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Systems Metabolic Engineering of Saccharomyces cerevisiae for the High-Level Production of (2S)-Eriodictyol.
Zhang, Siqi; Liu, Juan; Xiao, Zhiqiang; Tan, Xinjia; Wang, Yongtong; Zhao, Yifei; Jiang, Ning; Shan, Yang.
Afiliación
  • Zhang S; Longping Branch, College of Biology, Hunan University, Changsha 410125, China.
  • Liu J; Agriculture Product Processing Institute, Hunan Academy of Agricultural Sciences, Changsha 410125, China.
  • Xiao Z; Hunan Key Lab of Fruits & Vegetables Storage, Processing, Quality and Safety, Hunan Agricultural Products Processing Institute, Changsha 410125, China.
  • Tan X; Longping Branch, College of Biology, Hunan University, Changsha 410125, China.
  • Wang Y; Agriculture Product Processing Institute, Hunan Academy of Agricultural Sciences, Changsha 410125, China.
  • Zhao Y; Hunan Key Lab of Fruits & Vegetables Storage, Processing, Quality and Safety, Hunan Agricultural Products Processing Institute, Changsha 410125, China.
  • Jiang N; Department of Life Sciences, Chalmers University of Technology, SE412 96 Gothenburg, Sweden.
  • Shan Y; Longping Branch, College of Biology, Hunan University, Changsha 410125, China.
J Fungi (Basel) ; 10(2)2024 Jan 31.
Article en En | MEDLINE | ID: mdl-38392791
ABSTRACT
(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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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Fungi (Basel) Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Fungi (Basel) Año: 2024 Tipo del documento: Article País de afiliación: China