Name: Ji Yoon Kim<br />Enzyme Experiment<br />Name: Ji Yoon Kim<br />Partners: Eun Jeong, Na Young<br />Date of experiment: 6th December 2010<br />Factor that affects the speed of Catalase<br />Aim:  My aim is to see whether the amount of liver that is put inside the Hydrogen Peroxide affect the speed of reaction with catalase and hydrogen peroxide. <br />Hypothesis:  If we increase the amount of liver that is put into the same amount of Hydrogen Peroxide more oxygen will be produced in the same period of time. The amount of catalase that reacts with the substrate (Hydrogen Peroxide) increases when we put more liver inside. Therefore when we increase the amount of liver more oxygen will be produced in the same period of time.<br />Variables:<br />Input variable:  The amount of liver will be our input variable. We will change it by measuring the weight of liver and putting different amount of liver in Hydrogen Peroxide. We will be using 3, 9, 15 grams of liver.<br />Output variable:  The out put variable will be the amount of oxygen produced. We will measure it by attaching a gas collection cylinder to the rubber tubing and putting it on the conical flask.<br />Control variables:<br />Control variable 1:  Type of Liver. We will keep it same by using the same type of liver, which would be chicken liver.<br />Control variable 2:  Amount of Hydrogen Peroxide. We will keep it same by using the same amount of hydrogen peroxide every time. We will use 50ml of hydrogen peroxide each time.<br />Control variable 3:  Concentration of Hydrogen Peroxide. We will keep it same by using the same concentration of Hydrogen peroxide each experiment. We will use 1% of hydrogen peroxide each time.<br />Control variable 4: Time. We will keep it same by recording data in the same time. We will record our data in 30 seconds interval, up to 3 minutes.<br />Materials:<br />-Liver (81 grams)<br />-1% Hydrogen Peroxide (450ml)<br />-50ml Measuring Cylinder<br />-250ml Conical Flask<br />-Rubber Tubing<br />-100ml Gas collection cylinder<br />-Stopwatch<br />-Electric balance<br />Diagram:<br />Picture 1<br />Electric Balance71120031750<br />Rubber Tubing<br />100ml Gas Collection Cylinder<br /> 250ml Conical Flask<br />Method:<br />Set up equipments as shown in Picture 1
Cut the liver in 3 gram
Weigh the liver to check that the weight of the liver is 3 grams
Put 50 ml of Hydrogen Peroxide into the Measuring cylinder
Put the measured Hydrogen Peroxide in to the conical flask
Put the cut liver into the Hydrogen Peroxide
As soon as the liver is inside, put the rubber tubing on to the conical flask (air tight)

Enzyme experiment

  • 1.
    Name: Ji YoonKim<br />Enzyme Experiment<br />Name: Ji Yoon Kim<br />Partners: Eun Jeong, Na Young<br />Date of experiment: 6th December 2010<br />Factor that affects the speed of Catalase<br />Aim: My aim is to see whether the amount of liver that is put inside the Hydrogen Peroxide affect the speed of reaction with catalase and hydrogen peroxide. <br />Hypothesis: If we increase the amount of liver that is put into the same amount of Hydrogen Peroxide more oxygen will be produced in the same period of time. The amount of catalase that reacts with the substrate (Hydrogen Peroxide) increases when we put more liver inside. Therefore when we increase the amount of liver more oxygen will be produced in the same period of time.<br />Variables:<br />Input variable: The amount of liver will be our input variable. We will change it by measuring the weight of liver and putting different amount of liver in Hydrogen Peroxide. We will be using 3, 9, 15 grams of liver.<br />Output variable: The out put variable will be the amount of oxygen produced. We will measure it by attaching a gas collection cylinder to the rubber tubing and putting it on the conical flask.<br />Control variables:<br />Control variable 1: Type of Liver. We will keep it same by using the same type of liver, which would be chicken liver.<br />Control variable 2: Amount of Hydrogen Peroxide. We will keep it same by using the same amount of hydrogen peroxide every time. We will use 50ml of hydrogen peroxide each time.<br />Control variable 3: Concentration of Hydrogen Peroxide. We will keep it same by using the same concentration of Hydrogen peroxide each experiment. We will use 1% of hydrogen peroxide each time.<br />Control variable 4: Time. We will keep it same by recording data in the same time. We will record our data in 30 seconds interval, up to 3 minutes.<br />Materials:<br />-Liver (81 grams)<br />-1% Hydrogen Peroxide (450ml)<br />-50ml Measuring Cylinder<br />-250ml Conical Flask<br />-Rubber Tubing<br />-100ml Gas collection cylinder<br />-Stopwatch<br />-Electric balance<br />Diagram:<br />Picture 1<br />Electric Balance71120031750<br />Rubber Tubing<br />100ml Gas Collection Cylinder<br /> 250ml Conical Flask<br />Method:<br />Set up equipments as shown in Picture 1
  • 2.
    Cut the liverin 3 gram
  • 3.
    Weigh the liverto check that the weight of the liver is 3 grams
  • 4.
