化学
酶
生物催化
对映体
烯丙基重排
催化作用
组合化学
有机化学
立体异构
对映体过量
立体化学
动力学分辨率
生物化学
氨基酸
酶催化
营业额
定向进化
加合物
双加氧酶
作者
Teng Yuan,Mengxi Zhang,Linqi Cheng,Xinzhe Zheng,Shiyu Jiang,Xiongyi Huang,Han Xiao
摘要
Nonheme iron enzymes rank among nature's most versatile catalysts for molecular functionalization. Their flexible coordination environments provide a unique platform for expanding the scope of new-to-nature metalloenzymatic catalysis. Leveraging this feature, we herein present a novel biocatalytic strategy for synthesizing N-protected α-amino acids via 1,3-nitrogen migration. Specifically, we demonstrate that the nonheme iron enzyme isopenicillin N synthase (IPNS) from Aspergillus nidulans generates an iron-nitrene intermediate capable of aminating benzylic and allylic α-C-H bonds of carboxylic acids. Directed evolution has been performed to optimize the IPNS variant to accommodate a broad range of azanyl esters, yielding α-amino acids (24 examples) with up to 92% yield, 1477 total turnover number (TTN), and 99% enantiomeric excess (ee).
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