Team:Tianjin/Project/Experiment/TetA

From 2013.igem.org

(Difference between revisions)
(Endogenous Induce&Resistance Selection)
Line 235: Line 235:
                     </li>
                     </li>
                     <li>  
                     <li>  
-
                         <a href="https://2013.igem.org/Team:Tianjin/Project/Experiment/TetA">TetA</a>  
+
                         <a href="https://2013.igem.org/Team:Tianjin/Project/Experiment/TetA">Endogenous Induce&Resistance Selection</a>  
                     </li>
                     </li>
                 </ul>  
                 </ul>  

Revision as of 23:14, 27 September 2013

Experiment

Endogenous Induce&Resistance Selection



Here, we want to test the resistance against tetracycline of Alk-Sensor induced by endogenous alkanes.

We put the alkane producing module into cells to test the function of TetA:


Construct:

Left: No.60: TetA downstream of Palkm and AlkR downstream of J23103, are cloned into vector PSB1C3 and there’s a alkane producing vector PSB3K3.

Right: No.61: We construct a blank vector PSB3K3 without NPDC and AAR as blank control, and the other vector PSB1C3 is the same as No.60.


Characterization:

Strains of No.60 are cultured in LB medium for about 12 hours. Add 17μg/mL Kan, 12μg/mL Cm and 12μg/mL Tc respectively. After that, inoculate into 3 ml LB medium for an overnight cultures at 37 ℃ with 220rpm shaking.


Result:

Alkane producing E.coli can grow in tube but blank vector E.coli cannot grow .

Conclusion:

Synthesized alkanes induce the expression of alkR, which enables E.coli to survive under the pressure of Tetracycline.


Thus, we can get a 3×3 matrix, with promoter strength from weak, medium to strong, and plasmid copy number from small, medium to large.



Retrieved from "http://2013.igem.org/Team:Tianjin/Project/Experiment/TetA"