Phosphatases are enzymes that catalyse the removal of phosphate from other molecules, releasing inorganic phosphate ( $$\(\mathrm{P}_{\mathrm{i}}\)$$ ). A phosphatase can be extracted from mung bean seedlings, Vigna radiata. A student found a published method to extract phosphatase from mung bean seedlings. - Use a pestle and mortar to grind mung bean seedlings, with a small volume of distilled water, to make a paste. - Add distilled water to the paste to make a mixture with a total volume of $$\(50 \mathrm{~cm}^{3}\)$$. - Filter the mixture and put the filtrate into a clean centrifuge tube. - Centrifuge the filtrate until a solid pellet is formed, as shown in Fig. 1.2. - Pour the liquid extract containing phosphatase into a clean test-tube. Describe how the student could use the dilutions from (c) and a colorimeter to estimate the concentration of phenolphthalein in a reaction mixture. . . . .
Exam No:9700_s25_qp_52 Year:2025 Question No:1(d)
Answer:

Knowledge points:
3.1.1 state that enzymes are globular proteins that catalyse reactions inside cells (intracellular enzymes) or are secreted to catalyse reactions outside cells (extracellular enzymes)
3.1.2 explain the mode of action of enzymes in terms of an active site, enzyme–substrate complex, lowering of activation energy and enzyme specificity, including the lock-and-key hypothesis and the induced-fit hypothesis
3.1.3 investigate the progress of enzyme-catalysed reactions by measuring rates of formation of products using catalase and rates of disappearance of substrate using amylase
3.1.4 outline the use of a colorimeter for measuring the progress of enzyme-catalysed reactions that involve colour changes
3.2.1.1 temperature
3.2.1.2 pH (using buffer solutions)
3.2.1.3 enzyme concentration
3.2.1.4 substrate concentration
3.2.1.5 inhibitor concentration
3.2.2 explain that the maximum rate of reaction (Vmax) is used to derive the Michaelis-Menten constant (Km) which is used to compare the affinity of different enzymes for their substrates
3.2.3 explain the effects of inhibitors, both competitive and non- competitive, on the rate of enzyme activity
3.2.4 investigate the difference in activity between an enzyme immobilised in alginate and the same enzyme free in solution, and state the advantages of using immobilised enzymes
Solution:
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