Latest revision as of 14:04, 30 October 2015

Ferment It Yourself

iGEM Paris-Bettencourt 2O15

August
September

August 10th

Design primers

Gene PHO85

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

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

- Homology tail on gene PHO85
- Kanamycin resistance binding

Gene PHO80

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

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

- Homology tail on gene PHO80
- Kanamycin resistance binding

Gene FRT + PHO85

5’Primer of Kanamycin resistance gene with tails using to transformation with the PHO85 gene of the yeast, including FRT sequence to delete both of PHO80 and PHO85.
5’-TATCATTATATATACATGGCTACGGTTTTTCGCTGACGGGCTGCGGAAGTTCCTATTC TCTAGAAAGTATAGGAACTTCATAATCATTTGCATCCATACATTTTGATGGC-3’

3’Primer of Kanamycin resistance gene with tails using to transformation with the PHO85 gene of the yeast, including FRT sequence to delete both of PHO80 and PHO85.
3’-AAGGGATATATAGCGCGGCAAACTGGGCAAACTTGAGCAATACCACTTCAAGGATAT GAAAGATCTCTTATCCTTGAAGCAGCAGTATAGCGACCAGCATTC-5’

- Homology tail on gene PHO85
- FRT sequence
- Kanamycin resistance binding

August 12nd

Culture

Inoculate 100µL of Saccharomyces cerevisiae SK1 on YPD medium overnight (at 30°C).
This yeast will be transformed.

PCR

3 PCR were realized on HO-Poly-KanMX4-HO plasmid to create a Kanamycin resistance marker, thanks to 3 pairs 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

Figure 1 : PCR cycle

August 13th

PCR Purification

Protocol : PCR purification

Result of PCR (August 12th)

The PCR product are then revealed with a gel electrophoresis.
We expected bands around 1.300bp. The band corresponding to marker with FRT is bigger than the two others strips because these have just the Kanamycin resistance with tails, and no FRT sequences.

Figure 2 :Result of PCR

Pre-culture

Plated one colony of Saccharomyces cerevisiae SK1 in 5mL liquid YPD medium and let's grow overnight.

August 14th

Transformation of yeast

Protocol: Heat shock transformation for yeast

August 17th

Result of plates:

There is a culture in plates.

The negative control is not well. The no change yeast grow in the YPD medium with the antibiotic.
We will repeat this control on an agar plate and not in a liquid medium.

We analyze anyway down results, the results of the new control will allow us to validate the result of our experiment or search which are our error and try again.

The positive control is well, yeast multiply on YPD medium plate without antibiotic. Yeasts are not dead, so the culture on other agar mediums are not contamination.

We see more colonies on the plates with yeast transforming PHO85 and FRT+PHO85.

We look only few colonies in the plates with yeast transforming PHO80.

The result is well, transformation works.

Figure 3 : Negative control

Figure 4 : Positive control and result of transformation

Design primers

We design primers to verifie our results on the plates.
Thanks to the colony PCR, we might determinate if the resistance is integrated into the yeast DNA.
Primer 5'-3' PHO80
ATCATAAGACGAGGATATCCTTTGGAG

Primer 3'-5' PHO80
CTCAATCATGATTGCTTTCATAATACCCC

Primer 5'-3' PHO85
TATCATTATATATACATGGCTACGGTTTTTCG

Primer 3'-5' PHO85
AAGGGATATATAGCGCGGCAAACTG

Primer 5'-3' FRT+PHO85
TATCATTATATATACATGGCTACGGTTTTTCG

Primer 3'-5' FRT+PHO85
AAGGGATATATAGCGCGGCAAACTG

August 18th

Verification of the new negative control

The verification of the negative control is good, any colony is watching. We can continue our experiments, it will be validated.

Figure 5 : Result of the new negative control

FRT problems

The transformation with the FRT may be run well, but the plasmid with the gene coding for flippase works only for E. coli. We can't use this plasmid because it will be rejected by the yeast.
Other transformation with CreLox system is possible.
CreLox is a gene which have the same fonction than the FRT, it not cut by the flippase but by the Cre recombinase.

We design two primers for the new transformation with CreLox system.

Primer 5'-3' CreLox + PHO85

5’-TATCATTATATATACATGGCTACGGTTTTTCGCTGACGGGCTGCGATAACTTCGTATAGCATACATTATACGAAGTTATATAATCATTTGCATCCATACATTTTGATGGC-3’

Primer 3'-5' CreLox + PHO85

3’-AAGGGATATATAGCGCGGCAAACTGGGCAAACTTGAGCAATACCAATAACTTCGTATAGCATACATTATACGAAGTTATCAGCAGTATAGCGACCAGCATTC-5’

- Homology tail on gene PHO85
- CreLox sequence
- Kanamycin resistance binding

August 19th

Colony PCR

Protocol:

	PHO80	PHO85	FRT+ PHO85
dreamTaq 2X (µL)	3	3	3
H2O DNAse Free (µL)	9	9	9
Colony	1	1	1
PHO80 5'Primer (µL)		0.5
PHO80 3'Primer (µL)		0.5
PHO85 5'Primer (µL)	0.5		0.5
PHO85 3'Primer (µL)	0.5		0.5

Figure 6 : Colony PCR cycle

August 20th

Result of colony PCR (August 19th)

We see bands smaller than 500bp, but not the fragments we expected : this is probably contaminations. We start again the same PCR colony. There is DNA in holes too, which didn't migrate, probably the genomic DNA.

Figure 7 : Electrophoresis PCR colony

Colony PCR

Same to August 19th.

Result of second colony PCR

Figure 8 : second electrophoresis colony PCR

The DNA Ladder is good but DNA of PCR did not migrate. The ADN is in the holes. We think that the yeasts walls being thicker simple thermic shock does not break it. We will be carry a lysis whith NaOH in yeast, to push out DNA, to the primer can be fixed on it.

August 24th

Yeast lysis with NaOH

Protocol: Yeast lysis with NaOH
After the lysis of yeast we realize the new PCR in normal condition, the same as August 12nd.

August 25th

Result of PCR (August 24th)

Figure 9 : Third electrophoresis colony PCR with NaOH lysis

The DNA ladder migrate, but there was any amplification of the both genes.
We tested two PCR mix : the first did not work. The positive control worked with the second PCR mix. It is composed of HO plasmid and the oligos using for PHO85 gene.

August 26th

Colony PCR

To make the colony PCR, we need to lysis yeasts' wall. We realized the lysis with NaOH, but it did not work. So we realize a new lysis using the " DNeasy Blood and Tissue Kit" with the zymolyase enzyme on the non-transformed yeasts to verifie the melting temperature of primers (try between 55°C and 65°C) and if the amplification of the genes work.

