• Title of article

    Purification and characterization of catalase from sprouted black gram (Vigna mungo) seeds

  • Author/Authors

    Kandukuri، نويسنده , , Sai Srikar and Noor، نويسنده , , Ayesha and Ranjini، نويسنده , , S. Shiva and Vijayalakshmi، نويسنده , , M.A.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2012
  • Pages
    5
  • From page
    50
  • To page
    54
  • Abstract
    Black gram (Vigna mungo) is a legume which belongs to Fabaceae family. It is a rich source of protein. It has been known to have interesting small molecule antioxidant activity. However, its enzymatic antioxidant properties have not been explored much. In the present work we studied catalase, a principal antioxidant enzyme from black gram seeds. Day four sprouted black gram seeds were found to have a significant catalase content approximately of 15,240 U/g seeds. IMAC (Seph 4B-IDA-Zn(II)) was used for purifying this catalase, a purification fold of 106 and a high specific activity of 25,704 U/mg was obtained. The Km and Vmax of the purified catalase were found to be 16.2 mM and 2.5 μmol/min. The effect of inhibitors like Sodium azide (NaN3) and EDTA and different metal ions on catalase activity were studied. NaN3, Fe3+and Cu2+ were found to have profound inhibitory effects on the enzyme activity. Other metal ions like Ni2+, Ca2+, Mg2+ and Mn2+ had both enhancing and inhibitory effects. The enzyme showed optimal activity at a temperature of 40 °C and pH 7.0. It was stable over a broad range of pH 6.0–10.0 and had a half life of 7 h 30 min at 50 °C.
  • Keywords
    IMAC , enzyme purification , Catalase
  • Journal title
    Journal of Chromatography B
  • Serial Year
    2012
  • Journal title
    Journal of Chromatography B
  • Record number

    1469737