Duan Yangyang, Du Wenyu, Song Zhijun, Chen Ridao, Xie Kebo, Liu Jimei, Chen Dawei, Dai Jungui
State Key Laboratory of Bioactive Substance and Function of Natural Medicines, CAMS Key Laboratory of Enzyme and Biocatalysis of Natural Drugs, NHC Key Laboratory of Biosynthesis of Natural Products, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
Acta Pharm Sin B. 2023 Jan;13(1):271-283. doi: 10.1016/j.apsb.2022.05.015. Epub 2022 May 20.
Astragalosides are the main active constituents of traditional Chinese medicine Huang-Qi, of which cycloastragenol-type glycosides are the most typical and major bioactive compounds. This kind of compounds exhibit various biological functions including cardiovascular protective, neuroprotective, etc. Owing to the limitations of natural sources and the difficulties encountered in chemical synthesis, re-engineering of biosynthetic machinery will offer an alternative and promising approach to producing astragalosides. However, the biosynthetic pathway for astragalosides remains elusive due to their complex structures and numerous reaction types and steps. Herein, guided by transcriptome and phylogenetic analyses, a cycloartenol synthase and four glycosyltransferases catalyzing the committed steps in the biosynthesis of such bioactive astragalosides were functionally characterized from . AmCAS1, the first reported cycloartenol synthase from genus, is capable of catalyzing the formation of cycloartenol; AmUGT15, AmUGT14, AmUGT13, and AmUGT7 are four glycosyltransferases biochemically characterized to catalyze 3--xylosylation, 3--glucosylation, 25--glucosylation/-xylosylation and 2--glucosylation of cycloastragenol glycosides, respectively. These findings not only clarified the crucial enzymes for the biosynthesis and the molecular basis for the structural diversity of astragalosides in plants, also paved the way for further completely deciphering the biosynthetic pathway and constructing an artificial pathway for their efficient production.
黄芪甲苷是传统中药黄芪的主要活性成分,其中环黄芪醇型糖苷是最典型和主要的生物活性化合物。这类化合物具有多种生物学功能,包括心血管保护、神经保护等。由于天然来源的限制和化学合成中遇到的困难,对生物合成机制进行重新设计将为黄芪甲苷的生产提供一种替代且有前景的方法。然而,由于黄芪甲苷结构复杂、反应类型和步骤众多,其生物合成途径仍不明确。在此,在转录组和系统发育分析的指导下,从[具体植物名称]中对催化此类生物活性黄芪甲苷生物合成关键步骤的一种环阿屯醇合酶和四种糖基转移酶进行了功能表征。AmCAS1是首次报道的来自[属名]属的环阿屯醇合酶,能够催化环阿屯醇的形成;AmUGT15、AmUGT14、AmUGT13和AmUGT7是四种经生化表征的糖基转移酶,分别催化环黄芪醇糖苷的3-O-木糖基化、3-O-葡萄糖基化、25-O-葡萄糖基化/木糖基化和2-O-葡萄糖基化。这些发现不仅阐明了[具体植物名称]植物中黄芪甲苷生物合成的关键酶及其结构多样性的分子基础,也为进一步完全破译生物合成途径和构建其高效生产的人工途径铺平了道路。