Identification of prebiotic fructooligosaccharide metabolism in Lactobacillus plantarum WCFS1 through microarrays

D.M. Saulnier, D. Molenaar, W.M. de Vos, G. Gibson, S. Kolida

Research output: Contribution to journalArticleAcademicpeer-review

206 Citations (Scopus)

Abstract

Short-chain fructooligosaccharides (scFOS) and other prebiotics are used to selectively stimulate the growth and activity of lactobacilli and bifidobacteria in the colon. However, there is little information on the mechanisms whereby prebiotics exert their specific effects upon such microorganisms. To study the genomic basis of scFOS metabolism in Lactobacillus plantarum WCFS1, two-color microarrays were used to screen for differentially expressed genes when grown on scFOS compared to glucose (control). A significant up-regulation (8- to 60-fold) was observed with a set of only five genes located in a single locus and predicted to encode a sucrose phosphoenolpyruvate transport system (PTS), a ß-fructofuranosidase, a fructokinase, an -glucosidase, and a sucrose operon repressor. Several other genes were slightly overexpressed, including pyruvate dehydrogenase. For the latter, no detectable activity in L. plantarum under various growth conditions has been previously reported. A mannose-PTS likely to encode glucose uptake was 50-fold down-regulated as well as, to a lower extent, other PTSs. Chemical analysis of the different moieties of scFOS that were depleted in the growth medium revealed that the trisaccharide 1-kestose present in scFOS was preferentially utilized, in comparison with the tetrasaccharide nystose and the pentasaccharide fructofuranosylnystose. The main end products of scFOS fermentation were lactate and acetate. This is the first example in lactobacilli of the association of a sucrose PTS and a ß-fructofuranosidase that could be used for scFOS degradation.
Original languageEnglish
Pages (from-to)1753-1765
JournalApplied and Environmental Microbiology
Volume73
Issue number6
DOIs
Publication statusPublished - 2007

Keywords

  • lactic-acid bacteria
  • beta-fructofuranosidase
  • gastrointestinal-tract
  • catabolite repression
  • glucose kinase
  • gene
  • bifidobacteria
  • acidophilus
  • modulation
  • probiotics

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