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High-yield production of protopanaxadiol from sugarcane molasses by metabolically engineered Saccharomyces cerevisiae
BACKGROUND: Ginsenosides are Panax plant-derived triterpenoid with wide applications in cardiovascular protection and immunity-boosting. However, the saponins content of Panax plants is fairly low, making it time-consuming and unsustainable by direct extraction. Protopanaxadiol (PPD) is a common pre...
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/PMC9636795/ https://www.ncbi.nlm.nih.gov/pubmed/36335407 http://dx.doi.org/10.1186/s12934-022-01949-4 |
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author | Zhu, Yuan Li, Jianxiu Peng, Longyun Meng, Lijun Diao, Mengxue Jiang, Shuiyuan Li, Jianbin Xie, Nengzhong |
author_facet | Zhu, Yuan Li, Jianxiu Peng, Longyun Meng, Lijun Diao, Mengxue Jiang, Shuiyuan Li, Jianbin Xie, Nengzhong |
author_sort | Zhu, Yuan |
collection | PubMed |
description | BACKGROUND: Ginsenosides are Panax plant-derived triterpenoid with wide applications in cardiovascular protection and immunity-boosting. However, the saponins content of Panax plants is fairly low, making it time-consuming and unsustainable by direct extraction. Protopanaxadiol (PPD) is a common precursor of dammarane-type saponins, and its sufficient supply is necessary for the efficient synthesis of ginsenoside. RESULTS: In this study, a combinational strategy was used for the construction of an efficient yeast cell factory for PPD production. Firstly, a PPD-producing strain was successfully constructed by modular engineering in Saccharomyces cerevisiae BY4742 at the multi-copy sites. Then, the INO2 gene, encoding a transcriptional activator of the phospholipid biosynthesis, was fine-tuned to promote the endoplasmic reticulum (ER) proliferation and improve the catalytic efficiency of ER-localized enzymes. To increase the metabolic flux of PPD, dynamic control, based on a carbon-source regulated promoter P(HXT1), was introduced to repress the competition of sterols. Furthermore, the global transcription factor UPC2-1 was introduced to sterol homeostasis and up-regulate the MVA pathway, and the resulting strain BY-V achieved a PPD production of 78.13 ± 0.38 mg/g DCW (563.60 ± 1.65 mg/L). Finally, sugarcane molasses was used as an inexpensive substrate for the first time in PPD synthesis. The PPD titers reached 1.55 ± 0.02 and 15.88 ± 0.65 g/L in shake flasks and a 5-L bioreactor, respectively. To the best of our knowledge, these results were new records on PPD production. CONCLUSION: The high-level of PPD production in this study and the successful comprehensive utilization of low-cost carbon source -sugarcane molassesindicate that the constructed yeast cell factory is an excellent candidate strain for the production of high-value-added PPD and its derivativeswith great industrial potential. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-022-01949-4. |
format | Online Article Text |
id | pubmed-9636795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96367952022-11-06 High-yield production of protopanaxadiol from sugarcane molasses by metabolically engineered Saccharomyces cerevisiae Zhu, Yuan Li, Jianxiu Peng, Longyun Meng, Lijun Diao, Mengxue Jiang, Shuiyuan Li, Jianbin Xie, Nengzhong Microb Cell Fact Research BACKGROUND: Ginsenosides are Panax plant-derived triterpenoid with wide applications in cardiovascular protection and immunity-boosting. However, the saponins content of Panax plants is fairly low, making it time-consuming and unsustainable by direct extraction. Protopanaxadiol (PPD) is a common precursor of dammarane-type saponins, and its sufficient supply is necessary for the efficient synthesis of ginsenoside. RESULTS: In this study, a combinational strategy was used for the construction of an efficient yeast cell factory for PPD production. Firstly, a PPD-producing strain was successfully constructed by modular engineering in Saccharomyces cerevisiae BY4742 at the multi-copy sites. Then, the INO2 gene, encoding a transcriptional activator of the phospholipid biosynthesis, was fine-tuned to promote the endoplasmic reticulum (ER) proliferation and improve the catalytic efficiency of ER-localized enzymes. To increase the metabolic flux of PPD, dynamic control, based on a carbon-source regulated promoter P(HXT1), was introduced to repress the competition of sterols. Furthermore, the global transcription factor UPC2-1 was introduced to sterol homeostasis and up-regulate the MVA pathway, and the resulting strain BY-V achieved a PPD production of 78.13 ± 0.38 mg/g DCW (563.60 ± 1.65 mg/L). Finally, sugarcane molasses was used as an inexpensive substrate for the first time in PPD synthesis. The PPD titers reached 1.55 ± 0.02 and 15.88 ± 0.65 g/L in shake flasks and a 5-L bioreactor, respectively. To the best of our knowledge, these results were new records on PPD production. CONCLUSION: The high-level of PPD production in this study and the successful comprehensive utilization of low-cost carbon source -sugarcane molassesindicate that the constructed yeast cell factory is an excellent candidate strain for the production of high-value-added PPD and its derivativeswith great industrial potential. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-022-01949-4. BioMed Central 2022-11-05 /pmc/articles/PMC9636795/ /pubmed/36335407 http://dx.doi.org/10.1186/s12934-022-01949-4 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 Zhu, Yuan Li, Jianxiu Peng, Longyun Meng, Lijun Diao, Mengxue Jiang, Shuiyuan Li, Jianbin Xie, Nengzhong High-yield production of protopanaxadiol from sugarcane molasses by metabolically engineered Saccharomyces cerevisiae |
title | High-yield production of protopanaxadiol from sugarcane molasses by metabolically engineered Saccharomyces cerevisiae |
title_full | High-yield production of protopanaxadiol from sugarcane molasses by metabolically engineered Saccharomyces cerevisiae |
title_fullStr | High-yield production of protopanaxadiol from sugarcane molasses by metabolically engineered Saccharomyces cerevisiae |
title_full_unstemmed | High-yield production of protopanaxadiol from sugarcane molasses by metabolically engineered Saccharomyces cerevisiae |
title_short | High-yield production of protopanaxadiol from sugarcane molasses by metabolically engineered Saccharomyces cerevisiae |
title_sort | high-yield production of protopanaxadiol from sugarcane molasses by metabolically engineered saccharomyces cerevisiae |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636795/ https://www.ncbi.nlm.nih.gov/pubmed/36335407 http://dx.doi.org/10.1186/s12934-022-01949-4 |
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