Venturi V, Otten M, Korse V, Brouwer B, Leong J, Weisbeek P
Department of Molecular Cell Biology, University of Utrecht, The Netherlands.
Gene. 1995 Mar 21;155(1):83-8. doi: 10.1016/0378-1119(94)00868-s.
A previous study [Venturi et al., Mol. Microbiol. 10 (1993) 63-73] demonstrated that the siderophore regulatory gene pfrA of Pseudomonas putida (Pp) WCS358 is highly similar and interchangeable with the alginate regulatory gene algQ (algR2) of P. aeruginosa (Pa). The algQ gene is physically linked to two other alginate regulators in the Pa chromosome, namely algR (algR1), a response regulator, and algP (algR3), a histone-like gene. In this study, we have identified the same genes and a similar genetic organization in the Pp chromosome. The two genes linked to pfrA, designated pprA and pprB, are similar to algR and algP, respectively. Chromosomal mutants of pprA and pprB were constructed showing that unlike pfrA, the two newly identified regulators are not involved in siderophore regulation. The pprA gene complemented a Pa algR mutant phenotype, suggesting that it could be involved in alginate gene regulation. The WCS358 strain is not producing alginate, but we demonstrated by Southern analysis that it also possesses, in addition to pprA and pprB, algD and algU (algT) gene homologs, two genes essential for alginate biosynthesis. Using an algD-xylE transcriptional fusion, we observed that the algD promoter is active in strain WCS358 and absolutely requires pfrA. The possibility that all five genes of Pp WCS358 are involved in alginate biosynthesis is discussed.
先前的一项研究[文图里等人,《分子微生物学》10(1993)63 - 73]表明,恶臭假单胞菌(Pp)WCS358的铁载体调节基因pfrA与铜绿假单胞菌(Pa)的藻酸盐调节基因algQ(algR2)高度相似且可互换。algQ基因在Pa染色体上与另外两个藻酸盐调节因子物理相连,即作为应答调节因子的algR(algR1)和类组蛋白基因algP(algR3)。在本研究中,我们在Pp染色体中鉴定出了相同的基因和相似的基因组织。与pfrA相连的两个基因,分别命名为pprA和pprB,分别与algR和algP相似。构建了pprA和pprB的染色体突变体,结果表明,与pfrA不同,这两个新鉴定的调节因子不参与铁载体调节。pprA基因互补了Pa algR突变体表型,表明它可能参与藻酸盐基因调节。WCS358菌株不产生藻酸盐,但我们通过Southern分析证明,除了pprA和pprB之外,它还拥有algD和algU(algT)基因同源物,这两个基因是藻酸盐生物合成所必需的。使用algD - xylE转录融合,我们观察到algD启动子在WCS358菌株中具有活性,并且绝对需要pfrA。本文讨论了Pp WCS358的所有五个基因都参与藻酸盐生物合成的可能性。