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In vitro gastrointestinal digestion study of two wheat cultivars and evaluation of xylanase supplementation

BACKGROUND: The filamentous fungus Talaromyces versatilis is known to improve the metabolizable energy of wheat-based poultry diets thanks to its ability to produce a pool of CAZymes and particularly endo-β(1,4)-xylanases. In order to appreciate their in vivo mode of action, the supplementation effe...

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Autores principales: Lafond, Mickael, Bouza, Bernard, Eyrichine, Sandrine, Rouffineau, Friedrich, Saulnier, Luc, Giardina, Thierry, Bonnin, Estelle, Preynat, Aurélie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362821/
https://www.ncbi.nlm.nih.gov/pubmed/25785187
http://dx.doi.org/10.1186/s40104-015-0002-7
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author Lafond, Mickael
Bouza, Bernard
Eyrichine, Sandrine
Rouffineau, Friedrich
Saulnier, Luc
Giardina, Thierry
Bonnin, Estelle
Preynat, Aurélie
author_facet Lafond, Mickael
Bouza, Bernard
Eyrichine, Sandrine
Rouffineau, Friedrich
Saulnier, Luc
Giardina, Thierry
Bonnin, Estelle
Preynat, Aurélie
author_sort Lafond, Mickael
collection PubMed
description BACKGROUND: The filamentous fungus Talaromyces versatilis is known to improve the metabolizable energy of wheat-based poultry diets thanks to its ability to produce a pool of CAZymes and particularly endo-β(1,4)-xylanases. In order to appreciate their in vivo mode of action, the supplementation effect of two of its xylanases, XynD and XynB from families GH10 and GH11 respectively, have been evaluated on two different wheat cultivars Caphorn and Isengrain, which were chosen amongst 6 varieties for their difference in non starch polysaccharides content and arabinoxylan composition. RESULTS: Polysaccharides digestion was followed during 6 h along the digestive tract using the TNO gastrointestinal model-1, to mimic monogastric metabolism. Polysaccharide degradation appeared to occur mainly at the jejunal level and was higher with Isengrain than with Caphorn. For both cultivars, XynD and XynB supplementation increased notably the amount of reducing end sugars into the jejuno-ileal dialysates, which has been confirmed by a valuable increase of the soluble glucose into the jejunal dialysates. CONCLUSIONS: The amounts of arabinose and xylose into the dialysates and ileal deliveries increased consequently mainly for Caphorn, suggesting that XynD and XynB supplementation in wheat-based diet could alleviate the anti-nutritional effects of arabinoxylans by limiting the physical entrapment of starch and could increase the available metabolizable energy.
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spelling pubmed-43628212015-03-18 In vitro gastrointestinal digestion study of two wheat cultivars and evaluation of xylanase supplementation Lafond, Mickael Bouza, Bernard Eyrichine, Sandrine Rouffineau, Friedrich Saulnier, Luc Giardina, Thierry Bonnin, Estelle Preynat, Aurélie J Anim Sci Biotechnol Research BACKGROUND: The filamentous fungus Talaromyces versatilis is known to improve the metabolizable energy of wheat-based poultry diets thanks to its ability to produce a pool of CAZymes and particularly endo-β(1,4)-xylanases. In order to appreciate their in vivo mode of action, the supplementation effect of two of its xylanases, XynD and XynB from families GH10 and GH11 respectively, have been evaluated on two different wheat cultivars Caphorn and Isengrain, which were chosen amongst 6 varieties for their difference in non starch polysaccharides content and arabinoxylan composition. RESULTS: Polysaccharides digestion was followed during 6 h along the digestive tract using the TNO gastrointestinal model-1, to mimic monogastric metabolism. Polysaccharide degradation appeared to occur mainly at the jejunal level and was higher with Isengrain than with Caphorn. For both cultivars, XynD and XynB supplementation increased notably the amount of reducing end sugars into the jejuno-ileal dialysates, which has been confirmed by a valuable increase of the soluble glucose into the jejunal dialysates. CONCLUSIONS: The amounts of arabinose and xylose into the dialysates and ileal deliveries increased consequently mainly for Caphorn, suggesting that XynD and XynB supplementation in wheat-based diet could alleviate the anti-nutritional effects of arabinoxylans by limiting the physical entrapment of starch and could increase the available metabolizable energy. BioMed Central 2015-02-15 /pmc/articles/PMC4362821/ /pubmed/25785187 http://dx.doi.org/10.1186/s40104-015-0002-7 Text en © Lafond et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lafond, Mickael
Bouza, Bernard
Eyrichine, Sandrine
Rouffineau, Friedrich
Saulnier, Luc
Giardina, Thierry
Bonnin, Estelle
Preynat, Aurélie
In vitro gastrointestinal digestion study of two wheat cultivars and evaluation of xylanase supplementation
title In vitro gastrointestinal digestion study of two wheat cultivars and evaluation of xylanase supplementation
title_full In vitro gastrointestinal digestion study of two wheat cultivars and evaluation of xylanase supplementation
title_fullStr In vitro gastrointestinal digestion study of two wheat cultivars and evaluation of xylanase supplementation
title_full_unstemmed In vitro gastrointestinal digestion study of two wheat cultivars and evaluation of xylanase supplementation
title_short In vitro gastrointestinal digestion study of two wheat cultivars and evaluation of xylanase supplementation
title_sort in vitro gastrointestinal digestion study of two wheat cultivars and evaluation of xylanase supplementation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362821/
https://www.ncbi.nlm.nih.gov/pubmed/25785187
http://dx.doi.org/10.1186/s40104-015-0002-7
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