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异源表达和 II 类细菌素的抗菌潜力。

Heterologous expression and antimicrobial potential of class II bacteriocins.

机构信息

The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kongens Lyngby, Denmark.

出版信息

Gut Microbes. 2024 Jan-Dec;16(1):2369338. doi: 10.1080/19490976.2024.2369338. Epub 2024 Jun 20.

Abstract

Gut bacteria are known to produce bacteriocins to inhibit the growth of other bacteria. Consequently, bacteriocins have attracted increased attention as potential microbiome-editing tools. In this study we examine the inhibitory spectrum of 75 class II bacteriocins against 48 representative gut microbiota species. The bacteriocins were heterologously expressed in and evaluated and assays revealed 22 bacteriocins to inhibit at least one species and showed selective inhibition patterns against species implicated in certain disorders and diseases. Three bacteriocins were selected for assessment on mouse feces. Based on 16S rRNA sequencing of the cultivated feces we showed that the two bacteriocins: Actifencin (#13) and Bacteroidetocin A (#22) selectively inhibited the growth of and , respectively. The probiotic: Nissle 1917 was engineered to express these two bacteriocins in mice. However, the selective inhibitory patterns found in the and experiments could not be observed . Our study describes a methodology for heterologous high throughput bacteriocin expression and screening and elucidates the inhibitory patterns of class II bacteriocins on the gut microbiota.

摘要

肠道细菌已知会产生细菌素来抑制其他细菌的生长。因此,细菌素作为潜在的微生物组编辑工具引起了越来越多的关注。在这项研究中,我们检查了 75 种 II 类细菌素对 48 种代表性肠道微生物物种的抑制谱。这些细菌素在 中异源表达,并通过 和 实验进行评估,结果显示 22 种细菌素至少能抑制一种物种,并对某些疾病和病症中涉及的物种表现出选择性抑制模式。选择了三种细菌素进行小鼠粪便的 评估。基于培养粪便的 16S rRNA 测序,我们表明两种细菌素:Actifencin(#13)和 Bacteroidetocin A(#22)分别选择性地抑制了 和 的生长。将益生菌:Nissle 1917 工程化以在小鼠中表达这两种细菌素。然而,在 和 实验中发现的选择性抑制模式无法观察到。我们的研究描述了一种用于异源高通量细菌素表达和筛选的方法,并阐明了 II 类细菌素对肠道微生物群的抑制模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5462/11195462/962fb3a80f2f/KGMI_A_2369338_F0001_OC.jpg

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