Difference between revisions of "Team:UFMG Brazil/Results"

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<h3>Results</h3>
 
<h3>Results</h3>
  
<p> DNA coding sequence of Mouse interferon-beta (IFN-beta) linked to signal peptide that allow protein secretion and latency-associated peptide (LAP) that possibilite IFN activation only in inflammatory site was designed with optimized codons for expression in <i>Leishmania</i> host (Figure 1).<br/></p>
+
<p> DNA coding sequence of Mouse IFN-β linked to signal peptide that allow protein secretion and latency-associated peptide (LAP) that possibilite IFNactivation only in inflammatory site was designed with optimized codons for expression in <i>Leishmania</i> host (Figure 1).<br/></p>
  
 
<img class="centered-image" src="https://static.igem.org/mediawiki/2015/b/b3/Ufmg-brazil-results00.png"/>
 
<img class="centered-image" src="https://static.igem.org/mediawiki/2015/b/b3/Ufmg-brazil-results00.png"/>
  
<h5> <b>Figure 1</b> - LAP-IFN-beta synthetic gene synthetized. Highlighted in green is signal peptide for secretion and highlighted in purple is LAP sequence.</h5><br/><br/>
+
<h5> <b>Figure 1</b> - LAP-IFN-β synthetic gene synthetized. Highlighted in green is signal peptide for secretion and highlighted in purple is LAP sequence.</h5><br/><br/>
  
<p> The final sequence was synthesized by IDT (California, USA) in pUC_IDT standard vector with resistance to ampicillin. <i>E. coli</i> strain DH10b/TOP10 was transformed with the plasmid and resistant colonies were observed after incubation by 16 hours at 37 oC (Figure 2).<br/></p>
+
<p> The final sequence was synthesized by IDT (California, USA) in pUC_IDT standard vector with resistance to ampicillin. <i>E. coli</i> strain DH10b/TOP10 was transformed with the plasmid and resistant colonies were observed after incubation by 16 hours at 37° C (Figure 2).<br/></p>
  
 
<img class="centered-image" src="https://static.igem.org/mediawiki/2015/d/d8/Ufmg-brazil-results01.png"/>
 
<img class="centered-image" src="https://static.igem.org/mediawiki/2015/d/d8/Ufmg-brazil-results01.png"/>
  
<h5><b>Figure 2</b> - Plate of E. coli colonies transformed with pUC_IDT vector containing recombinant IFN-beta. Red arrows label positive colonies.</h5><br/><br/>
+
<h5><b>Figure 2</b> - Plate of <i>E. coli</i> colonies transformed with pUC_IDT vector containing recombinant IFN-β. Red arrows label positive colonies.</h5><br/><br/>
  
 
<p>Miniprep to recover the plasmids were carried out and the quality of extraction was confirmed by 1.2% agarose gel stained with SYBR Safe DNA Gel Stain from Invitrogen (Waltham, USA) (Figure 3).<br/></p>
 
<p>Miniprep to recover the plasmids were carried out and the quality of extraction was confirmed by 1.2% agarose gel stained with SYBR Safe DNA Gel Stain from Invitrogen (Waltham, USA) (Figure 3).<br/></p>
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<img class="centered-image" src="https://static.igem.org/mediawiki/2015/2/27/Ufmg-brazil-results02.png"/>
 
<img class="centered-image" src="https://static.igem.org/mediawiki/2015/2/27/Ufmg-brazil-results02.png"/>
  
<h5><b>Figure 3</b> - Electrophoresis in 1.2% agorose gel of plasmid pUC_IDT containing recombinant IFN-beta. Labels of lanes: 1) Molecular weight markers; 2) Negative control; 3 and 4) Plasmids recovered by miniprep protocol.</h5><br/><br/>
+
<h5><b>Figure 3</b> - Electrophoresis in 1.2% agarose gel of plasmid pUC_IDT containing recombinant IFN-β. Labels of lanes: 1) Molecular weight markers; 2) Negative control; 3 and 4) Plasmids recovered by miniprep protocol.</h5><br/><br/>
  
