Difference: ProtocolsPhageTiters (2 vs. 3)

Revision 32020-02-24 - JeffreyBarrick

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META TOPICPARENT name="ProtocolPhageLysate"

Determining Phage Titer

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  1. Add each sample to a top agar aliquot. Quickly mix by pipetting up and down or gently vortexing. Avoid bubbles. Pour the entire contents of test tube on top of an LB plate and rapidly rotate the plate around so that the agar covers the entire surface evenly before it cools.
  2. Let the plates cool ~15-30 minutes at room temperature and then transfer to an incubator at 30C or 37C.
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Expected Results

T6-plaques-1E6.png Phage T6 plaques after overnight growth at 37C of a 106 dilution of lysate. Plaques for most E. coli T-even phages resemble these. They reach a maximum size and then stop spreading.
T7-plaques-1E4.png Phage T7 plaques after overnight growth at 37C of a 104 dilution of a freezer stock. T7 plaques continue to grow. Incubate the plates at 30C if you want to slow plaque growth.
T7-plaques-1E2.png Phage T7 plaques after overnight growth at 37C of a 102 dilution of a freezer stock. The phage has lysed all bacteria in this plate. The remaining colonies (small if they are embedded in the top agar and large if they reach the surface) are derived from mutant bacterial cells that have become resistant to the phage.
 

Example of Calculating Phage Titer

Since you are plating 100 l of each stock you should multiply by 10 and also by the dilution of the tube that gave a countable number of plaques to determine the PFU/ml in the original lysate. So, if there were 25 plaques in the 100 l you mixed in of the 106 dilution, then the lysate would have 2.5×108 PFU/ml. \ No newline at end of file

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