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Activation of the glnA, glnK, and nac Promoters as Escherichia coli Undergoes the Transition from Nitrogen Excess Growth to Nitrogen Starvation

机译:大肠埃希氏菌从过量氮生长到饥饿饥饿的过渡过程中glnA,glnK和nac启动子的激活

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摘要

The nitrogen-regulated genes and operons of the Ntr regulon of Escherichia coli are activated by the enhancer-binding transcriptional activator NRI∼P (NtrC∼P). Here, we examined the activation of the glnA, glnK, and nac promoters as cells undergo the transition from growth on ammonia to nitrogen starvation and examined the amplification of NRI during this transition. The results indicate that the concentration of NRI is increased as cells become starved for ammonia, concurrent with the activation of Ntr genes that have less- efficient enhancers than does glnA. A diauxic growth pattern was obtained when E. coli was grown on a low concentration of ammonia in combination with arginine as a nitrogen source, consistent with the hypothesis that Ntr genes other than glnA become activated only upon amplification of the NRI concentration.
机译:大肠杆菌的Ntr调节子的氮调节基因和操纵子被增强子结合转录激活因子NRI-P(NtrC-P)激活。在这里,我们检查了glnA,glnK和nac启动子的激活情况,因为细胞经历了从氨气增长到氮饥饿的转变,并考察了NRI在此转变过程中的扩增。结果表明,随着细胞对氨的缺乏,NRI的浓度会增加,同时激活具有比glnA效率低的增强子的Ntr基因。当大肠杆菌在低浓度的氨水和精氨酸作为氮源的条件下生长时,可得到双辅助生长模式,这与以下假设相符:除glnA以外的其他Ntr基因仅在NRI浓度增加时才被激活。

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