Difference between revisions of "Team:British Columbia/Notebook"

 
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   <!-- page content -->
 
   <!-- page content -->
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   <div id="in-content" class="container">
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    <div class="container">
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    <div>
 
       <div>
 
       <div>
 
         <img src="https://static.igem.org/mediawiki/2018/a/a5/T--British_Columbia--NB-Hdg.png"  style="height:70px; margin-top:30px;margin-left:50px;">
 
         <img src="https://static.igem.org/mediawiki/2018/a/a5/T--British_Columbia--NB-Hdg.png"  style="height:70px; margin-top:30px;margin-left:50px;">
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         <div class="col-sm-1"></div>
 
         <div class="col-sm-1"></div>
 
         <div class="col-sm-10">
 
         <div class="col-sm-10">
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           <ul class="nav nav-tabs nav-justified">
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           <ul id="notebook-nav" class="nav nav-tabs nav-justified">
−
             <li class="active"><a href="#naringenin">Naringenin Notebook</a></li>
+
             <li class="active nav-item"><a href="#naringenin">Naringenin Notebook</a></li>
−
             <li><a href="#biosensor">Biosensor Notebook</a></li>
+
             <li class="nav-item"><a href="#biosensor">Biosensor Notebook</a></li>
−
             <li><a href="#kaempferol">Kaempferol Notebook</a></li>
+
             <li class="nav-item"><a href="#kaempferol">Kaempferol Notebook</a></li>
 
           </ul>
 
           </ul>
 
         </div>
 
         </div>
 
       </div>
 
       </div>
  
−
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+
       <div class="tab-content left-buffer right-buffer">
 
         <div id="naringenin" class="tab-pane fade in active">
 
         <div id="naringenin" class="tab-pane fade in active">
−
           <h3>Naringenin Notebook</h3>
+
           <h3 style="margin-left:50px;">Naringenin Notebook</h3>
 
           <!-- NARINGENIN NOTEBOOK CONTENT GOES HERE -->
 
           <!-- NARINGENIN NOTEBOOK CONTENT GOES HERE -->
 +
<p>
 +
We kindly received the following from UBC iGEM distribution kit of 2018:
 +
<br>
 +
 +
Constitutive promoter + RBS
 +
BBa_K880005
 +
~70 BP
 +
Spring 2018 Distribution
 +
Plate 2, Well 3F
 +
pSB1C3 (Cm)
 +
       
 +
<br>
 +
 
 +
 +
BBa_K880005
 +
~70 BP
 +
Spring 2018 Distribution
 +
Plate 2, Well 3F
 +
pSB1C3 (Cm)
 +
 +
<br>
 +
 +
 +
4CL
 +
BBa_K801093
 +
~1700 BP
 +
Spring 2018 Distribution
 +
Plate 2, Well 17D
 +
pSB1C3 (Cm)
 +
 +
<br>
 +
 +
 +
RBS+TAL
 +
BBa_K1033000
 +
~1600
 +
Spring 2018 Distribution
 +
Plate 4, Well 6C
 +
pSB1C3 (Cm)
 +
</p>
 +
 +
<br>
 +
<p>First, TAL and 4CL with RBS (ribosomal binding site) to combine them:</p>
 +
<ul>
 +
<li>4CL digest with EcoRI + SpeI </li>
 +
<li>TAL digest with EcoRI + Xbal</li>
 +
<li>Ligation of both digestion with T4 ligase </li>
 +
<li> E. coli transformation via heat shock method</li>
 +
<li>Spread on CMB-LB agar plate and incubate at 37 C° overnight </li>
 +
<li>PCR and gel electrophoresis to analyze if successful </li>
 +
<li> Take positive colonies and place in LB with CMP incubate for 16 hours at 37*C </li>
 +
<li> Plasmid obtained</li>
 +
</ul>
 +
 +
<br>
 +
<p>Second, we will take bio bricks of CHS + CHI with RBS (ribosomal binding site): </p>
 +
<ul>
 +
<li>CHS digest with EcoRI and SpeI </li>
 +
<li> CHI digest with EcoRI and Xbal </li>
 +
<li> Ligation of both digestion with T4 ligase </li>
 +
<li> E. coli transformation via heat shock method </li>
 +
<li> Spread on CMB-LB agar plate at 37c° overnight </li>
 +
<li> PCR and gel electrophoresis to analyze if successful </li>
 +
<li> Take positive colonies and place in LB with CMP incubate for 16 hours at 37 C°</li>
 +
<li> Plasmid obtained</li>
 +
</ul>
 +
 +
<br>
 +
<p>Third, combine the two plasmids previously prepared:</p>
 +
<ul>
 +
<li> 4CL – TAL digest by EcoRI and SpeI</li>
 +
<li>CHS-CHI with EcoRI and Xbal </li>
 +
<li> Dephosphorylate CHS-CHI </li>
 +
<li> Ligate the two together with T4 ligation </li>
 +
<li> Add GFP via digestion and then ligation* </li>
 +
<li> E. coli transformation via heat shock method </li>
 +
<li> PCR and gel electrophoresis to analyze if successful </li>
 +
<li> Take positive colonies and place in LB and CMP incubate for 16 hours at 37 C°</li>
 +
</ul>
 +
 +
 +
<p>Protocol for cloning promoter-RBS-4CL in pSB1C3<p>
 +
A.      Restriction enzyme digest
 +
1.      Prepare the master mix in a microfuge tube by combining the following:
 +
Component
 +
Volume to add (ul)
 +
10X NEB Buffer 2.1
 +
6
 +
NEB PstI restriction enzyme
 +
4
 +
Autoclaved distilled water
 +
26
 +
TOTAL
 +
36
 +
 +
2.      Zip-spin the master mix to collect all liquid at the bottom of the tube
 +
3.      With a pipette set to 25 ul, pipette each reaction up and down several times to mix
 +
4.      Vortex the master mix thoroughly
 +
5.      Zip-spin the master mix again
 +
6.      Aliquot the master mix into 3 aliquots of 14 ul (discard the remaining master mix)
 +
7.      Label the three tubes containing the aliquots as follows:
 +
a.      P-RBS
 +
b.      4CL
 +
c.      PDC (positive digest control)
 +
 +
 +
 +
 
