合理设计
合成生物学
工作流程
蛋白质工程
计算生物学
饱和突变
生化工程
定向进化
计算机科学
代谢工程
突变
底盘
生物传感器
组合化学
生物
生物技术
迭代设计
定向分子进化
系统生物学
生物合成
基因组工程
工程设计过程
药物设计
设计策略
对偶(语法数字)
工程类
生物化学
作者
L Wang,Zenglin Zhang,Boran Zhang,Shengqi Gao,Wei Tao,Yingying Chen,Xuyang Zhu,Yinghao Huang,Jing Wu,S Chen,Kang Zhang
标识
DOI:10.1021/acs.jafc.6c00566
摘要
Developing microbial platforms for 2′-fucosyllactose (2′-FL) production requires meticulous enzyme engineering to eliminate byproducts such as difucosyllactose (DFL). Here, we establish a synthetic biology platform for high-titer, byproduct-free 2′-FL biosynthesis using the strictly regioselective α-1,2-fucosyltransferase BKHT. We employed a dual protein engineering strategy: rational computational design (incorporating structural, evolutionary, and stability predictions) and semirational screening powered by an engineered l -fucose-responsive biosensor (FcsR-P fcsK ). Through promoter and vector optimization, this low-noise biosensor enabled efficient screening of saturation mutagenesis libraries. Iterative combinatorial assembly of the identified beneficial mutations yielded an optimized quintuple mutant, M5 (L36P–I58V–E261G–S317D–K324H). In a 3 L bioreactor, an Escherichia coli chassis expressing M5 achieved a record 2′-FL titer of 124.25 g/L from glucose, with no detectable DFL. This integrated workflow combining rational design and biosensor-guided screening provides a robust framework for constructing advanced microbial cell factories.
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