Team:LZU-China/Notebook

From 2013.igem.org

(Difference between revisions)
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/*** center alone ***/
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     <div class="main-center" id="main-center">
     <div class="main-center" id="main-center">
         <div class="center-left" id="center-left">
         <div class="center-left" id="center-left">
-
         <h1>指导老师</h1>
+
         <a href="#h-events"><h1>Events</h1></a>
-
         <h1>学生</h1>
+
         <a href="#h-mcp"><h1>MCP</h1></a>
 +
            <a href="#h-bc"><h2>Bacteria Culture</h2></a>
 +
            <a href="#h-vp"><h2>Violacein Protocols</h2></a>
 +
            <a href="#h-fap"><h2>FAP</h2></a>
         </div>
         </div>
          
          
         <div class="center-right">
         <div class="center-right">
-
         ==Events==
+
        
-
===July 1-14===
+
<h2> <span class="mw-headline" id="h-events">Events</span></h2>
-
Amplified IκB fragment from the Plasmid of  by Polymerase Chain Reaction(PCR).
+
<h3> <span class="mw-headline" id="July_1-14">July 1-14</span></h3>
 +
<p>Amplified IκB fragment from the Plasmid of  by Polymerase Chain Reaction(PCR).
 +
</p>
 +
<h3> <span class="mw-headline" id="July_15-25">July 15-25</span></h3>
 +
<p>Amplified GFP fragment from the Plasmid of pEGFP-N1 by Polymerase Chain Reaction(PCR).
 +
</p>
 +
<div class="thumb tright"><div class="thumbinner" style="width:182px;"> <div class="thumbcaption">Interchanged</div></div></div>
 +
<h3> <span class="mw-headline" id="July_25-August_1">July 25-August 1</span></h3>
 +
<p>BIT Team's member Zhou Xiaoyu visited our lab. We designed and constructed IκB-GFP fusion fragments together.
 +
</p>
 +
<h3> <span class="mw-headline" id="August_1-15">August 1-15</span></h3>
 +
<p>Used Overlap PCR techniques to build IκB-GFP fusion fragment.
 +
</p>
 +
<div class="thumb tright"><div class="thumbinner" style="width:182px;">  <div class="thumbcaption">Interchanged</div></div></div>
 +
<h3> <span class="mw-headline" id="August_3-4">August 3-4</span></h3>
 +
<p>LZU-China Team member Li Xiaomeng was invited to interchange with the Peking iGEM 2013 Team.
 +
</p>
 +
<div class="thumb tright"><div class="thumbinner" style="width:182px;"><div class="thumbcaption">Interchanged</div></div></div>
 +
<h3> <span class="mw-headline" id="August_4-11_Interchange_and_Helping_BIT">August 4-11 Interchange and Helping BIT </span></h3>
 +
<p>LZU-China Team member Li Xiaomeng was invited to interchange with the BIT iGEM 2013 Team. And help them to characterize and construct a part of Cr sensor.
 +
</p>
-
===July 15-25===
 
-
Amplified GFP fragment from the Plasmid of pEGFP-N1 by Polymerase Chain Reaction(PCR).
 
-
[[Image:LZU_China and BIT team-zhou.png|right|frame|Interchanged]]
 
-
===July 25-August 1===
+
<img src="https://static.igem.org/mediawiki/2013/1/18/IMG_0102.jpg"/>
-
BIT Team's member Zhou Xiaoyu visited our lab. We designed and constructed IκB-GFP fusion fragments together.
+
<img src="https://static.igem.org/mediawiki/2013/1/1e/IMG_6942.jpg"/>
 +
<img src="https://static.igem.org/mediawiki/2013/7/71/IMG_6943.jpg"/>
-
===August 1-15===
 
-
Used Overlap PCR techniques to build IκB-GFP fusion fragment.
 
-
[[Image:LZU_China and Peking team-lxm.png|right|frame|Interchanged]]
 
-
===August 3-4===
 
-
LZU-China Team member Li Xiaomeng was invited to interchange with the Peking iGEM 2013 Team.
 
-
[[Image:LZU_China and BIT team-lxm.png|right|frame|Interchanged]]
 
-
===August 4-11 Interchange and Helping BIT ===
 
-
LZU-China Team member Li Xiaomeng was invited to interchange with the BIT iGEM 2013 Team. And help them to characterize and construct a part of Cr sensor.
 
-
===August 16-30===
+
 
-
The primers synthesized two complementary single stranded DNA with NF-κB binding element. And then combined a completely DNA fragment.
+
<h3> <span class="mw-headline" id="August_16-30">August 16-30</span></h3>
 +
<p>The primers synthesized two complementary single stranded DNA with NF-κB binding element. And then combined a completely DNA fragment.
Used restriction enzymolysis, connection, and transformation to build NF-κB-IκB-GFP fragment.
Used restriction enzymolysis, connection, and transformation to build NF-κB-IκB-GFP fragment.
-
 
+
</p>
-
===September 1-16===
+
<h3> <span class="mw-headline" id="September_1-16">September 1-16</span></h3>
-
Put our part into the backbone with the BioBrick prefix and suffix. And sequenced the Plasmid which will be shipped to iGEM.
+
<p>Put our part into the backbone with the BioBrick prefix and suffix. And sequenced the Plasmid which will be shipped to iGEM.
-
 
+
</p><p><br />
-
 
+
</p>
-
 
+
<h2> <span class="mw-headline" id="h-mcp">Molecular Cloning Protocols</span></h2>
-
==Molecular Cloning Protocols==
+
<h3> <span class="mw-headline" id="Digestion">Digestion</span></h3>
-
===Digestion===
+
<h4> <span class="mw-headline" id="Material">Material</span></h4>
-
====Material====
+
<ul><li>EcoRI, BglII, PstI, XhoI, SpeI,XhoI,FD buffer,FD Green buffer, DNA,sterile water
-
*EcoRI, BglII, PstI, XhoI, SpeI,XhoI,FD buffer,FD Green buffer, DNA,sterile water
+
</li></ul>
-
 
