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Bacterial pathogens must be able to both recognize suitable niches within the host for colonization and successfully compete with commensal flora for nutrients in order to establish infection. Ethanolamine (EA) is a major component of mammalian and bacterial membranes and may be used by pathogens as...
ORGANISM(S): Escherichia coli 
Ethanolamine metabolism and inflammation Raw sequence reads
Isotopic model of ethanolamine metabolism in E. coli, used for 13C-flux calculations.
2024-06-28 | MODEL2403010002 | BioModels
Jallet2024 - iDJ1518 - Genome-scale model of ethanolamine metabolism in Escherichia coli
2024-06-25 | MODEL2403010003 | BioModels
Bacterial microcompartments (BMCs) represent prokaryotic counterparts to the eukaryotic organelles. BMCs act as intracellular microbioreactors that spatially insulate targeted pathways and enhance their kinetics through metabolic channelling effects. Some strains of E. coli natively bear an ethanola...
ORGANISM(S): Escherichia coli 
2024-07-02 | PXD048973 | Pride
Ethanolamine-induced assembly of microcompartments is required for Fusobacterium nucleatum virulence
Metabolic control of B-ALL cells by ethanolamine-induced autophagy
Many pathogenic bacteria use proteinaceous ethanolamine-utilization microcompartments (Eut BMCs) to facilitate the catabolism of ethanolamine, an abundant nutrient in the mammalian gut. The ability to metabolize ethanolamine gives pathogens a competitive edge over commensal microbiota which can driv...
ORGANISM(S): Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) Bacteria 
2025-10-06 | PXD059040 | Pride
Many bacteria metabolize ethanolamine as a nutrient source through cytoplasmic organelles named bacterial microcompartments (BMCs). Here we investigated the molecular assembly, regulation, and function of BMCs in Fusobacterium nucleatum – a Gram-negative oral pathobiont that is associated with adver...
ORGANISM(S): Fusobacterium nucleatum subsp. nucleatum ATCC 23726 
2024-12-12 | GSE280934 | GEO
The effect of ethanolamine phosphate phosphorylase knockout on hepatic gene expression
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