scholarly article | Q13442814 |
P2093 | author name string | Mark P Brynildsen | |
Kristin J Adolfsen | |||
Wen Kang Chou | |||
P2860 | cites work | Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection | Q22122301 |
NO-mediated cytoprotection: instant adaptation to oxidative stress in bacteria | Q24536030 | ||
Nitric oxide dioxygenase: an enzymic function for flavohemoglobin | Q24644801 | ||
Antimicrobial reactive oxygen and nitrogen species: concepts and controversies | Q28283086 | ||
Mycobacterium tuberculosis catalase and peroxidase activities and resistance to oxidative killing in human monocytes in vitro | Q28369434 | ||
The proteasome of Mycobacterium tuberculosis is required for resistance to nitric oxide | Q28487442 | ||
A kinetic platform to determine the fate of nitric oxide in Escherichia coli | Q28487462 | ||
The yjeB (nsrR) gene of Escherichia coli encodes a nitric oxide-sensitive transcriptional regulator | Q28768625 | ||
Absolute metabolite concentrations and implied enzyme active site occupancy in Escherichia coli | Q29615316 | ||
Nitric oxide and macrophage function | Q29615327 | ||
Carbon catabolite repression in bacteria: many ways to make the most out of nutrients | Q29615329 | ||
A comprehensive library of fluorescent transcriptional reporters for Escherichia coli | Q33251466 | ||
The 4-cysteine zinc-finger motif of the RNA polymerase regulator DksA serves as a thiol switch for sensing oxidative and nitrosative stress | Q33739903 | ||
Alkyl hydroperoxide reductase is the primary scavenger of endogenous hydrogen peroxide in Escherichia coli | Q33997228 | ||
Hydrogen peroxide fluxes and compartmentalization inside growing Escherichia coli | Q33997234 | ||
Efficient characterization of high-dimensional parameter spaces for systems biology. | Q34020133 | ||
Deciphering nitric oxide stress in bacteria with quantitative modeling | Q34033314 | ||
Alternative respiratory pathways of Escherichia coli: energetics and transcriptional regulation in response to electron acceptors | Q34064912 | ||
Flavorubredoxin, an inducible catalyst for nitric oxide reduction and detoxification in Escherichia coli | Q34105928 | ||
Respiratory detoxification of nitric oxide by the cytochrome c nitrite reductase of Escherichia coli | Q43964495 | ||
A mechanism by which nitric oxide accelerates the rate of oxidative DNA damage in Escherichia coli | Q44489409 | ||
Escherichia coli Hmp, an "oxygen-binding flavohaemoprotein", produces superoxide anion and self-destructs | Q45039278 | ||
Identification and molecular analysis of oxyR-regulated promoters important for the bacterial adaptation to oxidative stress | Q46451759 | ||
Metabolic control of persister formation in Escherichia coli | Q46473831 | ||
Reduced hydroperoxidase (HPI and HPII) activity in the Deltafur mutant contributes to increased sensitivity to UVA radiation in Escherichia coli. | Q46476066 | ||
An integrated network analysis identifies how ArcAB enables metabolic oscillations in the nitric oxide detoxification network of Escherichia coli. | Q47909181 | ||
Flavin-dependent alkyl hydroperoxide reductase from Salmonella typhimurium. 1. Purification and enzymatic activities of overexpressed AhpF and AhpC proteins | Q50140552 | ||
Persister Heterogeneity Arising from a Single Metabolic Stress. | Q51816586 | ||
Catalases HPI and HPII in Escherichia coli are induced independently. | Q54790507 | ||
The nitrosative stress response of Staphylococcus aureus is required for resistance to innate immunity | Q57426590 | ||
Loss of DksA leads to multi-faceted impairment of nitric oxide detoxification by Escherichia coli | Q58571753 | ||
Steady-state and Transient Kinetics ofEscherichia coliNitric-oxide Dioxygenase (Flavohemoglobin) | Q59599927 | ||
The flavohaemoglobin (HMP) of Escherichia coli generates superoxide in vitro and causes oxidative stress in vivo | Q71034286 | ||
Nitric oxide diffusion in membranes determined by fluorescence quenching | Q71097843 | ||
Kinetics of nitric oxide and hydrogen peroxide production and formation of peroxynitrite during the respiratory burst of human neutrophils | Q72315469 | ||
Flavohemoglobin Hmp affords inducible protection for Escherichia coli respiration, catalyzed by cytochromes bo' or bd, from nitric oxide | Q74071486 | ||
Modeling the reactions of superoxide and myeloperoxidase in the neutrophil phagosome: implications for microbial killing | Q79317154 | ||
DksA-DnaJ redox interactions provide a signal for the activation of bacterial RNA polymerase | Q93079740 | ||
Control of redox balance by the stringent response regulatory protein promotes antioxidant defenses of Salmonella. | Q34299203 | ||
DksA affects ppGpp induction of RpoS at a translational level | Q34316573 | ||
Direct inhibition by nitric oxide of the transcriptional ferric uptake regulation protein via nitrosylation of the iron | Q34429282 | ||
