The basic setup is as follows:
We are using partitioned petri dishes, with growth medium on one side and empty on the other. The side with growth medium has a standard amount of fungal colony placed on it, the blank side has a 2 ml microcentrifuge vial with either water, ethanol, d-3-carene, or (hopefully) CS2 or a CS2/Ethanol solution.
A tiny hole has been burned through the top of the centrifuge tube to ensure that the compounds elute. We have had no trouble getting reliable rates with ethanol and d-3-carene, but the CS2 elutes in minutes.
The idea is that the (synthetically derived) headspace volatiles are influencing fungal growth in some way. We performed the exact same experimental design using partitioned petri dishes with fungal colonies and yeast colonies, and showed that the presence of yeast-produced volatiles enhanced fungal growth.
When we performed a GC of the headspace volatiles produced by yeasts, we came up with ethanol, d-3-carene, and CS2.
Thoughts? Our main problem is just making a CS2/Ethanol solution, or finding some way to work with the CS2 so that it doesnt elute within minutes. Ideally the solution or compound would volatilize gradually over about 15 days.
thanks.