Difference between revisions of "Team:IISc-Bangalore/Assembly"

 
(48 intermediate revisions by 3 users not shown)
Line 2: Line 2:
 
<html>
 
<html>
 
     <ol id="inPageNav">
 
     <ol id="inPageNav">
−
<li><a href="#biobrick-transformations">BioBrick Transformations</a></li>
+
<li><a href="#biobrick-transformations">Transformations<img src="https://static.igem.org/mediawiki/2017/6/68/T--IISc-Bangalore--navbar_bullet.png" /></a></li>
−
<li><a href="#plasmid-isolation">Plasmid Isolation</a></li>
+
<li><a href="#plasmid-isolation">Plasmid Isolation<img src="https://static.igem.org/mediawiki/2017/6/68/T--IISc-Bangalore--navbar_bullet.png" /></a></li>
−
<li><a href="#pcrs">PCRs</a></li>
+
<li><a href="#pcrs">PCRs<img src="https://static.igem.org/mediawiki/2017/6/68/T--IISc-Bangalore--navbar_bullet.png" /></a></li>
−
<li><a href="#restriction-digests">Restriction digests</a></li>
+
<li><a href="#restriction-digests">Restriction digests<img src="https://static.igem.org/mediawiki/2017/6/68/T--IISc-Bangalore--navbar_bullet.png" /></a></li>
−
<li><a href="#ligations">Ligations</a></li>
+
<li><a href="#ligations">Ligations<img src="https://static.igem.org/mediawiki/2017/6/68/T--IISc-Bangalore--navbar_bullet.png" /></a></li>
−
<li><a href="#screening">Screening</a></li>
+
<li><a href="#screening">Screening<img src="https://static.igem.org/mediawiki/2017/6/68/T--IISc-Bangalore--navbar_bullet.png" /></a></li>
 
     </ol>
 
     </ol>
  
 
<div id="contentMain">
 
<div id="contentMain">
 +
 +
<img src="https://static.igem.org/mediawiki/2017/9/96/T--IISc-Bangalore--Header--assemb.svg" id="headerImg" />
  
 
<h1 id="biobrick-transformations">BioBrick Transformations</h1>
 
<h1 id="biobrick-transformations">BioBrick Transformations</h1>
  
−
<p>The five BioBricks we are using are transformed into <i>E. coli</i> strain DH5α — chosen for its <i>recA</i> and <i>endA</i> mutations that allow for high-yield minipreps.</p>
+
<p>The five BioBricks we are using were transformed into <i>E. coli</i> strain DH5α — chosen for its <i>recA</i> and <i>endA</i> mutations that allow for high-yield minipreps.</p>
  
−
<h2>INSERT IMAGES OF PLATES</h2>
+
<h2>Transformations for T7 expression system</h2>
  
−
<h1 id="plasmid-isolation">Plasmid Isolation</h1>
+
<figure>
 +
<IMG SRC="https://static.igem.org/mediawiki/2017/3/38/T--IISc-Bangalore--t7-plates.png" width="70%">
 +
<br>
 +
<figurecaption>
 +
<b>Figure 1</b>: BBa_K525998 and BBa_K731721
 +
</figurecaption>
 +
</figure>
  
−
<p>Minipreps are performed from three colonies on each plate to confirm the presence of the plasmid. One colony from each positive transformants is used to make a glycerol stock.</p>
+
<h2>Transformations for sfGFP-SpyCatcher</h2>
  
−
<h2>INSERT GEL IMAGES</h2>
+
<figure>
 +
<IMG SRC="https://static.igem.org/mediawiki/2017/2/21/T--IISc-Bangalore--sfGFP-SpyCatcher-plates.png" width="70%">
 +
<br>
 +
<figurecaption>
 +
<b>Figure 2</b>: BBa_K1650037 and BBa_K1321337
 +
</figurecaption>
 +
</figure>
  
−
<h1 id="pcrs">PCRs: Adding Restriction Sites and Linkers</h1>
+
<h2>Transformations for mCherry</h2>
−
Our assembly begins with our PCRs: using carefully-designed primers with 5'-overhangs, we add restriction sites, linkers and other features to our parts of interest. Since most of our PCRs have such overhangs, our annealing temperature changes after the first few cycles — our PCR cycle parameters account for this variation. In addition, we used NEB's Q5 MasterMix and NEB's Phusion polymerase, both high-fidelity DNA polymerases which have a higher annealing temperature than usual.
+
 
