Catalase Lab

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The purpose of this experiment is to examine the effect of Concentration of Catalase enzyme (E or E/2) and Concentration of Hydrogen Peroxide on the Mean Reaction Rate (ppm O2 evolved/min) and estimate the affinity of Catalase enzyme for Hydrogen Peroxide using Michaelis-Menton enzyme kinetics model by determining the Km and Vmax.
The results indicated that Catalase Enzyme Concentration and Concentration of Hydrogen Peroxide do affect the Mean Reaction Rate (ppm O2 evolved/min). The Figure 1 showed that Catalase enzyme E (Full Strength Enzyme Extract) graph has higher Mean Reaction Rate compared to Catalase enzyme E/2 (Half-Strength Enzyme Extract) graph. This is because, there were greater number of active sites accessible for the enzyme-substrate complex to be formed in the Catalase enzyme E compared to Catalase enzyme E/2 as the E/2 solution has been diluted with buffer and has one-half of the enzyme concentration. Catalase is very important because, it is an enzyme responsible for accelerating the lysis of Hydrogen Peroxide into water and Oxygen. If they were not present or had decreased in affinity for their substrate,
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As the amount of 3% Hydrogen Peroxide used was increased from 1ml to 2ml, 4ml and 5ml, the Mean Reaction Rate increased. When the concentration of Hydrogen Peroxide is doubled from 3% to 6%, the Mean Reaction Rate also went up. The Mean Reaction Rate for 5ml of 6% Hydrogen Peroxide was approximately 27293.9 ppm O2 evolved/min, which was higher compared to 5ml of 3% Hydrogen Peroxide that produced approximately 23126.5 ppm O2 evolved/min even though the same 5ml volume of substrate were used (Table 2, Figure 1). The increase in Mean Reaction Rate occurs because the more substrate, the more chance of collisions and effective collisions resulting in the more formation of enzyme-substrate