First we obtained a tributyrin agar plate and we used the aseptic technique to inoculate the tributyrin agar plate with a loopful of bacteria from our agar slant culture.


We then incubated the inoculated plate upside-down at 35 degrees Celsius for two days.
When we came back to lab two days later, we took out our plate from the incubator and examined the plate for a clear area around our bacteria growth (as indicated on the left). We did not see a clear area around our bacteria growth so this indicates that our bacteria are not able to digest a triglyceride.
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