 +
<figure>
 +
<IMG SRC="https://static.igem.org/mediawiki/2017/9/9d/T--IISc-Bangalore--BBa_J18932.png" width="35%">
 +
<br>
 +
<figurecaption>
 +
<b>Figure 3 </b>: BBa_J18932
 +
</figurecaption>
 +
</figure>
 +
 
 +
<h1 id="plasmid-isolation">Plasmid Isolation</h1>
 +
 
 +
<p>Minipreps were performed using three colonies on each transformation plate to confirm the presence of the plasmid. One positive transformant for each BioBrick was used to make a glycerol stock.</p>
 +
 
 +
<h1 id="pcrs">PCRs</h1>
 +
<p>Our assembly begins with our PCRs: using carefully-designed primers with 5'-overhangs, we add restriction sites, linkers and other features to our parts of interest. Since most of our PCRs have such overhangs, our annealing temperature changes after the first few cycles — our PCR cycle parameters account for this variation. In addition, we used NEB's Q5 MasterMix and NEB's Phusion polymerase, both high-fidelity DNA polymerases which have a higher annealing temperature than usual.</p>
  
 
<h2>PCRs for the T7 expression backbone</h2>
 
<h2>PCRs for the T7 expression backbone</h2>
  
−
<table>
+
<table class="fch">
 
<tr>
 
<tr>
 
<th colspan="2">PCR 1 — T7 Expression Backbone (Piece 1)</th>
 
<th colspan="2">PCR 1 — T7 Expression Backbone (Piece 1)</th>
Line 41: Line 69:
 
</tr>
 
</tr>
 
<tr>
 
<tr>
−
<td>Splits the CmR gene, includes NcoI site</td>
+
<td>Amplifies the CmR gene, includes NcoI site</td>
 
</tr>
 
</tr>
 
<tr>
 
<tr>
Line 53: Line 81:
 
<th>Amplicon size</th>
 
<th>Amplicon size</th>
 
<td>886 bp</td>
 
<td>886 bp</td>
−
</tr>
 
−
<tr>
 
−
<th>Polymerase</th>
 
−
<td>Q5 polymerase</td>
 
 
</tr>
 
</tr>
 
</table>
 
</table>
  
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/7/72/T--IISc-Bangalore--PCR1.png" width="100%">
 +
<figurecaption> PCR1 product</figurecaption>
 +
</figure>
  
−
 
+
<table class="fch">
−
<table>
+
 
<tr>
 
<tr>
 
<th colspan="2">PCR 2 — T7 Expression Backbone (Piece 2)</th>
 
<th colspan="2">PCR 2 — T7 Expression Backbone (Piece 2)</th>
Line 86: Line 113:
 
<th>Amplicon size</th>
 
<th>Amplicon size</th>
 
<td>1533 bp</td>
 
<td>1533 bp</td>
−
</tr>
 
−
<tr>
 
−
<th>Polymerase</th>
 
−
<td>Q5 polymerase</td>
 
 
</tr>
 
</tr>
 
</table>
 
</table>
 +
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/b/b7/T--IISc-Bangalore--PCR2.png" width="100%">
 +
<figurecaption>PCR2 product</figurecaption>
 +
</figure>
  
 
<h2>PCRs for sfGFP-SpyCatcher</h2>
 
<h2>PCRs for sfGFP-SpyCatcher</h2>
  
−
<table>
+
<table class="fch">
 
<tr>
 
<tr>
 
<th colspan="2">PCR 3 — sfGFP</th>
 
<th colspan="2">PCR 3 — sfGFP</th>
Line 119: Line 147:
 
<th>Amplicon size</th>
 
<th>Amplicon size</th>
 
<td>753 bp</td>
 
<td>753 bp</td>
−
</tr>
 
−
<tr>
 
−
<th>Polymerase</th>
 
−
<td>Q5 polymerase</td>
 
 
</tr>
 
</tr>
 
</table>
 
</table>
  
−
<h2>PCR 4: SpyCatcher</h2>
+
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/c/cf/T--IISc-Bangalore--PCR3.png" width="100%">
 +
<figurecaption>PCR3 product</figurecaption>
 +
</figure>
  
