Difference between revisions of "Team:Kent/Notebook"

Line 96: Line 96:
 
</div>
 
</div>
  
<a name="day1"></a><h4> Day 1 Wet lab <i>22/06/15</i> </h4>
+
<a class="anchor" id="top" name="day1"></a><h4> Day 1 Wet lab <i>22/06/15</i> </h4>
 
<p><li> Made LB plates </li>
 
<p><li> Made LB plates </li>
 
       <li> Made LB broth </li>
 
       <li> Made LB broth </li>
Line 102: Line 102:
 
</p>
 
</p>
  
<a name="day2"></a><h4> Day 2 Wet lab <i>23/06/15</i> </h4>
+
<a class="anchor" id="top"name="day2"></a><h4> Day 2 Wet lab <i>23/06/15</i> </h4>
 
<p><li> Set up Top10 overnight, VS45 overnight, US348 overnight </li>
 
<p><li> Set up Top10 overnight, VS45 overnight, US348 overnight </li>
 
       <li> Meeting with advisors to discuss progress </li>
 
       <li> Meeting with advisors to discuss progress </li>
 
</p>
 
</p>
  
<a name="day3"></a><h4> Day 3 Wet lab <i>24/06/15</i></h4>
+
<a class="anchor" id="top" name="day3"></a><h4> Day 3 Wet lab <i>24/06/15</i></h4>
 
<p><li> Filter sterilise the buffer</li>
 
<p><li> Filter sterilise the buffer</li>
 
       <li> 250ml no antibiotic broth, put top10 cells in</li>
 
       <li> 250ml no antibiotic broth, put top10 cells in</li>
Line 115: Line 115:
  
  
<a name="day4"></a><h4> Day 4 Wet lab <i> 25/06/15 </i> </h4>
+
<a class="anchor" id="top" name="day4"></a><h4> Day 4 Wet lab <i> 25/06/15 </i> </h4>
 
<p> <li> Transformation </li>
 
<p> <li> Transformation </li>
 
       <li> Prepare SBC media </li>
 
       <li> Prepare SBC media </li>
Line 121: Line 121:
 
</p>
 
</p>
  
<a name="day5"></a><h4> Day 5 Wet lab <i> 26/06/15 </i> </h4>
+
<a class="anchor" id="top" name="day5"></a><h4> Day 5 Wet lab <i> 26/06/15 </i> </h4>
 
<p><li> Calculated competent cell efficiency </li>
 
<p><li> Calculated competent cell efficiency </li>
 
       <li> Agarose gel formation </li>
 
       <li> Agarose gel formation </li>
Line 127: Line 127:
 
</p>
 
</p>
  
<a name="day6"></a><h4> Day 6 Wet lab <i> 29/06/15 </i> </h4>
+
<a class="anchor" id="top" name="day6"></a><h4> Day 6 Wet lab <i> 29/06/15 </i> </h4>
 
<p><li> Transforming linear PSB1C3 </li>
 
<p><li> Transforming linear PSB1C3 </li>
 
</p>
 
</p>
  
<a name="day7"></a><h4> Day 7 Wet lab <i> 30/06/15 </i> </h4>
+
<a class="anchor" id="top" name="day7"></a><h4> Day 7 Wet lab <i> 30/06/15 </i> </h4>
 
<p><li> Miniprep of PSB1A3 plasmid </li>
 
<p><li> Miniprep of PSB1A3 plasmid </li>
 
       <li> Gel electrophoresis of a large quantity of PSB1C3 </li>
 
       <li> Gel electrophoresis of a large quantity of PSB1C3 </li>
Line 141: Line 141:
 
</div>
 
</div>
  
<a name="day8"></a><h4> Day 8 Wet lab <i> 01/07/15 </i> </h4>
+
<a class="anchor" id="top" name="day8"></a><h4> Day 8 Wet lab <i> 01/07/15 </i> </h4>
 
<p> <li> Gel electrophoresis of the purified DNA extracted </li>
 
<p> <li> Gel electrophoresis of the purified DNA extracted </li>
 
<li> Transformation of pSB1A3 circular plasmid to VS45 cells (competent) </li>
 
<li> Transformation of pSB1A3 circular plasmid to VS45 cells (competent) </li>
 
<li> Digest of all pSB1C3 plasmids </li> </p>
 
<li> Digest of all pSB1C3 plasmids </li> </p>
  
<a name="day9"></a><h4> Day 9 Wet lab <i> 02/07/15 </i> </h4>
+
<a class="anchor" id="top" name="day9"></a><h4> Day 9 Wet lab <i> 02/07/15 </i> </h4>
 
<p> <li> Competent cells transformation efficiency </li>
 
<p> <li> Competent cells transformation efficiency </li>
 
<li> Mini-prep of 1MS340 to get pSB1C3 plasmid </li>
 
<li> Mini-prep of 1MS340 to get pSB1C3 plasmid </li>
Line 152: Line 152:
 
<li> Quantification of the digest. Added sample buffer to each digest </li>  </p>
 
<li> Quantification of the digest. Added sample buffer to each digest </li>  </p>
  
<a name="day10"></a><h4> Day 10 Wet lab <i> 03/07/15 </i> </h4>
+
<a class="anchor" id="top" name="day10"></a><h4> Day 10 Wet lab <i> 03/07/15 </i> </h4>
 
<p> <li> Transformation efficiency </li>
 
<p> <li> Transformation efficiency </li>
 
</p>
 
</p>
  
<a name="day11"></a><h4> Day 11 Wet lab <i> 06/07/15 </i></h4>
+
<a class="anchor" id="top" name="day11"></a><h4> Day 11 Wet lab <i> 06/07/15 </i></h4>
 
<p><li> TOP10 cells containing pSB1A3 with limonene synthase were cultured overnight on AMP plates </li>
 
<p><li> TOP10 cells containing pSB1A3 with limonene synthase were cultured overnight on AMP plates </li>
 
<li>Colonies of VS45 containing pSB1A3 were patched onto chloramphenicol plates </li>
 
<li>Colonies of VS45 containing pSB1A3 were patched onto chloramphenicol plates </li>
 
