Extraction and Purification of Pseudomonas aeruginosa Lipopolysaccharide Isolated from Wound Infection

Authors

  • Israa M. Subhi Department of Biology, College of Science, University of Baghdad, Baghdad, Iraq. Author
    • ayaid K. Zgair Department of Biology, College of Science, University of Baghdad, Baghdad, Iraq. Author
      • Jenan A. Ghafil Department of Biology, College of Science, University of Baghdad, Baghdad, Iraq. Author

        Keywords:

        Gel filtration chromatography, hotEDTA, Lipopolysaccharide, Pseudomonas aeruginosa, Sephadex G-200, VITEK 2 system.

        Abstract

        Samples were obtained from patients suffering from burns and wounds and then identified using the biochemical tests and the VITEK 2 fluorescent system. The tests confirmed the presence of Pseudomonas aeruginosa. Antibiotic susceptibility testing showed that the isolate was sensitive to piperacillin, ceftazidime, cefepime, imipenem, meropenem, amikacin, gentamicin, tobramycin, ciprofloxacin and levofloxacin while resistant to ampicillin, cefazolin, ceftriaxone, tigecycline and trimethoprim/sulfamethoxazole. The lipopolysaccharide (LPS) was extracted by the hotEDTA method and partially purified by gel filtration chromatography using the Sephadex G-200.

         

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        Published

        2017-01-12

        Issue

        Section

        Research article

        How to Cite

        [1]
        Israa M. Subhi et al. trans. 2017. Extraction and Purification of Pseudomonas aeruginosa Lipopolysaccharide Isolated from Wound Infection. World Journal of Experimental Biosciences. 5, 1 (Jan. 2017), 5–8.

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