Making plate lysates-PDF

Materials

Host culture
Petri plates containing solid culture medium appropriate for the host bacterium
Aliquots of molten soft agar for overlays (4 – 5 ml each, enough to cover one plate), held at ~50 ºC in a heat block or water bath
Tubes, tube racks, pipettors, sterile tips
Aseptic working area (near a flame or in an aseptic cabinet)

SM buffer (100 mM NaCl, 25 mM Tris-HCl pH 7.5, 8 mM MgSO4, 0.01% (w/v) gelatin) or sterile liquid culture medium
25 ml serological pipettes and bulb or Pipetboy
Falcon tubes (15 or 50 ml, depending on amount of lysate)
10 ml syringes and 0.22 μm syringe filters
Tube racks
Aseptic working area (near a flame or in an aseptic cabinet)

Label 1-5 plates for each phage isolate you will be propagating. The number of plates depends on how much lysate you need, but generally 1 plate will yield about 6-7 ml of lysate. Label the plate(s) with the phage isolate name.
Aliquot 4 ml of top agar into tubes and keep in the heat block. Make enough aliquots depending on how many plates per phage isolate you will be propagating.
In a second set of tubes, add 100 μl of host culture and 100 μl of appropriately diluted phage. Mix briefly.
Ideally, a plate lysate should be inoculated with enough phage to cause nearly-confluent lysis: the plate should be covered in plaques, with just a lacey remnant of the lawn visible. This usually translates into 10⁴ – 10⁵ PFU/plate for a standard 10-cm Petri plate, depending on the size of the plaques. Therefore, it is helpful to know at least the approximate titer of the phage stock or pickate you are using to inoculate the plate lysates. If you do not know, make your best guess on the phage concentration, remembering it is better to be too high than too low.
Pour a top agar aliquot into a tube containing the host culture/phage mixture, vortex briefly and pour over the appropriately labeled plate. Allow the lawns to set for 5 min, then invert and incubate as appropriate for your host organism.

Place the plate face-up and, using a pipette, flood the plate with 6-8 ml of broth or SM buffer. Use the pipette to GENTLY disrupt the lawn surface and then aspirate the resulting slurry back into the same pipette. Be tidy! Don’t slosh the lysate out of the plate! You only want to disrupt the soft top agar layer…do not gouge into the firmer bottom agar layer.
Place the lysate into a clean 15 or 50 ml Falcon tube and label it with the isolate name.
To avoid cross-contaminating your phage isolates, flood plates and transfer the slurry to tubes one isolate at a time. Periodically wipe the work surface with sanitizer or EtOH.
Centrifuge the lysates at 10,000 x g, 10 min.
Filter sterilize the phage-containing supernatant.
1. Remove a 10 ml syringe from its wrapper and remove the plunger from the syringe; place the syringe barrel on the bench and stand the plunger upright.
2. Place a 0.22 μm syringe filter onto the syringe barrel, and twist until it is locked on securely.
3. Pour the supernatant lysate into the syringe barrel, avoid disturbing the pelleted agar and cell debris.
4. Holding the tip of the syringe over a new tube, place the syringe plunger back into the barrel, and press to force the phage lysate through the filter.
5. Label the new tube containing the filter-sterilized phage lysate with the isolate name and date. Store at 4 ºC.