Futile cycling increases sensitivity toward oxidative stress in Escherichia coli

被引:56
作者
Adolfsen, Kristin J. [1 ]
Brynildsen, Mark P. [1 ]
机构
[1] Princeton Univ, Dept Chem & Biol Engn, Princeton, NJ 08544 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Reactive oxygen species; Oxidative stress; Futile cycle; Hydrogen peroxide; Metabolism; ALKYL HYDROPEROXIDE REDUCTASE; NEUTROPHIL NADPH OXIDASE; ENDOGENOUS HYDROGEN-PEROXIDE; SITE-DIRECTED MUTAGENESIS; SUPEROXIDE-DISMUTASE; MYCOBACTERIUM-TUBERCULOSIS; CATALASE KATA; REPAIR; DNA; METABOLISM;
D O I
10.1016/j.ymben.2015.02.006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Reactive oxygen species (ROS) are toxic molecules utilized by the immune system to combat invading pathogens. Recent evidence suggests that inefficiencies in ATP production or usage can lead to increased endogenous ROS production and sensitivity to oxidative stress in bacteria. With this as inspiration, and knowledge that ATP is required for a number of DNA repair mechanisms, we hypothesized that futile cycling would be an effective way to increase sensitivity to oxidative stress. We developed a mixed integer linear optimization framework to identify experimentally-tractable futile cycles, and confirmed metabolic modeling predictions that futile cycling depresses growth rate, and increases both O-2 consumption and ROS production per biomass generated. Further, intracellular ATP was decreased and sensitivity to oxidative stress increased in all actively cycling strains compared to their catalytically inactive controls. This research establishes a fundamental connection between ATP metabolism, endogenous ROS production, and tolerance toward oxidative stress in bacteria. (C) 2015 International Metabolic Engineering Society. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:26 / 35
页数:10
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