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首页> 外文期刊>Applied Microbiology and Biotechnology >Construction of a sodA :: luxCDABE fusion Escherichia coli: comparison with a katG fusion strain through their responses to oxidative stresses
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Construction of a sodA :: luxCDABE fusion Escherichia coli: comparison with a katG fusion strain through their responses to oxidative stresses

机译:sodA :: luxCDABE融合大肠杆菌的构建:通过对氧化应激的反应与katG融合菌株进行比较

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摘要

A recombinant bioluminescent Escherichia coli strain, EBHJ, (sodA::luxCDABE), containing the promoter for the manganese superoxide dismutase (sodA) gene fused to the Vibrio fischeri luxCDABE operon, was successfully constructed and characterized. Redox-cycling agents, such as paraquat and chromium. strongly induced a sodA- regulated response in dose-dependent manners, resulting in an increase of the bioluminescence. In a comparison with an existing oxidative stress responsive strain, DPD2511 (katG::luxCDABE), which is sensitive to H2O2, the mechanism of chemicals that cause oxidative damage was elucidated via the key transcriptional factors involved in induction of the sodA and katG promoters, i.e. SoxRS and OxyR, respectively. It was found that responses from the katG- and sodA-based strains were significantly different dependent upon the chemicals being tested. Therefore, EBHJ, alone or in parallel with DPD2511, can be used to characterize and monitor chemicals that cause oxidative damage. [References: 18]
机译:成功构建并鉴定了重组生物发光大肠杆菌菌株EBHJ(sodA :: luxCDABE),该菌株含有与费氏弧菌luxCDABE操纵子融合的锰超氧化物歧化酶(sodA)基因的启动子。氧化还原循环剂,例如百草枯和铬。以剂量依赖性方式强烈诱导sodA调节的反应,导致生物发光的增加。与现有的对H2O2敏感的氧化应激反应菌株DPD2511(katG :: luxCDABE)进行比较,通过诱导sodA和katG启动子的关键转录因子阐明了引起氧化损伤的化学物质的机制,即分别为SoxRS和OxyR。已经发现,基于katG和sodA的菌株的响应明显不同,取决于所测试的化学品。因此,EBHJ可以单独使用,也可以与DPD2511并行使用,以表征和监控引起氧化损伤的化学物质。 [参考:18]

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