Venturi V, Ottevanger C, Leong J, Weisbeek P J
Department of Molecular Cell Biology, University of Utrecht, The Netherlands.
Mol Microbiol. 1993 Oct;10(1):63-73. doi: 10.1111/j.1365-2958.1993.tb00904.x.
Genes encoding biosynthesis of pseudobactin 358 (a microbial iron transport agent) and its cognate outer membrane receptor protein, PupA, are transcribed only under iron limitation in plant growth-promoting Pseudomonas putida WCS358. Two cosmid clones were identified from a gene bank of WCS358 DNA which could independently and in an iron-dependent manner activate transcription from a WCS358 siderophore gene promoter in heterologous Pseudomonas strain A225. The functional region of one of the clones was localized by subcloning, transposon Tn3Gus mutagenesis, and DNA sequencing. Genomic transposon insertion mutants in the functional region lost the capacity to activate a siderophore gene promoter fusion transcriptionally; furthermore, these mutants no longer produced pseudobactin 358. The activating region consisted of a single gene designated pfrA (Pseudomonas ferric regulator). The pfrA gene codes for a single polypeptide, PfrA, of approximately 18 kDa, which has 58% identity to AlgQ (also known as AlgR2), a positive regulator involved in transcriptionally regulating alginate biosynthesis in Pseudomonas aeruginosa. Cross-complementation studies between the pfrA gene of P. putida and the algQ gene of P. aeruginosa revealed that pfrA can restore mucoidy (alginate production) in an algQ mutant and that algQ could poorly complement a pfrA genomic mutant. It is concluded that PfrA is involved in the positive regulation of siderophore biosynthetic genes in response to iron limitation; furthermore, pfrA and algQ appeared to be interchangeable between P. putida and P. aeruginosa.
编码假单胞菌素358(一种微生物铁转运剂)及其同源外膜受体蛋白PupA生物合成的基因,仅在促进植物生长的恶臭假单胞菌WCS358处于铁限制条件下时才会转录。从WCS358 DNA基因文库中鉴定出两个黏粒克隆,它们能够以铁依赖性方式独立激活异源假单胞菌菌株A225中WCS358铁载体基因启动子的转录。通过亚克隆、转座子Tn3Gus诱变和DNA测序确定了其中一个克隆的功能区域。功能区域中的基因组转座子插入突变体失去了转录激活铁载体基因启动子融合的能力;此外,这些突变体不再产生假单胞菌素358。激活区域由一个名为pfrA(假单胞菌铁调节因子)的单一基因组成。pfrA基因编码一种约18 kDa的单一多肽PfrA,它与AlgQ(也称为AlgR2)具有58%的同一性,AlgQ是一种参与转录调节铜绿假单胞菌藻酸盐生物合成的正调节因子。恶臭假单胞菌的pfrA基因与铜绿假单胞菌的algQ基因之间的交叉互补研究表明,pfrA可以恢复algQ突变体中的黏液性(藻酸盐产生),而algQ对pfrA基因组突变体的互补作用较差。得出的结论是,PfrA参与了对铁限制响应的铁载体生物合成基因的正调节;此外,pfrA和algQ在恶臭假单胞菌和铜绿假单胞菌之间似乎是可互换的。