<li> Overnight digest of miniprepped pSBIC3 using ECORI and PSTl </li> </p>
 
<li> Overnight digest of miniprepped pSBIC3 using ECORI and PSTl </li> </p>
  
<a name="day12"></a><h4> Day 12 Wet lab <i> 07/07/15 </i></h4>
+
<a class="anchor" id="top" name="day12"></a><h4> Day 12 Wet lab <i> 07/07/15 </i></h4>
 
<p><li> Agarose gel of overnight digest - no bands were visible </li>
 
<p><li> Agarose gel of overnight digest - no bands were visible </li>
 
<li> Set up overnight cultures of pSBIC3 and pSBIA3 to be miniprepped the next day </li>
 
<li> Set up overnight cultures of pSBIC3 and pSBIA3 to be miniprepped the next day </li>
 
<li> Set up an overnight digest of pSBIC3 </li>
 
<li> Set up an overnight digest of pSBIC3 </li>
  
<a name="day13"></a><h4> Day 13 Wet lab <i> 08/07/15 </i> </h4>
+
<a class="anchor" id="top" name="day13"></a><h4> Day 13 Wet lab <i> 08/07/15 </i> </h4>
 
<p> <li> Agarose gel of overnight digest - no bands were visible</li>
 
<p> <li> Agarose gel of overnight digest - no bands were visible</li>
 
<li> Miniprep of pSBIA3 and pSBIC3 </li>
 
<li> Miniprep of pSBIA3 and pSBIC3 </li>
Line 175: Line 175:
 
</div>
 
</div>
  
<a name="day14"></a><h4> Day 14 Wet lab <i> 09/07/15 </i></h4>
+
<a class="anchor" id="top" name="day14"></a><h4> Day 14 Wet lab <i> 09/07/15 </i></h4>
 
<p> <li> Agarose gel of digested pSBIA3 and pSBIC3 - no bands were visible</li>
 
<p> <li> Agarose gel of digested pSBIA3 and pSBIC3 - no bands were visible</li>
 
<li>Overnight cultures of MS349 containing pSBIA3 LIMS and MS340 containing pSBIC3 were set up, ready to be miniprepped</li></p>
 
<li>Overnight cultures of MS349 containing pSBIA3 LIMS and MS340 containing pSBIC3 were set up, ready to be miniprepped</li></p>
  
<a name="day15"></a><h4> Day 15 Wet lab <i> 10/07/15 </i></h4>
+
<a class="anchor" id="top" name="day15"></a><h4> Day 15 Wet lab <i> 10/07/15 </i></h4>
 
<p> <li> Miniprep of plasmids pSBIA3 and pSBIC3 </li></p>
 
<p> <li> Miniprep of plasmids pSBIA3 and pSBIC3 </li></p>
  
<a name="day16"></a><h4> Day 16 Wet lab <i> 13/07/15 </i></h4>
+
<a class="anchor" id="top" name="day16"></a><h4> Day 16 Wet lab <i> 13/07/15 </i></h4>
 
<p> <li> Overnight cultures of MS349 containing pSBIA3 LIMS and MS340 containing pSBIC3 were set up, ready to be miniprepped </li>
 
<p> <li> Overnight cultures of MS349 containing pSBIA3 LIMS and MS340 containing pSBIC3 were set up, ready to be miniprepped </li>
 
<li> Overnight digest of miniprepped plasmids pSBIA3 and pSBIC3 using the enzymes ECORI and PSTI </li></p>
 
<li> Overnight digest of miniprepped plasmids pSBIA3 and pSBIC3 using the enzymes ECORI and PSTI </li></p>
  
<a name="day17"></a><h4> Day 17 Wet lab <i> 14/07/15 </i></h4>
+
<a class="anchor" id="top" name="day17"></a><h4> Day 17 Wet lab <i> 14/07/15 </i></h4>
 
<p><li> Agarose gel of digested plasmids pSBIA3 and pSBIC3 - it finally worked!!! </li>
 
<p><li> Agarose gel of digested plasmids pSBIA3 and pSBIC3 - it finally worked!!! </li>
 
<li> Miniprep of overnight cultures </li>
 
<li> Miniprep of overnight cultures </li>
Line 193: Line 193:
 
<li> Overnight cultures of Top10 cells containing pVS72</p>
 
<li> Overnight cultures of Top10 cells containing pVS72</p>
  
<a name="day18"></a><h4> Day 18 Wet lab <i> 15/07/15 </i></h4>
+
<a class="anchor" id="top" name="day18"></a><h4> Day 18 Wet lab <i> 15/07/15 </i></h4>
 
<p><li> Miniprepped pVS72 </li>
 
<p><li> Miniprepped pVS72 </li>
 
<li> Transformation of VS45 with pVS72 </li>
 
<li> Transformation of VS45 with pVS72 </li>
Line 204: Line 204:
 
     <img src="https://static.igem.org/mediawiki/2015/e/e0/Team_Kent_JamesPractical.jpg" style="float: right; width: 50%; margin-right: 1%;  class="sideimage"/>
 
     <img src="https://static.igem.org/mediawiki/2015/e/e0/Team_Kent_JamesPractical.jpg" style="float: right; width: 50%; margin-right: 1%;  class="sideimage"/>
 
</div>
 
</div>
<a name="day19"></a><h4> Day 19 Wet lab <i> 16/07/15 </i></h4>
+
<a class="anchor" id="top" name="day19"></a><h4> Day 19 Wet lab <i> 16/07/15 </i></h4>
 
<p><li> Counted the overnight colonies of VS45 with pVS72 </li>
 
<p><li> Counted the overnight colonies of VS45 with pVS72 </li>
 
<li> Calculated the transformation efficiency </li></p>
 
<li> Calculated the transformation efficiency </li></p>
  
  
<a name="day20"></a><h4> Day 20 <i> 17/07/15 </i></h4>
+
<a class="anchor" id="top" name="day20"></a><h4> Day 20 <i> 17/07/15 </i></h4>
 
<p><li> No wet lab was carried out on this day as we focussed on dry lab tasks </li></p>
 
<p><li> No wet lab was carried out on this day as we focussed on dry lab tasks </li></p>
  
