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The most common way to produce an LI is to Mix up a wedge or dish of thoroughly clean mycelium on agar with sterile h2o and draw it right into a syringe. To accomplish this, insert a number of cc/ml of sterile h2o on to the agar plate by using a syringe and gently scrape mycelium Using the syringe needle or an inoculating needle/loop.Reports have s

tony, so I inocuylate the grain that is over the bottome of the bag. Once the mycelium if all white, I crack up the grain and mix while in the substrate then hold out?In case you inoculated one particular substrate with two species, they would most likely duke it out, and the much better just one would get. I assume they could also choose sides and