Genetic manipulation of a metabolic enzyme and a transcriptional regulator increasing succinate excretion from unicellular cyanobacterium

被引:58
|
作者
Osanai, Takashi [1 ,2 ]
Shirai, Tomokazu [3 ]
Iijima, Hiroko [1 ,2 ]
Nakaya, Yuka [1 ,3 ]
Okamoto, Mami [3 ]
Kondo, Akihiko [3 ,4 ]
Hirai, Masami Y. [1 ]
机构
[1] RIKEN Ctr Sustainable Resource Sci, Yokohama, Kanagawa 2300045, Japan
[2] Meiji Univ, Sch Agr, Dept Agr Chem, Kawasaki, Kanagawa 2148571, Japan
[3] RIKEN, Biomass Engn Program, Yokohama, Kanagawa, Japan
[4] Kobe Univ, Grad Sch Engn, Dept Chem Sci & Engn, Kobe, Hyogo 657, Japan
来源
基金
日本科学技术振兴机构;
关键词
cyanobacteria; metabolism; metabolomics; sigma factor; succinate; SYNECHOCYSTIS SP PCC-6803; SIGMA-FACTOR; HYDROGEN-PRODUCTION; ESCHERICHIA-COLI; ACID PRODUCTION; PHOSPHOENOLPYRUVATE CARBOXYLASE; PYRUVATE-CARBOXYLASE; RESPONSE REGULATOR; CARBON METABOLISM; OVEREXPRESSION;
D O I
10.3389/fmicb.2015.01064
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Succinate is a building block compound that the U.S. Department of Energy (DOE) has declared as important in biorefineries, and it is widely used as a commodity chemical. Here, we identified the two genes increasing succinate production of the unicellular cyanobacterium Synechocystis sp. PCC 6803. Succinate was excreted under dark, anaerobic conditions, and its production level increased by knocking out ackA, which encodes an acetate kinase, and by overexpressing sigE, which encodes an RNA polymerase sigma factor. Glycogen catabolism and organic acid biosynthesis were enhanced in the mutant lacking ackA and overexpressing sigE leading to an increase in succinate production reaching five times of the wild-type levels. Our genetic and metabolomic analyses thus demonstrated the effect of genetic manipulation of a metabolic enzyme and a transcriptional regulator on succinate excretion from this cyanobacterium with the data based on metabolomic technique.
引用
收藏
页数:10
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