• Title of article

    Purification of α-Amylase from Bacillus sp. GHA1 and Its Partial Characterization

  • Author/Authors

    A. Ahmadi ، نويسنده , , S. Ghobadi، نويسنده , , K. Khajeh، نويسنده , , B. Nomanpour and A. Badoei Dalfard، نويسنده ,

  • Issue Information
    ماهنامه با شماره پیاپی سال 2010
  • Pages
    9
  • From page
    432
  • To page
    440
  • Abstract
    Bacillus sp. GHA1 was isolated from water samples and screened for the production of α-amylase. Maximum production of amylase by this strain occurs at 42 ºC, pH 6.5 and 72 h after cultivation in production medium. The enzyme was purified through successive applications of ammonium sulfate precipitation, ion exchange and hydrophobic interaction chromatography, resulting in a single band with an apparent molecular weight of 66 kDa, as judged by SDS-PAGE. Calcium analysis of the purified enzyme revealed that it contained three metal ions per molecule. The new extracellular α-amylase is active in a wide range of pH with its maximum activity at pH values 5.5-8.0. The optimum temperature for enzyme activity is 57 ºC and the presence of calcium has relatively low influence on its activity and thermostability. The Bacillus sp. GHA1 α-amylase with these properties may be suitable for use in detergent and food industries
  • Keywords
    ?-amylase , Bacillus sp. GHA1 , pH profile , Broad range of pH , Industrial applications
  • Journal title
    Journal of the Iranian Chemical Society (JICS)
  • Serial Year
    2010
  • Journal title
    Journal of the Iranian Chemical Society (JICS)
  • Record number

    666947