Remazol blue removal and EPS production by Pseudomonas aeruginosa and Ochrobactrum sp.

• Autorzy: Kilic N.K. , Donmez G.
• Języki publikacji: EN

Abstrakty

EN

Pseudomonas aeruginosa and Ochrobactrum sp. were tested according to EPS production at different pH, temperatures, Remazol Blue concentrations, and incubation periods. Optimum pH was 7 for P. aeruginosa and 8 for Ochrobactrum sp. according to the highest EPS amount. P. aeruginosa produced the highest EPS (456.4 mg·l⁻¹) after incubation for 48 h (40ºC) and Ochrobactrum sp. gave the highest yield (404.6 mg·l⁻¹) after incubation for 72 h (30ºC). P. aeruginosa had a low capacity to remove Remazol Blue (12.5%); however, Ochrobactrum sp. had a significant potential to remove Remazol Blue yielded as 89.4%.

• Wydawca: -
• Czasopismo: Polish Journal of Environmental Studies
• Rocznik: 2012
• Tom: 21
• Numer: 1
• Opis fizyczny: p.123-128,fig.,ref.

Twórcy

autor

Kilic N.K.

• Department of Biology, Faculty of Science, Ankara University, 06100 Besevler, Ankara, Turkey

autor

Donmez G.

Bibliografia

• 1. SIRIANUNTAPIBOON S., SRISORNSAK P. Removal of disperse dyes from textile wastewater using bio-sludge. Biores. Technol. 98, 1057, 2007.
• 2. CLARKE E.A., ANLIKER R. Organic dyes and Pigments. In: Hand-book of environmental chemistry, anthropogenic compounds part A, Springer vol. 3. New York, pp. 181-215, 1980.
• 3. AKSU Z. Application of biosorption for the removal of organic pollutants: a review, Process Biochem. 40, 997, 2005.
• 4. ALLEGRE, C., MOULIN P., MAISSEU M., CHARBIT F. Treatment and reuse of reactive dyeing effluents. J. Memb. Sci. 269, 15, 2006.
• 5. CRINI G. Non-conventional low-cost adsorbents for dye removal: A review. Biores. Technol. 97, 1061, 2006.
• 6. NIGAM P., BANAT I.M., SINGH D., MARCHANT R. Microbial process for the decolorization of textile effluents containing azo, diazo and reactive dyes. Process Biochem. 31, 435, 1995.
• 7. DÖNMEZ G. Bioaccumulation of the reactive textile dyes by Candida tropicalis growing in molasses medium. Enzyme. Microbial. Technol. 30, 363, 2002.
• 8. KHEHRA M.S., SAINI H.S., SHARMA D.K., CHADHA B.S., CHIMNI S.S. Biodegradation of azo dye C.I. Acid Red 88 by an anoxic-aerobic sequential bioreactor. Dyes. Pigment. 70, 1, 2006.
• 9. SADETTİN S., DÖNMEZ G. Simultaneous bioaccumulation of reactive dye and chromium(VI) by using thermophil Phormidium sp. Enzyme Microbial. Technol. 41, 175, 2007.
• 10. KILIÇ N.K., NIELSEN J.L., YÜCE M., DÖNMEZ G. Characterization of a simple bacterial consortium for effective treatment of wastewaters with reactive dyes and Cr(VI), Chemosphere 67, 826, 2007.
• 11. CASAS N., BLANQUEZ P., GABARRAELL X., VICENT T., CAMINAL G., SARA M. Degradation of orange G by laccase: fungal versus enzymatic process. Environ. Technol. 28, 1103, 2007.
• 12. LODATO A., ALFIERI F., OLIVIERI G., DI DONATO A., MARZOCCHELLA A., SALATINO P. Azo-dye conversion by means of Pseudomonas sp. OX1. Enzyme. Microbial. Technol. 41, 646, 2007.
• 13. SHAH V., GARG N., MADAMWAR D. An integrated process of textile dye removal and hydrogen evolution using cyanobacterium, Phormidium valderianum. W.J. Microbial. Biotechnol. 17, 499, 1999.
• 14. CHEN, B. Understanding decolorization characteristics of reactive azo dyes by Pseudomonas luteola: toxicity and kinetics. Process Biochem. 38, 437, 2002.
• 15. ZHANG D., WANG J., PAN X. Cadmium sorption by EPSs produced by anaerobic sludge under sulfate-reducing conditions. J. Hazard. Mater. B138, 589, 2006.
• 16. HUGENHOLTZ J., LOOIJESTEIJIN E., STARRENBURG M., DIJKEMA C. Analysis of sugar metabolism in an EPS producing Lactococcus lactis by 31P NMR. J. Biotechnol. 77, 17, 2000.
• 17. CZACZYK K., MYSZKA K. Biosynthesis of Extracellular Polymeric Substances (EPS) and Its Role in Microbial Biofilm Formation. Pol. J. Environ. Stud. 16, (6), 799, 2007.
• 18. IYER A., MODY K., JHA B. Accumulation of hexavalent chromium by an exopolysaccharide producing marine Enterobacter cloaceae. Marine Poll. Bull. 49, 974, 2004.
• 19. OZDEMIR G., OZTURK T., CEYHAN N., ISLER R., COSAR T. Heavy metal biosorption by biomass of Ochrobactrum antropi producing exopolysaccharide in activated sludge. Biores. Technol. 90, 71, 2003.
• 20. WACKEROW-KOUZOVA N.D. Ochrobactrum intermedium ANKI, a nitrogen-fixing bacterium able to decolorize azobenzene. Appl. Biochem. Microbiol. 43, 403, 2007.
• 21. CÉRANTOLA S., BOUNÉRY J., SEGONDS C., MARTY N., MONTROZİE H. Exopolysaccharide production by mucoid and non-mucoid strains of Burkholderia cepacia. FEMS Microbiol. Lett. 185, 243, 2000.
• 22. DUBOIS M., GILLES K.A., HAMILTON J.K., REBERS P.A., SMITH F. Colorimetric method for determination of sugars and related substances. Anal. Chem. 28, 350, 1956.
• 23. KILIÇ N.K., DÖNMEZ G. Environmental conditions affecting exopolysaccharide production by Pseudomonas aeruginosa, Micrococcus sp., and Ochrobactrum sp. J. Hazard. Mater. 154, 1019, 2008.
• 24. KAZY S.K., SAR P., SINGH S.P., SEN A.K., D’SOUZA S.F. Extracellular polysaccharide of a copper-sensitive and a copper-resistant Pseudomonas aeruginosa strain: synthesis, chemical nature and copper binding. W. J. Microbial. Biotechnol. 18, 583, 2002.
• 25. VELASCO S., ÅRSKÖLD E., PAESE M., GRAGE H., IRASTORZA A., RĹDSTRÖM P., VAN NIEL E.W.J. Environmental factors influencing growth of and exopolysaccharide formation by Pedicoccus parvulus 2.6. Int. J. Food Microbiol. 111, 252, 2006.
• 26. LEE W.Y., PARK Y., AHN J.K., KA K.H., PARK S.Y. Factors influencing the production of endopolysaccharide and exopolysaccharide from Ganoderma applanatum. Enzyme. Microbial. Technol. 40, 249, 2007.
• 27. NANDAL K., SEHRAWAT A.R., YADAV A.S., VASHISHAT R.K., BOORA K.S. High temperatureinduced changes in exopolysaccharides, lipopolysaccharides and protein profile of heat-resistant mutants of Rhizobium sp. (Cajanus). Microbiol. Res., 160, 367, 2005.