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发现去甲二氢愈创木酸 A:L 型的特异性生长抑制剂。

Discovery of Demurilactone A: A Specific Growth Inhibitor of L-Form .

机构信息

The Centre for Bacterial Cell Biology, Biosciences Institute, Medical School, Newcastle University, Newcastle Upon Tyne NE2 4AX, U.K.

Odyssey Therapeutics Inc, The Biosphere, Draymans Way, Newcastle Helix, Newcastle Upon Tyne NE4 5BX, U.K.

出版信息

ACS Infect Dis. 2022 Nov 11;8(11):2253-2258. doi: 10.1021/acsinfecdis.2c00220. Epub 2022 Oct 21.

Abstract

Metabolic profiling of the extracts from a library of actinobacteria led to the identification of a novel polyketide, demurilactone A, produced by strain DEM21308. The structure of the compound was assigned based on a detailed investigation of 1D/2D NMR spectra and HR-MS. Whole genome DNA sequencing, followed by bioinformatics analysis and insertional mutagenesis, identified type I polyketide synthases encoded by the gene cluster to direct the biosynthesis of this polyene macrolide. While the number of modules is consistent with the carbon backbone of the assigned structure, some discrepancies were identified in the domain organization of five modules. Close investigation of the amino acid sequences identified several mutations in the conserved motifs of nonfunctional domains. Furthermore, the absolute configuration of hydroxy-bearing stereocenters was proposed based on analyses of the ketoreductase domains. Remarkably, although demurilactone A has little detectable activity against normal-walled bacteria, it specifically inhibits the growth of cell wall-deficient "L-form" at a minimum inhibitory concentration value of 16 μg/mL. Time-lapse microscopy analyses revealed that demurilactone affects membrane dynamics, probably by reducing membrane fluidity. This compound could be a powerful reagent for studying long-standing questions about the involvement of L-forms in recurrent infection.

摘要

从放线菌文库的提取物代谢特征分析中,鉴定出一种新型多烯大环内酯化合物,demurilactone A,由菌株 DEM21308 产生。该化合物的结构基于对 1D/2D NMR 谱和高分辨质谱(HR-MS)的详细研究进行了指定。通过全基因组 DNA 测序,然后进行生物信息学分析和插入诱变,确定了由 基因簇编码的 I 型聚酮合酶,指导该多烯大环内酯的生物合成。虽然模块的数量与指定结构的碳骨架一致,但在五个模块的结构域组织中发现了一些差异。对氨基酸序列的仔细研究确定了非功能结构域中保守基序的几个突变。此外,根据酮还原酶结构域的分析,提出了含有羟基的手性中心的绝对构型。值得注意的是,尽管 demurilactone A 对正常壁细菌几乎没有检测到活性,但它特异性地抑制细胞壁缺陷的“L 型”的生长,最低抑菌浓度值为 16 μg/mL。时程显微镜分析表明,demurilactone 影响膜动力学,可能通过降低膜流动性。这种化合物可能是研究关于 L 型在反复感染中作用的长期存在问题的有力试剂。

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