Preview

Enzyme Lab Write Up

Good Essays
Open Document
Open Document
854 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Enzyme Lab Write Up
Vaishnavi Kothapalli
Mrs. Manning
Honors Biology
30 November 2012

TITLE:
The Reaction Rate of Catalase in Various Concentrations of Hydrogen Peroxide

QUESTION:
How long does the catalase take to float to the top of a cup filled with different amounts of hydrogen peroxide concentration?

PREDICTION: A prediction that can be made for this experiment is that the higher the concentration, the faster time it takes the catalase to react with the solution. As the concentration increases from 1% to 100%, the average reaction rate of the catalase will decrease, as the catalase will speed up the reaction. MATERIALS:
90 mL clear, plastic Solo cups filter paper bottle of regular hydrogen peroxide
1%, 25%, 50%, 75%, and 100% substrate concentration tweezers timer permanent marker pen/pencil paper for data

PROCEDURE: The experiment begins with five beakers full of various substrate concentrations. To begin the lab, gather five plastic, Solo cups and label them 1%, 25%, 50%, 75%, and 100% with the permanent marker. Then, fill each cup with 75 mL of regular hydrogen peroxide. After, lightly dip the filter paper into the 1% substrate concentration till it is completely covered. Further, dip the covered paper into the cup labeled 1% (make sure the filter paper is completely submerged and has sunk to the bottom of the cup). After the filter paper is at the bottom of the cup, begin the timer, and time how long it takes the filter paper to rise to the top. After the paper has risen, gently remove it with tweezers and dispose of it properly. Record the time taken by the filter paper to rise to the top by creating a data table on your paper. Do this again for four more trials and record data. Repeat this process with 25%, 50%, 75%, and 100% substrate concentrations. After finishing up with the experiment, make sure to record your data and calculate the averages for each percent of substrate concentration.

MACROSCOPIC QUALITATIVE OBSERVATIONS:

You May Also Find These Documents Helpful

  • Better Essays

    Purpose/Problem: There are four parts to the Enzyme Catalyst lab - Activity A, B, C, and D. In activity A, the characteristics of enzyme actions will be observed. The main purposes are to determine the rate of an enzyme catalyzed reaction, to study the characteristics of an enzyme mediated reaction, and to observe the effect of heat on enzyme activity. The purpose of activity B is to use the Titration Protocol to determine the initial amount of H2O2 present in a solution. The amount will be the baseline for activities C and D. The purpose of activity C is to determine the rate at which H2O2 spontaneously decomposes when exposed to room temperatures and ambient light for 24 hours. The purpose of activity D is to determine the rate at which catalase decomposes H2O2. After adding H2SO4 for different time lashes, etc., the resulting data will be graphed at which the catalase decomposed by catalase.…

    • 2040 Words
    • 9 Pages
    Better Essays
  • Good Essays

    Hold in liquid for about three-seconds and then touch the disk to the inside of the beaker to remove excess drops of liquid.…

    • 591 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Easy Peasy

    • 401 Words
    • 2 Pages

    4. Different concentrations of hydrogen peroxide solution were added to each test tube using a pipette. (5mL of 6%, 3% and 1.5%)…

    • 401 Words
    • 2 Pages
    Good Essays
  • Good Essays

    The prediction for the effects of temperature on the enzyme activity was that the reaction’s rate would increase as the temperature increased, until they go over the optimum temperature where the enzymes denature and the reaction’s rate quickly drops to zero. At 5 degree C the rate is 0.00059mole PNP/min. This then increases to 0.01031mmoles PNP/min at a temperature of 50 degree C. The rate then drops drastically to -0.00215moles PNP/min. This point is where the enzymes have been denatured and have no activity, shown as the last point on the fig 8 and 9, do not fit on the graph. The optimum temperature was about 47 degree C. The core body temperature is only about 37 degree C and thus these enzymes are operating below their optimum temperature.…

    • 521 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Enzyme Lab Report

    • 492 Words
    • 2 Pages

    The results of our experiment showed the solutions in both tube 1 and tube 2 increasing in absorbency in the first eight minutes but then tube 1 continued to increase while tube 2 began to balance out. Tube 3, our blank, managed to stay at 0nm the entire twenty minutes. From this data, we can conclude that our hypothesis was supported that EDTA had a greater change in absorption over PTU.…

    • 492 Words
    • 2 Pages
    Good Essays
  • Powerful Essays

    (Click on the Save a Copy button on the panel above to save your report)…

    • 1209 Words
    • 5 Pages
    Powerful Essays
  • Good Essays

    Enzyme Lab Report

    • 1060 Words
    • 5 Pages

    Problem: How can we demonstrate how enzymes work? What happens if we alter the environment of an enzyme?…

