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. 2004 Jan 20;101(3):745-50.
doi: 10.1073/pnas.0307741100. Epub 2004 Jan 12.

Prominent roles of the NorR and Fur regulators in the Escherichia coli transcriptional response to reactive nitrogen species

Affiliations

Prominent roles of the NorR and Fur regulators in the Escherichia coli transcriptional response to reactive nitrogen species

Partha Mukhopadhyay et al. Proc Natl Acad Sci U S A. .

Abstract

We examined the genomewide transcriptional responses of Escherichia coli treated with nitrosylated glutathione or the nitric oxide (NO)-generator acidified sodium nitrite (NaNO(2)) during aerobic growth. These assays showed that NorR, a homolog of NO-responsive transcription factors in Ralstonia eutrophus, and Fur, the global repressor of ferric ion uptake, are major regulators of the response to reactive nitrogen species. In contrast, SoxR and OxyR, regulators of the E. coli defenses against superoxide-generating compounds and hydrogen peroxide, respectively, have minor roles. Moreover, additional regulators of the E. coli response to reactive nitrogen species remain to be identified because several of the induced genes were regulated normally in norR, fur, soxRS, and oxyR mutant strains. We propose that the E. coli transcriptional response to reactive nitrogen species is a composite response mediated by the modification of multiple transcription factors containing iron or redox-active cysteines, some specifically designed to sense NO and its derivatives and others that are collaterally activated by the reactive nitrogen species.

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Figures

Fig. 1.
Fig. 1.
Primer extension assays of norV, fes, ydiE, grxA, ahpC, katG, sodA, uspA, hmpA, and ygbA expression in wild-type and isogenic regulatory mutants. The parent MG1655 and Δfur, ΔnorR, ΔoxyR, ΔsoxRS, and ΔmetR mutant strains were grown to OD600 = 0.4–0.6 in LB medium, pH 6. Cultures were split, and aliquots were left untreated or treated with 1 mM H2O2, NaNO2, or GSNO. After 5 min, total RNA was isolated from each untreated and treated culture. All assays were carried out by using 5 μg of the same RNA preparation.
Fig. 2.
Fig. 2.
Primer extension assays of norV, ydiE, soxS, grxA, hmpA, and ygbA expression in wild-type cells treated with 0.01, 0.1, 1, and 5 mM GSNO or NaNO2 for 5 min (A) or with 1 mM GSNO or NaNO2 for 5, 10, 20, 30, 40, 50, 60, or 90 min (B). MG1655 cells were grown to OD600 = 0.4 in LB medium, pH 6. Aliquots of the cultures were left untreated or treated with the indicated concentrations of GSNO or NaNO2 and harvested after the indicated times. Total RNA was isolated from 15 ml of each untreated and treated culture, and 5 μg of each RNA sample was used in each primer extension reaction by using primers to the indicated genes.
Fig. 3.
Fig. 3.
Primer extension assays of norV expression in aerobic and anaerobic wild-type cells treated with 1 mM NaNO2. MG1655 cells were grown aerobically to OD600 = 0.1, 0.4, and 1.0 or anaerobically to OD600 = 0.4 and treated with 1 mM NaNO2 for 0, 5, 20, 60, 90, 120, 150, or 180 min. Total RNA was isolated from 15–30 ml of each untreated and treated culture; 5 μg of each RNA sample was used in each primer extension reaction using the norV-specific primer, and 1 μg of each RNA sample was used in Northern analysis for the 6S RNA.

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