Cargando…
Photosynthetically produced sucrose by immobilized Synechocystis sp. PCC 6803 drives biotransformation in E. coli
BACKGROUND: Whole-cell biotransformation is a promising emerging technology for the production of chemicals. When using heterotrophic organisms such as E. coli and yeast as biocatalysts, the dependence on organic carbon source impairs the sustainability and economic viability of the process. As a pr...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795604/ https://www.ncbi.nlm.nih.gov/pubmed/36575466 http://dx.doi.org/10.1186/s13068-022-02248-1 |
_version_ | 1784860297569239040 |
---|---|
author | Tóth, Gábor Szilveszter Siitonen, Vilja Nikkanen, Lauri Sovic, Lucija Kallio, Pauli Kourist, Robert Kosourov, Sergey Allahverdiyeva, Yagut |
author_facet | Tóth, Gábor Szilveszter Siitonen, Vilja Nikkanen, Lauri Sovic, Lucija Kallio, Pauli Kourist, Robert Kosourov, Sergey Allahverdiyeva, Yagut |
author_sort | Tóth, Gábor Szilveszter |
collection | PubMed |
description | BACKGROUND: Whole-cell biotransformation is a promising emerging technology for the production of chemicals. When using heterotrophic organisms such as E. coli and yeast as biocatalysts, the dependence on organic carbon source impairs the sustainability and economic viability of the process. As a promising alternative, photosynthetic cyanobacteria with low nutrient requirements and versatile metabolism, could offer a sustainable platform for the heterologous production of organic compounds directly from sunlight and CO(2). This strategy has been applied for the photoautotrophic production of sucrose by a genetically engineered cyanobacterium, Synechocystis sp. PCC 6803 strain S02. As the key concept in the current work, this can be further used to generate organic carbon compounds for different heterotrophic applications, including for the whole-cell biotransformation by yeast and bacteria. RESULTS: Entrapment of Synechocystis S02 cells in Ca(2+)-cross-linked alginate hydrogel beads improves the specific sucrose productivity by 86% compared to suspension cultures during 7 days of cultivation under salt stress. The process was further prolonged by periodically changing the medium in the vials for up to 17 days of efficient production, giving the final sucrose yield slightly above 3000 mg l(−1). We successfully demonstrated that the medium enriched with photosynthetically produced sucrose by immobilized Synechocystis S02 cells supports the biotransformation of cyclohexanone to ε-caprolactone by the E. coli WΔcscR Inv:Parvi strain engineered to (i) utilize low concentrations of sucrose and (ii) perform biotransformation of cyclohexanone to ε-caprolactone. CONCLUSION: We conclude that cell entrapment in Ca(2+)-alginate beads is an effective method to prolong sucrose production by the engineered cyanobacteria, while allowing efficient separation of the cells from the medium. This advantage opens up novel possibilities to create advanced autotroph–heterotroph coupled cultivation systems for solar-driven production of chemicals via biotransformation, as demonstrated in this work by utilizing the photosynthetically produced sucrose to drive the conversion of cyclohexanone to ε-caprolactone by engineered E. coli. |
format | Online Article Text |
id | pubmed-9795604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97956042022-12-29 Photosynthetically produced sucrose by immobilized Synechocystis sp. PCC 6803 drives biotransformation in E. coli Tóth, Gábor Szilveszter Siitonen, Vilja Nikkanen, Lauri Sovic, Lucija Kallio, Pauli Kourist, Robert Kosourov, Sergey Allahverdiyeva, Yagut Biotechnol Biofuels Bioprod Research BACKGROUND: Whole-cell biotransformation is a promising emerging technology for the production of chemicals. When using heterotrophic organisms such as E. coli and yeast as biocatalysts, the dependence on organic carbon source impairs the sustainability and economic viability of the process. As a promising alternative, photosynthetic cyanobacteria with low nutrient requirements and versatile metabolism, could offer a sustainable platform for the