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(13)C-metabolic flux analysis of ethanol-assimilating Saccharomyces cerevisiae for S-adenosyl-l-methionine production
BACKGROUND: Saccharomyces cerevisiae is a host for the industrial production of S-adenosyl-l-methionine (SAM), which has been widely used in pharmaceutical and nutritional supplement industries. It has been reported that the intracellular SAM content in S. cerevisiae can be improved by the addition...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977476/ https://www.ncbi.nlm.nih.gov/pubmed/29855316 http://dx.doi.org/10.1186/s12934-018-0935-6 |
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author | Hayakawa, Kenshi Matsuda, Fumio Shimizu, Hiroshi |
author_facet | Hayakawa, Kenshi Matsuda, Fumio Shimizu, Hiroshi |
author_sort | Hayakawa, Kenshi |
collection | PubMed |
description | BACKGROUND: Saccharomyces cerevisiae is a host for the industrial production of S-adenosyl-l-methionine (SAM), which has been widely used in pharmaceutical and nutritional supplement industries. It has been reported that the intracellular SAM content in S. cerevisiae can be improved by the addition of ethanol during cultivation. However, the metabolic state in ethanol-assimilating S. cerevisiae remains unclear. In this study, (13)C-metabolic flux analysis ((13)C-MFA) was conducted to investigate the metabolic regulation responsible for the high SAM production from ethanol. RESULTS: The comparison between the metabolic flux distributions of central carbon metabolism showed that the metabolic flux levels of the tricarboxylic acid cycle and glyoxylate shunt in the ethanol culture were significantly higher than that of glucose. Estimates of the ATP balance from the (13)C-MFA data suggested that larger amounts of excess ATP was produced from ethanol via increased oxidative phosphorylation. The finding was confirmed by the intracellular ATP level under ethanol-assimilating condition being similarly higher than glucose. CONCLUSIONS: These results suggest that the enhanced ATP regeneration due to ethanol assimilation was critical for the high SAM accumulation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-018-0935-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5977476 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59774762018-06-06 (13)C-metabolic flux analysis of ethanol-assimilating Saccharomyces cerevisiae for S-adenosyl-l-methionine production Hayakawa, Kenshi Matsuda, Fumio Shimizu, Hiroshi Microb Cell Fact Research BACKGROUND: Saccharomyces cerevisiae is a host for the industrial production of S-adenosyl-l-methionine (SAM), which has been widely used in pharmaceutical and nutritional supplement industries. It has been reported that the intracellular SAM content in S. cerevisiae can be improved by the addition of ethanol during cultivation. However, the metabolic state in ethanol-assimilating S. cerevisiae remains unclear. In this study, (13)C-metabolic flux analysis ((13)C-MFA) was conducted to investigate the metabolic regulation responsible for the high SAM production from ethanol. RESULTS: The comparison between the metabolic flux distributions of central carbon metabolism showed that the metabolic flux levels of the tricarboxylic acid cycle and glyoxylate shunt in the ethanol culture were significantly higher than that of glucose. Estimates of the ATP balance from the (13)C-MFA data suggested that larger amounts of excess ATP was produced from ethanol via increased oxidative phosphorylation. The finding was confirmed by the intracellular ATP level under ethanol-assimilating condition being similarly higher than glucose. CONCLUSIONS: These results suggest that the enhanced ATP regeneration due to ethanol assimilation was critical for the high SAM accumulation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-018-0935-6) contains supplementary material, which is available to authorized users. BioMed Central 2018-05-31 /pmc/articles/PMC5977476/ /pubmed/29855316 http://dx.doi.org/10.1186/s12934-018-0935-6 Text en © The Author(s) 2018 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 Hayakawa, Kenshi Matsuda, Fumio Shimizu, Hiroshi (13)C-metabolic flux analysis of ethanol-assimilating Saccharomyces cerevisiae for S-adenosyl-l-methionine production |
title | (13)C-metabolic flux analysis of ethanol-assimilating Saccharomyces cerevisiae for S-adenosyl-l-methionine production |
title_full | (13)C-metabolic flux analysis of ethanol-assimilating Saccharomyces cerevisiae for S-adenosyl-l-methionine production |
title_fullStr | (13)C-metabolic flux analysis of ethanol-assimilating Saccharomyces cerevisiae for S-adenosyl-l-methionine production |
title_full_unstemmed | (13)C-metabolic flux analysis of ethanol-assimilating Saccharomyces cerevisiae for S-adenosyl-l-methionine production |
title_short | (13)C-metabolic flux analysis of ethanol-assimilating Saccharomyces cerevisiae for S-adenosyl-l-methionine production |
title_sort | (13)c-metabolic flux analysis of ethanol-assimilating saccharomyces cerevisiae for s-adenosyl-l-methionine production |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977476/ https://www.ncbi.nlm.nih.gov/pubmed/29855316 http://dx.doi.org/10.1186/s12934-018-0935-6 |
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