         </div>
 
         </div>
 
         <div id="biosensor" class="tab-pane fade">
 
         <div id="biosensor" class="tab-pane fade">
−
           <h3>Biosensor Notebook</h3>
+
           <h3 style="margin-left:50px;">Biosensor Notebook</h3>
 
           <!-- BIOSENSOR NOTEBOOK CONTENT GOES HERE -->
 
           <!-- BIOSENSOR NOTEBOOK CONTENT GOES HERE -->
 +
<h3 style="margin-left:70px;">July</h3>
 +
  <ul>
 +
    <li>26:
 +
      <ul>
 +
        <li>Transformed RFP + RBS into DH5a</li>
 +
        <li>Transformed GFP + RBS into DH5a</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>27:
 +
      <ul>
 +
        <li>Inoculated RFP + RBS in 25mg/uL of CM-25</li>
 +
        <li>Inoculated GFP + RBS in 25mg/uL of CM-25</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>28:
 +
      <ul>
 +
        <li>Miniprepped RFP + RBS</li>
 +
        <li>Miniprepped GFP + RBS</li>
 +
        <li>Digested RFP + RBS  with ECOR1 and XBA1 to obtain 8.96uL of DNA at 111.16ng/uL</li>
 +
        <li>Digested GFP + RBS with ECOR1 and XBA1 to obtain 12.8uL of DNA at 78.1ng/uL</li>
 +
        <li>Eventually discarded both digests as we did not use them</li>
 +
      </ul>
 +
    </li>
 +
  </ul>
 +
  <hr>
 +
  <h3 style="margin-left:70px;">August</h3>
 +
  <ul>
 +
    <li>7:
 +
      <ul>
 +
        <li>Transformed Bba_E0020 into DH5a</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>8:
 +
      <ul>
 +
        <li>Inoculated CFP strains with  25mg/uL of CM-25</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>9:
 +
      <ul>
 +
        <li>Digested CFP with ECOR1 + XBA1 to obtain 8.77uL of DNA at 114.0ng/uL</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>15:
 +
      <ul>
 +
        <li>Transformed RFP into DH5a</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>16:
 +
      <ul>
 +
        <li>Inoculated RFP in 25mg/uL of CM-25</li>
 +
        <li>Miniprepped and digested RFP with ECOR1 + XBA1 to obtain 9.14uL of DNA at 109.4ng/uL</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>18:
 +
      <ul>
 +
        <li>Transformed Bba_E0040 (GFP) into DH5a</li>
 +
        <li>Transformed Bba_l15016 (CFP + RBS) into DH5a</li>
 +
        <li>Synthesized parts from IDT were resuspended in 1X TBE</li>
 +
        <ul>
 +
          <li>FdeR</li>
 +
          <li>Pt181-repressor</li>
 +
          <li>Pt181-GP2</li>
 +
          <li>GP2</li>
 +
          <li>Antisense</li>
 +
        </ul>
 +
        <li>RFP, RFP+RBS, CFP, GFP+RBS have all been digested</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>19:
 +
      <ul>
 +
        <li>Transformed Bba_E0040 (GFP) into DH5a</li>
 +
        <li>Transfroemd CFP + RBS  into DH5a</li>
 +
        <li>Both transformations were unsuccessful</li>
 +
      </ul>
 +
    </li>
 +
 +
 +
    <li>20
 +
      <ul>
 +
        <li>OD of DH5a competent cells was 0.69</li>
 +
        <li>Pelleted competent cells using 0.1M CaCl2</li>
 +
        <li>Transformed Bba_E0040 (GFP) into DH5a</li>
 +
        <li>Transformed Bba_I5016 (CFP + RBS) into DH5a</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>21:
 +
      <ul>
 +
        <li>OD of DH5a competent cells was 0.53</li>
 +
        <li>Pelleted competent cells using 0.1M CaCl2</li>
 +
        <li>Positive and Negative controls did not function properly</li>
 +
        <li>Realized glycerol was not added</li>
 +
        <li>Re-setup experiment</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>23:
 +
      <ul>
 +
        <li>Reaction cleanup using ABM kit, involving:</li>
 +
        <ul>
 +
          <li>GP2</li>
 +
          <li>E+S</li>
 +
          <li>Pt181-GP2</li>
 +
          <li>FdeR</li>
 +
        </ul>
 +
        <li>Transformed Bba_E0040 (GFP) into DH5a</li>
 +
        <li>Transformed Bba_I15016 (CFP + RBS) into DH5a</li>
 +
        <li>Both transformations were unsuccessful</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>24
 +
      <ul>
 +
        <li>Ran plasmid PSB1C3 digested with X+P, with 1X TAE buffer</li>
