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Recommended: Enzyme lab abstract
The Change on O2 Bubbles Produced When Changing the Environment of an Enzyme. Introduction Lab 5 Exploring Enzyme Activity we are provided a chance to understand how the enzyme catalase can turn a toxic product hydrogen peroxide into a non-toxic product. We will be utilizing a potato in this experiment because it contains the enzyme catalase. In order to understand how this enzyme works we first need to know the information of enzyme, active site, substrate and how they all come together. Enzymes are used to catalyze or speed up a chemical reaction. Substrates are molecules that an enzyme pushes itself onto. The active site is a 3D shape that allows the pieces of the substrate and the enzyme to come together like a puzzle piece forming the The enzyme that we are using to see a chemical reaction is known as catalase located into the potato. This enzyme is then going to act upon the substrate in this case hydrogen peroxide. When these two come together forming the enzyme substrate complex we will begin to see the chemical reaction carried out. The question then becomes what happens to the enzyme catalase when its exposed to extreme temperatures versus room temperature? Will it speed up? Slow down? Or fail to work in general? For my experiment I compared the difference in O2 bubbles when one potato was heated and another was at room temperature. My hypothesis is that when the potato is heated to an extreme temperature the enzyme catalase would be altered to much stopping the catalyzed ability to work with hydrogen peroxide resulting in no chemical reaction. My reasoning for this is because the enzyme is being cooked for too long changing the form and structure of the potato and causing the catalase to lose its potential to push itself onto the We measured and marked our test tubes at 6 cm high. We filled both test tubes with warm water to the 6 cm mark and placed one potato in each tube. We placed one potato on the heat block and another on the test tube rack for 20 minutes. After the 20 minutes we measured the temperature of both test tubes. Then we emptied the water from the test tubes and added hydrogen peroxide to the same 6 cm mark. We placed both tubes back on the rack and observed the amount of O2 bubbles being produce by each potato. Results The findings of this experiment showed that the production of O2 bubbles with a potato at 20o Celsius were far greater than the potato exposed to temperature of 77o Celsius. As you can see looking at Figure 1 the 20o caused large amounts of fizzing (O2) bubbles while 77o produced no fizzing at all.
The purpose of this study is to analyze the activity of the enzyme, catalase, through our understanding
In both solutions of catalase there is a steady increase in reaction relative to the hydrogen peroxide concentration as it increases. A significant jump is observed in the carrot catalase solution between .25% and .5% whereas the pinto bean catalase solution has a steady increase. Each solution doesn’t generate much more reaction to the next increment of hydrogen peroxide concentration, 1%. In general it stayed level. This continued to be a trend for the pinto bean catalase solution, plateauing through to the 6% concentration of hydrogen peroxide. This is known as the point of saturation.
Method: [IMAGE] Equipment needed: Ruler Measuring Cylinder Scalpel Tongs Pipette Thermometer Tri-pod Stop-clock Gauze Delivery Tube Bunsen Burner Beaker Matches/Lighter Potato Hydrogen Peroxide Solution (20%) Water Lead Nitrate The skin of the potato was removed using a scalpel and then cut into 1cm², using a ruler to measure the size of each cube, four cubes are required for each experiment, and therefore at least 36 cubes are required for the full experiment to take place. Fill a beaker half way with water, and place a thermometer in the water. Allow the thermometer to warm to room temperature to gather an accurate reading, and measure the temperature, using the thermometer. A measuring cylinder was used to put 10ml of Hydrogen Peroxide Solution into a
Investigating the Effect of Substrate Concentration on Catalase Reaction. Planning -Aim : The aim of the experiment is to examine how the concentration of the substrate (Hydrogen Peroxide, H2O2) affects the rate of reaction. the enzyme (catalase).
Conclusion In my conclusion, the potatoes with the lowest concentration gained the most mass, and would become hard relating back to the Turgor theory I stated earlier. In contrast to this, the potatoes in the most concentrated solution lost the most weight thus becoming plasmolysed and limp also relating back to the background I have mentioned earlier. Evaluation In general the experiment was succesful the results were consistent and also were in accordance with the theories made at the start.. The experiment could have been improved by: · More subjects used instead of potatoes · More potatoes · Wider time ranger · Different molarities Using this variety of methods could have improved the experiemnt, however I was generally satisfied with the results of this osmosis experiement.
