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Transcriptional Profiling and Molecular Characterization of the yccT Mutant Link: A Novel STY1099 Protein with the Peroxide Stress Response and Cell Division of Salmonella enterica Serovar Enteritidis

机译:转录特征和yccT突变链接的分子表征:一种新型STY1099蛋白具有过氧化物应激反应和肠炎沙门氏菌肠炎沙门氏菌的细胞分裂

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摘要

Uncharacterized protein STY1099, encoded by the gene, was previously identified as the most altered (i.e., upregulated) protein among the ZnO nanoparticle (NP) stimulon of serovar Enteritidis. Here we combined various stress response-related assays with functional genetics, global transcriptomic and proteomic analyses to characterize the gene and its STY1099 product. Exposure of . Enteritidis to H O (i.e., hydrogen peroxide) resulted in a significant ( < 0.0001) upregulation of the gene, whereas exposure to paraquat (i.e., superoxide) did not alter the expression of the gene. The ∆ mutant of Enteritidis exposed to 0.75 mM H O , showed significantly reduced ( < 0.05) viability compared to the wild type strain. Further, comparative transcriptome analyses supported by Co-immunoprecipitation (Co-IP) assay revealed that STY1099 protein plays a role in redox homeostasis during the peroxide stress assault via involvement in the processes of respiratory nitrate reductase, oxidoreductase activities, cellular uptake and stress response. In addition, we found that the STY1099 protein has the monopolar subcellular location and that it interacts with key cell division proteins, MinD, and FtsH, as well as with a rod shape-determining protein MerB.
机译:该基因编码的未鉴定蛋白STY1099先前被鉴定为是ZnO纳米颗粒(NP)刺激物中变化最大(即上调)的蛋白。 肠炎沙门氏菌。在这里,我们将各种与应激反应相关的测定与功能遗传学,整体转录组和蛋白质组学分析相结合,以鉴定该基因及其STY1099产品。的接触 。肠杆菌对H O(即过氧化氢)导致该基因显着(<0.0001)上调,而暴露于百草枯(即超氧化物)不会改变该基因的表达。与野生型菌株相比,暴露于0.75 mM H O的肠炎沙门氏菌的Δ突变体显示出明显降低的生存力(<0.05)。此外,由免疫共沉淀(Co-IP)分析支持的比较转录组分析显示,STY1099蛋白在过氧化物应激攻击过程中通过参与呼吸硝酸盐还原酶,氧化还原酶活性,细胞摄取和应激反应的过程在氧化还原稳态中起作用。此外,我们发现STY1099蛋白具有单极亚细胞位置,并且与关键的细胞分裂蛋白MinD和FtsH以及杆状决定蛋白MerB相互作用。

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