Ochsner Urs A, Johnson Zaiga, Vasil Michael L
Department of Microbiology, University of Colorado Health Sciences Center, 4200 E Ninth Avenue, Campus Box B175, Denver, CO 80262, USA1.
Microbiology (Reading). 2000 Jan;146 ( Pt 1):185-198. doi: 10.1099/00221287-146-1-185.
A gene cluster similar to haem iron uptake loci of bacterial pathogens was identified in Pseudomonas aeruginosa. This phu locus ('Pseudomonas haem uptake') consisted of the phuR receptor gene and the phuSTUVW operon encoding a typical ABC transporter. Expression of phuR and phuSTUVW from mapped transcriptional-start sites occurred under iron-restricted growth conditions and was directly controlled by the Fur protein. Binding of Fur was demonstrated by DNase footprinting of two adjacent 'Fur boxes' that overlapped both the phuR and phuSTUVW promoters. Two tandem repeats of 154 bp were identified downstream of the phuSTUVW operon, each of which contained a strong Fur-dependent promoter driving expression of iron-regulated RNAs antisense to phuSTUVW. Mutant strains with deletions in phuR and phuSTUV showed greatly reduced growth with either haem or haemoglobin as the only iron source: the defects were complemented by plasmids harbouring the phuR or the phuSTUV genes, respectively. Deletions of phuW or of the tandem repeats had only minor effects on haem utilization. The remaining haem and haemoglobin uptake still observed in the deltaphuR or deltaphuSTUV deletion mutants was due to a second haem-acquisition system, has, which was also under the direct control of Fur. This second haem-receptor gene, hasR, was identified upstream of and in an operon with hasA, encoding a haem-binding extracellular protein. A deltahasR mutant also exhibited decreased utilization of haem and haemoglobin, and a deltaphuR deltahasR double mutant was virtually unable to take up either compound. Both the PhuR and HasR proteins were detected in the outer-membrane fraction of P. aeruginosa grown in low-iron media. Taken together, the evidence suggests that the phu and has loci encode two distinct systems required for the acquisition of haem and haemoglobin in P. aeruginosa.
在铜绿假单胞菌中鉴定出一个与细菌病原体血红素铁摄取位点相似的基因簇。这个phu位点(“假单胞菌血红素摄取”)由phuR受体基因和编码典型ABC转运蛋白的phuSTUVW操纵子组成。在铁限制生长条件下,从定位的转录起始位点开始表达phuR和phuSTUVW,并且直接受Fur蛋白控制。通过对两个相邻的“Fur框”进行DNase足迹分析证明了Fur的结合,这两个“Fur框”与phuR和phuSTUVW启动子都重叠。在phuSTUVW操纵子下游鉴定出两个154 bp的串联重复序列,每个重复序列都包含一个强大的依赖Fur的启动子,驱动与phuSTUVW反义的铁调节RNA的表达。phuR和phuSTUV中存在缺失的突变菌株,以血红素或血红蛋白作为唯一铁源时生长大大减少:这些缺陷分别由携带phuR或phuSTUV基因的质粒互补。phuW或串联重复序列的缺失对血红素利用只有轻微影响。在deltaphuR或deltaphuSTUV缺失突变体中仍观察到的剩余血红素和血红蛋白摄取是由于第二个血红素获取系统has,它也受Fur的直接控制。这个第二个血红素受体基因hasR,在与hasA同一个操纵子中且位于hasA上游,hasA编码一种结合血红素的细胞外蛋白。一个deltahasR突变体也表现出血红素和血红蛋白利用减少,而一个deltaphuR deltahasR双突变体几乎无法摄取这两种化合物。在低铁培养基中生长的铜绿假单胞菌的外膜部分检测到了PhuR和HasR蛋白。综上所述,证据表明phu和has位点编码了铜绿假单胞菌获取血红素和血红蛋白所需的两个不同系统。