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discovery experiment
CHARLES PEPIN (STUDENT), MELBOURNE FL , CHARLES MARZZACCO (RETIRED), MELBOURNE FL
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Introduction
Enzyme catalysis1 is an important topic which is often neglected in introductory chemistry
courses. In this paper, we present a simple experiment involving the yeast-catalyzed fermentation
of sugars. The experiment is easy to carry out, does not require expensive equipment and is
suitable for introductory chemistry courses.
The sugars used in this study are sucrose and lactose (disaccharides), and glucose, fructose
and galactose (monosaccharides). Lactose, glucose and fructose were obtained from a health
food store and the galactose from Carolina Science Supply Company. The sucrose was obtained
at the grocery store as white sugar. The question that we wanted to answer was “Do all sugars
undergo yeast fermentation at the same rate?”
Sugar fermentation results in the production of ethanol and carbon dioxide. In the case of
sucrose, the fermentation reaction is:
\[C_{12}H_{22}O_{11}(aq)+H_2 O\overset{Yeast\:Enzymes}
{\longrightarrow}4C_{2}H_{5}OH(aq) + 4CO_{2}(g)\]
The hydrolysis of sucrose results in the formation of glucose and fructose, while lactose
produces glucose and galactose.
The enzymes sucrase and lactase are capable of catalyzing the hydrolysis of sucrose and lactose,
respectively.
\[C_{6}H_{12}O_{6}(aq)\overset{Yeast Enzymes}{\longrightarrow}2C_{2}H_{5}OH(aq) +
2CO_{2}(g)\]
Experiment
In our experiments 20.0 g of the sugar was dissolved in 100 mL of tap water. Next 7.0 g of Red
Star® Quick-Rise Yeast was added to the solution and the mixture was microwaved for 15
seconds at full power in order to fully activate the yeast. (The microwave power is 1.65 kW.)
This resulted in a temperature of about 110 oF (43 oC) which is in the recommended temperature
range for activation. The cap was loosened to allow the carbon dioxide to escape. The mass of
the reaction mixture was measured as a function of time. The reaction mixture was kept at
ambient temperature, and no attempt at temperature control was used. Each package of Red Star
Quick-Rise Yeast has a mass of 7.0 g so this amount was selected for convenience. Other brands
of baker’s yeast could have been used.
This method of studying chemical reactions has been reported by Lugemwa and Duffy et
al.2,3 We used a balance good to 0.1 g to do the measurements. Although fermentation is an
anaerobic process, it is not necessary to exclude oxygen to do these experiments. Lactose
and galactose dissolve slowly. Mild heat using a microwave greatly speeds up the process. When
using these sugars, allow the sugar solutions to cool to room temperature before adding the yeast
and microwaving for an additional 15 seconds.
However, when the reactions go to completion, the lactose, lactase and yeast mixture gives off
only about half as much CO2 as the sucrose and yeast mixture. This suggests that one of the two
sugars that result when lactose undergoes hydrolysis does not undergo yeast fermentation. In
order to verify this, we compared the rates of fermentation of glucose and galactose using yeast
and found that in the presence of yeast glucose readily undergoes fermentation while no
fermentation occurs in galactose.
Fig. 2. Comparison of the mass of CO2 released vs time for the fermentation of sucrose, glucose
and fructose. Each 20 g sugar sample was dissolved in 100 mL of water and then 7.0 g of yeast
was added.
Fig. 3. Comparison of the mass of CO2 released vs time for the fermentation of 20.0 g of glucose
and 10.0 g of glucose. Each sugar sample was dissolved in 100 mL of water and then 7.0 g of
yeast was added.
Fig. 4. Comparison of the mass of CO2 released vs time for the fermentation of two 20.0 g
samples of glucose dissolved in 100 mL of water. One had 7.0 g of yeast and the other had 3.5 g
of yeast.
Discussion
In hindsight, the observation that the rate of fermentation is dependent on the concentration of
yeast but independent of the concentration of sugar is not surprising. Enzyme saturation can be
explained to students in very simple terms. A molecule such as glucose is rather small compared
to a typical enzyme. Enzymes are proteins with large molar masses that are typically greater than
100,000 g/mol.1 Clearly, there are many more glucose molecules in the reaction mixture than
enzyme molecules. The large molecular ratio of sugar to enzyme clearly means that every
enzyme site is occupied by a sugar molecule. Thus, doubling or halving the sugar concentration
cannot make a significant difference in the initial rate of the reaction. On the other hand,
doubling the concentration of the enzyme should double the rate of reaction since you are
doubling the number of enzyme sites.
The experiments described here are easy to perform and require only a balance good to 0.1 g and
a timer. The results of these experiments can be discussed at various levels of sophistication and
are consistent with enzyme kinetics as described by the Michaelis-Menten model.1 The
experiments can be extended to look at the effect of temperature on the rate of reaction. For
enzyme reactions such as this, the reaction does not take place if the temperature is too high
because the enzymes get denatured. The effect of pH and salt concentration can also be
investigated.
References
1. Jeremy M. Berg, John L. Tymoczko and Lubert Stryer, Biochemistry, 6th edition, W.H.
Freeman and Company, 2007, pages 205-237.
2. Fugentius Lugemwa, Decomposition of Hydrogen Peroxide, Chemical Educator, April
2013, pages 85-87.
3. Daniel Q. Duffy, Stephanie A. Shaw, William D. Bare, Kenneth A. Goldsby, More
Chemistry in a Soda Bottle, A Conservation of Mass Activity, Journal of Chemical
Education, August 1995, pages 734-736.
4. Jessica L Epstein, Matthew Vieira, Binod Aryal, Nicolas Vera and Melissa Solis,
Developing Biofuel in the Teaching Laboratory: Ethanol from Various Sources, Journal
of Chemical Education, April 2010, pages 708–710.