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Transcriptional analysis of oligosaccharide utilization by Bifidobacterium lactis Bl-04

BACKGROUND: Probiotic bifidobacteria in combination with prebiotic carbohydrates have documented positive effects on human health regarding gastrointestinal disorders and improved immunity, however the selective routes of uptake remain unknown for most candidate prebiotics. The differential transcri...

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Detalles Bibliográficos
Autores principales: Andersen, Joakim M, Barrangou, Rodolphe, Hachem, Maher Abou, Lahtinen, Sampo J, Goh, Yong Jun, Svensson, Birte, Klaenhammer, Todd R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684542/
https://www.ncbi.nlm.nih.gov/pubmed/23663691
http://dx.doi.org/10.1186/1471-2164-14-312
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author Andersen, Joakim M
Barrangou, Rodolphe
Hachem, Maher Abou
Lahtinen, Sampo J
Goh, Yong Jun
Svensson, Birte
Klaenhammer, Todd R
author_facet Andersen, Joakim M
Barrangou, Rodolphe
Hachem, Maher Abou
Lahtinen, Sampo J
Goh, Yong Jun
Svensson, Birte
Klaenhammer, Todd R
author_sort Andersen, Joakim M
collection PubMed
description BACKGROUND: Probiotic bifidobacteria in combination with prebiotic carbohydrates have documented positive effects on human health regarding gastrointestinal disorders and improved immunity, however the selective routes of uptake remain unknown for most candidate prebiotics. The differential transcriptomes of Bifidobacterium animalis subsp. lactis Bl-04, induced by 11 potential prebiotic oligosaccharides were analyzed to identify the genetic loci involved in the uptake and catabolism of α- and β-linked hexoses, and β-xylosides. RESULTS: The overall transcriptome was modulated dependent on the type of glycoside (galactosides, glucosides or xylosides) utilized. Carbohydrate transporters of the major facilitator superfamily (induced by gentiobiose and β-galacto-oligosaccharides (GOS)) and ATP-binding cassette (ABC) transporters (upregulated by cellobiose, GOS, isomaltose, maltotriose, melibiose, panose, raffinose, stachyose, xylobiose and β-xylo-oligosaccharides) were differentially upregulated, together with glycoside hydrolases from families 1, 2, 13, 36, 42, 43 and 77. Sequence analysis of the identified solute-binding proteins that determine the specificity of ABC transporters revealed similarities in the breadth and selectivity of prebiotic utilization by bifidobacteria. CONCLUSION: This study identified the differential gene expression for utilization of potential prebiotics highlighting the extensive capabilities of Bifidobacterium lactis Bl-04 to utilize oligosaccharides. Results provide insights into the ability of this probiotic microbe to utilize indigestible carbohydrates in the human gastrointestinal tract.
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spelling pubmed-36845422013-06-18 Transcriptional analysis of oligosaccharide utilization by Bifidobacterium lactis Bl-04 Andersen, Joakim M Barrangou, Rodolphe Hachem, Maher Abou Lahtinen, Sampo J Goh, Yong Jun Svensson, Birte Klaenhammer, Todd R BMC Genomics Research Article BACKGROUND: Probiotic bifidobacteria in combination with prebiotic carbohydrates have documented positive effects on human health regarding gastrointestinal disorders and improved immunity, however the selective routes of uptake remain unknown for most candidate prebiotics. The differential transcriptomes of Bifidobacterium animalis subsp. lactis Bl-04, induced by 11 potential prebiotic oligosaccharides were analyzed to identify the genetic loci involved in the uptake and catabolism of α- and β-linked hexoses, and β-xylosides. RESULTS: The overall transcriptome was modulated dependent on the type of glycoside (galactosides, glucosides or xylosides) utilized. Carbohydrate transporters of the major facilitator superfamily (induced by gentiobiose and β-galacto-oligosaccharides (GOS)) and ATP-binding cassette (ABC) transporters (upregulated by cellobiose, GOS, isomaltose, maltotriose, melibiose, panose, raffinose, stachyose, xylobiose and β-xylo-oligosaccharides) were differentially upregulated, together with glycoside hydrolases from families 1, 2, 13, 36, 42, 43 and 77. Sequence analysis of the identified solute-binding proteins that determine the specificity of ABC transporters revealed similarities in the breadth and selectivity of prebiotic utilization by bifidobacteria. CONCLUSION: This study identified the differential gene expression for utilization of potential prebiotics highlighting the extensive capabilities of Bifidobacterium lactis Bl-04 to utilize oligosaccharides. Results provide insights into the ability of this probiotic microbe to utilize indigestible carbohydrates in the human gastrointestinal tract. BioMed Central 2013-05-10 /pmc/articles/PMC3684542/ /pubmed/23663691 http://dx.doi.org/10.1186/1471-2164-14-312 Text en Copyright © 2013 Andersen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Andersen, Joakim M
Barrangou, Rodolphe
Hachem, Maher Abou
Lahtinen, Sampo J
Goh, Yong Jun
Svensson, Birte
Klaenhammer, Todd R
Transcriptional analysis of oligosaccharide utilization by Bifidobacterium lactis Bl-04
title Transcriptional analysis of oligosaccharide utilization by Bifidobacterium lactis Bl-04
title_full Transcriptional analysis of oligosaccharide utilization by Bifidobacterium lactis Bl-04
title_fullStr Transcriptional analysis of oligosaccharide utilization by Bifidobacterium lactis Bl-04
title_full_unstemmed Transcriptional analysis of oligosaccharide utilization by Bifidobacterium lactis Bl-04
title_short Transcriptional analysis of oligosaccharide utilization by Bifidobacterium lactis Bl-04
title_sort transcriptional analysis of oligosaccharide utilization by bifidobacterium lactis bl-04
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684542/
https://www.ncbi.nlm.nih.gov/pubmed/23663691
http://dx.doi.org/10.1186/1471-2164-14-312
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