnol. Bioeng. 24 (1982) 2001
43. Leven L., and Schnurer A. Effect of temperature on biological degradation of phenols, benzoate and phthalates under methanogenic conditions. Int. Biodeterioration Biodegradation 55 (2005) 153
44. Margesin R., Bergauer P., and Gander S. Degradation of phenol and toxicity of phenolic compounds: a comparison of cold-tolerant Arthrobacter sp. and mesophilic Pseudomonas putida. Extremophiles 8 (2004) 201
45. Armenante P.M., Fava F., and Kafkewitz D. Effect of yeast extract on growth kinetics during aerobic biodegradation of chlorobenzoic acids. Biotechnol. Bioeng. 47 (1995) 227
46. Harayama S., Kok M., and Neidle E.L. Functional and evolutionary relationships among diverse oxygenases. Ann. Rev. Microbiol. 46 (1992) 565
47. Garcia-Valdes E., Cozar E., Rotger R., Lalucat J., and Ursing J. New naphthalene-degrading marine Pseudomonas strains. Appl. Environ. Microbiol. 54 (1988) 2478
48. Ji G., and Silver S. Bacterial resistance for heavy metal of environmental concern. J. Ind. Microbiol. 14 (1995) 61
49. Van der Meer J.R., de Vos W.M., Harayama S., and Zehnder A.J.B. Molecular mechanisms of genetic adaptation to xenobiotic compounds. Microbiol. Rev. 56 (1992) 677
50. Assinder S.J., and Williams P.A. Comparison of the meta pathway operons on NAH plasmid pWW60-22 and TOL plasmid pWW53-4 and its evolutionary significance. J. General Microbiol. 134 (1988) 2769
51. Harayama S., and Rekik M. Bacterial aromatic ring cleavage enzymes are classified into two different gene families. J. Biol. Chem. 264 (1989) 15328
52. Nakai C., Kagamiyama H., Nozaki M., Nakazawa T., Inouye S., Ebina Y., and Nakazawa A. Complete nucleotide sequence of the metapyrocatechase gene on the TOL plasmid of Pseudomonas putida mt-2. J. Biol. Chem. 258 (1983) 2923
53. Williams P.A., and Murray K. Metabolism of benzoate and the methylbenzoates by Pseudomonas putida (arvilla) mt-2: evidence for the existence of a TOL plasmid. J. Bacteriol. 125 (1974) 416
54. Heesche-Wagner K., Schwarz T., and Kaufmann M. Phenol degradation by an enterobacterium: a Klebsiella strain carries a TOL-like plasmid and a gene encoding a novel phenol hydroxylase. Can. J. Microbiol. 45 (1999) 162
55. Dua M., Singh A., Sethunathan N., and Johri A.K. Biotechnology and bioremediation: successes and limitations. Appl. Microbiol. Biotechnol. 59 (2002) 143
56. K. Suzuki, N. Ogawa and K. Miyashita, Expression of 2-halobenzoate dioxygenase genes (cbdSABC) involved in the degradation of benzoate and 2-halobenzoate in Burkholderia sp. TH2, Gene 262 (2001) 137.