In vitro digestibility of galactooligosaccharides: Effect of the structural features on their intestinal degradation

Small intestinal brush border membrane vesicles from pig were used to digest galactooligosaccharides from lactose (GOS) and from lactulose (OsLu). Dissimilar hydrolysis rates were detected after digestion. Predominant glycosidic linkages and monomeric composition affected the resistance to intestinal digestive enzymes. The β(1→3) GOS mixture was the most susceptible to hydrolysis (50.2%), followed by β(1→4) (34.9%), whereas β(1→6) linkages were highly resistant to digestion (27.1%). Monomeric composition provided a better resistance in β(1→6) OsLu (22.8%) compared to β(1→6) GOS (27.1%). This was also observed for β-galactosyl fructoses and β-galactosyl glucoses, where the presence of fructose provided higher resistance to digestion. Thus, the resistance to small intestinal digestive enzymes highly depends upon the structure and composition of prebiotics. Increasing knowledge in this regard could contribute to the future synthesis of new mixtures of carbohydrates, highly resistant to digestion and with potential to be tailored prebiotics with specific properties, targeting, for instance, specific probiotic species.

Saved in:
Bibliographic Details
Main Authors: Ferreira-Lazarte, Alvaro, Gallego-Lobillo, Pablo, Moreno, F. Javier, Villamiel, Mar, Hernández-Hernández, Oswaldo
Other Authors: Agencia Estatal de Investigación (España)
Format: artículo biblioteca
Language:English
Published: American Chemical Society 2019
Subjects:Prebiotics, Galactooligosaccharides, Glycosidic linkages, In vitro digestion model,
Online Access:http://hdl.handle.net/10261/193606
http://dx.doi.org/10.13039/501100011033
http://dx.doi.org/10.13039/501100003329
Tags: Add Tag
No Tags, Be the first to tag this record!
id dig-cial-es-10261-193606
record_format koha
spelling dig-cial-es-10261-1936062020-04-15T04:30:31Z In vitro digestibility of galactooligosaccharides: Effect of the structural features on their intestinal degradation Ferreira-Lazarte, Alvaro Gallego-Lobillo, Pablo Moreno, F. Javier Villamiel, Mar Hernández-Hernández, Oswaldo Agencia Estatal de Investigación (España) Ministerio de Ciencia, Innovación y Universidades (España) Ministerio de Economía y Competitividad (España) Moreno, F. Javier [0000-0002-7637-9542] Villamiel, Mar [0000-0001-6847-8359] Prebiotics Galactooligosaccharides Glycosidic linkages In vitro digestion model Small intestinal brush border membrane vesicles from pig were used to digest galactooligosaccharides from lactose (GOS) and from lactulose (OsLu). Dissimilar hydrolysis rates were detected after digestion. Predominant glycosidic linkages and monomeric composition affected the resistance to intestinal digestive enzymes. The β(1→3) GOS mixture was the most susceptible to hydrolysis (50.2%), followed by β(1→4) (34.9%), whereas β(1→6) linkages were highly resistant to digestion (27.1%). Monomeric composition provided a better resistance in β(1→6) OsLu (22.8%) compared to β(1→6) GOS (27.1%). This was also observed for β-galactosyl fructoses and β-galactosyl glucoses, where the presence of fructose provided higher resistance to digestion. Thus, the resistance to small intestinal digestive enzymes highly depends upon the structure and composition of prebiotics. Increasing knowledge in this regard could contribute to the future synthesis of new mixtures of carbohydrates, highly resistant to digestion and with potential to be tailored prebiotics with specific properties, targeting, for instance, specific probiotic species. This work has been funded by the Ministry of Economy and Competitiveness (MINECO) of Spain with Projects AGL2014-53445-R and AGL2017-84614-C2-1-R. Peer reviewed 2019-10-28T13:13:49Z 2019-10-28T13:13:49Z 2019 artículo http://purl.org/coar/resource_type/c_6501 Journal of Agricultural and Food Chemistry 67(16): 4662-4670 (2019) 0021-8561 http://hdl.handle.net/10261/193606 10.1021/acs.jafc.9b00417 1520-5118 http://dx.doi.org/10.13039/501100011033 http://dx.doi.org/10.13039/501100003329 30986057 en #PLACEHOLDER_PARENT_METADATA_VALUE# #PLACEHOLDER_PARENT_METADATA_VALUE# #PLACEHOLDER_PARENT_METADATA_VALUE# info:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/AGL2014-53445-R AGL2017-84614-C2-1-R/AEI/10.13039/501100011033 info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/AGL2017-84614-C2-1-R Postprint http://dx.doi.org/10.1021/acs.jafc.9b00417 Sí open American Chemical Society
