A cinnamyl alcohol dehydrogenase–like scaffold organizes monoterpenoid indole alkaloid biosynthesis · D. Gao et al.
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Di Gao (高笛)1,2†, Scott Galeung Alexander Mann3†, Binbin Chen (陈彬彬)4,5†, Yuanwei Gou (苟源蔚)1,2†, Cong Chen (陈聪)1,2†, Chong Qiao (乔崇)2†, Jorge Jonathan Oswaldo Garza- Garcia3†, Mohammadamin Shahsavarani ( ) 3, Xiaojing Jiang (姜小晶)1,2, Hannah Caroline Tran3, Jingfei Bao (包竟飞)1, Mathew Bailey Richardson3, Jianing Li (李佳宁)1,2, Jacob Owen Perley3, Jaewook Hwang (황재욱)3, Feng Dong (董峰)1, Chang Dong (董昌)2, Lei Huang (黄磊)1,2, Vincenzo De Luca6, Yajie Wang (王雅婕)4,5*, Yang Qu (曲洋)3*, Jiazhang Lian (连佳长)1,2,7,8,9* Biosynthesis of ∼3000 monoterpenoid indole alkaloids (MIAs), including the anticancer drug vinblastine, involves the highly unstable intermediate strictosidine aglycone. Its formation by strictosidine β- glucosidase (sgD) and subsequent conversion by geissoschizine synthase (gs) occur in spatially separated compartments, representing a major biosynthesis bottleneck. …
摘自《科学》(Science)第393卷 第6813期 · 2026年8月20日,D. Gao et al.。仅引用开头一小段供了解文章,版权归原刊所有,全文请阅读原刊。