首页> 美国卫生研究院文献>Journal of Bacteriology >The napF and narG Nitrate Reductase Operons in Escherichia coli Are Differentially Expressed in Response to Submicromolar Concentrations of Nitrate but Not Nitrite
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The napF and narG Nitrate Reductase Operons in Escherichia coli Are Differentially Expressed in Response to Submicromolar Concentrations of Nitrate but Not Nitrite

机译:响应于亚微摩尔浓度的硝酸盐而非亚硝酸盐差异表达大肠杆菌中的napF和narG硝酸盐还原酶操纵子

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摘要

Escherichia coli synthesizes two biochemically distinct nitrate reductase enzymes, a membrane-bound enzyme encoded by the narGHJI operon and a periplasmic cytochrome c-linked nitrate reductase encoded by the napFDAGHBC operon. To address why the cell makes these two enzymes, continuous cell culture techniques were used to examine napF and narG gene expression in response to different concentrations of nitrate and/or nitrite. Expression of the napF-lacZ and narG-lacZ reporter fusions in strains grown at different steady-state levels of nitrate revealed that the two nitrate reductase operons are differentially expressed in a complementary pattern. The napF operon apparently encodes a “low-substrate-induced” reductase that is maximally expressed only at low levels of nitrate. Expression is suppressed under high-nitrate conditions. In contrast, the narGHJI operon is only weakly expressed at low nitrate levels but is maximally expressed when nitrate is elevated. The narGHJI operon is therefore a “high-substrate-induced” operon that somehow provides a second and distinct role in nitrate metabolism by the cell. Interestingly, nitrite, the end product of each enzyme, had only a minor effect on the expression of either operon. Finally, nitrate, but not nitrite, was essential for repression of napF gene expression. These studies reveal that nitrate rather than nitrite is the primary signal that controls the expression of these two nitrate reductase operons in a differential and complementary fashion. In light of these findings, prior models for the roles of nitrate and nitrite in control of narG and napF expression must be reconsidered.
机译:大肠杆菌合成两种生物化学上不同的硝酸盐还原酶,一种是由narGHJI操纵子编码的膜结合酶,另一种是由napFDAGHBC操纵子编码的周质细胞色素c-连锁的硝酸盐还原酶。为了解决为什么细胞产生这两种酶的原因,连续细胞培养技术被用来检查napF和narG基因表达,以响应不同浓度的硝酸盐和/或亚硝酸盐。 napF-lacZ和narG-lacZ报告基因融合体在不同硝酸盐稳态水平下生长的菌株中的表达表明,两个硝酸盐还原酶操纵子以互补模式差异表达。 napF操纵子显然编码“低底物诱导的”还原酶,其仅在低水平的硝酸盐下最大表达。在高硝酸盐条件下表达受到抑制。相反,narGHJI操纵子仅在低硝酸盐水平下弱表达,而在硝酸盐升高时最大表达。因此,narGHJI操纵子是“高底物诱导的”操纵子,以某种方式在细胞的硝酸盐代谢中提供了第二种独特的作用。有趣的是,每种酶的终产物亚硝酸盐对任一操纵子的表达只产生很小的影响。最后,硝酸盐而非亚硝酸盐对抑制napF基因表达至关重要。这些研究表明,硝酸盐而不是亚硝酸盐是以差异和互补方式控制这两个硝酸盐还原酶操纵子表达的主要信号。根据这些发现,必须重新考虑硝酸盐和亚硝酸盐在narG和napF表达控制中的作用的先前模型。

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