<a name="day21"></a><h4> Day 21 Wet lab <i> 20/07/15 </i></h4>
+
<a class="anchor" id="top" name="day21"></a><h4> Day 21 Wet lab <i> 20/07/15 </i></h4>
 
<p><li>Fresh LB agar plates containing Chloramphenicol and Ampicillin were produced </li>
 
<p><li>Fresh LB agar plates containing Chloramphenicol and Ampicillin were produced </li>
 
<li> Transformed VS45 with pVS72 colonies were streaked onto fresh Chloramphenicol/Ampicillin plates<br> and incubated overnight </li></p>
 
<li> Transformed VS45 with pVS72 colonies were streaked onto fresh Chloramphenicol/Ampicillin plates<br> and incubated overnight </li></p>
  
<a name="day22"></a><h4> Day 22 Wet lab <i> 21/07/15 </i></h4>
+
<a class="anchor" id="top" name="day22"></a><h4> Day 22 Wet lab <i> 21/07/15 </i></h4>
 
<p><li> Congo red plates with 0.2% L-Arabinose were made </li>
 
<p><li> Congo red plates with 0.2% L-Arabinose were made </li>
 
<li> 500ml LB broth containing 0.2% L-Arabinose was made </li>
 
<li> 500ml LB broth containing 0.2% L-Arabinose was made </li>
 
<li> Overnight culture of VS45 with pVS72 in LB broth with 0.2% L-Arabinose </li></p>
 
<li> Overnight culture of VS45 with pVS72 in LB broth with 0.2% L-Arabinose </li></p>
  
<a name="day23"></a><h4> Day 23 Wet lab <i> 22/07/15 </i></h4>
+
<a class="anchor" id="top" name="day23"></a><h4> Day 23 Wet lab <i> 22/07/15 </i></h4>
 
<p><li> VS45 with pVS72 was plated on the Congo Red plates </li>
 
<p><li> VS45 with pVS72 was plated on the Congo Red plates </li>
 
<li> Culture preparation for TEM </li>
 
<li> Culture preparation for TEM </li>
  
<a name="day24"></a><h4> Day 24 Wet lab <i> 23/07/15 </i></h4>
+
<a class="anchor" id="top" name="day24"></a><h4> Day 24 Wet lab <i> 23/07/15 </i></h4>
 
<p><li> TEM imaging </li></p>
 
<p><li> TEM imaging </li></p>
  
<a name="day25"></a><h4> Day 25 <i> 24/07/15 </i></h4>
+
<a class="anchor" id="top" name="day25"></a><h4> Day 25 <i> 24/07/15 </i></h4>
 
<p><li> Dry lab day </li></p>
 
<p><li> Dry lab day </li></p>
  
<a name="day26"></a><h4> Day 26 <i> 27/07/15 </i></h4>
+
<a class="anchor" id="top" name="day26"></a><h4> Day 26 <i> 27/07/15 </i></h4>
 
<p><li> Transformation of Top10 cells with pVS105 (negative control plasmid), streaked onto Ampicillin LB plates </li>
 
<p><li> Transformation of Top10 cells with pVS105 (negative control plasmid), streaked onto Ampicillin LB plates </li>
 
<li> Transformation of VS45 with pVS72, streaked onto Chloramphenicol/Ampicillin LB plates </li>
 
<li> Transformation of VS45 with pVS72, streaked onto Chloramphenicol/Ampicillin LB plates </li>
 
<li> Produced plates containing Congo Red, Ampicillin plates and inducing Chloramphenicol/Ampicillin plates (containing Arabinose) <br> and non-inducing Chloramphenicol/Ampicillin plates </li></p>
 
<li> Produced plates containing Congo Red, Ampicillin plates and inducing Chloramphenicol/Ampicillin plates (containing Arabinose) <br> and non-inducing Chloramphenicol/Ampicillin plates </li></p>
  
<a name="day27"></a><h4> Day 27 <i> 28/07/15 </i></h4>
+
<a class="anchor" id="top" name="day27"></a><h4> Day 27 <i> 28/07/15 </i></h4>
 
<p><li> Made Chloramphenicol broth and made Ampicillin broth </li>
 
<p><li> Made Chloramphenicol broth and made Ampicillin broth </li>
 
<li>Resuspended Top10 with pVS105 in Amp broth </li>
 
<li>Resuspended Top10 with pVS105 in Amp broth </li>
 
<li>Resuspended VS45 with pVS72 in Chloramphenicol and Ampicillin broth </li></p>
 
<li>Resuspended VS45 with pVS72 in Chloramphenicol and Ampicillin broth </li></p>
  
<a name="day28"></a><h4> Day 28 <i> 29/07/15 </i></h4>
+
<a class="anchor" id="top" name="day28"></a><h4> Day 28 <i> 29/07/15 </i></h4>
 
<p><li>Miniprepped Top 10 cells containing pVS105 </li>
 
<p><li>Miniprepped Top 10 cells containing pVS105 </li>
 
<li> Diluted VS45 with pVS72 to OD<sub>600</sub> of 0.1 in 3ml of LB </li>
 
<li> Diluted VS45 with pVS72 to OD<sub>600</sub> of 0.1 in 3ml of LB </li>
 
<li> Spot plated 5μl of VS45 onto inducing plates (containing Arabinose and IPTG),<br> non-inducing plates and Congo red plates (both inducing and non-inducing) </li></p>
 
<li> Spot plated 5μl of VS45 onto inducing plates (containing Arabinose and IPTG),<br> non-inducing plates and Congo red plates (both inducing and non-inducing) </li></p>
  
<a name="day29"></a><h4> Day 29 <i> 30/07/15 </i></h4>
+
<a class="anchor" id="top" name="day29"></a><h4> Day 29 <i> 30/07/15 </i></h4>
 
<p><li>Transformed VS45 competent cells with the negative control plasmid (pVS105) </li></p>
 
<p><li>Transformed VS45 competent cells with the negative control plasmid (pVS105) </li></p>
  
<a name="day30"></a><h4> Day 30 <i> 31/07/15 </i></h4>
+
<a class="anchor" id="top" name="day30"></a><h4> Day 30 <i> 31/07/15 </i></h4>
 
<p><li> Weekend cultures of the negative control plasmid in VS45 were set up </li>
 
