Difference between revisions of "Team:US AFRL CarrollHS/Experiments"

 
(14 intermediate revisions by 2 users not shown)
Line 1: Line 1:
−
{{US_AFRL_CarrollHS/WikiStripDown}} {{US_AFRL_CarrollHS/Layout!}} {{US_AFRL_CarrollHS/Bootstrap1}} {{US_AFRL_CarrollHS/Bootstrap2}} {{US_AFRL_CarrollHS/Bootstrap3}} {{US_AFRL_CarrollHS/Bootstrap4}} {{US_AFRL_CarrollHS/Bootstrap8}} {{US_AFRL_CarrollHS/navbar}} {{US_AFRL_CarrollHS/hero}} {{US_AFRL_CarrollHS/footer}}  
+
{{US_AFRL_CarrollHS/WikiStripDown}} {{US_AFRL_CarrollHS/Layout!}} {{US_AFRL_CarrollHS/Bootstrap1}} {{US_AFRL_CarrollHS/Bootstrap2}} {{US_AFRL_CarrollHS/Bootstrap3}} {{US_AFRL_CarrollHS/Bootstrap4}} {{US_AFRL_CarrollHS/Bootstrap8}} {{US_AFRL_CarrollHS/navbar}} {{US_AFRL_CarrollHS/hero}}  
 
<html>
 
<html>
  
−
<div class="column full_size">
+
<div class="hero">
 +
      <img src="https://static.igem.org/mediawiki/2018/3/30/T--US_AFRL_CarrollHS--ExperimentsHeader.jpg" alt="Experiments" style="margin-top: 30px;">
 +
</div>
  
−
<h1>Experiments</h1>
+
<div class="background">
−
<p>Describe the research, experiments, and protocols you used in your iGEM project. These should be detailed enough for another team to repeat your experiments.</p>
+
<div class="row"><h1>Transformations</h1></div>
 +
<div class="row"><h2>BI21 Cells:</h2></div>
 +
<p>
 +
<ol>
 +
<div class="row"><li>Thaw 50 µL vial of BL21 cells on ice</li></div>
 +
<div class="row"><li>Inoculate 2µL DNA into 50µL BL21 cells</li></div>
 +
<ul>
 +
<div class="row"><li>incubate on ice for 30 minutes</li></div>
 +
<div class="row"><li>heat shock at 42℃ for 10 seconds</li></div>
 +
<div class="row"><li>incubate on ice for 5m</li></div>
 +
</ul>
 +
<div class="row"><li>Inoculate 250µL LB into vial</li></div>
 +
<ul>
 +
<div class="row"><li>incubate at 37℃ with shaking for 1.5 hours</li></div>
 +
</ul>
 +
<div class="row"><li>Plate 1x/9x</li></div>
 +
</ol>
 +
</p>
  
 +
<div class="row"><h2>JM109 Cells:</h3></div>
 
<p>
 
<p>
−
Please remember to put all characterization and measurement data for your parts on the corresponding Registry part pages.  
+
<ol>
 +
<div class="row"><li>Thaw vial of JM109 cells on ice</li></div>
 +
<div class="row"><li>Label 14 mL Falcon tube & plane on ice</li></div>
 +
<div class="row"><li>Inoculate 50 µL JM109 cells into Falcon tube</li></div>
 +
<div class="row"><li>Inoculate 2µL DNA into 50µL JM109 cells</li></div>
 +
<ul>
 +
<div class="row"><li>incubate on ice for 20m</li></div>
 +
<div class="row"><li>heat shock at 42℃ for 45 seconds</li></div>
 +
</ul>
 +
<div class="row"><li>Inoculate 950µL LB into vial</li></div>
 +
<ul>
 +
<div class="row"><li>incubate at 37℃ with shaking for 1.5 hours</li></div>
 +
</ul>
 +
<div class="row"><li>Plate 1x/9x</li></div>
 +
</ol>
 
