Team:Yale/Our Project/Notebook/Week 5

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<li id="nb"><a href="https://2010.igem.org/Team:Yale/Our Project/Notebook/Week 7">week 7</a></li>
<li id="nb"><a href="https://2010.igem.org/Team:Yale/Our Project/Notebook/Week 7">week 7</a></li>
<li id="nb"><a href="https://2010.igem.org/Team:Yale/Our Project/Notebook/Week 8">week 8</a></li>
<li id="nb"><a href="https://2010.igem.org/Team:Yale/Our Project/Notebook/Week 8">week 8</a></li>
 +
<li id="nb"><a href="https://2010.igem.org/Team:Yale/Our Project/Notebook/Week 9">week 9</a></li>
<li><a href="https://2010.igem.org/Team:Yale/Our Project/Protocols">protocols</a></li>
<li><a href="https://2010.igem.org/Team:Yale/Our Project/Protocols">protocols</a></li>
<li><a href="https://2010.igem.org/Team:Yale/Our Project/Safety">safety</a></li>
<li><a href="https://2010.igem.org/Team:Yale/Our Project/Safety">safety</a></li>
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<li>Ran colony PCR of colonies 1B-9B from ligation attempt #2 according to the same protocol as used on <a href="https://2010.igem.org/Team:Yale/Our_Project/Notebook/Week_4"> 7/1</a>.</li>
<li>Ran colony PCR of colonies 1B-9B from ligation attempt #2 according to the same protocol as used on <a href="https://2010.igem.org/Team:Yale/Our_Project/Notebook/Week_4"> 7/1</a>.</li>
  <li>Then ran a 1.0% agarose gel of the nine PCR reaction solutions against a 1 kb ladder, but the resulting gel failed to show any evidence of either insert or vector, so will have to rely on sequencing and digests of miniprepped plasmids.</li>
  <li>Then ran a 1.0% agarose gel of the nine PCR reaction solutions against a 1 kb ladder, but the resulting gel failed to show any evidence of either insert or vector, so will have to rely on sequencing and digests of miniprepped plasmids.</li>
-
       Gel of colony PCR from ligation attempt #2 Lane 1: 1 kb ladder, Lanes 3-11:PCR products from colonies 1B-9B, in order<br/>
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<div align="center">
 +
<img src="https://static.igem.org/mediawiki/2010/0/0a/Yale-ligation-products.jpg" />
 +
</div>
 +
       <div id="caption">Gel of colony PCR from ligation attempt #2 Lane 1: 1 kb ladder, Lanes 3-11:PCR products from colonies 1B-9B, in order</div>
        
        
-
<li>Miniprepped liquid cultures grown from colonies of first ligation attempt (colonies 1A-4A) and second ligation attempt (colonies 1B-9B) according to <a href="https://2010.igem.org/Team:Yale/Our_Project/Protocols"> standard miniprep protocol.</a> </li>
+
<li>Miniprepped liquid cultures grown from colonies of first ligation attempt (colonies 1A-4A) and second ligation attempt (colonies 1B-9B) according to <a href="https://2010.igem.org/Team:Yale/Our_Project/Protocols"> standard miniprep protocol</a> </li>
</ul>
</ul>
<i>This day's activities are also recorded on page 47 and 48 of the hard copy lab notebook. </i>
<i>This day's activities are also recorded on page 47 and 48 of the hard copy lab notebook. </i>
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<li>The diagnostic 1.0% agarose gel was run at 90 V vs. a 1 kb ladder. Each of the thirteen samples gave one diffuse band around 3 kb and no evidence of the 3.6 kb phsABC fragment, so both ligation attempts #1 and #2 were unsuccessful.</li>
<li>The diagnostic 1.0% agarose gel was run at 90 V vs. a 1 kb ladder. Each of the thirteen samples gave one diffuse band around 3 kb and no evidence of the 3.6 kb phsABC fragment, so both ligation attempts #1 and #2 were unsuccessful.</li>
-
       Gel of XbaI and SpeI double digest of plasmids from ligation attempts #1 and #2 Lane 1: 1 kb ladder, Lanes 2-5:1A-4A, Lanes 6-14: 1B-9B <br/>
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 +
<div align="center">
 +
<img src="https://static.igem.org/mediawiki/2010/9/93/Yale-digest-gel.jpg" />
 +
</div>
 +
       <div id="caption">Gel of XbaI and SpeI double digest of plasmids from ligation attempts #1 and #2 Lane 1: 1 kb ladder, Lanes 2-5:1A-4A, Lanes 6-14: 1B-9B </div>
        
