Identification of bacterial strains able to produce CLNA isomers for a possible application in the elaboration of new functional food products
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Tipo de documento: | Dissertação |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.14/20130 |
Resumo: | Functional food products consist of a modified foodstuff that can provide additional health and well-being benefits beyond their basic nutrition. In vitro and in vivo studies have reported that conjugated linolenic acid (CLNA) exerts anti-inflammatory, anti-cancer, anti-obesity and antioxidant activities. This group of conjugated isomers is naturally present in vegetable oils and ruminant meat and milk fat, however, lactobacilli, bifidobacteria and propionibacteria strains have revealed the capacity to produce CLNA isomers. Thus, the aim of this work was to identify CLNA producing strains, among a total of 12 Lactobacillus and 3 Bifidobacterium strains, that could be applied in the future formulation of new functional food products. CLA and CLNA microbial producing ability have been related to the presence of the linoleate isomerase (LAI) gene. Therefore, after the optimization of bacterial growth conditions, it was performed a molecular detection assay of LAI gene in Lactobacillus strains. Lactobacillus brevis D24, Lactobacillus plantarum D36 and Lactobacillus plantarum 299v revealed a positive result for the presence of LAI gene. In order to test strains for their CLNA producing ability, selected strains were first tested for their capacity to produce CLA isomers given previous evidence, experimental knowledge and chemical similarity with CLNA group of isomers. Low concentrations of CLA were detected, even for the positive LAI gene strains, although LA reduction rate was considerably high. Two strategies were then applied in order to optimize CLA production: addition of LA to the pre-inocula and inocula and addition of LA after 7 h of incubation. Despite the efforts, CLA production continued to be low in comparison to the percentages of LA reduction. LA was detected in strains’ pellet fatty acid composition, suggesting that the substrate could be being incorporated in the membrane. The amount of LA absorbed did not correspond to the level of substrate that was reduced, therefore, it was concluded that LA must have been converted into other unexpected compounds through an alternative transformation pathway not yet described. Among the strains tested, B. breve NCIMB 702258 was the only strain to demonstrate CLA-producing capacity. Further assays showed that this strain was also able to convert -LNA into CLNA isomers, even in a food matrix (1.6% reduced-fat milk). Therefore, B. breve NCIMB 702258 has the potential to be applied in the elaboration of CLA and CLNA enriched products, however, the organoleptic characteristics will need to be optimized. |
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Identification of bacterial strains able to produce CLNA isomers for a possible application in the elaboration of new functional food productsDomínio/Área Científica::Ciências Agrárias::Biotecnologia Agrária e AlimentarFunctional food products consist of a modified foodstuff that can provide additional health and well-being benefits beyond their basic nutrition. In vitro and in vivo studies have reported that conjugated linolenic acid (CLNA) exerts anti-inflammatory, anti-cancer, anti-obesity and antioxidant activities. This group of conjugated isomers is naturally present in vegetable oils and ruminant meat and milk fat, however, lactobacilli, bifidobacteria and propionibacteria strains have revealed the capacity to produce CLNA isomers. Thus, the aim of this work was to identify CLNA producing strains, among a total of 12 Lactobacillus and 3 Bifidobacterium strains, that could be applied in the future formulation of new functional food products. CLA and CLNA microbial producing ability have been related to the presence of the linoleate isomerase (LAI) gene. Therefore, after the optimization of bacterial growth conditions, it was performed a molecular detection assay of LAI gene in Lactobacillus strains. Lactobacillus brevis D24, Lactobacillus plantarum D36 and Lactobacillus plantarum 299v revealed a positive result for the presence of LAI gene. In order to test strains for their CLNA producing ability, selected strains were first tested for their capacity to produce CLA isomers given previous evidence, experimental knowledge and chemical similarity with CLNA group of isomers. Low concentrations of CLA were detected, even for the positive LAI gene strains, although LA reduction rate was considerably high. Two strategies were then applied in order to optimize CLA production: addition of LA to the