Glucose uptake regulation in <it>E. coli </it>by the small RNA SgrS: comparative analysis of <it>E. coli </it>K-12 (JM109 and MG1655) and <it>E. coli </it>B (BL21)
2010
Ng Weng-Ian | Negrete Alejandro | Shiloach Joseph
<p>Abstract</p> <p>Background</p> <p>The effect of high glucose concentration on the transcription levels of the small RNA SgrS and the messenger RNA ptsG, (encodin<it>g </it>the glucose transporter IICB<sup>Glc</sup>), was studied in both <it>E. coli </it>K-12 (MG1655 and JM109) and <it>E. coli </it>B (BL21). It is known that the transcription level of <it>sgrS </it>increases when <it>E. coli </it>K-12 (MG1655 and JM109) is exposed to the non-metabolized glucose alpha methyl glucoside (αMG) or when the bacteria with a defective glycolysis pathway is grown in presence of glucose. The increased level of sRNA SgrS reduces the level of the ptsG mRNA and consequently lowers the level of the glucose transporter IICB<sup>Glc</sup>. The suggested trigger for this action is the accumulation of the corresponding phospho-sugars.</p> <p>Results</p> <p>In the course of the described work, it was found that <it>E. coli </it>B (BL21) and <it>E. coli </it>K-12 (JM109 and MG1655) responded similarly to αMG: both strains increased <it>SgrS </it>transcription and reduced <it>ptsG </it>transcription. However, the two strains reacted differently to high glucose concentration (40 g/L). <it>E. coli </it>B (BL21) reacted by increasing <it>sgrS </it>transcription and reducing <it>ptsG </it>transcription while <it>E. coli </it>K-12 (JM109 and MG1655) did not respond to the high glucose concentration, and, therefore, transcription of <it>sgrS </it>was not detected and ptsG mRNA level was not affected.</p> <p>Conclusions</p> <p>The results suggest that <it>E. coli </it>B (BL21) tolerates high glucose concentration not only by its more efficient central carbon metabolism, but also by controlling the glucose transport into the cells regulated by the sRNA SgrS, which may suggest a way to control glucose consumption and increase its efficient utilization.</p>
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