    Put 50 mlof Hydrogen Peroxide into the Measuring cylinder
  • 5.
    Put the measuredHydrogen Peroxide in to the conical flask
  • 6.
    Put the cutliver into the Hydrogen Peroxide
  • 7.
    As soon asthe liver is inside, put the rubber tubing on to the conical flask (air tight)
  • 8.
    Time 3 minutewith a stop watch
  • 9.
    Measure the amountof Oxygen produced in 30 seconds intervals
  • 10.
    Record data in30 seconds intervals
  • 11.
  • 12.
    Repeat 2~11 with9g and 15g of liverResults:<br />Table 1: Amount of oxygen produced in different liver mass<br />Amount of Liver (grams)Number of TrialAmount of gas produced every 30 seconds (cm3)30s60s90s120s150s180s31689111415246791113361014162024Average5810121517911018274054672111724344353391625364560Average10172537476015110192940546721018283948593101525354557Average101727384961<br />Graph 1:<br />Amount of liver (g)<br />Conclusion:<br />In the graph shown above we could see that there was a clear difference of amount of Hydrogen Peroxide between 3 grams with 9 grams and 3 grams with 15. However there wasn’t a big difference between 9 grams and 15 grams of liver. We could see that on average, there wasn't a difference until 1 minute but after 1 minute there were one or two cm3 differences. Although there wasn’t a great difference on average between 9 grams of liver and 15 grams of liver we could see that the more the amount of liver the more the oxygen was produced. There were about 1~2cm3 increase from 9 to 15 grams. Because if we increase the amount of liver there will be more catalase reacting with Hydrogen Peroxide more oxygen was produced. I think there wasn’t a great difference between the result of 9 grams and 15 grams because of the amount of Hydrogen Peroxide. Although there was more catalase in 15 grams of liver I think there was little amount of Hydrogen Peroxide to react with. Another reason I think is because of the surface area of the liver that is touching the Hydrogen Peroxide. Although the liver was heavier the surface are that touched the Hydrogen Peroxide could have had not much difference. Therefore our hypothesis is somewhat correct. The amount of oxygen produced increased from 3 grams to 9 grams, but there wasn’t a great difference from 9 to 15 grams.<br />I don’t think my data is reliable enough because of the way we have measured the amount of oxygen produced. When we put the rubber tubing on the conical flask I have figured out that there was a 3~5 cm3 increase in the gas law syringe. Every trial the amount of gas increased differed. Sometimes the gas increased by 3cm3, sometimes the gas increased by 4cm3, and at most it increased by 5cm3 when we put the rubber tubing on to the conical flask. On average they increased by 4cm3. Because the data isn’t reliable the conclusion is not reliable also. There were only one or two cm3 difference between 9 grams and 15 grams. The one or two difference could have been from when we have put the rubber tubing on to the conical flask.<br />Evaluation:<br />I think overall our method is a reliable method to collect data however; there are some parts that are not reliable. The method may not give a reliable data because when we put the glass tubing the oxygen inside the conical flask may move to the gas collection cylinder and increase the value. The increased amount may vary depending on how hard we have pressed the rubber tubing. The method may not be reliable because on step 7 it is said to put the rubber tubing on as soon as we put the liver inside. The method does not specify whether ‘inside’ means inside the conical flask or when the liver touched the hydrogen peroxide. There were some errors that occurred during our experiment. When we did our experiment, we have left out the Hydrogen Peroxide in the sun for quite a long time. This could have had an effect on our data because when Hydrogen Peroxide is left in the sun the Hydrogen Peroxide can become dilute and slower the reaction. This will cause the amount of oxygen produced to be lower than what it should. Another error is that we sometimes used one piece or two pieces of liver. This could have had an effect on our data. This could have cause more oxygen to be produced because the more the pieces, the larger the surface area and the more the catalase reacts with Hydrogen Peroxide. <br />To improve the method I think we should first clarify the word inside. I think step 7 should be changed to ‘as soon as the liver touched the Hydrogen Peroxide’, put the rubber tubing on to the conical flask (air tight). I think to make our data reliable we should take note of the increase of gas when we put the rubber tubing on to the conical flask and subtract the value to each recording. For example for 3grams of liver trial 1 if the increase value on the gas collection cylinder was 4cm3, we should subtract to each recording by 4. Therefore the result would be 2, 4, 5, 7, 10, 11. By subtracting the increased value of the gas law syringe when the rubber tubing was put on the conical flask we could increase the reliability of our result. To solve the errors occurred during the experiment, I think we should state in the method to cover Hydrogen Peroxide with dark cloth to stop the reaction with the light when we are not using the Hydrogen Peroxide. To solve the problem with different surface areas, I think we should state in the method to cut the liver in one piece. By doing this we could solve the problem with larger surface area, which could have caused the value to be higher.<br />We could test different factors that affect the speed of the catalase. We could test whether the amount of Hydrogen Peroxide affects the speed of the catalase. We could also test different types of livers. We could test which animal’s liver has the fastest reaction. We could also test the concentration of the Hydrogen peroxide.<br />