Department of Chemical and Biomolecular Engineering, University of California, Berkeley, CA, United States.
Department of Chemical and Biomolecular Engineering, University of California, Berkeley, CA, United States.
Methods Enzymol. 2024;704:143-172. doi: 10.1016/bs.mie.2024.06.002. Epub 2024 Jun 29.
The isonitrile group is a compact, electron-rich moiety coveted for its commonplace as a building block and bioorthogonal functionality in synthetic chemistry and chemical biology. Hundreds of natural products containing an isonitrile group with intriguing bioactive properties have been isolated from diverse organisms. Our recent discovery of a conserved biosynthetic gene cluster in some Actinobacteria species highlighted a novel enzymatic pathway to isonitrile formation involving a non-heme iron(II) and α-ketoglutarate-dependent dioxygenase. Here, we focus this chapter on recent advances in understanding and probing the biosynthetic machinery for isonitrile synthesis by non-heme iron(II) and α-ketoglutarate-dependent dioxygenases. We will begin by describing how to harness isonitrile enzymatic machinery through heterologous expression, purification, synthetic strategies, and in vitro biochemical/kinetic characterization. We will then describe a generalizable strategy to probe the mechanism for isonitrile formation by combining various spectroscopic methods. The chapter will also cover strategies to study other enzyme homologs by implementing coupled assays using biosynthetic pathway enzymes. We will conclude this chapter by addressing current challenges and future directions in understanding and engineering isonitrile synthesis.
异腈基是一种紧凑、富电子的部分,因其在合成化学和化学生物学中作为构建块和生物正交官能团的普遍存在而备受追捧。从各种生物体中分离出了数百种含有异腈基的具有有趣生物活性的天然产物。我们最近在一些放线菌物种中发现了一个保守的生物合成基因簇,这突出了一种涉及非血红素铁(II)和α-酮戊二酸依赖性双加氧酶的新型异腈形成酶促途径。在本章中,我们将重点介绍近年来在理解和探索非血红素铁(II)和α-酮戊二酸依赖性双加氧酶参与的异腈合成生物合成机制方面的进展。我们将首先描述如何通过异源表达、纯化、合成策略和体外生化/动力学表征来利用异腈酶促机制。然后,我们将描述一种通过结合各种光谱方法来探测异腈形成机制的通用策略。该章节还将涵盖通过使用生物合成途径酶实施偶联测定来研究其他酶同源物的策略。最后,我们将讨论在理解和设计异腈合成方面当前的挑战和未来的方向。