Beynon J, Cannon M, Buchanan-Wollaston V, Cannon F
Cell. 1983 Sep;34(2):665-71. doi: 10.1016/0092-8674(83)90399-9.
We have determined the precise point of transcription initiation for five nif (nitrogen fixation) operons of Klebsiella pneumoniae and sequenced the promoters. Our results show that nifF is transcribed in the opposite direction to that previously proposed for nif genes, that nifM is transcribed from two promoters, and that there is a promoter preceding nifU but not nifX, and we present a revised map of nif transcripts. The nif promoters have a characteristic structure of 26 bp located between positions--1 and --26 upstream of the site of transcription initiation: CTGG..8bp...TTGCA...9bp...Py(+1). This structure, which has two regions of conserved sequence, shows no homology to the "consensus promoter" of enteric bacteria. Our results suggest that the--10 homology is equivalent to a "Pribnow box" for promoters expressed under nitrogen-starved conditions and that the--23 homology confers activator specificity on the nif promoters.
我们已确定了肺炎克雷伯菌五个固氮(nif)操纵子转录起始的精确位点,并对其启动子进行了测序。我们的结果表明,nifF的转录方向与先前对nif基因所提出的方向相反,nifM由两个启动子转录,并且在nifU之前存在一个启动子而nifX之前没有,我们还给出了nif转录本的修订图谱。nif启动子在转录起始位点上游-1至-26位之间具有一个26 bp的特征结构:CTGG..8bp...TTGCA...9bp...Py(+1)。这种具有两个保守序列区域的结构与肠道细菌的“共有启动子”没有同源性。我们的结果表明,-10同源序列相当于在氮饥饿条件下表达的启动子的“普里布诺框”,而-23同源序列赋予nif启动子激活剂特异性。