        
  <li>During digestion prepped plasmid samples for sequencing. Each sample contained 3 μL of plasmid soln (average concentration of 96 ng/μL), 2 μL of 4 mM VF2 (forward primer), and 13 μL of distilled water. Intended to follow up with reverse sequencing of more promising samples, but gel results made it a moot point. </li>
  <li>During digestion prepped plasmid samples for sequencing. Each sample contained 3 μL of plasmid soln (average concentration of 96 ng/μL), 2 μL of 4 mM VF2 (forward primer), and 13 μL of distilled water. Intended to follow up with reverse sequencing of more promising samples, but gel results made it a moot point. </li>
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<ul>
<ul>
<li>Needed more phsABC, so ran five PCR reactions to amplify it from plasmid pSB74. Reaction mixture contents were the same as the DMSO variant used on <a href="https://2010.igem.org/Team:Yale/Our_Project/Notebook/Week_4">6/30 </a>as was the thermocycler protocol (phs50). The results were then run on a gel</li>
<li>Needed more phsABC, so ran five PCR reactions to amplify it from plasmid pSB74. Reaction mixture contents were the same as the DMSO variant used on <a href="https://2010.igem.org/Team:Yale/Our_Project/Notebook/Week_4">6/30 </a>as was the thermocycler protocol (phs50). The results were then run on a gel</li>
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       Gel of PCR amplified phsABC Extreme right lane:1 kb ladder, all other lanes PCR reaction mixtures and their spillover
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<div align="center">
 +
<img src="https://static.igem.org/mediawiki/2010/a/ac/Yale-pcr-gel.jpg" />
 +
</div>
 +
       <div id="caption">Gel of PCR amplified phsABC Extreme right lane:1 kb ladder, all other lanes PCR reaction mixtures and their spillover</div>
        