<p>Plasmids containing IFN-beta were used as DNA template in a PCR with specific primers pair to the synthetic gene (Figure 4). The forward primer had restriction site of enzyme XbaI in the 5’ region and the reverse oligonucleotide sequence had site of BamHI in the 5’ region.<br/></p>
+
<p>Plasmids containing IFN-β were used as DNA template in a PCR with specific primers pair to the synthetic gene (Figure 4). The forward primer had restriction site of enzyme <i>Xba</i>I in the 5’ region and the reverse oligonucleotide sequence had site of <i>Bam</i>HI in the 5’ region.<br/></p>
  
 
<img class="centered-image" src="https://static.igem.org/mediawiki/2015/f/f8/Ufmg-brazil-results03.png"/>
 
<img class="centered-image" src="https://static.igem.org/mediawiki/2015/f/f8/Ufmg-brazil-results03.png"/>
  
<h5><b>Figure 4</b> - Electrophoresis in 1.2% agarose gel of IFN-beta PCR product containing restriction sites to XbaI and BamHI enzymes. The molecular weight of correct PCR product should be 1461 base pairs. Labels of lanes: 1) Molecular weight markers; 2, 3 and 4) Positive PCR for three transformed E. coli colonies; 5) Negative control. </h5><br/><br/>
+
<h5><b>Figure 4</b> - Electrophoresis in 1.2% agarose gel of IFN-β a PCR product containing restriction sites to <i>Xba</i>I and <i>Bam</i>HI enzymes. The molecular weight of correct PCR product should be 1461 base pairs. Labels of lanes: 1) Molecular weight markers; 2, 3 and 4) Positive PCR for three transformed <i>E. coli</i> colonies; 5) Negative control.</h5><br/><br/>
  
<p>The PCR product was joined with pGEM-T easy vector from Promega (Fitchburg, USA). E. coli DH10b/TOP10 were transformed with the ligated product (Figure 5) or pLpNEO vector specific to Leishmania expression. After resistant bacteria selection and cultivation in liquid medium, miniprep protocol was performed to recovered the plasmids (Figures 6 and 7).<br/></p>
+
<p>The PCR product was joined with pGEM-T Easy vector from Promega (Fitchburg, USA). <i>E. coli</i> DH10b/TOP10 were transformed with the ligated product (Figure 5) or pLpNEO vector specific to <i>Leishmania</i> expression. After resistant bacteria selection and cultivation in liquid medium, miniprep protocol was performed to recovered the plasmids (Figures 6 and 7).<br/></p>
  
 
<img class="centered-image" src="https://static.igem.org/mediawiki/2015/0/0e/Ufmg-brazil-results05.png"/>
 
<img class="centered-image" src="https://static.igem.org/mediawiki/2015/0/0e/Ufmg-brazil-results05.png"/>
  
<h5><b>Figure 5</b> - Plate of E. coli colonies transformed with pGEM-T easy vector containing recombinant IFN-beta. Red arrows label positive colonies. </h5><br/><br/>
+
<h5><b>Figure 5</b> - Plate of <i>E. coli</i> colonies transformed with pGEM-T Easy vector containing recombinant IFN-β. Red arrows label positive colonies. </h5><br/><br/>
  
 
<img class="centered-image" src="https://static.igem.org/mediawiki/2015/0/01/Ufmg-brazil-results06.png"/>
 
<img class="centered-image" src="https://static.igem.org/mediawiki/2015/0/01/Ufmg-brazil-results06.png"/>
  