heterologous production of organic compounds directly from sunlight and CO(2). This strategy has been applied for the photoautotrophic production of sucrose by a genetically engineered cyanobacterium, Synechocystis sp. PCC 6803 strain S02. As the key concept in the current work, this can be further used to generate organic carbon compounds for different heterotrophic applications, including for the whole-cell biotransformation by yeast and bacteria. RESULTS: Entrapment of Synechocystis S02 cells in Ca(2+)-cross-linked alginate hydrogel beads improves the specific sucrose productivity by 86% compared to suspension cultures during 7 days of cultivation under salt stress. The process was further prolonged by periodically changing the medium in the vials for up to 17 days of efficient production, giving the final sucrose yield slightly above 3000 mg l(−1). We successfully demonstrated that the medium enriched with photosynthetically produced sucrose by immobilized Synechocystis S02 cells supports the biotransformation of cyclohexanone to ε-caprolactone by the E. coli WΔcscR Inv:Parvi strain engineered to (i) utilize low concentrations of sucrose and (ii) perform biotransformation of cyclohexanone to ε-caprolactone. CONCLUSION: We conclude that cell entrapment in Ca(2+)-alginate beads is an effective method to prolong sucrose production by the engineered cyanobacteria, while allowing efficient separation of the cells from the medium. This advantage opens up novel possibilities to create advanced autotroph–heterotroph coupled cultivation systems for solar-driven production of chemicals via biotransformation, as demonstrated in this work by utilizing the photosynthetically produced sucrose to drive the conversion of cyclohexanone to ε-caprolactone by engineered E. coli. BioMed Central 2022-12-27 /pmc/articles/PMC9795604/ /pubmed/36575466 http://dx.doi.org/10.1186/s13068-022-02248-1 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 Tóth, Gábor Szilveszter Siitonen, Vilja Nikkanen, Lauri Sovic, Lucija Kallio, Pauli Kourist, Robert Kosourov, Sergey Allahverdiyeva, Yagut Photosynthetically produced sucrose by immobilized Synechocystis sp. PCC 6803 drives biotransformation in E. coli |
title | Photosynthetically produced sucrose by immobilized Synechocystis sp. PCC 6803 drives biotransformation in E. coli |
title_full | Photosynthetically produced sucrose by immobilized Synechocystis sp. PCC 6803 drives biotransformation in E. coli |
title_fullStr | Photosynthetically produced sucrose by immobilized Synechocystis sp. PCC 6803 drives biotransformation in E. coli |
title_full_unstemmed | Photosynthetically produced sucrose by immobilized Synechocystis sp. PCC 6803 drives biotransformation in E. coli |
title_short | Photosynthetically produced sucrose by immobilized Synechocystis sp. PCC 6803 drives biotransformation in E. coli |
title_sort | photosynthetically produced sucrose by immobilized synechocystis sp. pcc 6803 drives biotransformation in e. coli |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795604/ https://www.ncbi.nlm.nih.gov/pubmed/36575466 http://dx.doi.org/10.1186/s13068-022-02248-1 |
work_keys_str_mv | AT tothgaborszilveszter photosyntheticallyproducedsucrosebyimmobilizedsynechocystissppcc6803drivesbiotransformationinecoli AT siitonenvilja photosyntheticallyproducedsucrosebyimmobilizedsynechocystissppcc6803drivesbiotransformationinecoli AT nikkanenlauri photosyntheticallyproducedsucrosebyimmobilizedsynechocystissppcc6803drivesbiotransformationinecoli AT soviclucija photosyntheticallyproducedsucrosebyimmobilizedsynechocystissppcc6803drivesbiotransformationinecoli AT kalliopauli photosyntheticallyproducedsucrosebyimmobilizedsynechocystissppcc6803drivesbiotransformationinecoli AT kouristrobert photosyntheticallyproducedsucrosebyimmobilizedsynechocystissppcc6803drivesbiotransformationinecoli AT kosourovsergey photosyntheticallyproducedsucrosebyimmobilizedsynechocystissppcc6803drivesbiotransformationinecoli AT allahverdiyevayagut photosyntheticallyproducedsucrosebyimmobilizedsynechocystissppcc6803drivesbiotransformationinecoli |