Phytic acid dosage

We dose the phytic acid in the fermented rice with the kit " Phytic Acid (Total Phosphorus) Assay Kit ".

August 27th

Result of PCR (August 26th)

Figure 10 : Electrophoresis colony PCR with temperature gradient on non-transformed yeasts lysed by the zymolyase

We made a PCR gradient on non-transformed yeast to know exactly wich temperature is better to a good fixation of the primers on the DNA.
The amplification failed, we supposed it is because our MasterMix did not work. We will try this PCR again.

Phytic acid dosage

We dose the phytic acid in fermented rice.
After analysis, the fermented rice have very little quantity of phosphorus and of phytic acid.
[Phosphorus] : 0.0758 mg/100g of rice.
[Phytic acid] : 0.269 mg/100g of rice.

Figure 11 : Phosphorus calibration curve for titration of phytic acid in fermented rice

Result of second PCR

Figure 12 : Second electrophoresis colony PCR with temperature gradient (non-transformed yeast)

We watch bands for the gene PHO80, at the good size : 882bp. But the gene PHO85, there was no amplifiction, and the positive control is negative : we only see aband bigger than 10,000bp and it is not what we expected.
We try again this PCR to see if the no amplification of the gene PHO85 it is a manipulation error or not.

August 28th

Phytic acid dosage in different strains

Figure 13 : Phosphorus calibration curve + results of OD in some strains

Figure 14 : Results of acid phytic dosage on fermented rice

Results of PCR

Figure 15 : Third electrophoresis gradient PCR (non-transformed yeast)

We watch bands for the both of genes, but not at the same temperatures. Thanks to the gradient, we can suppose that oligos have not exactly the same melting temperature, and it may be the reason why the previous PCR failed.
The controle postive with the HO plasmid worked, the band matches with the PHO85 gene size (1020bp).

Figure 16 : Electrophoresis PCR transformed yeasts

The positive control is negative, PCR does not therefore our work.

Transformation

We transform the yeast Saccharomyces cerevisiae SK1 with the resistance to geneticin and the Cre gene. We delete the PHO 85 genes and we replace it by the resistance gene.

Figure 17 :Principle of Cre recombinase

The Cre gene is the sequence that little be cut thanks Cre recombinase and recombined the gene without the sequence between the Cre sequences.

August 30th

Transformation on yeasts with Cre gene

First step, we realize the PCR of Cre and RFP gene with primers (created by Amaury) and plasmid containing RFP. We amplified the gene, its promoter and its terminater.
Protocol : PCR

Second step, we make PCR purification, and check the result with electrophoresis.
Protocol : PCR purification

Third step, we transformed yeast that is already integrated the resistance instead of PHO85 gene. We introduce the Cre and RFP genes instead of PHO80 gene
Protocol : Transformation of yeast

Fourth step, we cultived the transforming yeasts in YPD agar medium with geneticin overnight.

PCR and result

We did electrophoresis of transformation product. It's revealed bands around 10,000bp, while we expected 1,000bp. We think the DNA extraction in yeast doesn't work, and these bands are contamination.

Figure 18 : Colony PCR on transformed yeast with RFP

September 1st

Result of transformation

We watching any culture on plates YPD + Geneticin. The yeast are not resistant to geneticin, they had not introduced the resistance gene. Transformation does not work.

September 2nd

Transformation

We start again the transformation of august 28th, with the same protocol.

Titration of phytic acid

We test the quantity of phytic acid different strains, at dilution 1/5, 1/50 and 1/500.
Strains : g15,37 / g15,55 / g15,56 / g15,57 / g15,58 / Sook dall + HCl / Sook rice + HCl.

September 4th

After the transformation of September 2nd, any culture is observable on plates. The tansformation are not function. We restart transformation, but we transform with Cre and RFP genes. It is more interesting because we not forced to simply remove the resistance gene, we can make a double identification. It helps to identify yeast that is already integrated in place of the resistance gene PHO85 (they cultivate on agar with geneticin) and we also integrate the RFP in place of PHO80 gene (they will be red).

September 8th

PCR to product cassette Cre/RFP

We restart PCR with Cre sequence and RFP gene.

Figure 19 : Electrophoresis of Cre and RFP amplification

We see only one band. We can continue experiments with this sample and realize the transformation.

Analysis of results of titration phytic acid of September 2nd

We test the quantity of phytic acid different strains, at dilution 1/5, 1/50 and 1/500.
Strains : g15,37 / g15,55 / g15,56 / g15,57 / g15,58 / Sook dall + HCl / Sook rice + HCl. We start to do the phosphorus scale.

Figure 20 : Phosphorus calibration curve

With calculations of the protocol, we can determine the concentration in our samples.
Protocol : Titration of phytic acid

Figure 21 : Table of results

Concentrations are very low. There are less to 1mg/100g d’idli.

September 11th

Transformation

We did the transformation on strain Saccharomyces cerevisiae SK1, using the protocol of heat shock yeast transformation.

September 14th

Genomic DNA extraction of transformed yeast

We try to extract genomic DNA of transformed yeast with the "Blood & Tissue extraction Kit"
We make PCR on it.

Result of PCR

The gel electrophoresis revealed any bands. We might suppose that the transformation did not work, but it's probably that we don't succeed to extract the yeast's DNA which prevent us to verify our results.

September 15th

Plate of yeast transformed with RFP

Figure 22 : Transformed S. cerevisiae SK1 on YPD agar + geneticin

Colonies are not isolated, we cannot distinguish all of them. The culture that was inoculate was too concentrate. We make suspensions low concentrate and inoculate again on YPD medium with geneticin at 200µg/mL.

September 16th

Plate of yeast transformed with RFP

Figure 23 : Transformed S. cerevisiae SK1 on YPD agar + geneticin

All colonies are the same, but there is no red coloration.
These result can be explicated by the fact that when this gene is introduced in the genomic DNA, it's not revealed, whereas it is in a plasmid.

Test new transformed yeast

We test our new transformed yeast which deletion of PHO80 and PHO85 genes and compare with yeast transformed previously (first with the geneticin resistance gene in place PHO85 gene and second with the geneticin resistance gene in place PHO80). We put this yeast in YPD + geneticin medium (YPD + geneticinn for always keep the selection). We have grown the yeast with six concentration of phytic acid (0.005, 0.01, 0.02, 0.04, 0.1, 0.2 g/mL). We also realize a scale with phytic acid and YPD medium + geneticin.
Scale: C(phytic acid;YPD) (g.mL-1) 0,005 0,01 0,02 0,04 0,1

Figure 24 :Table manipulation

We don’t have enough reagents in our kit to do all manipulations we want, and it is too late to buy it. We choose to delete three concentrations by strain and in the scale.