</p>
 
</p>
 +
<br>
 +
</div>
  
 +
<img src="https://static.igem.org/mediawiki/2018/e/e1/T--US_AFRL_CarrollHS--_WhiteNavyDNA.png" style="width: 100%;">
 +
 +
 +
<div class="background2">
 +
<div class="row"><h1>Electrophoresis/Gel Protocols</h2></div>
 +
<div class="row"><h2>1% Agarose Electrophoresis Gel</h3></div>
 +
<ol>
 +
<div class="row"><li>Add 0.35 g agarose to 35 mL 1x TAE in 100mL conical flask</li></div>
 +
<div class="row"><li>Heat in microwave for 35 seconds</li></div>
 +
<div class="row"><li>Swirl and heat in microwave for 25 seconds</li></div>
 +
<div class="row"><li>Swirl and heat in microwave for 15 seconds</li></div>
 +
<div class="row"><li>Swirl and heat in microwave for 7 seconds</li></div>
 +
<div class="row"><li>Swirl and ensure no ‘floaties’ </li></div>
 +
<div class="row"><li>Cool outside of conical flask with water until ‘hand not’</li></div>
 +
<div class="row"><li>Pour into gel mold and add well comb</li></div>
 +
</ol>
 +
 +
 +
<div class="row"><h2>Gel Extraction</h3></div>
 +
<ol>
 +
<div class="row"><li>Use ethanol-wiped scalpel to excise appropriate bands</li></div>
 +
<div class="row"><li>Mix and incubate at 50°C for 10 min</li></div>
 +
<ul>
 +
<div class="row"><li>Vortex every 2 mins until gel slice is completely dissolved</li></div>
 +
</ul>
 +
<div class="row"><li>Place nucleospin column into 2mL collection tube</li></div>
 +
<ul>
 +
<div class="row"><li>Add sample</li></div>
 +
<div class="row"><li>Centrifuge at 11,000 xg for 1 minute</li></div>
 +
<div class="row"><li>Discard throughflow and place column back in same tube</li></div>
 +
</ul>
 +
<div class="row"><li>Add 700 mL Buffer NT3</li></div>
 +
<ul>
 +
<div class="row"><li>Centrifuge at 11,000 xg for 1 minute</li></div>
 +
<div class="row"><li>Discard throughflow and place column back in same tube</li></div>
 +
</ul>
 +
<div class="row"><li>Repeat step 4</li></div>
 +
<div class="row"><li>Centrifuge at 11,000 xg for another minute</li></div>
 +
<ul>
 +
<div class="row"><li>To remove buffer</li></div>
 +
<ul>
 +
<div class="row"><li>Discard throughflow</li></div>
 +
<div class="row"><li>Centrifuge at 11,00 xg for add minute</li></div>
 +
<div class="row"><li>Place column in a clean, labelled 1.5 mL tube </li></div>
 +
</ul>
 +
</ul>
 +
<div class="row"><li>Add 25 mL prewarmed (50°C) Buffer NE</li></div>
 +
<ul>
 +
<div class="row"><li>Incubate at 50°C for 5 min</li></div>
 +
<div class="row"><li>Centrifuge at 50 xg for 1 minute</li></div>
 +
<div class="row"><li>Centrifuge at 11,000 xg for 1 minute</li></div>
 +
</ul>
 +
</ol>
 +
<br>
 
</div>
 
</div>
  
  
 +
<img src="https://static.igem.org/mediawiki/2018/6/6a/T--US_AFRL_CarrollHS--_NavyWhiteDNA.png" style="width: 100%;">
  
−
<div class="column two_thirds_size">
+
 
−
<h3>What should this page contain?</h3>
+
<div class= "background">
 +
<div class="row"><h1>Plasmid Transformation Protocol</h2></div>
 +
<ol>
 +
<div class="row"><li>Aliquot 1 ml media into 1.5 mL tubes</li></div>
 
<ul>
 
<ul>
−
<li> Protocols </li>
+
<div class="row">   <li>Place in 42°C waterbath</li></div>
−
<li> Experiments </li>
+
−
<li> Documentation of the development of your project </li>
+
 
</ul>
 
</ul>
 +
<div class="row"><li>Prechill labelled 14 mL round-bottom falcon tubes</li></div>
 +
<ul>
 +
  <div class="row"> <li>Add mL cell culture to tube</li></div>
 +
  <div class="row"> <li>Add appropriate amount of ligase rxh (2-2.5 L)</li> </div>
 +
  <div class="row"> <li>Incubate in nice for 20 minutes</li></div>
 +
</ul>
 +
<div class="row"><li>Heat shock cells by placing at 42℃ for 45 seconds in waterbath </li></div>
 +
<ul>
 +
<div class="row">  <li>Place on ice for 2 minutes</li></div>
 +
</ul>
 +
<div class="row"><li>Add 950 mL preheated media to each tube</li></div>
 +
<ul>
 +
<div class="row"><li>Incubate at 37℃ with 215 rpm shaking for 1.5 hr -> 20 minutes</li></div>
 +
</ul>
 +
</ol>
 +
<div class="row"><h2>Plating</h2></div>
 +
<ol>
 +
<div class="row"><li>Plate on LB-antibiotic plates</li></div>
 +
<ul>
 +
<div class="row"><li>Plate 100 ml for 1x transformation</li> </div>
 +
<div class="row"><li>Plate 100 mL 9x centrifuge remaining transformation at 2000 xg for 5 minutes and resuspended pellet in 100 L media </li></div>
 +
</ol>
 +
</div>
  
 +
<img src="https://static.igem.org/mediawiki/2018/e/e1/T--US_AFRL_CarrollHS--_WhiteNavyDNA.png" style="width: 100%;">
 +
 +
<div class="background2">
 +
<div class="row"><h1>Plates Protocol</h1></div>
 +
<ol>
 +
<div class="row"><li>Follow LB Agar Recipe </li></div>
 +
  <ul>
 +
<div class="row">  <li>Make sure to put stirring bar in water</li></div>
 +
<div class="row">  <li>Needed to make into homogenous gel</li></div>
 +
<div class="row">  <li>Needs to be sterile</li></div>
 +
  </ul>
 +
<div class="row"><li>Put into Autoclave </li></div>
 +
  <ul>
 +
<div class="row">  <li>Lid should not be too tight</li></div>
 +
  </ul>
 +
<div class="row"><li>Put in ice bath 42°C</li></div>
 +
  <ul>
 +
<div class="row">  <li>Cool till not burning hand</li></div>
 +
<div class="row">  <li>Put on stirring plate</li></div>
 +
  </ul>
 +
<div class="row"><li>Put sterilized plates in Lamenia shield</li></div>
 +
<div class="row"><li>Using micropipette put .5 mL of chlor. And amp. agar solution</li></div>
 +
  <ul>
 +
<div class="row">  <li>1000x dilution</li></div>
 +
<div class="row">  <li>Amp. has to be defrosted in dark drawer</li></div>
 +
  </ul>
 +
<div class="row"><li>Pour solution into plates</li></div>
 +
  <ul>
 +
<div class="row">  <li>Thin layer fill bottom</li></div>
 +
<div class="row">  <li>Take lid slightly off to prevent condensation</li></div>
 +
<br>
 