Protection against deleterious nitrogen compounds: role of σS-dependent small RNAs encoded adjacent to sdiA. | Q34526027 | ||
Nutrient transitions are a source of persisters in Escherichia coli biofilms | Q35131052 | ||
Futile cycling increases sensitivity toward oxidative stress in Escherichia coli | Q35602663 | ||
Catalase (KatA) and alkyl hydroperoxide reductase (AhpC) have compensatory roles in peroxide stress resistance and are required for survival, persistence, and nasal colonization in Staphylococcus aureus | Q35634601 | ||
A Kinetic Platform to Determine the Fate of Hydrogen Peroxide in Escherichia coli | Q35834574 | ||
ppGpp is the major source of growth rate control in E. coli | Q36015916 | ||
Why do bacteria use so many enzymes to scavenge hydrogen peroxide? | Q36147012 | ||
Nitric oxide potentiates hydrogen peroxide-induced killing of Escherichia coli. | Q36365394 | ||
Antimicrobial actions of the NADPH phagocyte oxidase and inducible nitric oxide synthase in experimental salmonellosis. I. Effects on microbial killing by activated peritoneal macrophages in vitro | Q36368785 | ||
Discovery and dissection of metabolic oscillations in the microaerobic nitric oxide response network of Escherichia coli | Q36742674 | ||
DksA-Dependent Transcriptional Regulation in Salmonella Experiencing Nitrosative Stress | Q36750337 | ||
Redundant hydrogen peroxide scavengers contribute to Salmonella virulence and oxidative stress resistance. | Q37247851 | ||
A novel protein protects bacterial iron-dependent metabolism from nitric oxide | Q37253002 | ||
Antimicrobial mechanisms of phagocytes and bacterial evasion strategies | Q37445493 | ||
The EcoCyc database: reflecting new knowledge about Escherichia coli K-12. | Q37556663 | ||
Bacterial manipulation of innate immunity to promote infection. | Q37675898 | ||
Hydrogen peroxide: a Jekyll and Hyde signalling molecule | Q37942731 | ||
Connecting the chemical and biological properties of nitric oxide | Q37997080 | ||
Bioconversion of lignocellulose: inhibitors and detoxification. | Q38077292 | ||
A reassessment of the FNR regulon and transcriptomic analysis of the effects of nitrate, nitrite, NarXL, and NarQP as Escherichia coli K12 adapts from aerobic to anaerobic growth | Q38317337 | ||
A novel mechanism for upregulation of the Escherichia coli K-12 hmp (flavohaemoglobin) gene by the 'NO releaser', S-nitrosoglutathione: nitrosation of homocysteine and modulation of MetR binding to the glyA-hmp intergenic region. | Q38332558 | ||
NsrR targets in the Escherichia coli genome: new insights into DNA sequence requirements for binding and a role for NsrR in the regulation of motility | Q38351703 | ||
Oxidative stress modulates the nitric oxide defense promoted by Escherichia coli flavorubredoxin | Q39352823 | ||
The steady-state internal redox state (NADH/NAD) reflects the external redox state and is correlated with catabolic adaptation in Escherichia coli | Q39495135 | ||
NO sensing by FNR: regulation of the Escherichia coli NO-detoxifying flavohaemoglobin, Hmp. | Q39647563 | ||
Flavohemoglobin Hmp protects Salmonella enterica serovar typhimurium from nitric oxide-related killing by human macrophages. | Q39655749 | ||
Nitric oxide, nitrite, and Fnr regulation of hmp (flavohemoglobin) gene expression in Escherichia coli K-12. | Q39842767 | ||
Utilization of gluconate by Escherichia coli. A role of adenosine 3′:5′-cyclic monophosphate in the induction of gluconate catabolism | Q39966592 | ||
Control of the Sequential Utilization of Glucose and Fructose by Escherichia coli | Q40009152 | ||
Nontargeted Metabolomics Reveals the Multilevel Response to Antibiotic Perturbations. | Q40216617 | ||
Experimental and computational assessment of conditionally essential genes in Escherichia coli | Q41063583 | ||
An ensemble-guided approach identifies ClpP as a major regulator of transcript levels in nitric oxide-stressed Escherichia coli | Q41139105 | ||
Construction and Experimental Validation of a Quantitative Kinetic Model of Nitric Oxide Stress in Enterohemorrhagic Escherichia coli O157:H7. | Q41704567 | ||
The nitric oxide reductase of enterohaemorrhagic Escherichia coli plays an important role for the survival within macrophages | Q43451353 | ||
Pro-oxidative synergic bactericidal effect of NO: kinetics and inhibition by nitroxides | Q43523659 | ||
P433 | issue | 14 | |
P921 | main subject | prioritization | Q11888847 |
P577 | publication date | 2019-06-21 | |
P1433 | published in | Journal of Bacteriology | Q478419 |
P1476 | title | Transcriptional Regulation Contributes to Prioritized Detoxification of Hydrogen Peroxide over Nitric Oxide | |
P478 | volume | 201 |
Q92758270 | Flavohaemoglobin: the pre-eminent nitric oxide-detoxifying machine of microorganisms | cites work | P2860 |
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