化学
加氧酶
基质(水族馆)
立体化学
替代(逻辑)
催化作用
底物特异性
合理设计
双加氧酶
酶
组合化学
生物化学
纳米技术
海洋学
材料科学
计算机科学
程序设计语言
地质学
作者
Takahiro Mori,Ziheng Yu,Hui Tao,Ikuro Abe
出处
期刊:Organic Letters
[American Chemical Society]
日期:2022-02-23
卷期号:24 (8): 1737-1741
被引量:5
标识
DOI:10.1021/acs.orglett.2c00409
摘要
The Fe- and 2-oxoglutarate-dependent oxygenase SptF is a promising powerful biocatalys with unusual catalytic versatility and promiscuity. The site-specific random substitution of N150, I63, and N65, which are involved in substrate interactions, generated three compounds that were not produced by the SptF wild type. The substrate binding mode was dramatically altered by the introduction of only one or two substitutions. These results provide insights into the engineering of Fe- and 2-oxoglutarate-dependent oxygenases for chemoenzymatic syntheses of bioactive compounds.
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