</div>
 
</div>
  
−
<div class="column third_size">
+
 
−
<div class="highlight decoration_A_full">
+
<img src="https://static.igem.org/mediawiki/2018/6/6a/T--US_AFRL_CarrollHS--_NavyWhiteDNA.png" style="width: 100%;">
−
<h3>Inspiration</h3>
+
 
 +
 
 +
<div class="background">
 +
<div class="row"><h1>QIA Prep Spin Mini Prep Kit</h1></div>
 +
<ol>
 +
<div class="row"><li>Example for 18 mL LB add</li></div>
 
<ul>
 
<ul>
−
<li><a href="https://2014.igem.org/Team:Colombia/Protocols">2014 Colombia </a></li>
+
<div class="row">   <li>18 L20 mg/ L Kanamycin (antibiotic)</li></div>
−
<li><a href="https://2014.igem.org/Team:Imperial/Protocols">2014 Imperial </a></li>
+
<div class="row">   <li>18 L 50 mg/ L ampicillin</li></div>
−
<li><a href="https://2014.igem.org/Team:Caltech/Project/Experiments">2014 Caltech </a></li>
+
 
</ul>
 
</ul>
 +
<div class="row"><li>Aliquot 3.5 mL into labelled round bottom falcon tubes</li></div>
 +
<div class="row"><li>Using sterile toothpicks- pick a single colony forming unit (cfu) and inoculate tube</li></div>
 +
  <ul>
 +
<div class="row">  <li>Incubate overnight at 37°C with 215 rpm shaking</li></div>
 +
  </ul>
 +
<div class="row"><li>To 100 mL 60% glycerol stock, add 300mL overnight culture to appropriately labelled tube</li></div>
 +
  <ul>
 +
<div class="row">  <li>Store at -80°C</li></div>
 +
  </ul>
 +
<div class="row"><li>Pellet remaining cells by centrifugation in 1.5 mL tube at 13,2000 rpm for 1 min</li></div>
 +
  <ul>
 +
<div class="row">  <li>Discard supernatant and repeat</li></div>
 +
  </ul>
 +
<div class="row"><li>Resuspend pellet in Buffer P1 250 mL </li></div>
 +
  <ul>
 +
<div class="row">  <li>Add 250 L Buffer, P2 and mix by inverting 10x</li></div>
 +
<div class="row">  <li>Add 350 L Buffer N3 and immediately mix by inverting 10x</li></div>
 +
  </ul>
 +
<div class="row"><li>Centrifuge at 13, 200 rpm for 10 minute</li></div>
 +
<div class="row"><li>Pipet supernatant into labelled QIA prep spin column</li></div>
 +
  <ul>
 +
<div class="row">  <li>Centrifuge at 13, 200 rpm for 1 minute</li></div>
 +
<div class="row">  <li>Discard thoroughflow </li></div>
 +
  </ul>
 +
<div class="row"><li>Wash column by adding .5 mL Buffer PB *regular for low copy number plasmids*</li></div>
 +
  <ul>
 +
<div class="row">  <li>Centrifuge at 13, 200 rpm for 1 minute</li></div>
 +
<div class="row">  <li>Discard thoroughflow </li></div>
 +
  </ul>
 +
<div class="row"><li>Wash by adding .75 mL Buffer PE</li></div>
 +
  <ul>
 +
<div class="row">  <li>Centrifuge at 13, 200 rpm for 1 minute</li></div>
 +
<div class="row">  <li>Discard thoroughflow </li></div>
 +
<div class="row">  <li>Centrifuge for an addition minute to ensure removal of residual wash buffer</li></div>
 +
  </ul>
 +
<div class="row"><li>Place spin column in a clean, labelled 1.5 mL tube </li></div>
 +
  <ul>
 +
<div class="row">  <li>Add 50 LEB to center of column & let stand for 1 minute at room temperature</li></div>
 +
<div class="row">  <li>Centrifuge at 12,000 rpm for 1 minute</li></div>
 +
<div class="row">  <li>Store at -20℃</li></div>
 +
  </ul>
 +
</ol>
 
