Difference between revisions of "Team:Paris Bettencourt/Notebook/Phytase"

Line 86: Line 86:
 
<tr>
 
<tr>
 
<td>H2O DNAse Free (µL)</td>
 
<td>H2O DNAse Free (µL)</td>
<td>45</td>
+
<td align="center">45</td>
<td>45</td>
+
<td align="center">45</td>
<td>45</td>
+
<td align="center">45</td>
 
</tr>
 
</tr>
 
<tr>
 
<tr>
 
<td>Resistance plasmid (µL)</td>
 
<td>Resistance plasmid (µL)</td>
<td>1</td>
+
<td align="center">1</td>
<td>1</td>
+
<td align="center">1</td>
<td>1</td>
+
<td align="center">1</td>
 
</tr>
 
</tr>
 
<tr>
 
<tr>
 
<td>PHO80 5'Primer (µL)</td>
 
<td>PHO80 5'Primer (µL)</td>
<td> </td>
+
<td align="center"> </td>
<td>2</td>
+
<td align="center">2</td>
<td> </td>
+
<td align="center"> </td>
 
</tr>
 
</tr>
<tr>
+
<tr align="center">
 
<td>PHO80 3'Primer (µL)</td>
 
<td>PHO80 3'Primer (µL)</td>
 
<td> </td>
 
<td> </td>

Revision as of 16:28, 14 August 2015

Background

Aims

Results

Cobalamin (vitamin B12) deficiency is widely spread in India, due to diet that is mostly vegetarian. We aimed at introducing a high-level cobalamin producer to the rice batter. Tadaa.

5/08/15

Design primers


Gene PHO85

5’Primer of Kan resistance gene with tails use to transformation with the PHO85 gene of the yeast.
5’-TATCATTATATATACATGGCTACGGTTTTTCGCTGACGGGCTGCGATAATCATTTGCA
TCCATACATTTTGATGGC
-3’

3’Primer of Kan resistance gene with tails use to transformation with the PHO85 gene of the yeast.
3’-AAGGGATATATAGCGCGGCAAACTGGGCAAACTTGAGCAATACCACAGCAGTATAG
CGACCAGCATTC
-5’

- tail homologie PHO85
- Primer Kan

Gene PHO80

5’Primer of Kan resistance gene with tails use to transformation with the PHO80 gene of the yeast.
5’-ATCATAAGACGAGGATATCCTTTGGAGACTCATAGAAATCATAATCATTTGCATCCAT
ACATTTTGATGGC
-3’

3’Primer of Kan resistance gene with tails use to transformation with the PHO80 gene of the yeast.
3’-CTCAATCATGATTGCTTTCATAATACCCCACGAAAAATCACAGCAGTATAGCGACCA
GCATTC
-5’

- tail homologie PHO80
- Primer Kan

Gene FRT + PHO85

5’Primer of Kan resistance gene with tails use to transformation with the PHO85 gene of the yeast, including FRT sequence to can delete both of PHO80 an PHO85.
5’-TATCATTATATATACATGGCTACGGTTTTTCGCTGACGGGCTGCGGAAGTTCCTATTC
TCTAGAAAGTATAGGAACTTC
ATAATCATTTGCATCCATACATTTTGATGGC-3’

3’Primer of Kan resistance gene with tails use to transformation with the PHO85 gene of the yeast, including FRT sequence to can delete both of PHO80 an PHO85.
3’-AAGGGATATATAGCGCGGCAAACTGGGCAAACTTGAGCAATACCACTTCAAGGATAT
GAAAGATCTCTTATCCTTGAAG
CAGCAGTATAGCGACCAGCATTC-5’

- tail homologie PHO85
- FRT
- Primer Kan

12/08/15

Culture

The saccharomyces cerevisiae SK1 was thaw and sow 100µL of it on YPD medium overnight. (at 30°C)
This yeast will be transformed.

PCR

3 PCR were realized on OH plasmid to create a Kanamicine resistance marker, thanks to 3 pair of primers wich have tails we’ll be use to knock out genes PHO80, PHO85 and both in the yeast.

Protocol:
PHO80 PHO85 FRT+ PHO85
Master mix (µL) 50 50 50
H2O DNAse Free (µL) 45 45 45
Resistance plasmid (µL) 1 1 1
PHO80 5'Primer (µL) 2
PHO80 3'Primer (µL) 2
PHO85 5'Primer (µL) 2
PHO85 3'Primer (µL) 2
PHO85 + FRT 5'Primer (µL) 2
PHO85 + FRT 3'Primer (µL) 2