 +
        <li>Ran plasmid PSB1C3 digested with E+S, with 1X TAE buffer</li>
 +
        <li>Ran plasmid PSB1C3 digested with E+P, with 1X TAE buffer</li>
 +
        <li>Purified with ABM kit:</li>
 +
        <ul>
 +
          <li>X+P</li>
 +
          <li>E+P</li>
 +
          <li>E+S</li>
 +
          <li>CFP</li>
 +
          <li>GFP+RBS</li>
 +
          <li>RFP+RBS</li>
 +
          <li>RFP</li>
 +
        </ul>
 +
        <li>Inoculated CFP and GFP in 25mg/uL of CM-25</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>25:
 +
      <ul>
 +
        <li>Miniprepped CFP+RBS and GFP (concentration 149ng/uL)</li>
 +
      </ul>
 +
      <li>27:
 +
        <ul>
 +
          <li>Ligated FdeR and Repressor DNA into RFP vector</li>
 +
          <li>Ligated FdER and Repressor DNA into E+S vector</li>
 +
          <li>Ligated pt181-GP2 and GP2 DNA into E+P</li>
 +
          <li>Ligated antisense DNA into X+P</li>
 +
        </ul>
 +
      </li>
 +
 +
      <li>29:
 +
        <ul>
 +
          <li>Transformed in DH5a:
 +
            RFP - FdeR, RFP - Repressor, E+S - FdeR, E+S - Repressor, CFP - Repressor, CFP - FdeR, E+P - Pt181-GP2, E+P - GP2, X+P - Antisense
 +
          </li>
 +
        </ul>
 +
      </li>
 +
 +
      <li>30:
 +
        <ul>
 +
          <li>Inoculated in 25mg/uL of CM25:
 +
            RFP - FdeR, RFP - Repressor, E+S - FdeR, E+S - Repressor, CFP - Repressor, CFP - FdeR, E+P - Pt181-GP2, E+P - GP2, X+P - Antisense
 +
          </li>
 +
        </ul>
 +
      </li>
 +
 +
      <li>31:
 +
        <ul>
 +
          <li>Miniprepped:
 +
            RFP - FdeR, RFP - Repressor, E+S - FdeR, E+S - Repressor, CFP - Repressor, CFP - FdeR, E+P - Pt181-GP2, E+P - GP2, X+P - Antisense
 +
          </li>
 +
        </ul>
 +
      </li>
 +
 +
    </ul>
 +
 +
    <hr>
 +
 +
    <h3 style="margin-left:70px;">September</h3>
 +
    <li>4:
 +
      <ul>
 +
        <li>Digested:
 +
          RFP - FdeR, RFP - Repressor, E+S - FdeR, E+S - Repressor, CFP - Repressor, CFP - FdeR, E+P - Pt181-GP2, E+P - GP2, X+P - Antisense
 +
        </li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>5:
 +
      <ul>
 +
        <li>Ran Gel Electrophoresis In 1X TBE buffer on:
 +
          RFP - FdeR, RFP - Repressor, E+S - FdeR, E+S - Repressor, CFP - Repressor, CFP - FdeR, E+P - Pt181-GP2, E+P - GP2, X+P - Antisense
 +
        </li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>7:
 +
      <ul>
 +
        <li>Double checked digestions with BamH1 + ECOR1  + Pst1 of strains:
 +
          RFP - FdeR, E+S-FdeR
 +
        </li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>13:
 +
      <ul>
 +
        <li>Transformed RFP - FdeR2 into DHd5a</li>
 +
        <li>Digested GFP Vector using: E+P, E+X, E+S</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>20:
 +
      <ul>
 +
        <li>Ran Gel Electrophoresis on: GFP Vector + (E+P, E+X, E+S)</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>22:
 +
      <ul>
 +
        <li>Purified: GFP - E+P, GFP - E+S</li>
 +
        <li>Digested Repressor (from IDT) using E+S</li>
 +
        <li>Ligated repressor with E+S vector, pt181 GP2 and GP2 with E+P digested vector. Antisense ligated with X+P vector</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>23:
 +
      <ul>
 +
        <li>Inoculated: E+S - Rep Lig 1, E+P - pt181GP2 Lig, E+P - GP2 Lig, Antisense - X+P Lig</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>24:
 +
      <ul>
 +
        <li>Miniprepped: E+S - Rep Lig 1, E+P - pt181GP2 Lig, E+P - GP2 Lig, Antisense - X+P Lig</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>24:
 +
      <ul>
 +
        <li>Digested with E+P: E+S - Rep Lig 1, E+P - pt181GP2 Lig, E+P - GP2 Lig, Antisense - X+P Lig</li>
 +
      </ul>
 +
    </li>
 +
 +
    <li>25:
 +
      <ul>
 +
        <li>Performed Gel Electrophoresis of DNA strains: E+S - Rep Lig 1, E+P - pt181GP2 Lig, E+P - GP2 Lig, Antisense - X+P Lig</li>
 +
      </ul>
 +
    </li>
 +
    <hr>
 