</div>
 
</div>
 +
 +
<img src="https://static.igem.org/mediawiki/2018/e/e1/T--US_AFRL_CarrollHS--_WhiteNavyDNA.png" style="width: 100%;">
 +
 +
 +
<div class="background2">
 +
 +
<div class="row"><h1>Making Motility Plates</h1></div>
 +
<ol>
 +
<div class="row"><li>Follow Motility Plate Recipe </li></div>
 +
  <ul>
 +
<div class="row"><li>Recipe</li></div>
 +
  <ul>
 +
  <div class="row"><li>5 grams of Tryptone </li></div>
 +
  <div class="row"><li>2.5 grams of NaCl</li></div>
 +
  <div class="row"><li>1.25 grams of Agar </li></div>
 +
  <div class="row"><li>500 mL H2O</li></div>
 +
  </ul>
 +
<div class="row"><li>Make sure to put stirring bar in water</li></div>
 +
<div class="row"><li>Needed to make into homogenous gel</li></div>
 +
<div class="row"><li>Needs to be sterile</li></div>
 +
  </ul>
 +
 +
<div class="row"><li>Put into Autoclave</li></div>
 +
<ul>
 +
<div class="row"><li>Lid should not be too tight</li></div>
 +
</ul>
 +
 +
<div class="row"><li>Put in water bath 42°C</li></div>
 +
  <ul>
 +
  <div class="row"><li>Cool till not burning hand</li></div>
 +
  <div class="row"><li>Put on stirring plate</li></div>
 +
  </ul>
 +
<div class="row"><li>Put sterilized plates in Lamenia shield</li></div>
 +
<div class="row"><li>Pour solution into plates</li></div>
 +
  <ul>
 +
  <div class="row"><li>Thin layer fill bottom</li></div>
 +
  <div class="row"><li>Take lid slightly off to prevent condensation</li></div>
 +
  </ul>
 +
 +
</ol>
 +
 
