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Removal of the product from the culture medium strongly enhances free fatty acid production by genetically engineered Synechococcus elongatus
BACKGROUND: Cyanobacterial mutants engineered for production of free fatty acids (FFAs) secrete the products to the medium and hence are thought to be useful for biofuel production. The dAS1T mutant constructed from Synechococcus elongatus PCC 7942 has indeed a large capacity of FFA production, whic...
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/PMC5452621/ https://www.ncbi.nlm.nih.gov/pubmed/28580015 http://dx.doi.org/10.1186/s13068-017-0831-z |
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author | Kato, Akihiro Takatani, Nobuyuki Ikeda, Kazutaka Maeda, Shin-ichi Omata, Tatsuo |
author_facet | Kato, Akihiro Takatani, Nobuyuki Ikeda, Kazutaka Maeda, Shin-ichi Omata, Tatsuo |
author_sort | Kato, Akihiro |
collection | PubMed |
description | BACKGROUND: Cyanobacterial mutants engineered for production of free fatty acids (FFAs) secrete the products to the medium and hence are thought to be useful for biofuel production. The dAS1T mutant constructed from Synechococcus elongatus PCC 7942 has indeed a large capacity of FFA production, which is comparable to that of triacylglycerol production in green algae, but the yield of secreted FFAs is low because the cells accumulate most of the FFAs intracellularly and eventually die of their toxicity. To increase the FFA productivity, enhancement of FFA secretion is required. RESULTS: Growth of dAS1T cells but not WT cells was inhibited in a liquid medium supplemented with 0.13 g L(−1) of palmitic acid. This suggested that when FFA accumulates in the medium, it would inhibit the release of FFA from the cell, leading to FFA accumulation in the cell to a toxic level. To remove FFAs from the medium during cultivation, an aqueous-organic two-phase culture system was developed. When the dAS1T culture was overlaid with isopropyl myristate (IM), the final cell density, cellular chlorophyll content, and the photosynthetic yield of PSII were greatly improved. The total amount of extracellular FFA was more than three times larger than that in the control culture grown without IM, with most of the secreted FFAs being recovered in the IM layer. The cellular FFA content was decreased by more than 85% by the presence of the IM layer. Thus, the two-phase culture system effectively facilitated FFA secretion out of the cell. An average FFA excretion rate of 1.5 mg L(−1) h(−1) was attained in the 432 h of cultivation, with a total amount of excreted FFA being 0.64 g L(−1) of culture. These figures were more than three times higher than those reported previously for the cyanobacteria-based FFA production systems. CONCLUSIONS: Removal of FFA from the culture medium is important for improving the productivity of the FFA production system using cyanobacteria. Further increase in productivity would require an increase in both the rates of FFA production in the cell and active FFA export across the plasma membrane. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-017-0831-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5452621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54526212017-06-02 Removal of the product from the culture medium strongly enhances free fatty acid production by genetically engineered Synechococcus elongatus Kato, Akihiro Takatani, Nobuyuki Ikeda, Kazutaka Maeda, Shin-ichi Omata, Tatsuo Biotechnol Biofuels Research BACKGROUND: Cyanobacterial mutants engineered for production of free fatty acids (FFAs) secrete the products to the medium and hence are thought to be useful for biofuel production. The dAS1T mutant constructed from Synechococcus elongatus PCC 7942 has indeed a large capacity of FFA production, which is comparable to that of triacylglycerol production in green algae, but the yield of secreted FFAs is low because the cells accumulate most of the FFAs intracellularly and eventually die of their toxicity. To increase the FFA productivity, enhancement of FFA secretion is required. RESULTS: Growth of dAS1T cells but not WT cells was inhibited in a liquid medium supplemented with 0.13 g L(−1) of palmitic acid. This suggested that when FFA accumulates in the medium, it would inhibit the release of FFA from the cell, leading to FFA accumulation in the cell to a toxic level. To remove FFAs from the medium during cultivation, an aqueous-organic two-phase culture system was developed. When the dAS1T culture was overlaid with isopropyl myristate (IM), the final cell density, cellular chlorophyll content, and the photosynthetic yield of PSII were greatly improved. The total amount of extracellular FFA was more than three times larger than that in the control culture grown without IM, with most of the secreted FFAs being recovered in the IM layer. The cellular FFA content was decreased by more than 85% by the presence of the IM layer. Thus, the two-phase culture system effectively facilitated FFA secretion out of the cell. An average FFA excretion rate of 1.5 mg L(−1) h(−1) was attained in the 432 h of cultivation, with a total amount of excreted FFA being 0.64 g L(−1) of culture. These figures were more than three times higher than those reported previously for the cyanobacteria-based FFA production systems. CONCLUSIONS: Removal of FFA from the culture medium is important for improving the productivity of the FFA production system using cyanobacteria. Further increase in productivity would require an increase in both the rates of FFA production in the cell and active FFA export across the plasma membrane. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-017-0831-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-05-31 /pmc/articles/PMC5452621/ /pubmed/28580015 http://dx.doi.org/10.1186/s13068-017-0831-z 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 Kato, Akihiro Takatani, Nobuyuki Ikeda, Kazutaka Maeda, Shin-ichi Omata, Tatsuo Removal of the product from the culture medium strongly enhances free fatty acid production by genetically engineered Synechococcus elongatus |
title | Removal of the product from the culture medium strongly enhances free fatty acid production by genetically engineered Synechococcus elongatus |
title_full | Removal of the product from the culture medium strongly enhances free fatty acid production by genetically engineered Synechococcus elongatus |
title_fullStr | Removal of the product from the culture medium strongly enhances free fatty acid production by genetically engineered Synechococcus elongatus |
title_full_unstemmed | Removal of the product from the culture medium strongly enhances free fatty acid production by genetically engineered Synechococcus elongatus |
title_short | Removal of the product from the culture medium strongly enhances free fatty acid production by genetically engineered Synechococcus elongatus |
title_sort | removal of the product from the culture medium strongly enhances free fatty acid production by genetically engineered synechococcus elongatus |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452621/ https://www.ncbi.nlm.nih.gov/pubmed/28580015 http://dx.doi.org/10.1186/s13068-017-0831-z |
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