Jensen P R, Michelsen O
Department of Microbiology, Technical University of Denmark, Lyngby.
J Bacteriol. 1992 Dec;174(23):7635-41. doi: 10.1128/jb.174.23.7635-7641.1992.
The membrane-bound H(+)-ATPase plays a key role in free-energy transduction of biological systems. We report how the carbon and energy metabolism of Escherichia coli changes in response to deletion of the atp operon that encodes this enzyme. Compared with the isogenic wild-type strain, the growth rate and growth yield were decreased less than expected for a shift from oxidative phosphorylation to glycolysis alone as a source of ATP. Moreover, the respiration rate of a atp deletion strain was increased by 40% compared with the wild-type strain. This result is surprising, since the atp deletion strain is not able to utilize the resulting proton motive force for ATP synthesis. Indeed, the ratio of ATP concentration to ADP concentration was decreased from 19 in the wild type to 7 in the atp mutant, and the membrane potential of the atp deletion strain was increased by 20%, confirming that the respiration rate was not controlled by the magnitude of the opposing membrane potential. The level of type b cytochromes in the mutant cells was 80% higher than the level in the wild-type cells, suggesting that the increased respiration was caused by an increase in the expression of the respiratory genes. The atp deletion strain produced twice as much by-product (acetate) and exhibited increased flow through the tricarboxylic acid cycle and the glycolytic pathway. These three changes all lead to an increase in substrate level phosphorylation; the first two changes also lead to increased production of reducing equivalents. We interpret these data as indicating that E. coli makes use of its ability to respire even if it cannot directly couple this ability to ATP synthesis; by respiring away excess reducing equivalents E. coli enhances substrate level ATP synthesis.
膜结合H(+) -ATP酶在生物系统的自由能转导中起关键作用。我们报告了编码该酶的atp操纵子缺失时,大肠杆菌的碳代谢和能量代谢如何变化。与同基因野生型菌株相比,生长速率和生长产量的降低幅度小于仅从氧化磷酸化转变为糖酵解作为ATP来源时预期的降幅。此外,与野生型菌株相比,atp缺失菌株的呼吸速率提高了40%。这一结果令人惊讶,因为atp缺失菌株无法利用产生的质子动力势进行ATP合成。实际上,ATP浓度与ADP浓度的比值从野生型的19降至atp突变体的7,atp缺失菌株的膜电位增加了20%,这证实了呼吸速率不受相反膜电位大小的控制。突变细胞中b型细胞色素的水平比野生型细胞中的水平高80%,表明呼吸增加是由呼吸基因表达增加引起的。atp缺失菌株产生的副产物(乙酸)是原来的两倍,并且通过三羧酸循环和糖酵解途径的通量增加。这三个变化都导致底物水平磷酸化增加;前两个变化还导致还原当量的产生增加。我们将这些数据解释为表明大肠杆菌即使不能将呼吸能力直接与ATP合成偶联,也会利用其呼吸能力;通过呼吸消耗过量的还原当量,大肠杆菌增强了底物水平的ATP合成。