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Integrated Continuous Bioprocess Development for ACE-Inhibitory Peptide Production by Lactobacillus helveticus Strains in Membrane Bioreactor
Production of bioactive peptides (BAPs) by Lactobacillus species is a cost-effective approach compared to the use of purified enzymes. In this study, proteolytic Lactobacillus helveticus strains were used for milk fermentation to produce BAPs capable of inhibiting angiotensin converting enzyme (ACE)...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546403/ https://www.ncbi.nlm.nih.gov/pubmed/33102467 http://dx.doi.org/10.3389/fbioe.2020.585815 |
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author | Raveschot, Cyril Deracinois, Barbara Bertrand, Emmeline Flahaut, Christophe Frémont, Marc Drider, Djamel Dhulster, Pascal Cudennec, Benoit Coutte, François |
author_facet | Raveschot, Cyril Deracinois, Barbara Bertrand, Emmeline Flahaut, Christophe Frémont, Marc Drider, Djamel Dhulster, Pascal Cudennec, Benoit Coutte, François |
author_sort | Raveschot, Cyril |
collection | PubMed |
description | Production of bioactive peptides (BAPs) by Lactobacillus species is a cost-effective approach compared to the use of purified enzymes. In this study, proteolytic Lactobacillus helveticus strains were used for milk fermentation to produce BAPs capable of inhibiting angiotensin converting enzyme (ACE). Fermented milks were produced in bioreactors using batch mode, and the resulting products showed significant ACE-inhibitory activities. However, the benefits of fermentation in terms of peptide composition and ACE-inhibitory activity were noticeably reduced when the samples (fermented milks and non-fermented controls) were subject to simulated gastrointestinal digestion (GID). Introducing an ultrafiltration step after fermentation allowed to prevent this effect of GID and restored the effect of fermentation. Furthermore, an integrated continuous process for peptide production was developed which led to a 3 fold increased peptide productivity compared to batch production. Using a membrane bioreactor allowed to generate and purify in a single step, an active ingredient for ACE inhibition. |
format | Online Article Text |
id | pubmed-7546403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75464032020-10-22 Integrated Continuous Bioprocess Development for ACE-Inhibitory Peptide Production by Lactobacillus helveticus Strains in Membrane Bioreactor Raveschot, Cyril Deracinois, Barbara Bertrand, Emmeline Flahaut, Christophe Frémont, Marc Drider, Djamel Dhulster, Pascal Cudennec, Benoit Coutte, François Front Bioeng Biotechnol Bioengineering and Biotechnology Production of bioactive peptides (BAPs) by Lactobacillus species is a cost-effective approach compared to the use of purified enzymes. In this study, proteolytic Lactobacillus helveticus strains were used for milk fermentation to produce BAPs capable of inhibiting angiotensin converting enzyme (ACE). Fermented milks were produced in bioreactors using batch mode, and the resulting products showed significant ACE-inhibitory activities. However, the benefits of fermentation in terms of peptide composition and ACE-inhibitory activity were noticeably reduced when the samples (fermented milks and non-fermented controls) were subject to simulated gastrointestinal digestion (GID). Introducing an ultrafiltration step after fermentation allowed to prevent this effect of GID and restored the effect of fermentation. Furthermore, an integrated continuous process for peptide production was developed which led to a 3 fold increased peptide productivity compared to batch production. Using a membrane bioreactor allowed to generate and purify in a single step, an active ingredient for ACE inhibition. Frontiers Media S.A. 2020-09-25 /pmc/articles/PMC7546403/ /pubmed/33102467 http://dx.doi.org/10.3389/fbioe.2020.585815 Text en Copyright © 2020 Raveschot, Deracinois, Bertrand, Flahaut, Frémont, Drider, Dhulster, Cudennec and Coutte. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Raveschot, Cyril Deracinois, Barbara Bertrand, Emmeline Flahaut, Christophe Frémont, Marc Drider, Djamel Dhulster, Pascal Cudennec, Benoit Coutte, François Integrated Continuous Bioprocess Development for ACE-Inhibitory Peptide Production by Lactobacillus helveticus Strains in Membrane Bioreactor |
title | Integrated Continuous Bioprocess Development for ACE-Inhibitory Peptide Production by Lactobacillus helveticus Strains in Membrane Bioreactor |
title_full | Integrated Continuous Bioprocess Development for ACE-Inhibitory Peptide Production by Lactobacillus helveticus Strains in Membrane Bioreactor |
title_fullStr | Integrated Continuous Bioprocess Development for ACE-Inhibitory Peptide Production by Lactobacillus helveticus Strains in Membrane Bioreactor |
title_full_unstemmed | Integrated Continuous Bioprocess Development for ACE-Inhibitory Peptide Production by Lactobacillus helveticus Strains in Membrane Bioreactor |
title_short | Integrated Continuous Bioprocess Development for ACE-Inhibitory Peptide Production by Lactobacillus helveticus Strains in Membrane Bioreactor |
title_sort | integrated continuous bioprocess development for ace-inhibitory peptide production by lactobacillus helveticus strains in membrane bioreactor |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546403/ https://www.ncbi.nlm.nih.gov/pubmed/33102467 http://dx.doi.org/10.3389/fbioe.2020.585815 |
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