Media and Passaging

Minimal Media Recipe

LeMaster-Richards Minimal Media (LeMaster and Richards, 1982)

Final Volume	Water	4x Minimal Salts	2M MgSO4	Trace Minerals (4000x)	Glucose (if needed)
10ml	7.5ml	2.5ml	10ul	2.5ul	xxul
100ml	75ml	25ml	100ul	25ul	xxul
250ml	180ml	62.5ml	250ul	62.5ul	xxul

• Glycerol should be added to a final concentration of xx% (or xx% if using a double amount).

If using:

• • Black cells in 10ml: xxul (xxul for double amount)
  • Green cells in 10ml: xxul (xxul for double amount)
  • Red cells in 10ml: xxul (xxul for double amount)
  • Green and Orange cells in 10ml: xxul (xxul for double amount)
  • Red and Blue cells in 10ml: xxul (xxul for double amount)

Cell Aliquots

Using Cell Passaging E. coli Aliquots

Aliquot Color	For 10^7 cells, use:	Strain Number	Genotype	Grows in:	Fluorescence	Frozen Date
Black	xxxxx	S-734	Wild Type	All	None	xxxx
Green	18.25ul	S-735	Δppc	LB; glycerol; succinate; a-keto	sfGFP	xxxx
Red	Example	S-736	Δppc	LB; glycerol; succinate; a-keto	DSRed-Express2	xxxx
Blue	Example	S-737	Δfbp	LB; glucose; galactose	sfGFP	xxxx
Orange	11.55ul	S-738	Δfbp	LB; glucose; galactose	DSRed-Express2	xxxx

Phage Passaging Protocol

1. Prepare 10ml of appropriate media
2. Add cells
3. Incubate in shaking incubator for 1 hour
4. Add xxx PFU of phage
5. Incubate in shaking incubator for 23 hours
6. Add additional sugars, if applicable
7. Incubate in shaking incubator for 23-24 hours
8. Add xxul chloroform into 3 labeled microcentrifuge tubes. Label 3 additional tubes and set aside.
9. Add 1ml of incubated cells + phage into each tube.
10. Vortex for 15 seconds each.
11. Put in microcentrifuge and spin down, 3 minutes at max speed.
12. Pipet out 800ul into the previously labeled, empty tube. Put into phage box in the refrigerator.
13. If the passage is dividable by 5, do a plaque assay to correct the number of added PFU for the next passage.