Schellhorn H E, Hassan H M
Department of Microbiology, North Carolina State University, Raleigh 27695-7624.
J Bacteriol. 1988 Sep;170(9):4286-92. doi: 10.1128/jb.170.9.4286-4292.1988.
Escherichia coli produces two distinct species of catalase, hydroperoxidases I and II, which differ in kinetic properties and regulation. To further examine catalase regulation, a lacZ fusion was placed into one of the genes that is involved in catalase synthesis. Transductional mapping revealed the fusion to be either allelic with or very close to katE, a locus which together with katF controls the synthesis of the aerobically inducible hydroperoxidase (hydroperoxidase II). katE was expressed under anaerobic conditions at levels that were approximately one-fourth of those found in aerobically grown cells and was found to be induced to higher levels in early-stationary-phase cells relative to levels of exponentially growing cells under both anaerobic and aerobic conditions. katE was fully expressed in air and was not further induced when the growth medium was sparged with 100% oxygen. Expression of katE was unaffected by the addition of hydrogen peroxide or by the presence of additional lesions in oxyR or sodA, indicating that it is not part of the oxyR regulon. When katF::Tn10 was introduced into a katE::lacZ strain, beta-galactosidase synthesis was largely eliminated and was no longer inducible, suggesting that katF is a positive regulator of katE expression.
大肠杆菌产生两种不同的过氧化氢酶,即过氧化氢酶I和II,它们在动力学特性和调控方面存在差异。为了进一步研究过氧化氢酶的调控,将一个lacZ融合基因导入参与过氧化氢酶合成的一个基因中。转导作图显示该融合基因要么与katE等位,要么与katE非常接近,katE是一个与katF共同控制需氧诱导型过氧化氢酶(过氧化氢酶II)合成的基因座。katE在厌氧条件下的表达水平约为需氧生长细胞中的四分之一,并且发现在早期稳定期细胞中相对于厌氧和好氧条件下指数生长细胞的水平被诱导到更高水平。katE在空气中完全表达,当生长培养基用100%氧气鼓泡时不再进一步诱导。katE的表达不受过氧化氢添加或oxyR或sodA中其他损伤的影响,表明它不是oxyR调节子的一部分。当将katF::Tn10导入katE::lacZ菌株时,β-半乳糖苷酶的合成基本消除且不再可诱导,这表明katF是katE表达的正调控因子。