English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Single cell fluorescence imaging of glycan uptake by intestinal bacteria

MPS-Authors
/persons/resource/persons210443

Hehemann,  Jan-Hendrik
University Bremen - MPI Joint Research Group for Marine Glycobiology, Max Planck Institute for Marine Microbiology, Max Planck Society;

/persons/resource/persons210710

Reintjes,  Greta
Department of Molecular Ecology, Max Planck Institute for Marine Microbiology, Max Planck Society;

/persons/resource/persons210230

Amann,  Rudolf
Department of Molecular Ecology, Max Planck Institute for Marine Microbiology, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)

Hehemann_2019.pdf
(Publisher version), 2MB

Supplementary Material (public)
There is no public supplementary material available
Citation

Hehemann, J.-H., Reintjes, G., Klassen, L., Smith, A. D., Ndeh, D., Arnosti, C., et al. (2019). Single cell fluorescence imaging of glycan uptake by intestinal bacteria. The ISME Journal, 13(7), 1883-1889. doi:10.1038/s41396-019-0406-z.


Cite as: https://hdl.handle.net/21.11116/0000-0005-C1E4-F
Abstract
Microbes in the intestines of mammals degrade dietary glycans for energy
and growth. The pathways required for polysaccharide utilization are
functionally diverse; moreover, they are unequally dispersed between
bacterial genomes. Hence, assigning metabolic phenotypes to genotypes
remains a challenge in microbiome research. Here we demonstrate that
glycan uptake in gut bacteria can be visualized with fluorescent glycan
conjugates (FGCs) using epifluorescence microscopy. Yeast alpha-mannan
and rhamnogalacturonan-II, two structurally distinct glycans from the
cell walls of yeast and plants, respectively, were fluorescently labeled
and fed to Bacteroides thetaiotaomicron VPI-5482. Wild-type cells
rapidly consumed the FGCs and became fluorescent; whereas, strains that
had deleted pathways for glycan degradation and transport were
non-fluorescent. Uptake of FGCs, therefore, is direct evidence of
genetic function and provides a direct method to assess specific glycan
metabolism in intestinal bacteria at the single cell level.