Title of article :
Arg-94 is crucial to the catalysis of 3-isopropylmalate dehydrogenase from Thermus thermophilus HB8
Author/Authors :
Fujita، نويسنده , , Masaaki and Toyooka، نويسنده , , Yumiko and Tamegai، نويسنده , , Hideyuki and Eguchi، نويسنده , , Tadashi and Kakinuma، نويسنده , , Katsumi، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2000
Abstract :
The crucial role of Arg-94 in 3-isopropylmalate (IPM) dehydrogenase from Thermus thermophilus HB8 was elucidated by replacing the residue to lysine with site-directed mutagenesis. The kcat value of the R94K mutant enzyme for IPM was significantly reduced to 1/170 compared with that of native enzyme, whereas the Km for IPM was not much changed. It appeared that the major role of Arg-94 in exerting the enzymatic activity is not for the substrate recognition, but for the reaction catalysis, in such a way that Arg-94 facilitates stabilization of the transition-state in the decarboxylation step.
Keywords :
Thermus thermophilus HB-8 , 3-isopropylmalate dehydrogenase , site-directed mutagenesis , catalytic residue
Journal title :
Journal of Molecular Catalysis B Enzymatic
Journal title :
Journal of Molecular Catalysis B Enzymatic