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Amylase Temperature

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The Effect of Temperature on the Enzymatic Activity of Amylase
Enzymes are biological molecules or proteins that act as catalysts and help complex reactions occur everywhere in life. The enzyme and the substrate are in the same area, closely together. The enzyme grabs on to the substrate at a special area called the active site. The combination is called the enzyme/ substrate complex. After this, the substrate is changed. It can either be broken down or combined with another molecule to make something new. When this is complete, you will have the enzyme, still unchanged, and the product. The enzyme then releases the product. When the enzyme lets go, it returns to its original shape. It is then ready to work on another molecular substrate. In …show more content…
It can also be found in molds, bacteria and yeasts. Some amylase can also be found in the tissues and organs of the human body. Amylase is an enzyme that acts as a catalyst to hydrolyze carbohydrates. The role of amylase in plants is for breaking down starches Amylase assists in the initial development of the plant, before it is able to use energy from photosynthesis. The amylase enzymes begin their role in plant development as the plants seed begins to germinate. What effect could temperature have on amylase activity? I will test my question by analyzing enzyme activity at different temperatures and compare them. Temperature will affect the enzyme amylase rate. An increase in temperature will increase the enzyme amylase …show more content…
First we decided on meaningful time intervals to take samples. My lab partner and I decided to make 1-minute intervals. We then prepared test tubes for each time point by adding exactly one drop of IKI into each of the nine test tubes that we used. After adding the drops, we prepared our reaction flask by adding exactly fifty milliliters of starch solution as a substrate. The substrate was provided at a concentration of sixty micrograms over microliters. Our reaction proceeded at room temperature for our control experiment. At time zero, before adding the enzyme, we removed exactly 2.5 ml of substrate from our reaction flask and added it into our test tube labeled 0. After this, we added exactly 1 ml of enzyme extract into our reaction flask. We swirled the solution and then immediately started the stopwatch. For each time point, we removed exactly 2.5 ml of solution and transferred it into a test tube (labeled accordingly). The control tube had the highest concentration of starch because the enzyme had not broken down the starch. As we went on, minute-by-minute, the color of the test tube solution became lighter and lighter until the solution was transparent. This indicated that the longer the enzyme was mixed with the starch concentration, the more the concentration became broken down by this amylase enzyme. We then repeated the exact same

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