         </div>
 
         </div>
 +
 
         <div id="kaempferol" class="tab-pane fade">
 
         <div id="kaempferol" class="tab-pane fade">
−
           <h3>Kaempferol Notebook</h3>
+
           <h3 style="margin-left:50px;">Kaempferol Notebook</h3>
−
          <!-- KAEMPFEROL NOTEBOOK CONTENT GOES HERE -->
+
       
 +
<p>
 +
<b> We kindly received the following from UBC iGEM distribution kit of 2018: </b>
 +
<br>
 +
 
 +
Constitutive promoter + RBS
 +
BBa_K880005
 +
~70 BP
 +
Spring 2018 Distribution
 +
Plate 2, Well 3F
 +
pSB1C3 (Cm)
 +
       
 +
<br>
 +
 
 +
 
 +
F3H
 +
BBa_K1497009
 +
~1107 BP
 +
Spring 2018 Distribution
 +
Plate 2, Well 12I
 +
pSB1C3 (Cm)
 +
 
 +
<br>
 +
 
 +
 
 +
RBS
 +
BBa_B0034
 +
~12 BP
 +
Spring 2018 Distribution
 +
Plate 4, Well 1N
 +
pSB1C3 (Cm)
 +
 
 +
<br>
 +
 
 +
Double Terminator
 +
BBa_B0015
 +
~129 BP
 +
Spring 2018 Distribution
 +
Plate 3, Well 3F
 +
pSB1C3 (Cm)
 +
</p>
 +
<br>
 +
<p>
 +
<b> Parts we've synthesized ourselves: </b>
 +
 
 +
 
 +
 
 +
<br>
 +
 
 +
FLS1
 +
BBa_K2700000
 +
~1011 BP
 +
pSB1C3 (Cm)
 +
</p>
 +
 
 +
<h3 style="margin-left:70px;">July</h3>
 +
  <ul>
 +
    <li>25:
 +
      <ul>
 +
        <li>Transformed F3H into DH5a</li>
 +
        <li>Transformed K880005 into DH5a</li>
 +
        <li>Transformed B0034 into DH5a</li>
 +
        <li>Transformed B0015 into DH5a</li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>26:
 +
      <ul>
 +
        <li>Inoculated F3H in 25mg/uL of CM-25</li>
 +
        <li>Inoculated K880005 in 25mg/uL of CM-25</li>
 +
        <li>Inoculated B0034 in 25mg/uL of CM-25</li>
 +
        <li>Inoculated B0015 in 25mg/uL of CM-25</li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>27:
 +
      <ul>
 +
        <li>Miniprepped F3H</li>
 +
        <li>Miniprepped K880005</li>
 +
        <li>Miniprepped B0034</li>
 +
        <li>Miniprepped B0015</li>
 +
      </ul>
 +
    </li>
 +
  </ul>
 +
 
