Kang Aram, Tan Mui Hua, Ling Hua, Chang Matthew Wook
Division of Chemical and Biomolecular Engineering, School of Chemical and Biomedical Engineering, Nanyang Technological University, 62 Nanyang Drive, Singapore 637459, Singapore.
Mol Biosyst. 2013 Feb 2;9(2):285-95. doi: 10.1039/c2mb25259g. Epub 2012 Dec 7.
Despite many prior studies on microbial response to oxidative stress, our understanding of microbial tolerance against oxidative stress is currently limited to aerobic conditions, and few engineering strategies have been devised to resolve toxicity issues of oxidative stress under anaerobic conditions. Since biological processes, such as anaerobic fermentation, are frequently hampered by toxicity arising from oxidative stress, increased microbial tolerance against oxidative stress improves the overall productivity and yield of biological processes. Here, we show a systems-level analysis of oxidative stress response of Escherichia coli under anaerobic conditions, and present an engineering strategy to improve oxidative stress tolerance. First, we identified essential cellular mechanisms and regulatory factors underlying oxidative stress response under anaerobic conditions using a transcriptome analysis. In particular, we showed that nitrogen metabolisms and respiratory pathways were differentially regulated in response to oxidative stress under anaerobic and aerobic conditions. Further, we demonstrated that among transcription factors with oxidative stress-derived perturbed activity, the deletion of arcA and arcB significantly improved oxidative stress tolerance under aerobic and anaerobic conditions, respectively, whereas fnr was identified as an essential transcription factor for oxidative stress tolerance under anaerobic conditions. Moreover, we showed that oxidative stress increased the intracellular NADH : NAD(+) ratio under aerobic and anaerobic conditions, which indicates a regulatory role of NADH in oxidative stress tolerance. Based on this finding, we demonstrated that increased NADH availability through fdh1 overexpression significantly improved oxidative stress tolerance under aerobic conditions. Our results here provide novel insight into better understanding of cellular mechanisms underlying oxidative stress tolerance under anaerobic conditions, and into developing strain engineering strategies to enhance microbial tolerance against oxidative stress towards improved biological processes.
尽管之前有许多关于微生物对氧化应激反应的研究,但我们目前对微生物对氧化应激的耐受性的理解仅限于有氧条件,并且很少有工程策略被设计用于解决厌氧条件下氧化应激的毒性问题。由于生物过程,如厌氧发酵,经常受到氧化应激产生的毒性的阻碍,提高微生物对氧化应激的耐受性可以提高生物过程的整体生产力和产量。在这里,我们展示了对大肠杆菌在厌氧条件下氧化应激反应的系统水平分析,并提出了一种提高氧化应激耐受性的工程策略。首先,我们使用转录组分析确定了厌氧条件下氧化应激反应背后的基本细胞机制和调控因子。特别是,我们表明氮代谢和呼吸途径在厌氧和好氧条件下对氧化应激的反应中受到不同的调节。此外,我们证明,在氧化应激导致活性受到干扰的转录因子中,arcA和arcB的缺失分别在好氧和厌氧条件下显著提高了氧化应激耐受性,而fnr被确定为厌氧条件下氧化应激耐受性的必需转录因子。此外,我们表明氧化应激在好氧和厌氧条件下都会增加细胞内NADH : NAD(+)的比率,这表明NADH在氧化应激耐受性中具有调节作用。基于这一发现,我们证明通过过表达fdh1增加NADH的可用性在好氧条件下显著提高了氧化应激耐受性。我们的研究结果为更好地理解厌氧条件下氧化应激耐受性的细胞机制,以及开发菌株工程策略以增强微生物对氧化应激的耐受性从而改善生物过程提供了新的见解。