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.
引用
收藏
页数:13
相关论文
共 50 条
  • [31] High-titer production of 13R-manoyl oxide in metabolically engineered Saccharomyces cerevisiae
    Chuanbo Zhang
    Haiyan Ju
    Chun-Zhe Lu
    Fanglong Zhao
    Jingjing Liu
    Xiaoyan Guo
    Yufen Wu
    Guang-Rong Zhao
    Wenyu Lu
    Microbial Cell Factories, 18
  • [32] A modular engineering strategy for high-level production of protopanaxadiol from ethanol by Saccharomyces cerevisiae
    Zhao, Fanglong
    Bai, Peng
    Nan, Weihua
    Li, Dashuai
    Zhang, Chuanbo
    Lu, Chunzhe
    Qi, Haishan
    Lu, Wenyu
    AICHE JOURNAL, 2019, 65 (03) : 866 - 874
  • [33] Biosynthesis of adipic acid in metabolically engineered Saccharomyces cerevisiae
    Xi Zhang
    Yingli Liu
    Jing Wang
    Yunying Zhao
    Yu Deng
    Journal of Microbiology, 2020, 58 : 1065 - 1075
  • [34] Biosynthesis of adipic acid in metabolically engineered Saccharomyces cerevisiae
    Zhang, Xi
    Liu, Yingli
    Wang, Jing
    Zhao, Yunying
    Deng, Yu
    JOURNAL OF MICROBIOLOGY, 2020, 58 (12) : 1065 - 1075
  • [35] D-Lactic Acid Production from Sugarcane Bagasse by Genetically Engineered Saccharomyces cerevisiae
    Sornlek, Warasirin
    Sae-Tang, Kittapong
    Watcharawipas, Akaraphol
    Wongwisansri, Sriwan
    Tanapongpipat, Sutipa
    Eurwilaichtr, Lily
    Champreda, Verawat
    Runguphan, Weerawat
    Schaap, Peter J.
    Dos Santos, Vitor A. P. Martins
    JOURNAL OF FUNGI, 2022, 8 (08)
  • [36] Lipid engineering combined with systematic metabolic engineering of Saccharomyces cerevisiae for high-yield production of lycopene
    Ma, Tian
    Shi, Bin
    Ye, Ziling
    Li, Xiaowei
    Liu, Min
    Chen, Yun
    Xia, Jiang
    Nielsen, Jens
    Deng, Zixin
    Liu, Tiangang
    METABOLIC ENGINEERING, 2019, 52 : 134 - 142
  • [37] Efficient production of glycyrrhetinic acid in metabolically engineered Saccharomyces cerevisiae via an integrated strategy
    Caixia Wang
    Xinyao Su
    Mengchu Sun
    Mengting Zhang
    Jiajia Wu
    Jianmin Xing
    Ying Wang
    Jianping Xue
    Xia Liu
    Wei Sun
    Shilin Chen
    Microbial Cell Factories, 18
  • [38] Production of L-ascorbic acid by metabolically engineered Saccharomyces cerevisiae and Zygosaccharomyces bailii
    Sauer, M
    Branduardi, P
    Valli, M
    Porro, D
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (10) : 6086 - 6091
  • [39] Ergosterol production from molasses by genetically modified Saccharomyces cerevisiae
    Xiuping He
    Xuena Guo
    Nan Liu
    Borun Zhang
    Applied Microbiology and Biotechnology, 2007, 75 : 55 - 60
  • [40] BIOSYNTHESIS OF INVERTASE BY SACCHAROMYCES-CEREVISIAE WITH SUGARCANE MOLASSES AS SUBSTRATE
    BOKOSSA, IP
    KRASTANOV, AI
    ROCHKOVA, Z
    ANGELOV, A
    WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY, 1993, 9 (06): : 662 - 663