Author:
Zhu Yuan,Li Jianxiu,Peng Longyun,Meng Lijun,Diao Mengxue,Jiang Shuiyuan,Li Jianbin,Xie Nengzhong
Abstract
Abstract
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 PHXT1, 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
Funder
National Natural Science Foundation of China
Science and Technology of Guangxi Zhuang Autonomous
Innovation Project of Guangxi Graduate Education
Agriculture Research System of China
Science and Technology Service Network Initiative of Chinese Academy of Sciences
National Natural Science Foundation of Guangxi
Science foundation Project of Guangxi Academy of Sciences
Innovation-driven development project of Guangxi
Publisher
Springer Science and Business Media LLC
Subject
Applied Microbiology and Biotechnology,Bioengineering,Biotechnology
Reference54 articles.
1. Choi HI, Waminal NE, Park HM, Kim NH, Choi BS, Park M, Choi D, Lim YP, Kwon SJ, Park BK, et al. Major repeat components covering one-third of the ginseng (Panax ginseng C.A. Meyer) genome and evidence for allotetraploidy. Plant J. 2014;77:906–16.
2. Jeffreys LN, Girvan HM, McLean KJ, Munro AW. Chapter eight-characterization of cytochrome P450 enzymes and their applications in synthetic biology. In: Scrutton N, editor. Methods Enzymol, vol. 608. Academic Press; 2018. p. 189–261.
3. Zhang H, Xu HL, Fu WW, Xin Y, Li MW, Wang SJ, Yu XF, Sui DY. 20(S)-Protopanaxadiol induces human breast cancer MCF-7 apoptosis through a caspase-mediated pathway. Asian Pac J Cancer Prev. 2014;15:7919–23.
4. Han BH, Park MH, Han YN, Woo LK, Sankawa U, Yahara S, Tanaka O. Degradation of ginseng saponins under mild acidic conditions. Planta Med. 1982;44:146–9.
5. Bae E, Han MJ, Kim E, Kim D. Transformation of ginseng saponins to ginsenoside Rh2 by acids and human intestinal bacteria and biological activities of their transformants. Arch Pharmacal Res. 2004;27:61–7.
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