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Cell factory for γ-aminobutyric acid (GABA) production using Bifidobacterium adolescentis

BACKGROUND: Bifidobacteria are gram-positive, probiotic, and generally regarded as safe bacteria. Techniques such as transformation, gene knockout, and heterologous gene expression have been established for Bifidobacterium, indicating that this bacterium can be used as a cell factory platform. Howev...

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Autores principales: Altaib, Hend, Kozakai, Tomoya, Badr, Yassien, Nakao, Hazuki, El-Nouby, Mahmoud A. M., Yanase, Emiko, Nomura, Izumi, Suzuki, Tohru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903651/
https://www.ncbi.nlm.nih.gov/pubmed/35255900
http://dx.doi.org/10.1186/s12934-021-01729-6
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author Altaib, Hend
Kozakai, Tomoya
Badr, Yassien
Nakao, Hazuki
El-Nouby, Mahmoud A. M.
Yanase, Emiko
Nomura, Izumi
Suzuki, Tohru
author_facet Altaib, Hend
Kozakai, Tomoya
Badr, Yassien
Nakao, Hazuki
El-Nouby, Mahmoud A. M.
Yanase, Emiko
Nomura, Izumi
Suzuki, Tohru
author_sort Altaib, Hend
collection PubMed
description BACKGROUND: Bifidobacteria are gram-positive, probiotic, and generally regarded as safe bacteria. Techniques such as transformation, gene knockout, and heterologous gene expression have been established for Bifidobacterium, indicating that this bacterium can be used as a cell factory platform. However, there are limited previous reports in this field, likely because of factors such as the highly anaerobic nature of this bacterium. Bifidobacterium adolescentis is among the most oxygen-sensitive Bifidobacterium species. It shows strain-specific gamma-aminobutyric acid (GABA) production. GABA is a potent bioactive compound with numerous physiological and psychological functions. In this study, we investigated whether B. adolesentis could be used for mass production of GABA. RESULTS: The B. adolescentis 4–2 strain isolated from a healthy adult human produced approximately 14 mM GABA. It carried gadB and gadC, which encode glutamate decarboxylase and glutamate GABA antiporter, respectively. We constructed pKKT427::P(ori)-gadBC and pKKT427::P(gap)-gadBC plasmids carrying gadBC driven by the original gadB (ori) and gap promoters, respectively. Recombinants of Bifidobacterium were then constructed. Two recombinants with high production abilities, monitored by two different promoters, were investigated. GABA production was improved by adjusting the fermentation parameters, including the substrate concentration, initial culture pH, and co-factor supplementation, using response surface methodology. The optimum initial cultivation pH varied when the promoter region was changed. The ori promoter was induced under acidic conditions (pH 5.2:4.4), whereas the constitutive gap promoter showed enhanced GABA production at pH 6.0. Fed-batch fermentation was used to validate the optimum fermentation parameters, in which approximately 415 mM GABA was produced. The conversion ratio of glutamate to GABA was 92–100%. CONCLUSION: We report high GABA production in recombinant B. adolescentis. This study provides a foundation for using Bifidobacterium as a cell factory platform for industrial production of GABA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-021-01729-6.
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spelling pubmed-89036512022-03-18 Cell factory for γ-aminobutyric acid (GABA) production using Bifidobacterium adolescentis Altaib, Hend Kozakai, Tomoya Badr, Yassien Nakao, Hazuki El-Nouby, Mahmoud A. M. Yanase, Emiko Nomura, Izumi Suzuki, Tohru Microb Cell Fact Research BACKGROUND: Bifidobacteria are gram-positive, probiotic, and generally regarded as safe bacteria. Techniques such as transformation, gene knockout, and heterologous gene expression have been established for Bifidobacterium, indicating that this bacterium can be used as a cell factory platform. However, there are limited previous reports in this field, likely because of factors such as the highly anaerobic nature of this bacterium. Bifidobacterium adolescentis is among the most oxygen-sensitive Bifidobacterium species. It shows strain-specific gamma-aminobutyric acid (GABA) production. GABA is a potent bioactive compound with numerous physiological and psychological functions. In this study, we investigated whether B. adolesentis could be used for mass production of GABA. RESULTS: The B. adolescentis 4–2 strain isolated from a healthy adult human produced approximately 14 mM GABA. It carried gadB and gadC, which encode glutamate decarboxylase and glutamate GABA antiporter, respectively. We constructed pKKT427::P(ori)-gadBC and pKKT427::P(gap)-gadBC plasmids carrying gadBC driven by the original gadB (ori) and gap promoters, respectively. Recombinants of Bifidobacterium were then constructed. Two recombinants with high production abilities, monitored by two different promoters, were investigated. GABA production was improved by adjusting the fermentation parameters, including the substrate concentration, initial culture pH, and co-factor supplementation, using response surface methodology. The optimum initial cultivation pH varied when the promoter region was changed. The ori promoter was induced under acidic conditions (pH 5.2:4.4), whereas the constitutive gap promoter showed enhanced GABA production at pH 6.0. Fed-batch fermentation was used to validate the optimum fermentation parameters, in which approximately 415 mM GABA was produced. The conversion ratio of glutamate to GABA was 92–100%. CONCLUSION: We report high GABA production in recombinant B. adolescentis. This study provides a foundation for using Bifidobacterium as a cell factory platform for industrial production of GABA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-021-01729-6. BioMed Central 2022-03-07 /pmc/articles/PMC8903651/ /pubmed/35255900 http://dx.doi.org/10.1186/s12934-021-01729-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Altaib, Hend
Kozakai, Tomoya
Badr, Yassien
Nakao, Hazuki
El-Nouby, Mahmoud A. M.
Yanase, Emiko
Nomura, Izumi
Suzuki, Tohru
Cell factory for γ-aminobutyric acid (GABA) production using Bifidobacterium adolescentis
title Cell factory for γ-aminobutyric acid (GABA) production using Bifidobacterium adolescentis
title_full Cell factory for γ-aminobutyric acid (GABA) production using Bifidobacterium adolescentis
title_fullStr Cell factory for γ-aminobutyric acid (GABA) production using Bifidobacterium adolescentis
title_full_unstemmed Cell factory for γ-aminobutyric acid (GABA) production using Bifidobacterium adolescentis
title_short Cell factory for γ-aminobutyric acid (GABA) production using Bifidobacterium adolescentis
title_sort cell factory for γ-aminobutyric acid (gaba) production using bifidobacterium adolescentis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903651/
https://www.ncbi.nlm.nih.gov/pubmed/35255900
http://dx.doi.org/10.1186/s12934-021-01729-6
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