Technische Universität Berlin, Institut für Chemie, Strasse des 17. Juni 124, 10623, Berlin, Germany.
Angew Chem Int Ed Engl. 2017 Mar 27;56(14):3770-3821. doi: 10.1002/anie.201609079. Epub 2017 Mar 21.
Nonribosomal peptide synthetases (NRPSs) are large multienzyme machineries that assemble numerous peptides with large structural and functional diversity. These peptides include more than 20 marketed drugs, such as antibacterials (penicillin, vancomycin), antitumor compounds (bleomycin), and immunosuppressants (cyclosporine). Over the past few decades biochemical and structural biology studies have gained mechanistic insights into the highly complex assembly line of nonribosomal peptides. This Review provides state-of-the-art knowledge on the underlying mechanisms of NRPSs and the variety of their products along with detailed analysis of the challenges for future reprogrammed biosynthesis. Such a reprogramming of NRPSs would immediately spur chances to generate analogues of existing drugs or new compound libraries of otherwise nearly inaccessible compound structures.
非核糖体肽合成酶(NRPSs)是一种大型多酶复合体,能够组装具有丰富结构和功能多样性的多种肽类化合物。这些肽类化合物包括 20 多种已上市的药物,如抗菌药物(青霉素、万古霉素)、抗肿瘤化合物(博来霉素)和免疫抑制剂(环孢素)。在过去的几十年中,生物化学和结构生物学的研究已经深入了解了非核糖体肽的高度复杂的组装线。这篇综述提供了关于 NRPSs 的基础机制及其产物多样性的最新知识,并对未来重新编程生物合成所面临的挑战进行了详细分析。这种对 NRPSs 的重新编程将立即为生成现有药物的类似物或原本几乎无法获得的化合物结构的新化合物库提供机会。