酶
生物催化
合成生物学
生物化学
化学
代谢工程
酿酒酵母
生物合成
肽
大肠杆菌
模块化设计
焊剂(冶金)
代谢途径
组合化学
计算生物学
生物
催化作用
计算机科学
有机化学
基因
离子液体
操作系统
作者
Wenli Kang,T. Ma,Min Liu,Jiale Qu,Zhenjun Liu,Huawei Zhang,Bin Shu,Shuai Fu,Juncai Ma,Louis Tung Faat Lai,Sicong He,Jianan Y. Qu,Shannon Wing‐Ngor Au,Byung‐Ho Kang,Wilson Chun Yu Lau,Zixin Deng,Jiang Xia,Tiangang Liu
标识
DOI:10.1038/s41467-019-12247-w
摘要
Abstract Enzymatic reactions in living cells are highly dynamic but simultaneously tightly regulated. Enzyme engineers seek to construct multienzyme complexes to prevent intermediate diffusion, to improve product yield, and to control the flux of metabolites. Here we choose a pair of short peptide tags (RIAD and RIDD) to create scaffold-free enzyme assemblies to achieve these goals. In vitro, assembling enzymes in the menaquinone biosynthetic pathway through RIAD–RIDD interaction yields protein nanoparticles with varying stoichiometries, sizes, geometries, and catalytic efficiency. In Escherichia coli , assembling the last enzyme of the upstream mevalonate pathway with the first enzyme of the downstream carotenoid pathway leads to the formation of a pathway node, which increases carotenoid production by 5.7 folds. The same strategy results in a 58% increase in lycopene production in engineered Saccharomyces cerevisiae . This work presents a simple strategy to impose metabolic control in biosynthetic microbe factories.
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