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放线菌:发现新型抗生素候选物的宝库。

Actinomycetes: Treasure trove for discovering novel antibiotic candidates.

作者信息

Yi Rexing, Shi Yutong, Cao Xun, Pan Chengqian

机构信息

Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

College of Food Science and Engineering, Ningbo University, Ningbo, 315832, China.

出版信息

Eur J Med Chem. 2025 Mar 15;286:117317. doi: 10.1016/j.ejmech.2025.117317. Epub 2025 Jan 25.

Abstract

Actinomycetes are an important source of secondary metabolites such as antibiotics and other active natural products. Many well-known antibiotics, such as streptomycin, oxytetracycline, and tetracycline, are produced by actinomycetes. Different types of antibiotics have distinct mechanisms of action against microorganisms: inhibit protein synthesis, inhibit nucleic acid synthesis, or inhibit cell wall synthesis. For decades, actinomycetes have played a crucial role in clinical treatment for major diseases such as pathogenic bacterial infections, serving as one of the most significant sources of new discoveries. However, due to extensive use of antibiotics, the types and numbers of drug-resistant bacteria, represented by multidrug resistant (MDR) and extensively drug resistant (XDR) bacteria, have increased dramatically in clinical settings, posing a significant threat to human survival. Therefore, there is an urgent need to search for structurally novel antibacterial natural products and develop new antibiotics. In this review, a total of 170 antibacterial secondary metabolites from actinomycetes, published in the 54 literatures (2020 to September 2024) and some synthetic analogs, are discussed with emphasis on their structures and biological activities.

摘要

放线菌是抗生素和其他活性天然产物等次级代谢产物的重要来源。许多知名抗生素,如链霉素、土霉素和四环素,都是由放线菌产生的。不同类型的抗生素对微生物有不同的作用机制:抑制蛋白质合成、抑制核酸合成或抑制细胞壁合成。几十年来,放线菌在治疗致病性细菌感染等重大疾病的临床治疗中发挥了关键作用,是最重要的新发现来源之一。然而,由于抗生素的广泛使用,以多重耐药(MDR)和广泛耐药(XDR)细菌为代表的耐药菌的种类和数量在临床环境中急剧增加,对人类生存构成了重大威胁。因此,迫切需要寻找结构新颖的抗菌天然产物并开发新的抗生素。在这篇综述中,我们讨论了2020年至2024年9月发表的54篇文献中报道的来自放线菌的170种抗菌次级代谢产物以及一些合成类似物,重点介绍了它们的结构和生物活性。

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