Figure 25 :New table manipulation

Figure 26 :Result of test

Result analysis: We have only optic density result below zero. Normally is no possible. We suppose the reagents of the kit are old and it not work. Would have had to do again the tests but there is not reagents and time anymore.

@@ Line 1: / Line 1: @@
 {{Paris_Bettencourt/header}}
 {{Paris_Bettencourt/menu}}
-{{Paris_Bettencourt/phytaseBanner}}
+{{Paris_Bettencourt/banner|page_id=notebook|page_name=Notebook - Phytase}}
 <html>
-<h1>August 8th</h1>
+<div id="notebookMenu">
+  <ul>
+    <li><a href="#august">August</a></li>
+    <li><a href="#september">September</a></li>
+  </ul>
+</div>
+<div id="notebookContent">
+<a name="august" class="anchor"></a>
+<h1 class="date one">August 10th</h1>
 <h2>Design primers</h2>
 <h3>Gene PHO85</h3>
@@ Line 10: / Line 20: @@
 <br>5’-<span style="color:#9A1717">TATCATTATATATACATGGCTACGGTTTTTCGCTGACGGGCTGCG</span><span style="color:#179A89">ATAATCATTTGCA
-<br>TCCATACATTTTGATGGC </span>-3’
+TCCATACATTTTGATGGC </span>-3’
 <br>
@@ Line 16: / Line 26: @@
 <br>3’-<span style="color:#9A1717">AAGGGATATATAGCGCGGCAAACTGGGCAAACTTGAGCAATACCA</span><span style="color:#179A89">CAGCAGTATAG
-<br>CGACCAGCATTC</span>-5’
+CGACCAGCATTC</span>-5’
 <br>
-<br><span style="color:#9A1717"> -&nbsp;tail homology PHO85 </span>
+<br><span style="color:#9A1717"> -&nbsp;Homology tail on gene PHO85</span>
-<br><span style="color:#179A89"> -&nbsp;Primer Kanamycin </span><br>
+<br><span style="color:#179A89"> -&nbsp;Kanamycin resistance binding</span><br>
 <br><h3>Gene PHO80</h3>
@@ Line 27: / Line 37: @@
 <br>5’-<span style="color:#9A1717">ATCATAAGACGAGGATATCCTTTGGAGACTCATAGAAATC</span><span style="color:#179A89">ATAATCATTTGCATCCAT
-<br>ACATTTTGATGGC</span>-3’
+ACATTTTGATGGC</span>-3’
 <br>
@@ Line 34: / Line 44: @@
 <br>3’-<span style="color:#9A1717">CTCAATCATGATTGCTTTCATAATACCCCACGAAAAATCA</span><span style="color:#179A89">CAGCAGTATAGCGACCA
-<br>GCATTC</span>-5’
+GCATTC</span>-5’
 <br>
-<br><span style="color:#9A1717"> -&nbsp;tail homology PHO80 </span>
+<br><span style="color:#9A1717"> -&nbsp;Homology tail on gene PHO80</span>
-<br><span style="color:#179A89"> -&nbsp;Primer Kanamycin </span><br>
+<br><span style="color:#179A89"> -&nbsp;Kanamycin resistance binding</span><br>
 <br><h3>Gene FRT + PHO85</h3>
@@ Line 46: / Line 56: @@
 <br>5’-<span style="color:#9A1717">TATCATTATATATACATGGCTACGGTTTTTCGCTGACGGGCTGCG</span><span style="color:#36C40F">GAAGTTCCTATTC
-<br>TCTAGAAAGTATAGGAACTTC</span><span style="color:#179A89">ATAATCATTTGCATCCATACATTTTGATGGC</span>-3’
+TCTAGAAAGTATAGGAACTTC</span><span style="color:#179A89">ATAATCATTTGCATCCATACATTTTGATGGC</span>-3’
@@ Line 54: / Line 64: @@
-<br>GAAAGATCTCTTATCCTTGAAG</span><span style="color:#179A89">CAGCAGTATAGCGACCAGCATTC</span>-5’
+GAAAGATCTCTTATCCTTGAAG</span><span style="color:#179A89">CAGCAGTATAGCGACCAGCATTC</span>-5’
 <br>
-<br><span style="color:#9A1717"> -&nbsp;tail homology PHO85 </span>
+<br><span style="color:#9A1717"> -&nbsp;Homology tail on gene PHO85</span>
-<br><span style="color:#36C40F"> -&nbsp;FRT</span>
+<br><span style="color:#36C40F"> -&nbsp;FRT sequence</span>
-<br><span style="color:#179A89"> -&nbsp;Primer Kanamycin </span><br>
+<br><span style="color:#179A89"> -&nbsp;Kanamycin resistance binding</span><br>
-<br><h1>August 12nd</h1>
+<br><h1 class="date one">August 12nd</h1>
 <h2>Culture</h2>
-Inoculate 100µL of <i>Saccharomyces cerevisiae SK1</i> on YPD medium overnight (at 30°C).
+<p>Inoculate 100µL of <i>Saccharomyces cerevisiae SK1</i> on YPD medium overnight (at 30°C).
 <br>This yeast will be transformed.<br>
 <br><h2>PCR</h2>
 PCR were realized on HO-Poly-KanMX4-HO plasmid to create a Kanamycin resistance marker, thanks to 3 pairs of primers wich have tails we’ll be use to knock out genes PHO80, PHO85 and both in the yeast.<br>
+</p>
 <br>
 <b>Protocol:</b>
@@ Line 135: / Line 146: @@
 </table></div>
-<div class="column-right"><img src="https://static.igem.org/mediawiki/2015/6/69/ParisBettencourt_Cycle_pcr_cassette_kanR.png" width="550px">
+<div class="column-right"><img src="https://static.igem.org/mediawiki/2015/3/3d/ParisBettencourt_Cycle_PCRnormal000000.png" width="550px">
-<p class="legend"><b>Figure 1:</b>Times and temp of PCR</p></div>
+<p class="legend"><b>Figure 1 :</b> PCR cycle</p></div>
 <div style="clear:both"></div>
-<br><h1>August 13rd</h1>
-<h2>PCR purification</h2>
-<B>Protocol : </B>
+<br><h1 class="date one">August 13th</h1>
-<li><u>Dilute</u> PCR product (5 or 10 times ?) with the resuspension  buffer<br></li>
+<h2>PCR Purification</h2>
-<li><u>Pour</u> it in a purification column<br></li>
+<b>Protocol</b> :
-<li><u>Centrifuge</u> 30sec at 14K rpm<br></li>
+<a href="https://2015.igem.org/Team:Paris_Bettencourt/Protocols/PCR_purification"> PCR purification </a>
-<li><u>Throw</u> the filtrat<br></li>
-<li><u>Add</u> 700µL of EtOH (washing solution)<br></li>
-<li><u>Centrifuge</u> 30sec at 14K rpm<br></li>
-<li><u>Throw</u> the filtrat<br></li>
-<li><u>Add</u> 500µLof washing solution<br></li>
-<li><u>Centrifuge</u> 30sec at 14K rpm<br></li>
-<li><u>Throw</u> the filtrat<br></li>
-<li><u>Centrifuge</u> 30sec at 14K rpm<br></li>
-<li><u>Throw</u> the filtrat<br></li>
-<li><u>Put</u> the column in a Eppendorf<br></li>
-<li><u>Add</u> 45µL of RNAse/DNAse free water right on the membrane<br></li>
-<li><u>Wait</u> 2min<br></li>
-<li><u>Centrifuge</u> 2min at 10K rpm<br></li>
-<br>
-<h2>PCR control with an electrophoresis</h2><br>
 <br>
+<h2>Result of PCR (August 12th)</h2><br>
-<div class="column-right">We expected bands around 1.300bp.
+<div class="column-right"><p>The PCR product are then revealed with a<a href="https://2015.igem.org/Team:Paris_Bettencourt/Protocols/Gel_Electrophoresis"> gel electrophoresis.</a><br>
-The band corresponding to marker with FRT is bigger than the two others strips because these have just the Kanamycin resistance with tails, and no FRT sequences.<br></div>
+We expected bands around 1.300bp.
+The band corresponding to marker with FRT is bigger than the two others strips because these have just the Kanamycin resistance with tails, and no FRT sequences.</p><br></div>
-<div class="column-left"><img src="https://static.igem.org/mediawiki/2015/e/e0/ParisBettencourt_ElectrophoresisPCRKanResistance.png" width="350px"><br>