+
<h4> <span class="mw-headline" id="Digestion_temperature">Digestion temperature</span></h4>
-
====Digestion temperature====
+
<ul><li>37℃
-
*37℃
+
</li></ul>
-
 
+
<h4> <span class="mw-headline" id="Time_period">Time period</span></h4>
-
====Time period====
+
<ol><li>Plasmid: 10-30min(the higher the concentration, the longer time it takes.
-
#Plasmid: 10-30min(the higher the concentration, the longer time it takes.
+
</li><li>DNA fragment:1-2h(the higher the concentration, the longer time it takes.Since it is more difficult to digest DNA than plasmid, digesting DNA requires more time.
-
#DNA fragment:1-2h(the higher the concentration, the longer time it takes.Since it is more difficult to digest DNA than plasmid, digesting DNA requires more time.
+
</li></ol>
-
 
+
<h4> <span class="mw-headline" id="System_amount">System amount</span></h4>
-
====System amount====
+
<ol><li>50ul system is preferred if there is subsequent operations. If digestion is only for identification, 20ul system is used.  
-
#50ul system is preferred if there is subsequent operations. If digestion is only for identification, 20ul system is used.  
+
</li><li>During the double digestion, the optimum buffer system which is suitable for both enzymes should be utilized. Without such shared system, digestion of two different enzymes is usually separated.  
-
#During the double digestion, the optimum buffer system which is suitable for both enzymes should be utilized. Without such shared system, digestion of two different enzymes is usually separated.  
+
</li></ol>
-
 
+
<h4> <span class="mw-headline" id="System">System</span></h4>
-
====System====
+
<dl><dd><dl><dd><dl><dd><table border="1">
-
 
+
<tr>
-
:::{|border=1
+
<td width="200">Enzyme
-
|width="200"|Enzyme
+
</td><td width="150">1μl
-
|width="150"|1μl
+
</td></tr>
-
|-
+
<tr>
-
|10×FD Buffer or FD Green buffer||2μl
+
<td>10×FD Buffer or FD Green buffer</td><td>2μl
-
|-
+
</td></tr>
-
|DNA ||≤1μg
+
<tr>
-
|-
+
<td>DNA </td><td>≤1μg
-
|Sterile water||up to 20μl
+
</td></tr>
-
|}
+
<tr>
-
 
+
<td>Sterile water</td><td>up to 20μl
-
===Gel extraction===
+
</td></tr></table></dd></dl></dd></dl></dd></dl>
-
 
+
<h3> <span class="mw-headline" id="Gel_extraction">Gel extraction</span></h3>
-
====Material====
+
<h4> <span class="mw-headline" id="Material_2">Material</span></h4>
-
*Agarose Gel DNA Extraction Kit (centrifugation)
+
<ul><li>Agarose Gel DNA Extraction Kit (centrifugation)
-
 
+
</li></ul>
-
====Experimental Procedure====
+
<h4> <span class="mw-headline" id="Experimental_Procedure">Experimental Procedure</span></h4>
-
#Add 500uL balance liquid(BL) to the spin column(CA2). Centrifuge at 12,000 x g for 1 min at room temperature. Discard the flow-through and put the column back to the collection tube.(optional)
+
<ol><li>Add 500uL balance liquid(BL) to the spin column(CA2). Centrifuge at 12,000 x g for 1 min at room temperature. Discard the flow-through and put the column back to the collection tube.(optional)
-
#Excise the DNA fragment from the agarose gel and weigh it in a clean centrifuge tube (A gel slice of 100 mg approximately equals to 100 μL).
+
</li><li>Excise the DNA fragment from the agarose gel and weigh it in a clean centrifuge tube (A gel slice of 100 mg approximately equals to 100 µL).
-
#Add 3 volume of sol solution(PN) to the centrifuge tube and incubate the mixture at 50℃ for 10 min with mixing the tube by tapping the bottom of the tube occationally till the gel has melted completely. Cool the tube to RT.
+
</li><li>Add 3 volume of sol solution(PN) to the centrifuge tube and incubate the mixture at 50℃ for 10 min with mixing the tube by tapping the bottom of the tube occationally till the gel has melted completely. Cool the tube to RT.
-
#Transfer the mixture to an spin column (CA2) within a collection tube. Centrifuge at 12,000 x g for 1 min at room temperature. Discard the flow-through and put the column back to the collection tube.
+
</li><li>Transfer the mixture to an spin column (CA2) within a collection tube. Centrifuge at 12,000 x g for 1 min at room temperature. Discard the flow-through and put the column back to the collection tube.
-
#Add 600 μL DNA Wash Buffer (PW) to the column and centrifuge at 12,000 x g for 1 min at room temperature. Discard the flow through and put the column back to the collection tube.
+
</li><li>Add 600 µL DNA Wash Buffer (PW) to the column and centrifuge at 12,000 x g for 1 min at room temperature. Discard the flow through and put the column back to the collection tube.
-
#Repeat step 5.
+
</li><li>Repeat step 5.
-
#Put the column back to the collection tube. Centrifuge at 12,000 x g for 2 min at room temperature to discard the PW totally. Keep the lid open for several minutes.
+
</li><li>Put the column back to the collection tube. Centrifuge at 12,000 x g for 2 min at room temperature to discard the PW totally. Keep the lid open for several minutes.
-
#Put the column back to the clean collection tube. Add ddH2O to the column vacantly and keep it at room temperature for 2 minutes. Centrifuge at 12,000 x g for 2 min at room temperature to collect the DNA solution.
+
</li><li>Put the column back to the clean collection tube. Add ddH2O to the column vacantly and keep it at room temperature for 2 minutes. Centrifuge at 12,000 x g for 2 min at room temperature to collect the DNA solution.
-
#Transfer the eluted solution to CA2 and keep it at room temperature for 2minutes. Centrifuge at 12,000 x g for 2 min at room temperature.  
+
</li><li>Transfer the eluted solution to CA2 and keep it at room temperature for 2minutes. Centrifuge at 12,000 x g for 2 min at room temperature.  
-
#Gel electrophoresis to verify the correctness and concentration of bands.
+
</li><li>Gel electrophoresis to verify the correctness and concentration of bands.
-
 
