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
Link To Document :
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