+<div class="column-left"><img src="https://static.igem.org/mediawiki/2015/e/ef/Paris_BettencourtPremier_PCR.png" width="350px"><br>
-<p class="legend"><b>Figure 2:</b>Result of PCR.</p></div>
+<p class="legend"><b>Figure 2 :</b>Result of PCR</p></div>
 <div style="clear:both"></div>
 <br><h2>Pre-culture</h2>
-Swo one colony of <i>Saccharomyces cerevisiae SK1</i> in 5mL liquid YPD medium and let's grow overnight.<br>
+Plated one colony of <i>Saccharomyces cerevisiae SK1</i> in 5mL liquid YPD medium and let's grow overnight.<br>
-<br><h1>August 14th</h1>
+<br><h1 class="date one">August 14th</h1>
 <h2>Transformation of yeast</h2>
-<b>Protocol :</b>
+<b>Protocol</b>:
-<ul>
+<a href="https://2015.igem.org/Team:Paris_Bettencourt/Protocols/Heat_shock_transformation_for_yeast"> Heat shock transformation for yeast </a>
-<li>After growth, determine the titer of the yeast culture by using spectrophotometer : pipette 10µL of cells into 1mL of wtaer in spectrophotometer cuvette and measure the OD at 600nm.<br></li>
-<li>Add 2.5x10<sup>8</sup> cells to 50mL of 2X YPD in a culture flask.<br></li>
-<li>Incubate the flask in a shaking incubator at 30°C until the cell culture is at least 2x10<sup>7</sup> cells.mL<sup>-1</sup><br></li>
-<li>Denature 1mL of carrier DNA at 99°C for 5min and chill immediately in ice.<br></li>
-<li>Harvest the yeast cells by centrifugation at 3,000g for 5min.<br></li>
-<li>Resuspend the pellet in 25mL of sterile water and centrifuge at 3,000g for 5min at 20°C. Repeat this wash with sterile water 2 times.<br></li>
-<li>Resuspend the last pellet in 1mL of sterile water.<br></li>
-<li>Transfer the cell suspension to a 1.5mL microcentrifuge tube.<br></li>
-<li>Centrifuge for 30s at 13,000g and discard the supernatant.<br></li>
-<li>Resuspend the cells in 1mL of sterile water and pipette 100µL samples into 1.5mL microcentrifuge tubes, one for each transformation.<br></li>
-<li>For each transformation :<br></li>
-<ul>
-     <li>240µL of PEG 3350 (50% (w/v))<br></li>
-     <li>36µL of LiAc 1.0M<br></li>
-     <li>50µL of single-stranded carrier DNA (2.0mg.mL<sup>-1</sup>)<br></li>
-     <li>6µL of PCR product <br></li>
-     <li>28µL of water DNAse Free<br></li>
-</ul>
-<li>Place the tubes at 42°C for 40min.<br></li>
-<li>Centrifuge the tubes at 13,000g for 30s in a microcentrifuge tube and remove the supernatant.<br></li>
-<li>Pipette 1mL of YPD liquid medium into the transformation tube, and vortex mix to resuspend pellet.<br></li>
-<li>Incubate 3h at 30°C to ensure good antibiotic expression.<br></li>
-<li>Plate 2, 20 and 200µL of the cell suspension onto YPD medium with 200µm.mL<sup>-1</sup> antibiotic G418.<br></li>
-<li>Incubate the plates at 30°C for 3 days.<br></li>
-</ul><br>
-<br><h1>August 17th</h1>
+<br><h1 class="date one">August 17th</h1>
 <h2>Result of plates:</h2>
 There is a culture in plates.<br>
-<div class="column-right">
+<div class="column-right"><p>
-The negative control is not good. The no change yeast grow in the YPD medium with the antibiotic. We will repeat this control on an agar plate and not in a liquid medium.<br>
+The negative control is not well. The no change yeast grow in the YPD medium with the antibiotic.<br> We will repeat this control on an agar plate and not in a liquid medium.<br><br>
 We analyze anyway down results, the results of the new control will allow us to validate the result of our experiment or search which are our error and try again.<br>
-<br><br><br><br><br><br><br><br>
+<br><br><br><br><br>
-The positive control is good, yeast to multiply of YPD agar without antibiotic. Yeast is not dead, if we observe of other agar is not a contamination.<br>
+The positive control is well, yeast multiply on YPD medium plate without antibiotic. Yeasts are not dead, so the culture on other agar mediums are not contamination.<br><br>
-We see more colonies on the plates with yeast transforming PHO85 and FRT+PHO85.<br>
+We see more colonies on the plates with yeast transforming PHO85 and FRT+PHO85.<br><br>
 We look only few colonies in the plates with yeast transforming PHO80.<br><br>
-The result is good transformation is perform well.</div>
+The result is well, transformation works.</p></div>
-<div class="column-left"><img src="https://static.igem.org/mediawiki/2015/b/b8/Paris-bettencourt-g%C3%A9lose65.png" width="300px"><br>
+<div class="column-left"><img src="https://static.igem.org/mediawiki/2015/c/c7/Paris-bettencourt-controle884.png" width="300px"><br>
-<p class="legend"><b>Figure 3:</b>Negative control</p>
+<p class="legend"><b>Figure 3 : </b>Negative control</p>
 <img src="https://static.igem.org/mediawiki/2015/b/b8/Paris-bettencourt-g%C3%A9lose65.png" width="300px">
-<p class="legend"><b>Figure 4:</b>positive control and Result of transformation</p></div>
+<p class="legend"><b>Figure 4 : </b>Positive control and result of transformation</p></div>
 <div style="clear:both"></div>
-<h2>Verification of the results</h2>
+<h2>Design primers</h2>
-Thanks to the colony PCR, to determinate if the resistance is integrated.<br>
+We design primers to verifie our results on the plates.<br>
-Create the primer:<br>
+Thanks to the colony PCR, we might determinate if the resistance is integrated into the yeast DNA.<br>
 Primer 5'-3' PHO80<br>
-<span style="color:#179A89">ATCATAAGACGAGGATATCCTTTGGAG</span><br>
+<span style="color:#179A89">ATCATAAGACGAGGATATCCTTTGGAG</span><br><br>
 Primer 3'-5' PHO80<br>
-<span style="color:#179A89">CTCAATCATGATTGCTTTCATAATACCCC</span><br>
+<span style="color:#179A89">CTCAATCATGATTGCTTTCATAATACCCC</span><br><br>
 Primer 5'-3' PHO85<br>
-<span style="color:#179A89">TATCATTATATATACATGGCTACGGTTTTTCG</span><br>
+<span style="color:#179A89">TATCATTATATATACATGGCTACGGTTTTTCG</span><br><br>
 Primer 3'-5' PHO85<br>
-<span style="color:#179A89">AAGGGATATATAGCGCGGCAAACTG</span><br>
+<span style="color:#179A89">AAGGGATATATAGCGCGGCAAACTG</span><br><br>
 Primer 5'-3' FRT+PHO85<br>
-<span style="color:#179A89">TATCATTATATATACATGGCTACGGTTTTTCG</span><br>
+<span style="color:#179A89">TATCATTATATATACATGGCTACGGTTTTTCG</span><br><br>
 Primer 3'-5' FRT+PHO85<br>
-<span style="color:#179A89">AAGGGATATATAGCGCGGCAAACTG</span><br>
+<span style="color:#179A89">AAGGGATATATAGCGCGGCAAACTG</span><br><br>
-<br><h1>August 18th</h1>
-<div class="column-right">The verification of the negative control is good, any colony is watching. We can continue our experiments, it will be validated.</div><br>