+
</li></ol>
-
====Important Notes====
+
<h4> <span class="mw-headline" id="Important_Notes">Important Notes</span></h4>
-
#If the balance liquid turns turbid, incubate it at 37℃ for several minutes.  
+
<ol><li>If the balance liquid turns turbid, incubate it at 37℃ for several minutes.  
-
#When cutting the gel, keep the UV irradiation time period as short as possible, otherwise DNA would be damaged.
+
</li><li>When cutting the gel, keep the UV irradiation time period as short as possible, otherwise DNA would be damaged.
-
#For those DNA fragment shorter than 100bp or larger than 10kb, the sol solution volume should be increased as well as the time period for adsorption and elution.  
+
</li><li>For those DNA fragment shorter than 100bp or larger than 10kb, the sol solution volume should be increased as well as the time period for adsorption and elution.  
-
#Recovery depends on the initial DNA amount and elution volume. The less the DNA, the less the elution volume, the smaller of recovery.
+
</li><li>Recovery depends on the initial DNA amount and elution volume. The less the DNA, the less the elution volume, the smaller of recovery.
-
 
+
</li></ol>
-
===PCR===
+
<h3> <span class="mw-headline" id="PCR">PCR</span></h3>
-
====Reagents====
+
<h4> <span class="mw-headline" id="Reagents">Reagents</span></h4>
-
*KOD-Plus-Neo
+
<ul><li>KOD-Plus-Neo
-
*Tap enzymes
+
</li><li>Tap enzymes
-
 
+
</li></ul>
-
====Experiment system====
+
<h4> <span class="mw-headline" id="Experiment_system">Experiment system</span></h4>
-
*Experiment system with KOD enzymes (Mostly 50uL)
+
<ul><li>Experiment system with KOD enzymes (Mostly 50uL)
-
 
+
</li></ul>
-
*Experiment system with taq enzymes:  
+
<ul><li>Experiment system with taq enzymes:  
-
 
+
</li></ul>
-
*Reaction temperature:
+
<ul><li>Reaction temperature:
-
        Two-step method:
+
</li></ul>
-
        Predenature
+
<pre>        Two-step method:
-
          94℃,2min
+
        Predenature
-
        Denature and extension
+
          94℃,2min
-
          {
+
        Denature and extension
-
          98℃ 10sec
+
-
          68℃ 30sec/kb
+
-
          }
+
-
                        &times; 25-45 cycles
+
-
          4℃
+
-
----
+
-
        Three-step method:
+
-
        Predenature
+
-
          94℃,2min
+
-
        Denature,annealing and extension
+
-
          98℃ 10sec 
+
           {
           {
-
           (Tm-5)℃  30sec
+
           98℃ 10sec
-
          68℃ 30sec/kb
+
          68℃ 30sec/kb
-
          }
+
          }
                         &times; 25-45 cycles
                         &times; 25-45 cycles
-
          4℃
+
          4℃
-
 
+
</pre>
-
====Important Notes====
+
<hr />
-
#KOD enzymes should be operated in ice.
+
<pre>        Three-step method:
-
#Two-step method is preferred if primer Tm is relatively high.  
+
        Predenature
-
#1.2% agarose gel is used to separate 1kb-5kb DNA; 0.8% agarose gel is used to separate 3k-10k DNA; 2.5-3% agarose gel is used to separate DNA longer than 100bp.  
+
          94℃,2min
-
#PCR reaction system varies from 20uL to 100uL. Under most cases, 20uL system is preferred as long as PCR is for identification only. However, when subsequent experiments such as tailing, digestion which require certain amount of DNA are necessary, 50uL system is usually preferred.  
+
        Denature,annealing and extension
-
#KOD enzymes are preferred if the purpose of PCR is for gene amplification. At the same time, PCR for identification or tailing usually requires taq enzymes.
+
          98℃ 10sec 
-
 
+
        {
-
===PCR Purification===
+
        (Tm-5)℃  30sec
-
====Reagents====
+
          68℃  30sec/kb
-
*LifeFeng DNA PCR purification kit
+
          }
-
====Experimental Procedure====
+
                      &times; 25-45 cycles
-
#Transfer PCR system (< 250uL)  to 1.5mL microcentrifuge tube. Add 5 volume Buffer PD and mix. Have a quick centrifugation to remove the liquid on lid.  
+
          4℃
-
#Transfer the mixture to DNA spin column (A4) and put it in a collection tube.  
+
</pre>
-
#Centrifuge at 7000g for 1 minute and replace the collection tube with a new collection tube.  
+
<h4> <span class="mw-headline" id="Important_Notes_2">Important Notes</span></h4>
-
#To wash, add 500uL Buffer WB to the spin column (A4) and centrifuge at 7000g for 1 minute. Discard the flow-through and place the column back in the same tube.  
+
<ol><li>KOD enzymes should be operated in ice.
-
#Repeat step 4.
+
</li><li>Two-step method is preferred if primer Tm is relatively high.  
-
#Centrifuge at 12,000g for 2 minutes.
+
</li><li>1.2% agarose gel is used to separate 1kb-5kb DNA; 0.8% agarose gel is used to separate 3k-10k DNA; 2.5-3% agarose gel is used to separate DNA longer than 100bp.  
-
#Place spin column in a clean 1.5 ml microcentrifuge tube.
+
</li><li>PCR reaction system varies from 20uL to 100uL. Under most cases, 20uL system is preferred as long as PCR is for identification only. However, when subsequent experiments such as tailing, digestion which require certain amount of DNA are necessary, 50uL system is usually preferred.  
-
#To elute DNA, add ddwater (>30uL) to the center of the membrane. Let the column stand for 1-2 min and centrifuge the column for 1 min at 12,000g.  
+
</li><li>KOD enzymes are preferred if the purpose of PCR is for gene amplification. At the same time, PCR for identification or tailing usually requires taq enzymes.
-
#Add elution liquid back to spin column and centrifuge at 12,000g for 1 min. ( Inoculating ddwater at 65℃ prior would improve the elution efficiency )
+
</li></ol>
-
#Gel electrophoresis to verify the concentration of bands.  
+
<h3> <span class="mw-headline" id="PCR_Purification">PCR Purification</span></h3>
-
====Important Notes====
+
<h4> <span class="mw-headline" id="Reagents_2">Reagents</span></h4>
-
*Buffer PD contains irritant compounds, thus be careful not to avoid contamination of skin.
+
<ul><li>LifeFeng DNA PCR purification kit
-
 
