Low-Salt LB 1.5% Agar Plates
MATERIALS
Reagents
Agar (BD Bacto, dehydrated; BD 214010)
NaCl (Merck 1.06404)
Tryptone (BD 211705)
Yeast extract (BD 212750)
Equipment
Autoclave
Bunsen burner (FIREBOY safety; Integra 144000) or match (see Step 5)
Erlenmeyer flask (2-L)
Magnetic stirrer
Magnetic stirring bar (50-mm)
Petri dishes (100-mm × 15-mm; Fisher Scientific FB0875713)
METHOD
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Place a magnetic stirring bar in a 2-L Erlenmeyer flask and add the following:
Reagent Quantity Agar 15 g Tryptone 10 g Yeast extract 5 g NaCl 5 g H2O to 1000 mL -
Mix briefly and autoclave for 20 min at 120°C and 15 psi.
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Place the flask on a magnetic stirrer and stir at low speed.
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Avoid stirring too fast, as this generates bubbles that are fastidious to remove (see Step 5).
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Wait for the liquid to cool down until you can barely touch the flask with your hand.
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This corresponds to a temperature of ∼60°C.
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Pour the melted medium into Petri dishes (replacing the lid each time), aiming to pour about 25 mL per plate.
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With a little practice, you will be able to gauge this amount. Should bubbles form on the surface of the plates, quickly apply the flame of a Bunsen burner (or even that of a match) on the surface of the plate to pop the bubbles. Be careful not to melt the plastic of the dishes in the process.
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Once the agar has hardened, turn the plates upside down, stacking them in piles.
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Inverting the plates prevents vapor condensation on the lids and stops H2O droplets from falling on the surface of the agar.
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Leave the plates for 3–4 d at room temperature to allow them to dry slightly.
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Store the plates at 4°C.
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Most types of plates can be used for several months provided that they are protected from drying and contamination.
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