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GROWING GOURMET - Anto2ni.it

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90<br />

CULTURING MUSHROOM MYCELIUM ON AGAR MEDIA<br />

Malt Extract, Yeast Agar<br />

1000 millil<strong>it</strong>ers (1 l<strong>it</strong>er) water<br />

20 grams agar agar<br />

20 grams barley malt sugar<br />

2 gram yeast (nutr<strong>it</strong>ional)<br />

1 gram peptone (optional, soybean derived)<br />

(The above medium is abbreviated as MYA.<br />

W<strong>it</strong>h the peptone, which is not cr<strong>it</strong>ical for most<br />

of the species described in this book, this medium<br />

is designated MYPA.)<br />

Potato, Dextrose, Yeast Agar<br />

1000 millil<strong>it</strong>ers (1 l<strong>it</strong>er) water<br />

300 grams of potatoes (i. e. the broth from boiling<br />

potatoes in 2-3 l<strong>it</strong>ers of water for 1 hour)<br />

20 grams agar agar<br />

10 grams dextrose<br />

2 grams yeast<br />

1 gram peptone (optional, soybean derived)<br />

(This medium is designated PDYA, or<br />

PDYPA if peptone is added. Note that only the<br />

broth from boiling the potatoes is used-the potatoes<br />

are discarded. The total volume of the<br />

media should equal 1 l<strong>it</strong>er.)<br />

Oatmeal, Malt, Yeast Enriched Agar<br />

1000 millil<strong>it</strong>ers water (1 l<strong>it</strong>er)<br />

80 grams instant oatmeal<br />

20 grams agar agar<br />

10 grams malt sugar<br />

2 grams yeast<br />

(This rich medium is called OMYA. The<br />

oatmeal does not have to be filtered out although<br />

some prefer to do so.)<br />

Dog Food Agar<br />

1000 millil<strong>it</strong>ers water (1 l<strong>it</strong>er)<br />

20 grams dry food*<br />

20 grams agar agar<br />

* Dog food was first used as a component for agar medium by<br />

the late Dr. Steven Pollock.<br />

Corn Meal, Yeast, Glucose Agar<br />

1000 millil<strong>it</strong>ers water (1 l<strong>it</strong>er)<br />

20 grams agar agar<br />

10 grams cornmeal<br />

5 grams malt or glucose<br />

1 gram yeast<br />

(This medium is known as CMYA and is<br />

widely used by mycological laboratories for<br />

storing cultures and is not as nutr<strong>it</strong>ious as the<br />

other above-described formulas.)<br />

The pH of the above media formulations, after<br />

sterilizing, generally falls between 5.5-6. 8.<br />

This media can be further fortified w<strong>it</strong>h the add<strong>it</strong>ion<br />

of 3-5 grams of the end-substrate (in most<br />

cases hardwood sawdust) upon which mushrooms<br />

willbeproduced. If samples of soil ordung are desired,<br />

they first must be pre-boiled for 1-2 hours<br />

before adding to any of the above formulas. One<br />

potential advantage of the add<strong>it</strong>ion of these endsubstrate<br />

components is a significant reduction in<br />

the "lag period. "The lag period is seen when<br />

mushroommyceliumencountersunfarniliarcomponents.<br />

(See Leatham & Griffin, 1984; Raaska<br />

1990). This simple step can greatly accelerate<br />

the mushroom life cycle, decreasing the duration<br />

of colonization prior to fru<strong>it</strong>ing.<br />

The dry components are mixed together,<br />

placed into a flask, to which 1 l<strong>it</strong>er of water is<br />

added. This cultivator finds that well-water,<br />

spring water, or mineral water works well.<br />

Chlorinated water is not recommended. Purchasing<br />

distilled water is unnecessary in my<br />

opinion. Once the media has been thoroughly<br />

mixed, the media flask is placed into a pressure<br />

cooker. The top of the media flask is e<strong>it</strong>her<br />

stopped w<strong>it</strong>h non-absorbent cotton, wrapped in<br />

aluminum foil, or, if equipped w<strong>it</strong>h a screw cap,<br />

the cap is loosely tightened. Sterilize for 45<br />

minutes @ 15 psi or @ 2500 F<br />

Pressure cookers or sterilizers that do not re-<br />

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