+
</li></ul>
-
===DNA Ligation===
+
<h4> <span class="mw-headline" id="Experimental_Procedure_2">Experimental Procedure</span></h4>
-
====Experimental Procedures====
+
<ol><li>Transfer PCR system (&lt; 250uL)  to 1.5mL microcentrifuge tube. Add 5 volume Buffer PD and mix. Have a quick centrifugation to remove the liquid on lid.  
-
#Set up the following reaction in a microcentrifuge tube on ice.
+
</li><li>Transfer the mixture to DNA spin column (A4) and put it in a collection tube.  
-
#Gently mix the reaction by pipetting up and down and microfuge briefly.
+
</li><li>Centrifuge at 7000g for 1 minute and replace the collection tube with a new collection tube.  
-
#For cohesive (sticky) ends, incubate at 16°C overnight or room temperature for 10 minutes.
+
</li><li>To wash, add 500uL Buffer WB to the spin column (A4) and centrifuge at 7000g for 1 minute. Discard the flow-through and place the column back in the same tube.  
-
#For blunt ends or single base overhangs, incubate at 16°C overnight or room temperature for 2 hours  
+
</li><li>Repeat step 4.
-
#Chill on ice and transform 1-5 μl of the reaction into 50 μl competent cells.
+
</li><li>Centrifuge at 12,000g for 2 minutes.
-
====Ligation System====
+
</li><li>Place spin column in a clean 1.5 ml microcentrifuge tube.
-
:::{| border=1  
+
</li><li>To elute DNA, add ddwater (&gt;30uL) to the center of the membrane. Let the column stand for 1-2 min and centrifuge the column for 1 min at 12,000g.  
-
|width="200"| COMPONENT
+
</li><li>Add elution liquid back to spin column and centrifuge at 12,000g for 1 min. ( Inoculating ddwater at 65℃ prior would improve the elution efficiency )
-
|width="100"| 20 μl REACTION
+
</li><li>Gel electrophoresis to verify the concentration of bands.  
-
|-
+
</li></ol>
-
| 10X T4 DNA Ligase Buffer
+
<h4> <span class="mw-headline" id="Important_Notes_3">Important Notes</span></h4>
-
| 2 μl
+
<ul><li>Buffer PD contains irritant compounds, thus be careful not to avoid contamination of skin.
-
|-
+
</li></ul>
-
| Vector DNA  
+
<h3> <span class="mw-headline" id="DNA_Ligation">DNA Ligation</span></h3>
-
| 0.025 pmol
+
<h4> <span class="mw-headline" id="Experimental_Procedures">Experimental Procedures</span></h4>
-
|-
+
<ol><li>Set up the following reaction in a microcentrifuge tube on ice.
-
| Insert DNA
+
</li><li>Gently mix the reaction by pipetting up and down and microfuge briefly.
-
| 0.076 pmol
+
</li><li>For cohesive (sticky) ends, incubate at 16°C overnight or room temperature for 10 minutes.
-
|-
+
</li><li>For blunt ends or single base overhangs, incubate at 16°C overnight or room temperature for 2 hours  
-
| T4 DNA Ligase
+
</li><li>Chill on ice and transform 1-5 μl of the reaction into 50 μl competent cells.
-
| 1μl
+
</li></ol>
-
|-
+
<h4> <span class="mw-headline" id="Ligation_System">Ligation System</span></h4>
-
| Nuclease-free water
+
<dl><dd><dl><dd><dl><dd><table border="1">
-
| to 20 μl
+
<tr>
-
|}
+
<td width="200"> COMPONENT
-
 
+
</td><td width="100"> 20 μl REACTION
-
 
+
</td></tr>
-
== Bacteria Culture ==
+
<tr>
-
===Strain===
+
<td> 10X T4 DNA Ligase Buffer
-
 
+
</td><td> 2 μl
-
#DH5a (F- endA1 glnV44 thi-1 recA1 relA1 gyrA96 deoR nupG Φ80dlacZΔM15 Δ(lacZYA-argF)U169, hsdR17(rK- mK+), λ–)use for cloning
+
</td></tr>
-
#BL21(DE3) (fhuA2 [lon] ompT gal (λ DE3) [dcm] ?hsdS,λ DE3 = λ sBamHIo ?EcoRI-B int::(lacI::PlacUV5::T7 gene1) i21 ?nin5) use for expressing
+
<tr>
-
 
+
<td> Vector DNA
-
===Medium===
+
</td><td> 0.025 pmol
-
====LB Medium====
+
</td></tr>
-
:::{|border=1
+
<tr>
-
|width="100"|NaCl
+
<td> Insert DNA
-
|width="150"|10g
+
</td><td> 0.076 pmol
-
|-
+
</td></tr>
-
|Tryptone
+
<tr>
-
|10g
+
<td> T4 DNA Ligase
-
|-
+
</td><td> 1μl
-
|Yeast Extract
+
</td></tr>
-
|5 g
+
<tr>
-
|-
+
<td> Nuclease-free water
-
|Water
+
</td><td> to 20 μl
-
|up to 1000mL
+
</td></tr></table></dd></dl></dd></dl></dd></dl>
-
|}
+
<p><br />
-
 
