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IclR 家族转录调节因子 XyrR 控制 sp. ATCC 39006 中的浮选、运动性、抗生素生产和毒力。

The IclR-family transcriptional regulator XyrR controls flotation, motility, antibiotic production and virulence in sp. ATCC 39006.

作者信息

Sandoval Carlo Miguel Castro, Salmond George P C

机构信息

Department of Biochemistry, University of Cambridge, Cambridge, United Kingdom.

Institute of Crop Science, University of the Philippines Los Baños, Los Baños, Laguna, Philippines.

出版信息

Front Microbiol. 2025 Jan 15;15:1500889. doi: 10.3389/fmicb.2024.1500889. eCollection 2024.

Abstract

The opportunistic pathogen sp. ATCC 39006 (S39006) is a rod-shaped, motile, Gram-negative bacterium that produces a 𝛽-lactam antibiotic (a carbapenem) and a bioactive red-pigmented tripyrrole antibiotic, prodigiosin. It is also the only known enterobacterium that naturally produces intracellular gas vesicles (GVs), enabling cells to float in static water columns. Regulation of GVs and secondary metabolites in S39006 can be coordinated but such pleiotropy is still poorly understood. To uncover novel inputs to this complex regulatory network, we used transposon mutagenesis to identify a mutant with an insertion in an IclR-type transcriptional regulator gene. The mutant showed diminished production of carbapenem, prodigiosin, GVs and cellulase. Furthermore, the mutant also showed increased swimming and swarming motilities but exhibited attenuated virulence and ability to kill the nematode . Using differential expression analysis of the intracellular proteomes of the wild type and mutant, we confirmed that the mutation negatively impacted expression of the corresponding GV, carbapenem and prodigiosin gene clusters. In contrast, flagellar and chemotaxis proteins were overexpressed, consistent with the increased motility of the mutant. We also found that the proteins encoded by a putative operon, involved in xylonate catabolism and transport, showed a 5- to 7-fold increase in expression. Finally, we show that IclR is a repressor of xylonate catabolism in S39006 and suggest that xylonate is potentially involved in controlling carbapenem and prodigiosin biosynthesis. Our results indicate that IclR is a global regulator that controls antibiotic biosynthesis, flotation through modulating GV assembly, and has pleiotropic impacts on the physiology and virulence of S39006. Based on these findings, we propose the designation of this IclR-family transcriptional regulator as XyrR (lonate esponse egulator).

摘要

机会致病菌sp. ATCC 39006(S39006)是一种杆状、可运动的革兰氏阴性菌,能产生一种β-内酰胺抗生素(一种碳青霉烯)和一种具有生物活性的红色色素三吡咯抗生素灵菌红素。它也是唯一已知的能天然产生细胞内气体囊泡(GVs)的肠杆菌,使细胞能够漂浮在静止的水柱中。S39006中GVs和次级代谢产物的调控可以相互协调,但这种多效性仍知之甚少。为了揭示这个复杂调控网络的新输入,我们使用转座子诱变来鉴定一个在IclR型转录调节基因中发生插入的突变体。该突变体显示碳青霉烯、灵菌红素、GVs和纤维素酶的产量减少。此外,该突变体还表现出游泳和群集运动能力增强,但毒力减弱且杀死线虫的能力降低。通过对野生型和突变体细胞内蛋白质组的差异表达分析,我们证实该突变对相应的GV、碳青霉烯和灵菌红素基因簇的表达产生了负面影响。相比之下,鞭毛蛋白和趋化蛋白过度表达,这与突变体运动能力增强一致。我们还发现,一个假定的操纵子编码的蛋白质参与木糖酸盐分解代谢和转运,其表达增加了5至7倍。最后,我们表明IclR是S39006中木糖酸盐分解代谢的阻遏物,并表明木糖酸盐可能参与控制碳青霉烯和灵菌红素的生物合成。我们的结果表明,IclR是一种全局调节因子,通过调节GV组装来控制抗生素生物合成、漂浮,并对S39006的生理学和毒力具有多效性影响。基于这些发现,我们建议将这个IclR家族转录调节因子命名为XyrR(木糖酸盐反应调节因子)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e11a/11778176/9490139c755d/fmicb-15-1500889-g001.jpg

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