The bacterium has developed various strategies to sense and respond to the complex stresses encountered during its transmission and pathogenic processes. PurR is a common transcriptional regulator of purine biosynthesis among microorganisms, and it modulates the transcription level of the operon to suppress the production of hypoxanthine nucleotide (IMP). This study aims to understand the functions and regulatory mechanisms of in . Firstly, we constructed a knockout mutant of strain 201 and compared certain phenotypes of the null mutant (201-Δ) and the wild-type strain (201-WT). The results show that deleting has no significant impact on the biofilm formation, growth rate, or viability of under different stress conditions (heat and cold shock, high salinity, and hyperosmotic pressure). Although the cytotoxicity of the knockout mutant on HeLa and 293 cells is reduced, the animal-challenging test found no difference of the virulence in mice between 201-Δ and 201-WT. Furthermore, RNA-seq and EMSA analyses demonstrate that PurR binds to the promoter regions of at least 15 genes in strain 201, primarily involved in purine biosynthesis, along with others not previously observed in other bacteria. Additionally, RNA-seq results suggest the presence of 11 potential operons, including a newly identified co-transcriptional T6SS cluster. Thus, aside from its role as a regulator of purine biosynthesis, in may have additional regulatory functions.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673613PMC
http://dx.doi.org/10.3390/microorganisms11112801DOI Listing

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