Potter Kevin C, Jia Meirong, Hong Young J, Tantillo Dean, Peters Reuben J
Roy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University , Ames, Iowa 50011, United States.
Department of Chemistry, University of California , Davis, California 95616, United States.
Org Lett. 2016 Mar 4;18(5):1060-3. doi: 10.1021/acs.orglett.6b00181. Epub 2016 Feb 15.
Through site-directed mutagenesis targeted at identification of the catalytic base in the rice (Oryza sativa) syn-copalyl diphosphate synthase OsCPS4, changes to a single residue (H501) were found to induce rearrangement rather than immediate deprotonation of the initially formed bicycle, leading to production of the novel compound syn-halimadienyl diphosphate. These mutational results are combined with quantum chemical calculations to provide insight into the underlying reaction mechanism.
通过定点诱变来鉴定水稻(Oryza sativa)顺式-柯巴基二磷酸合酶OsCPS4中的催化碱基,发现单一残基(H501)的变化会诱导重排,而不是使最初形成的双环立即去质子化,从而产生新化合物顺式-哈利马二烯基二磷酸。这些突变结果与量子化学计算相结合,以深入了解潜在的反应机制。