Hi Dianne,
This sounds like it will be an excellent project. Here are some things you should consider:
1. Do you have access to a microbiology laboratory? This experiment really should be done in a regular laboratory. Have you every grown fungi in a laboratory before?
2. Do you have a method for testing for fungal inhibition? There are two standard methods and the following article describes a new method that you could use if you had access to the equipment. With the radial growth method, the test fungicide (in this case, papaya seed extract) is added to the cooled potato dextrose agar just before the agar plates are poured. The test organism is inoculated onto the center of the plate and the growth of the fungal colony is measured in centimeters after 3 days of incubation. In the dry weight method, the Botrytis is grown in a liquid culture medium for 3 days and the fungus is then filtered and dried before it is weighed. The third new method requires a microplate reader and preparation of a standard suspension of fungal spores. You can choose just one method for your experiment.
http://www.apsnet.org/pd/pdfs/2003/0317-04R.pdf
3. Do you have cultures of the two test organisms? How will you maintain the stock cultures? One very important point that is mentioned in the reference above is that the culture used to test for fungicide activity must be actively growing when it is transferred to the test medium. The automated method uses spores.
4. For your experiment, you should use more than one concentration of papaya seed extract. I would recommend using between 3 and 7 different concentrations. You should also run the samples in duplicate or triplicate. If at all possible, run the experiment more than one time. What is your independent variable in this experiment? What is the dependent variable? What will you use for controls?
I hope these suggestions will help. Please let us know if you have any questions.
Donna Hardy