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The Gene yggE Functions in Restoring Physiological Defects of Escherichia coli Cultivated under Oxidative Stress Conditions†

机译:基因yggE在恢复氧化应激条件下培养的大肠杆菌的生理缺陷中的功能†

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摘要

DNA microarray analysis showed that yfiD, yggB, and yggE genes were up-regulated when superoxide dismutase (SOD)-deficient Escherichia coli IM303 (I4) was cultivated under the oxidative stress generated by photoexcited TiO2, and pYFD, pYGB, and pYGE were constructed by inserting the respective genes into a pUC 19 vector. The content of reactive oxygen species (ROS) in IM303 (I4) cells carrying pYGE was reduced to 31% of ROS content in the control cells with pUC 19. In the culture of wild-type strain, E. coli MM294, in the medium with paraquat (10 μmol/l), maximum specific growth rate of the cells with pYGE was about five times higher than that of the control cells, with a decreased ROS content in the former cells. The introduction of pYGE also suppressed the occurrence of the cells with altered amino acid requirement in the culture of MM294 cells with paraquat.
机译:DNA微阵列分析显示,在光激发TiO2产生的氧化胁迫下培养超氧化物歧化酶(SOD)缺陷的大肠杆菌IM303(I4)时,yfiD,yggB和yggE基因上调,并构建了pYFD,pYGB和pYGE通过将各个基因插入pUC 19载体中。在携带pYGE的IM303(I4)细胞中,带有pYGE的IM303(I4)细胞中的活性氧(ROS)含量降至对照细胞中ROS含量的31%。在培养基中培养野生型大肠杆菌MM294使用百草枯(10μmol/ l)时,pYGE细胞的最大比生长速率比对照细胞高约5倍,前者的ROS含量降低。 pYGE的引入还抑制了百草枯MM294细胞培养中氨基酸需求改变的细胞的发生。

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