IGEM:UNAM/2009/Notebook/Modeling logbook Claudia/2010/09/25: Difference between revisions

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|style="background-color: #EEE"|[[Image:igem-logo-150px.png|150px]]<span style="font-size:22px;"> iGEM Project name 1</span>
|style="background-color: #EEE"|[[Image:TeamLogo.jpg|350px]]<span style="font-size:19px;"> UNAM-Genomics-Mexico team</span>
|style="background-color: #F2F2F2" align="center"|<html><img src="/images/9/94/Report.png" border="0" /></html> [[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>[[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]]<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>}}
|style="background-color: #F2F2F2" align="center"|<html><img src="/images/9/94/Report.png" border="0" /></html> [[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>[[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]]<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>}}
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Revision as of 14:24, 9 October 2010

UNAM-Genomics-Mexico team <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>

Repeated experiment:Working on J23101 promoter: Ligation to P0451/Lumazine/LuxY

Due to the first attempt to ligate P0451, Lumazine and LuxY to promoter J23101 failed, I am going to repeat the experiment.

Ligation Procedure:Promoter J23101 with P0451 (RBS+cI repressor)/Lumazine and LuxY

1. Prepare the ligation mixture taking into account the quantity of the DNA insert -P0451 (RBS+cI repressor),LuxY and Lumazine- and the receiver DNA -plasmid harboring the promoter J23101-. This can be check in the following gel.

Gel for ligations. Lane1:Ladder. Lane2: plasmid harboring the promoter J23101 dephosphatated (SpeI/PstI). Lane3: Lumazine PCR amplified product from Mr.Gene plasmid (XbaI/PstI). Lane4:P0451 colony 6 (XbaI/PstI). Lane5:LuxY purification from Mr.Gene plasmid (XbaI/PstI).
  • Ligation mixture: P0451(RBS+cI repressor)
Reactive Quantity
DNA insert (P0451:RBS+cI repressor) 4μL
DNA plasmid (plasmid harboring the promoter J23101) 2μL
Buffer 10X T4 Ligase 2μL
Enzyme T4 Ligase 1μL
HPLC Up to a final volume of 20 μL of the mixture (11μL)
  • Ligation mixture: Lumazine/LuxY
Reactive Quantity
DNA insert (Lumazine/LuxY) 5μL
DNA plasmid (plasmid harboring the promoter J23101) 2μL
Buffer 10X T4 Ligase 2μL
Enzyme T4 Ligase 1μL
HPLC Up to a final volume of 20 μL of the mixture (10μL)

2. Incubate the sample at 16°C overnight.

3. Transform the cells. Click here for the protocol.

4. Culture the cells in the proper selective medium, in our case LB + Kanamycin.

5. Incubate the petri dishes at 37°C overnight.

6. Re-culture the resultant colonies in the proper selective medium; incubate them at 37°C overnight.

7. Analyze the colonies with Colony PCR to confirm that they contain the correct ligation

The primers that I am using are:

Forward (5'->3'): Preffix primer.

Reverse:(5'->3'): Suffix primer.

These primers would amplify LuxY, Lumazine and P0451:RBS+cI repressor plus promoter J23101, if the ligation was correctly done.

Repeated experiment:Working on cI inverter construction and fusion to pSB1T3 backbone. LovTAP repressor activity:reporter system

Due to the first attempt to ligate K098991 (cI regulated promoter+RBS+GFP) and P0451(RBS+cI repressor) inside plasmid pSB1C3 failed, I am going to ligate them in plasmid pSB1T3.

Ligation Procedure: P0451 + K098991 to plasmid pSB1T3

1. Prepare the ligation mixture taking into account the quantity of the DNA insertS -K098991 and P0451- and the receiver DNA -plasmid pSB1T3-. This can be check in the following gel. Quantity loaded 3μL.

Restriction enzyme assays. Lane1:Ladder. Lane4:Plasmid pSB1T3. Lane11:P0451 colony 6 (EcoRI/SpeI) .Lane12: K098991 colony 8 (XbaI/PstI). The other lanes are samples from other experiments
  • Ligation mixture 1
Reactive Quantity
DNA inserts (K098991 and P0451) 4μL each
DNA plasmid (pSB1T3) 2μL
Buffer 10X T4 Ligase 2μL
Enzyme T4 Ligase 1μL
HPLC Up to a final volume of 20 μL of the mixture (7μL)


  • Ligation mixture 2
Reactive Quantity
DNA inserts (K098991+ P0451) 5μL each
DNA plasmid (pSB1C3) 3μL
Buffer 10X T4 Ligase 2μL
Enzyme T4 Ligase 1μL
HPLC Up to a final volume of 20 μL of the mixture (4μL)


2. Incubate the sample at 16°C overnight.

3. Transform the cells. Click here for the protocol.

4. Culture the cells in the proper selective medium, in our case LB + Kanamycin.

5. Incubate the petri dishes at 37°C overnight.

6. Re-culture the resultant colonies in the proper selective medium; incubate them at 37°C overnight.

7. Analyze the colonies with Colony PCR to confirm that they contain the correct ligation

The primers that I am using are:

Forward (5'->3'): Preffix primer.

Reverse:(5'->3'): Suffix primer.

These primers would amplify the whole cI inverter, if the ligation was correctly done.


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