Department of Chemistry, Indiana University, Bloomington, Indiana 47405, United States.
Chem Rev. 2023 Aug 23;123(16):10381-10431. doi: 10.1021/acs.chemrev.3c00215. Epub 2023 Jul 31.
The ability to site-selectively modify equivalent functional groups in a molecule has the potential to streamline syntheses and increase product yields by lowering step counts. Enzymes catalyze site-selective transformations throughout primary and secondary metabolism, but leveraging this capability for non-native substrates and reactions requires a detailed understanding of the potential and limitations of enzyme catalysis and how these bounds can be extended by protein engineering. In this review, we discuss representative examples of site-selective enzyme catalysis involving functional group manipulation and C-H bond functionalization. We include illustrative examples of native catalysis, but our focus is on cases involving non-native substrates and reactions often using engineered enzymes. We then discuss the use of these enzymes for chemoenzymatic transformations and target-oriented synthesis and conclude with a survey of tools and techniques that could expand the scope of non-native site-selective enzyme catalysis.
选择性地在分子中修饰等效官能团的能力有可能通过降低步骤数来简化合成并提高产物收率。酶在初级和次级代谢过程中催化选择性转化,但要将这种能力用于非天然底物和反应,需要详细了解酶催化的潜力和限制,以及如何通过蛋白质工程来扩展这些限制。在这篇综述中,我们讨论了涉及官能团修饰和 C-H 键功能化的代表性酶选择性催化实例。我们包括了天然催化的说明性实例,但我们的重点是涉及非天然底物和反应的情况,这些反应通常使用工程酶。然后,我们讨论了这些酶在化学酶转化和定向合成中的应用,并以可扩展非天然选择性酶催化范围的工具和技术调查作为结束。