Salinas P C, Tolmasky M E, Crosa J H
Department of Microbiology and Immunology, School of Medicine, Oregon Health Sciences University, Portland 97201.
Proc Natl Acad Sci U S A. 1989 May;86(10):3529-33. doi: 10.1073/pnas.86.10.3529.
We have identified a 110-kDa polypeptide that has a trans-acting regulatory activity on the expression of the pJM1 plasmid iron-uptake genes in Vibrio anguillarum. This protein is encoded by the angR gene and maps in a 3.6-kilobase-pair pJM1 DNA region located downstream of the iron transport genes. Full expression of this gene occurs under iron-limiting conditions and requires a 2.9-kilobase-pair upstream region in cis that maps within the coding region of the OM2 outer membrane protein, essential for the transport of iron into the cell cytosol. Determination of the siderophore anguibactin levels as well as analysis of specific transcripts for anguibactin biosynthetic genes demonstrated that AngR and another transcriptional activator, Taf, regulate in a synergistic fashion the level of anguibactin production by activation of transcription of the anguibactin biosynthetic genes under iron-limiting conditions.
我们已经鉴定出一种110 kDa的多肽,它对鳗弧菌中pJM1质粒铁摄取基因的表达具有反式作用调节活性。该蛋白由angR基因编码,定位于铁转运基因下游一个3.6千碱基对的pJM1 DNA区域。该基因在铁限制条件下实现完全表达,并且需要位于OM2外膜蛋白编码区域内的一个2.9千碱基对的顺式上游区域,这对于铁转运到细胞质中至关重要。对铁载体anguibactin水平的测定以及对anguibactin生物合成基因特定转录本的分析表明,AngR和另一种转录激活因子Taf在铁限制条件下通过激活anguibactin生物合成基因的转录,以协同方式调节anguibactin的产生水平。