Team:Groningen/Lab/experiments/Motility assay

From 2013.igem.org

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<h1>Motility assay</h1>
<h1>Motility assay</h1>
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<p>A motility assay is done for <i>Bacillus subtilis</i> of different knockout strains as well as a wild type strain.  
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To test the difference in motility between the wild type <i>Bacillus subtilis</i> 168 strain and the both knockout strains, &Delta;CheY and &Delta;CheY&Delta;Des, a motility test is done.
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<p>This is to determine how different the knockouts move compared to the wild type <i>B. subtilis</i>.
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The plates are inoculated in 25&deg;C, 30&deg;C and 37&deg;C to determine the different behaviour of the strain at different temperatures. We expect the wildtype to be more motile than the knockout strains.  
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<p>The results will be used to determine if the temperature controlled strain works as desired, moving more as a CheY knockout in warm environments and more as a wild type in cold environments.
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The design we used for our motility assay is a simple one. The LB agar plates are made with the normal amount of LB-broth as nutrient, but with a reduced amount of agar. Low concentrations of agar are needed to allow movement through the medium, but when the concentrations are getting too low the observed movement can be caused by dispersal and turbulence during movement.
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<p>The design of the motility assay is a simple one. LB agar Plates are made with the normal amount of LB-broth as nutrients but with a reduced amount of agar.  
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To determine in which medium the strains have a higher motility two concentrations of agar are tested, 0.4% and 0.7%. For the reproducibility of the project, it is decided to pipet 13 ml agar to all of the plates.  
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<p>Different concentrations are used to find out the optimal amount of agar to show the motility.
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On every plate 10 &micro;l of liquid culture at an OD<sub>600</sub> of 0.4. Two different approaches are used for injecting the samples on the agar; one is to pipet it directly in the gel, the other one is to inject the sample on top of the agar.  
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Low concentrations are needed to allow movement through the medium but too low and the observed movement can be caused by dispersal and turbulence during movement.  
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The assay is performed in triplo for each strain and approach, and the plates are inoculated for 16 hours. The bacteria that are motile should spread out over the agar creating a cloudy look while the non-motile bacteria should stay at the spot. How quickly the bacteria spread from their spot to the edge can be used as an indicator of how fast they move.  
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The concentrations that are used are, 0.4% agar and 0.7% agar. The plates contained 13 ml agar.
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<p>The plates are inoculated in the center with the strain that is to be tested. This is done with 10 ul of liquid culture at an OD<sub>600</sub> of 0.4. The inoculation was done by sticking the pipette in to the agar, injecting the sample in to it, and by injecting the sample on top of the agar.  
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<p>For each strain 9 plates of each agar concentration and inoculation method is made. Three of the plates per treatment are placed in a 37&deg;C stove and three placed in a 30&deg;C stove and three placed in a 27&deg;C stove to grow.
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<p>The colonies are left to grow for 16 hours. Then how the colonies spread on the plates are observed every hour. The bacteria that are more motile should spread out over the agar creating a cloudy look while the non-motile bacteria should stay in the center, close together.
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<p>How quickly the bacteria spread from the center to the edge can be used as an indicator of how fast they move.  
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Revision as of 16:05, 4 October 2013

Motility assay

To test the difference in motility between the wild type Bacillus subtilis 168 strain and the both knockout strains, ΔCheY and ΔCheYΔDes, a motility test is done. The plates are inoculated in 25°C, 30°C and 37°C to determine the different behaviour of the strain at different temperatures. We expect the wildtype to be more motile than the knockout strains. The design we used for our motility assay is a simple one. The LB agar plates are made with the normal amount of LB-broth as nutrient, but with a reduced amount of agar. Low concentrations of agar are needed to allow movement through the medium, but when the concentrations are getting too low the observed movement can be caused by dispersal and turbulence during movement. To determine in which medium the strains have a higher motility two concentrations of agar are tested, 0.4% and 0.7%. For the reproducibility of the project, it is decided to pipet 13 ml agar to all of the plates. On every plate 10 µl of liquid culture at an OD600 of 0.4. Two different approaches are used for injecting the samples on the agar; one is to pipet it directly in the gel, the other one is to inject the sample on top of the agar. The assay is performed in triplo for each strain and approach, and the plates are inoculated for 16 hours. The bacteria that are motile should spread out over the agar creating a cloudy look while the non-motile bacteria should stay at the spot. How quickly the bacteria spread from their spot to the edge can be used as an indicator of how fast they move.