Development of a Synthetic Malonyl-CoA Sensor in Saccharomyces cerevisiae for Intracellular Metabolite Monitoring and Genetic Screening

被引:125
|
作者
Li, Sijin [1 ,2 ]
Si, Tong [2 ]
Wang, Meng [1 ,3 ]
Zhao, Huimin [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Univ Illinois, Energy Biosci Inst, Urbana, IL 61801 USA
[2] Univ Illinois, Inst Genom Biol, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Chem & Biomol Engn, Urbana, IL 61801 USA
[4] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[5] Univ Illinois, Dept Biochem, Urbana, IL 61801 USA
[6] Univ Illinois, Dept Bioengn, Urbana, IL 61801 USA
来源
ACS SYNTHETIC BIOLOGY | 2015年 / 4卷 / 12期
关键词
malonyl-CoA; genetic sensor; genome-wide library; high-throughput screening; 3-hydroxypropionic acid; ESCHERICHIA-COLI; 3-HYDROXYPROPIONIC ACID; GLYCEROL PRODUCTION; REGULATOR SYSTEM; HIGHLY EFFICIENT; DESIGN; YEAST; IDENTIFICATION; CONSTRUCTION; BIOSENSORS;
D O I
10.1021/acssynbio.5b00069
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Genetic sensors capable of converting key metabolite levels to fluorescence signals enable the monitoring of intracellular compound concentrations in living cells, and emerge as an efficient tool in high-throughput genetic screening. However, the development of genetic sensors in yeasts lags far behind their development in bacteria. Here we report the design of a malonyl-CoA sensor in Saccharomyces cerevisiae using an adapted bacterial transcription factor FapR and its corresponding operator fapO to gauge intracellular malonyl-CoA levels. By combining this sensor with a genome-wide overexpression library, we identified two novel gene targets that improved intracellular malonyl-CoA concentration. We further utilized the resulting recombinant yeast strain to produce a valuable compound, 3-hydroxypropionic acid, from malonyl-CoA and enhanced its titer by 120%. Such a genetic sensor provides a powerful approach for genome-wide screening and could further improve the synthesis of a large range of chemicals derived from malonyl-CoA in yeast.
引用
收藏
页码:1308 / 1315
页数:8
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