+
</p>
-
====SOB Medium====
+
<h2> <span class="mw-headline" id="h-bc"> Bacteria Culture </span></h2>
-
:::{|border=1
+
<h3> <span class="mw-headline" id="Strain">Strain</span></h3>
-
|width="100"|Tryptone
+
<ol><li>DH5a (F- endA1 glnV44 thi-1 recA1 relA1 gyrA96 deoR nupG Φ80dlacZΔM15 Δ(lacZYA-argF)U169, hsdR17(rK- mK+), λ–)use for cloning
-
|width="150"|20g
+
</li><li>BL21(DE3) (fhuA2 [lon] ompT gal (λ DE3) [dcm] ∆hsdS,λ DE3 = λ sBamHIo ∆EcoRI-B int::(lacI::PlacUV5::T7 gene1) i21 ∆nin5) use for expressing
-
|-
+
</li></ol>
-
|Yeast extract
+
<h3> <span class="mw-headline" id="Medium">Medium</span></h3>
-
|5g
+
<h4> <span class="mw-headline" id="LB_Medium">LB Medium</span></h4>
-
|-
+
<dl><dd><dl><dd><dl><dd><table border="1">
-
|NaCl
+
<tr>
-
|0.5g
+
<td width="100">NaCl
-
|-
+
</td><td width="150">10g
-
|1M KCl
+
</td></tr>
-
|2.5ml
+
<tr>
-
|-
+
<td>Tryptone
-
|ddH2O
+
</td><td>10g
-
|up to 1000 ml
+
</td></tr>
-
|}
+
<tr>
-
::Adjust pH to 7.0 with 10N NaOH, autoclave to sterilize, and add 10 ml of 1 M MgCl2 before use
+
<td>Yeast Extract
-
 
+
</td><td>5 g
-
===Antibiotics===
+
</td></tr>
-
:::{|border=1
+
<tr>
-
|width="70"|
+
-
|width="150"| Storage
+
-
|width="100"|Use
+
-
|-
+
-
|width="70"|Kana
+
-
|width="150"|50 mg/ml(Water)
+
-
|50 μg/ml
+
-
|-
+
-
|Amp||50 mg/ml(Water)||50 μg/ml
+
-
|-
+
-
|Tet||10 mg/ml (Alcohol)||10 μg/ml
+
-
|-
+
-
|Cm||34 mg/ml (Alcohol)||68 μg/ml
+
-
|}
+
-
 
+
-
 
+
-
===Transformation===
+
-
 
+
-
#Remove competent cells from freezer and allow to thaw
+
-
#Add 3-5 μl of DNA to the cells
+
-
#Incubate on ice for 30 min
+
-
#Heat shock the cells at 37°C for 1.5 mins
+
-
#Add 500 μl of SOB medium, and incubate in a shaker at 37°C for 1 hour
+
-
#Centrifuge for 3 min at 3,000 g, remove and keep 100 μl of the supernatant, and pour away the rest
+
-
#Re-suspend the pellet in the 100 μl of supernatant that was removed earlier
+
-
#Spread All onto one plate with corresponding antibotics, and then pour the rest onto another. Incubate the plates overnight at 37°C.
+
-
 
+
-
==Violacein Protocols==
+
-
===Induction and Extraction===
+
-
#Incubate the monoclonal from medium in a shaker at 37°C overnight
+
-
#Add 0.1% Arabinose, 1mM Ferrous ammonium sulfate and 40 μM to start induction for another 6 hours
+
-
#Centrifuge for 1 min at 10000rpm, remove the LB Medium
+
-
#Add 800 μL 10%SDS and break cells using ultrasound
+
-
#Add 800 μL ethyl acetate to extract violacein/deoxyviolacein
+
-
#Use rotovap to concentrate violacein and resuspend with methanol
+
-
 