−
<table>
+
<table class="fch">
 
<tr>
 
<tr>
 
<th colspan="2">PCR 4 — SpyCatcher</th>
 
<th colspan="2">PCR 4 — SpyCatcher</th>
Line 152: Line 179:
 
<th>Amplicon size</th>
 
<th>Amplicon size</th>
 
<td>450 bp</td>
 
<td>450 bp</td>
−
</tr>
 
−
<tr>
 
−
<th>Polymerase</th>
 
−
<td>Q5 polymerase</td>
 
 
</tr>
 
</tr>
 
</table>
 
</table>
 +
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/5/52/T--IISc-Bangalore--PCR4.png" width="100%">
 +
<figurecaption>PCR4 product</figurecaption>
 +
</figure>
  
 
<h2>PCRs for 6xHis-mCherry</h2>
 
<h2>PCRs for 6xHis-mCherry</h2>
  
−
<table>
+
<table class="fch">
 
<tr>
 
<tr>
 
<th colspan="2">PCR 5 — mCherry</th>
 
<th colspan="2">PCR 5 — mCherry</th>
Line 185: Line 213:
 
<th>Amplicon size</th>
 
<th>Amplicon size</th>
 
<td>735 bp</td>
 
<td>735 bp</td>
−
</tr>
 
−
<tr>
 
−
<th>Polymerase</th>
 
−
<td>Q5 polymerase</td>
 
 
</tr>
 
</tr>
 
</table>
 
</table>
  
−
<table>
+
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/b/b7/T--IISc-Bangalore--PCR5.png" width="100%">
 +
<figurecaption>PCR5 product</figurecaption>
 +
</figure>
 +
 
 +
<table class="fch">
 
<tr>
 
<tr>
 
<th colspan="2">PCR 6 — mCherry</th>
 
<th colspan="2">PCR 6 — mCherry</th>
Line 216: Line 245:
 
<th>Amplicon size</th>
 
<th>Amplicon size</th>
 
<td>753 bp</td>
 
<td>753 bp</td>
−
</tr>
 
−
<tr>
 
−
<th>Polymerase</th>
 
−
<td>Q5 polymerase</td>
 
 
</tr>
 
</tr>
 
</table>
 
</table>
 +
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/6/6e/T--IISc-Bangalore--PCR6.png" width="100%">
 +
<figurecaption>PCR6 product</figurecaption>
 +
</figure>
  
 
<h2>PCRs for mCherry-SpyTag</h2>
 
<h2>PCRs for mCherry-SpyTag</h2>
  
−
<table>
+
<table class="fch">
 
<tr>
 
<tr>
 
<th colspan="2">PCR 7 — mCherry-SpyTag</th>
 
<th colspan="2">PCR 7 — mCherry-SpyTag</th>
Line 250: Line 280:
 
<td>732 bp</td>
 
<td>732 bp</td>
 
</tr>
 
</tr>
−
<tr>
+
 
−
<th>Polymerase</th>
+
−
<td>Q5 polymerase</td>
+
−
</tr>
+
 
</table>
 
</table>
 +
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/f/fb/T--IISc-Bangalore--assembly-PCR7.png" width="100%">
 +
<figurecaption>
 +
PCR7 product
 +
</figurecaption>
 +
</figure>
  
 
<h1 id="restriction-digests">Restriction Digests</h1>
 
<h1 id="restriction-digests">Restriction Digests</h1>
−
<table>
+
 
 +
<h2>Restriction digests for T7 expression backbone</h2>
 +
 
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/7/72/T--IISc-Bangalore--PCR1.png" width="100%">
 +
<figurecaption>
 +
Double-digest PCR1 product with NcoI and HindIII (D1)
 +
</figurecaption>
 +
</figure>
 +
 
 +
 
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/b/b7/T--IISc-Bangalore--PCR2.png" width="100%">
 +
<figurecaption>
 +
Double-digest PCR2 product with NheI and NcoI (D2)
 +
</figurecaption>
 +
</figure>
 +
 
 +
<h2>Restriction digests for sfGFP-SpyCatcher</h2>
 +
 
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/c/cf/T--IISc-Bangalore--PCR3.png" width="100%">
 +
<figurecaption>
 +
Double-digest PCR3 product with HindIII and BamHI (D3)
 +
</figurecaption>
 +
</figure>
 +
 
