How does the structure of sugar affect the rate of fermentation?

Background Information:
Living things need to obtain energy in order to sustain their presence by performing their vital activities. For most of the vital activities energy is a must have concept. Cellular respiration is an example fort he process of obtaining energy in the form of ATP (Adenosine Triphosphate)There are two main processes to obtain energy by respiration. They are classified as Aerobic and Anaerobic respiration which are distincted by the use of oxygen.
Anaerobic respiration also stated as fermentation is the process to obtain ATP without the use of Oxygen. The process where yeast converts sugar into ethyl alcohol and carbondioxide is called ethyl alcohol fermentation. This is a result of the absence of oxygen for yeast to convert the organic substance (sugar) into cellular energy. This is considered an anaerobic process.
Yeast, as a member of the fungi family is neither an animal nor a plant,it is an eukaryotic micro organism. In ethyl alcohol fermentation sugar fungi form of yeast is used. The conversion of sugar into carbon dioxide and alcohol provides energy for the yeast cells. Glucose, sucrose, lactose and fructose are the sugars that are often used to perform experiments and observe the process of fermentation.

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Glucose is a type of sugar and a subcategory of the monosaccharides. It’s molecular formula is C6H12O6 . Sucrose is a subcategory of disaccharides as a combination of glucose and fructose. It’s molecular formula is C12H22O11. Lactose is another disaccharide derived from glucose and galactose with molecular formula C12H22O11 which makes it an isomer of sucrose. Fructose is a monosaccharide that is also known as fruit sugar and mostly bonds with glucose to form sucrose. It’s molecular formula is also C6H12O6.
The overall process of ethyl alcohol fermentation is the conversion of sugar into CO2 and alcohol (CH3CH2OH). The reaction is shown for glucose is as shown below ;
The simplicity of the chemical reaction is not preserved in reality and the products are far more complex that it is shown in the reaction. Sugar is also incorporated into other unmentioned products such as yeast biomass,acids and glycerol. This fermentation which was done using glucose as sugar was an example for the fermentation of a monosaccharide. Even though the process does dffer slightly,the amount of the released carbon dioxide and alcohol does change through monosaccharides and disaccharides.
The first step of alcoholic fermentation is the cleavage of glycosidic bonds between glucose and fructose by the enzyme invertase. Then glucose molecules are broken down into two pyruvate molecules by glycolysis. Thus as shown in the reaction above,glycolysis causes the reduction of NAD+ to NADH,ADP is converted into ATP and water molecules via substrate-level phosphorylation.
In the background researches of the previous experiments, it was estimated that different sugars would release different amounts of CO2. Glucose was expected to produce more carbon dioxide than other types of sugar because of it’s 6-Carbon structure. Sucrose was expected to be the runner up producer of carbon dioxide after Glucose because of it’s formation by the combination of glucose and fructose. It has also been considered that the attachment of a 5-Carbon sugar to a 6-Carbon sugar would limit the production of CO2. Fructose was not considered to have a major importance in the experiment but it was estimated that it would evolve some carbon dioxide. The smallest expectation was made on lactose because of it’s complex structure and the absence of enzymes that can break down galactose.
As the results, it was seen that in adequate amount of time both glucose and sucrose reached the maximum amount of CO2 release however sucrose reached it faster. Fructose produced a small amount of CO2 where lactose produced almost none.
Therefore it was stated that the structural differences between different types of sugar effects the CO2 release rate during the fermentation process of yeast.
Aim: To investigate the different fermentation rates of different sugars by measuring the CO2 release.
Research Question: How does the structure of sugar affect the rate of fermentation?
Variables:

Independent Variable

Type of sugar

Glucose,Fructose and Lactose were used.

Dependent Variable

Rate of ethyl alcohol fermentation

It depended on the structure of the sugar used.

Controlled Variable

Temperature

It was done in room temperature (38-40 ºC).

 

Amount of sugar

The amount of sugar was kept constant at 5 mg.

