首页> 外文期刊>Journal of bacteriology >The ptsH, ptsI, and crr genes of the Escherichia coli phosphoenolpyruvate-dependent phosphotransferase system: a complex operon with several modes of transcription.
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The ptsH, ptsI, and crr genes of the Escherichia coli phosphoenolpyruvate-dependent phosphotransferase system: a complex operon with several modes of transcription.

机译:大肠杆菌磷酸烯醇丙酮酸依赖性磷酸转移酶系统的ptsH,ptsI和crr基因:具有多种转录模式的复杂操纵子。

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摘要

The ptsH, ptsI, and crr genes, coding for three of the proteins of the phosphoenolpyruvate-dependent phosphotransferase system (PTS) (HPr, enzyme I, and enzyme IIIGlc, respectively) have been studied by determination of their nucleotide sequence and analysis of their expression. The three genes constitute an operon, but analysis of the ptsH, ptsI, and crr transcripts by Northern (RNA) blotting revealed the existence of three major mRNA species. One encompassed the three cistrons, a second one the ptsH gene and part of the ptsI gene, and the third one only the distal gene crr. The short crr transcripts were initiated inside the ptsI open reading frame at points which were identified by S1 mapping. Expression of the genes was studied in vivo by using operon and protein fusions between the lacZ gene and the ptsH, ptsI, or crr gene on IncW low-copy-number plasmids. The present study showed that (i) the ptsH, ptsI, and crr genes exhibited high basal expression, (ii) transcription of the ptsH and ptsI genes was stimulated threefold by the cyclic AMP-cyclic AMP receptor protein complex and also by growth on glucose, but only in the presence of an active enzyme IIGlc, (iii) crr-specific expression was not sensitive to the complex or to growth on glucose, and (iv) under the growth conditions tested, the major part of crr transcription was initiated from internal promoters.
机译:已通过确定核苷酸序列并对其进行分析,研究了编码磷酸烯醇丙酮酸依赖性磷酸转移酶系统(PTS)的三种蛋白质的ptsH,ptsI和crr基因(分别为HPr,酶I和酶IIIGlc)。表达。这三个基因组成一个操纵子,但是通过Northern(RNA)印迹对ptsH,ptsI和crr转录本进行的分析显示,存在三种主要的mRNA。一个包含三个顺反子,第二个包含ptsH基因和部分ptsI基因,第三个仅包含远端基因crr。简短的crr转录本在ptsI开放阅读框内由S1映射确定的点启动。通过使用lacZ基因与IncW低拷贝数质粒上的ptsH,ptsI或crr基因之间的操纵子和蛋白质融合体,在体内研究了基因的表达。本研究表明(i)ptsH,ptsI和crr基因表现出较高的基础表达;(ii)环状AMP-环状AMP受体蛋白复合物以及葡萄糖的生长刺激了ptsH和ptsI基因的转录三倍,但仅在存在活性酶IIGlc的情况下,(iii)crr特异性表达对复合物或葡萄糖生长不敏感;(iv)在测试的生长条件下,crr转录的主要部分从内部推动者。

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