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Physiology of bacterial growth
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What Affects the Rate of Breakdown of Hydrogen Peroxide by Enzymes Aim === The aim of this experiment is to find out how temperature and concentration affect the breakdown of hydrogen peroxide by an enzyme (yeast). I hope to achieve reliable results that will confirm my predictions. Prediction ========== I predict that if the concentration is high in the yeast then the speed of oxygen produced in the reaction with hydrogen peroxide will also be high. This is because the amount of yeast that can react with the hydrogen peroxide can get no higher and will have the maximum affect on the reaction. If the concentration is more in favour of water then the amount of oxygen produced will be slow because there is not as much yeast to react with the hydrogen peroxide, giving less oxygen. If the temperature is not in favour of the limits to the yeast then the amount of oxygen produced will be small because the enzyme will have denatured. If the temperature is in favour of the yeast then the amount of oxygen produced will be high because it is at the prime temperature for the yeast to react. I predict that if I double the amount of yeast then I will get double the amount of oxygen produced because I am doubling the rate of which the particles collide. I predict that if I double the amount of water in the yeast then the oxygen will have decreased by double because I am halving the amount of yeast particles the can react. Independent Variable ==================== This is what I'm going to be changing in the experiment and this will be the temperature and the concentration of the yeast. There are several variables in this experiment, they are: · Amount Used - Too much or too little of the hydrogen peroxide causes the reaction to speed up/slow down producing different amounts of oxygen. If the amount of either hydrogen peroxide or yeast is different in any of the sections in the experiment then the results
2. A test tube was then filled with 35ml of yeast and placed in the
For example, substrate concentration, enzyme concentration, and temperature could all be factors that affected the chemical reactions in our experiment. The concentration of substrate, in this case, would not have an affect on how the bovine liver catalase and the yeast would react. The reason why is because in both instances, the substrate (hydrogen peroxide) concentration was 1.5%. Therefore, the hydrogen peroxide would saturate the enzyme and produce the maximum rate of the chemical reaction. The other factor that could affect the rate of reaction is enzyme concentration. Evidently, higher concentrations of catalase in the bovine liver produced faster reactions, and the opposite occurs for lower concentrations of catalase. More enzymes in the catalase solution would collide with the hydrogen peroxide substrate. However, the yeast would react slower than the 400 U/mL solution, but faster than the 40 U/mL. Based on this evidence, I would conclude that the yeast has a higher enzyme concentration than 40 U/mL, but lower than 400
· I also predict that when my results are put on to a graph they will
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.
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The Effect of Surface Area on the Rate of Reaction Between Catalase from a Potato and Hydrogen Peroxide Aim To find out the relationship between the surface area of a potato chip and the rate of reaction when hydrogen peroxide is put in with it. Variables As I do this experiment the thing I am going to be changing is the surface area of the potato chip, first I will put it in the beaker as a whole (3cm chip) then I will start cutting it into smaller pieces and repeating the experiment. I will keep the temperature the same throughout all the experiments also I will keep the amount and concentration of hydrogen peroxide the same, the amount of potato and the same brand of potato. By doing this I will make it a fair test. Prediction I predict that the bigger the surface area the quicker the 10 cubic cm of hydrogen peroxide gas will be produced.
Input variables In this experiment there are two main factors that can affect the rate of the reaction. These key factors can change the rate of the reaction by either increasing it or decreasing it. These were considered and controlled so that they did not disrupt the success of the experiment. Temperature-
I will be studying varying concentrations of ethanol and their effect on fermentation of saccharomyces cerevisiae, which is a yeast commonly known as brewer’s yeast. The first step of alcohol fermentation begins with glycolysis, which is the process of breaking down glucose molecules, the breakdown of glucose through glycolysis forms two pyruvate molecules, and two carbon dioxide molecules. The final steps of fermentation are anaerobic, occurring without oxygen. Pyruvate is split into carbon dioxide and two carbon acetaldehydes. Then electrons and hydrogen are transferred from NADH to the acetaldehyde, then 2 NAD+ and EtOH are formed. NAD+ is regenerated to continue glycolysis, but no additional ATP is produced. The final net products of fermentation are two ATP from glycolysis, 2 CO2, and two EtOH molecules per glucose (Starr et. al. 2016). The chemical formula for fermentation is C6H12O C2 H5 OH + CO2. Yeast cells are able to
Investigating the Effect of Temperature on the Fermentation of Yeast To fully investigate the effect of temperature on the rate of fermentation of yeast Background Information Yeast is a single-cell fungus, occurring in the soil and on plants, commonly used in the baking and alcohol industries. Every living thing requires energy to survive and through respiration, glucose is converted into energy. There are two types of respiration available to living cells are: 1.
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.
Investigate the Effect of pH on Immobilised Yeast Cells on the Breakdown of Hydrogen Peroxide
Dependent Variable ------------------ Rate at which the bubbles of oxygen rise, which will be calculated by observing how many bubbles of oxygen rise to the surface of a measuring cylinder (by means of downward displacement) in one minute. This will be measured in bubbles per ten seconds. Control variables: ¨ Volume of substrate used: 100ml ¨ Temperature: taken place at room temperature 21 degrees centigrade ¨ Type of substrate used: Hydrogen peroxide ¨ Mass of meat used: 5g ¨ Amount of water in the test tube in which the oxygen bubbles downward displaces in the water. This is so the time taken for each individual bubble to effectively rise to the bottom of the test tube will take the same amount of time.
There were five test solutions used in this experiment, water being the control, which were mixed with a yeast solution to cause fermentation. A 1ml pipetman was used to measure 1 ml of each of the test solutions and placed them in separated test tubes. The 1 ml pipetman was then used to take 1ml of the yeast solution, and placed 1ml of yeast into the five test tubes all containing 1 ml of the test solutions. A 1ml graduated pipette was placed separately in each of the test tubes and extracted 1ml of the solutions into it. Once the mixture was in the pipette, someone from the group placed a piece of parafilm securely on the open end of the pipette and upon completion removed the top part of the graduated pipette.