<p><li> Weekend cultures of the negative control plasmid in VS45 were set up </li>
 
<li> London meetup </li></p>
 
<li> London meetup </li></p>
  
<a name="day31"></a><h4> Day 31 <i> 03/08/15 </i></h4>
+
<a class="anchor" id="top" name="day31"></a><h4> Day 31 <i> 03/08/15 </i></h4>
 
<p><li> Dry lab </li> </p>
 
<p><li> Dry lab </li> </p>
  
<a name="day32"></a><h4> Day 32 <i> 04/08/15 </i></h4>
+
<a class="anchor" id="top" name="day32"></a><h4> Day 32 <i> 04/08/15 </i></h4>
 
<p><li> LB plates were made </li>
 
<p><li> LB plates were made </li>
 
<li> Transformations of cultures were spotted onto Chl + Amp plates (both inducing and non-inducing) and Congo Red. </li>
 
<li> Transformations of cultures were spotted onto Chl + Amp plates (both inducing and non-inducing) and Congo Red. </li>
 
<li> Plates were incubated overnight </li></p>
 
<li> Plates were incubated overnight </li></p>
  
<a name="day33"></a><h4> Day 33 <i> 05/08/15 </i></h4>  
+
<a class="anchor" id="top" name="day33"></a><h4> Day 33 <i> 05/08/15 </i></h4>  
 
<p><li> Overnight plates were checked for contamination </li>
 
<p><li> Overnight plates were checked for contamination </li>
 
<li> pVS105 and pVS72 were transformed into VS45 </li>
 
<li> pVS105 and pVS72 were transformed into VS45 </li>
 
<li> Transformations were plated and incubated overnight </li>
 
<li> Transformations were plated and incubated overnight </li>
  
<a name="day34"></a><h4> Day 34 <i> 06/08/15 </i></h4>
+
<a class="anchor" id="top" name="day34"></a><h4> Day 34 <i> 06/08/15 </i></h4>
 
<p><li> Overnight cultures were set up </li></p>
 
<p><li> Overnight cultures were set up </li></p>
  
<a name="day35"></a><h4> Day 35 <i> 07/08/15 </i></h4>
+
<a class="anchor" id="top" name="day35"></a><h4> Day 35 <i> 07/08/15 </i></h4>
 
<p><li> The colonies did not grow overnight, therefore more colonies were set up in the morning, with the OD being checked in the evening </li>
 
<p><li> The colonies did not grow overnight, therefore more colonies were set up in the morning, with the OD being checked in the evening </li>
 
<li> The transformation of pVS105 and pVS72 into VS45 was repeated </li>  
 
<li> The transformation of pVS105 and pVS72 into VS45 was repeated </li>  
 
<li> Transformed cells were plated out, and incubated overnight </li></p>
 
<li> Transformed cells were plated out, and incubated overnight </li></p>
  
<a name="day36"></a><h4> Day 36 <i>10/08/15</i></h4>
+
<a class="anchor" id="top" name="day36"></a><h4> Day 36 <i>10/08/15</i></h4>
 
<p><li> Plasmids were digested </li>
 
<p><li> Plasmids were digested </li>
 
<li> Agarose gel of the digested plasmids was run </li>
 
<li> Agarose gel of the digested plasmids was run </li>
 
<li> Colonies were set up as overnight cultures in LB </li></p>
 
<li> Colonies were set up as overnight cultures in LB </li></p>
  
<a name="day37"></a><h4> Day 37 <i>11/08/15</i></h4>
+
<a class="anchor" id="top" name="day37"></a><h4> Day 37 <i>11/08/15</i></h4>
 
<p><li> The OD of the overnight cultures was checked </li>
 
<p><li> The OD of the overnight cultures was checked </li>
 
<li> pSBIA3 and pSBIC3 was transformed into Top10 cells </li>  
 
<li> pSBIA3 and pSBIC3 was transformed into Top10 cells </li>  
Line 286: Line 286:
 
<li> The cultures of both plasmids were spot plated onto separate plates, ready for imaging </li></p>
 
<li> The cultures of both plasmids were spot plated onto separate plates, ready for imaging </li></p>
  
<a name="day38"></a><h4> Day 38 <i> 12/08/15 </i></h4>
+
<a class="anchor" id="top" name="day38"></a><h4> Day 38 <i> 12/08/15 </i></h4>
 
<p><li>pSBIA3 was re-transformed into Top10 cells </li>  
 
<p><li>pSBIA3 was re-transformed into Top10 cells </li>  
 
<li> PCR of pSBIC3 and pVS72 </li> </p>
 
<li> PCR of pSBIC3 and pVS72 </li> </p>
  
<a name="day39"></a><h4> Day 39 <i> 13/08/15 </i></h4>
+
<a class="anchor" id="top" name="day39"></a><h4> Day 39 <i> 13/08/15 </i></h4>
 
<p><li> PCR was repeated </li>  
 
<p><li> PCR was repeated </li>  
 
<li> Scanned the streaked Congo Red plates </li></p>
 
<li> Scanned the streaked Congo Red plates </li></p>
  
<a name="day40"></a><h4> Day 40 <i> 14/08/15 </i></h4>
+
<a class="anchor" id="top" name="day40"></a><h4> Day 40 <i> 14/08/15 </i></h4>
 
<p><li> Purified the PCR product </li>
 
<p><li> Purified the PCR product </li>
 
<li> Digested the PCR product </li>
 
<li> Digested the PCR product </li>
 
<li> Quantified the plasmid </li> </p>
 
<li> Quantified the plasmid </li> </p>
  
<a name="day41"></a><h4> Day 41 <i> 17/08/15 </i></h4>
+
<a class="anchor" id="top" name="day41"></a><h4> Day 41 <i> 17/08/15 </i></h4>
 
<p><li> Ligations of pSBIC3 and pVS72 </li>
 
<p><li> Ligations of pSBIC3 and pVS72 </li>
 
<li> Agarose gel to check the digest worked </li>
 
<li> Agarose gel to check the digest worked </li>
Line 305: Line 305:
 
