Growth time to log phase for a vat of yeast after innoculation of warm sterile medium is a few hours at most. They really get rocking. Fermenting yeast evlove large volumes of carbon dioxide gas. DO NOT SEAL the vessel! Use a fementation lock (bubbler) for one-way gas conduction.
(As an aside, can you get progessively evolve yeast to grow on "metabolially inert" sucralose sugar substitute by culturing on agar gradients or with high and increasing sucralose concentrations in solution, culturing to exhaustion in low sugar?)
Plate dilute pure yeast culture on a Petri dish. You will grow separated individual colonies with reasonably uniform density (OK - Poisson distribution, but we're talking kids). Do it again, but grow them under a black light hard above the plate (Pyrex is transparent here). A blacklight goes to 345 nm. Do you kill them all off (no fair if it overheated the plate) ? We are in business! Otherwise use a shorter wavelength lamp and be very careful about being burned, especially eyes.
http://www.minershop.com/html/blacklight.html
http://en.wikipedia.org/wiki/Ultraviolet
Photochemistry and Photobiology 81(5) 1047 (2005)
http://phot.allenpress.com/photonlin...5-08-09-RA-645
Expose the yeast after it starts growing. Reproducing cells are most vulnerable. "Mitogenesis causes mutagenesis," Bruce Ames (he of the Ames test.) Are growing yeast in air (aerobic metabolism) more vulnerable than growing yeast in unventilated containment (anaerobic fermentation)?
You can go fancy, as below, or simply regulate total exposure by total time of irradiation. There's a lot of experimentation and exploration possible. Does continuous vs. periodic exposure make a difference? Lots of dimmer vs. less time but more intense? You may want a very dense plating and shoot for 99+% lethality to rapidly breed resistance. Intensity from an infinitely long line source varies as the inverse distance, not the inverse squared distance. Or bulk irradate the bottle of solution culture until it is almost sterilized. Regrow, rezap. Reculture in a new bottle, zap some more.
Make a stepped stack of thin UV-absorbing films. Can you get a gradient of growth of the yeast underneath?. Culture the most zapped colony, replate, repeat the cycle a few times. Do the resulting yeast tolerate much more UV exposure? Are they the same color as when you began?
Raw polycarbonate film cuts off at 220 nm.
A 0.13 mm Mylar (PET) film cuts off at 320 nm.
UV-absorbing polycarbonate film cuts off at 380 nm.
Or go for a stepped stack of very thin, very slightly aluminized or chromed otherwise UV-transparent films as a broadband neutral density filter.
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Uncle Al
http://www.mazepath.com/uncleal/
(Toxic URL! Unsafe for children and most mammals)
http://www.mazepath.com/uncleal/qz4.htm