Galimand M, Gamper M, Zimmermann A, Haas D
Mikrobiologisches Institut, Eidgenössische Technische Hochschule, Zürich, Switzerland.
J Bacteriol. 1991 Mar;173(5):1598-606. doi: 10.1128/jb.173.5.1598-1606.1991.
A mutant of Pseudomonas aeruginosa was characterized which could not grow anaerobically with nitrate as the terminal electron acceptor or with arginine as the sole energy source. In this anr mutant, nitrate reductase and arginine deiminase were not induced by oxygen limitation. The anr mutation was mapped in the 60-min region of the P. aeruginosa chromosome. A 1.3-kb chromosomal fragment from P. aeruginosa complemented the anr mutation and also restored anaerobic growth of an Escherichia coli fnr deletion mutant on nitrate medium, indicating that the 1.3-kb fragment specifies an FNR-like regulatory protein. The arcDABC operon, which encodes the arginine deiminase pathway enzymes of P. aeruginosa, was rendered virtually noninducible by a deletion or an insertion in the -40 region of the arc promoter. This -40 sequence (TTGAC....ATCAG) strongly resembled the consensus FNR-binding site (TTGAT....ATCAA) of E. coli. The cloned arc operon was expressed at low levels in E. coli; nevertheless, some FNR-dependent anaerobic induction could be observed. An FNR-dependent E. coli promoter containing the consensus FNR-binding site was expressed well in P. aeruginosa and was regulated by oxygen limitation. These findings suggest that P. aeruginosa and E. coli have similar mechanisms of anaerobic control.
对一株铜绿假单胞菌突变体进行了表征,该突变体在以硝酸盐作为末端电子受体进行厌氧生长或仅以精氨酸作为能源时无法生长。在这个anr突变体中,硝酸盐还原酶和精氨酸脱亚氨酶不会因氧限制而被诱导。anr突变被定位在铜绿假单胞菌染色体的60分钟区域。来自铜绿假单胞菌的一个1.3 kb染色体片段互补了anr突变,并且还恢复了大肠杆菌fnr缺失突变体在硝酸盐培养基上的厌氧生长,这表明该1.3 kb片段指定了一种FNR样调节蛋白。编码铜绿假单胞菌精氨酸脱亚氨酶途径酶的arcDABC操纵子,由于在arc启动子的 -40区域缺失或插入而几乎无法被诱导。这个 -40序列(TTGAC....ATCAG)与大肠杆菌的共有FNR结合位点(TTGAT....ATCAA)非常相似。克隆的arc操纵子在大肠杆菌中低水平表达;然而,可以观察到一些FNR依赖的厌氧诱导。一个包含共有FNR结合位点的FNR依赖的大肠杆菌启动子在铜绿假单胞菌中表达良好,并受氧限制调控。这些发现表明铜绿假单胞菌和大肠杆菌具有相似的厌氧控制机制。