Capability of Lactobacillus plantarum IFPL935 to catabolize Flavan-3-ol compounds and complex phenolic extracts

Lactobacillus plantarum IFPL935 was incubated with individual monomeric flavan-3-ols and dimeric A-and B-type procyanidins to identify new metabolites and to determine the effect of compound structural features on bacterial growth and catabolism. Complex extracts rich in A-type proanthocyanidins and phenolic acids from cranberry were also tested. The results showed that L. plantarum IFPL935 exhibited higher resistance to nongalloylated monomeric flavan-3-ols, A-type dimeric procyanidins, and cranberry extract than to (-)-epicatechin-3-O- gallate and B-type dimeric procyanidins. Despite these findings, the strain was capable of rapidly degrading (-)-epicatechin-3-O-gallate, but not A- or B-type dimeric procyanidins. However, it was able to produce large changes in the phenolic profile of the cranberry extract mainly due to the catabolism of hydroxycinnamic and hydroxybenzoic acids. Of most relevance was the fact that L. plantarum IFPL935 cleaved the heterocyclic ring of monomeric flavan-3-ols, giving rise to 1-(3',4'-dihydroxyphenyl)-3-(2>,4>,6>- trihydroxyphenyl)propan-2-ol, activity exhibited by only a few human intestinal bacteria. © 2012 American Chemical Society.

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Main Authors: Sánchez-Patán, Fernando, Tabasco, Raquel, Monagas Juan, María Josefina, Requena, Teresa, Peláez, Carmen, Moreno-Arribas, M. Victoria, Bartolomé, Begoña
Other Authors: Comunidad de Madrid
Format: artículo biblioteca
Published: American Chemical Society 2012
Subjects:Cranberry extract, Grape seed extract, A-type procyanidins, B-type procyanidins, Flavan-3-ols, Microbial catabolism, Lactobacillus,
Online Access:http://hdl.handle.net/10261/101249
http://dx.doi.org/10.13039/501100004837
http://dx.doi.org/10.13039/501100000780
http://dx.doi.org/10.13039/501100003339
http://dx.doi.org/10.13039/100012818
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spelling dig-cial-es-10261-1012492018-09-19T08:29:26Z Capability of Lactobacillus plantarum IFPL935 to catabolize Flavan-3-ol compounds and complex phenolic extracts Sánchez-Patán, Fernando Tabasco, Raquel Monagas Juan, María Josefina Requena, Teresa Peláez, Carmen Moreno-Arribas, M. Victoria Bartolomé, Begoña Comunidad de Madrid Ministerio de Ciencia e Innovación (España) European Commission Consejo Superior de Investigaciones Científicas (España) Cranberry extract Grape seed extract A-type procyanidins B-type procyanidins Flavan-3-ols Microbial catabolism Lactobacillus Lactobacillus plantarum IFPL935 was incubated with individual monomeric flavan-3-ols and dimeric A-and B-type procyanidins to identify new metabolites and to determine the effect of compound structural features on bacterial growth and catabolism. Complex extracts rich in A-type proanthocyanidins and phenolic acids from cranberry were also tested. The results showed that L. plantarum IFPL935 exhibited higher resistance to nongalloylated monomeric flavan-3-ols, A-type dimeric procyanidins, and cranberry extract than to (-)-epicatechin-3-O- gallate and B-type dimeric procyanidins. Despite these findings, the strain was capable of rapidly degrading (-)-epicatechin-3-O-gallate, but not A- or B-type dimeric procyanidins. However, it was able to produce large changes in the phenolic profile of the cranberry extract mainly due to the catabolism of hydroxycinnamic and hydroxybenzoic acids. Of most relevance was the fact that L. plantarum IFPL935 cleaved the heterocyclic ring of monomeric flavan-3-ols, giving rise to 1-(3',4'-dihydroxyphenyl)-3-(2>,4>,6>- trihydroxyphenyl)propan-2-ol, activity exhibited by only a few human intestinal bacteria. © 2012 American Chemical Society. This work has been funded by the Spanish Ministry for Science and Innovation (AGL2009-13361-C02-00, AGL2010-17499, and CSD2007-00063 Consolider Ingenio 2010 FUN-C-FOOD Projects), the Comunidad de Madrid (ALIBIRD P2009/AGR- 1469 Project), and CYTED (IBEROFUN 110AC0386). F.S.-P. is the recipient of a contract from the JAE-Doc Program (CSIC). R.T. thanks the Danone Institute for a fellowship award. Peer Reviewed 2014-08-27T07:27:08Z 2014-08-27T07:27:08Z 2012 2014-08-27T07:27:08Z artículo http://purl.org/coar/resource_type/c_6501 doi: 10.1021/jf3006867 issn: 0021-8561 e-issn: 1520-5118 Journal of Agricultural and Food Chemistry 60(29): 7142-7151 (2012) http://hdl.handle.net/10261/101249 10.1021/jf3006867 http://dx.doi.org/10.13039/501100004837 http://dx.doi.org/10.13039/501100000780 http://dx.doi.org/10.13039/501100003339 http://dx.doi.org/10.13039/100012818 #PLACEHOLDER_PARENT_METADATA_VALUE# S2009/AGR-1469/ALIBIRD none 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
