Isolation, Screening and Characterization of Hyaluronidase Producing Bacteria

Authors

  • Anindita Nayak Department of Microbiology, Orissa University of Agriculture and Technology, Bhubaneswar751 003, Orissa, India
  • Poluri Ellaiah Pharmaceutical Biotechnology Division, College of Pharmaceutical Sciences, Andhra University, Visakhapatnam-530 003, A.P., India
  • Prasana Kumar Panda University Department of Pharmaceutical Sciences, Utkal University, Bhubaneswar 751004. Orissa, India
  • Sabuj Sahoo University Department of Pharmaceutical Sciences, Utkal University, Bhubaneswar 751004. Orissa, India
  • Sashi Kanta Dash Department of Microbiology, Orissa University of Agriculture and Technology, Bhubaneswar- 751 003, Orissa, India
  • Sashi Kanta Patel University Department of Pharmaceutical Sciences, Utkal University, Bhubaneswar 751004. Orissa, India
  • Satyaranjan Mishra University Department of Pharmaceutical Sciences, Utkal University, Bhubaneswar 751004. Orissa, India
Abstract:

      Hyaluronidase has a panoramic use in biotechnology processes and therapy due to its therapeutic, pathophysiological, physiological and biological importance. Since much of the preparations of hyaluronidases are from animal source (bovine and ovine testicular sources) with limited sources of microbial origin, that prompted the authors to screen and isolate a new promising bacterial strain with higher yield followed by its characterization employing detailed taxonomic studies. The newly isolated strain was identified based upon their micro- and macro-morphological, cultural, physiological and biochemical parameters. Twenty isolates from different pathological samples were primarily selected and further screened for their hyaluronidase producing capabilities by measuring reduction in turbidity and hydrolyzed zone of substrate hyaluronic acid. Four isolates showing marked reduction in turbidity (A600 nm) and hydrolyzed zones were selected and subjected to secondary screening by shake flask fermentation. Isolate SII9 (Dental caries specimen) exhibited maximum hyaluronidase activity (117 U/ml) when compared to the reference Streptococcus mitis MTCC*2695 (106 U/ml). A close scrutiny of the literature revealed that the characteristics of our isolate SII9 are mostly identical to S. equi subsp. equisimilis with few differences and thus designated as S. equi SED 9.

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Journal title

volume 5  issue 2

pages  95- 102

publication date 2009-04-01

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