 +
<li>28:
 +
      <ul>
 +
        <li>Digested F3H with XbaI and SpeI</li>
 +
        <li>Digested K880005 with SpeI and Pst1</li>
 +
        <li>Digested B0034 with EcoR1 and Xba1</li>
 +
        <li>Digested B0015 with EcoR1 and Xba1</li>
 +
      </ul>
 +
    </li>
 +
  </ul>
 +
 
 +
  <hr>
 +
  <h3 style="margin-left:70px;">August</h3>
 +
  <ul>
 +
    <li>2:
 +
      <ul>
 +
        <li>Ran gel and purified all samples
 +
        <li>Ligate F3H (insert, 5uL) and K880005 (vector, 2uL) with T4 ligase </li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>7:
 +
      <ul>
 +
        <li> transformed F3H and K880005</li>
 +
        <li> Digested RFP in pSB1C3; ran gel and purified </li>
 +
        <li> Digested synthesized FLS1 with Ecor1 and Pst1 </li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>10:
 +
      <ul>
 +
        <li> inoculated F3H and K880005 </li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>15:
 +
      <ul>
 +
      <li> Miniprepped F3H + K880005</li>
 +
      <li> Gel ran and get purified for RFP/pSB1C3, F3H + K880005, B0034, B0015</li>
 +
      <li> gel ran and PCR purified for FLS1</li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>16:
 +
      <ul>
 +
        <li> Redigested F3H with XbaI and SpeI (gel failed on the 15th, needed to redo cloning) </li>
 +
        <li> Redigested K880005 with SpeI and Pst1</li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>17:
 +
      <ul>
 +
        <li> Ligated RFP/pSB1C3 (vector, 2uL) with FLS1 (insert, 4uL) </li>
 +
        <li> Ligated FLS1 (vector, 2uL) with B0015 (insert, 4uL) </li>
 +
        <li> purified and religated F3H+K880005
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>19:
 +
      <ul>
 +
        <li>Transformed FLS1 + pSB1C3 into DH5a</li>
 +
        <li>Transformed FLS1 + B0015 into DH5a</li>
 +
        <li>Transformed F3H + K880005 into DH5a</li>
 +
      </ul>
 +
    </li>
 +
 
 +
 
 +
    <li>20
 +
      <ul>
 +
        <li> Inoculate all samples </li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>21:
 +
      <ul>
 +
        <li> Miniprep all samples </li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>24
 +
      <ul>
 +
        <li>Ran diagnostic gel for all samples, F3H + K880005 failed again, everything else fine </li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>25:
 +
      <ul>
 +
        <li> Took originally miniprepped F3H and digested with XbaI and SpeI </li>
 +
      </ul>
 +
 
 +
      <li>27:
 +
        <ul>
 +
          <li> Gel purified F3H </li>
 +
          <li> ligated with previously digested B0034 </li>
 +
        </ul>
 +
      </li>
 +
 
 +
     
 +
    <hr>
 +
 
 +
    <h3 style="margin-left:70px;">September</h3>
 +
    <li>5:
 +
      <ul>
 +
        <li> Transformed F3H + B0034</li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>5:
 +
      <ul>
 +
        <li> Inoculated F3H + B0034 </li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>7:
 +
      <ul>
 +
        <li> Miniprepped F3H + B0034 </li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>10:
 +
      <ul>
 +
        <li> Ran F3H + B0034 on gel and gel purified (cloning successful!)
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>15:
 +
      <ul>
 +
        <li> Used glycerol stock K880005 and streaked on LB+Cm plate</li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>16:
 +
      <ul>
 +
        <li> Inoculated K880005</li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>17:
 +
      <ul>
 +
        <li>Miniprepped K880005</li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>19:
 +
      <ul>
 +
        <li>Digested K880005 with Spe1 + Pst1</li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>20:
 +
      <ul>
 +
        <li>Ran K880005 in gel and gel purified</li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>23:
 +
      <ul>
 +
        <li> Digested FLS1 + B0015 with Pst1 + Spe1 </li>
 +
        <li> Digested F3H + B0034 with Xba1 + Pst1 </li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>24:
 +
      <ul>
 +
        <li> Gel eletrophoresis and gel purified FLS1 + B0015 </li>
 +
        <li> Gel eletrophoresis and gel purified F3H + B0034 </li>
 +
      </ul>
 +
    </li>
 +
 
 +
    <li>29:
 +
      <ul>
 +
        <li> Ligation of F3H + B0034 (insert, 6uL) and K880005 (vector, 2uL)</li>
 +
      </ul>
 +
    </li>
 +
    <hr>
 +
 
 +
 
 +
    <h3 style="margin-left:70px;">October</h3>
 +
 
 +
  <li>1:
 +
      <ul>
 +
        <li> Transformation of k880005 + F3H + B0034</li>
 +
      </ul>
 +
    </li>
 +
 
