• Through a series of heterologous complementation experiments, enzyme assays, gene fusions, and transport experiments we show that the R. leguminosarum kinase is capable of directly phosphorylating rhamnose and rhamnulose, whereas the Sinorhizobium meliloti kinase does not have rhamnose kinase activity. (umanitoba.ca)
  • This suggests that this proteins face may play a role in a protein-protein interaction that affects rhamnose transport. (umanitoba.ca)
  • We showed that the infection of the host is characterised by an enhancement of functions associated with antibiotic and glucans catabolism functions but a reduction of sulfate assimilation process in T. maritimum . (biomedcentral.com)
  • phosphorylation of rhamnose, and an unknown interaction with the rhamnose ABC transporter. (umanitoba.ca)
  • Structures of intact shells have been determined for three functionally distinct: BMC types, carboxysomes, the GRM2 organelles involved in choline catabolism and a metabolosome of unknown function. (wikipedia.org)
  • Overview: Rhamnose utilization in GapMind is based on MetaCyc pathway I via L-rhamnulose 1-phosphate aldolase ( link ), pathway II via 2-keto-3-deoxy-L-rhamnonate aldolase ( link ), and pathway III via 2,4-diketo-3-deoxyrhamnonate hydrolase ( link ). (lbl.gov)
  • In pathway III, rhamnose is also oxidized and dehydrated to 2-dehydro-3-deoxy-L-rhamnonate, but then, dehydrogenase LRA5 forms 2,4-didehydro-3-deoxy-L-rhamnonate and hydrolase LRA6 forms L-lactate and pyruvate. (lbl.gov)
  • The major constituent monosaccharides of these polysaccharides are glucose, xylose, and arabinose, while smaller amounts of galactose, glucuronic acid, rhamnose and mannose are also present. (biomedcentral.com)
  • The major monosaccharide constituents of lignocellulose are D-glucose, D-xylose, and L-arabinose, while smaller amounts of D-galactose, D-galacturonic acid, L-rhamnose and D-mannose are also present. (biomedcentral.com)
  • Sucrose and other sugars, such as xylose, rhamnose and arabinose, are present in very low concentrations, and it is widely accepted that S. cerevisiae strains do not use these sugars as carbon or energy sources during alcoholic fermentation (Bisson, 1993). (moam.info)
  • Carbon catabolism serves fungi with energy in the form of reducing equivalents and ATP, as well as essential precursor metabolites for biosynthesis, such as glucose-6-phosphate and fructose-6-phosphate [ 1 ]. (biomedcentral.com)
  • However, in fruiting bodies only hexose catabolism occurs, and no accumulation of other sugars was observed. (biomedcentral.com)
  • Structures of intact shells have been determined for three functionally distinct: BMC types, carboxysomes, the GRM2 organelles involved in choline catabolism and a metabolosome of unknown function. (wikipedia.org)