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通过细菌基因组挖掘揭示四环素家族天然产物的分子图谱。

Uncovering the Molecular Landscape of Tetracycline Family Natural Products through Bacterial Genome Mining.

作者信息

Wang Haiyan, Wang Lijun, Li Dong, Fan Keqiang, Yang Yingzhe, Cao Haolan, Sun Jianing, Ren Jinwei, Liu Yao, Xiang Lijun, Li Weishu, Pan Minghui, Hu Huitao, Chen Yihua, Xu Zhengren, Huang Ying, Wang Weishan, Pan Guohui

机构信息

State Key Laboratory of Microbial Diversity and Innovative Utilization, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.

University of Chinese Academy of Sciences, Beijing 101408, China.

出版信息

J Am Chem Soc. 2025 May 7;147(18):15100-15114. doi: 10.1021/jacs.4c17551. Epub 2025 Apr 26.

Abstract

Tetracycline (TC) family natural products have attracted significant attention due to their diverse chemical structures and important role in drug development. As one of the most successful classes of drugs, TC antibiotics have been used clinically for over 70 years and remain crucial in treating infections. Despite their importance, systematic exploration of novel TC natural products has been limited, leaving the molecular landscape of the TC family poorly understood and hindering further development of these compounds for therapeutic applications. Here, we developed a targeted strategy to identify TC biosynthetic gene clusters (BGCs) based on specific cyclase signatures involved in assembling the TC scaffold. This led to the discovery of 82 representative BGCs with the potential to produce structurally diverse TCs. Among them, we uncovered three groups of novel natural products─misiomycins, varsomycins, and hibarimicins J-L─and identified their biosynthetic pathways. These compounds display distinctive structural features, with misiomycin A and hibarimicin L among the most highly modified TCs identified to date. Misiomycin A biosynthesis involves extensive glycosylation, while biosynthesis of varsomycin A, featuring a unique six-membered lactone ring structure, requires the coordinated action of two TC BGCs. The biosynthesis of hibarimicins J-L, derived from TC monomer dimerization, undergoes complex oxidative modifications involving seven oxygenases. Several TCs exhibited potent activity against drug-resistant Gram-positive pathogens. Our work further expands the structural diversity within the TC family and underscores the potential of these BGCs for generating new TC structures, providing valuable insights for the discovery and development of novel TC-based therapeutics.

摘要

四环素(TC)家族天然产物因其多样的化学结构以及在药物开发中的重要作用而备受关注。作为最成功的药物类别之一,TC抗生素已在临床应用超过70年,在治疗感染方面仍然至关重要。尽管它们很重要,但对新型TC天然产物的系统探索却很有限,导致对TC家族的分子格局了解不足,阻碍了这些化合物在治疗应用方面的进一步发展。在此,我们开发了一种靶向策略,基于参与组装TC支架的特定环化酶特征来鉴定TC生物合成基因簇(BGC)。这导致发现了82个具有产生结构多样的TC潜力的代表性BGC。其中,我们发现了三组新型天然产物——米西霉素、瓦尔索霉素和日向霉素J-L,并确定了它们的生物合成途径。这些化合物具有独特的结构特征,米西霉素A和日向霉素L是迄今为止鉴定出的修饰程度最高的TC之一。米西霉素A的生物合成涉及广泛的糖基化,而具有独特六元内酯环结构的瓦尔索霉素A的生物合成需要两个TC BGC的协同作用。日向霉素J-L由TC单体二聚化衍生而来,其生物合成经历了涉及七种氧化酶的复杂氧化修饰。几种TC对耐药革兰氏阳性病原体表现出强效活性。我们的工作进一步扩展了TC家族内的结构多样性,并强调了这些BGC在产生新的TC结构方面的潜力,为新型基于TC的治疗药物的发现和开发提供了有价值的见解。

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