</div>
 
</div>
  
 +
<img src="https://static.igem.org/mediawiki/2018/6/6a/T--US_AFRL_CarrollHS--_NavyWhiteDNA.png" style="width: 100%;">
 +
 +
<div class="background">
 +
 +
<div class="row"><h1>Making TSA Plates</h1></div>
 +
<ol>
 +
<div class="row"><li>Follow TSA Plate Recipe </li></div>
 +
  <ul>
 +
<div class="row"><li>Recipe</li></div>
 +
  <ul>
 +
  <div class="row"><li>30 g of TSB</li></div>
 +
  <div class="row"><li>15 g of Agar</li></div>
 +
  <div class="row"><li>1 Liter of H20 18 mΩ</li></div>
 +
  </ul>
 +
<div class="row"><li>Make sure to put stirring bar in water</li></div>
 +
<div class="row"><li>Needed to make into homogenous gel</li></div>
 +
<div class="row"><li>Needs to be sterile</li></div>
 +
  </ul>
 +
 +
<div class="row"><li>Put into Autoclave</li></div>
 +
<ul>
 +
<div class="row"><li>Lid should not be too tight</li></div>
 +
</ul>
 +
 +
<div class="row"><li>Put in water bath 42°C</li></div>
 +
  <ul>
 +
  <div class="row"><li>Cool till not burning hand</li></div>
 +
  <div class="row"><li>Put on stirring plate</li></div>
 +
  </ul>
 +
<div class="row"><li>Put sterilized plates in Lamenia shield</li></div>
 +
<div class="row"><li>Pour solution into plates</li></div>
 +
  <ul>
 +
  <div class="row"><li>Thin layer fill bottom</li></div>
 +
  <div class="row"><li>Take lid slightly off to prevent condensation</li></div>
 +
  </ul>
 +
 +
</ol>
 +
 +
</div>
 +
 +
 +
<img src="https://static.igem.org/mediawiki/2018/e/e1/T--US_AFRL_CarrollHS--_WhiteNavyDNA.png" style="width: 100%;">
 +
 +
<div class="background2">
 +
 +
<div class="row"><h1>Yarrowia Testing</h1></div>
 +
<div class="row"><h2>Growing Yarrowia Culture</h2></div>
 +
<ol>
 +
<div class="row"><li>Pipette 5 mL of TSB into a culture tube</li></div>
 +
 +
<div class="row"><li>Use a wand to swipe a colony of Yarrowia from an already grown plate of Yarrowia</li></div>
 +
<div class="row"><li>Place wand with colony of Yarrowia into culture tube</li></div>
 +
  <ul>
 +
  <div class="row"><li>Flick wand for 15 seconds</li></div>
 +
  </ul>
 +
<div class="row"><li>Incubate overnight at 27°C with 200 rpm shaking</li></div>
 +
 +
</ol>
 +
 +
<div class="row"><h2>Preparing Chitinase Testing Enzyme</h2></div>
 +
<ol>
 +
<div class="row"><li>Measure out 2 g of chitinase from Streptomyces Griseus  </li></div>
 +
  <ul>
 +
  <div class="row"><li>Place into 2 mL microcentrifuge tube</li></div>
 +
  </ul>
 +
<div class="row"><li>Resuspend chitinase</li></div>
 +
  <ul>
 +
  <div class="row"><li>Pipette 0.100 mL of PBS into tube</li></div>
 +
  <div class="row"><li>Vortex tube for 15 seconds</li></div>
 +
  </ul>
 +
<div class="row"><li>Store in -20°C freezer</li></div>
 +
 +
</ol>
 +
 +
 +
<div class="row"><h2>Chitinase Testing Against Yarrowia</h2></div>
 +
<ol>
 +
<div class="row"><li>Dilute Yarrowia culture 1:000</li></div>
 +
  <ul>
 +
  <div class="row"><li>Use 1.5 mL microcentrifuge tube</li></div>
 +
    <ul>
 +
    <div class="row"><li>Pipette .999 mL of TSB into tube</li></div>
 +
    <div class="row"><li>Pipette .001 mL of grown Yarrowia culture into tube</li></div>
 +
    <div class="row"><li>Inoculate tube by flicking 4-6 times</li></div>
 +
    </ul>
 +
  </ul>
 +
<div class="row"><li>Pipette .300 mL of diluted Yarrowia culture on TSA plate</li></div>
 +
  <ul>
 +
  <div class="row"><li>Use L-spreader to spread diluted Yarrowia culture</li></div>
 +
  <div class="row"><li>Let plates dry in fume hood for 30 minutes</li></div>
 +
  </ul>
 +
<div class="row"><li>Perform steps 4-6 a total of 3 times on 3 separate TSA plates</li></div>
 +
 +
<div class="row"><li>Using a pipette, spot 4 0.005 mL spots of chitinase enzyme on plate</li></div>
 +
  <ul>
 +
  <div class="row"><li>2 spots diluted to 10 mg/mL</li></div>
 +
  <div class="row"><li>2 spots diluted 5 mg/mL</li></div>
 +
  </ul>
 +
 +
<div class="row"><li>Using a pipette, spot 6 0.005 mL spots of chitinase enzyme on plate</li></div>
 +
  <ul>
 +
  <div class="row"><li>2 spots diluted to 10 mg/mL</li></div>
 +
  <div class="row"><li>2 spots diluted 1 mg/mL</li></div>
 +
  <div class="row"><li>2 spots diluted 0.1 mg/mL</li></div>
 +
  </ul>
 +
<div class="row"><li>Using a pipette, spot 4 0.005 mL spots of chitinase enzyme on plate</li></div>
 +
  <ul>
 +
  <div class="row"><li>2 spots diluted to 0.1 mg/mL</li></div>
 +
  <div class="row"><li>2 spots diluted 0.01 mg/mL</li></div>
 +
  </ul>
 +
 +
<div class="row"><li>Use one plate without Yarrowia as a negative control</li></div>
 +
 +
<div class="row"><li>Take one plate with Yarrowia spread and pipette 4 0.005 mL spots of PBS</li></div>
 +
  <ul>
 +
  <div class="row"><li>Use plate as positive control</li></div>
 +
  </ul>
 +
 +
<div class="row"><li>Cover plates with a plastic bag and place all plates into an incubator</li></div>
 +
  <ul>
 +
  <div class="row"><li>Incubate overnight at 27°Ce</li></div>
 +
  </ul>
 +
 +
</ol>
 +
 +
 +
 +
<div class="row"><h2>Chitinase And Cinnamaldehyde Spotting Testing Against Yarrowia</h2></div>
 +
<ol>
 +
<div class="row"><li>Pipette 0.300 mL of diluted Yarrowia culture on TSA plate</li></div>
 +
  <ul>
 +
  <div class="row"><li>Use L-spreader to spread diluted Yarrowia culture</li></div>
 +
  <div class="row"><li>Let plates dry in fume hood for 30 minutes</li></div>
 +
  </ul>
 +
<div class="row"><li>Make discs</li></div>
 +
  <ul>
 +
  <div class="row"><li>Using a holepunch, create 100 discs</li></div>
 +
  <div class="row"><li>Wrap discs in aluminum foil</li></div>
 +
  <div class="row"><li>Autoclave discs</li></div>
 +
  </ul>
 +
<div class="row"><li>Soak 25 discs in each of the following</li></div>
 +
  <ul>
 +
  <div class="row"><li>Chitinase enzyme from Streptomyces Griseus diluted to 10 mg/mL in 1/32 diluted cinnamaldehyde</li></div>
 +
  <div class="row"><li>Chitinase enzyme from Streptomyces Griseus diluted to 5 mg/mL with 1/32 diluted cinnamaldehyde</li></div>
 +
  <div class="row"><li>Chitinase enzyme from Streptomyces Griseus diluted to 10 mg/mL with 1/32 diluted cinnamaldehyde</li></div>
 +
  <div class="row"><li>Chitinase enzyme from Streptomyces Griseus diluted to 5 mg/mL with 1/64 diluted cinnamaldehyde</li></div>
 +
  </ul>
 +
<div class="row"><li>Place 4 of each of the previous discs on Yarrowia covered TSA plates</li></div>
 +
 +
 +
<div class="row"><li>Cover plates with a plastic bag and place plates in incubator</li></div>
 +
  <ul>
 +
  <div class="row"><li>Incubate overnight at 27°C</li></div>
 +
  </ul>
 +
 +
</ol>
 +
 +
</div>
 +
 +
 +
<img src="https://static.igem.org/mediawiki/2018/6/6a/T--US_AFRL_CarrollHS--_NavyWhiteDNA.png" style="width: 100%;">
 +
 +
<div class="background">
 +
 +
<div class="row"><h1>Biofilm Assay Testing With Cinnamaldehyde</h1></div>
 +
 +
<div class="row"><h2>Growing a Biofilm</h2></div>
 +
<ol>
 +
<div class="row"><li>Grow a culture of the wild-type Nissle overnight in a rich medium (i.e. LB)</li></div>
 +
<div class="row"><li>Dilute the overnight culture 1:100 into fresh medium for biofilm assays.</li></div>
 +
<div class="row"><li>Add 100 μL of the dilution per well in a 96 well dish. </li></div>
 +
<div class="row"><li>Add cinnamaldehyde at different volumes to create the desired concentrations</li></div>
 +
<div class="row"><li>Incubate the microtiter plate for 4-24 hrs at 37°C.</li></div>
 +
</ol>
 +
 +
 +
<div class="row"><h2>Staining the Biofilm</h2></div>
 +
<ol>
 +
<div class="row"><li>After incubation, dump out cells by turning the plate over and shaking out the liquid.</li></div>
 +
<div class="row"><li>Gently submerge the plate in a small tub of water (i.e., use the bottoms of pipette tip boxes for P1000 pipetman as the tub). Shake out water. Repeat this process a two more  times. This step helps remove unattached cells and media components that can be stained in the next step, and significantly lowers background staining.</li></div>
 +
<div class="row"><li>Add 125 μL of a 0.1% solution of crystal violet in water to each well of the microtiter plate. Wear gloves and a lab coat while making the solution. Use caution when weighing out the CV as the powder is hydroscopic and readily stains clothing, skin, etc.</li></div>
 +
<div class="row"><li>Incubate the microtiter plate at room temperature for 10-15 min.</li></div>
 +
<div class="row"><li>Rinse the plate 3-4 times with water by submerging in a tub of water as outlined above, shake out and blot vigorously on a stack of paper towels to rid the plate of all excess cells and dye.</li></div>
 +
<div class="row"><li>Turn the microtiter plate upside down and dry for a few hours or overnight.</li></div>
 +
<div class="row"><li>For qualitative assays, the wells can be photographed when dry.</li></div>
 +
</ol>
 +
 +
<div class="row"><h2>Quantifying the Biofilm</h2></div>
 +
 +
<ol>
 +
<div class="row"><li>Add 125 μL of 30% acetic acid in water to each well of the microtiter plate to solubilize the CV.</li></div>
 +
<div class="row"><li>Incubate the microtiter plate at room temperature for 10-15 min.</li></div>
 +
<div class="row"><li>Transfer 125 μL of the solubilized CV to a new flat bottomed microtiter dish.</li></div>
 +
<div class="row"><li>Quantify absorbance in a plate reader at 550 nm using 30% acetic acid in water as the blank.</li></div>
 +
</ol>
 +
 +
<div class="row"><p><i>Procedure is a modified form of NCBI’s Microtiter Dish Biofilm Formation Assay <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182663/">(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182663/)</a></i></p></div>
 +
 +
</div>
  
