High-yield production of protopanaxadiol from sugarcane molasses by metabolically engineered Saccharomyces cerevisiae

被引:8
作者
Zhu, Yuan [1 ,2 ]
Li, Jianxiu [2 ]
Peng, Longyun [2 ]
Meng, Lijun [2 ]
Diao, Mengxue [2 ]
Jiang, Shuiyuan [3 ]
Li, Jianbin [1 ]
Xie, Nengzhong [2 ]
机构
[1] Guangxi Univ, Coll Light Ind & Food Engn, 100 Daxue Rd, Nanning 530004, Peoples R China
[2] Guangxi Acad Sci, State Key Lab Nonfood Biomass & Enzyme Technol, Natl Engn Res Ctr Nonfood Biorefinery, Guangxi Biomass Engn Technol Res Ctr, 98 Daling Rd, Nanning 530007, Peoples R China
[3] Guangxi Zhuangzu Autonomous Reg & Chinese Acad Sc, Guangxi Inst Bot, Guilin 541006, Peoples R China
基金
中国国家自然科学基金;
关键词
Protopanaxadiol; Terpenoids; Synthetic biology; Sugarcane molasses; Saccharomyces cerevisiae; HIGH-LEVEL PRODUCTION; GINSENOSIDE RG(3); ESCHERICHIA-COLI; SAPONINS; ETHANOL; BIOSYNTHESIS; GENE; TRANSFORMATION; EXPRESSION; MEMBRANES;
D O I
10.1186/s12934-022-01949-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
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页数:13
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