Deletion of the aroK gene is essential for high shikimic acid accumulation through the shikimate pathway in E. coli

被引:38
作者
Chen, Kai [1 ]
Dou, Jie [1 ]
Tang, Shirui [1 ]
Yang, Yishun [1 ]
Wang, Hui [1 ]
Fang, Hongqing [2 ]
Zhou, Changlin [1 ]
机构
[1] China Pharmaceut Univ, Sch Life Sci & Technol, Nanjing 210009, Peoples R China
[2] Acad Mil Med Sci, Inst Biotechnol, Beijing 100071, Peoples R China
关键词
Arok gene; Antisense RNA interference; Gene deletion; Shikimate kinase; CARBOHYDRATE PHOSPHOTRANSFERASE SYSTEM; ESCHERICHIA-COLI; LIMITED CONDITIONS; STRAIN LACKING; QUINIC ACID; PHOSPHOENOLPYRUVATE; BIOSYNTHESIS; GLUCOSE; TRANSPORT; DESIGN;
D O I
10.1016/j.biortech.2012.05.100
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Shikimic acid (SA) is an important metabolic intermediate with diverse commercial applications. In this work, antisense RNA interference and gene deletion were carried out to inactivate the aroK gene in an SA-producing Escherichia coli strain, DHPYA-T7. In this strain, the aroL, ptsHIcrr and ydiB genes are deleted, and the tktA, glk, aroE and aroB genes are overexpressed. Flask cultivations of the DHPYA-T7 derivative strains showed that the accumulation of SA increased 2.69-fold after aroK gene deletion (DHPYAAS-T7) and 1.29-fold after antisense RNA interference (DHPYAS-T7). Furthermore, the activity of shikimate kinase in DHPYAAS-T7 was 0.21-fold of that in strain DHPYAS-T7. In a 10-L fermentation, SA accumulation increased to 1850 mg L-1 in strain DHPYAAS-T7, which is a 1.5-fold increase over that in strain DHPYAS-T7. These results demonstrate that aroK gene inactivation in DHPYA-T7 leads to high SA accumulation, especially when this inactivation is caused by chromosomal deletion. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:141 / 147
页数:7
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