20.109(F07): Growth of phage materials
From OpenWetWare
Introduction
Protocols
In advance of this lab, a bacterial host (namely XL1-blue) was infected with the modified M13 phage called "3-12." Though the precise details of the 3-12 modification are still unpublished, it was isolated from a screen for changes in the M13 p8 that enable the phage to bind a metal (Iridium). Today you will harvest the phage from the supernatant of the infected bacterial culture and then titer it.
Part 1: Phage purification
- Spin 2 eppendorf tubes with infected cells in a room temperature microfuge, 1 minute at full speed.
- Remove the supernatant to clean fresh eppendorf tubes.
- Use your P1000 to measure the volume, then add a 1/6th volume of 20% PEG-8000/2.5M NaCl solution.
- Invert to mix then incubate on ice 60 minutes.
- Spin in a room temperature microfuge, 15 minutes at full speed. A white pellet should be visible...these are your precipitated phage.
- Remove the supernatant by aspiration (carefully so as not to disturb the pellet) or using your P1000.
- Spin the tubes 1 minute more to pellet any droplets stuck to the walls of the tube and use your P200 to remove the last drops of liquid from the pellet.
- Resuspend the pellet in 100 ul sterile H2O, pool the volumes of both eppendorf tubes into one and add a 1/6th volume of 20% PEG-8000/2.5M NaCl solution.
- Invert to mix then incubate on ice, 15 minutes.
- Balance your sample against that of another group, or against an eppendorf with water. Spin in a room temperature microfuge, 10 minutes at full speed.
- Aspirate the supernatant and resuspend the pellet in 100 ul sterile H2O.
- If the solution looks at all cloudy, spin in a room temperature 1 minute more and move supernatant with the phage to a new eppendorf tube.
Part 2: Titering phage
DONE!