 +
  <li>2:
 +
      <ul>
 +
        <li> Inoculation of k880005 + F3H + B0034</li>
 +
      </ul>
 +
    </li>
 +
   
 +
  <li>3:
 +
      <ul>
 +
        <li> Miniprep of k880005 + F3H + B0034</li>
 +
      </ul>
 +
    </li>
 +
 
 +
  <li>4:
 +
      <ul>
 +
        <li> Digest of k880005 + F3H + B0034</li>
 +
      </ul>
 +
    </li>
 +
 
 
         </div>
 
         </div>
  
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Latest revision as of 03:46, 18 October 2018

Naringenin Notebook

We kindly received the following from UBC iGEM distribution kit of 2018:
Constitutive promoter + RBS BBa_K880005 ~70 BP Spring 2018 Distribution Plate 2, Well 3F pSB1C3 (Cm)
BBa_K880005 ~70 BP Spring 2018 Distribution Plate 2, Well 3F pSB1C3 (Cm)
4CL BBa_K801093 ~1700 BP Spring 2018 Distribution Plate 2, Well 17D pSB1C3 (Cm)
RBS+TAL BBa_K1033000 ~1600 Spring 2018 Distribution Plate 4, Well 6C pSB1C3 (Cm)


First, TAL and 4CL with RBS (ribosomal binding site) to combine them:

  • 4CL digest with EcoRI + SpeI
  • TAL digest with EcoRI + Xbal
  • Ligation of both digestion with T4 ligase
  • E. coli transformation via heat shock method
  • Spread on CMB-LB agar plate and incubate at 37 C° overnight
  • PCR and gel electrophoresis to analyze if successful
  • Take positive colonies and place in LB with CMP incubate for 16 hours at 37*C
  • Plasmid obtained

Second, we will take bio bricks of CHS + CHI with RBS (ribosomal binding site):

  • CHS digest with EcoRI and SpeI
  • CHI digest with EcoRI and Xbal
  • Ligation of both digestion with T4 ligase
  • E. coli transformation via heat shock method
  • Spread on CMB-LB agar plate at 37c° overnight
  • PCR and gel electrophoresis to analyze if successful
  • Take positive colonies and place in LB with CMP incubate for 16 hours at 37 C°
  • Plasmid obtained

Third, combine the two plasmids previously prepared:

  • 4CL – TAL digest by EcoRI and SpeI
  • CHS-CHI with EcoRI and Xbal
  • Dephosphorylate CHS-CHI
  • Ligate the two together with T4 ligation
  • Add GFP via digestion and then ligation*
  • E. coli transformation via heat shock method
  • PCR and gel electrophoresis to analyze if successful
  • Take positive colonies and place in LB and CMP incubate for 16 hours at 37 C°

Protocol for cloning promoter-RBS-4CL in pSB1C3

A. Restriction enzyme digest 1. Prepare the master mix in a microfuge tube by combining the following: Component Volume to add (ul) 10X NEB Buffer 2.1 6 NEB PstI restriction enzyme 4 Autoclaved distilled water 26 TOTAL 36 2. Zip-spin the master mix to collect all liquid at the bottom of the tube 3. With a pipette set to 25 ul, pipette each reaction up and down several times to mix 4. Vortex the master mix thoroughly 5. Zip-spin the master mix again 6. Aliquot the master mix into 3 aliquots of 14 ul (discard the remaining master mix) 7. Label the three tubes containing the aliquots as follows: a. P-RBS b. 4CL c. PDC (positive digest control)

Biosensor Notebook

July

  • 26:
    • Transformed RFP + RBS into DH5a
    • Transformed GFP + RBS into DH5a
  • 27:
    • Inoculated RFP + RBS in 25mg/uL of CM-25
    • Inoculated GFP + RBS in 25mg/uL of CM-25
  • 28:
    • Miniprepped RFP + RBS
    • Miniprepped GFP + RBS
    • Digested RFP + RBS with ECOR1 and XBA1 to obtain 8.96uL of DNA at 111.16ng/uL
    • Digested GFP + RBS with ECOR1 and XBA1 to obtain 12.8uL of DNA at 78.1ng/uL
    • Eventually discarded both digests as we did not use them

