de Lorenzo V, Wee S, Herrero M, Neilands J B
J Bacteriol. 1987 Jun;169(6):2624-30. doi: 10.1128/jb.169.6.2624-2630.1987.
The promoter region of the pColV-K30-encoded operon specifying biosynthesis and transport of the siderophore aerobactin was subjected to deletion analysis to determine the smallest DNA sequence affording iron regulation of a iucA'-'lacZ gene fusion. A 78-base-pair (bp) region containing the main (P1) promoter retained the character of inducibility under iron starvation. A 250-bp fragment carrying this sequence was examined for protection against DNase I by the Fur protein, the product of a gene (fur) required for negative control of several iron-regulated functions. The DNase I footprints, in the presence of various divalent heavy-metal ions added as corepressors, revealed two contiguous binding sites with different lengths and affinities for Fur. Increased concentrations of the protein appeared to elicit formation of repressor oligomers which bind to the upstream and downstream regions of the P1 promoter in a metal-dependent fashion, but with a presently undefined stoichiometry. The primary site for Fur binding spans 31 bp and contains two overlapping symmetry dyads which share the sequence 5'-TCATT-3'. It also contains extensive homology with a 19-bp consensus sequence for iron-regulated genes as deduced from comparison with the fhuA and fepA putative promoter sequences.
对编码铁载体气杆菌素生物合成与转运的pColV-K30操纵子的启动子区域进行缺失分析,以确定赋予iucA'-'lacZ基因融合体铁调节功能的最小DNA序列。包含主要(P1)启动子的一个78碱基对(bp)区域在铁饥饿条件下仍保留诱导特性。对携带该序列的一个250 bp片段进行检测,以观察它是否能被Fur蛋白保护免受DNase I的作用,Fur蛋白是几个铁调节功能的负调控所需基因(fur)的产物。在添加了作为共阻遏物的各种二价重金属离子的情况下,DNase I足迹揭示了两个相邻的、对Fur具有不同长度和亲和力的结合位点。蛋白质浓度的增加似乎引发了阻遏物寡聚体的形成,这些寡聚体以金属依赖的方式结合到P1启动子的上游和下游区域,但目前化学计量关系尚不明确。Fur结合的主要位点跨度为31 bp,包含两个重叠的对称二元体,其共有序列为5'-TCATT-3'。通过与fhuA和fepA推定启动子序列比较推导得出,它还与铁调节基因的一个19 bp共有序列具有广泛的同源性。