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/5/52/T--IISc-Bangalore--PCR4.png" width="100%">
 +
<figurecaption>
 +
Double-digest PCR4 product with BamHI and NheI (D4)
 +
</figurecaption>
 +
</figure>
 +
 
 +
<h2>Restriction digest for 6xHis-mCherry</h2>
 +
 
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/6/6e/T--IISc-Bangalore--PCR6.png" width="100%">
 +
<figurecaption>
 +
Double-digest PCR6 product with HindIII and NheI (D6)
 +
</figurecaption>
 +
</figure>
 +
 
 +
<h2>Restriction digests for mCherry-SpyTag</h2>
 +
 
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/0/0a/T--IISc-Bangalore--assembly-oligo-1.png" width="100%">
 +
<figurecaption>
 +
Double-digest Oligo 1 with HindIII and NdeI (DO1)
 +
</figurecaption>
 +
</figure>
 +
 
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/f/fb/T--IISc-Bangalore--assembly-PCR7.png" width="100%">
 +
<figurecaption>
 +
Double-digest PCR7 product with NdeI and BamHI (D7)
 +
</figurecaption>
 +
</figure>
 +
 
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/a/a0/T--IISc-Bangalore--assembly-oligo-2.png" width="100%">
 +
<figurecaption>
 +
Double-digest Oligo 2 with BamHI and NheI (DO2)
 +
</figurecaption>
 +
</figure>
 +
 
 +
<h2>Gel-purification of our digested products</h2>
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/c/c9/T--IISc-Bangalore--gel-purification.png" width="100%">
 +
<br>
 +
<figurecaption>
 +
<b>Figure 4</b>: Digested PCR products (D1, D2, D3, D4, D6, DO1, DO2)
 +
</figurecaption>
 +
</figure>
 +
 
 +
<table width="100%">
 
<tr>
 
<tr>
 
<th colspan="8">Restriction enzymes used in our assembly</th>
 
<th colspan="8">Restriction enzymes used in our assembly</th>
Line 373: Line 482:
 
<td>37°C</td>
 
<td>37°C</td>
 
<td>80°C</td>
 
<td>80°C</td>
 +
</tr>
 +
<tr>
 +
<td>NdeI</td>
 +
<td>CA\TATG</td>
 +
<td>75</td>
 +
<td>100</td>
 +
<td>100</td>
 +
<td>100</td>
 +
<td>37°C</td>
 +
<td>65°C</td>
 
</tr>
 
</tr>
 
<tr>
 
<tr>
Line 395: Line 514:
 
</tr>
 
</tr>
 
<tr>
 
<tr>
−
<td colspan="8">* denotes star activity| NOTE ADD NdeI TOO</td>
+
<td colspan="8">* denotes star activity</td>
 
</tr>
 
</tr>
 
 
 
</table>
 
</table>
  
−
<h1 id="ligation">Multi-Ligation: Coming Full Circle</h1>
+
<h1 id="ligations">Multi-Ligation</h1>
−
<h1 id="screening">Screening Transformants: Colony PCR with VF2/VR</h1>
+
  
 +
<h2>Ligating sfGFP-SpyCatcher</h2>
 +
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/b/b5/T--IISc-Bangalore--C1234.png" width="80%">
 +
<br>
 +
<figurecaption>
 +
Plasmid map of BBa_K2319000 (sfGFP-SpyCatcher)
 +
</figurecaption>
 +
</figure>
 +
 +
<h2>Ligating 6xHis-mCherry</h2>
 +
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/a/a4/T--IISc-Bangalore--assembly-C126-linear.png" width="80%">
 +
<figurecaption>
 +
Plasmid map of BBa_K2319009 (6xHis-mCherry)
 +
</figurecaption>
 +
</figure>
 +
 +
<h1 id="screening">Screening Transformants</h1>
 +
<p>We screened 30 transformants from each plate using colony PCR with primers VF2 and VR, which we standardized using Taq polymerase (annealing temperature of 56°C).</p>
 +
 +
<figure>
 +
<img src="https://static.igem.org/mediawiki/2017/1/19/T--IISc-Bangalore--colony-PCR.png" width="100%">
 +
<br>
 +
<figurecaption>
 +
<b>Figure 6 </b>: Colony PCR of sfGFP-SpyCatcher colonies (B1-B21) and 6xHis-mCherry colonies (D1-D21)
 +
</figurecaption>
 +
</figure>
 +
 +
<p>We obtained the expected band (~1.5 kb) for one of the thirty sfGFP-SpyCatcher colonies tested while none of the thirty 6xHis-mCherry colonies tested gave the expected band (> 1.1 kb). After plasmid isolation from this positive clone, we transformed BL21 (DE3) to continue with our protein experiments.</p>
 +
 +
<h2>Other parts</h2>
 +
<p>Due to the failure of our assemblies for the other BioBricks, we were not able to submit these parts on time, but we have submitted the designs for future teams to use.</p>
 
