Holtel A, Goldenberg D, Giladi H, Oppenheim A B, Timmis K N
National Research Centre for Biotechnology, Gesellschaft für Biotechnologische Forschung mbH, Braunschweig, Germany.
J Bacteriol. 1995 Jun;177(11):3312-5. doi: 10.1128/jb.177.11.3312-3315.1995.
Regulation of the xyl gene operons of the Pseudomonas putida TOL plasmid is mediated by the products of the downstream clustered and divergently oriented xylR and xylS regulatory genes. The xylR-xylS intergenic region contains the xylR and xylS promoters Pr and Ps, respectively. A binding site for the XylR activator protein is located upstream of Ps and overlapping Pr. DNase I footprint experiments showed that one of these sites, which overlaps the recognition site for XylR activator, as well as an AT-rich region comprising the Ps promoter consensus were protected by integration host factor (IHF). IHF was found to act negatively in the in vivo activation of the Ps promoter, since the activity of a Ps promoter::lacZ fusion was elevated in an Escherichia coli mutant lacking IHF. In contrast, no alteration in the synthesis of XylR protein in the E. coli IHF-deficient mutant was detected.
恶臭假单胞菌TOL质粒木糖基因操纵子的调控由下游成簇且方向相反的木糖R和木糖S调控基因的产物介导。木糖R - 木糖S基因间区域分别包含木糖R启动子Pr和木糖S启动子Ps。木糖R激活蛋白的结合位点位于Ps上游且与Pr重叠。DNA酶I足迹实验表明,这些位点之一与木糖R激活剂的识别位点重叠,以及包含Ps启动子共有序列的富含AT的区域受到整合宿主因子(IHF)的保护。发现IHF在Ps启动子的体内激活中起负作用,因为在缺乏IHF的大肠杆菌突变体中,Ps启动子::lacZ融合体的活性升高。相反,在大肠杆菌IHF缺陷突变体中未检测到木糖R蛋白合成的改变。