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Converting Phenylacetone Monooxygenase into Phenylcyclohexanone Monooxygenase by Rational Design:Towards Practical Baeyer-Villiger Monooxygenases

机译:通过合理设计将苯丙酮单加氧酶转化为苯环己酮单加氧酶:迈向实用的拜尔-维利格单加氧酶

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摘要

A homology model of the most frequently used, but thermally somewhat labile, Baeyer–Villiger monooxygenase, cyclohexanone monooxygenase (CHMO) has been derived on the basis of the recently published crystal structure of the thermally stable phenylacetone monooxygenase (PAMO). This has led to the identification of a structural element crucial for substrate acceptance and stereoselectivity, namely an arginine-interacting loop near the active site. A bulge in this loop occurring in PAMO (but not in CHMO) has been eliminated by mutation, enhancing the range of substrate acceptance and enantioselectivity of Baeyer–Villiger reactions while maintaining high thermal stability.
机译:根据最近发表的热稳定苯丙酮单加氧酶(PAMO)的晶体结构,得出了最常用但热不稳定的Baeyer-Villiger单加氧酶,环己酮单加氧酶(CHMO)的同源性模型。这导致鉴定对于底物接受和立体选择性至关重要的结构元素,即活性位点附近的精氨酸相互作用环。通过突变消除了PAMO(而不是CHMO中)出现的该循环中的凸起,从而在维持高热稳定性的同时,增强了Baeyer-Villiger反应的底物接受范围和对映选择性。

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