</div>
 
</div>
  
Line 409: Line 561:
 
   changeHash: true     
 
   changeHash: true     
 
});
 
});
 +
 +
var height = $('#headerImg').height();
 +
    window.onscroll = function() {myFunction()};
 +
 +
    function myFunction() {
 +
        if (document.body.scrollTop > height || document.documentElement.scrollTop > height) {
 +
            $("#inPageNav").fadeIn(200);
 +
        } else {
 +
            $("#inPageNav").fadeOut(200);
 +
        }
 +
    }
 
</script>
 
</script>
  
 
</html>
 
</html>

Latest revision as of 02:23, 2 November 2017

  1. Transformations
  2. Plasmid Isolation
  3. PCRs
  4. Restriction digests
  5. Ligations
  6. Screening

BioBrick Transformations

The five BioBricks we are using were transformed into E. coli strain DH5α — chosen for its recA and endA mutations that allow for high-yield minipreps.

Transformations for T7 expression system


Figure 1: BBa_K525998 and BBa_K731721

Transformations for sfGFP-SpyCatcher


Figure 2: BBa_K1650037 and BBa_K1321337

Transformations for mCherry


Figure 3 : BBa_J18932

Plasmid Isolation

Minipreps were performed using three colonies on each transformation plate to confirm the presence of the plasmid. One positive transformant for each BioBrick was used to make a glycerol stock.

PCRs

Our assembly begins with our PCRs: using carefully-designed primers with 5'-overhangs, we add restriction sites, linkers and other features to our parts of interest. Since most of our PCRs have such overhangs, our annealing temperature changes after the first few cycles — our PCR cycle parameters account for this variation. In addition, we used NEB's Q5 MasterMix and NEB's Phusion polymerase, both high-fidelity DNA polymerases which have a higher annealing temperature than usual.

PCRs for the T7 expression backbone

PCR 1 — T7 Expression Backbone (Piece 1)
Template BBa_K525998 (T7 promoter+RBS)
Forward primer gactaccacggcatgatgaacctgaatcgc
Amplifies the CmR gene, includes NcoI site
Reverse primer gaattcAAGCTTtttctcctctttccctatagtgagtcg
Adds HindIII site downstream
Amplicon size 886 bp
PCR1 product
PCR 2 — T7 Expression Backbone (Piece 2)
Template BBa_K731721 (T7 terminator)
Forward primer gtatcacgaggcagaatttcag
Keeps the NheI site
Reverse primer gagaatatgtttttcgtctcagcc
Splits the CmR gene, includes NcoI site
Amplicon size 1533 bp
PCR2 product

PCRs for sfGFP-SpyCatcher

PCR 3 — sfGFP
Template BBa_K1321337 (sfGFP in Freiburg format)
Forward primer gaattcAAGCTTatgACCGGTcgtaaaggcgaagagctgttc
Adds BBa_K2319001 (HindIII+ATG+AgeI scar) upstream
Reverse primer gGAATTCggatccTGACCCTCCtttgtacagttcatccataccatg
Adds Gly-Gly-Ser and BamHI site downstream
Amplicon size 753 bp
PCR3 product
PCR 4 — SpyCatcher
Template BBa_K1650037 (SpyCatcher)
Forward primer GAATTAggatccGGGAGTAGCtcttattatcatcatcaccatcacc
Adds BamHI and Gly-Ser-Ser upstream
Reverse primer gacgtcGCTAGCTTAaatatgagcatcgcccttgg
Adds stop codon (TAA) and NheI site downstream
Amplicon size 450 bp
PCR4 product

