...
首页> 外文期刊>FEMS Microbiology Letters >Growth-phase-dependent expression of the operon coding for the glycosylated autotransporter adhesin AIDA-I of pathogenic Escherichia coli
【24h】

Growth-phase-dependent expression of the operon coding for the glycosylated autotransporter adhesin AIDA-I of pathogenic Escherichia coli

机译:致病性大肠杆菌糖基化自转运粘附素AIDA-1编码操纵子的生长阶段依赖性表达

获取原文
获取原文并翻译 | 示例

摘要

The adhesin involved in diffuse adherence (AIDA-I) is an autotransporter found in pathogenic strains of Escherichia coli causing diarrhea in humans and pigs. The AIDA-I protein is glycosylated by a specific enzyme, the AIDA-associated heptosyltransferase (Aah). The aah gene is immediately upstream of the aidA gene, suggesting that they form an operon. However, the mechanisms of regulation of the aah and aidA genes are unknown. Using a clinical E. coli isolate expressing AIDA-I, we identified two putative promoters 149 and 128 nucleotides upstream of aah. Using qRT-PCR, we observed that aah and aidA are transcribed in a growth-dependent fashion, mainly at the start of the stationary phase. Western blotting confirmed that protein expression follows the same pattern. Using a fusion to a reporter gene, we observed that the regulation of the isolated aah promoter matched this transcription and expression pattern. Lastly, we found glucose to be a repressor and nutrient starvation to be an inducer. Taken together, our results suggest that, in the strain and the conditions we studied, aah-aidA is transcribed as a bicistronic message from a promoter upstream of aah, with maximal expression under conditions of nutrient limitation such as high cell density.
机译:参与弥漫性粘附的粘附素(AIDA-1)是一种在大肠杆菌致病性菌株中引起人类和猪腹泻的自转运蛋白。 AIDA-1蛋白被一种特定的酶糖基化,该酶与AIDA相关的庚糖基转移酶(Aah)。 aah基因位于aidA基因的上游,表明它们形成操纵子。但是,调控aah和aidA基因的机制尚不清楚。使用表达AIDA-1的临床大肠杆菌分离株,我们鉴定了aah上游的两个推定的启动子149和128个核苷酸。使用qRT-PCR,我们观察到aah和aidA以依赖于生长的方式转录,主要在固定相开始时进行。蛋白质印迹证实蛋白质表达遵循相同的模式。使用与报告基因的融合,我们观察到分离的aah启动子的调控与该转录和表达模式匹配。最后,我们发现葡萄糖是阻遏物,营养不足是诱导物。两者合计,我们的结果表明,在我们研究的菌株和条件下,aah-aidA作为双顺反子信息从aah上游的启动子转录,在营养限制(例如高细胞密度)的条件下具有最大表达。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号