Conversion of NO2 to NO by reduced coenzyme F420 protects mycobacteria from nitrosative damage.
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Metabolic engineering of cofactor F420 production in Mycobacterium smegmatisUnexpected abundance of coenzyme F(420)-dependent enzymes in Mycobacterium tuberculosis and other actinobacteriaNitrogen dioxide is a positive regulator of plant growth.Rv0132c of Mycobacterium tuberculosis encodes a coenzyme F420-dependent hydroxymycolic acid dehydrogenaseF420H2-dependent degradation of aflatoxin and other furanocoumarins is widespread throughout the actinomycetalesThe genome of the ammonia-oxidizing Candidatus Nitrososphaera gargensis: insights into metabolic versatility and environmental adaptations.Tat-dependent translocation of an F420-binding protein of Mycobacterium tuberculosis.Mycobacterial survival strategies in the phagosome: defence against host stresses.Biosynthetic versatility and coordinated action of 5'-deoxyadenosyl radicals in deazaflavin biosynthesisNo effect of pure oxygen inhalation on headache induced by glyceryl trinitrate.SIRT3 Mediates the Antioxidant Effect of Hydrogen Sulfide in Endothelial Cells.Physiology, Biochemistry, and Applications of F420- and Fo-Dependent Redox Reactions.F420H2 Is Required for Phthiocerol Dimycocerosate Synthesis in Mycobacteria.Genetic-and-Epigenetic Interspecies Networks for Cross-Talk Mechanisms in Human Macrophages and Dendritic Cells during MTB Infection.The redox cofactor F420 protects mycobacteria from diverse antimicrobial compounds and mediates a reductive detoxification system.Proteomics and comparative genomics of Nitrososphaera viennensis reveal the core genome and adaptations of archaeal ammonia oxidizers.Differentiating between live and dead Mycobacterium smegmatis using autofluorescence.Oxidative Phosphorylation as a Target Space for Tuberculosis: Success, Caution, and Future Directions.Cloning, expression, purification, crystallization and preliminary X-ray studies of the C-terminal domain of Rv3262 (FbiB) from Mycobacterium tuberculosis.Substrate specificity of the deazaflavin-dependent nitroreductase from Mycobacterium tuberculosis responsible for the bioreductive activation of bicyclic nitroimidazoles.Discovery and characterization of an F420-dependent glucose-6-phosphate dehydrogenase (Rh-FGD1) from Rhodococcus jostii RHA1.Elongation of the Poly-γ-glutamate Tail of F420 Requires Both Domains of the F420:γ-Glutamyl Ligase (FbiB) of Mycobacterium tuberculosis.Maximizing bactericidal activity with combinations of bioreduced drugs.OsmC proteins of Mycobacterium tuberculosis and Mycobacterium smegmatis protect against organic hydroperoxide stress.Systems level mapping of metabolic complexity in Mycobacterium tuberculosis to identify high-value drug targets.Nitrogen dioxide regulates organ growth by controlling cell proliferation and enlargement in Arabidopsis.Nitrogen dioxide is reduced to NO by F420C-C bond forming radical SAM enzymes involved in the construction of carbon skeletons of cofactors and natural products.Renewable Molecular Flasks with NADH Models: Combination of Light-Driven Proton Reduction and Biomimetic Hydrogenation of Benzoxazinones.
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Conversion of NO2 to NO by reduced coenzyme F420 protects mycobacteria from nitrosative damage.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 26 March 2009
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vedecký článok
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vetenskaplig artikel
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Conversion of NO2 to NO by red ...... teria from nitrosative damage.
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Conversion of NO2 to NO by red ...... teria from nitrosative damage.
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Conversion of NO2 to NO by red ...... teria from nitrosative damage.
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Conversion of NO2 to NO by red ...... teria from nitrosative damage.
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Conversion of NO2 to NO by red ...... teria from nitrosative damage.
@en
Conversion of NO2 to NO by red ...... teria from nitrosative damage.
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Conversion of NO2 to NO by red ...... teria from nitrosative damage.
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Biswarup Mukhopadhyay
Endang Purwantini
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10.1073/PNAS.0812883106
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P577
2009-03-26T00:00:00Z