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A versatile and scalable strategy for glycoprofiling bifidobacterial consumption of human milk oligosaccharides

Human milk contains approximately 200 complex oligosaccharides believed to stimulate the growth and establishment of a protective microbiota in the infant gut. The lack of scalable analytical techniques has hindered the measurement of bacterial metabolism of these and other complex prebiotic oligosa...

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Autores principales: LoCascio, Riccardo G., Niñonuevo, Milady R., Kronewitter, Scott R., Freeman, Samara L., German, J. Bruce, Lebrilla, Carlito B., Mills, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815754/
https://www.ncbi.nlm.nih.gov/pubmed/21261928
http://dx.doi.org/10.1111/j.1751-7915.2008.00072.x
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author LoCascio, Riccardo G.
Niñonuevo, Milady R.
Kronewitter, Scott R.
Freeman, Samara L.
German, J. Bruce
Lebrilla, Carlito B.
Mills, David A.
author_facet LoCascio, Riccardo G.
Niñonuevo, Milady R.
Kronewitter, Scott R.
Freeman, Samara L.
German, J. Bruce
Lebrilla, Carlito B.
Mills, David A.
author_sort LoCascio, Riccardo G.
collection PubMed
description Human milk contains approximately 200 complex oligosaccharides believed to stimulate the growth and establishment of a protective microbiota in the infant gut. The lack of scalable analytical techniques has hindered the measurement of bacterial metabolism of these and other complex prebiotic oligosaccharides. An in vitro, multi‐strain, assay capable of measuring kinetics of bacterial growth and detailed oligosaccharide consumption analysis by FTICR‐MS was developed and tested simultaneously on 12 bifidobacterial strains. For quantitative consumption, deuterated and reduced human milk oligosaccharide (HMO) standards were used. A custom software suite developed in house called Glycolyzer was used to process the large amounts of oligosaccharide mass spectra automatically with (13)C corrections based on de‐isotoping protocols. High growth on HMOs was characteristic of Bifidobacterium longum biovar infantis strains, which consumed nearly all available substrates, while other bifidobacterial strains tested, B. longum bv. longum, B. adolescentis, B. breve and B. bifidum, showed low or only moderate growth ability. Total oligosaccharide consumption ranged from a high of 87% for B. infantis JCM 7009 to only 12% for B. adolescentis ATCC 15703. A detailed analysis of consumption glycoprofiles indicated strain‐specific capabilities towards differential metabolism of milk oligosaccharides. This method overcomes previous limitations in the quantitative, multi‐strain analysis of bacterial metabolism of HMOs and represents a novel approach towards understanding bacterial consumption of complex prebiotic oligosaccharides.
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spelling pubmed-38157542014-02-12 A versatile and scalable strategy for glycoprofiling bifidobacterial consumption of human milk oligosaccharides LoCascio, Riccardo G. Niñonuevo, Milady R. Kronewitter, Scott R. Freeman, Samara L. German, J. Bruce Lebrilla, Carlito B. Mills, David A. Microb Biotechnol Research Articles Human milk contains approximately 200 complex oligosaccharides believed to stimulate the growth and establishment of a protective microbiota in the infant gut. The lack of scalable analytical techniques has hindered the measurement of bacterial metabolism of these and other complex prebiotic oligosaccharides. An in vitro, multi‐strain, assay capable of measuring kinetics of bacterial growth and detailed oligosaccharide consumption analysis by FTICR‐MS was developed and tested simultaneously on 12 bifidobacterial strains. For quantitative consumption, deuterated and reduced human milk oligosaccharide (HMO) standards were used. A custom software suite developed in house called Glycolyzer was used to process the large amounts of oligosaccharide mass spectra automatically with (13)C corrections based on de‐isotoping protocols. High growth on HMOs was characteristic of Bifidobacterium longum biovar infantis strains, which consumed nearly all available substrates, while other bifidobacterial strains tested, B. longum bv. longum, B. adolescentis, B. breve and B. bifidum, showed low or only moderate growth ability. Total oligosaccharide consumption ranged from a high of 87% for B. infantis JCM 7009 to only 12% for B. adolescentis ATCC 15703. A detailed analysis of consumption glycoprofiles indicated strain‐specific capabilities towards differential metabolism of milk oligosaccharides. This method overcomes previous limitations in the quantitative, multi‐strain analysis of bacterial metabolism of HMOs and represents a novel approach towards understanding bacterial consumption of complex prebiotic oligosaccharides. Blackwell Publishing Ltd 2009-05 2009-04-17 /pmc/articles/PMC3815754/ /pubmed/21261928 http://dx.doi.org/10.1111/j.1751-7915.2008.00072.x Text en Copyright © 2008 The Authors. Journal compilation © 2008 Society for Applied Microbiology and Blackwell Publishing Ltd
spellingShingle Research Articles
LoCascio, Riccardo G.
Niñonuevo, Milady R.
Kronewitter, Scott R.
Freeman, Samara L.
German, J. Bruce
Lebrilla, Carlito B.
Mills, David A.
A versatile and scalable strategy for glycoprofiling bifidobacterial consumption of human milk oligosaccharides
title A versatile and scalable strategy for glycoprofiling bifidobacterial consumption of human milk oligosaccharides
title_full A versatile and scalable strategy for glycoprofiling bifidobacterial consumption of human milk oligosaccharides
title_fullStr A versatile and scalable strategy for glycoprofiling bifidobacterial consumption of human milk oligosaccharides
title_full_unstemmed A versatile and scalable strategy for glycoprofiling bifidobacterial consumption of human milk oligosaccharides
title_short A versatile and scalable strategy for glycoprofiling bifidobacterial consumption of human milk oligosaccharides
title_sort versatile and scalable strategy for glycoprofiling bifidobacterial consumption of human milk oligosaccharides
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815754/
https://www.ncbi.nlm.nih.gov/pubmed/21261928
http://dx.doi.org/10.1111/j.1751-7915.2008.00072.x
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