Metabolic fluxes for nutritional flexibility of Mycobacterium tuberculosis.
Ontology highlight
ABSTRACT: The co-catabolism of multiple host-derived carbon substrates is required by Mycobacterium tuberculosis (Mtb) to successfully sustain a tuberculosis infection. However, the metabolic plasticity of this pathogen and the complexity of the metabolic networks present a major obstacle in identifying those nodes most amenable to therapeutic interventions. It is therefore critical that we define the metabolic phenotypes of Mtb in different conditions. We applied metabolic flux analysis using stable isotopes and lipid fingerprinting to investigate the metabolic network of Mtb growing slowly in our steady-state chemostat system. We demonstrate that Mtb efficiently co-metabolises either cholesterol or glycerol, in combination with two-carbon generating substrates without any compartmentalisation of m
SUBMITTER: Borah K
PROVIDER: S-EPMC8094261 | biostudies-literature | 2021 May
REPOSITORIES: biostudies-literature
ACCESS DATA