Grant C C, Vasil M L
J Bacteriol. 1986 Dec;168(3):1112-9. doi: 10.1128/jb.168.3.1112-1119.1986.
Analysis of RNA isolated from Pseudomonas aeruginosa PA103 and PAKS grown under Fe2+-limiting (0.08 microgram/ml) and Fe2+-sufficient (10 micrograms/ml) conditions demonstrated that exotoxin A (ETA) expression is regulated by Fe2+ at the level of transcription. S1 nuclease mapping revealed two 5' termini of the tox transcript, 89 base pairs (bp) (S1A) and 62 bp (S1B) 5' to the ETA initiation codon. There appeared to be no consensus promoter sequence for either tox transcript. An 8-bp direct repeat was found 5' to the start of transcript S1A. Transcript S1B mapped 8 bp upstream of a dodecamer sequence conserved between the ETA and phospholipase C genes of P. aeruginosa. Multicopy plasmids in which the expression of ETA is directed from the Escherichia coli trp promoter (ptrpETA-RSF1010) or the tox promoter (pCMtox) were constructed and mobilized into a Tox-P. aeruginosa strain, WR5. WR5 synthesized and secreted high levels of ETA when it was expressed from the E. coli trp promoter; however, the synthesis of ETA from its own promoter in this strain was very low. These and other data suggest that the expression of ETA is under a positive control mechanism. A fusion of the ETA promoter fragment to lacZ was constructed. Use of this fusion plasmid revealed that this DNA fragment directed the synthesis of beta-galactosidase in E. coli at very low levels and that the synthesis of beta-galactosidase from this fusion in E. coli was not regulated by Fe2+.
对从在铁离子限制(0.08微克/毫升)和铁离子充足(10微克/毫升)条件下生长的铜绿假单胞菌PA103和PAKS中分离出的RNA进行分析,结果表明外毒素A(ETA)的表达在转录水平受铁离子调控。S1核酸酶图谱分析揭示了tox转录本的两个5'末端,在ETA起始密码子上游89个碱基对(bp)(S1A)和62 bp(S1B)处。这两种tox转录本似乎都没有共有启动子序列。在转录本S1A起始位点上游5'处发现了一个8 bp的直接重复序列。转录本S1B定位于铜绿假单胞菌ETA基因和磷脂酶C基因之间保守的十二聚体序列上游8 bp处。构建了多拷贝质粒,其中ETA的表达由大肠杆菌色氨酸启动子(ptrpETA-RSF1010)或tox启动子(pCMtox)指导,并将其导入铜绿假单胞菌Tox-菌株WR5。当ETA从大肠杆菌色氨酸启动子表达时,WR5合成并分泌高水平的ETA;然而,该菌株中ETA从其自身启动子的合成非常低。这些以及其他数据表明ETA的表达处于正调控机制之下。构建了ETA启动子片段与lacZ的融合体。使用该融合质粒表明,该DNA片段在大肠杆菌中指导β-半乳糖苷酶的合成水平非常低,并且该融合体在大肠杆菌中β-半乳糖苷酶的合成不受铁离子调控。