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我们循环往复——酶辅助因子再生的策略。

Round, round we go - strategies for enzymatic cofactor regeneration.

机构信息

Institute of Microbiology, ETH Zürich, Vladimir-Prelog-Weg 1-5/10, 8093 Zürich, Switzerland.

出版信息

Nat Prod Rep. 2020 Oct 1;37(10):1316-1333. doi: 10.1039/d0np00004c. Epub 2020 Jun 25.

Abstract

Covering: up to the beginning of 2020Enzymes depending on cofactors are essential in many biosynthetic pathways of natural products. They are often involved in key steps: catalytic conversions that are difficult to achieve purely with synthetic organic chemistry. Hence, cofactor-dependent enzymes have great potential for biocatalysis, on the condition that a corresponding cofactor regeneration system is available. For some cofactors, these regeneration systems require multiple steps; such complex enzyme cascades/multi-enzyme systems are (still) challenging for in vitro biocatalysis. Further, artificial cofactor analogues have been synthesised that are more stable, show an altered reaction range, or act as inhibitors. The development of bio-orthogonal systems that can be used for the production of modified natural products in vivo is an ongoing challenge. In light of the recent progress in this field, this review aims to provide an overview of general strategies involving enzyme cofactors, cofactor analogues, and regeneration systems; highlighting the current possibilities for application of enzymes using some of the most common cofactors.

摘要

涵盖

截至 2020 年初 依赖辅因子的酶在天然产物的许多生物合成途径中是必不可少的。它们通常参与关键步骤:仅用合成有机化学难以实现的催化转化。因此,在有相应的辅因子再生系统的情况下,依赖辅因子的酶具有很大的生物催化潜力。对于一些辅因子,这些再生系统需要多个步骤;对于体外生物催化来说,如此复杂的酶级联/多酶体系仍然具有挑战性。此外,已经合成了更稳定、反应范围改变或起抑制剂作用的人工辅因子类似物。开发可用于体内生产修饰天然产物的生物正交系统是一个持续的挑战。鉴于该领域的最新进展,本综述旨在概述涉及酶辅因子、辅因子类似物和再生系统的一般策略;强调了使用一些最常见的辅因子应用酶的当前可能性。

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