August

  • 7:
    • Transformed Bba_E0020 into DH5a
  • 8:
    • Inoculated CFP strains with 25mg/uL of CM-25
  • 9:
    • Digested CFP with ECOR1 + XBA1 to obtain 8.77uL of DNA at 114.0ng/uL
  • 15:
    • Transformed RFP into DH5a
  • 16:
    • Inoculated RFP in 25mg/uL of CM-25
    • Miniprepped and digested RFP with ECOR1 + XBA1 to obtain 9.14uL of DNA at 109.4ng/uL
  • 18:
    • Transformed Bba_E0040 (GFP) into DH5a
    • Transformed Bba_l15016 (CFP + RBS) into DH5a
    • Synthesized parts from IDT were resuspended in 1X TBE
      • FdeR
      • Pt181-repressor
      • Pt181-GP2
      • GP2
      • Antisense
    • RFP, RFP+RBS, CFP, GFP+RBS have all been digested
  • 19:
    • Transformed Bba_E0040 (GFP) into DH5a
    • Transfroemd CFP + RBS into DH5a
    • Both transformations were unsuccessful
  • 20
    • OD of DH5a competent cells was 0.69
    • Pelleted competent cells using 0.1M CaCl2
    • Transformed Bba_E0040 (GFP) into DH5a
    • Transformed Bba_I5016 (CFP + RBS) into DH5a
  • 21:
    • OD of DH5a competent cells was 0.53
    • Pelleted competent cells using 0.1M CaCl2
    • Positive and Negative controls did not function properly
    • Realized glycerol was not added
    • Re-setup experiment
  • 23:
    • Reaction cleanup using ABM kit, involving:
      • GP2
      • E+S
      • Pt181-GP2
      • FdeR
    • Transformed Bba_E0040 (GFP) into DH5a
    • Transformed Bba_I15016 (CFP + RBS) into DH5a
    • Both transformations were unsuccessful
  • 24
    • Ran plasmid PSB1C3 digested with X+P, with 1X TAE buffer
    • Ran plasmid PSB1C3 digested with E+S, with 1X TAE buffer
    • Ran plasmid PSB1C3 digested with E+P, with 1X TAE buffer
    • Purified with ABM kit:
      • X+P
      • E+P
      • E+S
      • CFP
      • GFP+RBS
      • RFP+RBS
      • RFP
    • Inoculated CFP and GFP in 25mg/uL of CM-25
  • 25:
    • Miniprepped CFP+RBS and GFP (concentration 149ng/uL)
  • 27:
    • Ligated FdeR and Repressor DNA into RFP vector
    • Ligated FdER and Repressor DNA into E+S vector
    • Ligated pt181-GP2 and GP2 DNA into E+P
    • Ligated antisense DNA into X+P
  • 29:
    • Transformed in DH5a: RFP - FdeR, RFP - Repressor, E+S - FdeR, E+S - Repressor, CFP - Repressor, CFP - FdeR, E+P - Pt181-GP2, E+P - GP2, X+P - Antisense
  • 30:
    • Inoculated in 25mg/uL of CM25: RFP - FdeR, RFP - Repressor, E+S - FdeR, E+S - Repressor, CFP - Repressor, CFP - FdeR, E+P - Pt181-GP2, E+P - GP2, X+P - Antisense
  • 31:
    • Miniprepped: RFP - FdeR, RFP - Repressor, E+S - FdeR, E+S - Repressor, CFP - Repressor, CFP - FdeR, E+P - Pt181-GP2, E+P - GP2, X+P - Antisense

September

  • 4:
    • Digested: RFP - FdeR, RFP - Repressor, E+S - FdeR, E+S - Repressor, CFP - Repressor, CFP - FdeR, E+P - Pt181-GP2, E+P - GP2, X+P - Antisense
  • 5:
    • Ran Gel Electrophoresis In 1X TBE buffer on: RFP - FdeR, RFP - Repressor, E+S - FdeR, E+S - Repressor, CFP - Repressor, CFP - FdeR, E+P - Pt181-GP2, E+P - GP2, X+P - Antisense
  • 7:
    • Double checked digestions with BamH1 + ECOR1 + Pst1 of strains: RFP - FdeR, E+S-FdeR
  • 13:
    • Transformed RFP - FdeR2 into DHd5a
    • Digested GFP Vector using: E+P, E+X, E+S
  • 20:
    • Ran Gel Electrophoresis on: GFP Vector + (E+P, E+X, E+S)
  • 22:
    • Purified: GFP - E+P, GFP - E+S
    • Digested Repressor (from IDT) using E+S
    • Ligated repressor with E+S vector, pt181 GP2 and GP2 with E+P digested vector. Antisense ligated with X+P vector
  • 23:
    • Inoculated: E+S - Rep Lig 1, E+P - pt181GP2 Lig, E+P - GP2 Lig, Antisense - X+P Lig
  • 24:
    • Miniprepped: E+S - Rep Lig 1, E+P - pt181GP2 Lig, E+P - GP2 Lig, Antisense - X+P Lig
  • 24:
    • Digested with E+P: E+S - Rep Lig 1, E+P - pt181GP2 Lig, E+P - GP2 Lig, Antisense - X+P Lig
  • 25:
    • Performed Gel Electrophoresis of DNA strains: E+S - Rep Lig 1, E+P - pt181GP2 Lig, E+P - GP2 Lig, Antisense - X+P Lig