<li> Sample preparation for imaging</li></p>
 
<li> Sample preparation for imaging</li></p>
  
<a name="day42"></a><h4> Day 42 <i> 18/08/15 </i></h4>
+
<a class="anchor" id="top" name="day42"></a><h4> Day 42 <i> 18/08/15 </i></h4>
 
<p><li> Overnight cultures of the transformed ligations were made </li> </p>
 
<p><li> Overnight cultures of the transformed ligations were made </li> </p>
  
<a name="day43"></a><h4> Day 43 <i> 19/08/15 </i></h4>
+
<a class="anchor" id="top" name="day43"></a><h4> Day 43 <i> 19/08/15 </i></h4>
 
<p><li> The overnight cultures were miniprepped </li>
 
<p><li> The overnight cultures were miniprepped </li>
 
<li> Plasmids digested </li>
 
<li> Plasmids digested </li>
 
<li> Transformation of plasmids into VS45 </li></p>
 
<li> Transformation of plasmids into VS45 </li></p>
  
<a name="day44"></a><h4> Day 44 <i> 20/08/15 </i></h4>
+
<a class="anchor" id="top" name="day44"></a><h4> Day 44 <i> 20/08/15 </i></h4>
 
<p><li> Agarose gel of digested plasmids </li>  
 
<p><li> Agarose gel of digested plasmids </li>  
 
<li> Overnight cultures of ligations of pSBIC3 and pVS72 </li></p>
 
<li> Overnight cultures of ligations of pSBIC3 and pVS72 </li></p>
  
<a name="day45"></a><h4> Day 45 <i> 21/08/15 </i></h4>  
+
<a class="anchor" id="top" name="day45"></a><h4> Day 45 <i> 21/08/15 </i></h4>  
 
<p><li> Overnight cultures were miniprepped </li>
 
<p><li> Overnight cultures were miniprepped </li>
 
<li> Ligations of pSBIC3 and pVS72 </li>   
 
<li> Ligations of pSBIC3 and pVS72 </li>   
Line 323: Line 323:
 
<li> Transformation of the fragments into competent cells, incubated over the weekend </li></p>
 
<li> Transformation of the fragments into competent cells, incubated over the weekend </li></p>
  
<a name="day46"></a><h4> Day 46 <i> 24/08/15 </i> </h4>  
+
<a class="anchor" id="top" name="day46"></a><h4> Day 46 <i> 24/08/15 </i> </h4>  
 
<p><li> Gibson assembly of fragments containing CsgAss, Sup35NM and Cytochrome b<sub>562</sub>, followed by transformation into competent cells</li>  
 
<p><li> Gibson assembly of fragments containing CsgAss, Sup35NM and Cytochrome b<sub>562</sub>, followed by transformation into competent cells</li>  
 
<li> Digest of ligations</li>
 
<li> Digest of ligations</li>
 
<li> Agarose gel of digest </li></p>
 
<li> Agarose gel of digest </li></p>
  
<a name="day47"></a><h4> Day 47 <i> 25/08/15 </i> </h4>  
+
<a class="anchor" id="top" name="day47"></a><h4> Day 47 <i> 25/08/15 </i> </h4>  
 
<p><li> PCR </li>  
 
<p><li> PCR </li>  
 
<li> Overnight cultures of the Gibson Assembled fragments </li>  
 
<li> Overnight cultures of the Gibson Assembled fragments </li>  
Line 334: Line 334:
 
<li> Agarose gel of the digest </li> </p>  
 
<li> Agarose gel of the digest </li> </p>  
  
<a name="day48"></a><h4> Day 48 <i> 26/08/15 </i></h4>  
+
<a class="anchor" id="top" name="day48"></a><h4> Day 48 <i> 26/08/15 </i></h4>  
 
<p><li> Gibson Assembly of fragments containing CsgAss and Sup35NM with pSBIA3 and Gibson Assembly of fragments containing CsgAss,<br> Sup35NM and Cytochrome b<sub>562</sub>, followed by transformation into competent cells  </li>  
 
<p><li> Gibson Assembly of fragments containing CsgAss and Sup35NM with pSBIA3 and Gibson Assembly of fragments containing CsgAss,<br> Sup35NM and Cytochrome b<sub>562</sub>, followed by transformation into competent cells  </li>  
 
<li> Agarose gel of PCR product </li>  
 
<li> Agarose gel of PCR product </li>  
Line 340: Line 340:
 
<li> Digest of PCR product </li> </p>
 
<li> Digest of PCR product </li> </p>
  
<a name="day49"></a><h4> Day 49 <i> 27/08/15 </i> </h4>  
+
<a class="anchor" id="top" name="day49"></a><h4> Day 49 <i> 27/08/15 </i> </h4>  
 
<p><li> Agarose gel of digest </li>  
 
<p><li> Agarose gel of digest </li>  
 
<li> Double digest of plasmids pSBIC3 and pSBIA3 </li></p>  
 
<li> Double digest of plasmids pSBIC3 and pSBIA3 </li></p>  
  
  
<a name="day50"></a><h4> Day 50 <i> 28/08/15 </i> </h4>  
+
<a class="anchor" id="top" name="day50"></a><h4> Day 50 <i> 28/08/15 </i> </h4>  
 
<p><li> Miniprep of plasmids pSBIC3 and pSBIA3 </li>  
 
<p><li> Miniprep of plasmids pSBIC3 and pSBIA3 </li>  
 
<li> Digest of miniprepped plasmids </li>  
 
<li> Digest of miniprepped plasmids </li>  
 
<li> Agarose gel of miniprepped plasmids </li>  
 
<li> Agarose gel of miniprepped plasmids </li>  
  
<a name="day51"></a><h4> Day 51 <i> 01/09/15 </i> </h4>
+
<a class="anchor" id="top" name="day51"></a><h4> Day 51 <i> 01/09/15 </i> </h4>
 
<p> <li> Digest of pVS72 and agarose gel </li>  
 
<p> <li> Digest of pVS72 and agarose gel </li>  
  
<a name="day52"></a><h4> Day 52 <i> 02/09/15 </i></h4>  
+
<a class="anchor" id="top" name="day52"></a><h4> Day 52 <i> 02/09/15 </i></h4>  
 
