Here at the Faculty of Life Sciences in the University of Manchester we have a number of researchers using Drosophila melanogaster as a model organism. Our media staff make fly food in a pressurised vessel, bringing it up to 99C under constant mechanical stirring before cooling it and adding preservatives. The recipe we use produces a highly viscous liquid that has proved the death of many stirring mechanisms. We are now in the process of replacing our media maker and have been wrestling with the problem that a pressurised vessel means that the stirring has to be done through indirect magnetic induction, which seems more prone to mechanical breakdown, whereas a non-pressurised vessel means you can have a directly-driven stronger stirring mechanism but you then run the risk of fluid loss through evaporation or extremely vigorous boiling, which often overboils the vessel.
Our recipe is:
Total Volume 10.00 l
Water 8.70 l
Yeast 434.78 g
Glucose 689.57 g
Agar 72.17 g
Maize 626.09 g
Propionic Acid 26.09 ml
Nipagin 234.78 ml
How does this compare to anyone else's recipe? What mechanical solution do you use, and what volume of vials or bottles do you produce in a week?
Thanks,
Geoff Blunt
Greg_A (not verified)
Hi Geoff,
We provide two sizes to our researchers, in 50 ml vials we use 9.5ml of food and in 500ml bottles we use 72ml of food. The media kitchen makes between 30-40 litres each week in a big old pot and it’s manually stirred with a wooden spoon (which is also was how it was made back at Warwick University when I worked there a few years ago), not magnetically stirred in a mediaclave.
The recipe is the Dundee Formula:
Water 10 litres
Live Yeast 57g
Glucose 786g
Agar 107g
Maize 714g
Propionic Acid 32 ml
Nipagin 27g equivalent dissolved in ethanol and added when cooling
Regards,
Greg.
Greg Anderson
Centre Laboratory Manager
Wellcome Trust Centre for Cell Biology
University Of Edinburgh