Reducing acetate excretion from E. coli K-12 by over-expressing the small RNA SgrS

被引:23
作者
Negrete, Alejandro [1 ]
Majdalani, Nadim [2 ]
Phue, Je-Nie [1 ]
Shiloach, Joseph [1 ]
机构
[1] NIDDK, Biotechnol Core Lab, NIH, Bethesda, MD 20892 USA
[2] NCI, Mol Biol Lab, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
HIGH-CELL-DENSITY; ESCHERICHIA-COLI; GLUCOSE-TRANSPORTER; TRANSCRIPTIONAL ACTIVATOR; METABOLIC PATHWAYS; MESSENGER-RNA; GROWTH; ACCUMULATION; PTSG; PHOSPHOENOLPYRUVATE;
D O I
10.1016/j.nbt.2011.11.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
When exposed to the nonmetabolized glucose derivative alpha methyl glucoside (alpha MG), both Escherichia coli K-12 (JM109 and MG1655) and E. coli B (BL21) respond by reducing the concentration of the mRNA of the ptsG gene which is responsible for the biosynthesis of the glucose transporter EIICBglu. This occurs through the over-expression of the noncoding small RNA SgrS, which interacts specifically with the mRNA of the ptsG gene and prevents its translation. However, when these bacteria are exposed to a glucose concentration of 40 g/L, over-expression of SgrS is observed only in E. coli B (BL21). Unlike E. coli K-12 (JM109 and MG1655), which are affected by high glucose concentration and produce higher levels of acetate, E. coli B (BL21) is not affected. Based on this information, it was assumed that overexpression of SgrS enables E. coli B (BL21) to reduce its acetate excretion by controlling the glucose transport. When SgrS was over-expressed in both E. coli K-12 strains from a multicopy plasmid, it was possible to reduce their acetate excretion levels to those seen in E. coli B. This observation opens a new approach towards controlling bacterial metabolism through the use of noncoding RNA.
引用
收藏
页码:269 / 273
页数:5
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