+
-
===HPLC===
+
-
*Column: C18, 15cm
+
-
 
+
-
*Mobile phase: 75% methanol, 25% ddH2O
+
-
 
+
-
*Injection volume: 20 μL
+
-
 
+
-
*Speed: 0.5 mL/min
+
-
 
+
-
*Detection: 230 nm
+
-
 
+
-
 
+
-
 
+
-
==Fatty Acid Protocols==
+
-
 
+
-
#Transfer a fresh transformed colony to 5ml LB liquid medium and shake at 37℃ overnight(12h).
+
-
#Add seed broth to 50-100ml LB medium(volume ratio is 3% and loaded liquid is 20%) and shake until the OD600 reaches 0.6 or so. Add inducer of appropriate concentration to induce gene expression.
+
-
#Continue shake culture for another 20h. Contrifuge at 8,000 for 5min. Collect supernatant and bacteria sediment respectively (prepare 3 parallel samples, each 10ml).
+
-
#Extract the supernatant by chloroform-methanol(2:1) solution of the same volume (shake for 5min) place until stratification. Dry the lower organic layer at 50℃ for about 24h. Suspend the bacteria by 1ml ddH2O. Add 20ml chloroform-methanol solution and extract for another 2 times.(Attention: weigh the empty flask before drying).
+
-
#Weigh the crude extract and record the results. (For reference only)
+
-
#Dissolve the crude extract with 1ml methanol and add 2ml tetrafluoroboron. Methyl esterificate at 60℃ for 30min. After the reagent cools down, add 2ml N-hexane and extract for 2 times. Collect the upper layer and dry overnight at 50℃ (weigh the empty flask before drying as well).
+
-
#Add the crude bacteria extract to 1ml chloroform-methanol(2:1) solution and shake by vortex to extract the total lipid of the cells. Add 2ml methanol-water(4:1) as saponification reagent. Saponificate in 60℃ water bath for 1h. Then esterificate as the 6th step.
+
-
#Dissolve the obtained fatty acidmethyl ester(FAME)mixture with N-hexane(2mg/ml). Take 1ml sample for test.
+
-
#GC-MS condition:
+
-
::Sample injector temperature: 250℃;
+
-
::Detector temperature: 280℃;
+
-
::Temperature programming: begin at 100℃ and last 2min. Warm to 250℃ at the rate of 10℃/min and last 5min.
+
-
::Use C15 FAME as the interior label for quantification. (Quantity of C15 FAME depends on the sample concentration)
+
 +
<td>Water
 +
</td><td>up to 1000mL
 +
</td></tr></table></dd></dl></dd></dl></dd></dl>
 +
<h4> <span class="mw-headline" id="SOB_Medium">SOB Medium</span></h4>
 +
<dl><dd><dl><dd><dl><dd><table border="1">
 +
<tr>
 +
<td width="100">Tryptone
 +
</td><td width="150">20g
 +
</td></tr>
 +
<tr>
 +
<td>Yeast extract
 +
</td><td>5g
 +
</td></tr>
 +
<tr>
 +
<td>NaCl
 +
</td><td>0.5g
 +
</td></tr>
 +
<tr>
 +
<td>1M KCl
 +
</td><td>2.5ml
 +
</td></tr>
 +
<tr>
 +
<td>ddH2O
 +
</td><td>up to 1000 ml
 +
</td></tr></table></dd></dl></dd></dl></dd></dl>
 +
<dl><dd><dl><dd>Adjust pH to 7.0 with 10N NaOH, autoclave to sterilize, and add 10 ml of 1 M MgCl2 before use
 +
</dd></dl>
 +
</dd></dl>
 +
<h3> <span class="mw-headline" id="Antibiotics">Antibiotics</span></h3>
 +
<dl><dd><dl><dd><dl><dd><table border="1">
 +
<tr>
 +
<td width="70">
 +
</td><td width="150"> Storage
 +
</td><td width="100">Use
 +
</td></tr>
 +
<tr>
 +
<td width="70">Kana
 +
</td><td width="150">50 mg/ml(Water)
 +
</td><td>50 μg/ml
 +
</td></tr>
 +
<tr>
 +
<td>Amp</td><td>50 mg/ml(Water)</td><td>50 μg/ml
 +
</td></tr>
 +
<tr>
 +
<td>Tet</td><td>10 mg/ml (Alcohol)</td><td>10 μg/ml
 +
</td></tr>
 +
<tr>
 +
<td>Cm</td><td>34 mg/ml (Alcohol)</td><td>68 μg/ml
 +
</td></tr></table></dd></dl></dd></dl></dd></dl>
 +
<p><br />
 +
</p>
 +
<h3> <span class="mw-headline" id="Transformation">Transformation</span></h3>
 +
<ol><li>Remove competent cells from freezer and allow to thaw
 +
</li><li>Add 3-5 μl of DNA to the cells
 +
</li><li>Incubate on ice for 30 min
 +
</li><li>Heat shock the cells at 37°C for 1.5 mins
 +
</li><li>Add 500 μl of SOB medium, and incubate in a shaker at 37°C for 1 hour
 +
</li><li>Centrifuge for 3 min at 3,000 g, remove and keep 100 μl of the supernatant, and pour away the rest
 +
</li><li>Re-suspend the pellet in the 100 μl of supernatant that was removed earlier
 +
</li><li>Spread All onto one plate with corresponding antibotics, and then pour the rest onto another. Incubate the plates overnight at 37°C.
 +
</li></ol>
 +
<h2> <span class="mw-headline" id="h-vp">Violacein Protocols</span></h2>
 +
<h3> <span class="mw-headline" id="Induction_and_Extraction">Induction and Extraction</span></h3>
 +
<ol><li>Incubate the monoclonal from medium in a shaker at 37°C overnight
 +
</li><li>Add 0.1% Arabinose, 1mM Ferrous ammonium sulfate and 40 μM to start induction for another 6 hours
 +
</li><li>Centrifuge for 1 min at 10000rpm, remove the LB Medium
 +
</li><li>Add 800 μL 10%SDS and break cells using ultrasound
 +
</li><li>Add 800 μL ethyl acetate to extract violacein/deoxyviolacein
 +
</li><li>Use rotovap to concentrate violacein and resuspend with methanol
 +
</li></ol>
 +
<h3> <span class="mw-headline" id="HPLC">HPLC</span></h3>
 +
<ul><li>Column: C18, 15cm
 +
</li></ul>
 +
<ul><li>Mobile phase: 75% methanol, 25% ddH2O
 +
</li></ul>
 +
<ul><li>Injection volume: 20 μL
 +
</li></ul>
 +
<ul><li>Speed: 0.5 mL/min
 +
</li></ul>
 +
<ul><li>Detection: 230 nm
 +
</li></ul>
 +
<p><br />
 +
</p>
 +
<h2> <span class="mw-headline" id="h-fap">Fatty Acid Protocols</span></h2>
 +
<ol><li>Transfer a fresh transformed colony to 5ml LB liquid medium and shake at 37℃ overnight(12h).
 +
</li><li>Add seed broth to 50-100ml LB medium(volume ratio is 3% and loaded liquid is 20%) and shake until the OD600 reaches 0.6 or so. Add inducer of appropriate concentration to induce gene expression.
 +
</li><li>Continue shake culture for another 20h. Contrifuge at 8,000 for 5min. Collect supernatant and bacteria sediment respectively (prepare 3 parallel samples, each 10ml).
 +
</li><li>Extract the supernatant by chloroform-methanol(2:1) solution of the same volume (shake for 5min) place until stratification. Dry the lower organic layer at 50℃ for about 24h. Suspend the bacteria by 1ml ddH2O. Add 20ml chloroform-methanol solution and extract for another 2 times.(Attention: weigh the empty flask before drying).
 +
</li><li>Weigh the crude extract and record the results. (For reference only)
 +
</li><li>Dissolve the crude extract with 1ml methanol and add 2ml tetrafluoroboron. Methyl esterificate at 60℃ for 30min. After the reagent cools down, add 2ml N-hexane and extract for 2 times. Collect the upper layer and dry overnight at 50℃ (weigh the empty flask before drying as well).
 +
</li><li>Add the crude bacteria extract to 1ml chloroform-methanol(2:1) solution and shake by vortex to extract the total lipid of the cells. Add 2ml methanol-water(4:1) as saponification reagent. Saponificate in 60℃ water bath for 1h. Then esterificate as the 6th step.
 +
</li><li>Dissolve the obtained fatty acidmethyl ester(FAME)mixture with N-hexane(2mg/ml). Take 1ml sample for test.
 +
</li><li>GC-MS condition:
 +
</li></ol>
 +
<dl><dd><dl><dd>Sample injector temperature: 250℃;
 +
</dd><dd>Detector temperature: 280℃;
 +
</dd><dd>Temperature programming: begin at 100℃ and last 2min. Warm to 250℃ at the rate of 10℃/min and last 5min.
 +
</dd><dd>Use C15 FAME as the interior label for quantification. (Quantity of C15 FAME depends on the sample concentration)
 +
</dd></dl>
 +
</dd></dl>
         </div>
         </div>
     </div>
     </div>

Revision as of 13:01, 27 September 2013

progect

Events

July 1-14

Amplified IκB fragment from the Plasmid of by Polymerase Chain Reaction(PCR).

