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      Fermentation of Fructooligosaccharides and Inulin by Bifidobacteria: a Comparative Study of Pure and Fecal Cultures

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          ABSTRACT

          The utilization of fructooligosaccharides (FOS) and inulin by 55 Bifidobacterium strains was investigated. Whereas FOS were fermented by most strains, only eight grew when inulin was used as the carbon source. Residual carbohydrates were analyzed by high-performance anion-exchange chromatography with pulsed amperometric detection after batch fermentation. A strain-dependent capability to degrade fructans of different lengths was observed. During batch fermentation on inulin, the short fructans disappeared first, and then the longer ones were gradually consumed. However, growth occurred through a single uninterrupted exponential phase without exhibiting polyauxic behavior in relation to the chain length. Cellular β-fructofuranosidases were found in all of the 21 Bifidobacterium strains tested. Four strains were tested for extracellular hydrolytic activity against fructans, and only the two strains which ferment inulin showed this activity. Batch cultures inoculated with human fecal slurries confirmed the bifidogenic effect of both FOS and inulin and indicated that other intestinal microbial groups also grow on these carbon sources. We observed that bifidobacteria grew by cross-feeding on mono- and oligosaccharides produced by primary inulin intestinal degraders, as evidenced by the high hydrolytic activity of fecal supernatants. FOS and inulin greatly affected the production of short-chain fatty acids in fecal cultures; butyrate was the major fermentation product on inulin, whereas mostly acetate and lactate were produced on FOS.

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          Author and article information

          Journal
          Applied and Environmental Microbiology
          Appl Environ Microbiol
          American Society for Microbiology
          0099-2240
          1098-5336
          October 2005
          October 2005
          : 71
          : 10
          : 6150-6158
          Affiliations
          [1 ]Department of Chemistry, University of Modena and Reggio Emilia, Modena, Italy
          [2 ]Department of Inorganic Chemistry, Analytical Chemistry, and Physical Chemistry, University of Parma, Parma, Italy
          [3 ]Department of Pharmaceutical Sciences, University of Bologna, Bologna, Italy
          Article
          10.1128/AEM.71.10.6150-6158.2005
          1265942
          16204533
          fb0d490e-f288-427c-808b-1246cfa6db8e
          © 2005

          https://journals.asm.org/non-commercial-tdm-license

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