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Using small molecules as a new challenge to redirect metabolic pathway
The presence of acetate in the bacterial medium leads to a reduction in the growth rate of cells and recombinant protein production. In this study, three compounds including propionic acid, lithium chloride and butyric acid were added to the medium which decreased acetate levels and enhanced recombi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162896/ https://www.ncbi.nlm.nih.gov/pubmed/28324386 http://dx.doi.org/10.1007/s13205-013-0185-6 |
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author | Morshedi, Dina Aliakbari, Farhang Nouri, Hamid Reza Lotfinia, Majid Fallahi, Jafar |
author_facet | Morshedi, Dina Aliakbari, Farhang Nouri, Hamid Reza Lotfinia, Majid Fallahi, Jafar |
author_sort | Morshedi, Dina |
collection | PubMed |
description | The presence of acetate in the bacterial medium leads to a reduction in the growth rate of cells and recombinant protein production. In this study, three compounds including propionic acid, lithium chloride and butyric acid were added to the medium which decreased acetate levels and enhanced recombinant protein production (alpha-synuclein). In fact, propionic acid and lithium chloride are both known as acetate kinase inhibitors. The results obtained in the case of butyric acid were similar to those of the two other compounds indicating that butyric acid may act through a mechanism similar to propionic acid and lithium chloride. Consequently, it was shown that the presence of each of these supplements (5–200 μM) increased recombinant alpha-synuclein production and cell density by approximately 10–15 %. HPLC analysis showed that the levels of acetate in the media containing the supplements were considerably less than those of the control. Furthermore, pH values remained almost constant in the supplemented cultures. Growing the bacteria at lower temperatures (25 °C) indicated that the positive effects of these supplements were not as effective as at higher temperatures (37 °C), presumably due to the adequate balance between oxygen and carbon consumption. This study can confirm the viewpoint regarding the harmful effects of acetate on the recombinant protein production and cell density. Besides, such methods represent easy and complementary ways to increase target recombinant protein production without negatively affecting host cell density, and requiring complex genetic manipulation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13205-013-0185-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4162896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-41628962014-09-22 Using small molecules as a new challenge to redirect metabolic pathway Morshedi, Dina Aliakbari, Farhang Nouri, Hamid Reza Lotfinia, Majid Fallahi, Jafar 3 Biotech Original Article The presence of acetate in the bacterial medium leads to a reduction in the growth rate of cells and recombinant protein production. In this study, three compounds including propionic acid, lithium chloride and butyric acid were added to the medium which decreased acetate levels and enhanced recombinant protein production (alpha-synuclein). In fact, propionic acid and lithium chloride are both known as acetate kinase inhibitors. The results obtained in the case of butyric acid were similar to those of the two other compounds indicating that butyric acid may act through a mechanism similar to propionic acid and lithium chloride. Consequently, it was shown that the presence of each of these supplements (5–200 μM) increased recombinant alpha-synuclein production and cell density by approximately 10–15 %. HPLC analysis showed that the levels of acetate in the media containing the supplements were considerably less than those of the control. Furthermore, pH values remained almost constant in the supplemented cultures. Growing the bacteria at lower temperatures (25 °C) indicated that the positive effects of these supplements were not as effective as at higher temperatures (37 °C), presumably due to the adequate balance between oxygen and carbon consumption. This study can confirm the viewpoint regarding the harmful effects of acetate on the recombinant protein production and cell density. Besides, such methods represent easy and complementary ways to increase target recombinant protein production without negatively affecting host cell density, and requiring complex genetic manipulation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13205-013-0185-6) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2013-11-30 2014-10 /pmc/articles/PMC4162896/ /pubmed/28324386 http://dx.doi.org/10.1007/s13205-013-0185-6 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Article Morshedi, Dina Aliakbari, Farhang Nouri, Hamid Reza Lotfinia, Majid Fallahi, Jafar Using small molecules as a new challenge to redirect metabolic pathway |
title | Using small molecules as a new challenge to redirect metabolic pathway |
title_full | Using small molecules as a new challenge to redirect metabolic pathway |
title_fullStr | Using small molecules as a new challenge to redirect metabolic pathway |
title_full_unstemmed | Using small molecules as a new challenge to redirect metabolic pathway |
title_short | Using small molecules as a new challenge to redirect metabolic pathway |
title_sort | using small molecules as a new challenge to redirect metabolic pathway |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162896/ https://www.ncbi.nlm.nih.gov/pubmed/28324386 http://dx.doi.org/10.1007/s13205-013-0185-6 |
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