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铜绿假单胞菌lasA基因:转录起始点的确定及启动子/调控区域分析

Pseudomonas aeruginosa lasA gene: determination of the transcription start point and analysis of the promoter/regulatory region.

作者信息

Freck-O'Donnell L C, Darzins A

机构信息

Department of Microbiology, Ohio State University, Columbus 43210.

出版信息

Gene. 1993 Jul 15;129(1):113-7. doi: 10.1016/0378-1119(93)90705-8.

Abstract

The elastolytic activity of the opportunistic pathogen Pseudomonas aeruginosa is due to the combined activities of at least three secreted proteins: elastase, LasA and alkaline protease. Transcription of both the lasA gene and the elastase structural gene, lasB, requires the transcriptional activator LasR. In order to localize the promoter elements involved in lasA expression, the transcription start point (tsp) for lasA was localized by S1 protection and primer extension analysis. The DNA sequence of the region upstream from the tsp was determined, and a putative sigma promoter was identified. Sequence comparison with the lasB promoter region revealed two areas of considerable homology which could act as potential binding sites for LasR or other, as yet unidentified, regulatory proteins.

摘要

机会致病菌铜绿假单胞菌的弹性蛋白酶活性归因于至少三种分泌蛋白的联合作用

弹性蛋白酶、LasA和碱性蛋白酶。lasA基因和弹性蛋白酶结构基因lasB的转录都需要转录激活因子LasR。为了定位参与lasA表达的启动子元件,通过S1保护和引物延伸分析确定了lasA的转录起始点(tsp)。测定了tsp上游区域的DNA序列,并鉴定出一个假定的σ启动子。与lasB启动子区域的序列比较揭示了两个具有相当同源性的区域,它们可能作为LasR或其他尚未鉴定的调节蛋白的潜在结合位点。

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