Mycology media

Yin-Tse Huang

Published: 2022-05-16 DOI: 10.17504/protocols.io.e6nvw536wvmk/v2

Abstract

Mycology media

Steps

1.

WA+C agar

Water agar + chloramphenicol (氯黴素 kill bacteria): As an environmental isolating media

AB
ComponentAmount
Agar20g
Chloramphenicol0.05g
DI water1000 ml

chloramphenicol is autoclavable

2.

PDA+C agar

potato dextrose agar + chloramphenicol (氯黴素 kill bacteria): Use when WA+C agar is not working

AB
ComponentAmount
PDA39g (or per instruction on label)
Agar5g
Chloramphenicol0.05g
DI water1000 ml
3.

quarter-strength PDA

  1. Less nutrient than regular PDA (1/4)

  2. For beetle-associated fungi isolation

AB
ComponentAmount
PDA9.75g (or per instruction on label)
Agar5g
DI water1000 ml
4.

MEA (malt extraction agar)

For isolate subculture

AB
ComponentAmount
MEA33.6g (or per instruction on label)
Agar5g
DI water1000 ml
5.

Emerson YpSs Agar : For chytrids

AB
ComponentAmount
Yeast extract4g
Soluble Starch15g
K2HPO41g
MgSO4 x 7H2O0.5g
Agar20g
DI water1000ml

Adujust pH to 7.0 +/- 0.2. Autoclave at 121ºC.

6.

10% Unclarified V8 Agar

  1. Combine 100 ml V8 juice and 900 ml of distilled water.
  2. Add 1g CaCO3and 0.05 g b-sitosterol and mix well. Leave stir bar in the flask for later mixing.
  3. Add 15g of agar.
  4. Autoclave at 15 psi for 20 minutes.
  5. Stir medium while dispensing to insure good mixing of CaCO3. 20% : 200 ml V8, 800ml d. water, 2g CaCO3, and 0.05g b-sitosterol.

15% : 150 ml V8, 850 ml d. water, 1.5g CaCO3, and 0.05g b-sitosterol.

Reference: Miller, P. M. 1955. V-8 juice agar as a general purpose medium for fungi and bacteria. Phytopathology 45:461-462.

7.

SceSel+ medium (Kaltseis et al.,2009)

For isolation of Scedosporium

AB
ComponentAmount
Malt extract6.25 g
maltose6.25 g
KH2PO41.25 g
yeast extract1 g
Magnesium Sulfate Heptahydrate0.625 g
soy peptone0.625 g
chloramphenicol0.1 g
ciprofloxacin0.1 g
streptomycin sulfate0.1 g
dichloran2 mg
benomyl6 mg
DI water1000ml

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