        
<li>Needed chloramphenicol plates for pSB1C3-based constructs, so mixed 350 μL of 50 μg/μL chloramphenicol with an autoclaved solution of 7.5 g agar and 12.5 g LB in 500 mL H2O and poured plates. </li>
<li>Needed chloramphenicol plates for pSB1C3-based constructs, so mixed 350 μL of 50 μg/μL chloramphenicol with an autoclaved solution of 7.5 g agar and 12.5 g LB in 500 mL H2O and poured plates. </li>
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Digestion Reaction Components
Digestion Reaction Components
</td></tr> <tr> <td>
</td></tr> <tr> <td>
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phsABC Digestion </td> <td> B0015 Digestion </td> <td>pSB1C3 Digestion
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phsABC Digestion </td> <td> B0015 Digestion </td> <td>pSB1C3 Digestionhttps://2010.igem.org/Main_Page
</td></tr> <tr> <td>
</td></tr> <tr> <td>
5 μL EcoRI Buffer 10x </td> <td>5 μL NEB Buffer 3 10x </td> <td> 5 μL EcoRI Buffer 10x
5 μL EcoRI Buffer 10x </td> <td>5 μL NEB Buffer 3 10x </td> <td> 5 μL EcoRI Buffer 10x
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<b>Ligation Attempt #4</b><br/>
<b>Ligation Attempt #4</b><br/>
<ul>
<ul>
-
<li>Concerns about enzyme activity led to reversing the order of the serial digestion of B0015 background so that the first digestion is XbaI (low salt buffer) and the second is EcoRI (high salt buffer). Will also omit the pre-ligation PCR purification step.<li/>
+
<li>Concerns about enzyme activity led to reversing the order of the serial digestion of B0015 background so that the first digestion is XbaI (low salt buffer) and the second is EcoRI (high salt buffer). Will also omit the pre-ligation PCR purification step.</li>
<li>Overnight digestion of ligation components--Set up the following digestions to run overnight at 37°C. The EcoRI was newly purchased as there was concern about the age of the previously used enzyme.</li>
<li>Overnight digestion of ligation components--Set up the following digestions to run overnight at 37°C. The EcoRI was newly purchased as there was concern about the age of the previously used enzyme.</li>
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<li>
<li>
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Fridays short content
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Friday 7/9--Ligation attempt #4 to join phsABC and B0015 terminator.
</li>
</li>
<a id="link" href="javascript:ReverseDisplay('friday')">See more/less</a>
<a id="link" href="javascript:ReverseDisplay('friday')">See more/less</a>
<div style="display:none;" id="friday">
<div style="display:none;" id="friday">
<!------------- Friday ------------->
<!------------- Friday ------------->
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Extra content
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<h4> Ligation Attempt #4</h4>
 +
<ul>
 +
<li>Removed both overnight digestions, the XbaI digestion of B0015 and the EcoRI and SpeI digestion of phsABC, from 7/8 from the incubator.</li>
 +
<li>Heatkilled enzymes of phsABC digest with 20 minutes at 80°C.</li>
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<li>Ran <a href="https://2010.igem.org/Team:Yale/Our_Project/Protocols/PCR_purify">PCR purification protocol </a>on XbaI digestion using microcentrifuge. In order to give a concentrated sample, eluted in only 35 μL of EB Buffer that had been heated at 50°C. Resulting concentration could not be determined as there was residual ethanol contamination.</li>
 +
<li>Ran EcoRI digestion of purified XbaI digest product at 37 °C, with components as follows. Digestion was run for an hour before addition of CIP, after which it was run for another hour. </li>
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<table> <tr> <td>
 +
<b>B0015 digestion with EcoRI</b>
 +
</td> </tr>
 +
<tr> <td>
 +
NEB EcoRI buffer </td><td> 5 μL
 +
</td> </tr>
 +
<tr> <td>
 +
BSA 100x </td><td> 0.5 μL
 +
</td> </tr>
 +
<tr> <td>
 +
NEB EcoRI </td><td>3.6 μL
 +
</td> </tr>
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<tr> <td>
 +
B0015 digested with XbaI </td><td>25 μL
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</td> </tr>
 +
<tr> <td>
 +
NEB Calf Intestinal Phosphatase </td><td>1 μL
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</td> </tr>
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<tr> <td>
 +
Sterile H2O </td><td> 15.9 μL
 +
</td> </tr>
 +
</table>
 +
 
