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Metabolic recycling of storage lipids promotes squalene biosynthesis in yeast
BACKGROUND: Metabolic rewiring in microbes is an economical and sustainable strategy for synthesizing valuable natural terpenes. Terpenes are the largest class of nature-derived specialized metabolites, and many have valuable pharmaceutical or biological activity. Squalene, a medicinal terpene, is u...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555684/ https://www.ncbi.nlm.nih.gov/pubmed/36224649 http://dx.doi.org/10.1186/s13068-022-02208-9 |
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author | Son, So-Hee Kim, Jae-Eung Moon, Soo Young Jang, In-Seung Yu, Byung Jo Lee, Ju Young |
author_facet | Son, So-Hee Kim, Jae-Eung Moon, Soo Young Jang, In-Seung Yu, Byung Jo Lee, Ju Young |
author_sort | Son, So-Hee |
collection | PubMed |
description | BACKGROUND: Metabolic rewiring in microbes is an economical and sustainable strategy for synthesizing valuable natural terpenes. Terpenes are the largest class of nature-derived specialized metabolites, and many have valuable pharmaceutical or biological activity. Squalene, a medicinal terpene, is used as a vaccine adjuvant to improve the efficacy of vaccines, including pandemic coronavirus disease 2019 (COVID-19) vaccines, and plays diverse biological roles as an antioxidant and anticancer agent. However, metabolic rewiring interferes with inherent metabolic pathways, often in a way that impairs the cellular growth and fitness of the microbial host. In particular, as the key starting molecule for producing various compounds including squalene, acetyl-CoA is involved in numerous biological processes with tight regulation to maintain metabolic homeostasis, which limits redirection of metabolic fluxes toward desired products. RESULTS: In this study, focusing on the recycling of surplus metabolic energy stored in lipid droplets, we show that the metabolic recycling of the surplus energy to acetyl-CoA can increase squalene production in yeast, concomitant with minimizing the metabolic interferences in inherent pathways. Moreover, by integrating multiple copies of the rate-limiting enzyme and implementing N-degron-dependent protein degradation to downregulate the competing pathway, we systematically rewired the metabolic flux toward squalene, enabling remarkable squalene production (1024.88 mg/L in a shake flask). Ultimately, further optimization of the fed-batch fermentation process enabled remarkable squalene production of 6.53 g/L. CONCLUSIONS: Our demonstration of squalene production via engineered yeast suggests that plant- or animal-based supplies of medicinal squalene can potentially be complemented or replaced by industrial fermentation. This approach will also provide a universal strategy for the more stable and sustainable production of high-value terpenes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13068-022-02208-9. |
format | Online Article Text |
id | pubmed-9555684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95556842022-10-13 Metabolic recycling of storage lipids promotes squalene biosynthesis in yeast Son, So-Hee Kim, Jae-Eung Moon, Soo Young Jang, In-Seung Yu, Byung Jo Lee, Ju Young Biotechnol Biofuels Bioprod Research BACKGROUND: Metabolic rewiring in microbes is an economical and sustainable strategy for synthesizing valuable natural terpenes. Terpenes are the largest class of nature-derived specialized metabolites, and many have valuable pharmaceutical or biological activity. Squalene, a medicinal terpene, is used as a vaccine adjuvant to improve the efficacy of vaccines, including pandemic coronavirus disease 2019 (COVID-19) vaccines, and plays diverse biological roles as an antioxidant and anticancer agent. However, metabolic rewiring interferes with inherent metabolic pathways, often in a way that impairs the cellular growth and fitness of the microbial host. In particular, as the key starting molecule for producing various compounds including squalene, acetyl-CoA is involved in numerous biological processes with tight regulation to maintain metabolic homeostasis, which limits redirection of metabolic fluxes toward desired products. RESULTS: In this study, focusing on the recycling of surplus metabolic energy stored in lipid droplets, we show that the metabolic recycling of the surplus energy to acetyl-CoA can increase squalene production in yeast, concomitant with minimizing the metabolic interferences in inherent pathways. Moreover, by integrating multiple copies of the rate-limiting enzyme and implementing N-degron-dependent protein degradation to downregulate the competing pathway, we systematically rewired the metabolic flux toward squalene, enabling remarkable squalene production (1024.88 mg/L in a shake flask). Ultimately, further optimization of the fed-batch fermentation process enabled remarkable squalene production of 6.53 g/L. CONCLUSIONS: Our demonstration of squalene production via engineered yeast suggests that plant- or animal-based supplies of medicinal squalene can potentially be complemented or replaced by industrial fermentation. This approach will also provide a universal strategy for the more stable and sustainable production of high-value terpenes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13068-022-02208-9. BioMed Central 2022-10-12 /pmc/articles/PMC9555684/ /pubmed/36224649 http://dx.doi.org/10.1186/s13068-022-02208-9 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 Son, So-Hee Kim, Jae-Eung Moon, Soo Young Jang, In-Seung Yu, Byung Jo Lee, Ju Young Metabolic recycling of storage lipids promotes squalene biosynthesis in yeast |
title | Metabolic recycling of storage lipids promotes squalene biosynthesis in yeast |
title_full | Metabolic recycling of storage lipids promotes squalene biosynthesis in yeast |
title_fullStr | Metabolic recycling of storage lipids promotes squalene biosynthesis in yeast |
title_full_unstemmed | Metabolic recycling of storage lipids promotes squalene biosynthesis in yeast |
title_short | Metabolic recycling of storage lipids promotes squalene biosynthesis in yeast |
title_sort | metabolic recycling of storage lipids promotes squalene biosynthesis in yeast |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555684/ https://www.ncbi.nlm.nih.gov/pubmed/36224649 http://dx.doi.org/10.1186/s13068-022-02208-9 |
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