代谢工程
聚酮
聚酮合酶
酵母
生物化学
生物合成
合成生物学
化学
基质(水族馆)
代谢途径
产量(工程)
酶
基因
蛋白质工程
ATP合酶
生物
基因组
生产过剩
酿酒酵母
效价
细菌
分子工程
作者
Wenping Wei,Mengfan Li,Gaopan Cai,Jiayun Xu,Ping Zhang,Tao Qian,Xiaochuan Chen,Haiyang Su,Yihui Zhu,Xiaohe Chu,Bang-Ce Ye,Wenping Wei,Mengfan Li,Gaopan Cai,Jiayun Xu,Ping Zhang,Tao Qian,Xiaochuan Chen,Haiyang Su,Yihui Zhu
标识
DOI:10.1021/acs.jafc.5c07541
摘要
The polyketides 6-methylsalicylic acid (6-MSA) exhibits good resistance to plant pathogens and considerable application potential. However, conventional methods, such as plant extraction, have limited its industrialization and green synthesis. Microbial synthesis of 6-MSA is a novel and efficient preparation method. In this study, Yarrowia lipolytica was engineered by introducing the 6-MSA synthase gene (6-MSAS) and its activating partner 4'-phosphopantetheinyl transferase, along with the enhancement of precursor synthesis and substrate utilization genes, combined with genome multicopy integration strategies, resulted in the titer of 6-MSA to 3.93 g/L. Finally, through the implementation of xylose-induced biosynthesis modules and fermentation, the titer of 6-MSA was increased to 5.71 g/L in shake flasks and 25.88 g/L in a 5 L bioreactor, representing the highest yield reported to date. This study successfully demonstrated the potential for the synthesis of 6-MSA catalyzed by polyketide synthase I (PKS I) in yeast through systematic metabolic engineering approaches.
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