−
<div class="clear"></div>
 
  
  
Line 43: Line 474:
  
 
</html>
 
</html>
 +
{{US_AFRL_CarrollHS/footer}}

Latest revision as of 22:07, 15 October 2018

Experiments

Transformations

BI21 Cells:

  1. Thaw 50 µL vial of BL21 cells on ice
  2. Inoculate 2µL DNA into 50µL BL21 cells
    • incubate on ice for 30 minutes
    • heat shock at 42℃ for 10 seconds
    • incubate on ice for 5m
  3. Inoculate 250µL LB into vial
    • incubate at 37℃ with shaking for 1.5 hours
  4. Plate 1x/9x

JM109 Cells:

  1. Thaw vial of JM109 cells on ice
  2. Label 14 mL Falcon tube & plane on ice
  3. Inoculate 50 µL JM109 cells into Falcon tube
  4. Inoculate 2µL DNA into 50µL JM109 cells
    • incubate on ice for 20m
    • heat shock at 42℃ for 45 seconds
  5. Inoculate 950µL LB into vial
    • incubate at 37℃ with shaking for 1.5 hours
  6. Plate 1x/9x


Electrophoresis/Gel Protocols

1% Agarose Electrophoresis Gel

  1. Add 0.35 g agarose to 35 mL 1x TAE in 100mL conical flask
  2. Heat in microwave for 35 seconds
  3. Swirl and heat in microwave for 25 seconds
  4. Swirl and heat in microwave for 15 seconds
  5. Swirl and heat in microwave for 7 seconds
  6. Swirl and ensure no ‘floaties’
  7. Cool outside of conical flask with water until ‘hand not’
  8. Pour into gel mold and add well comb

