天然有機化合物討論会講演要旨集
Online ISSN : 2433-1856
セッションID: P-31
会議情報
P-31 シダ植物由来の多機能型テルペン合成酵素が生成するmiltiradieneの酵素合成と多次元NMR解析(ポスター発表の部)
菅井 佳宣植野 陽平林 謙一郎豊増 知伸松本 定夏目 雅裕野崎 浩川出 洋
著者情報
会議録・要旨集 フリー

詳細
抄録
The complete genome of a lycophyte, Selaginella moellendorffii, has been sequenced and been available for extended research of functional genomics. S. moellendorffii genome contains putative 13 diterpene cyclase genes that are homologus to the angiosperm monofunctional cyclases and the moss and gymnosperm bifunctional cyclases. We cloned a possible diterpene cyclase gene SmBDTC that encodes a bifunctional enzyme catalyzing cyclization reaction of geranylgeranyl diphosphate (GGDP) to hydrocarbon product(s). The recombinant protein of SmBDTC expressed in Escherichia coli produced a single hydrocarbon product with the molecular mass of 272 from GGDP. A mutant of SmBDTC lacking ionization-initiated cyclization activity afforded copalyl diphosphate from GGDP. Although another mutant lacking protonation-initiated cyclization activity recognized both syn- and (+)-copalyl diphosphates, (+)-copalyl diphosphate as the native substrate of SmBDTC was determined. The SmBDTC product was enzymatically synthesized from [U-^<13>C_6] mevalonic acid, and all carbon atoms were fully labeled with ^<13>C isotope (>99%). The inverse gated-decoupling ^<13>C NMR spectrum of fully ^<13>C labeled compound confirmed 20 garbon signals. Two dimensional NMR spectrum (C-C COSY) and three-dimensional HCCH COSY spectrum demonstrated that SmBDTC catalyzed the production of miltiradiene, a biosynthetic precursor of tanshinones identified from the Chinese medicinal herb Salvta miltiorrhiza.
著者関連情報
© 2011 天然有機化合物討論会電子化委員会
前の記事 次の記事
feedback
Top