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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
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-
The results shown in table 1 clearly show that when the volume of yeast is increased in the milk solution, so does the rate of oxygen depletion and therefore the rate of eutrophication. It shows that when 2mL of yeast solution was added it took 32.86 minutes on average for the milk to be depleted of oxygen, while it took only 7.46 minutes on average for the 10mL of yeast to use up the oxygen present.
· I also predict that when my results are put on to a graph they will
Investigate the Effect of pH on Immobilised Yeast Cells on the Breakdown of Hydrogen Peroxide
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.
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.
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.
In our Biology Lab we did a laboratory experiment on fermentation, alcohol fermentation to be exact. Alcohol fermentation is a type of fermentation that produces the alcohol ethanol and CO2. In the experiment we estimated the rate of alcohol fermentation by measuring the rate of CO2 production. Both glycolysis and fermentation consist of a series of chemical reactions, each of which is catalyzed by a specific enzyme. Two of the tables substituted some of the solution glucose for two different types of solutions. They are as followed, Table #5 substituted glucose for sucrose and Table #6 substituted the glucose for pH4. The equation for alcohol fermentation consists of 6 Carbons 12 Hydrogens 6 Oxygen to produce 2 pyruvates plus 2 ATP then finally the final reaction will be 2 CO2 plus Ethanol. In the class our controlled numbers were at Table #1; their table had 15 mL Glucose, 10 mL RO water, and 10 mL of yeast which then they placed in an incubator at 37 degrees Celsius. We each then measured our own table’s fermentation flasks every 15 mins for an hour to compare to Table #1’s controlled numbers. At
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.
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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