July 15-25

Amplified GFP fragment from the Plasmid of pEGFP-N1 by Polymerase Chain Reaction(PCR).

Interchanged

July 25-August 1

BIT Team's member Zhou Xiaoyu visited our lab. We designed and constructed IκB-GFP fusion fragments together.

August 1-15

Used Overlap PCR techniques to build IκB-GFP fusion fragment.

Interchanged

August 3-4

LZU-China Team member Li Xiaomeng was invited to interchange with the Peking iGEM 2013 Team.

Interchanged

August 4-11 Interchange and Helping BIT

LZU-China Team member Li Xiaomeng was invited to interchange with the BIT iGEM 2013 Team. And help them to characterize and construct a part of Cr sensor.

August 16-30

The primers synthesized two complementary single stranded DNA with NF-κB binding element. And then combined a completely DNA fragment. Used restriction enzymolysis, connection, and transformation to build NF-κB-IκB-GFP fragment.

September 1-16

Put our part into the backbone with the BioBrick prefix and suffix. And sequenced the Plasmid which will be shipped to iGEM.


Molecular Cloning Protocols

Digestion

Material

  • EcoRI, BglII, PstI, XhoI, SpeI,XhoI,FD buffer,FD Green buffer, DNA,sterile water

Digestion temperature

  • 37℃

Time period

  1. Plasmid: 10-30min(the higher the concentration, the longer time it takes.
  2. DNA fragment:1-2h(the higher the concentration, the longer time it takes.Since it is more difficult to digest DNA than plasmid, digesting DNA requires more time.

System amount

  1. 50ul system is preferred if there is subsequent operations. If digestion is only for identification, 20ul system is used.
  2. During the double digestion, the optimum buffer system which is suitable for both enzymes should be utilized. Without such shared system, digestion of two different enzymes is usually separated.

System

Enzyme 1μl
10×FD Buffer or FD Green buffer2μl
DNA ≤1μg
Sterile waterup to 20μl

Gel extraction

Material

  • Agarose Gel DNA Extraction Kit (centrifugation)

Experimental Procedure

  1. Add 500uL balance liquid(BL) to the spin column(CA2). Centrifuge at 12,000 x g for 1 min at room temperature. Discard the flow-through and put the column back to the collection tube.(optional)
  2. Excise the DNA fragment from the agarose gel and weigh it in a clean centrifuge tube (A gel slice of 100 mg approximately equals to 100 µL).
  3. Add 3 volume of sol solution(PN) to the centrifuge tube and incubate the mixture at 50℃ for 10 min with mixing the tube by tapping the bottom of the tube occationally till the gel has melted completely. Cool the tube to RT.
  4. Transfer the mixture to an spin column (CA2) within a collection tube. Centrifuge at 12,000 x g for 1 min at room temperature. Discard the flow-through and put the column back to the collection tube.
  5. Add 600 µL DNA Wash Buffer (PW) to the column and centrifuge at 12,000 x g for 1 min at room temperature. Discard the flow through and put the column back to the collection tube.
  6. Repeat step 5.
  7. Put the column back to the collection tube. Centrifuge at 12,000 x g for 2 min at room temperature to discard the PW totally. Keep the lid open for several minutes.
  8. Put the column back to the clean collection tube. Add ddH2O to the column vacantly and keep it at room temperature for 2 minutes. Centrifuge at 12,000 x g for 2 min at room temperature to collect the DNA solution.
  9. Transfer the eluted solution to CA2 and keep it at room temperature for 2minutes. Centrifuge at 12,000 x g for 2 min at room temperature.
  10. Gel electrophoresis to verify the correctness and concentration of bands.

Important Notes

  1. If the balance liquid turns turbid, incubate it at 37℃ for several minutes.
  2. When cutting the gel, keep the UV irradiation time period as short as possible, otherwise DNA would be damaged.
  3. For those DNA fragment shorter than 100bp or larger than 10kb, the sol solution volume should be increased as well as the time period for adsorption and elution.
  4. Recovery depends on the initial DNA amount and elution volume. The less the DNA, the less the elution volume, the smaller of recovery.

PCR

Reagents

  • KOD-Plus-Neo
  • Tap enzymes

Experiment system

  • Experiment system with KOD enzymes (Mostly 50uL)
  • Experiment system with taq enzymes:
  • Reaction temperature:
        Two-step method:
        Predenature
          94℃,2min
        Denature and extension
          {
          98℃ 10sec 
          68℃ 30sec/kb
          }
                        × 25-45 cycles
          4℃

        Three-step method:
        Predenature
          94℃,2min
        Denature,annealing and extension
          98℃ 10sec   
         {
         (Tm-5)℃  30sec
          68℃  30sec/kb
          }
                       × 25-45 cycles
          4℃

Important Notes

  1. KOD enzymes should be operated in ice.
  2. Two-step method is preferred if primer Tm is relatively high.
  3. 1.2% agarose gel is used to separate 1kb-5kb DNA; 0.8% agarose gel is used to separate 3k-10k DNA; 2.5-3% agarose gel is used to separate DNA longer than 100bp.
  4. PCR reaction system varies from 20uL to 100uL. Under most cases, 20uL system is preferred as long as PCR is for identification only. However, when subsequent experiments such as tailing, digestion which require certain amount of DNA are necessary, 50uL system is usually preferred.
  5. KOD enzymes are preferred if the purpose of PCR is for gene amplification. At the same time, PCR for identification or tailing usually requires taq enzymes.

