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全球Gac/Rsm调控系统通过控制sp. NCIMB 10586中的MupR/I群体感应系统来激活莫匹罗星的生物合成。

Global Gac/Rsm regulatory system activates the biosynthesis of mupirocin by controlling the MupR/I quorum sensing system in sp. NCIMB 10586.

作者信息

Cai Yuyuan, Huang Peng, Venturi Vittorio, Xiong Runyao, Wang Zheng, Wang Wei, Huang Xianqing, Hu Hongbo, Zhang Xuehong

机构信息

State Key Laboratory of Microbial Metabolism, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.

International Centre for Genetic Engineering and Biotechnology, Trieste, Italy.

出版信息

Appl Environ Microbiol. 2025 Feb 19;91(2):e0189624. doi: 10.1128/aem.01896-24. Epub 2025 Jan 23.

Abstract

The biosynthesis of mupirocin, a clinically significant antibiotic produced by sp. NCIMB 10586, is activated by the -acyl homoserine lactone (AHL) MupR/I quorum sensing (QS) system. However, to date, limited research has focused on the influence of global regulators such as the GacS/A two-component system (TCS) on the MupR/I QS system or mupirocin biosynthesis. In this study, we characterized the regulatory components of the Gac/Rsm transduction system in the mupirocin-producing model strain NCIMB 10586 and investigated their interconnection with the MupR/I QS circuit and subsequent mupirocin biosynthesis. The production of mupirocin was hampered by either inactivation, inactivation, or the double-mutant of the sRNAs ( RsmY and RsmZ). Similarly, the expressions of and , and AHL synthesis significantly decreased in or mutants, indicating that the GacS/A system stimulates mupirocin biosynthesis via the MupR/I QS system. Five CsrA family proteins, RsmA/E/I/F/N, were found in strain NCIMB 10586, and the single and multiple mutants of showed different phenotypes with respect to mupirocin production. Our results revealed that mupirocin biosynthesis was likely to be negatively regulated by RsmA/E/I, but positively regulated by RsmF. Additionally, the RsmF protein was shown to interact with the 5' leader of mRNA. In summary, the Gac/Rsm system positively regulates the biosynthesis of mupirocin mainly through the MupR/I QS system, and the model of the regulatory mechanism is proposed. The elucidation of the Gac/Rsm-MupR/I regulatory pathway could help devise ways for improving mupirocin production through genetic engineering.IMPORTANCEThe Gac/Rsm regulatory system plays a global regulatory role in bacterial physiology and metabolism, including secondary metabolism. Mupirocin is a clinically important antibiotic, produced by sp. NCIMB 10586, whose biosynthesis is activated by the MupR/I quorum sensing system. Global regulators have important impacts on the gene expression of secondary metabolic gene clusters and QS genes, and the GacS/A two-component system is one of the main regulators across species, which significantly influences antibiotic production. Our study presented that the expressions of QS genes and gene cluster were downregulated in or mutants compared to the wild-type. The inactivation of in NCIMB 10586, encoding CsrA family proteins, showed different regulatory traits of mupirocin production, in which the RsmF protein could interact with the 5' UTR region of mRNA. These findings provide the understanding of the regulatory role of Gac/Rsm on mupirocin biosynthesis and QS system and lay foundations for further improving mupirocin production.

摘要

莫匹罗星是由 sp. NCIMB 10586 产生的一种具有临床意义的抗生素,其生物合成由 N-酰基高丝氨酸内酯(AHL)MupR/I 群体感应(QS)系统激活。然而,迄今为止,针对诸如 GacS/A 双组分系统(TCS)等全局调控因子对 MupR/I QS 系统或莫匹罗星生物合成的影响的研究有限。在本研究中,我们对莫匹罗星产生模型菌株 NCIMB 10586 中 Gac/Rsm 转导系统的调控成分进行了表征,并研究了它们与 MupR/I QS 回路以及随后的莫匹罗星生物合成之间的相互联系。sRNA(RsmY 和 RsmZ)的缺失、缺失或双突变均会阻碍莫匹罗星的产生。同样,在缺失或缺失突变体中,和的表达以及 AHL 合成均显著降低,这表明 GacS/A 系统通过 MupR/I QS 系统刺激莫匹罗星的生物合成。在菌株 NCIMB 10586 中发现了五种 CsrA 家族蛋白,即 RsmA/E/I/F/N,的单突变体和多突变体在莫匹罗星产生方面表现出不同的表型。我们的结果表明,莫匹罗星生物合成可能受到 RsmA/E/I 的负调控,但受到 RsmF 的正调控。此外,RsmF 蛋白被证明与 mRNA 的 5' 前导序列相互作用。总之,Gac/Rsm 系统主要通过 MupR/I QS 系统正向调控莫匹罗星的生物合成,并提出了调控机制模型。阐明 Gac/Rsm-MupR/I 调控途径有助于设计通过基因工程提高莫匹罗星产量的方法。

重要性

Gac/Rsm 调控系统在细菌生理和代谢(包括次级代谢)中发挥全局调控作用。莫匹罗星是一种由 sp. NCIMB 10586 产生的临床重要抗生素,其生物合成由 MupR/I 群体感应系统激活。全局调控因子对次级代谢基因簇和 QS基因的基因表达有重要影响,而 GacS/A 双组分系统是跨物种的主要调控因子之一,对抗生素产生有显著影响。我们的研究表明,与野生型相比,在缺失或缺失突变体中,QS 基因和基因簇的表达下调。在 NCIMB 10586 中编码 CsrA 家族蛋白的缺失显示出莫匹罗星产生的不同调控特征,其中 RsmF 蛋白可与 mRNA 的 5' UTR 区域相互作用。这些发现有助于理解 Gac/Rsm 对莫匹罗星生物合成和 QS 系统的调控作用,并为进一步提高莫匹罗星产量奠定基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe16/11837529/ca031cc9fb43/aem.01896-24.f001.jpg

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