Author/Authors :
Ebrahimi، M. نويسنده Department of Biochemistry and Biophysics,Islamic Azad University, Varamin-Pishva Branch,Varamin,Iran , , Hosseinkhani، S. نويسنده Faculty of Biological Sciences,Department of Biochemistry,Tarbiat Modares University,Tehran,Iran , , Heydari، A. نويسنده Faculty of Science,Department of Chemistry,Tarbiat Modares University,Tehran,Iran , , Akbari، J. نويسنده Faculty of Science,Department of Chemistry,Tarbiat Modares University,Tehran,Iran ,
Abstract :
We expressed and purified a recombinant P. pyralis luciferase with Nterminal Histags. The silanized Ni or Culoaded magnetic particles were prepared and used to assemble the Histagged P. pyralis luciferase. This enzyme immobilized on functionalized magnetic nanoparticles (MNPs) via electrostatic interactions of Histag with Ni2+/Cu2+ ions on the surface of MNPs using simple one step method. These particles were also used for purification of recombinant luciferase from crude extract of cell lysate. Effect of incubation time and amount of MNPs in bioluminescent activity were investigated to determine optimum condition for immobilization. Several properties of immobilized luciferase were studied and compared with free enzyme. Immobilization has shown different effects on Km for ATP and luciferin. In both immobilized form, Km(ATP) was increased while Km(luciferin) was shown decreases. Optimal temperature of both immobilized luciferase increased to 30 ºC while thermal stabilities have not shown significant differences compared to free enzyme. Both immobilized form inactivated after five consecutive reaction cycles.
Keywords :
P. pyralis , luciferase , magnetic nanoparticles , Immobilization , thermostability
