HI,

Swim is hobbying around with the mush's.

Last time when SWIM was extracting Harmine and had a lot of Harmaline left. He decided to add that to the mushroom substrate to see what happens. Nice thing is, that the substrate is now very shiny green under the UV. This would make it at least possible to see wether it is being metabolized if that fluoresence dissappears after some time (unless it is metaboilized in something that is fluorenscent green as well) even in the kitchen.

SWIM was following this post and tried to understand the biosynthesis of psilocybin a bit and has some vague idea of what it could become. This is not really my field though.

Does anybody has a view on this and the possible outcomes?

Also SWIM has acces to HPLC so SWIM could check and compare to either a simular mushflush with the same substrate without Harmaline and analyze the end result of both the fruiting bodies. It should be possible to see if some new compound was created and if Harmailne is still there and how much, but SWIM has no clue how to determine what that is then with his equipment.

SWIM will post his results asap. Would be nice to have some inspirational idea from the community.

Grtz