Gel Extraction

  1. Use ethanol-wiped scalpel to excise appropriate bands
  2. Mix and incubate at 50°C for 10 min
    • Vortex every 2 mins until gel slice is completely dissolved
  3. Place nucleospin column into 2mL collection tube
    • Add sample
    • Centrifuge at 11,000 xg for 1 minute
    • Discard throughflow and place column back in same tube
  4. Add 700 mL Buffer NT3
    • Centrifuge at 11,000 xg for 1 minute
    • Discard throughflow and place column back in same tube
  5. Repeat step 4
  6. Centrifuge at 11,000 xg for another minute
    • To remove buffer
      • Discard throughflow
      • Centrifuge at 11,00 xg for add minute
      • Place column in a clean, labelled 1.5 mL tube
  7. Add 25 mL prewarmed (50°C) Buffer NE
    • Incubate at 50°C for 5 min
    • Centrifuge at 50 xg for 1 minute
    • Centrifuge at 11,000 xg for 1 minute

Plasmid Transformation Protocol

  1. Aliquot 1 ml media into 1.5 mL tubes
    • Place in 42°C waterbath
  2. Prechill labelled 14 mL round-bottom falcon tubes
    • Add mL cell culture to tube
    • Add appropriate amount of ligase rxh (2-2.5 L)
    • Incubate in nice for 20 minutes
  3. Heat shock cells by placing at 42℃ for 45 seconds in waterbath
    • Place on ice for 2 minutes
  4. Add 950 mL preheated media to each tube
    • Incubate at 37℃ with 215 rpm shaking for 1.5 hr -> 20 minutes

Plating

  1. Plate on LB-antibiotic plates
    • Plate 100 ml for 1x transformation
    • Plate 100 mL 9x centrifuge remaining transformation at 2000 xg for 5 minutes and resuspended pellet in 100 L media

Plates Protocol

  1. Follow LB Agar Recipe
    • Make sure to put stirring bar in water
    • Needed to make into homogenous gel
    • Needs to be sterile
  2. Put into Autoclave
    • Lid should not be too tight
  3. Put in ice bath 42°C
    • Cool till not burning hand
    • Put on stirring plate
  4. Put sterilized plates in Lamenia shield
  5. Using micropipette put .5 mL of chlor. And amp. agar solution
    • 1000x dilution
    • Amp. has to be defrosted in dark drawer
  6. Pour solution into plates
    • Thin layer fill bottom
    • Take lid slightly off to prevent condensation

QIA Prep Spin Mini Prep Kit

  1. Example for 18 mL LB add
    • 18 L20 mg/ L Kanamycin (antibiotic)
    • 18 L 50 mg/ L ampicillin
  2. Aliquot 3.5 mL into labelled round bottom falcon tubes
  3. Using sterile toothpicks- pick a single colony forming unit (cfu) and inoculate tube
    • Incubate overnight at 37°C with 215 rpm shaking
  4. To 100 mL 60% glycerol stock, add 300mL overnight culture to appropriately labelled tube
    • Store at -80°C
  5. Pellet remaining cells by centrifugation in 1.5 mL tube at 13,2000 rpm for 1 min
    • Discard supernatant and repeat
  6. Resuspend pellet in Buffer P1 250 mL
    • Add 250 L Buffer, P2 and mix by inverting 10x
    • Add 350 L Buffer N3 and immediately mix by inverting 10x
  7. Centrifuge at 13, 200 rpm for 10 minute
  8. Pipet supernatant into labelled QIA prep spin column
    • Centrifuge at 13, 200 rpm for 1 minute
    • Discard thoroughflow
  9. Wash column by adding .5 mL Buffer PB *regular for low copy number plasmids*
    • Centrifuge at 13, 200 rpm for 1 minute
    • Discard thoroughflow
  10. Wash by adding .75 mL Buffer PE
    • Centrifuge at 13, 200 rpm for 1 minute
    • Discard thoroughflow
    • Centrifuge for an addition minute to ensure removal of residual wash buffer
  11. Place spin column in a clean, labelled 1.5 mL tube
    • Add 50 LEB to center of column & let stand for 1 minute at room temperature
    • Centrifuge at 12,000 rpm for 1 minute
    • Store at -20℃

Making Motility Plates

  1. Follow Motility Plate Recipe
    • Recipe
      • 5 grams of Tryptone
      • 2.5 grams of NaCl
      • 1.25 grams of Agar
      • 500 mL H2O
    • Make sure to put stirring bar in water
    • Needed to make into homogenous gel
    • Needs to be sterile
  2. Put into Autoclave
    • Lid should not be too tight
  3. Put in water bath 42°C
    • Cool till not burning hand
    • Put on stirring plate
  4. Put sterilized plates in Lamenia shield
  5. Pour solution into plates
    • Thin layer fill bottom
    • Take lid slightly off to prevent condensation

Making TSA Plates

  1. Follow TSA Plate Recipe
    • Recipe
      • 30 g of TSB
      • 15 g of Agar
      • 1 Liter of H20 18 mΩ
    • Make sure to put stirring bar in water
    • Needed to make into homogenous gel
    • Needs to be sterile
  2. Put into Autoclave
    • Lid should not be too tight
  3. Put in water bath 42°C
    • Cool till not burning hand
    • Put on stirring plate
  4. Put sterilized plates in Lamenia shield
  5. Pour solution into plates
    • Thin layer fill bottom
    • Take lid slightly off to prevent condensation

Yarrowia Testing

Growing Yarrowia Culture

  1. Pipette 5 mL of TSB into a culture tube
  2. Use a wand to swipe a colony of Yarrowia from an already grown plate of Yarrowia
  3. Place wand with colony of Yarrowia into culture tube
    • Flick wand for 15 seconds
  4. Incubate overnight at 27°C with 200 rpm shaking

