Transcriptional analysis of prebiotic uptake and catabolism by Lactobacillus acidophilus NCFM.
The human gastrointestinal tract can be positively modulated by dietary supplementation of probiotic bacteria in combination with prebiotic carbohydrates. Here differential transcriptomics and functional genomics were used to identify genes in Lactobacillus acidophilus NCFM involved in the uptake an...
Main Authors: | , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2012-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC3446993?pdf=render |
_version_ | 1818999201935130624 |
---|---|
author | Joakim Mark Andersen Rodolphe Barrangou Maher Abou Hachem Sampo J Lahtinen Yong-Jun Goh Birte Svensson Todd R Klaenhammer |
author_facet | Joakim Mark Andersen Rodolphe Barrangou Maher Abou Hachem Sampo J Lahtinen Yong-Jun Goh Birte Svensson Todd R Klaenhammer |
author_sort | Joakim Mark Andersen |
collection | DOAJ |
description | The human gastrointestinal tract can be positively modulated by dietary supplementation of probiotic bacteria in combination with prebiotic carbohydrates. Here differential transcriptomics and functional genomics were used to identify genes in Lactobacillus acidophilus NCFM involved in the uptake and catabolism of 11 potential prebiotic compounds consisting of α- and β-linked galactosides and glucosides. These oligosaccharides induced genes encoding phosphoenolpyruvate-dependent sugar phosphotransferase systems (PTS), galactoside pentose hexuronide (GPH) permease, and ATP-binding cassette (ABC) transporters. PTS systems were upregulated primarily by di- and tri-saccharides such as cellobiose, isomaltose, isomaltulose, panose and gentiobiose, while ABC transporters were upregulated by raffinose, Polydextrose, and stachyose. A single GPH transporter was induced by lactitol and galactooligosaccharides (GOS). The various transporters were associated with a number of glycoside hydrolases from families 1, 2, 4, 13, 32, 36, 42, and 65, involved in the catabolism of various α- and β-linked glucosides and galactosides. Further subfamily specialization was also observed for different PTS-associated GH1 6-phospho-β-glucosidases implicated in the catabolism of gentiobiose and cellobiose. These findings highlight the broad oligosaccharide metabolic repertoire of L. acidophilus NCFM and establish a platform for selection and screening of both probiotic bacteria and prebiotic compounds that may positively influence the gastrointestinal microbiota. |
first_indexed | 2024-12-20T22:13:40Z |
format | Article |
id | doaj.art-bb3264f72e83419f97fccc916deec2d4 |
institution | Directory Open Access Journal |
issn | 1932-6203 |
language | English |
last_indexed | 2024-12-20T22:13:40Z |
publishDate | 2012-01-01 |
publisher | Public Library of Science (PLoS) |
record_format | Article |
series | PLoS ONE |
spelling | doaj.art-bb3264f72e83419f97fccc916deec2d42022-12-21T19:25:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0179e4440910.1371/journal.pone.0044409Transcriptional analysis of prebiotic uptake and catabolism by Lactobacillus acidophilus NCFM.Joakim Mark AndersenRodolphe BarrangouMaher Abou HachemSampo J LahtinenYong-Jun GohBirte SvenssonTodd R KlaenhammerThe human gastrointestinal tract can be positively modulated by dietary supplementation of probiotic bacteria in combination with prebiotic carbohydrates. Here differential transcriptomics and functional genomics were used to identify genes in Lactobacillus acidophilus NCFM involved in the uptake and catabolism of 11 potential prebiotic compounds consisting of α- and β-linked galactosides and glucosides. These oligosaccharides induced genes encoding phosphoenolpyruvate-dependent sugar phosphotransferase systems (PTS), galactoside pentose hexuronide (GPH) permease, and ATP-binding cassette (ABC) transporters. PTS systems were upregulated primarily by di- and tri-saccharides such as cellobiose, isomaltose, isomaltulose, panose and gentiobiose, while ABC transporters were upregulated by raffinose, Polydextrose, and stachyose. A single GPH transporter was induced by lactitol and galactooligosaccharides (GOS). The various transporters were associated with a number of glycoside hydrolases from families 1, 2, 4, 13, 32, 36, 42, and 65, involved in the catabolism of various α- and β-linked glucosides and galactosides. Further subfamily specialization was also observed for different PTS-associated GH1 6-phospho-β-glucosidases implicated in the catabolism of gentiobiose and cellobiose. These findings highlight the broad oligosaccharide metabolic repertoire of L. acidophilus NCFM and establish a platform for selection and screening of both probiotic bacteria and prebiotic compounds that may positively influence the gastrointestinal microbiota.http://europepmc.org/articles/PMC3446993?pdf=render |
spellingShingle | Joakim Mark Andersen Rodolphe Barrangou Maher Abou Hachem Sampo J Lahtinen Yong-Jun Goh Birte Svensson Todd R Klaenhammer Transcriptional analysis of prebiotic uptake and catabolism by Lactobacillus acidophilus NCFM. PLoS ONE |
title | Transcriptional analysis of prebiotic uptake and catabolism by Lactobacillus acidophilus NCFM. |
title_full | Transcriptional analysis of prebiotic uptake and catabolism by Lactobacillus acidophilus NCFM. |
title_fullStr | Transcriptional analysis of prebiotic uptake and catabolism by Lactobacillus acidophilus NCFM. |
title_full_unstemmed | Transcriptional analysis of prebiotic uptake and catabolism by Lactobacillus acidophilus NCFM. |
title_short | Transcriptional analysis of prebiotic uptake and catabolism by Lactobacillus acidophilus NCFM. |
title_sort | transcriptional analysis of prebiotic uptake and catabolism by lactobacillus acidophilus ncfm |
url | http://europepmc.org/articles/PMC3446993?pdf=render |
work_keys_str_mv | AT joakimmarkandersen transcriptionalanalysisofprebioticuptakeandcatabolismbylactobacillusacidophilusncfm AT rodolphebarrangou transcriptionalanalysisofprebioticuptakeandcatabolismbylactobacillusacidophilusncfm AT maherabouhachem transcriptionalanalysisofprebioticuptakeandcatabolismbylactobacillusacidophilusncfm AT sampojlahtinen transcriptionalanalysisofprebioticuptakeandcatabolismbylactobacillusacidophilusncfm AT yongjungoh transcriptionalanalysisofprebioticuptakeandcatabolismbylactobacillusacidophilusncfm AT birtesvensson transcriptionalanalysisofprebioticuptakeandcatabolismbylactobacillusacidophilusncfm AT toddrklaenhammer transcriptionalanalysisofprebioticuptakeandcatabolismbylactobacillusacidophilusncfm |