Kato Takahiro, Lee Jung-Bum, Taura Futoshi, Kurosaki Fumiya
Nat Prod Commun. 2016 Sep;11(9):1221-1224.
Two genes involved in δ-guaiene biosynthesis in Aquilaria microcarpa, δ-guaiene synthase (GS) and famesyl diphosphate synthase (FPS), were overexpressed in Escherichia coli cells. Immunoblot analysis revealed that the concentration of GS-translated protein was rather low in the cells transformed by solely GS while appreciable accumulation of the recombinant protein was observed when GS was coexpressed with FPS. GS-transformed cells liberated only a trace amount of δ-guaiene (0.004 μg/mL culture), however, the concentration of the compound elevated to 0.08 pg/mL culture in the cells transformed by GS plus FPS. δ-Guaiene biosynthesis was markedly activated when E. coli cells coexpressing GS and FPS were incubated in enriched Terrific broth, and the content of the compound increased to approximately 0.6 μg/mL culture. These results suggest that coexpression of FPS and GS in E. coli is required for efficient δ- guaiene production in the bacterial cells, and the sesquiterpene-producing activity of the transformant is appreciably enhanced in the nutrients-enriched medium.
参与小果沉香中δ-愈创木烯生物合成的两个基因,即δ-愈创木烯合酶(GS)和法呢基二磷酸合酶(FPS),在大肠杆菌细胞中过表达。免疫印迹分析表明,仅由GS转化的细胞中GS翻译蛋白的浓度相当低,而当GS与FPS共表达时,观察到重组蛋白有明显积累。仅由GS转化的细胞仅释放微量的δ-愈创木烯(0.004μg/mL培养物),然而,在由GS加FPS转化的细胞中,该化合物的浓度升高至0.08μg/mL培养物。当共表达GS和FPS的大肠杆菌细胞在富集的Terrific肉汤中培养时,δ-愈创木烯生物合成被显著激活,该化合物的含量增加至约0.6μg/mL培养物。这些结果表明,在大肠杆菌中高效生产δ-愈创木烯需要FPS和GS共表达,并且在营养丰富的培养基中,转化体的倍半萜生产活性明显增强。