topic Cranberry extract
Grape seed extract
A-type procyanidins
B-type procyanidins
Flavan-3-ols
Microbial catabolism
Lactobacillus
Cranberry extract
Grape seed extract
A-type procyanidins
B-type procyanidins
Flavan-3-ols
Microbial catabolism
Lactobacillus
spellingShingle Cranberry extract
Grape seed extract
A-type procyanidins
B-type procyanidins
Flavan-3-ols
Microbial catabolism
Lactobacillus
Cranberry extract
Grape seed extract
A-type procyanidins
B-type procyanidins
Flavan-3-ols
Microbial catabolism
Lactobacillus
Sánchez-Patán, Fernando
Tabasco, Raquel
Monagas Juan, María Josefina
Requena, Teresa
Peláez, Carmen
Moreno-Arribas, M. Victoria
Bartolomé, Begoña
Capability of Lactobacillus plantarum IFPL935 to catabolize Flavan-3-ol compounds and complex phenolic extracts
description Lactobacillus plantarum IFPL935 was incubated with individual monomeric flavan-3-ols and dimeric A-and B-type procyanidins to identify new metabolites and to determine the effect of compound structural features on bacterial growth and catabolism. Complex extracts rich in A-type proanthocyanidins and phenolic acids from cranberry were also tested. The results showed that L. plantarum IFPL935 exhibited higher resistance to nongalloylated monomeric flavan-3-ols, A-type dimeric procyanidins, and cranberry extract than to (-)-epicatechin-3-O- gallate and B-type dimeric procyanidins. Despite these findings, the strain was capable of rapidly degrading (-)-epicatechin-3-O-gallate, but not A- or B-type dimeric procyanidins. However, it was able to produce large changes in the phenolic profile of the cranberry extract mainly due to the catabolism of hydroxycinnamic and hydroxybenzoic acids. Of most relevance was the fact that L. plantarum IFPL935 cleaved the heterocyclic ring of monomeric flavan-3-ols, giving rise to 1-(3',4'-dihydroxyphenyl)-3-(2>,4>,6>- trihydroxyphenyl)propan-2-ol, activity exhibited by only a few human intestinal bacteria. © 2012 American Chemical Society.
author2 Comunidad de Madrid
author_facet Comunidad de Madrid
Sánchez-Patán, Fernando
Tabasco, Raquel
Monagas Juan, María Josefina
Requena, Teresa
Peláez, Carmen
Moreno-Arribas, M. Victoria
Bartolomé, Begoña
format artículo
topic_facet Cranberry extract
Grape seed extract
A-type procyanidins
B-type procyanidins
Flavan-3-ols
Microbial catabolism
Lactobacillus
author Sánchez-Patán, Fernando
Tabasco, Raquel
Monagas Juan, María Josefina
Requena, Teresa
Peláez, Carmen
Moreno-Arribas, M. Victoria
Bartolomé, Begoña
author_sort Sánchez-Patán, Fernando
title Capability of Lactobacillus plantarum IFPL935 to catabolize Flavan-3-ol compounds and complex phenolic extracts
title_short Capability of Lactobacillus plantarum IFPL935 to catabolize Flavan-3-ol compounds and complex phenolic extracts
title_full Capability of Lactobacillus plantarum IFPL935 to catabolize Flavan-3-ol compounds and complex phenolic extracts
title_fullStr Capability of Lactobacillus plantarum IFPL935 to catabolize Flavan-3-ol compounds and complex phenolic extracts
title_full_unstemmed Capability of Lactobacillus plantarum IFPL935 to catabolize Flavan-3-ol compounds and complex phenolic extracts
title_sort capability of lactobacillus plantarum ifpl935 to catabolize flavan-3-ol compounds and complex phenolic extracts
publisher American Chemical Society
publishDate 2012
url http://hdl.handle.net/10261/101249
http://dx.doi.org/10.13039/501100004837
http://dx.doi.org/10.13039/501100000780
http://dx.doi.org/10.13039/501100003339
http://dx.doi.org/10.13039/100012818
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