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格罗莫霉素:一类由新型生物合成途径产生的前所未有的三萜类抗生素。

Gromomycins: An Unprecedented Class of Triterpene Antibiotics Produced by a Novel Biosynthetic Pathway.

作者信息

Tistechok Stepan, Bratiichuk Dmytro, Sucipto Hilda, Gummerlich Nils, Stierhof Marc, Gromyko Oleksandr, Fries Franziska, Fedorenko Victor, Müller Rolf, Zapp Josef, Myronovskyi Maksym, Luzhetskyy Andriy

机构信息

Department of Pharmaceutical Biotechnology, Saarland University, Bld. C2.3, 66123, Saarbrücken, Germany.

Helmholtz Institute for Pharmaceutical Research Saarland (HIPS), Helmholtz Centre for Infection Research (HZI), Saarland University, 66123, Saarbrücken, Germany.

出版信息

Angew Chem Int Ed Engl. 2025 May 26;64(22):e202422270. doi: 10.1002/anie.202422270. Epub 2025 Mar 27.

Abstract

The current situation with drug-resistant microbial pathogens is critical, dictating an acute need for novel efficient antibiotics. Herein, we report a new class of antibiotics named gromomycins with significant activity, especially against drug-resistant Gram-positive pathogens, including methicillin- and daptomycin-resistant Staphylococcus aureus. Gromomycins are pentacyclic triterpenes with a cyclic guanidino group forming the fifth six-membered ring. We have used transposon mutagenesis to identify the gromomycin biosynthetic gene cluster, since it could not be assigned by any available bioinformatics tools, highlighting its unique biosynthetic route. Using gene cluster engineering, feeding experiments, and LC-MS and NMR analyses we have proposed the biosynthetic pathway for gromomycins, which are the first bacterial triterpenes synthesized independently of the squalene pathway. They also exhibit a so far unprecedented cyclization route that utilizes a hexaprenylguanidine linear precursor. Leveraging our understanding of their biosynthesis, we have identified additional gromomycin producers, resulting in the isolation of novel bioactive derivatives.

摘要

耐药微生物病原体的现状危急,迫切需要新型高效抗生素。在此,我们报道了一类名为格罗霉素的新型抗生素,其具有显著活性,尤其对耐药革兰氏阳性病原体有效,包括耐甲氧西林和耐达托霉素的金黄色葡萄球菌。格罗霉素是具有环状胍基形成第五个六元环的五环三萜。由于任何可用的生物信息学工具都无法确定其基因,我们利用转座子诱变来鉴定格罗霉素生物合成基因簇,突出了其独特的生物合成途径。通过基因簇工程、饲喂实验以及液相色谱-质谱联用和核磁共振分析,我们提出了格罗霉素的生物合成途径,格罗霉素是首批独立于鲨烯途径合成的细菌三萜。它们还展现出一种迄今前所未有的环化途径,该途径利用六异戊二烯基胍线性前体。基于我们对其生物合成的理解,我们鉴定出了其他格罗霉素产生菌,从而分离出了新型生物活性衍生物。

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