-<div class="column-left"><img src="https://static.igem.org/mediawiki/2015/d/d8/Paris-bettencourt-g%C3%A9lose655584848.png" width="200px"><p class="legend"><b>Figure 5:</b>Result of the new negative control</p></div>
+<br><h1 class="date one">August 18th</h1>
+<h2>Verification of the new negative control</h2>
+<div class="column-right"><p>
+The verification of the negative control is good, any colony is watching. We can continue our experiments, it will be validated.
+</p></div><br>
+<div class="column-left">
+<img src="https://static.igem.org/mediawiki/2015/d/d8/Paris-bettencourt-g%C3%A9lose655584848.png" width="200px"><p class="legend"><b>Figure 5 : </b>Result of the new negative control
+</p></div>
 <div style="clear:both"></div>
-itihthowfojGJ£RGJDR£JQJHh$qjfhdqqqqqqqqqqqqqqqqqqqqq<br>
+<h2>FRT problems</h2>
+<p>
+The transformation with the FRT may be run well, but the plasmid with the gene coding for flippase works only for <i>E. coli</i>. We can't use this plasmid because it will be rejected by the yeast.<br>
+Other transformation with CreLox system is possible.<br>
+CreLox is a gene which have the same fonction than the FRT, it not cut by the flippase but by the Cre recombinase.
+</p><br><br>
+We design two primers for the new transformation with CreLox system.<br><br>
+Primer 5'-3' CreLox + PHO85<br>
+<br>5’-<span style="color:#9A1717">TATCATTATATATACATGGCTACGGTTTTTCGCTGACGGGCTGCG</span><span style="color:#36C40F">ATAACTTCGTATAGCATACATTATACGAAGTTAT</span><span style="color:#179A89">ATAATCATTTGCATCCATACATTTTGATGGC</span>-3’<br><br>
+Primer 3'-5' CreLox + PHO85<br>
+<br>3’-<span style="color:#9A1717">AAGGGATATATAGCGCGGCAAACTGGGCAAACTTGAGCAATACCA</span><span style="color:#36C40F">ATAACTTCGTATAGCATACATTATACGAAGTTAT</span><span style="color:#179A89">CAGCAGTATAGCGACCAGCATTC</span>-5’<br>
+<br><span style="color:#9A1717"> -&nbsp;Homology tail on gene PHO85</span>
+<br><span style="color:#36C40F"> -&nbsp;CreLox sequence</span>
+<br><span style="color:#179A89"> -&nbsp;Kanamycin resistance binding</span><br>
+<br><h1 class="date one">August 19th</h1>
+<h2>Colony PCR</h2>
+<b>Protocol:</b>
+<br>
+<div class="column-left">
+<table borercolor="black">
+<tr>
+<td> </td>
+<td><b>PHO80</b></td>
+<td><b>PHO85</b></td>
+<td><b>FRT+ PHO85</b></td>
+</tr>
+<tr>
+<td><b>dreamTaq 2X (µL)</b></td>
+<td align="center">3</td>
+<td align="center">3</td>
+<td align="center">3</td>
+</tr>
+<tr>
+<td><b>H2O DNAse Free (µL)</b></td>
+<td align="center">9</td>
+<td align="center">9</td>
+<td align="center">9</td>
+</tr>
+<tr>
+<td><b> Colony </b></td>
+<td align="center">1</td>
+<td align="center">1</td>
+<td align="center">1</td>
+</tr>
+<tr>
+<td><b>PHO80 5'Primer (µL)</b></td>
+<td align="center"> </td>
+<td align="center">0.5</td>
+<td align="center"> </td>
+</tr>
+<tr>
+<td><b>PHO80 3'Primer (µL)</b></td>
+<td> </td>
+<td align="center">0.5</td>
+<td> </td>
+</tr>
+<tr>
+<td><b>PHO85 5'Primer (µL)</b></td>
+<td align="center">0.5</td>
+<td> </td>
+<td align="center">0.5</td>
+</tr>
+<tr>
+<td><b>PHO85 3'Primer (µL)</b></td>
+<td align="center">0.5</td>
+<td> </td>
+<td align="center">0.5</td>
+</tr>
+</table></div>
+<div class="column-right">
+<img src="https://static.igem.org/mediawiki/2015/6/69/ParisBettencourt_Cycle_PCR_colony00000.png" width="550px">
+<p class="legend"><b>Figure 6 :</b> Colony PCR cycle</p></div>
+<div style="clear:both"></div>
+<br><h1 class="date one">August 20th</h1>
+<h2>Result of colony PCR (August 19th)</h2>
+<div class="column-left"><br><br><p>
+We see bands smaller than 500bp, but not the fragments we expected : this is probably contaminations. We start again the same PCR colony. There is DNA in holes too, which didn't migrate, probably the genomic DNA.
+</p></div>
+<div class="column-right">
+<img src="https://static.igem.org/mediawiki/2015/3/30/Paris_bettencoursPCR_rg%C3%AEZH.png" width="550px">
+<p class="legend"><b>Figure 7 :</b> Electrophoresis PCR colony</p></div>
+<div style="clear:both"></div>
+<br><h2>Colony PCR</h2>
+Same to August 19th.
+<br><h2>Result of second colony PCR</h2>
+<div class="column-left">
+<img src="https://static.igem.org/mediawiki/2015/c/c4/ParisbettencoursPCR_colony_sans_lise.png" width="550px">
+<p class="legend"><b>Figure 8 :</b> second electrophoresis colony PCR</p></div>
+<div class="column-right"><p>
+The DNA Ladder is good but DNA of PCR did not migrate. The ADN is in the holes. We think that the yeasts walls being thicker simple thermic shock does not break it. We will be carry a lysis whith NaOH in yeast, to push out DNA, to the primer can be fixed on it.
+</p></div>
+<div style="clear:both"></div>
+<br><h1 class="date one">August 24th</h1>
+<h2>Yeast lysis with NaOH</h2>
+<b>Protocol:</b> <a href="https://2015.igem.org/Team:Paris_Bettencourt/Protocols/Yeast_lysis_with_NaOH"> Yeast lysis with NaOH</a><br>
+After the lysis of yeast we realize the new PCR in normal condition, the same as August 12nd. <br>
+<br><h1 class="date one">August 25th</h1>
+<h2>Result of PCR (August 24th)</h2>
+<div class="column-left">
+<img src="https://static.igem.org/mediawiki/2015/0/06/ParisBettencourt_PCR_colony_25.08.png" width="550px">
+<p class="legend"><b>Figure 9 :</b> Third electrophoresis colony PCR with NaOH lysis</p></div>
+<div class="column-right"><p>
+The DNA ladder migrate, but there was any amplification of the both genes.<br>
+We tested two PCR mix : the first did not work. The positive control worked with the second PCR mix. It is composed of HO plasmid and the oligos using for PHO85 gene.
+</p></div>
+<div style="clear:both"></div>
+<br><h1 class="date one">August 26th</h1>
+<h2>Colony PCR</h2>
+<p>To make the colony PCR, we need to lysis yeasts' wall. We realized the lysis with NaOH, but it did not work.
+So we realize a new lysis using the   "<a href="https://2015.igem.org/Team:Paris_Bettencourt/Protocols/yeast-dna-extraction-dneasy-blood-and-tissue-kit"> DNeasy Blood and Tissue Kit</a>" with the zymolyase enzyme on the non-transformed yeasts to verifie the melting temperature of primers (try between 55°C and 65°C) and if the amplification of the genes work.</p><br>
+<h2>Phytic acid dosage</h2>
+We dose the phytic acid in the fermented rice with the kit "<a href="https://2015.igem.org/Team:Paris_Bettencourt/Protocols/titration-acid-phytic"> Phytic Acid (Total Phosphorus) Assay Kit </a>".