(Table 1)
Hypothesis:
If the structural complexity of the sugar increases,the rate of ethyl alcohol fermentation increases.
Material & Method
1. Materials

100 ml pure water (x4)
5 mg yeast (x4)
5 mg Fructose
5 mg Lactose
5 mg Glucose
100 ml beakers (x4, %5)
500 ml beaker
Tube (x4)
Syrnge (x4)
Vernier competer inference
Logger pro
Vernier CO2 Gas sensor
250 mL respiration chamber
Thermometer
Heater
Beral pipettes

2. Method
I. 5 mg of Fructose, Glucose and Lactose was measured separately.
II. Measured sugars were put into separated beakers.
III. 500 ml ofpure water was heated until it reached 38-40ºC and kept constant.
IV. 5 mg of yeast was put into tubes.
V. 25 ml of pure water was put into tubes which were filled with yeast (x4)
VI. Filled tubes were put into the pre-heated 500 ml beaker for 10 minutes.
VII. 2 ml of yeast solution was measured each tube using the syringes.
VIII. All of the solutions were added in to the chamber separately and CO2 sensor was put on the chamber.
IX. Amount of C02 release was calculated for each beaker.
X. All steps were repeated for 5 trials.
3. Design
Data Table (Raw Data):

Fructose

Time

Carbon Diocide Release

 

Trial 1

Trial 2

Trial 3

Trial 4

Trial 5

Mean Average

 

0 s.

0

0

0

0

0

0

 

20 s.

0

0

0

0

0

0

 

40 s.

821

830

825

820

820

823. 2

 

60 s.

877

883

873

875

879

877. 4

 

80 s.

921

918

920

925

922

921. 2

 

100 s.

959

957

960

962

958

959. 2

 

120 s.

981

985

980

982

980

981. 6

 

140 s.

994

999

993

992

995

994. 6

 

160 s.

1006

1004

1003

1007

1000

1004

 

180 s.

1009

1011

1007

1005

1010

1008. 4

 

200 s.

1016

1019

1014

1017

1015

1016. 2

 

220 s.

1018

1023

1020

1017

1019

1019. 4

 

240 s.

1022

1025

1027

1025

1020

1023. 8

 

(Table 2)

Glucose

Time

Carbon Dioxide Release

 

Trial 1

Trial 2

Trial 3

Trial 4

Trial 5

Mean Average

 

0 s.

0

0

0

0

0

0

 

20 s.

0

0

0

0

0

0

 

40 s.

1873

1870

1876

1875

1871

1873

 

60 s.

2113

2110

2114

2012

2015

2072. 8

 

80 s.

2313

2315

2310

2311

2314

2312. 6

 

100 s.

2443

2440

2445

2442

2443

2442. 6

 

120 s.

2563

2560

2566

2562

2564

2563

 

140 s.

2651

2652

2556

2550

2555

2592. 8

 

160 s.

2745

2744

2746

2743

2748

2745. 2

 

180 s.

2800

2800

2802

2805

2801

2801. 6

 

200 s.

2839

2840

2842

2835

2841

2839. 4

 

220 s.

2870

2872

2868

2873

2869

2870. 4

 

240 s.

2893

2895

2891

2890

2896

2893

 

(Table 3)

Lactose

Time

Carbon Dioxide Release

 

Trial 1

Trial 2

Trial 3

Trial 4

Trial 5

Mean Average

 

0 s.

0

0

0

0

0

0

 

20 s.

0

0

0

0

0

0

 

40 s.

679

680

677

681

680

679. 4

 

60 s.

744

745

743

748

745

745

 

80 s.

804

805

803

800

808

804

 

100 s.

851

855

848

850

852

851. 2

 

120 s.

895

900

897

890

892

894. 8

 

140 s.

922

925

917

930

920

922. 8

 

160 s.

943

940

945

946

941

943

 

180 s.

961

960

956

967

959

960. 6

 

200 s.

976

980

970

966

981

974. 6

 

220 s.

983

985

980

988

979

983

 

240 s.

994

990

992

995

989

992

 

(Table 4)

Water

Time

Carbon Dioxide Release

 

Trial 1

Trial 2

Trial 3

Trial 4

Trial 5

Mean Average

 

0 s.

0

0

0

0

0

0

 

20 s.

0

0

0

0

0

0

 

40 s.

757

756

758

750

760

756. 2

 

60 s.

876

877

880

873

875

876. 2

 

80 s.

970

973

967

977

963

970

 

100 s.

1022

1024

1020

1027

1017

1022

 

120 s.

1054

1055

1060

1052

1057

1055. 6

 

140 s.

1082

1080

1095

1079

1083

1083. 8

 

160 s.

1109

1109

1111

1107

1109

1109

 

180 s.

1124

1127

1120

1131

1125

1125. 4

 

200 s.

