Mycobacterium tuberculosis nitrogen assimilation and host colonization require aspartate.
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The complex amino acid diet of Francisella in infected macrophagesMycobacterial genes essential for the pathogen's survival in the hostMycobacterium tuberculosis exploits asparagine to assimilate nitrogen and resist acid stress during infectionUnravelling the Secrets of Mycobacterial Cidality through the Lens of AntisenseEmerging Approaches to Tuberculosis Drug Development: At Home in the Metabolome.Higher resource level promotes virulence in an environmentally transmitted bacterial fish pathogen.Whole genome sequencing distinguishes between relapse and reinfection in recurrent leprosy cases.Manipulation of the mononuclear phagocyte system by Mycobacterium tuberculosis.Importance of branched-chain amino acid utilization in Francisella intracellular adaptationComprehensive insights into transcriptional adaptation of intracellular mycobacteria by microbe-enriched dual RNA sequencingMycobacterium tuberculosis metabolismDefining the nitrogen regulated transcriptome of Mycobacterium smegmatis using continuous cultureMycobacteria, metals, and the macrophageGlutamate Dehydrogenase Is Required by Mycobacterium bovis BCG for Resistance to Cellular Stress.Essential roles of methionine and S-adenosylmethionine in the autarkic lifestyle of Mycobacterium tuberculosis.A central role for aspartate in Mycobacterium tuberculosis physiology and virulence.Minding the gaps: metabolomics mends functional genomics.Importance of Metabolic Adaptations in Francisella Pathogenesis.Nitrogen metabolism in Mycobacterium tuberculosis physiology and virulence.Illumination of growth, division and secretion by metabolic labeling of the bacterial cell surface.Integration of Metabolomics and Transcriptomics Reveals a Complex Diet of Mycobacterium tuberculosis during Early Macrophage Infection.Metabolic crosstalk between host and pathogen: sensing, adapting and competing.Amino acid capture and utilization within the Mycobacterium tuberculosis phagosome.Mycobacterium tuberculosis in the Face of Host-Imposed Nutrient Limitation.Acetate Dissimilation and Assimilation in Mycobacterium tuberculosis Depend on Carbon Availability.Dynamic exometabolome analysis reveals active metabolic pathways in non-replicating mycobacteria.Deciphering the metabolic response of Mycobacterium tuberculosis to nitrogen stress.Lipid metabolism and its implication in mycobacteria-host interaction.Amino Acids As Mediators of Metabolic Cross Talk between Host and Pathogen.Updated and standardized genome-scale reconstruction of Mycobacterium tuberculosis H37Rv, iEK1011, simulates flux states indicative of physiological conditions.
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Mycobacterium tuberculosis nitrogen assimilation and host colonization require aspartate.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 29 September 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Mycobacterium tuberculosis nitrogen assimilation and host colonization require aspartate.
@en
Mycobacterium tuberculosis nitrogen assimilation and host colonization require aspartate.
@nl
type
label
Mycobacterium tuberculosis nitrogen assimilation and host colonization require aspartate.
@en
Mycobacterium tuberculosis nitrogen assimilation and host colonization require aspartate.
@nl
prefLabel
Mycobacterium tuberculosis nitrogen assimilation and host colonization require aspartate.
@en
Mycobacterium tuberculosis nitrogen assimilation and host colonization require aspartate.
@nl
P2093
P2860
P50
P356
P1476
Mycobacterium tuberculosis nitrogen assimilation and host colonization require aspartate.
@en
P2093
Alexandre Gouzy
Antonio Peixoto
Florence Levillain
Ting-Di Wu
Yannick Poquet
P2860
P2888
P304
P356
10.1038/NCHEMBIO.1355
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P577
2013-09-29T00:00:00Z