Gas Production by Yeast.
First Experiment
Apparatus
The apparatus we used in the first experiment are as follows: Syringe, fresh yeast, three solutions of glucose at concentrations of 1%, 5% and 10%, enamel dish, boss head, small crystallising dish, glass rod, spatula, 10cm measuring cylinder, stop clock, thermometers and a water bath.
Prediction
I predict that as I increase the concentration of glucose, the more bubbles will be produced.
Method
My partner and I placed one spatula of fresh yeast into a glass beaker, 5cm3 of 1% glucose was added to the beaker slowly bit at a time, my partner and I mixed the two together thoroughly. When the glucose and yeast were mixed together well, we drew 5cm3 of the mixture into a syringe we then made sure that the mixture was not near the nozzle by pulling the plunger back as far as it could go. We both filled a water bath with warm water at a temp of 35oC and placed the syringe in the bath, a boss head was used to hold the syringe down. My partner then started the stop clock and I was on hand to count the number of bubbles produced each minute. I intended to work out an average number of three readings. After washing the equipment out we intended to repeat the experiment with 5% and 10% concentrations of glucose.
First Experiment
Apparatus
The apparatus we used in the first experiment are as follows: Syringe, fresh yeast, three solutions of glucose at concentrations of 1%, 5% and 10%, enamel dish, boss head, small crystallising dish, glass rod, spatula, 10cm measuring cylinder, stop clock, thermometers and a water bath.
Prediction
I predict that as I increase the concentration of glucose, the more bubbles will be produced.
Method
My partner and I placed one spatula of fresh yeast into a glass beaker, 5cm3 of 1% glucose was added to the beaker slowly bit at a time, my partner and I mixed the two together thoroughly. When the glucose and yeast were mixed together well, we drew 5cm3 of the mixture into a syringe we then made sure that the mixture was not near the nozzle by pulling the plunger back as far as it could go. We both filled a water bath with warm water at a temp of 35oC and placed the syringe in the bath, a boss head was used to hold the syringe down. My partner then started the stop clock and I was on hand to count the number of bubbles produced each minute. I intended to work out an average number of three readings. After washing the equipment out we intended to repeat the experiment with 5% and 10% concentrations of glucose.