    • 1060 Words
    • 5 Pages
    Good Essays
  • Satisfactory Essays

    Enzymes Lab Report

    • 371 Words
    • 2 Pages

    Explain in detail the procedure that you followed (including amount of substrate, enzyme etc, and the whole procedure including incubation times) (3 Points)…

    • 371 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Peroxidase Lab

    • 823 Words
    • 4 Pages

    The materials needed for this experiment were four medium sized tubes, a spectrophotometer, a buffer with a pH of 5, H2O2, Peroxidase, and Guaiacol Dye. We as a group had four tubes labeled two, three, four, and five. In the tube labeled two we had a solution of 2.0 mL of H2O2 and 1.0 mL of Guaiacol Dye for a total solution of 3.0 mL. In the tube labeled three we had a solution of 4.0 mL buffer and 1.0 mL Peroxidase for a total of 5.0 mL solution. In the tube labeled four we had a solution of 2.0 mL H2O2 and 1.0 mL Guaiacol Dye for a total of 3.0 mL solution. Last, in the tube labeled five we had a solution of 4.0 mL buffer and 1.0 mL Peroxidase for a total solution of 5.0 mL. We then set the spectrophotometer to a value of zero, using a blank containing buffer, H2O2, and Guaiacol Dye. After that, tubes two and three were mixed together and tubes four and five were mixed together for a large solution of with a total of 8.0 mL. Once the two solutions are mixed clean the tube with a Kim Wipe, so all fingerprints are removed. Place the tube with solutions of four and five in the ice bath for twenty minutes. While placing the tube in the spectrophotometer make sure the white strip that is on the tube is facing the direction of the person who is handling placing the tube I the spectrophotometer. Furthermore, just let the spectrophotometer act on the solution for the desired length of time while recording the data at each specific…

    • 823 Words
    • 4 Pages
    Good Essays
  • Good Essays

    |Hot Water |Hot water splashing or spilling on |Safety glasses and aprons were worn |…

    • 929 Words
    • 4 Pages
    Good Essays
  • Satisfactory Essays

    Enzyme Lab Quiz

    • 293 Words
    • 2 Pages

    a. Temperature affects the rate at which substrate and enzyme molecules collide. If the temperature is greater than the optimal the activation site denatures which makes binding more difficult. Lower temps make it so that the enzymes and substrates attach at a slower rate, diminishing product formation.…

    • 293 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Enzyme Lab

    • 1242 Words
    • 6 Pages

    6. Measure 10 mL of hydrogen peroxide. (diluted with water by 25, 75, 50 percent)…

    • 1242 Words
    • 6 Pages
    Good Essays
  • Better Essays

    enzyme report

    • 684 Words
    • 3 Pages

    In this lab we used a solution of lactase to test the chemical and physiological properties of this particular enzyme and determined whether the lactase came from human cells or bacterial cells. In the statistical analysis statistical formulas and techniques are used to analyze the significance of a set of data and the validity of the conclusions made based on that data. These are some terms and definitions that will be crucial to understanding the validity of this experiment. An enzyme is a protein that acts as a catalyst to lower the activation energy required for reactions to progress in the cells. Null hypothesis states that there will be no difference between the result of two separate variables A and B. The null hypothesis states in regards to the enzyme experiment that lactase will not bind preferentially, or more specifically, to maltose or lactose. Before a null hypothesis can be rejected we must notice a large difference between glucose produced from maltose versus lactose. Alternate Hypothesis states the opposite of null in that there will be differences between the results of A and B. Probability is an indication of likelihood very similar to a percent chance. All probabilities are between 0 and 1, with probability zero indicating an event is impossible and one indicating an event is certain to occur. T-value or t-Test is what is used to determine whether or not the null hypothesis is valid. This t-value can be used to create a p value which in turn will determine whether the results are statistically significant or not. Based on what I know about the effect of temperature on the enzymatic activity of lactase, I hypothesize that higher temperatures will cause denaturing in the enzyme causing it to be less effective and lower temperatures will more conducive to enzymatic activity, and a higher pH will be more conducive to enzymatic activity.…

    • 684 Words
    • 3 Pages
    Better Essays
  • Good Essays

    Enzyme Lab Write Up

    • 724 Words
    • 3 Pages

    Enzymes are proteins that are involved in all the chemical processes in living things. As they are made of proteins they are affected by pH and temperature. Enzymes are catalysts; they speed up chemical reactions without being changed themselves. Digestive enzymes speed up the breakdown of large food molecules into smaller ones so that the blood can absorb them. Enzymes turn a large starch molecule into thousands of tiny glucose molecules. Enzymes end in 'ase'. There are thousands of enzymes in our body but each enzyme is only specialised to do one thing, for example carbohydraise enzymes digest carbohydrates, protease enzymes digest protein.…

    • 724 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    Aim: In this investigation I will try to find how long it takes for the filter paper disc to rise up whilst varying the amounts of concentration of catalyse.…

    • 571 Words
    • 3 Pages
    Satisfactory Essays