Analysis of glycerol and dihydroxyacetone metabolism in Enterococcus faecium.
Cindy StaerckValentin WasselinAurélie Budin-VerneuilIsabelle RincéMargherita CacaciMarkus WeigelCaroline GiraudTorsten HainAxel HartkeEliette Riboulet-BissonPublished in: FEMS microbiology letters (2021)
Glycerol (Gly) can be dissimilated by two pathways in bacteria. Either this sugar alcohol is first oxidized to dihydroxyacetone (DHA) and then phosphorylated or it is first phosphorylated to glycerol-3-phosphate (GlyP) followed by oxidation. Oxidation of GlyP can be achieved by NAD-dependent dehydrogenases or by a GlyP oxidase. In both cases, dihydroxyacetone phosphate is the product. Genomic analysis showed that Enterococcus faecium harbors numerous genes annotated to encode activities for the two pathways. However, our physiological analyses of growth on glycerol showed that dissimilation is limited to aerobic conditions and that despite the presence of genes encoding presumed GlyP dehydrogenases, the GlyP oxidase is essential in this process. Although E. faecium contains an operon encoding the phosphotransfer protein DhaM and DHA kinase, which are required for DHA phosphorylation, it is unable to grow on DHA. This operon is highly expressed in stationary phase but its physiological role remains unknown. Finally, data obtained from sequencing of a transposon mutant bank of E. faecium grown on BHI revealed that the GlyP dehydrogenases and a major intrinsic family protein have important but hitherto unknown physiological functions.
Keyphrases
- fatty acid
- genome wide
- single cell
- hydrogen peroxide
- protein kinase
- protein protein
- biofilm formation
- amino acid
- bioinformatics analysis
- genome wide identification
- binding protein
- gene expression
- pseudomonas aeruginosa
- big data
- escherichia coli
- nitric oxide
- high intensity
- cystic fibrosis
- transcription factor
- mass spectrometry
- tyrosine kinase
- electron transfer
- low density lipoprotein
- visible light