热稳定性
生物转化
定向进化
化学
蔗糖
异构酶
生物化学
糖
生物合成
葡萄糖-6-磷酸异构酶
蛋白质工程
酶
溶剂
发酵
分子动力学
动力学
组合化学
作者
Hao Meng,Chao Li,Qian Shen,Xi-rong Liu,Chun-ling Zeng,Fang Yang,Xiaojuan Zhao,Jin‐lan Xia
标识
DOI:10.1021/acs.jafc.5c09800
摘要
Isomaltulose, a functional reducing sugar with promising applications, is biosynthesized from sucrose using sucrose isomerase (SIase). Nonetheless, the practical application of SIase has been hindered by its instability and reduced activity. In this study, we modified Pantoea dispersa SIase (PdSIase) by truncating certain flexible regions, resulting in PdSIaseΔ32, which exhibited a 2.29-fold increase in activity. Additionally, a high-throughput screening platform was designed to facilitate the directed evolution of PdSIaseΔ32, leading to the identification of PdSIaseΔ32-V300D/D330T, which demonstrated a 1.7-fold improvement in half-life at 45 °C. Structural modeling and molecular dynamics simulations revealed that the enhanced thermostability stemmed from the formation of new hydrogen bonds between the chains. Importantly, the bioconversion of 800 g/L sucrose with PdSIaseΔ32-V300D/D330T resulted in the production of 791.2 g/L isomaltulose, achieving a conversion rate of 98.9%. Our findings provide a fast screening tool and a theoretical foundation for advancing SIases, thereby facilitating the large-scale biosynthesis of isomaltulose.
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