雷巴迪甙A
甜叶菊
甜菊苷
糖苷键
化学
糖苷
糖基转移酶
甜菊醇
产量(工程)
酶
食品科学
立体化学
生物化学
材料科学
医学
替代医学
病理
冶金
作者
Baodang Guo,Zhiwei Deng,Fei Meng,Qingfu Wang,Yan Zhang,Zhenbo Yuan,Yijian Rao
标识
DOI:10.1021/acs.jafc.2c01209
摘要
Owing to zero-calorie and advanced organoleptic properties similar to sucrose, the plant-derived rebaudioside M (Reb M) has been considered as a next generation sweetener. However, a low content of Reb M in Stevia rebaudiana Bertoni and low enzymatic activity of UGT76G1, which is an uridine diphosphate glucose (UDPG)-dependent glycosyltransferase with the ability to glycosylate rebaudioside D (Reb D) to produce Reb M through the formation of β-1,3 glycosidic bond, restrict its commercial usage. To improve the catalytic activity of UGT76G1, a variant UGT76G1-T284S/M88L/L200A was obtained by structure-guided evolution, whose catalytic activity toward Reb D increased by 2.38 times compared with UGT76G1-T284S. This allowed us to prepare Reb M on a large-scale with a great yield of 90.50%. Moreover, molecular dynamics simulation illustrated that UGT76G1-T284S/M88L/L200A reduced distances from Reb D to catalytic residues and UDPG. Hence, we report an efficient method for the potential scale production of Reb M in this study.
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