| 摘要 |
cDNAs encoding E-alpha-bisabolene synthase, delta-selinene synthase and gamma-humulene synthase from Grand Fir (Abies grandis) have been isolated and sequenced, and the corresponding amino acid sequences have been determined. Accordingly, isolated DNA sequences (SEQ ID No:12 and SEQ ID No:19 and SEQ ID No:23) are provided which code for the expression of E-alpha-bisabolene synthase (SEQ ID No:13), delta-selinene synthase (SEQ ID No:20) and gamma-humulene synthase (SEQ ID No: 24), respectively, from Grand Fir (Abies grandis). In other aspects, replicable recombinant cloning vehicles are provided which code for E-alpha-bisabolene synthase, delta-selinene synthase and gamma-humulene synthase, or for a base sequence sufficiently complementary to at least a portion of E-alpha-bisabolene synthase, delta-selinene synthase or gamma-humulene synthase DNA or RNA to enable hybridization therewith. In yet other aspects, modified host cells are provided that have been transformed, transfected, infected and/or injected with a recombinant cloning vehicle and/or DNA sequence encoding E-alpha-bisabolene synthase, delta-selinene synthase or gamma-humulene synthase. Thus, systems and methods are provided for the recombinant expression of the aforementioned recombinant sesquiterpene synthases that may be used to facilitate their production, isolation and purification in significant amounts. Recombinant E-alpha-bisabolene synthase, delta-selinene synthase and gamma-humulene synthase may be used to obtain expression or enhanced expression of E-alpha-bisabolene synthase, delta-selinene synthase and gamma-humulene synthase in plants, or may be otherwise employed for the regulation or expression of E-alpha-bisabolene synthase, delta-selinene synthase and gamma-humulene synthase. |
