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生物合成
大肠杆菌
氨基酸
生物化学
氨酰tRNA合成酶
化学
蛋白质生物合成
翻译(生物学)
计算生物学
功能(生物学)
蛋白质工程
生物
合成生物学
转移RNA
突变
芳香族氨基酸
HEK 293细胞
肽序列
氨基酰基tRNA合成酶
代谢工程
蛋白质结构
酿酒酵母
氨基酸残基
基因组
药物发现
酶
绿色荧光蛋白
定向进化
大肠杆菌蛋白质类
基因
作者
Jingxuan Zhang,Keying Yu,Yan Xu,W. R. Zhao,Yulian Li,Ying Wang,Florian P. Seebeck,Xiaohua Chen,Cangsong Liao
标识
DOI:10.1038/s41467-025-63679-6
摘要
Genetic code expansion (GCE) has significantly enhanced the diversity of proteins in the biological world, leading to a wide range of applications. Despite the advances in GCE, the cost of noncanonical amino acids (ncAAs) remains one of the major obstacles for large-scale production. In situ biosynthesis of ncAAs from commercial precursors offers a promising solution to this challenge, yet only a few biosynthetic pathways have been reported. Here, we present a platform that couples the biosynthesis of aromatic ncAAs with genetic code expansion in E. coli, enabling the production of proteins and peptides containing ncAAs. Forty ncAAs are synthesized from aryl aldehydes by the biosynthetic pathway, while nineteen ncAAs are incorporated into superfolder GFP using three orthogonal translation systems. The platform's versatility is demonstrated by the production of macrocyclic peptides and antibody fragments. We envision that the platform will facilitate the production of peptides, enzymes, and antibody fragments containing ncAAs.
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