TY - JOUR
T1 - Increased Cordycepin Production in Yarrowia lipolytica Using Combinatorial Metabolic Engineering Strategies
AU - Song, Zeqi
AU - Lin, Wenbo
AU - Duan, Xiyu
AU - Song, Liping
AU - Wang, Chong
AU - Yang, Hui
AU - Lu, Xiangyang
AU - Ji, Xiaojun
AU - Tian, Yun
AU - Liu, Huhu
N1 - Publisher Copyright:
© 2023 American Chemical Society
PY - 2023/3/17
Y1 - 2023/3/17
N2 - As the first nucleoside antibiotic discovered in fungi, cordycepin, with its various biological activities, has wide applications. At present, cordycepin is mainly obtained from the natural fruiting bodies of Cordyceps militaris. However, due to long production periods, low yields, and low extraction efficiency, harvesting cordycepin from natural C. militaris is not ideal, making it difficult to meet market demands. In this study, an engineered Yarrowia lipolytica YlCor-18 strain, constructed by combining metabolic engineering strategies, achieved efficient de novo cordycepin production from glucose. First, the cordycepin biosynthetic pathway derived from C. militaris was introduced into Y. lipolytica. Furthermore, metabolic engineering strategies including promoter, protein, adenosine triphosphate, and precursor engineering were combined to enhance the synthetic ability of engineered strains of cordycepin. Fermentation conditions were also optimized, after which, the production titer and yields of cordycepin in the engineered strain YlCor-18 under fed-batch fermentation were improved to 4362.54 mg/L and 213.85 mg/g, respectively, after 168 h. This study demonstrates the potential of Y. lipolytica as a cell factory for cordycepin synthesis, which will serve as the model for the green biomanufacturing of other nucleoside antibiotics using artificial cell factories.
AB - As the first nucleoside antibiotic discovered in fungi, cordycepin, with its various biological activities, has wide applications. At present, cordycepin is mainly obtained from the natural fruiting bodies of Cordyceps militaris. However, due to long production periods, low yields, and low extraction efficiency, harvesting cordycepin from natural C. militaris is not ideal, making it difficult to meet market demands. In this study, an engineered Yarrowia lipolytica YlCor-18 strain, constructed by combining metabolic engineering strategies, achieved efficient de novo cordycepin production from glucose. First, the cordycepin biosynthetic pathway derived from C. militaris was introduced into Y. lipolytica. Furthermore, metabolic engineering strategies including promoter, protein, adenosine triphosphate, and precursor engineering were combined to enhance the synthetic ability of engineered strains of cordycepin. Fermentation conditions were also optimized, after which, the production titer and yields of cordycepin in the engineered strain YlCor-18 under fed-batch fermentation were improved to 4362.54 mg/L and 213.85 mg/g, respectively, after 168 h. This study demonstrates the potential of Y. lipolytica as a cell factory for cordycepin synthesis, which will serve as the model for the green biomanufacturing of other nucleoside antibiotics using artificial cell factories.
KW - Yarrowia lipolytica
KW - combinatorial metabolic engineering
KW - cordycepin
KW - fermentation optimization
KW - green biomanufacturing
UR - http://www.scopus.com/inward/record.url?scp=85148336404&partnerID=8YFLogxK
U2 - 10.1021/acssynbio.2c00570
DO - 10.1021/acssynbio.2c00570
M3 - 文章
C2 - 36791366
AN - SCOPUS:85148336404
SN - 2161-5063
VL - 12
SP - 780
EP - 787
JO - ACS Synthetic Biology
JF - ACS Synthetic Biology
IS - 3
ER -