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Enhanced production of sucrose in the fast-growing cyanobacterium Synechococcus elongatus UTEX 2973
Cyanobacteria are attractive microbial hosts for production of chemicals using light and CO(2). However, their low productivity of chemicals is a major challenge for commercial applications. This is mostly due to their relatively slow growth rate and carbon partitioning toward biomass rather than pr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962321/ https://www.ncbi.nlm.nih.gov/pubmed/31942010 http://dx.doi.org/10.1038/s41598-019-57319-5 |
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author | Lin, Po-Cheng Zhang, Fuzhong Pakrasi, Himadri B. |
author_facet | Lin, Po-Cheng Zhang, Fuzhong Pakrasi, Himadri B. |
author_sort | Lin, Po-Cheng |
collection | PubMed |
description | Cyanobacteria are attractive microbial hosts for production of chemicals using light and CO(2). However, their low productivity of chemicals is a major challenge for commercial applications. This is mostly due to their relatively slow growth rate and carbon partitioning toward biomass rather than products. Many cyanobacterial strains synthesize sucrose as an osmoprotectant to cope with salt stress environments. In this study, we harnessed the photosynthetic machinery of the fast-growing cyanobacterium Synechococcus elongatus UTEX 2973 to produce sucrose under salt stress conditions and investigated if the high efficiency of photosynthesis can enhance the productivity of sucrose. By expressing the sucrose transporter CscB, Synechococcus 2973 produced 8 g L(−1) of sucrose with a highest productivity of 1.9 g L(−1) day(−1) under salt stress conditions. The salt stress activated the sucrose biosynthetic pathway mostly via upregulating the sps gene, which encodes the rate-limiting sucrose-phosphate synthase enzyme. To alleviate the demand on high concentrations of salt for sucrose production, we further overexpressed the sucrose synthesis genes in Synechococcus 2973. The engineered strain produced sucrose with a productivity of 1.1 g L(−1) day(−1) without the need of salt induction. The engineered Synechococcus 2973 in this study demonstrated the highest productivity of sucrose in cyanobacteria. |
format | Online Article Text |
id | pubmed-6962321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69623212020-01-23 Enhanced production of sucrose in the fast-growing cyanobacterium Synechococcus elongatus UTEX 2973 Lin, Po-Cheng Zhang, Fuzhong Pakrasi, Himadri B. Sci Rep Article Cyanobacteria are attractive microbial hosts for production of chemicals using light and CO(2). However, their low productivity of chemicals is a major challenge for commercial applications. This is mostly due to their relatively slow growth rate and carbon partitioning toward biomass rather than products. Many cyanobacterial strains synthesize sucrose as an osmoprotectant to cope with salt stress environments. In this study, we harnessed the photosynthetic machinery of the fast-growing cyanobacterium Synechococcus elongatus UTEX 2973 to produce sucrose under salt stress conditions and investigated if the high efficiency of photosynthesis can enhance the productivity of sucrose. By expressing the sucrose transporter CscB, Synechococcus 2973 produced 8 g L(−1) of sucrose with a highest productivity of 1.9 g L(−1) day(−1) under salt stress conditions. The salt stress activated the sucrose biosynthetic pathway mostly via upregulating the sps gene, which encodes the rate-limiting sucrose-phosphate synthase enzyme. To alleviate the demand on high concentrations of salt for sucrose production, we further overexpressed the sucrose synthesis genes in Synechococcus 2973. The engineered strain produced sucrose with a productivity of 1.1 g L(−1) day(−1) without the need of salt induction. The engineered Synechococcus 2973 in this study demonstrated the highest productivity of sucrose in cyanobacteria. Nature Publishing Group UK 2020-01-15 /pmc/articles/PMC6962321/ /pubmed/31942010 http://dx.doi.org/10.1038/s41598-019-57319-5 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lin, Po-Cheng Zhang, Fuzhong Pakrasi, Himadri B. Enhanced production of sucrose in the fast-growing cyanobacterium Synechococcus elongatus UTEX 2973 |
title | Enhanced production of sucrose in the fast-growing cyanobacterium Synechococcus elongatus UTEX 2973 |
title_full | Enhanced production of sucrose in the fast-growing cyanobacterium Synechococcus elongatus UTEX 2973 |
title_fullStr | Enhanced production of sucrose in the fast-growing cyanobacterium Synechococcus elongatus UTEX 2973 |
title_full_unstemmed | Enhanced production of sucrose in the fast-growing cyanobacterium Synechococcus elongatus UTEX 2973 |
title_short | Enhanced production of sucrose in the fast-growing cyanobacterium Synechococcus elongatus UTEX 2973 |
title_sort | enhanced production of sucrose in the fast-growing cyanobacterium synechococcus elongatus utex 2973 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962321/ https://www.ncbi.nlm.nih.gov/pubmed/31942010 http://dx.doi.org/10.1038/s41598-019-57319-5 |
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