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大肠杆菌依赖NADH的亚硝酸还原酶基因启动子的位置和序列及其受氧气、Fnr蛋白和亚硝酸盐的调控

Location and sequence of the promoter of the gene for the NADH-dependent nitrite reductase of Escherichia coli and its regulation by oxygen, the Fnr protein and nitrite.

作者信息

Jayaraman P S, Peakman T C, Busby S J, Quincey R V, Cole J A

机构信息

Department of Biochemistry, University of Birmingham, U.K.

出版信息

J Mol Biol. 1987 Aug 20;196(4):781-8. doi: 10.1016/0022-2836(87)90404-9.

Abstract

The DNA sequence containing the start of the Escherichia coli nirB gene is reported. The N-terminal amino acid sequence of purified NADH-dependent nitrite reductase coincided with that predicted from the DNA sequence, confirming that nirB is the structural gene for nitrite reductase apoprotein and identifying the translation start point. Using nuclease S1 mapping, the sole transcription startpoint for the nirB gene was found 23 or 24 base-pairs upstream from the ATG initiation codon. By subcloning successively smaller DNA fragments into a beta-galactosidase expression vector plasmid, we located the promoter within a sequence bounded by a TaqI site at +14 with respect to the transcription startpoint and a HpaII site at -208. Measurements in vivo of beta-galactosidase expression and RNA levels due to nirB promoter activity showed that this promoter was activated during anaerobic growth. Optimal activity was found only after anaerobic growth in the presence of nitrite. The sequence of the nirB promoter is compared with sequences found at other anaerobically activated promoters.

摘要

已报道了包含大肠杆菌nirB基因起始部分的DNA序列。纯化的依赖NADH的亚硝酸还原酶的N端氨基酸序列与从DNA序列预测的序列一致,证实nirB是亚硝酸还原酶脱辅基蛋白的结构基因,并确定了翻译起始点。通过核酸酶S1图谱分析,发现nirB基因的唯一转录起始点位于ATG起始密码子上游23或24个碱基对处。通过将相继更小的DNA片段亚克隆到β-半乳糖苷酶表达载体质粒中,我们将启动子定位在相对于转录起始点位于+14的TaqI位点和位于-208的HpaII位点界定的序列内。对由于nirB启动子活性导致的β-半乳糖苷酶表达和RNA水平进行的体内测量表明,该启动子在厌氧生长期间被激活。仅在厌氧生长且存在亚硝酸盐的情况下才发现最佳活性。将nirB启动子的序列与在其他厌氧激活启动子处发现的序列进行了比较。

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