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Proteomic characterization of Mycobacterium tuberculosis subjected to carbon starvation
by
Leach, Damon T.
, Devlin, Kaylyn L.
, Lamichhane, Gyanu
, Beatty, Kimberly E.
, Stratton, Kelly G.
, Lin, Vivian S.
in
Acids
/ Antibiotic resistance
/ Antibiotics
/ Arabinogalactan
/ Bacteria
/ Bacterial Proteins - metabolism
/ Biosynthesis
/ Carbon
/ Carbon - metabolism
/ Cell culture
/ Cell Wall - metabolism
/ Cell walls
/ Chromatography
/ Dormancy
/ Drug metabolism
/ Environmental conditions
/ Enzymes
/ Glycerol
/ Humans
/ Hypoxia
/ infectious disease
/ Infectious diseases
/ Lipid metabolism
/ Mass spectrometry
/ Metabolism
/ Mycobacteriology
/ Mycobacterium tuberculosis
/ Mycobacterium tuberculosis - genetics
/ Mycobacterium tuberculosis - metabolism
/ Oxidative metabolism
/ Oxidative phosphorylation
/ Pandemics
/ Particle size
/ Pathogens
/ Peptides
/ Peptidoglycans
/ Phenotypes
/ Phosphorylation
/ Pore size
/ Proteins
/ Proteome - metabolism
/ Proteomes
/ Proteomics
/ Proteomics - methods
/ Research Article
/ Scientific imaging
/ Special Series: Microbial Dormancy
/ Tuberculosis
2025
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Proteomic characterization of Mycobacterium tuberculosis subjected to carbon starvation
by
Leach, Damon T.
, Devlin, Kaylyn L.
, Lamichhane, Gyanu
, Beatty, Kimberly E.
, Stratton, Kelly G.
, Lin, Vivian S.
in
Acids
/ Antibiotic resistance
/ Antibiotics
/ Arabinogalactan
/ Bacteria
/ Bacterial Proteins - metabolism
/ Biosynthesis
/ Carbon
/ Carbon - metabolism
/ Cell culture
/ Cell Wall - metabolism
/ Cell walls
/ Chromatography
/ Dormancy
/ Drug metabolism
/ Environmental conditions
/ Enzymes
/ Glycerol
/ Humans
/ Hypoxia
/ infectious disease
/ Infectious diseases
/ Lipid metabolism
/ Mass spectrometry
/ Metabolism
/ Mycobacteriology
/ Mycobacterium tuberculosis
/ Mycobacterium tuberculosis - genetics
/ Mycobacterium tuberculosis - metabolism
/ Oxidative metabolism
/ Oxidative phosphorylation
/ Pandemics
/ Particle size
/ Pathogens
/ Peptides
/ Peptidoglycans
/ Phenotypes
/ Phosphorylation
/ Pore size
/ Proteins
/ Proteome - metabolism
/ Proteomes
/ Proteomics
/ Proteomics - methods
/ Research Article
/ Scientific imaging
/ Special Series: Microbial Dormancy
/ Tuberculosis
2025
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Proteomic characterization of Mycobacterium tuberculosis subjected to carbon starvation
by
Leach, Damon T.
, Devlin, Kaylyn L.
, Lamichhane, Gyanu
, Beatty, Kimberly E.
, Stratton, Kelly G.
, Lin, Vivian S.
in
Acids
/ Antibiotic resistance
/ Antibiotics
/ Arabinogalactan
/ Bacteria
/ Bacterial Proteins - metabolism
/ Biosynthesis
/ Carbon
/ Carbon - metabolism
/ Cell culture
/ Cell Wall - metabolism
/ Cell walls
/ Chromatography
/ Dormancy
/ Drug metabolism
/ Environmental conditions
/ Enzymes
/ Glycerol
/ Humans
/ Hypoxia
/ infectious disease
/ Infectious diseases
/ Lipid metabolism
/ Mass spectrometry
/ Metabolism
/ Mycobacteriology
/ Mycobacterium tuberculosis
/ Mycobacterium tuberculosis - genetics
/ Mycobacterium tuberculosis - metabolism
/ Oxidative metabolism
/ Oxidative phosphorylation
/ Pandemics
/ Particle size
/ Pathogens
/ Peptides
/ Peptidoglycans
/ Phenotypes
/ Phosphorylation
/ Pore size
/ Proteins
/ Proteome - metabolism
/ Proteomes
/ Proteomics
/ Proteomics - methods
/ Research Article
/ Scientific imaging
/ Special Series: Microbial Dormancy
/ Tuberculosis
2025
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Proteomic characterization of Mycobacterium tuberculosis subjected to carbon starvation
Journal Article
Proteomic characterization of Mycobacterium tuberculosis subjected to carbon starvation
2025
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Overview
Tuberculosis is a devastating human disease that kills over 1.2 million people a year. This disease is caused by the bacterial pathogen Mycobacterium tuberculosis ( Mtb ). Mtb excels at surviving in the human host by entering a non-replicating, dormant state. The current work investigated the proteomic changes that Mtb undergoes in response to carbon starvation, a culture condition that models dormancy. The authors found broad effects of carbon starvation on the proteome, with the relative abundance of 37% of proteins significantly altered. Protein changes related to cell wall biosynthesis, metabolism, and drug susceptibility are discussed. Proteins associated with a carbon starvation phenotype are identified, and results are compared to other dormancy models, including hypoxia.
Publisher
American Society for Microbiology
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