PCRs for 6xHis-mCherry

PCR 5 — mCherry
Template BBa_J18932 (mCherry RFP)
Forward primer CACCATCATCACCATGTGAGCAAAGGCGAGGAAG
Adds 5xHis upstream
Reverse primer cgtatgGCTAGCTTATTTATACAGTTCATCCATGCCG
Adds stop codon (TAA) and NheI site downstream
Amplicon size 735 bp
PCR5 product
PCR 6 — mCherry
Template Product of PCR5
Forward primer aattcgAAGCTTATGCACCACCATCATCACCATGTGAG
Adds HindIII, a start codon (ATG) and His upstream
Reverse primer cgtatgGCTAGCTTATTTATACAG
Keeps stop codon (TAA) and NheI site downstream
Amplicon size 753 bp
PCR6 product

PCRs for mCherry-SpyTag

PCR 7 — mCherry-SpyTag
Template BBa_J18932 (mCherry RFP)
Forward primer CACCATCATCACCATGTGAGCAAAGGCGAGGAAG
Adds 5xHis upstream
Reverse primer accgatGGATCCtttatacagttcatccatgccg
Adds BamHI site downstream
Amplicon size 732 bp
PCR7 product

Restriction Digests

Restriction digests for T7 expression backbone

Double-digest PCR1 product with NcoI and HindIII (D1)
Double-digest PCR2 product with NheI and NcoI (D2)

Restriction digests for sfGFP-SpyCatcher

Double-digest PCR3 product with HindIII and BamHI (D3)
Double-digest PCR4 product with BamHI and NheI (D4)

Restriction digest for 6xHis-mCherry

Double-digest PCR6 product with HindIII and NheI (D6)

Restriction digests for mCherry-SpyTag

Double-digest Oligo 1 with HindIII and NdeI (DO1)
Double-digest PCR7 product with NdeI and BamHI (D7)
Double-digest Oligo 2 with BamHI and NheI (DO2)

Gel-purification of our digested products


Figure 4: Digested PCR products (D1, D2, D3, D4, D6, DO1, DO2)
Restriction enzymes used in our assembly
Restriction Enzyme Sequence Activity in NEBuffers (%) Incubation temperature Heat inactivation
1.1 2.1 3.1 CutSmart
AgeI A\CCGGT 100 75 25 75 37°C 65°C
AgeI-HF A\CCGGT 100 50 10 100 37°C 65°C
BamHI G\GATCC 75* 100* 100 100* 37°C —
BamHI-HF G\GATCC 100 50 10 100 37°C —
HindIII A\AGCTT 25 100 50 50 37°C 80°C
HindIII-HF A\AGCTT 10 100 10 100 37°C 80°C
HindIII A\AGCTT 25 100 50 50 37°C 80°C
HindIII-HF A\AGCTT 10 100 10 100 37°C 80°C
NcoI C\CATGG 100 100 100 100 37°C 80°C
NcoI-HF C\CATGG 50 100 10 100 37°C 80°C
NdeI CA\TATG 75 100 100 100 37°C 65°C
NheI G\CTAGC 100 100 10 100 37°C 65°C
NheI-HF G\CTAGC 100 25 10 100 37°C 80°C
* denotes star activity

Multi-Ligation

Ligating sfGFP-SpyCatcher


Plasmid map of BBa_K2319000 (sfGFP-SpyCatcher)

Ligating 6xHis-mCherry

Plasmid map of BBa_K2319009 (6xHis-mCherry)

Screening Transformants

We screened 30 transformants from each plate using colony PCR with primers VF2 and VR, which we standardized using Taq polymerase (annealing temperature of 56°C).


Figure 6 : Colony PCR of sfGFP-SpyCatcher colonies (B1-B21) and 6xHis-mCherry colonies (D1-D21)

We obtained the expected band (~1.5 kb) for one of the thirty sfGFP-SpyCatcher colonies tested while none of the thirty 6xHis-mCherry colonies tested gave the expected band (> 1.1 kb). After plasmid isolation from this positive clone, we transformed BL21 (DE3) to continue with our protein experiments.

Other parts

Due to the failure of our assemblies for the other BioBricks, we were not able to submit these parts on time, but we have submitted the designs for future teams to use.