    • Kaempferol Notebook

    We kindly received the following from UBC iGEM distribution kit of 2018:
    Constitutive promoter + RBS BBa_K880005 ~70 BP Spring 2018 Distribution Plate 2, Well 3F pSB1C3 (Cm)
    F3H BBa_K1497009 ~1107 BP Spring 2018 Distribution Plate 2, Well 12I pSB1C3 (Cm)
    RBS BBa_B0034 ~12 BP Spring 2018 Distribution Plate 4, Well 1N pSB1C3 (Cm)
    Double Terminator BBa_B0015 ~129 BP Spring 2018 Distribution Plate 3, Well 3F pSB1C3 (Cm)


    Parts we've synthesized ourselves:
    FLS1 BBa_K2700000 ~1011 BP pSB1C3 (Cm)

    July

    • 25:
      • Transformed F3H into DH5a
      • Transformed K880005 into DH5a
      • Transformed B0034 into DH5a
      • Transformed B0015 into DH5a
    • 26:
      • Inoculated F3H in 25mg/uL of CM-25
      • Inoculated K880005 in 25mg/uL of CM-25
      • Inoculated B0034 in 25mg/uL of CM-25
      • Inoculated B0015 in 25mg/uL of CM-25
    • 27:
      • Miniprepped F3H
      • Miniprepped K880005
      • Miniprepped B0034
      • Miniprepped B0015
  • 28:
    • Digested F3H with XbaI and SpeI
    • Digested K880005 with SpeI and Pst1
    • Digested B0034 with EcoR1 and Xba1
    • Digested B0015 with EcoR1 and Xba1

    • August

    • 2:
      • Ran gel and purified all samples
      • Ligate F3H (insert, 5uL) and K880005 (vector, 2uL) with T4 ligase
    • 7:
      • transformed F3H and K880005
      • Digested RFP in pSB1C3; ran gel and purified
      • Digested synthesized FLS1 with Ecor1 and Pst1
    • 10:
      • inoculated F3H and K880005
    • 15:
      • Miniprepped F3H + K880005
      • Gel ran and get purified for RFP/pSB1C3, F3H + K880005, B0034, B0015
      • gel ran and PCR purified for FLS1
    • 16:
      • Redigested F3H with XbaI and SpeI (gel failed on the 15th, needed to redo cloning)
      • Redigested K880005 with SpeI and Pst1
    • 17:
      • Ligated RFP/pSB1C3 (vector, 2uL) with FLS1 (insert, 4uL)
      • Ligated FLS1 (vector, 2uL) with B0015 (insert, 4uL)
      • purified and religated F3H+K880005
    • 19:
      • Transformed FLS1 + pSB1C3 into DH5a
      • Transformed FLS1 + B0015 into DH5a
      • Transformed F3H + K880005 into DH5a
    • 20
      • Inoculate all samples
    • 21:
      • Miniprep all samples
    • 24
      • Ran diagnostic gel for all samples, F3H + K880005 failed again, everything else fine
    • 25:
      • Took originally miniprepped F3H and digested with XbaI and SpeI
    • 27:
      • Gel purified F3H
      • ligated with previously digested B0034

      • September

    • 5:
      • Transformed F3H + B0034
    • 5:
      • Inoculated F3H + B0034
    • 7:
      • Miniprepped F3H + B0034
    • 10:
      • Ran F3H + B0034 on gel and gel purified (cloning successful!)
    • 15:
      • Used glycerol stock K880005 and streaked on LB+Cm plate
    • 16:
      • Inoculated K880005
    • 17:
      • Miniprepped K880005
    • 19:
      • Digested K880005 with Spe1 + Pst1
    • 20:
      • Ran K880005 in gel and gel purified
    • 23:
      • Digested FLS1 + B0015 with Pst1 + Spe1
      • Digested F3H + B0034 with Xba1 + Pst1
    • 24:
      • Gel eletrophoresis and gel purified FLS1 + B0015
      • Gel eletrophoresis and gel purified F3H + B0034
    • 29:
      • Ligation of F3H + B0034 (insert, 6uL) and K880005 (vector, 2uL)

      • October

    • 1:
      • Transformation of k880005 + F3H + B0034
    • 2:
      • Inoculation of k880005 + F3H + B0034
    • 3:
      • Miniprep of k880005 + F3H + B0034
    • 4:
      • Digest of k880005 + F3H + B0034

    Plasmid Maintenance Notebook