 +
Followed with 20 minute heatkill at 80°C.<br/>
 +
 
 +
<li>In order to set up ligation, need concentration of B0015, but ethanol contaminant continues to preclude measurement. Will estimate that the purification between digestion steps resulted in a 50% loss of DNA, leaving behind a 10 ng/μL concentration. Will also, as usual, run different ligation trials with different ratios of insert to vector, which should help combat any issues if this estimate is inaccurate </li>
 +
<li>Set up the following ligation trials, with stoichiometric ratios of insert to vector (I:V) based on B0015 concentration estimate. Ran the ligations for 20 minutes at room temperature. </li>
 +
<table>
 +
<tr><td>
 +
<b>Ligation Reaction Components</b>
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</td></tr>
 +
<tr><td>
 +
Control Ligation</td> <td> 1:1 I:V </td> <td>2:1 I:V </td> <td> 3:1 I:V</td> <td> 4:1 I:V
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</td></tr>
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<tr><td>
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2 μL NEB T4 ligase buffer for all reactions
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</td></tr>
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<tr><td>
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1 μL NEB T4 ligase for all reactions
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</td></tr>
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<tr><td>
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5 μL B0015 solution for all reactions
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</td></tr>
 +
<tr><td>
 +
12 μL H<sub>2</sub>O </td> <td> 8.9 μL </td> <td>5.8 μL H<sub>2</sub>O </td> <td>2.7 μL H<sub>2</sub>O </td> <td> --
 +
</td></tr>
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<tr><td>
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-- </td> <td>3.1 μL phsABC </td> <td> 6.2μL phsABC </td> <td> 9.3 μL phsABC</td> <td> 12 μL phsABC
 +
</td> </tr>
 +
</table>
 +
<li> Following ligation, transformed 1 μL of each ligation reaction into commercial grade cells according to standard transformation protocol. Also transformed triple ligation reaction. </li>
 +
</ul>
 +
 
 +
<h4>Enzyme Activity Test</h4>
 +
 
 +
To test enzyme activity, will do single digests of B0015 with enzymes in question and then run them on a gel to see if the plasmid linearized. XbaI and EcoRI are old, so will test them first. For XbaI activity test, simply set aside 10 μL of digestion solution from overnight digestion. Testing of EcoRI required additional digests. Digests using both old and new EcoRI samples were run for two hours at 37 °C with the following components:<br/>
 +
<table>
 +
<tr><td>
 +
<b>EcoRI Activity </b>
 +
</td> </tr>
 +
<tr><td>
 +
NEB EcoRI buffer </td> <td> 5 μL
 +
</td> </tr>
 +
<tr><td>
 +
BSA 100x </td> <td>0.5 μL
 +
</td> </tr>
 +
<tr><td>
 +
NEB EcoRI </td> <td>3.6 μL
 +
</td> </tr>
 +
<tr><td>
 +
undigested B0015 </td> <td>3.8 μL ( 1 μg DNA)
 +
</td> </tr>
 +
<tr><td>
 +
Sterile H<sub>2</sub>O </td> <td>37.1 μL
 +
</td> </tr>
 +
</table>
 +
 
 +
Followed with 20 minute heatkill at 80°C.<br/>
 +
<ul>
 +
<li>Loaded all three enzyme activity tests on a 1.0% agarose gel and ran them at 90 V versus a 1 kb ladder and circular B0015 plasmid. </li>
 +
 
 +
Gel of single digests of B0015 Left to Right lane 1:1 kb ladder, lane 2: uncut circular B0015, its dimer, and lane 3 spillover, lane 3: XbaI digest of B0015, lane 4: old EcoRI digest of B0015, lane 5: new EcoRI digest of B0015<br/>
 +
 
 +
<li>Based on the results, all enzymes appeared to work, as they successfully created a linearized 3.2 kb fragment.</li>
 +
<div align="center">
 +
<img src="https://static.igem.org/mediawiki/2010/9/93/Yale-enzyme-test.jpg" />
 +
</div>
 +
 
 +
<i>Wetlab work for this day is also recorded on pages 54-57 of the hard copy lab notebook. </i>
 +
</ul>
 +
 
