Difference between revisions of "Team:NWU-CHINA/Expression"
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<h3>Expression</h3> | <h3>Expression</h3> | ||
| − | <p>After acquainted with the catabolic regulation mechanism of alkanes in Pseudomonas aeruginosa DN1, we need a reporter gene to show the condition of the cells after DN1 initiating the alkane catabolism pathway. Here, we chose the chromoprotein RFP (BBa_J00450). We linked it to the downstream of the AlkB2 promoter. After alkane released the inhibition of GntR to the AlkB2 promoter, the promoter plays a role in initiating the downstream gene and expressing the RFP. By this way, we can detect alkane.</p> | + | <p style="font-size:20px">After acquainted with the catabolic regulation mechanism of alkanes in Pseudomonas aeruginosa DN1, we need a reporter gene to show the condition of the cells after DN1 initiating the alkane catabolism pathway. Here, we chose the chromoprotein RFP (BBa_J00450). We linked it to the downstream of the AlkB2 promoter. After alkane released the inhibition of GntR to the AlkB2 promoter, the promoter plays a role in initiating the downstream gene and expressing the RFP. By this way, we can detect alkane.</p> |
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Latest revision as of 05:41, 1 November 2017
Expression
After acquainted with the catabolic regulation mechanism of alkanes in Pseudomonas aeruginosa DN1, we need a reporter gene to show the condition of the cells after DN1 initiating the alkane catabolism pathway. Here, we chose the chromoprotein RFP (BBa_J00450). We linked it to the downstream of the AlkB2 promoter. After alkane released the inhibition of GntR to the AlkB2 promoter, the promoter plays a role in initiating the downstream gene and expressing the RFP. By this way, we can detect alkane.
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