pre-inocula and inocula and addition of LA after 7 h of incubation. Despite the efforts, CLA production continued to be low in comparison to the percentages of LA reduction. LA was detected in strains’ pellet fatty acid composition, suggesting that the substrate could be being incorporated in the membrane. The amount of LA absorbed did not correspond to the level of substrate that was reduced, therefore, it was concluded that LA must have been converted into other unexpected compounds through an alternative transformation pathway not yet described. Among the strains tested, B. breve NCIMB 702258 was the only strain to demonstrate CLA-producing capacity. Further assays showed that this strain was also able to convert -LNA into CLNA isomers, even in a food matrix (1.6% reduced-fat milk). Therefore, B. breve NCIMB 702258 has the potential to be applied in the elaboration of CLA and CLNA enriched products, however, the organoleptic characteristics will need to be optimized.Os alimentos funcionais consistem em géneros alimentícios modificados capazes de providenciar benefícios adicionais para a saúde e bem-estar além da sua nutrição básica. Estudos in vitro e in vivo revelaram que o ácido linolénico conjugado (CLNA) exerce actividades anti-inflamatória, anti-cancerígena, anti-obesidade e antioxidante. Este grupo de isómeros conjugados está naturalmente presente em óleos vegetais e na gordura da carne e leite de ruminantes, contudo, estirpes dos géneros lactobacilli, bifidobacteria e propionibacteria têm demonstrado capacidade para produzirem isómeros de CLNA. Assim, o objectivo deste trabalho foi de se identificar estirpes produtoras de CLNA, entre um total de 12 estirpes Lactobacillus e 3 Bifidobacterium, que possam vir a ser aplicadas na formulação futura de novos produtos funcionais. A capacidade de produção de CLA e CLNA tem sido relacionada com a presença do gene da linoleato isomerase (LAI). Por isso, após a optimização das condições de crescimento, foi realizado um ensaio de detecção molecular do gene LAI em estirpes do género Lactobacillus. Lactobacillus brevis D24, Lactobacillus plantarum D36 e Lactobacillus plantarum 299v deram resultado positivo relativamente à presença do gene LAI. De forma a se testar a capacidade de produção de CLNA das estirpes, estirpes seleccionadas foram primeiro testadas quanto à sua capacidade de formação de isómeros de CLA dadas anteriores evidências, o conhecimento experimental e a similaridade química com o grupo de isómeros de CLNA. Baixas concentrações de CLA foram detectadas, mesmo para as estirpes com o gene LAI presente, embora as taxas de redução do LA tenham sido consideravelmente altas. Duas estratégias foram então depois tomadas de forma a se optimizar a produção de CLA: adição de LA aos pre-inóculos e inóculos e adição de LA após 7 h de incubação. Apesar das tentativas, a produção de CLA continuou a ser baixa comparando com a percentagem de redução do LA. Na composição de ácidos gordos do pellet das estirpes, foi detectada a presença de LA, o que sugeriu que o substrato pudesse estar sendo incorporado na membrana. A quantidade de LA absorvida não correspondia ao nível de substrato que foi reduzido, por isso foi concluído que o LA teria que estar a ser convertido em outros compostos não esperados através de uma via de transformação alternativa ainda não descrita. Entre as estirpes testadas, B. breve NCIMB 702258 foi a única que demonstrou a capacidade de produção de CLA. Ensaios posteriores revelaram que esta estirpe também era capaz de converter -LNA em isómeros de CLNA, mesmo numa matriz alimentar (leite meio gordo). Assim sendo, B. breve NCIMB 702258 tem o potencial para ser aplicada na elaboração de produtos enriquecidos em CLA e CLNA, contudo, as características organolépticas terão que ser optimizadas.Gomes, Ana Maria PereiraRodríguez-Alcalá, LuísPimentel, LígiaVeritati - Repositório Institucional da Universidade Católica PortuguesaFontes, Ana Luiza Rodrigues2016-05-17T09:50:38Z2015-12-0720152015-12-07T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://hdl.handle.net/10400.14/20130TID:201023130enginfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-12T17:25:54Zoai:repositorio.ucp.pt:10400.14/20130Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:16:37.867838Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Identification of bacterial strains able to produce CLNA isomers for a possible application in the elaboration of new functional food products |
title |
Identification of bacterial strains able to produce CLNA isomers for a possible application in the elaboration of new functional food products |
spellingShingle |