<p><li> Miniprep of pSBIC3 and pSBIA3 </li>  
 
<p><li> Miniprep of pSBIC3 and pSBIA3 </li>  
 
<li> Digest of the miniprepped plasmids </li>  
 
<li> Digest of the miniprepped plasmids </li>  
Line 359: Line 359:
 
<li> Gel extraction of the digested plasmids </li></p>  
 
<li> Gel extraction of the digested plasmids </li></p>  
  
<a name="day53"></a><h4> Day 53 <i> 03/09/15 </i> </h4>
+
<a class="anchor" id="top" name="day53"></a><h4> Day 53 <i> 03/09/15 </i> </h4>
 
<p><li>Gibson assembly </li>
 
<p><li>Gibson assembly </li>
 
<li> Transformation of the Gibson assembly products into Top10 cells </li>  
 
<li> Transformation of the Gibson assembly products into Top10 cells </li>  
Line 365: Line 365:
 
<li> Agarose gel of digested plasmid </li> </p>
 
<li> Agarose gel of digested plasmid </li> </p>
  
<a name="day54"></a><h4> Day 54 <i> 04/09/15 </i> </h4>
+
<a class="anchor" id="top" name="day54"></a><h4> Day 54 <i> 04/09/15 </i> </h4>
 
<p> <li> Overnight cultures of the Gibson Assembled products </li>  
 
<p> <li> Overnight cultures of the Gibson Assembled products </li>  
 
<li> Gibson assembly of fragments into pSBIA3 </li>  
 
<li> Gibson assembly of fragments into pSBIA3 </li>  
Line 374: Line 374:
 
<li> Stacey Symposium </li> </p>
 
<li> Stacey Symposium </li> </p>
  
<a name="day55"></a><h4> Day 55 <i> 05/09/15 </i></h4>
+
<a class="anchor" id="top" name="day55"></a><h4> Day 55 <i> 05/09/15 </i></h4>
 
<p><li> Gel extraction </li>  
 
<p><li> Gel extraction </li>  
 
<li> Digest of plasmids and Gibson assembled products </li>  
 
<li> Digest of plasmids and Gibson assembled products </li>  
Line 381: Line 381:
 
<li> Presentation at London iGEM meetup </li> </p>  
 
<li> Presentation at London iGEM meetup </li> </p>  
  
<a name="day56"></a><h4> Day 56 <i> 07/09/15 </i></h4>
+
<a class="anchor" id="top" name="day56"></a><h4> Day 56 <i> 07/09/15 </i></h4>
 
<p><li> Transformation of pSBIC3 and pSBIA3 into Top10 cells from the iGEM distribution kit </li>  
 
<p><li> Transformation of pSBIC3 and pSBIA3 into Top10 cells from the iGEM distribution kit </li>  
 
<li> PCR </li>  
 
<li> PCR </li>  
Line 390: Line 390:
 
</p>
 
</p>
  
<a name="day57"></a><h4> Day 57 <i> 08/09/15 </i></h4>  
+
<a class="anchor" id="top" name="day57"></a><h4> Day 57 <i> 08/09/15 </i></h4>  
 
<p><li> PCR purification </li>
 
<p><li> PCR purification </li>
 
<li> Ligation </li>  
 
<li> Ligation </li>  
Line 397: Line 397:
 
<li> Made plates </li></p>  
 
<li> Made plates </li></p>  
  
<a name="day58"></a><h4> Day 58 <i> 09/09/15 </i></h4>
+
<a class="anchor" id="top" name="day58"></a><h4> Day 58 <i> 09/09/15 </i></h4>
 
<p><li> Miniprep of pSBIC3 </li>
 
<p><li> Miniprep of pSBIC3 </li>
 
<li> Digest of pSBIC3 and heat inactivation of the enzymes at 80ºC </li>
 
<li> Digest of pSBIC3 and heat inactivation of the enzymes at 80ºC </li>
Line 403: Line 403:
 
<li> Overnight cultures of pSBIC3 in Top10 cells </p>
 
<li> Overnight cultures of pSBIC3 in Top10 cells </p>
  
<a name="day59"></a><h4> Day 59 <i> 10/09/15 </i></h4>
+
<a class="anchor" id="top" name="day59"></a><h4> Day 59 <i> 10/09/15 </i></h4>
 
<p><li> Miniprep of pSBIC3 </li>  
 
<p><li> Miniprep of pSBIC3 </li>  
 
<li> Digest of plasmid and heat inactivation of the enzymes used </li>  
 
<li> Digest of plasmid and heat inactivation of the enzymes used </li>  
Line 411: Line 411:
 
<li> Overnight cultures of Ligated products from 09/09/15</p>
 
<li> Overnight cultures of Ligated products from 09/09/15</p>
  
<a name="day60"></a><h4> Day 60 <i> 11/09/15 </i> </h4>  
+
<a class="anchor" id="top" name="day60"></a><h4> Day 60 <i> 11/09/15 </i> </h4>  
 
<li> Miniprep of ligated pSBIC3 with PCR products </li>  
 
<li> Miniprep of ligated pSBIC3 with PCR products </li>  
 
<li> Digest of the minipreps </li>
 
<li> Digest of the minipreps </li>
 
<li> Agarose gel of the digests </li> </p>  
 
<li> Agarose gel of the digests </li> </p>  
  
<a name="day61"></a><h4> Day 61 <i> 14/09/15 </i> </h4>  
+
<a class="anchor" id="top" name="day61"></a><h4> Day 61 <i> 14/09/15 </i> </h4>  
 
<li> Miniprep of our plasmids </li>  
 
<li> Miniprep of our plasmids </li>  
 
<li> Digest of our plasmids </li>  
 
<li> Digest of our plasmids </li>  

Revision as of 11:01, 15 September 2015


iGEM Kent 2015


Notebook

June

M T W T F S S
1 2 3 4 5 6 7
8 9 10 11 12 13 14
15 16 17 18 19 20 21
22 23 24 25 26 27 28
29 30

July

M T W T F S S
1 2 3 4 5
6 7 8 9 10 11 12
13 14 15 16 17 18 19
20 21 22 23 24 25 26
27 28 2930 31

August

M T W T F S S
1 2
3 4 5 6 7 8 9
10 11 12 13 14 15 16
17 18 19 20 21 22 23
24 25 2627 28 29 30
31

September

M T W T F S S
1 2 3 4 5 6
7 8 9 10 11 12 13
14 15 16 17 18 19 20
21 22 23 24 25 26 27
28 29 30

Day 1 Wet lab 22/06/15

  • Made LB plates
  • Made LB broth
  • TIPS autoclaved
  • Day 2 Wet lab 23/06/15