Investigating Factors that Affect the Rate of Catalase Action Investigation into the factors which affect the rate of catalase action. Planning Aim: To investigate the affect of concentration of the enzyme catalase on the decomposition reaction of hydrogen peroxide. The enzyme: Catalase is an enzyme found within the cells of many different plants and animals. In this case, it is found in celery.
The Effect of Surface Area on the Rate of Reaction Between Catalase from a Potato and Hydrogen Peroxide
Influence of Temperature on the Activity of Potato Catalase Hypothesis That the higher the temperature the higher the reaction rate of potato catalyse to a point were denaturing occurs in the enzyme and the reaction rate of the potato catalase drops off. Prediction The rate of Catalase activity will be faster at higher temperatures until a point, because at higher temperatures there are more chances of collisions between the enzyme's (Catalase) active site and the substrate (hydrogen peroxide). However the rate depends on the active site being able to join with the substrate, and at higher temperatures the enzyme can be denatured, which changes the shape of the active site which thus prevents the reaction from happening. At first, as the temperature increases the activity of the Potato catalase also increases this is because the collision rate of the enzyme with the hydrogen peroxide is increased.
Abstract: Enzymes are catalysts therefore we can state that they work to start a reaction or speed it up. The chemical transformed due to the enzyme (catalase) is known as the substrate. In this lab the chemical used was hydrogen peroxide because it can be broken down by catalase. The substrate in this lab would be hydrogen peroxide and the enzymes used will be catalase which is found in both potatoes and liver. This substrate will fill the active sites on the enzyme and the reaction will vary based on the concentration of both and the different factors in the experiment. Students placed either liver or potatoes in test tubes with the substrate and observed them at different temperatures as well as with different concentrations of the substrate. Upon reviewing observations, it can be concluded that liver contains the greater amount of catalase as its rates of reaction were greater than that of the potato.
The Effect of pH on the Activity of Catalase Planning Experimental Work Secondary Resources Catalase is a type of enzyme found in different types of foods such as potatoes, apples and livers. It speeds up the disintegration of hydrogen peroxide into water because of the molecule of hydrogen peroxide (H2O2) but it remains unchanged at the end of the reaction.
== = This experiment is based on the concept of Osmosis. Osmosis is the diffusion of water molecules from a region of high water concentration to a low water concentration through a semi permeable membrane (in this case, the cell potato cell membrane). The cell walls of the potato cells are semi permeable meaning that water molecules (which are small) can fit through but other bigger molecules such as glucose cannot pass through. The water molecules can flow both ways through the membrane, letting molecules both in and out.
We then put the stopwatch on and left them for half an hour. After we weighed each potato tube and recorded our results. We did the experiment twice. We did this to make sure our results were correct. Preliminary method: We did everything the same as in our other experiment except we
How the Concentration of the Substrate Affects the Reaction in the Catalase Inside Potato Cells Introduction Enzymes are made of proteins and they speed up reactions, this means that they act as catalysts. Hydrogen peroxide is a byproduct of our cell's activities and is very toxic. The enzymes in our bodies break down the hydrogen peroxide at certain temperatures they work best at body temperature, which is approximately 37 degrees. At high temperatures, the cells begin to denature. This means that the hydrogen peroxide is prevented from being broken down because they will not 'fit' into the enzyme.[IMAGE] Objective I am going to find out how the concentration of the substrate, hydrogen peroxide affects the reaction in the catalase inside the potato cells.
Hypothesis: If a test tube filled with 3% hydrogen peroxide and catalase solution, the room temperature will increase the activity. Freezer, refrigerator, and boiling water will have
An Investigation into the Decomposition of Hydrogen Peroxide Aim: To investigate the rate of decomposition of H2O2 with different amounts of catalyst (MnO2). Hypothesis: When H2O2 and a catalyst are mixed together, the catalyst would break down H2O2 into water and oxygen. This will result in bubbles being produced. With the data of these oxygen bubbles, the rate at which H2O2 decomposed could be found out. 2H2O2 (l) à2H2O + O2 The controlwould be to maintain the same temperature (room temperature) and to use the same amount of hydrogen peroxide (10ml) in all the tubes.