Identification of bacterial strains able to produce CLNA isomers for a possible application in the elaboration of new functional food products Fontes, Ana Luiza Rodrigues Domínio/Área Científica::Ciências Agrárias::Biotecnologia Agrária e Alimentar |
title_short |
Identification of bacterial strains able to produce CLNA isomers for a possible application in the elaboration of new functional food products |
title_full |
Identification of bacterial strains able to produce CLNA isomers for a possible application in the elaboration of new functional food products |
title_fullStr |
Identification of bacterial strains able to produce CLNA isomers for a possible application in the elaboration of new functional food products |
title_full_unstemmed |
Identification of bacterial strains able to produce CLNA isomers for a possible application in the elaboration of new functional food products |
title_sort |
Identification of bacterial strains able to produce CLNA isomers for a possible application in the elaboration of new functional food products |
author |
Fontes, Ana Luiza Rodrigues |
author_facet |
Fontes, Ana Luiza Rodrigues |
author_role |
author |
dc.contributor.none.fl_str_mv |
Gomes, Ana Maria Pereira Rodríguez-Alcalá, Luís Pimentel, Lígia Veritati - Repositório Institucional da Universidade Católica Portuguesa |
dc.contributor.author.fl_str_mv |
Fontes, Ana Luiza Rodrigues |
dc.subject.por.fl_str_mv |
Domínio/Área Científica::Ciências Agrárias::Biotecnologia Agrária e Alimentar |
topic |
Domínio/Área Científica::Ciências Agrárias::Biotecnologia Agrária e Alimentar |
description |
Functional food products consist of a modified foodstuff that can provide additional health and well-being benefits beyond their basic nutrition. In vitro and in vivo studies have reported that conjugated linolenic acid (CLNA) exerts anti-inflammatory, anti-cancer, anti-obesity and antioxidant activities. This group of conjugated isomers is naturally present in vegetable oils and ruminant meat and milk fat, however, lactobacilli, bifidobacteria and propionibacteria strains have revealed the capacity to produce CLNA isomers. Thus, the aim of this work was to identify CLNA producing strains, among a total of 12 Lactobacillus and 3 Bifidobacterium strains, that could be applied in the future formulation of new functional food products. CLA and CLNA microbial producing ability have been related to the presence of the linoleate isomerase (LAI) gene. Therefore, after the optimization of bacterial growth conditions, it was performed a molecular detection assay of LAI gene in Lactobacillus strains. Lactobacillus brevis D24, Lactobacillus plantarum D36 and Lactobacillus plantarum 299v revealed a positive result for the presence of LAI gene. In order to test strains for their CLNA producing ability, selected strains were first tested for their capacity to produce CLA isomers given previous evidence, experimental knowledge and chemical similarity with CLNA group of isomers. Low concentrations of CLA were detected, even for the positive LAI gene strains, although LA reduction rate was considerably high. Two strategies were then applied in order to optimize CLA production: addition of LA to the pre-inocula and inocula and addition of LA after 7 h of incubation. Despite the efforts, CLA production continued to be low in comparison to the percentages of LA reduction. LA was detected in strains’ pellet fatty acid composition, suggesting that the substrate could be being incorporated in the membrane. The amount of LA absorbed did not correspond to the level of substrate that was reduced, therefore, it was concluded that LA must have been converted into other unexpected compounds through an alternative transformation pathway not yet described. Among the strains tested, B. breve NCIMB 702258 was the only strain to demonstrate CLA-producing capacity. Further assays showed that this strain was also able to convert -LNA into CLNA isomers, even in a food matrix (1.6% reduced-fat milk). Therefore, B. breve NCIMB 702258 has the potential to be applied in the elaboration of CLA and CLNA enriched products, however, the organoleptic characteristics will need to be optimized. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-12-07 2015 2015-12-07T00:00:00Z 2016-05-17T09:50:38Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.14/20130 TID:201023130 |
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http://hdl.handle.net/10400.14/20130 |
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TID:201023130 |
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eng |
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eng |
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openAccess |
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application/pdf |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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