  • Set up Top10 overnight, VS45 overnight, US348 overnight
  • Meeting with advisors to discuss progress
  • Day 3 Wet lab 24/06/15

  • Filter sterilise the buffer
  • 250ml no antibiotic broth, put top10 cells in
  • Incubate until optical density is 0.6
  • Miniprep PSB1C3 plasmid
  • Day 4 Wet lab 25/06/15

  • Transformation
  • Prepare SBC media
  • Digest of PSB1c3 from MS348
  • Day 5 Wet lab 26/06/15

  • Calculated competent cell efficiency
  • Agarose gel formation
  • Gel electrophoresis
  • Day 6 Wet lab 29/06/15

  • Transforming linear PSB1C3
  • Day 7 Wet lab 30/06/15

  • Miniprep of PSB1A3 plasmid
  • Gel electrophoresis of a large quantity of PSB1C3
  • Meeting with advisors to discuss progress
  • Day 8 Wet lab 01/07/15

  • Gel electrophoresis of the purified DNA extracted
  • Transformation of pSB1A3 circular plasmid to VS45 cells (competent)
  • Digest of all pSB1C3 plasmids
  • Day 9 Wet lab 02/07/15

  • Competent cells transformation efficiency
  • Mini-prep of 1MS340 to get pSB1C3 plasmid
  • Gel extraction of big digest
  • Quantification of the digest. Added sample buffer to each digest
  • Day 10 Wet lab 03/07/15

  • Transformation efficiency
  • Day 11 Wet lab 06/07/15

  • TOP10 cells containing pSB1A3 with limonene synthase were cultured overnight on AMP plates
  • Colonies of VS45 containing pSB1A3 were patched onto chloramphenicol plates
  • Overnight digest of miniprepped pSBIC3 using ECORI and PSTl
  • Day 12 Wet lab 07/07/15

  • Agarose gel of overnight digest - no bands were visible
  • Set up overnight cultures of pSBIC3 and pSBIA3 to be miniprepped the next day
  • Set up an overnight digest of pSBIC3
  • Day 13 Wet lab 08/07/15

  • Agarose gel of overnight digest - no bands were visible
  • Miniprep of pSBIA3 and pSBIC3
  • Overnight digest of pSBIA3 and pSBIC3
  • Day 14 Wet lab 09/07/15

  • Agarose gel of digested pSBIA3 and pSBIC3 - no bands were visible
  • Overnight cultures of MS349 containing pSBIA3 LIMS and MS340 containing pSBIC3 were set up, ready to be miniprepped
  • Day 15 Wet lab 10/07/15

  • Miniprep of plasmids pSBIA3 and pSBIC3
  • Day 16 Wet lab 13/07/15

  • Overnight cultures of MS349 containing pSBIA3 LIMS and MS340 containing pSBIC3 were set up, ready to be miniprepped
  • Overnight digest of miniprepped plasmids pSBIA3 and pSBIC3 using the enzymes ECORI and PSTI
  • Day 17 Wet lab 14/07/15

  • Agarose gel of digested plasmids pSBIA3 and pSBIC3 - it finally worked!!!
  • Miniprep of overnight cultures
  • Gel extraction of both plasmids
  • Analytical gel using Hyperladder I to quantify the plasmid
  • Overnight cultures of Top10 cells containing pVS72

    Day 18 Wet lab 15/07/15

  • Miniprepped pVS72
  • Transformation of VS45 with pVS72
  • Made LB plates with Chloramphenicol and Ampicillin
  • Plated the transformed VS45 cells on the Chloramphenicol/Ampicillin plates
  • Agarose gel of leftover digested pSBIA3 and pSBIC3 from 14/07/15
  • Gel extraction of pSBIA3 and pSBIC3
  • Day 19 Wet lab 16/07/15

  • Counted the overnight colonies of VS45 with pVS72
  • Calculated the transformation efficiency
  • Day 20 17/07/15

  • No wet lab was carried out on this day as we focussed on dry lab tasks
  • Day 21 Wet lab 20/07/15

  • Fresh LB agar plates containing Chloramphenicol and Ampicillin were produced
  • Transformed VS45 with pVS72 colonies were streaked onto fresh Chloramphenicol/Ampicillin plates
    and incubated overnight
  • Day 22 Wet lab 21/07/15

  • Congo red plates with 0.2% L-Arabinose were made
  • 500ml LB broth containing 0.2% L-Arabinose was made
  • Overnight culture of VS45 with pVS72 in LB broth with 0.2% L-Arabinose
  • Day 23 Wet lab 22/07/15

  • VS45 with pVS72 was plated on the Congo Red plates
  • Culture preparation for TEM
  • Day 24 Wet lab 23/07/15

  • TEM imaging
  • Day 25 24/07/15

  • Dry lab day
  • Day 26 27/07/15

  • Transformation of Top10 cells with pVS105 (negative control plasmid), streaked onto Ampicillin LB plates
  • Transformation of VS45 with pVS72, streaked onto Chloramphenicol/Ampicillin LB plates
  • Produced plates containing Congo Red, Ampicillin plates and inducing Chloramphenicol/Ampicillin plates (containing Arabinose)
    and non-inducing Chloramphenicol/Ampicillin plates
  • Day 27 28/07/15

  • Made Chloramphenicol broth and made Ampicillin broth
  • Resuspended Top10 with pVS105 in Amp broth
  • Resuspended VS45 with pVS72 in Chloramphenicol and Ampicillin broth
  • Day 28 29/07/15

  • Miniprepped Top 10 cells containing pVS105
  • Diluted VS45 with pVS72 to OD600 of 0.1 in 3ml of LB
  • Spot plated 5μl of VS45 onto inducing plates (containing Arabinose and IPTG),
    non-inducing plates and Congo red plates (both inducing and non-inducing)
  • Day 29 30/07/15

