Enzyme Activity

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Enzyme Catalase Activity in Reaction with the Substrate Hydrogen Peroxide Abstract
We performed these experiments to observe the effects of enzymes on the rate of reactions. We tested and compared the activity of the enzyme catalase on the substrate H2O2 in various states and percentages, and observed the absorption values of the enzyme-substrate relationship at different concentrations. Our results show that the more substrate available, the quicker the reaction will happen except in one test, which might mean that a balanced concentration of the two is most beneficial. Introduction

The objectives of these experiments were to observe the effects of the enzyme-substrate relationships and to record our findings. Enzymes increase the rate of reactions by lowering the energy needed to activate the reaction (McNeil et al. 2013). Enzymes will work with substrates to produce reactions and products and they will bind together at an active site. They will only bond to with particular molecules and environmental factors can also affect their productivity. They are proteins, and proteins are made up of many amino acids (Brian et al. 2013). We used the enzyme catalase that occurs naturally in many organisms to study the qualitative and quantitative results of enzymatic activity. My hypothesis is that the findings in these experiments will show that the enzyme catalase will increase the rate of reaction with the substrate. Methods

In Activity 1 Procedure A, we had four test tubes filled with different components. The table below shows each tube’s components. In each test tube, we added 5.0 mL 3% H2O2. We recorded initial observations and checked frequently for changes.

Table 1.
Tube #| Contents|
1| 1 mL H2O|
2| ¼ × ¼” potato cube |
3| 1 mL Enz.|
4| 1 mL Enz boiled for 5 minutes, then cooled|

In Activity 1 Procedure B, we prepared two more test tubes with different substrates. In each empty tube we put 1 mL of enzyme. To that, we added the same substrate with different percentage levels. What we added to the test tubes is depicted in the chart below. We recorded our observations of these tubes and compared observations initially with those of minutes 4-5.

Table 2.
Tube #| Contents |
A| 1 mL Enz. + 5.0 mL1.5% H2O2|
B| 1 mL Enz. + 5.0 mL .75% H2O2|

In Activity 2 Procedure C, we filtered the catalase used in Procedures A and B with #4 filter paper. We made a black solution without the catalase and another with it to be compared in the spectrophotometer. The contents of the blank and cuvette #1 are shown below. We observed absorbance levels at 470 nm and measured the blank to subtract its values from those of cuvette #1. We measured the absorbance every minute for 5 minutes and recorded our observations. After the 5 minutes we removed them and observed differences.

Table 3.
Cuvette #| Contents |
Blank | 6.0 mL dH2O + .100 uL guaiacol + .150 uL H2O2|
1| 1.0 mL catalase + 5.0 mL dH2O + .100 uL guaiacol + .150 uL H2O2|

In Activity 2 Procedure D, we followed the same procedures as we did in Procedure C; however, the contents of the blank and cuvette were changed. The changes are shown in the table below.
Table 4.
Cuvette #| Contents |
Blank | 5 mL dH2O + .100 uL guaiacol + .300 uL H2O2|
1| 1.0 mL catalase + 4.0 mL dH2O + .100 uL guaiacol + .300 uL H2O2|

These methods came from the Biology 183 Introductory II Lab Manual. Results
The presence of an enzyme speeds up chemical reactions and is affected by the concentration of the substrate. We found that the results of reaction were much greater and happened faster with the presence of a greater amount of substrate and enzyme until there was too much substrate in relation to enzyme.

In Activity 1 Procedure A, we found that the more available substrate present, the faster the reaction would happen. More product was observed when there was increased substrate surface area. The table of results is depicted...
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