• Title of article

    Candida rugosa lipase Lip1–polyethyleneglycol interaction and the relation with its partition in aqueous two-phase systems

  • Author/Authors

    Bassani، نويسنده , , Georgina and Fuciٌos، نويسنده , , Pablo and Picَ، نويسنده , , Guillermo and Farruggia، نويسنده , , Beatriz، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2010
  • Pages
    6
  • From page
    532
  • To page
    537
  • Abstract
    The interaction between a lipase from Candida rugosa (Lip1) and polyethyleneglycols of different molecular masses was studied using fluorescence and circular dichroism approaches in order to be applied to the analysis of the enzyme partition mechanism in aqueous two-phase systems of polyethyleneglycol–potassium phosphate. The decrease of the partition coefficients with the polyethyleneglycol molecular mass showed that the enzyme partition is driven by the excluded volume effect and not by the enzyme–polymer interaction. The polymer did not affect the secondary and tertiary structure of the enzyme nor its biological activity. The lipase from Candida rugosa lyophilizate was partitioned in favour of the polyethyleneglycol rich phase; PEG 2000 being the system which showed the better enzyme recovery (78.26%) with a purification factor of 2.3. This method could be applied as a first step to isolate the enzyme from a culture medium with good recovery and without modifying the enzymatic capacity and the molecular structure.
  • Keywords
    Partition , conformational flexibility , Lipase , Candida rugosa , Aqueous two-phase systems
  • Journal title
    Colloids and Surfaces B Biointerfaces
  • Serial Year
    2010
  • Journal title
    Colloids and Surfaces B Biointerfaces
  • Record number

    1970950