Characterization and Identification of Phenol Degrading Bacteria Isolated from Industrial Waste Water in Oran (Algeria)

Authors

  • Maghnia D. Laboratory for Experimental Biotoxicology of Biodepollution and Phytoremediation, Department of Biology, Faculty of Science University of Oran Ahmed Ben Bella 1, Algeria
  • Bensoltane A. Laboratory for Experimental Biotoxicology of Biodepollution and Phytoremediation, Department of Biology, Faculty of Science University of Oran Ahmed Ben Bella 1, Algeria
  • Belarbi F. Laboratory for Experimental Biotoxicology of Biodepollution and Phytoremediation, Department of Biology, Faculty of Science University of Oran Ahmed Ben Bella 1, Algeria
  • Medouakh L. Laboratory for Experimental Biotoxicology of Biodepollution and Phytoremediation, Department of Biology, Faculty of Science University of Oran Ahmed Ben Bella 1, Algeria

DOI:

https://doi.org/10.38150/sajeb.10(2).p70-76

Abstract

Phenol is the major organic pollutant present in industrial waste water. Phe-nol biodegradation is the most efficient and cost-effective pollutants degra-dation technologies, it can also ensure a completely degradation of phenol on non toxic products .In this research our objective is to isolate a new bac-terial strains with the ability of degrading phenol at high concentrations. Four phenol-degrading bacterium strain were successfully isolated from the effluent of industrial wastewater collected from Telamine Lake in the indus-trial area in Oran. Based on their morphological, physiological and biochemi-cal characteristics, all the strains were characterized as a Gram-negative, strictly aerobic, no motile and short rod-shaped bacterium that utilize phe-nol as a sole carbon and energy source. 16S rRNA sequence analysis revealed that these strains ENP, ENP2, ENP3 and ENP4 were affiliated to Pseudomo-nas putida, Pseudomonas sp, Raoultella ornithinolytica and Klebisella Sp re-spectively in the group of Gammaproteo bacteria. All the strains were effi-cient in removing 99% of the initial 750 mg/L of phenol within 72 h and had a tolerance of phenol concentration as high as 1000 mg/L of phenol. Analysis of the gene of the largest subunit of the multi-component phenol hydrox-ylase (LmPH) in each isolate showed the presence of this one in all isolate and only the strains ENP1 and ENP2 had the Catechol 2,3-dioxygenases gene (C230). These results indicated that the strains ENP1, ENP2, ENP3 and ENP4 can be exploited for bioremediation of phenol. 

Author Biographies

Maghnia D., Laboratory for Experimental Biotoxicology of Biodepollution and Phytoremediation, Department of Biology, Faculty of Science University of Oran Ahmed Ben Bella 1, Algeria

Laboratory for Experimental Biotoxicology of Biodepollution and Phytoremediation, Department of Biology, Faculty of Science University of Oran Ahmed Ben Bella 1, Algeria 

Bensoltane A., Laboratory for Experimental Biotoxicology of Biodepollution and Phytoremediation, Department of Biology, Faculty of Science University of Oran Ahmed Ben Bella 1, Algeria

Laboratory for Experimental Biotoxicology of Biodepollution and Phytoremediation, Department of Biology, Faculty of Science University of Oran Ahmed Ben Bella 1, Algeria 

Belarbi F., Laboratory for Experimental Biotoxicology of Biodepollution and Phytoremediation, Department of Biology, Faculty of Science University of Oran Ahmed Ben Bella 1, Algeria

Laboratory for Experimental Biotoxicology of Biodepollution and Phytoremediation, Department of Biology, Faculty of Science University of Oran Ahmed Ben Bella 1, Algeria 

Medouakh L., Laboratory for Experimental Biotoxicology of Biodepollution and Phytoremediation, Department of Biology, Faculty of Science University of Oran Ahmed Ben Bella 1, Algeria

Laboratory for Experimental Biotoxicology of Biodepollution and Phytoremediation, Department of Biology, Faculty of Science University of Oran Ahmed Ben Bella 1, Algeria 

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Published

2020-04-19

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Research Articles