开发从核苷合成 2′3′-cGAMP 的多酶级联程序

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL
Martin Becker , Isabel Nowak , Katharina Hildebrand , Stephan Lütz , Katrin Rosenthal
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引用次数: 0

摘要

近年来,人们对多酶级联法合成药物活性成分的兴趣与日俱增。通过巧妙地选择酶,级联反应可在一次反应中完成多步合成,而无需纯化中间产物。本研究成功开发了一种五酶级联法,可在七个反应步骤中由腺苷和鸟苷形成环状 2′3′-GMP-AMP(2′3′-cGAMP)。首先,研究了激酶磷酸化核苷酸和核苷酸的底物范围,然后将其结合到酶级联中,由腺苷、鸟苷和多聚磷酸形成 2′3′-cGAMP。与初始鸟苷浓度相比,57%的底物被转化为 2′3′-cGAMP。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development of a multi-enzyme cascade for 2′3′-cGAMP synthesis from nucleosides†

Development of a multi-enzyme cascade for 2′3′-cGAMP synthesis from nucleosides†

Development of a multi-enzyme cascade for 2′3′-cGAMP synthesis from nucleosides†

The interest in multi-enzyme cascades for the synthesis of pharmaceutically relevant active ingredients has increased in recent years. Through a smart selection of enzymes, cascades enable multi-step synthesis in a one-pot reaction without the purification of intermediates. In this study, a five-enzyme cascade for the formation of cyclic 2′3′-GMP-AMP (2′3′-cGAMP) from adenosine and guanosine in seven reaction steps was successfully developed. First, the substrate scope of kinases for the phosphorylation of nucleosides and nucleotides was investigated, which were then combined in an enzyme cascade for 2′3′-cGAMP formation from adenosine, guanosine, and polyphosphate. An overall conversion of 57% of the substrates into 2′3′-cGAMP was achieved in relation to the initial guanosine concentration.

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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
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