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Systems Metabolic Engineering of Saccharomyces cerevisiae for the High-Level Production of (2S)-Eriodictyol

文献类型: 外文期刊

作者: Zhang, Siqi 1 ; Liu, Juan 1 ; Xiao, Zhiqiang 1 ; Tan, Xinjia 1 ; Wang, Yongtong 1 ; Zhao, Yifei 1 ; Jiang, Ning 1 ; Shan, Yang 1 ;

作者机构: 1.Hunan Univ, Coll Biol, Longping Branch, Changsha 410125, Peoples R China

2.Hunan Acad Agr Sci, Agr Prod Proc Inst, Changsha 410125, Peoples R China

3.Hunan Agr Prod Proc Inst, Hunan Key Lab Fruits & Vegetables Storage Proc Qua, Changsha 410125, Peoples R China

4.Chalmers Univ Technol, Dept Life Sci, SE-41296 Gothenburg, Sweden

关键词: flavonoid; (2S)-naringenin; (2S)-eriodictyol; metabolic engineering; metabolic balance

期刊名称:JOURNAL OF FUNGI ( 影响因子:4.7; 五年影响因子:5.2 )

ISSN:

年卷期: 2024 年 10 卷 2 期

页码:

收录情况: SCI

摘要: (2S)-eriodictyol (ERD) is a flavonoid widely found in citrus fruits, vegetables, and important medicinal plants with neuroprotective, cardioprotective, antidiabetic, and anti-obesity effects. However, the microbial synthesis of ERD is limited by complex metabolic pathways and often results in a low production performance. Here, we engineered Saccharomyces cerevisiae by fine-tuning the metabolism of the ERD synthesis pathway. The results showed that the ERD titer was effectively increased, and the intermediate metabolites levels were reduced. First, we successfully reconstructed the de novo synthesis pathway of p-coumaric acid in S. cerevisiae and fine-tuned the metabolic pathway using promoter engineering and terminator engineering for the high-level production of (2S)-naringenin. Subsequently, the synthesis of ERD was achieved by introducing the ThF3 ' H gene from Tricyrtis hirta. Finally, by multiplying the copy number of the ThF3 ' H gene, the production of ERD was further increased, reaching 132.08 mg L-1. Our work emphasizes the importance of regulating the metabolic balance to produce natural products in microbial cell factories.

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