+<br><h1 class="date one">August 27th</h1>
+<h2>Result of PCR (August 26th)</h2>
+<div class="column-right">
+<img src="https://static.igem.org/mediawiki/2015/c/ce/ParisBettencourt_PCR_colony_gradient_27.08.png" width="550px">
+<p class="legend"><b>Figure 10 :</b> Electrophoresis colony PCR with temperature gradient on non-transformed yeasts lysed by the zymolyase</p></div>
+<div class="column-left">
+<p>We made a PCR gradient on non-transformed yeast to know exactly wich temperature is better to a good fixation of the primers on the DNA. <br>
+The amplification failed, we supposed it is because our MasterMix did not work. We will try this PCR again.
+</p></div>
+<div style="clear:both"></div>
+<h2>Phytic acid dosage</h2>
+<div class="column-right"><p>
+We dose the phytic acid in fermented rice.<br>
+After analysis, the fermented rice have very little quantity of phosphorus and of phytic acid.<br>
+<b>[Phosphorus] :</b> 0.0758 mg/100g of rice.<br>
+<b>[Phytic acid] :</b> 0.269 mg/100g of rice.</p></div>
+<div class="column-left">
+<img src="https://static.igem.org/mediawiki/2015/0/09/ParisBettencourtPhyticAcidTitration1.png" width="550px">
+<p class="legend"><b>Figure 11 :</b> Phosphorus calibration curve for titration of phytic acid in fermented rice</p></div>
+<div style="clear:both"></div>
+<h2>Result of second PCR</h2>
+<div class="column-right">
+<img src="https://static.igem.org/mediawiki/2015/f/fe/ParisBettencourt_PCR_colony_gradient_27.08.15_%282%29.png" width="550px">
+<p class="legend"><b>Figure 12 :</b> Second electrophoresis colony PCR with temperature gradient (non-transformed yeast)</p></div>
+<div class="column-left">
+<p>We watch bands for the gene PHO80, at the good size : 882bp. But the gene PHO85, there was no amplifiction, and the positive control is negative : we only see aband bigger than 10,000bp and it is not what we expected.<br>We try again this PCR to see if the no amplification of the gene PHO85 it is a manipulation error or not.</p></div>
+<div style="clear:both"></div>
+<br><h1 class="date one">August 28th</h1>
+<h2>Phytic acid dosage in different strains</h2>
+<img src="https://static.igem.org/mediawiki/2015/3/3c/ParisBettencourtTitrationPhyticAcidCurve2.png" width="750px"><br><br>
+<img src="https://static.igem.org/mediawiki/2015/b/bb/ParisBettencourtTitrationPhyticAcidResultsOD2.png" width="1000px">
+<p class="legend"><b>Figure 13 :</b> Phosphorus calibration curve + results of OD in some strains</p><br>
+<img src="https://static.igem.org/mediawiki/2015/8/85/ParisBettencourtTitrationPhyticAcidResultsConcentration2.png" width="850px">
+<p class="legend"><b>Figure 14 :</b> Results of acid phytic dosage on fermented rice</p>
+<h2>Results of PCR</h2>
+<div class="column-left">
+<img src="https://static.igem.org/mediawiki/2015/2/2d/ParisBettencourtGel_28.08_gradient_4temp_80-85.png" width="550px">
+<p class="legend"><b>Figure 15 :</b> Third electrophoresis gradient PCR (non-transformed yeast)</p><br>
+</div>
+<div class="column-right"><p>We watch bands for the both of genes, but not at the same temperatures. Thanks to the gradient, we can suppose that oligos have not exactly the same melting temperature, and it may be the reason why the previous PCR failed.<br>
+The controle postive with the HO plasmid worked, the band matches with the PHO85 gene size (1020bp).
+</p></div>
+<div style="clear:both"></div>
+<br>
+<div class="column-left">
+<img src="https://static.igem.org/mediawiki/2015/3/37/ParisBettencourt_Gel_28.08_Gradient_yeast_transfo_2temp_80-85-FRT.png" width="300px">
+<p class="legend"><b>Figure 16 :</b> Electrophoresis PCR transformed yeasts</p><br>
+</div>
+<div class="column-right"><p>The positive control is negative, PCR does not therefore our work.
+</p></div>
+<div style="clear:both"></div>
+<h2>Transformation</h2>
+We transform the yeast <i>Saccharomyces cerevisiae SK1</i> with the resistance to geneticin and the <i>Cre</i> gene. We delete the PHO 85 genes and we replace it by the resistance gene.<br>
+<div class="column-right">
+<img src="https://static.igem.org/mediawiki/2015/e/e7/PARISBETTENCOURT_CRE.png" width="550px">
+<p class="legend"><b>Figure 17 :</b>Principle of Cre recombinase</p><br>
+</div>
+<div class="column-left"><p><br>The <i>Cre</i> gene is the sequence that little be cut thanks Cre recombinase and recombined the gene without the sequence between the Cre sequences.</p></div>
+<div style="clear:both"></div>
+<br>
+<br><h1 class="date one">August 30th</h1>
+<h2>Transformation on yeasts with <i>Cre</i> gene</h2>
+First step, we realize the PCR of <i>Cre</i> and <i>RFP</i> gene with primers (created by Amaury) and plasmid containing RFP. We amplified the gene, its promoter and its terminater.<br>
+<b>Protocol</b> :<a href="https://2015.igem.org/Team:Paris_Bettencourt/Protocols/PCR"> PCR</a><br>
+<br>
+Second step, we make PCR purification, and check the result with electrophoresis.<br>
+<b>Protocol</b> :<a href="https://2015.igem.org/Team:Paris_Bettencourt/Protocols/PCR_purification"> PCR purification</a>
+<br>
+<br>
+Third step, we transformed yeast that is already integrated the resistance instead of PHO85 gene. We introduce the <i>Cre</i> and <i>RFP</i> genes instead of PHO80 gene<br>
+<b>Protocol</b> :<a href="https://2015.igem.org/Team:Paris_Bettencourt/Protocols/Heat_shock_transformation_for_yeast"> Transformation of yeast</a><br>
+<br>
+Fourth step, we cultived the transforming yeasts in YPD agar medium with geneticin overnight.
+<br><br>
+</p>
+<h2>PCR and result</h2>
+<div class="column-left"></p>We did electrophoresis of transformation product. It's revealed bands around 10,000bp, while we expected 1,000bp. We think the DNA extraction in yeast doesn't work, and these bands are contamination.</div>
+<div class="column-right">
+<img src="https://static.igem.org/mediawiki/2015/b/bf/ParisBettencourt_PCRgelRFPCRE.png" width="400px">
+<p class="legend"><b>Figure 18 :</b> Colony PCR on transformed yeast with RFP</p></div>
+<div style="clear:both"></div>
+<a name="september" class="anchor"><h1></h1></a>
+<br><h1 class="date two">September 1st</h1>
+<h2>Result of transformation</h2>
+We watching any culture on plates YPD + Geneticin. The yeast are not resistant to geneticin, they had not introduced the resistance gene. Transformation does not work.