<h5><b>Figure 6</b> - Electrophoresis in 1.2% agarose gel of plasmid pGEM-T easy containing synthetic IFN-beta. Labels of lanes: 1) Molecular weight markers; 2, 3, 4 and 5) Plasmids recovered by miniprep protocol.</h5><br/><br/>
+
<h5><b>Figure 6</b> - Electrophoresis in 1.2% agarose gel of plasmid pGEM-T Easy containing synthetic IFN-β. Labels of lanes: 1) Molecular weight markers; 2, 3, 4 and 5) Plasmids recovered by miniprep protocol.</h5><br/><br/>
  
 
<img class="centered-image" src="https://static.igem.org/mediawiki/2015/7/78/Ufmg-brazil-results07.png"/>
 
<img class="centered-image" src="https://static.igem.org/mediawiki/2015/7/78/Ufmg-brazil-results07.png"/>

Revision as of 17:05, 18 September 2015




Project

Overview

Problem and
Solution

Chassis

Devices and
kill switch

Lab Work

Safety

Notebook

Protocols

Results

Modeling

Practices

Overview

Integrated Human
Practices

Public
Engagement

Synenergene

Overview

Application
Scenarios

Techno-moral

Team

Our Team

Attributions

Collaborations

Sponsors




Results

DNA coding sequence of Mouse IFN-β linked to signal peptide that allow protein secretion and latency-associated peptide (LAP) that possibilite IFN-β activation only in inflammatory site was designed with optimized codons for expression in Leishmania host (Figure 1).

Figure 1 - LAP-IFN-β synthetic gene synthetized. Highlighted in green is signal peptide for secretion and highlighted in purple is LAP sequence.


The final sequence was synthesized by IDT (California, USA) in pUC_IDT standard vector with resistance to ampicillin. E. coli strain DH10b/TOP10 was transformed with the plasmid and resistant colonies were observed after incubation by 16 hours at 37° C (Figure 2).

Figure 2 - Plate of E. coli colonies transformed with pUC_IDT vector containing recombinant IFN-β. Red arrows label positive colonies.


Miniprep to recover the plasmids were carried out and the quality of extraction was confirmed by 1.2% agarose gel stained with SYBR Safe DNA Gel Stain from Invitrogen (Waltham, USA) (Figure 3).

Figure 3 - Electrophoresis in 1.2% agarose gel of plasmid pUC_IDT containing recombinant IFN-β. Labels of lanes: 1) Molecular weight markers; 2) Negative control; 3 and 4) Plasmids recovered by miniprep protocol.


Plasmids containing IFN-β were used as DNA template in a PCR with specific primers pair to the synthetic gene (Figure 4). The forward primer had restriction site of enzyme XbaI in the 5’ region and the reverse oligonucleotide sequence had site of BamHI in the 5’ region.

Figure 4 - Electrophoresis in 1.2% agarose gel of IFN-β a PCR product containing restriction sites to XbaI and BamHI enzymes. The molecular weight of correct PCR product should be 1461 base pairs. Labels of lanes: 1) Molecular weight markers; 2, 3 and 4) Positive PCR for three transformed E. coli colonies; 5) Negative control.


The PCR product was joined with pGEM-T Easy vector from Promega (Fitchburg, USA). E. coli DH10b/TOP10 were transformed with the ligated product (Figure 5) or pLpNEO vector specific to Leishmania expression. After resistant bacteria selection and cultivation in liquid medium, miniprep protocol was performed to recovered the plasmids (Figures 6 and 7).

Figure 5 - Plate of E. coli colonies transformed with pGEM-T Easy vector containing recombinant IFN-β. Red arrows label positive colonies.


Figure 6 - Electrophoresis in 1.2% agarose gel of plasmid pGEM-T Easy containing synthetic IFN-β. Labels of lanes: 1) Molecular weight markers; 2, 3, 4 and 5) Plasmids recovered by miniprep protocol.


Figure 7 - Electrophoresis in 1.2% agarose gel of pLpNEO vector. Labels of lanes: 1) Molecular weight markers; 2 and 3) Plasmids recovered by miniprep protocol.