Catalase is one of the highly efficient enzymes. It is a tetramer made of four porphyrin rings and catalyzes the conversion of the DNA damaging agent Hydrogen Peroxide H2O2 into H2 and O2. Hence, when H2O2 is added to catalase in a test-tube, H2 and O2 will be produced whenever the enzyme is functional. Based on the activity of the enzyme and the presence of optimum conditions, the H2 and O2 released would vary with the amount being maximum for optimum conditions. The O2 released will cause bubbles.
Question 7: Being an enzyme in a living cell, it is selected evolutionarily to function at the pH of the cell, which is roughly 7.0. Hence the catalase will produce maximum bubbles at pH 7.0 in tube 8.
Question 8: Again being an enzyme in a living cell, it is selected to function at the temperature of the cell, which is around 37 degrees C. This temperature will vary based on the environment in which the potato grows. Thus it can vary from roughly 0 degrees C near Siberia to hot temperatures up to 50-60 degree C. But it will surely not be active at a temperature of 100 degree C in boiling water, where the protein will be almost completely denatured.
Question 9: In humans, the internal temperature is strictly regulated around 37 degree C. Hence the human catalase will definitely be most active at 37 degree C and produce most bubbles at this temperature.
please help me out! Effect of pH - Tube 7: 1 ml catalase + pH 3.0...
please help me out!
Negative and positive controls Tube 1: 1 ml Catalase + 3 ml distilled water Tube 2: 1 ml Catalase + 3 ml sucrose Tube 3: 1 ml Catalase + 3 ml H,O, Positive test produces bubbles; negative reaction does not bubble Question #1: State the NUMBER of the ONE tube that is the negative control: Question #2: Explain why no bubbles will appear in Tube 2: Effect of concentration - Tube 4: 1 ml catalase +...
Please Refer to This Lab Background: Procedure Only one group prepares each type of extract, and then shares the extract. Make enough for all of the groups. Cut a piece of the tissue to be tested, approximately 4x4 cm. Cut into smaller pieces; then grind in a mortar and pestle with a pinch of sand and 8 mL of deionized water to break the cell walls and release the catalase into solution. Place the mortar and pestle on the side...
What causes the lack of on in tube # 5 that is acting as the control tube? 13. What is the reason for using the control tube What is the reason for 5. used in this exercise 14. What is the relationship between the concentration of pepsin and enzyme activity, as observed on Figure 3-7? 15. How does an increase in the amount of the pepsin, in the test tube, enhance the interaction between pepsin and substrate, thus speeding up...
Write out your separation scheme for this experiment. 1. Heat 75 mL of water to 90 °C in a 250-mL beaker. 2. While the water is being heated, place 250 mg of salicylic acid, 1 drop of 85% phosphoric acid and 0.5 mL of acetic anhydride in a test tube. Add a boiling chip to the mixture and gently shake it in order to mix the reactants. 3. Heat the tube in the beaker of water at 85 - 90...
Foundations of Biological Sciences 1 Enzymes - 8 PART 4: THE EFFECT OF PH ON ENZYME ACTIVITY The pll scale measures the amount Another factor influencing the rate of enzyme catalysis is the pll of the of ons in a solution. The more solution. pH specifies the acidity or basicity of solution by measuring the the more acidic the solution and lower hydrogen ion consentation (H). Like temperature, pH affects the three- pH) dimensional shape of enzymes, thus regulating their...
PROCEDURE 1. Place a reaction tube into a 5-mL Erienmeyer and tare. Add between 0.275- 0.300g of salicylic acid. Record on the data sheet. 2. Transfer the reaction tube and 5-ml Erienmeyer to the hood. Add a boiling chip, 2 drops of 85% phosphoric acid, and about 0.70 mL of acetic anhydride to the reaction tube. Mix well. 3. Place a 50-ml beaker containing about 20-mls of water on a hot plate or in the sand bath. Allow the water...
are
theses correct?
please correct me if they are not.
Results Fe Test Tube 2: FeSCN (aa) SCN () Fe Chemical equation: Explanation: The equilibrium shifted toward the increased the due to the addition of Fe(NO,)) because it of the Test Tube 3: FESCN 0) SCN () (as Chemical equation: Fe(ag) Explanation: Test Tube 4: Chemical equation: Fe(agk FeSCN( (aq)h Explanation: Test Tube 5: Chemical equation: Fe"( SCN () FESCN 3+ + (sq) Explanation: Test Tube 6 Chemical equation: Fe(a...
Attached is the lab experiment. Here are the questions I need
help with:
1. What is the purpose of each of the following steps in this
experiment?
a. Adding solid NaCl to the reaction mixture
b. Repeated washings with water, sat'd NAHCO3, and brine
c. the pipet column chromatography
2. Which compound, cyclohexanol or cyclohexanone will have a
higher Rf on a TLC plate?
3. What is the advantage of using sodium hypochlorite as an
oxidant over CrO3 or Na2Cr2O7...
please help asap and the values are from the procedure there is no
additional info
QUESTION.
PROCEDURE 1. Obtain seven spectrophotometer tubes, three 5 mL pipets and seven 125 mL Erlenmeyer flasks. One for the blank and six sample test tubes. Make sure to label the test tubes with appropriated calculated concentration. Label one flask as NaSCN 2. Pipet 5 mL of 0.00020 M NaSCN into Erlenmeyer flask #1. Pipet 5 mL of 0.20 M Fe(NO3)3 into Erlenmeyer flask #1....
can
someone help me answer these 5 questions and figire this graph out
please?
Acid-Base Titration of a Weak Acid with a Strong Base: Determination of K. Introduction: You will be titrating a solution of a weak acid with 0.100 M NaOH, while monitoring the reaction using a pH meter. Weak acids have characteristic acid-ionization constants, K. The purpose of this lab is to use the titration to determine the value of this constant for the weak acid called “benzoic...