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Team:HZAU-China/Help
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| + | <h3 style="text-align:center">Interaction work:</h3> | ||
| + | <h3 style="text-align:center">pCusC, PpcoA sequencing and promoter test</h3> | ||
| + | <p class="highlighttext">Author：Tian Liu</p> | ||
| + | <p class="highlighttext"><span style="font-style:italic;"></span></p> | ||
| + | <p class="highlighttext">Experimental Background：</p> | ||
| + | <p class="highlighttext">iGEM encourage the communication between teams and help others. So, when we heard HUST-China has something wrong about their promoter, we decided to give a hand. The one problem they had is they tried many times but failed to sequencing those promoters in pET28a, and the other is they put mRFP under the promoter to do a promoter test but didn’t get result. So we got A&B promoters with mRFP from them.</p> | ||
| - | + | <p class="highlighttext"><span style="font-style:italic;">Proposes: </span></p> | |
| - | + | <p class="highlighttext">1. pCusC & PpcoA promoters sequencing</p> | |
| + | <p class="highlighttext">2. pCusC & PpcoA promoters test</p> | ||
| + | |||
| + | <p class="highlighttext"><span style="font-style:italic;">Materials and equipment:</span></p> | ||
| + | <p class="highlighttext">pCusC & PpcoA promoters with mRFP in pET28a plasmid</br> | ||
| + | LB medium</br> | ||
| + | Kanamycin</br> | ||
| + | Multifunctional microplate reader</br> | ||
| + | Shaking incubator </p> | ||
| + | |||
| + | <p class="highlighttext"><span style="font-style:italic;">Method:</span></p> | ||
| + | <p class="highlighttext"><span style="font-style:italic;">1. Sequencing</span></p> | ||
| + | <p class="highlighttext">We design the 5’-agatcgggctcgccacttcg-3’ as the reverse primer to sequencing the promoters. And Tsing Ke Biology Technology Company help us synthetize the primer and sequencing those plasmid.</p> | ||
| + | <p class="highlighttext">You can get the sequencing results of two samples at supplement 1.</p> | ||
| + | <p class="highlighttext">Analyzed the sample pCusC’s sequencing result, we find that the T7 promoter has not be digested , there is no pCusC in the plasmid, but mRFP has successful ligated. So we can observe the red is the red fluorescent protein expression by the T7 promoter. Therefore, in the subsequent promoter test, we abandoned the pCusC samples.</p> | ||
| + | <p class="highlighttext">In the PpcoA samples we successfully found PpcoA and mRFP. However, at the end of PpcoA‘s sequencing result, there is more 6bp than HUST’s sequence. We take PpcoA promoter to detection.</p> | ||
| + | |||
| + | <p class="highlighttext"><span style="font-style:italic;">2. Promoter test</span></p> | ||
| + | <p class="highlighttext">a. Add 2mL LB culture medium, 2uL Kanamycin (50mg/L) and 20uL bacterial samples to a 5mL centrifuge tube. Shaken overnight in the 37°C shaking incubator and set the rotational speed at 180 rpm/min.</p> | ||
| + | <p class="highlighttext">b. Add CuSO4 solution to induce in concentration of 0, 0.02, 0.1 and 1mM. Set three copies for each concentration as repetitions. Cultivate in the 37°C shaking incubator at the rotational speed of 180 rpm/min for 4 hours.</p> | ||
| + | <p class="highlighttext">c. Add 200uL bacterial samples from each centrifuge tube to the 96-well plate. Set two copies for each centrifuge tub as repetitions. Meanwhile, add LB culture medium containing and not containing 1.0mM CuSO4 as blank controls.</p> | ||
| + | <p class="highlighttext">d. Read the OD<sub>600</sub> and fluorescent intensity (with the emission wavelength at 607nM and excitation wavelength at 584nM) using a multifunctional microplate reader.</p> | ||
| + | <p class="highlighttext">e. Divided the fluorescent intensity result using the value of OD<sub>600</sub>. Record the data for compare and analysis. </p> | ||
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Revision as of 02:49, 18 October 2014
<!DOCTYPE html>
Help Each Other
Interaction work:
pCusC, PpcoA sequencing and promoter test
Author：Tian Liu
Experimental Background：
iGEM encourage the communication between teams and help others. So, when we heard HUST-China has something wrong about their promoter, we decided to give a hand. The one problem they had is they tried many times but failed to sequencing those promoters in pET28a, and the other is they put mRFP under the promoter to do a promoter test but didn’t get result. So we got A&B promoters with mRFP from them.
Proposes:
1. pCusC & PpcoA promoters sequencing
2. pCusC & PpcoA promoters test
Materials and equipment:
pCusC & PpcoA promoters with mRFP in pET28a plasmid LB medium Kanamycin Multifunctional microplate reader Shaking incubator
Method:
1. Sequencing
We design the 5’-agatcgggctcgccacttcg-3’ as the reverse primer to sequencing the promoters. And Tsing Ke Biology Technology Company help us synthetize the primer and sequencing those plasmid.
You can get the sequencing results of two samples at supplement 1.
Analyzed the sample pCusC’s sequencing result, we find that the T7 promoter has not be digested , there is no pCusC in the plasmid, but mRFP has successful ligated. So we can observe the red is the red fluorescent protein expression by the T7 promoter. Therefore, in the subsequent promoter test, we abandoned the pCusC samples.
In the PpcoA samples we successfully found PpcoA and mRFP. However, at the end of PpcoA‘s sequencing result, there is more 6bp than HUST’s sequence. We take PpcoA promoter to detection.
2. Promoter test
a. Add 2mL LB culture medium, 2uL Kanamycin (50mg/L) and 20uL bacterial samples to a 5mL centrifuge tube. Shaken overnight in the 37°C shaking incubator and set the rotational speed at 180 rpm/min.
b. Add CuSO4 solution to induce in concentration of 0, 0.02, 0.1 and 1mM. Set three copies for each concentration as repetitions. Cultivate in the 37°C shaking incubator at the rotational speed of 180 rpm/min for 4 hours.
c. Add 200uL bacterial samples from each centrifuge tube to the 96-well plate. Set two copies for each centrifuge tub as repetitions. Meanwhile, add LB culture medium containing and not containing 1.0mM CuSO4 as blank controls.
d. Read the OD600 and fluorescent intensity (with the emission wavelength at 607nM and excitation wavelength at 584nM) using a multifunctional microplate reader.
e. Divided the fluorescent intensity result using the value of OD600. Record the data for compare and analysis.