<!------------- Friday ------------->
<!------------- Friday ------------->
</div>
</div>
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<li>
<li>
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Saturday short content
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Saturday 7/10--Transformants from ligation attempts
</li>
</li>
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<a id="link" href="#" onclick="toggle_visibility('saturday'); return false;">See more</a>
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<div style="display:none" id="saturday">
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<a id="link" href="javascript:ReverseDisplay('saturday')">See more/less</a>
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<div style="display:none;" id="saturday">
<!------------- Saturday ------------->
<!------------- Saturday ------------->
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Extra content
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<b> Transformants from ligation attempts #3 an #4</b> <br/>
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<ul>
 +
<li> The plate from ligation attempt #3 shoed in excess of 100 differnt colonies. </li>
 +
<li> Plates from ligation attempt #4 had the following colony counts:</li>
 +
Control-- 5 colonies <br/>
 +
1:1--28 colonies <br/>
 +
2:1--38 colonies <br/>
 +
3:1--18 colonies <br/>
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4:1--27 colonies <br/>
 +
<li>Took colonies from various plates and used them to establish index plates on Amp LB, labeled as follow: eight colonies from triple ligation as #1-#8, four colonies from 1:1 as#9-#12, four colonies from 2:1 as #13-#16, four colonies from 3:1 as #17-#20, and four colonies from 4:1 as #21-#24.</li>
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<i>Wetlab work for this day is also recorded on page 58 of the hard copy lab notebook.</i>
<!------------- Saturday ------------->
<!------------- Saturday ------------->
</div>
</div>
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<li>
<li>
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Sunday short content
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Sunday 7/11--Prep for copper growth assays of transformants
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</li>
</li>
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<a id="link" href="#" onclick="toggle_visibility('sunday'); return false;">See more</a>
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<a id="link" href="javascript:ReverseDisplay('sunday')">See more/less</a>
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<div style="display:none" id="sunday">
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<div style="display:none;" id="sunday">
<!------------- Sunday ------------->
<!------------- Sunday ------------->
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Extra content
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<b>Ligation work </b> <br/>
 +
<ul>
 +
<li> Realize that mistakenly plated triple ligation reaction on ampicillin plate rather than the required chloramphenicol, so none of the colonies present are of value.  Fortunately still have transformation solution, so replate it, this time on a chloramphenicol </li>
 +
<li> Inoculated overnight liquid cultures of ligation attempt #4 transformants  (#9-#24 on index plates) for miniprep the following morning </li>
 +
<b>Growth assay prep work </b> <br/>
 +
<li> Want to see if pSB74 confers any copper resistance on <i>E. coli</i>, since it should help them precipitate nearby copper and thus reduce the copper concentration that they experience. </li>
 +
<li> Inoculated liquid cultures of  LE392 with pSB74 in ampicillin LB and untransformed LE392 in plain LB and left to grow overnight on shaker at 37˚C for growth assays the following day </li>
 +
<li> Prepared CuSO<sub>4</sub> solutions in LB.  Each well in the 96-well plate will have 225 uL of copper solution and 25 uL of cell solution, so the copper solution must have a CuSO<sub>4</sub> concentration that is 10/9 the desired final values. The copper solutions must also contain ampicillin and IPTG at the same levels as the cultures that will be introduced. The desired  CuSO<sub>4</sub> concentrations are those used in the wide and narrow concentration range trials on <a href="https://2010.igem.org/Team:Yale/Our_Project/Notebook"> 6/10 </a> and <a href="https://2010.igem.org/Team:Yale/Our_Project/Notebook/Week_2"> 6/14 </a>. </li>
 +
</ul>
 +
<i>Wetlab work for this day is also recorded on pages 59-61 of the hard copy lab notebook.</i>
<!------------- Sunday ------------->
<!------------- Sunday ------------->
</div>
</div>

Latest revision as of 02:51, 28 October 2010

iGEM Yale

lab notebook: week 5 (7/5 -7/11)

  • Monday 7/5--Colony PCR of Ligation Attempt #2 Transformants
  • See more/less
  • Tuesday 7/6--Analysis of Results of Ligation Attempts 1 & 2
  • See more/less
  • Wednesday 7/7--Triple ligation attempt--promoter + thiosulfate reductase + terminator
  • See more/less
  • Thursday 7/8--Further ligation efforts
  • See more/less
  • Friday 7/9--Ligation attempt #4 to join phsABC and B0015 terminator.
  • See more/less
  • Saturday 7/10--Transformants from ligation attempts
  • See more/less
  • Sunday 7/11--Prep for copper growth assays of transformants
  • See more/less