1131

1134

1131

1130

1137

1132. 6

 

220 s.

1143

1140

1145

1147

1141

1143. 2

 

240 s.

1154

1155

1150

1156

1155

1154

 

(Table 5)
Average Table (Processing Data):

Fructose

Time

CO2 Release

0

0

20

0

40

823. 2

60

877. 4

80

921. 2

100

959. 2

120

981. 6

140

994. 6

160

1004

180

1008. 4

200

1016. 2

220

1019. 4

240

1023. 8

Glucose

Time

CO2 Release

0

0

20

0

40

1873

60

2072. 8

80

2312. 6

100

2442. 6

120

2563

140

2592. 8

160

2745. 2

180

2801. 6

200

2839. 4

220

2870. 4

240

2893

Lactose

Time

CO2 Release

0

0

20

0

40

679. 4

60

745

80

804

100

851. 2

120

894. 8

140

922. 8

160

943

180

960. 6

200

974. 6

220

983

240

992

Water

Time

CO2 Release

0

0

20

0

40

756. 2

60

876. 2

80

970

100

1022

120

1055. 6

140

1083. 8

160

1109

180

1125. 4

200

1132. 6

220

1143. 2

240

1154

Calculation: The calculations for calculating the fermentation rate should be done using the formula (Final CO2 release-Initial CO2 release)(ppm)/Time(min). The calculations for the experiment is as following,

Fructose: (1023. 8-0)/4= 255,95
Glucose: (2893-0)/4=723,25
Lactose: (992-0)/4=248
Water: (1154-0)/4=288,5

Graphs
(Graph 1) Shows that the Final CO2 release of yeast with Fructose is 1023.
(Graph 2) Shows that the Final CO2 release of yeast with Glucose is 2893.
(Graph 3) Shows that the Final CO2 release of yeast with Lactose is 992.
(Graph 4) Shows that the Final CO2 release of yeast with water is 1154.
Conclusion and Evaluation
Conclusion
As it has been seen in the light of the datas taken during the experiment our hypothesis has been proven to be wrong. Because even though Glucose was a monosaccharide it’s fermentation rate has been measured higher than the Fructose who is a disaccharide. The complex structure of Frutose didn’t cause the fermentation rate to be higher. Thus the hypothesis haven’t been proven to be correct.
The information in the background information has led us to assume that the rate of the more complex sugar would be higher because the number of bonds was higher. But the principle monosaccharide Glucose had the highest fermentation rate n 4 minutes followed by the disaacharide Fructose.
The slowest fermentation rate was measured from the solution which consisted of only yeast and pure water. It was already estimated because Ethyl Alcohol Fermentation is focused on producing energy for yeast. But in the lacking of an energy providing substance such as sugar,enery can not be produced.
Thus,we can conclude our experiment by stating that the structural complexity of sugars affect the rate of ethyl alcohol fermentation however it is not the only factor that affects the rate when different types of sugars are used. The type of bonds is also an effective factor on the rate of ethyl alcohol fermentation.
Limitations:

Limitations

Sütun1

Deficiency on Temperature

While heating the 500ml beaker to 38ºC,it was a struggle to try to keep the

temperature around 39ºC and it may have affected the rate of

fermentation bacause it may have affected the solublity of the sugars in yeast solution.

Cleaning the Chamber

Cleaning of the chamber in switching between trials and

different sugars has also been a struggle because it couldn’t be

cleaned totally. Hence this may have affected the fermentation

rate because of the mixture of sugars.

Minimum value of syringe

The operation done by the syringe was a little value

but the it’s minimum value was hard to read.

Improvement
The lack of controlling during the heating of the 500 mL beaker caused a uncertainty of the datas of the experiment. We could have used a more precise heater and quickly used it in the solutions. The largest uncertainties were caused by person-based uncertanities. For example if more time was spent or some tools were used in cleaning the respiration chamber the datas of the experiment could have been more accurate. . One of the other limitations during the experiment was that the use of the syringe was hard because of it’s form.
If the stated limitations were decreased to minimum,the datas could have been more precise and accurate.
References

BiologyMad A-Level Biology. 02 Mar. 2009
Cohn, Don. (1999) Science in the Real World, Microbes in Action; How Long Will I Be Blue? Universityof Missouri
Brazillian archives of biology technology. vol. 51 no. 3 Curitiba May/June 2008

 

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