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Reversible bacterial immobilization based on the salt-dependent adhesion of the bacterionanofiber protein AtaA
BACKGROUND: Immobilization of microbial cells is an important strategy for the efficient use of whole-cell catalysts because it simplifies product separation, enables the cell concentration to be increased, stabilizes enzymatic activity, and permits repeated or continuous biocatalyst use. However, c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516326/ https://www.ncbi.nlm.nih.gov/pubmed/28720107 http://dx.doi.org/10.1186/s12934-017-0740-7 |
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author | Yoshimoto, Shogo Ohara, Yuki Nakatani, Hajime Hori, Katsutoshi |
author_facet | Yoshimoto, Shogo Ohara, Yuki Nakatani, Hajime Hori, Katsutoshi |
author_sort | Yoshimoto, Shogo |
collection | PubMed |
description | BACKGROUND: Immobilization of microbial cells is an important strategy for the efficient use of whole-cell catalysts because it simplifies product separation, enables the cell concentration to be increased, stabilizes enzymatic activity, and permits repeated or continuous biocatalyst use. However, conventional immobilization methods have practical limitations, such as limited mass transfer in the inner part of a gel, gel fragility, cell leakage from the support matrix, and adverse effects on cell viability and catalytic activity. We previously showed a new method for bacterial cell immobilization using AtaA, a member of the trimeric autotransporter adhesin family found in Acinetobacter sp. Tol 5. This approach is expected to solve the drawbacks of conventional immobilization methods. However, similar to all other immobilization methods, the use of support materials increases the cost of bioprocesses and subsequent waste materials. RESULTS: We found that the stickiness of the AtaA molecule isolated from Tol 5 cells is drastically diminished at ionic strengths lower than 10 mM and that it cannot adhere in deionized water, which also inhibits cell adhesion mediated by AtaA. Cells immobilized on well plates and polyurethane foam in a salt solution were detached in deionized water by rinsing and shaking, respectively. The detached cells regained their adhesiveness in a salt solution and could rapidly be re-immobilized. The cells expressing the ataA gene maintained their adhesiveness throughout four repeated immobilization and detachment cycles and could be repeatedly immobilized to polyurethane foam by a 10-min shake in a flask. We also demonstrated that both bacterial cells and a support used in a reaction could be reused for a different type of reaction after detachment of the initially immobilized cells from the support and a subsequent immobilization step. CONCLUSIONS: We invented a unique reversible immobilization method based on the salt-dependent adhesion of the AtaA molecule that allows us to reuse bacterial cells and supports by a simple manipulation involving a deionized water wash. This mitigates problems caused by the use of support materials and greatly helps to enhance the efficiency and productivity of microbial production processes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-017-0740-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5516326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55163262017-07-20 Reversible bacterial immobilization based on the salt-dependent adhesion of the bacterionanofiber protein AtaA Yoshimoto, Shogo Ohara, Yuki Nakatani, Hajime Hori, Katsutoshi Microb Cell Fact Research BACKGROUND: Immobilization of microbial cells is an important strategy for the efficient use of whole-cell catalysts because it simplifies product separation, enables the cell concentration to be increased, stabilizes enzymatic activity, and permits repeated or continuous biocatalyst use. However, conventional immobilization methods have practical limitations, such as limited mass transfer in the inner part of a gel, gel fragility, cell leakage from the support matrix, and adverse effects on cell viability and catalytic activity. We previously showed a new method for bacterial cell immobilization using AtaA, a member of the trimeric autotransporter adhesin family found in Acinetobacter sp. Tol 5. This approach is expected to solve the drawbacks of conventional immobilization methods. However, similar to all other immobilization methods, the use of support materials increases the cost of bioprocesses and subsequent waste materials. RESULTS: We found that the stickiness of the AtaA molecule isolated from Tol 5 cells is drastically diminished at ionic strengths lower than 10 mM and that it cannot adhere in deionized water, which also inhibits cell adhesion mediated by AtaA. Cells immobilized on well plates and polyurethane foam in a salt solution were detached in deionized water by rinsing and shaking, respectively. The detached cells regained their adhesiveness in a salt solution and could rapidly be re-immobilized. The cells expressing the ataA gene maintained their adhesiveness throughout four repeated immobilization and detachment cycles and could be repeatedly immobilized to polyurethane foam by a 10-min shake in a flask. We also demonstrated that both bacterial cells and a support used in a reaction could be reused for a different type of reaction after detachment of the initially immobilized cells from the support and a subsequent immobilization step. CONCLUSIONS: We invented a unique reversible immobilization method based on the salt-dependent adhesion of the AtaA molecule that allows us to reuse bacterial cells and supports by a simple manipulation involving a deionized water wash. This mitigates problems caused by the use of support materials and greatly helps to enhance the efficiency and productivity of microbial production processes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-017-0740-7) contains supplementary material, which is available to authorized users. BioMed Central 2017-07-18 /pmc/articles/PMC5516326/ /pubmed/28720107 http://dx.doi.org/10.1186/s12934-017-0740-7 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Yoshimoto, Shogo Ohara, Yuki Nakatani, Hajime Hori, Katsutoshi Reversible bacterial immobilization based on the salt-dependent adhesion of the bacterionanofiber protein AtaA |
title | Reversible bacterial immobilization based on the salt-dependent adhesion of the bacterionanofiber protein AtaA |
title_full | Reversible bacterial immobilization based on the salt-dependent adhesion of the bacterionanofiber protein AtaA |
title_fullStr | Reversible bacterial immobilization based on the salt-dependent adhesion of the bacterionanofiber protein AtaA |
title_full_unstemmed | Reversible bacterial immobilization based on the salt-dependent adhesion of the bacterionanofiber protein AtaA |
title_short | Reversible bacterial immobilization based on the salt-dependent adhesion of the bacterionanofiber protein AtaA |
title_sort | reversible bacterial immobilization based on the salt-dependent adhesion of the bacterionanofiber protein ataa |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516326/ https://www.ncbi.nlm.nih.gov/pubmed/28720107 http://dx.doi.org/10.1186/s12934-017-0740-7 |
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