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META TOPICPARENT |
name="ProtocolList" |
Measuring Lysis Timing of T7 Phage
Reagents / Materials:
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- For plating phages:
- LB Plates with w/ appropriate supplements and antibiotics
- LB Top Agar (LB + 0.8% Agar)
- Test tubes
- 55C Water bath or heat block
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Procedure:
- Add 500uL of an overnight culture of the E. coli host to 9.5mL of LB in a 250mL flask
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- Allow to grow for 1h @ 37C, 200RPM until culture density is 1-2e8 cells / mL (OD ~ 0.2-0.3)
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- Allow to grow for 1.5h @ 30C, 200RPM until culture density is 1-2e8 cells / mL (OD ~ 0.2-0.3)
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- Add 5e7 phages and incubate 5min without shaking at 37C* (may need to be shorter for some strains?) *30C for nsAA evolved strains
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- Dilute 100uL of culture into 900uL of media in an eppendorf tube, then transfer 10uL into 10mL fresh media pre-warmed to 37C* (10000x dilution total) (may need to adjust volumes?)
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- Dilute 100uL of culture into 900uL of media in an eppendorf tube, then transfer 10uL into 10mL fresh media pre-warmed to 37C* (10000x dilution total)
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- Plate samples at 1min timepoints from 5-15min (may depend on strain)
- plate 10uL of each dilution as described in Determining Phage Titers
- Probably don't need to set up dilutions for these (?)
- Plot titers over timepoints; 'lysis time' is timepoint just before titer begins to increase
References:
[1] Heineman, Richard H, and James J Bull. "Testing Optimality with Experimental Evolution: Lysis Time in a Bacteriophage." Evolution 61, no. 7 (2007): doi:10.1111/j.1558-5646.2007.00132.x.
-- ColinBrown - 14 Jun 2017 |