PCR Purification

Reagents

  • LifeFeng DNA PCR purification kit

Experimental Procedure

  1. Transfer PCR system (< 250uL) to 1.5mL microcentrifuge tube. Add 5 volume Buffer PD and mix. Have a quick centrifugation to remove the liquid on lid.
  2. Transfer the mixture to DNA spin column (A4) and put it in a collection tube.
  3. Centrifuge at 7000g for 1 minute and replace the collection tube with a new collection tube.
  4. To wash, add 500uL Buffer WB to the spin column (A4) and centrifuge at 7000g for 1 minute. Discard the flow-through and place the column back in the same tube.
  5. Repeat step 4.
  6. Centrifuge at 12,000g for 2 minutes.
  7. Place spin column in a clean 1.5 ml microcentrifuge tube.
  8. To elute DNA, add ddwater (>30uL) to the center of the membrane. Let the column stand for 1-2 min and centrifuge the column for 1 min at 12,000g.
  9. Add elution liquid back to spin column and centrifuge at 12,000g for 1 min. ( Inoculating ddwater at 65℃ prior would improve the elution efficiency )
  10. Gel electrophoresis to verify the concentration of bands.

Important Notes

  • Buffer PD contains irritant compounds, thus be careful not to avoid contamination of skin.

DNA Ligation

Experimental Procedures

  1. Set up the following reaction in a microcentrifuge tube on ice.
  2. Gently mix the reaction by pipetting up and down and microfuge briefly.
  3. For cohesive (sticky) ends, incubate at 16°C overnight or room temperature for 10 minutes.
  4. For blunt ends or single base overhangs, incubate at 16°C overnight or room temperature for 2 hours
  5. Chill on ice and transform 1-5 μl of the reaction into 50 μl competent cells.

Ligation System

COMPONENT 20 μl REACTION
10X T4 DNA Ligase Buffer 2 μl
Vector DNA 0.025 pmol
Insert DNA 0.076 pmol
T4 DNA Ligase 1μl
Nuclease-free water to 20 μl


Bacteria Culture

Strain

  1. DH5a (F- endA1 glnV44 thi-1 recA1 relA1 gyrA96 deoR nupG Φ80dlacZΔM15 Δ(lacZYA-argF)U169, hsdR17(rK- mK+), λ–)use for cloning
  2. BL21(DE3) (fhuA2 [lon] ompT gal (λ DE3) [dcm] ∆hsdS,λ DE3 = λ sBamHIo ∆EcoRI-B int::(lacI::PlacUV5::T7 gene1) i21 ∆nin5) use for expressing

Medium

LB Medium

NaCl 10g
Tryptone 10g
Yeast Extract 5 g
Water up to 1000mL

SOB Medium

Tryptone 20g
Yeast extract 5g
NaCl 0.5g
1M KCl 2.5ml
ddH2O up to 1000 ml
Adjust pH to 7.0 with 10N NaOH, autoclave to sterilize, and add 10 ml of 1 M MgCl2 before use

Antibiotics

Storage Use
Kana 50 mg/ml(Water) 50 μg/ml
Amp50 mg/ml(Water)50 μg/ml
Tet10 mg/ml (Alcohol)10 μg/ml
Cm34 mg/ml (Alcohol)68 μg/ml


Transformation

  1. Remove competent cells from freezer and allow to thaw
  2. Add 3-5 μl of DNA to the cells
  3. Incubate on ice for 30 min
  4. Heat shock the cells at 37°C for 1.5 mins
  5. Add 500 μl of SOB medium, and incubate in a shaker at 37°C for 1 hour
  6. Centrifuge for 3 min at 3,000 g, remove and keep 100 μl of the supernatant, and pour away the rest
  7. Re-suspend the pellet in the 100 μl of supernatant that was removed earlier
  8. Spread All onto one plate with corresponding antibotics, and then pour the rest onto another. Incubate the plates overnight at 37°C.

Violacein Protocols

Induction and Extraction

  1. Incubate the monoclonal from medium in a shaker at 37°C overnight
  2. Add 0.1% Arabinose, 1mM Ferrous ammonium sulfate and 40 μM to start induction for another 6 hours
  3. Centrifuge for 1 min at 10000rpm, remove the LB Medium
  4. Add 800 μL 10%SDS and break cells using ultrasound
  5. Add 800 μL ethyl acetate to extract violacein/deoxyviolacein
  6. Use rotovap to concentrate violacein and resuspend with methanol

HPLC

  • Column: C18, 15cm
  • Mobile phase: 75% methanol, 25% ddH2O
  • Injection volume: 20 μL
  • Speed: 0.5 mL/min
  • Detection: 230 nm


Fatty Acid Protocols

  1. Transfer a fresh transformed colony to 5ml LB liquid medium and shake at 37℃ overnight(12h).
  2. Add seed broth to 50-100ml LB medium(volume ratio is 3% and loaded liquid is 20%) and shake until the OD600 reaches 0.6 or so. Add inducer of appropriate concentration to induce gene expression.
  3. Continue shake culture for another 20h. Contrifuge at 8,000 for 5min. Collect supernatant and bacteria sediment respectively (prepare 3 parallel samples, each 10ml).
  4. Extract the supernatant by chloroform-methanol(2:1) solution of the same volume (shake for 5min) place until stratification. Dry the lower organic layer at 50℃ for about 24h. Suspend the bacteria by 1ml ddH2O. Add 20ml chloroform-methanol solution and extract for another 2 times.(Attention: weigh the empty flask before drying).
  5. Weigh the crude extract and record the results. (For reference only)
  6. Dissolve the crude extract with 1ml methanol and add 2ml tetrafluoroboron. Methyl esterificate at 60℃ for 30min. After the reagent cools down, add 2ml N-hexane and extract for 2 times. Collect the upper layer and dry overnight at 50℃ (weigh the empty flask before drying as well).
  7. Add the crude bacteria extract to 1ml chloroform-methanol(2:1) solution and shake by vortex to extract the total lipid of the cells. Add 2ml methanol-water(4:1) as saponification reagent. Saponificate in 60℃ water bath for 1h. Then esterificate as the 6th step.
  8. Dissolve the obtained fatty acidmethyl ester(FAME)mixture with N-hexane(2mg/ml). Take 1ml sample for test.
  9. GC-MS condition:
Sample injector temperature: 250℃;
Detector temperature: 280℃;
Temperature programming: begin at 100℃ and last 2min. Warm to 250℃ at the rate of 10℃/min and last 5min.
Use C15 FAME as the interior label for quantification. (Quantity of C15 FAME depends on the sample concentration)
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