Osamura Tatsuya, Kawakami Takuro, Kido Reiko, Ishii Masaharu, Arai Hiroyuki
Department of Biotechnology, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.
PLoS One. 2017 May 18;12(5):e0177957. doi: 10.1371/journal.pone.0177957. eCollection 2017.
Pseudomonas aeruginosa has one A-type (caa3) and multiple C-type (cbb3) cytochrome c oxidases as well as two quinol oxidases for aerobic respiration. The caa3 oxidase is highly efficient in creating a proton gradient across the cell membrane, but it is not expressed under normal growth conditions and its physiological role has not been investigated. In the present study, a mutant strain deficient in the coxBA-PA0107-coxC genes encoding caa3 exhibited normal growth under any test conditions, but it had low relative fitness under carbon starvation conditions, indicating that the expression of caa3 is advantageous under starvation conditions. A mutant that lacked four terminal oxidase gene clusters except for the cox genes was unable to grow aerobically because of low expression level of caa3. However, suppressor mutants that grew aerobically using caa3 as the only terminal oxidase emerged after aerobic subculturing. Analyses of the suppressor mutants revealed that a mutation of roxS encoding a sensor kinase of a two-component regulator RoxSR was necessary for the aerobic growth in synthetic medium. Two additional mutations in the 5'-flanking region of coxB were necessary for the aerobic growth in LB medium. Although the expression level of caa3 was higher in the suppressor mutants, their growth rates were lower than when the other terminal oxidases were utilized, suggesting that caa3 was not suited for utilization as the only terminal oxidase. Overexpression of the cox genes also inhibited the aerobic growth of the wild-type strain. These results indicate that caa3 is tightly regulated to be expressed only under starvation conditions at low level and it functions in cooperation with other terminal oxidases to facilitate survival in nutrient starvation conditions.
铜绿假单胞菌有一个 A 型(caa3)和多个 C 型(cbb3)细胞色素 c 氧化酶以及两个用于有氧呼吸的喹啉氧化酶。caa3 氧化酶在跨细胞膜产生质子梯度方面效率很高,但在正常生长条件下不表达,其生理作用尚未得到研究。在本研究中,编码 caa3 的 coxBA - PA0107 - coxC 基因缺失的突变株在任何测试条件下均表现出正常生长,但在碳饥饿条件下相对适应性较低,这表明 caa3 的表达在饥饿条件下具有优势。一个除了 cox 基因外缺少四个末端氧化酶基因簇的突变体由于 caa3 表达水平低而无法进行有氧生长。然而,在有氧传代培养后出现了以 caa3 作为唯一末端氧化酶进行有氧生长的抑制突变体。对抑制突变体的分析表明,编码双组分调节因子 RoxSR 的传感器激酶的 roxS 突变对于在合成培养基中进行有氧生长是必需的。coxB 的 5'侧翼区域的另外两个突变对于在 LB 培养基中进行有氧生长是必需的。尽管抑制突变体中 caa3 的表达水平较高,但其生长速率低于利用其他末端氧化酶时的生长速率,这表明 caa3 不适合作为唯一的末端氧化酶使用。cox 基因的过表达也抑制了野生型菌株的有氧生长。这些结果表明,caa3 受到严格调控,仅在饥饿条件下低水平表达,并且它与其他末端氧化酶协同作用,以促进在营养饥饿条件下的存活。