institution CIAL ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-cial-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del CIAL España
language English
topic Prebiotics
Galactooligosaccharides
Glycosidic linkages
In vitro digestion model
Prebiotics
Galactooligosaccharides
Glycosidic linkages
In vitro digestion model
spellingShingle Prebiotics
Galactooligosaccharides
Glycosidic linkages
In vitro digestion model
Prebiotics
Galactooligosaccharides
Glycosidic linkages
In vitro digestion model
Ferreira-Lazarte, Alvaro
Gallego-Lobillo, Pablo
Moreno, F. Javier
Villamiel, Mar
Hernández-Hernández, Oswaldo
In vitro digestibility of galactooligosaccharides: Effect of the structural features on their intestinal degradation
description Small intestinal brush border membrane vesicles from pig were used to digest galactooligosaccharides from lactose (GOS) and from lactulose (OsLu). Dissimilar hydrolysis rates were detected after digestion. Predominant glycosidic linkages and monomeric composition affected the resistance to intestinal digestive enzymes. The β(1→3) GOS mixture was the most susceptible to hydrolysis (50.2%), followed by β(1→4) (34.9%), whereas β(1→6) linkages were highly resistant to digestion (27.1%). Monomeric composition provided a better resistance in β(1→6) OsLu (22.8%) compared to β(1→6) GOS (27.1%). This was also observed for β-galactosyl fructoses and β-galactosyl glucoses, where the presence of fructose provided higher resistance to digestion. Thus, the resistance to small intestinal digestive enzymes highly depends upon the structure and composition of prebiotics. Increasing knowledge in this regard could contribute to the future synthesis of new mixtures of carbohydrates, highly resistant to digestion and with potential to be tailored prebiotics with specific properties, targeting, for instance, specific probiotic species.
author2 Agencia Estatal de Investigación (España)
author_facet Agencia Estatal de Investigación (España)
Ferreira-Lazarte, Alvaro
Gallego-Lobillo, Pablo
Moreno, F. Javier
Villamiel, Mar
Hernández-Hernández, Oswaldo
format artículo
topic_facet Prebiotics
Galactooligosaccharides
Glycosidic linkages
In vitro digestion model
author Ferreira-Lazarte, Alvaro
Gallego-Lobillo, Pablo
Moreno, F. Javier
Villamiel, Mar
Hernández-Hernández, Oswaldo
author_sort Ferreira-Lazarte, Alvaro
title In vitro digestibility of galactooligosaccharides: Effect of the structural features on their intestinal degradation
title_short In vitro digestibility of galactooligosaccharides: Effect of the structural features on their intestinal degradation
title_full In vitro digestibility of galactooligosaccharides: Effect of the structural features on their intestinal degradation
title_fullStr In vitro digestibility of galactooligosaccharides: Effect of the structural features on their intestinal degradation
title_full_unstemmed In vitro digestibility of galactooligosaccharides: Effect of the structural features on their intestinal degradation
title_sort in vitro digestibility of galactooligosaccharides: effect of the structural features on their intestinal degradation
publisher American Chemical Society
publishDate 2019
url http://hdl.handle.net/10261/193606
http://dx.doi.org/10.13039/501100011033
http://dx.doi.org/10.13039/501100003329
work_keys_str_mv AT ferreiralazartealvaro invitrodigestibilityofgalactooligosaccharideseffectofthestructuralfeaturesontheirintestinaldegradation
AT gallegolobillopablo invitrodigestibilityofgalactooligosaccharideseffectofthestructuralfeaturesontheirintestinaldegradation
AT morenofjavier invitrodigestibilityofgalactooligosaccharideseffectofthestructuralfeaturesontheirintestinaldegradation
AT villamielmar invitrodigestibilityofgalactooligosaccharideseffectofthestructuralfeaturesontheirintestinaldegradation
AT hernandezhernandezoswaldo invitrodigestibilityofgalactooligosaccharideseffectofthestructuralfeaturesontheirintestinaldegradation
_version_ 1777671351505518592