IGEM:PennState/2006/Growthmedia: Difference between revisions

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<h1>Growth Media and plates</h1>
=Media=


===<font color="red">LB Media</font>===
===<font color="red">LB Media</font>===

Revision as of 11:15, 8 August 2007

Growth Media and plates

LB Media

(Per L)

  • 10 g bactotryptone
  • 5 g yeast extract
  • 10 g NaCl
  • pH to 7.0 (~40uL 2M NaOH / L)

M9 Minimal Media

(SUPPLEMENTED W/ 0.1% YE) Final concentrations:

  • 1X M9 salts (autoclaved)
  • 1 mM MgSO4 (autoclaved)
  • 0.16% glycerol (autoclaved)
  • 0.148 μM thiamine/vitamin B1 (filter sterilized)
  • 0.1% casamino acids (filter sterilized)
  • 0.1% Yeast Extract (autoclaved)

Procedure:

1. These solutions should already be made, so add together w/sterile technique:

  • 200 mL 5X M9 salts
  • 1 mL 1 M MgSO4
  • 2.27 mL 70% glycerol
  • 50 μL thiamine (10mg/mL)
  • 5 mL casamino acids (200 mg/mL)
  • 10 mL 0.1g/mL Yeast Extract
  • 782 mL sterile dH2O .
  • 1 L M9 media (for plates just add 15 g bacto agar to recipe)

SOB Media

Final concentrations

  • 0.5% Yeast Extract
  • 2% Tryptone
  • 10mM NaCl
  • 2.5 mM KCl
  • 10 mM MgCl2
  • 10 mM MgSO4

Procedure

1. To 1 L, add:

  • 20 g bactotryptone
  • 5 g bacto-yeast extract
  • 0.5 g NaCl
  • 0.19 g KCl
  • Adjust to pH 7.0 w/ NaOH

2. Autoclave on slow exhaust for 25 min.

3. Add filter-sterilized MgCl2, MgSO4 solution to give final Mg2+ conc. of 20 mM (i.e. 10 mM MgCl2, 10 mM MgSO4)

SOC MEDIA SOB + 20 mM (final) glucose (aka dextrose)


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