  • Transformed VS45 competent cells with the negative control plasmid (pVS105)
  • Day 30 31/07/15

  • Weekend cultures of the negative control plasmid in VS45 were set up
  • London meetup
  • Day 31 03/08/15

  • Dry lab
  • Day 32 04/08/15

  • LB plates were made
  • Transformations of cultures were spotted onto Chl + Amp plates (both inducing and non-inducing) and Congo Red.
  • Plates were incubated overnight
  • Day 33 05/08/15

  • Overnight plates were checked for contamination
  • pVS105 and pVS72 were transformed into VS45
  • Transformations were plated and incubated overnight
  • Day 34 06/08/15

  • Overnight cultures were set up
  • Day 35 07/08/15

  • The colonies did not grow overnight, therefore more colonies were set up in the morning, with the OD being checked in the evening
  • The transformation of pVS105 and pVS72 into VS45 was repeated
  • Transformed cells were plated out, and incubated overnight
  • Day 36 10/08/15

  • Plasmids were digested
  • Agarose gel of the digested plasmids was run
  • Colonies were set up as overnight cultures in LB
  • Day 37 11/08/15

  • The OD of the overnight cultures was checked
  • pSBIA3 and pSBIC3 was transformed into Top10 cells
  • Glycerol stock solution of pVS105 and pVS72 was produced
  • Miniprep of pVS72 and pVS105
  • The cultures of both plasmids were spot plated onto separate plates, ready for imaging
  • Day 38 12/08/15

  • pSBIA3 was re-transformed into Top10 cells
  • PCR of pSBIC3 and pVS72
  • Day 39 13/08/15

  • PCR was repeated
  • Scanned the streaked Congo Red plates
  • Day 40 14/08/15

  • Purified the PCR product
  • Digested the PCR product
  • Quantified the plasmid
  • Day 41 17/08/15

  • Ligations of pSBIC3 and pVS72
  • Agarose gel to check the digest worked
  • Ligations were transformed into Top10 cells and plated out
  • Sample preparation for imaging
  • Day 42 18/08/15

  • Overnight cultures of the transformed ligations were made
  • Day 43 19/08/15

  • The overnight cultures were miniprepped
  • Plasmids digested
  • Transformation of plasmids into VS45
  • Day 44 20/08/15

  • Agarose gel of digested plasmids
  • Overnight cultures of ligations of pSBIC3 and pVS72
  • Day 45 21/08/15

  • Overnight cultures were miniprepped
  • Ligations of pSBIC3 and pVS72
  • Gibson assembly of fragments containing CsgAss and Sup35NM
  • Transformation of the fragments into competent cells, incubated over the weekend
  • Day 46 24/08/15

  • Gibson assembly of fragments containing CsgAss, Sup35NM and Cytochrome b562, followed by transformation into competent cells
  • Digest of ligations
  • Agarose gel of digest
  • Day 47 25/08/15

  • PCR
  • Overnight cultures of the Gibson Assembled fragments
  • Digest of Gibson Assembled fragments containing CsgAss and Sup35NM
  • Agarose gel of the digest
  • Day 48 26/08/15

  • Gibson Assembly of fragments containing CsgAss and Sup35NM with pSBIA3 and Gibson Assembly of fragments containing CsgAss,
    Sup35NM and Cytochrome b562, followed by transformation into competent cells
  • Agarose gel of PCR product
  • PCR purification of the product
  • Digest of PCR product
  • Day 49 27/08/15

  • Agarose gel of digest
  • Double digest of plasmids pSBIC3 and pSBIA3
  • Day 50 28/08/15

  • Miniprep of plasmids pSBIC3 and pSBIA3
  • Digest of miniprepped plasmids
  • Agarose gel of miniprepped plasmids
  • Day 51 01/09/15

  • Digest of pVS72 and agarose gel
  • Day 52 02/09/15

  • Miniprep of pSBIC3 and pSBIA3
  • Digest of the miniprepped plasmids
  • Agarose gel was run to check the digest had worked
  • Gel extraction of the digested plasmids
  • Day 53 03/09/15

  • Gibson assembly
  • Transformation of the Gibson assembly products into Top10 cells
  • Digest of pSBIC3
  • Agarose gel of digested plasmid
  • Day 54 04/09/15

  • Overnight cultures of the Gibson Assembled products
  • Gibson assembly of fragments into pSBIA3
  • Transformation into Top10 cells
  • Digested pVS72
  • Agarose gel
  • London meetup
  • Stacey Symposium
  • Day 55 05/09/15

  • Gel extraction
  • Digest of plasmids and Gibson assembled products
  • Agarose gel of digests
  • University of Kent open day
  • Presentation at London iGEM meetup
  • Day 56 07/09/15

  • Transformation of pSBIC3 and pSBIA3 into Top10 cells from the iGEM distribution kit
  • PCR
  • Transformation of ordered plasmids into Top10 and VS45
  • Miniprep of pSBIA3
  • Digest of pSBIC3 and pSBIA3, followed by an agarose gel
  • Diagnostic digest of pVS72 and pVS72 with cytochrome b562, followed by an agarose gel
  • Day 57 08/09/15

  • PCR purification
  • Ligation
  • Gibson Assembly
  • Transformation
  • Made plates
  • Day 58 09/09/15

  • Miniprep of pSBIC3
  • Digest of pSBIC3 and heat inactivation of the enzymes at 80ºC
  • Ligation of pSBIC3 with PCR products
  • Overnight cultures of pSBIC3 in Top10 cells

    Day 59 10/09/15

  • Miniprep of pSBIC3
  • Digest of plasmid and heat inactivation of the enzymes used
  • Ligation of pSBIC3 with PCR products
  • Gibson assembly of pSBIC3 with ordered fragments
  • Competent Top10 cell production
  • Overnight cultures of Ligated products from 09/09/15

    Day 60 11/09/15

  • Miniprep of ligated pSBIC3 with PCR products
  • Digest of the minipreps
  • Agarose gel of the digests
  • Day 61 14/09/15

  • Miniprep of our plasmids
  • Digest of our plasmids
  • Diagnostic Agarose gel to see if we have our biobricks