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细菌多环酮类天然产物的化学与生物合成。

Chemistry and biosynthesis of bacterial polycyclic xanthone natural products.

机构信息

State Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic and Developmental Sciences, School of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai 200240, China.

出版信息

Nat Prod Rep. 2022 Nov 16;39(11):2057-2095. doi: 10.1039/d2np00046f.

Abstract

Covering: up to the end of 2021Bacterial polycyclic xanthone natural products (BPXNPs) are a growing family of natural xanthones featuring a pentangular architecture with various modifications to the tricyclic xanthone chromophore. Their structural diversities and various activities have fueled biosynthetic and chemical synthetic studies. Moreover, their more potent activities than the clinically used drugs make them potential candidates for the treatment of diseases. Future unraveling of structure activity relationships (SARs) will provide new options for the (bio)-synthesis of drug analogues with higher activities. This review summarizes the isolation, structural elucidation and biological activities and more importantly, the recent strategies for the microbial biosynthesis and chemical synthesis of BPXNPs. Regarding their biosynthesis, we discuss the recent progress in enzymes that synthesize tricyclic xanthone, the protein candidates for structural moieties (methylene dioxygen bridge and nitrogen heterocycle), tailoring enzymes for methylation and halogenation. The chemical synthesis part summarizes the recent methodology for the division synthesis and coupling construction of achiral molecular skeletons. Ultimately, perspectives on the biosynthetic study of BPXNPs are discussed.

摘要

涵盖内容

截至 2021 年底。细菌多环黄烷酮天然产物 (BPXNPs) 是一类不断发展的天然黄烷酮家族,其特征为五角形结构,三环黄烷酮生色团具有各种修饰。它们的结构多样性和各种活性激发了生物合成和化学合成研究。此外,它们比临床使用的药物具有更强的活性,使它们成为治疗疾病的潜在候选药物。未来对结构活性关系 (SAR) 的揭示将为具有更高活性的药物类似物的 (生物) 合成提供新的选择。本综述总结了 BPXNPs 的分离、结构阐明、生物活性,更重要的是,微生物生物合成和化学合成的最新策略。关于它们的生物合成,我们讨论了合成三环黄烷酮的酶、结构部分(亚甲二氧基桥和氮杂环)的蛋白质候选物、用于甲基化和卤化的修饰酶的最新进展。化学合成部分总结了非手性分子骨架的分段合成和偶联构建的最新方法。最终,讨论了 BPXNPs 生物合成研究的展望。

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