热稳定性
化学
枯草芽孢杆菌
催化作用
酶
合理设计
定向进化
生物化学
组合化学
生物
材料科学
纳米技术
细菌
基因
遗传学
突变体
作者
Zijie Li,Yangfan Hu,Cheng Yu,Kangqing Fei,Liqun Shen,Yishi Liu,Nakanishi Hideki
标识
DOI:10.1002/biot.202400280
摘要
BACKGROUND: D-Allulose is one of the most well-known rare sugars widely used in food, cosmetics, and pharmaceutical industries. The most popular method for D-allulose production is the conversion from D-fructose catalyzed by D-allulose 3-epimerase (DAEase). To address the general problem of low catalytic efficiency and poor thermostability of wild-type DAEase, D-allulose biosensor was adopted in this study to develop a convenient and efficient method for high-throughput screening of DAEase variants. RESULTS: D-fructose in 1 h by Bacillus subtilis WB800 whole cells expressing this DAEase variant. Furthermore, the practicability of cell immobilization was evaluated and more than 80% relative activity of the immobilized cells was maintained from the second to seventh cycle. CONCLUSION: variant would be a potential candidate for the industrial production of D-allulose.
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