• Title of article

    High Level Expression ofRicinus communisCasbene Synthase inEscherichia coliand Characterization of the Recombinant Enzyme

  • Author/Authors

    Hill، نويسنده , , Alison M. and Cane، نويسنده , , David E. and Mau، نويسنده , , Christopher J.D. and West، نويسنده , , Charles A.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی 12 سال 1996
  • Pages
    7
  • From page
    283
  • To page
    289
  • Abstract
    Casbene synthase catalyzes the cyclization of geranylgeranyl diphosphate (2) to casbene (1), a diterpene phytoalexin with antibacterial and antifungal activity that is produced by seedlings of castor bean (Ricinus communisL.) in response to fungal attack. We report the high-level expression of casbene synthase cDNA inEscherichia colias insoluble inclusion bodies, the solubilization and refolding of active casbene synthase, and the kinetic and product analysis of the recombinant enzyme. To overcome problems apparently associated with the presence in the casbene synthase gene of rare Arg codons, as well as the intrinsic antibacterial activity of casbene itself, the casbene synthase gene was expressed in anE. colihost harboring the pSM102 vector that encodes thednaYgene fortArg(AGA/G), using an expression vector, pET-21d(+), carrying the tightly controlled T7lacpromoter.
  • Journal title
    Archives of Biochemistry and Biophysics
  • Serial Year
    1996
  • Journal title
    Archives of Biochemistry and Biophysics
  • Record number

    1608271