Ye R W, Haas D, Ka J O, Krishnapillai V, Zimmermann A, Baird C, Tiedje J M
Department of Microbiology, Michigan State University, East Lansing 48824, USA.
J Bacteriol. 1995 Jun;177(12):3606-9. doi: 10.1128/jb.177.12.3606-3609.1995.
The Pseudomonas aeruginosa gene anr, which encodes a structural and functional analog of the anaerobic regulator Fnr in Escherichia coli, was mapped to the SpeI fragment R, which is at about 59 min on the genomic map of P. aeruginosa PAO1. Wild-type P. aeruginosa PAO1 grew under anaerobic conditions with nitrate, nitrite, and nitrous oxide as alternative electron acceptors. An anr deletion mutant, PAO6261, was constructed. It was unable to grow with these alternative electron acceptors; however, its ability to denitrify was restored upon the introduction of the wild-type anr gene. In addition, the activities of two enzymes in the denitrification pathway, nitrite reductase and nitric oxide reductase, were not detectable under oxygen-limiting conditions in strain PAO6261 but were restored when complemented with the anr+ gene. These results indicate that the anr gene product plays a key role in anaerobically activating the entire denitrification pathway.
铜绿假单胞菌基因anr编码一种与大肠杆菌厌氧调节因子Fnr结构和功能类似的蛋白,该基因被定位到SpeI片段R上,此片段位于铜绿假单胞菌PAO1基因组图谱约59分钟处。野生型铜绿假单胞菌PAO1在厌氧条件下能够以硝酸盐、亚硝酸盐和一氧化二氮作为替代电子受体进行生长。构建了一个anr缺失突变体PAO6261。它无法利用这些替代电子受体进行生长;然而,在导入野生型anr基因后,其反硝化能力得以恢复。此外,在PAO6261菌株中,在限氧条件下无法检测到反硝化途径中两种酶(亚硝酸还原酶和一氧化氮还原酶)的活性,但在用anr+基因进行互补时,这些酶的活性得以恢复。这些结果表明,anr基因产物在厌氧激活整个反硝化途径中起关键作用。