+<br><h1 class="date two">September 2nd</h1>
+<h2> Transformation</h2>
+We start again the transformation of august 28th, with the same protocol.
+<h2>Titration of phytic acid</h2>
+We test the quantity of phytic acid different strains, at dilution 1/5, 1/50 and 1/500.<br>
+Strains : g15,37 / g15,55 / g15,56 / g15,57 / g15,58 / Sook dall + HCl / Sook rice + HCl.
+<br><h1 class="date two">September 4th</h1>
+After the transformation of September 2nd, any culture is observable on plates. The tansformation are not function. We restart transformation, but we transform with <i>Cre</i> and <i>RFP</i> genes. It is more interesting because we not forced to simply remove the resistance gene, we can make a double identification. It helps to identify yeast that is already integrated in place of the resistance gene PHO85 (they cultivate on agar with geneticin) and we also integrate the RFP in place of PHO80 gene (they will be red).
+<br><h1 class="date two">September 8th</h1>
+<h2>PCR to product cassette Cre/RFP</h2>
+We restart PCR with Cre sequence and RFP gene.<br>
+<div class="column-left">
+<br><img src="https://static.igem.org/mediawiki/2015/f/f3/ParisBettencourt_PCRelectrophoresisCRERFP.jpeg" width="450px">
+<p class="legend"><b>Figure 19 : </b>Electrophoresis of Cre and RFP amplification</p><br>
+</div>
+<div class="column-right"><p><br>We see only one band. We can continue experiments with this sample and realize the transformation.</p></div>
+<div style="clear:both"></div>
+<h2> Analysis of results of titration phytic acid of September 2nd</h2>
+We test the quantity of phytic acid different strains, at dilution 1/5, 1/50 and 1/500.<br>
+Strains : g15,37 / g15,55 / g15,56 / g15,57 / g15,58 / Sook dall + HCl / Sook rice + HCl.
+We start to do the phosphorus scale.<br><br>
+<img src="https://static.igem.org/mediawiki/2015/c/cb/ParisBettencourtTitrationPhyticAcidCurve3.png" width="500px">
+<p class="legend"><b>Figure 20 :</b> Phosphorus calibration curve</p>
+<br>
+With calculations of the protocol, we can determine the concentration in our samples.<br>
+<b>Protocol :</b><a href="https://2015.igem.org/Team:Paris_Bettencourt/Protocols#FSTitrationacidphytic"> Titration of phytic acid</a>
+<br><br>
+<img src="https://static.igem.org/mediawiki/2015/8/8f/ParisBettencourt_TAB85jdkshdjs6255666666.png" width="600px">
+<p class="legend"><b>Figure 21 :</b> Table of results</p>
+Concentrations are very low. There are less to 1mg/100g d’idli.
+<br><h1 class="date two">September 11th</h1>
+<h2>Transformation</h2>
+We did the transformation on strain <i>Saccharomyces cerevisiae SK1</i>, using the protocol of<a href="https://2015.igem.org/Team:Paris_Bettencourt/Protocols#HeatShockYeast"> heat shock yeast transformation</a>.
+<br><h1 class="date two">September 14th</h1>
+<h2>Genomic DNA extraction of transformed yeast</h2>
+We try to extract genomic DNA of transformed yeast with the <a href="https://2015.igem.org/Team:Paris_Bettencourt/Protocols#YeastDNAextractiondneasybloodandtissuekit"> "Blood & Tissue extraction Kit"</a>
+<br>
+We make PCR on it.
+<h2>Result of PCR</h2>
+The gel electrophoresis revealed any bands. We might suppose that the transformation did not work, but it's probably that we don't succeed to extract the yeast's DNA which prevent us to verify our results.
+<br><h1 class="date two">September 15th</h1>
+<h2>Plate of yeast transformed with RFP</h2>
+<div class="column-left">
+<img src="https://static.igem.org/mediawiki/2015/6/60/ParsBettencourt_PlateAMAURYRFPCRE.jpeg" width="300px">
+<p class="legend"><b>Figure 22 :</b> Transformed <i>S. cerevisiae SK1</i> on YPD agar + geneticin</p></div>
+<div class="column-right">Colonies are not isolated, we cannot distinguish all of them. The culture that was inoculate was too concentrate.
+We make suspensions low concentrate and inoculate again on YPD medium with geneticin at 200µg/mL.
+</div>
+<div style="clear:both"></div>
+<br><h1 class="date two">September 16th</h1>
+<h2>Plate of yeast transformed with RFP</h2>
+<div class="column-left">
+<img src="https://static.igem.org/mediawiki/2015/9/97/ParisBettencourt_PCRgelRFPCRE1.jpeg" width="300px">
+<p class="legend"><b>Figure 23 :</b> Transformed <i>S. cerevisiae SK1</i> on YPD agar + geneticin</p></div>
+<div class="column-right">All colonies are the same, but there is no red coloration.<br>
+These result can be explicated by the fact that when this gene is introduced in the genomic DNA, it's not revealed, whereas it is in a plasmid.
+</div>
+<div style="clear:both"></div>
+<h2>Test new transformed yeast</h2>
+We test our new transformed yeast which deletion of PHO80 and PHO85 genes and compare with yeast transformed previously (first with the geneticin resistance gene in place PHO85 gene and second with the  geneticin resistance gene in place PHO80). We put this yeast in YPD + geneticin medium (YPD + geneticinn for always keep the selection). We have grown the yeast with six concentration of phytic acid (0.005, 0.01, 0.02, 0.04, 0.1, 0.2 g/mL). We also realize a scale with phytic acid and YPD medium + geneticin. <br>
+Scale: C(phytic acid;YPD) (g.mL-1)	0,005	0,01	0,02	0,04	0,1 <br>
+<img src="https://static.igem.org/mediawiki/2015/1/15/PariBettencourt_1erTeste_acidejdphfiZV.png" width="1000px"><br>
+<p class="legend"><b>Figure 24 :</b>Table manipulation</p><br>
+We don’t have enough reagents in our kit to do all manipulations we want, and it is too late to buy it. We choose to delete three concentrations by strain and in the scale. <br>
+<img src="https://static.igem.org/mediawiki/2015/d/de/PariBettencourt_1erTeste_acide_phytiquerggrrrgrgert-jhtTH.png" width="1000px"><br>
+<p class="legend"><b>Figure 25 :</b>New table manipulation</p><br>
+<img src="https://static.igem.org/mediawiki/2015/b/bb/PariBettencourt_hghdhfuhgggkhgchggv.png" width="1000px"><br>
+<p class="legend"><b>Figure 26 :</b>Result of test</p><br>
+Result analysis: We have only optic density result below zero. Normally is no possible. We suppose the reagents of the kit are old and it not work. Would have had to do again the tests but there is not reagents and time anymore. <br>
+</div>
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Difference between revisions of "Team:Paris Bettencourt/Notebook/Phytase"

