详细信息
The yeast peroxisome: A dynamic storage depot and subcellular factory for squalene overproduction ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:The yeast peroxisome: A dynamic storage depot and subcellular factory for squalene overproduction
作者:Liu, Guo-Song[1];Li, Tian[1];Zhou, Wei[1];Jiang, Min[1];Tao, Xin-Yi[1];Liu, Min[1];Zhao, Ming[1];Ren, Yu-Hong[1];Gao, Bei[1];Wang, Feng-Qing[1];Wei, Dong-Zhi[1]
机构:[1]East China Univ Sci & Technol, Newworld Inst Biotechnol, State Key Lab Bioreactor Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China
年份:2020
卷号:57
起止页码:151
外文期刊名:METABOLIC ENGINEERING
收录:;EI(收录号:20194707707904);WOS:【SCI-EXPANDED(收录号:WOS:000506206200015)】;
基金:This work was financially supported by the National Natural Science Foundation of China (No. 31772007 and No. 21776075) and the Fundamental Research Funds for the Central University of China (No. 22221818014).
语种:英文
外文关键词:Synthetic biology; Saccharomyces cerevisiae; Peroxisome; Storage depot; Subcellular factory; Terpene
摘要:Engineering microbes to produce terpenes from renewable feedstock is a promising alternative to traditional production approaches. Generally, terpenes are not readily secreted by microbial cells, and their distribution within cells is usually obscure and often a restricting factor for the overproduction of terpenes due to the storage limitation. Here, we determined that squalene overproduced in the cytoplasm of Saccharomyces cerevisiae was distributed in a form similar to oil droplets. Interestingly, these suspected oil droplets were confirmed to be inflated peroxisomes that were swollen along with the production of squalene, indicating that peroxisomes in S. cerevisiae are dynamic depots for the storage of squalene. In view of this, harnessing peroxisomes as subcellular compartments for squalene synthesis was performed, achieving a 138-fold improvement in squalene titer (1312.82 mg/L) relative to the parent strain, suggesting that the peroxisome of S. cerevisiae is an efficient subcellular factory for the synthesis of terpenes. By dual modulation of cytoplasmic and peroxisomal engineering, the squalene titer was further improved to 1698.02 mg/L. After optimizing a two-stage fed-batch fermentation method, the squalene titer reached 11.00 g/L, the highest ever reported. This provides new insight into the synthesis and storage of squalene in peroxisomes and reveals the potential of harnessing peroxisomes to overproduce terpenes in S. cerevisiae through dual cytoplasmic-peroxisomal engineering.
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