肽
核糖体RNA
酶
蛋白质工程
核糖体蛋白
生物化学
化学
计算生物学
生物
核糖体
核糖核酸
基因
作者
Minuri S. Ratnayake,Mathias Henning Hansen,Max J. Cryle
出处
期刊:Structure
[Elsevier]
日期:2024-05-01
卷期号:32 (5): 520-522
标识
DOI:10.1016/j.str.2024.04.003
摘要
In a recent issue of Nature Chemical Biology, Folger et al. demonstrated a high-throughput approach for engineering peptide bond forming domains from non-ribosomal peptide synthesis. A non-ribosomal peptide synthetase module from surfactin biosynthesis was reprogrammed to accept a fatty acid substrate into peptide biosynthesis, thus illustrating the potential of this approach for generating novel bioactive peptides.
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