Preparing Chitinase Testing Enzyme

  1. Measure out 2 g of chitinase from Streptomyces Griseus
    • Place into 2 mL microcentrifuge tube
  2. Resuspend chitinase
    • Pipette 0.100 mL of PBS into tube
    • Vortex tube for 15 seconds
  3. Store in -20°C freezer

Chitinase Testing Against Yarrowia

  1. Dilute Yarrowia culture 1:000
    • Use 1.5 mL microcentrifuge tube
      • Pipette .999 mL of TSB into tube
      • Pipette .001 mL of grown Yarrowia culture into tube
      • Inoculate tube by flicking 4-6 times
  2. Pipette .300 mL of diluted Yarrowia culture on TSA plate
    • Use L-spreader to spread diluted Yarrowia culture
    • Let plates dry in fume hood for 30 minutes
  3. Perform steps 4-6 a total of 3 times on 3 separate TSA plates
  4. Using a pipette, spot 4 0.005 mL spots of chitinase enzyme on plate
    • 2 spots diluted to 10 mg/mL
    • 2 spots diluted 5 mg/mL
  5. Using a pipette, spot 6 0.005 mL spots of chitinase enzyme on plate
    • 2 spots diluted to 10 mg/mL
    • 2 spots diluted 1 mg/mL
    • 2 spots diluted 0.1 mg/mL
  6. Using a pipette, spot 4 0.005 mL spots of chitinase enzyme on plate
    • 2 spots diluted to 0.1 mg/mL
    • 2 spots diluted 0.01 mg/mL
  7. Use one plate without Yarrowia as a negative control
  8. Take one plate with Yarrowia spread and pipette 4 0.005 mL spots of PBS
    • Use plate as positive control
  9. Cover plates with a plastic bag and place all plates into an incubator
    • Incubate overnight at 27°Ce

Chitinase And Cinnamaldehyde Spotting Testing Against Yarrowia

  1. Pipette 0.300 mL of diluted Yarrowia culture on TSA plate
    • Use L-spreader to spread diluted Yarrowia culture
    • Let plates dry in fume hood for 30 minutes
  2. Make discs
    • Using a holepunch, create 100 discs
    • Wrap discs in aluminum foil
    • Autoclave discs
  3. Soak 25 discs in each of the following
    • Chitinase enzyme from Streptomyces Griseus diluted to 10 mg/mL in 1/32 diluted cinnamaldehyde
    • Chitinase enzyme from Streptomyces Griseus diluted to 5 mg/mL with 1/32 diluted cinnamaldehyde
    • Chitinase enzyme from Streptomyces Griseus diluted to 10 mg/mL with 1/32 diluted cinnamaldehyde
    • Chitinase enzyme from Streptomyces Griseus diluted to 5 mg/mL with 1/64 diluted cinnamaldehyde
  4. Place 4 of each of the previous discs on Yarrowia covered TSA plates
  5. Cover plates with a plastic bag and place plates in incubator
    • Incubate overnight at 27°C

Biofilm Assay Testing With Cinnamaldehyde

Growing a Biofilm

  1. Grow a culture of the wild-type Nissle overnight in a rich medium (i.e. LB)
  2. Dilute the overnight culture 1:100 into fresh medium for biofilm assays.
  3. Add 100 μL of the dilution per well in a 96 well dish.
  4. Add cinnamaldehyde at different volumes to create the desired concentrations
  5. Incubate the microtiter plate for 4-24 hrs at 37°C.

Staining the Biofilm

  1. After incubation, dump out cells by turning the plate over and shaking out the liquid.
  2. Gently submerge the plate in a small tub of water (i.e., use the bottoms of pipette tip boxes for P1000 pipetman as the tub). Shake out water. Repeat this process a two more times. This step helps remove unattached cells and media components that can be stained in the next step, and significantly lowers background staining.
  3. Add 125 μL of a 0.1% solution of crystal violet in water to each well of the microtiter plate. Wear gloves and a lab coat while making the solution. Use caution when weighing out the CV as the powder is hydroscopic and readily stains clothing, skin, etc.
  4. Incubate the microtiter plate at room temperature for 10-15 min.
  5. Rinse the plate 3-4 times with water by submerging in a tub of water as outlined above, shake out and blot vigorously on a stack of paper towels to rid the plate of all excess cells and dye.
  6. Turn the microtiter plate upside down and dry for a few hours or overnight.
  7. For qualitative assays, the wells can be photographed when dry.

Quantifying the Biofilm

  1. Add 125 μL of 30% acetic acid in water to each well of the microtiter plate to solubilize the CV.
  2. Incubate the microtiter plate at room temperature for 10-15 min.
  3. Transfer 125 μL of the solubilized CV to a new flat bottomed microtiter dish.
  4. Quantify absorbance in a plate reader at 550 nm using 30% acetic acid in water as the blank.

Procedure is a modified form of NCBI’s Microtiter Dish Biofilm Formation Assay (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182663/)

Contact us @iGEMLabPats or iGEM@carrollhs.org