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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
Catalase is a common enzyme that is produced in all living organisms. All living organisms are made up of cells and within the cells, enzymes function to increase the rate of chemical reactions. Enzymes function to create the same reactions using a lower amount of energy. The reactions of catalase play an important role to life, for example, it breaks down hydrogen peroxide into oxygen and water. Our group developed an experiment to test the rate of reaction of catalase in whole carrots and pinto beans with various concentrations of hydrogen peroxide. Almost all enzymes are proteins and proteins are made up of amino acids. The areas within an enzyme speed up the chemical reactions which are known as the active sites, and are also where the
This experiment was conducted to determine the effects of pH and temperature on peroxidase from a potato. The optimum temperature for peroxidase was determined to be 23°C, because it had a rate of absorbance of 0.3493, higher than the other temperatures evaluated. A temperature of 48°C is inefficient of speeding up peroxidase activity because its rate of absorbance was 0.001.
This is a type of reaction where a molecule is broken down into smaller pieces. It is called an anabolic reaction. This experiment is the breakdown of hydrogen peroxide to form water and oxygen in the air. Catalase is found in a cell organelle called the peroxisome. Peroxisomes in animal cells are occupied in the decomposition of
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.
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.
Purpose: This lab gives the idea about the enzyme. We will do two different experiments. Enzyme is a protein that made of strings of amino acids and it is helping to produce chemical reactions in the quickest way. In the first experiment, we are testing water, sucrose solution, salt solution, and hydrogen peroxide to see which can increase the bubbles. So we can understand that enzyme producing chemical reactions in the speed. In the second experiment, we are using temperature of room, boiling water, refrigerator, and freezer to see what will effect the enzyme.
This enzyme speeds up the break down of hydrogen peroxide into water and oxygen, as enzymes are biological catalysts. [IMAGE]The reaction: Hydrogen peroxide Water + Oxygen Catalase -------- [IMAGE] 2H2O2 2H2O + O2 Apparatus: Hydrogen Peroxide, Several sticks of celery, Stand, boss and clamp, 100ml conical flask, 25cm3 burette, 1800cm3 beaker, Rubber bung with delivery tube, Distilled water, Large container filled with water, 10cm3 measuring cylinder, 10cm3 syringe, 20cm3 syringe, Blender, Knife, Ceramic tile, Electronic balance (correct to 2 decimal places), Sieve, Stopwatch/timer. The variables: There are many possible variables in this investigation, such as pH, temperature, the concentration of substrate and the concentration of the enzyme.
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
With this information we were able to identify any patterns and similarities. Hypothesis: The higher the temperature of water, potato and H²O², the rate at which the Enzyme will work will be faster therefore producing more oxygen. The reaction will be the same without the catalase (potato). Therefore in both experiments the Enzyme will work more rapidly and produce more oxygen. Aim: To test the hypothesis.
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.
The reason for this is that as you increase the temperature of the enzyme and the substrate molecules you also increase the energy in the form of kinetic energy which they possess. Because the enzymes and substrate molecules are moving faster the chance of them colliding in a certain time and area is increased. Thus the chance of the hydrogen peroxide molecules binding with the Catalase molecules active site and reacting is higher. However after a certain point increasing the temperature will begin to hinder the activity of the potato catalase.
The Effect of Surface Area on the Rate of Reaction Between Catalase from a Potato and Hydrogen Peroxide
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.