Latest revision as of 14:04, 30 October 2015

Ferment It Yourself

iGEM Paris-Bettencourt 2O15

Notebook - Phytase

August 10th

Design primers

Gene PHO85

Gene PHO80

Gene FRT + PHO85

August 12nd

Culture

PCR

August 13th

PCR Purification

Result of PCR (August 12th)

Pre-culture

August 14th

Transformation of yeast

August 17th

Result of plates:

Design primers

August 18th

Verification of the new negative control

FRT problems

August 19th

Colony PCR

August 20th

Result of colony PCR (August 19th)

Colony PCR

Result of second colony PCR

August 24th

Yeast lysis with NaOH

August 25th

Result of PCR (August 24th)

August 26th

Colony PCR

Phytic acid dosage

August 27th

Result of PCR (August 26th)

Phytic acid dosage

Result of second PCR

August 28th

Phytic acid dosage in different strains

Results of PCR

Transformation

August 30th

Transformation on yeasts with Cre gene

PCR and result

September 1st

Result of transformation

September 2nd

Transformation

Titration of phytic acid

September 4th

September 8th

PCR to product cassette Cre/RFP

Analysis of results of titration phytic acid of September 2nd

September 11th

Transformation

September 14th

Genomic DNA extraction of transformed yeast

Result of PCR

September 15th

Plate of yeast transformed with RFP

September 16th

Plate of yeast transformed with RFP

Test new transformed yeast