Period 1
10/05/15
The Effect of Temperature on Rate of Enzyme Activity of Different Enzymes
Abstract/Purpose:
The main objective of this experiment was to determine how different factors, such as the type of enzyme and the temperatures that each of the enzymes were exposed to, could affect the rate of enzyme activity. In order to measure this, a potato enzyme and liver enzyme were placed in four different temperatures for 24 hours. Each enzyme was then placed in a test tube with hydrogen peroxide and the rate of enzyme activity was measured. The result was that the rate of enzyme activity decreased as the temperature increased for the liver enzyme, but increased for the potato enzyme.
Introduction/Hypothesis:
An enzyme is usually a protein that works as a catalyst, which is anything that helps to speed up, or catalyze, the chemical reaction (Bolster&Moss, n.d.). To speed up a chemical reaction, enzymes lower the activation energy, which is the initial energy required for a reaction to occur by applying heat. However, enzymes are very substrate-specific, only acting on specific reactants, which are the substrates, and consequently, enzymes are selective in the chemical reactions that they catalyze. Since an enzyme is a protein, each enzyme has a specific amino acid sequence, which determines its shape and eventually, the reactions that it will catalyze. In this way, an enzyme supports the biological theme that form fits function. Each substrate binds to the enzyme
Do enzyme reactions increase as the temperature is raised? It is proven that the rate of an enzyme reaction increases as the temperature is raised. But by how much? A ten-degree centigrade rise in temperature will increase by fifty to on hundred percent. There is a direct influence between enzyme activity and temperature. The question that was studied in Bio110 lab Enzyme Activity II was “Does temperature influence the activity of an enzyme?” The null hypothesis is; temperature does not significantly influence enzyme activity. The alternative hypothesis is; temperature does significantly influence enzyme activity. The alternative hypothesis is accepted. This is true because in our results in the Enzyme Activity II, showed that as temperature increases so does the activity of an enzyme.
The use of multiple test tubes and Parafilm was used for each experiment. Catechol, potato juice, pH 7 phosphate buffer, and stock potato extract 1:1 will be used to conduct the following experiments: temperature effect on enzyme activity, the effect of pH on enzyme action, the effect of enzyme concentration, and the effect of substrate concentration on enzyme activity. For the temperature effect on enzyme activity, three test tube were filled with three ml of pH 7 phosphate buffer and each test tube was labels 1.5 degrees Celsius, 20 °C, and 60 °C. The first test tube was placed in an ice-water bath, the second test tube was left at room temperature, and the third test tube was placed in approximately 60°C of warm water. After filling the test tubes with three ml of the
Enzymes are biological catalysts that speed up chemical reactions, without being used up or changed. Catalase is a globular protein molecule that is found in all living cells. A globular protein is a protein with its molecules curled up into a 'ball' shape. All enzymes have an active site. This is where another molecule(s) can bind with the enzyme. This molecule is known as the substrate. When the substrate binds with the enzyme, a product is produced. Enzymes are specific to their substrate, because the shape of their active site will only fit the shape of their substrate. It is said that the substrate is complimentary to their substrate.
The role of an enzyme is to catalyse reactions within a cell. The enzyme present in a potato (Solanum Tuberosum) is catechol oxidase. In this experiment, the enzyme activity was tested under different temperature and pH conditions. The objective of this experiment was to determine the ideal conditions under which catechol oxidase catalyses reactions. In order to do this, catechol was catalyzed by catechol oxidase into benzoquinone at diverse temperatures and pH values. The enzyme was exposed to its new environment for 5 minutes before the absorbance of the catechol oxidase was measured at 420 nm using a spectrophotometer. The use of a spectrophotometer was crucial for the collection of data in this experiment. When exposed to hot and cold temperatures, some enzymes were found to denature causing the activity to decrease. Similarly, when the pH was too high or low, then the catechol oxidase enzyme experienced a significant decrease in activity. It can be concluded after completing this experiment that the optimal pH for catechol oxidase is 7 and that the prime temperature is 20º C. Due to the fact that the catechol oxidase was only tested under several different temperatures and pH values, it is always possible to get a more precise result by decreasing the increments between the test values. However, our experiment was able to produce accurate results as to the
Hypothesis: If the temperature increases, then rate of the chemical reaction will increase as well, and if the temperature decreases, then the rate of reaction will also decrease.
As stated in the introduction, three conditions that may affect enzyme activity are salinity, temperature, and pH. In experiment two, we explored how temperature can affect enzymatic activity. Since most enzymes function best at their optimum temperature or room temperature, it was expected that the best reaction is in this environment. The higher the temperature that faster the reaction unless the enzyme is denatured because it is too hot. Similarly, pH and salinity can affect enzyme activity.
Enzymes are specific-type proteins that act as a catalyst by lowering the activation energy of a reaction. Each enzyme binds closely to the substrate; this greatly increases the reaction rate of the bounded substrate. Amylase enzyme, just like any other enzyme, has an optimum PH and temperature range in which it is most active, and in which the substrate binds most easily.
The purpose of this experiment was to record catalase enzyme activity with different temperatures and substrate concentrations. It was hypothesized that, until all active sites were bound, as the substrate concentration increased, the reaction rate would increase. The first experiment consisted of five different substrate concentrations, 0.8%, 0.4%, 0.2%, 0.1%, and 0% H2O2. The second experiment was completed using 0.8% substrate concentration and four different temperatures of enzymes ranging from cold to boiled. It was hypothesized that as the temperature increased, the reaction rate would increase. This would occur until the enzyme was denatured. The results from the two experiments show that the more substrate concentration,
In the exercise # 2 we observed the effect of substrate concentration, enzyme concentration, pH and temperature on enzyme activity. All the data showed that once potato extract was added to catechol and water the reaction varied dependent on the level of catechol. As in
Enzymes are proteins catalysts, in which the enzyme speeds up reactions. Enzymes speed up reactions by lowering the activation energy. The enzyme or catalyst is not consumed in the reaction; therefore, the enzyme can be reused (Areda, 2017). Activation energy is the energy needed to start a chemical reaction (Reece, 2017). In other words, the activation energy is kind of like a barrier, in which enzymes help decrease the amount of energy needed to start the chemical reactions. Enzymes have unique shapes and one part of the enzyme that has a specific shape is the active site. The active site is where the substrate (reactant) binds with the enzyme. When the enzyme and substrate attach they form what is know as the enzyme-substrate complex. This
Enzymes are very efficient catalysts for biochemical reactions. They speed up reactions by providing an alternative reaction pathway of lower activation energy. Like all catalysts, enzymes take part in the reaction - that is how they provide an alternative reaction pathway. But they do not undergo permanent changes and so remain unchanged at the end of the reaction. They can only alter the rate of reaction, not the position of the equilibrium. Enzymes are usually highly selective, catalyzing specific reactions only. This specificity is due to the shapes of the enzyme molecules.
The reaction rate of an enzyme can be affected by many factors, and the purpose of this experiment was to find out how an increasing substrate concentration influences the rate of an enzyme activity; we obtained data from recording the absorbance of the samples which contain the same amount of potato juice (enzyme oxidase) and different amount of catechol (substrate) while holding pH and temperature constant. Our findings illustrate that the rate of enzyme activity is only influenced by substrate concentration at low level of substrate concentration, and as substrate
: Enzymes are made up of proteins and their function is mainly determined by their structure. The primary structure of an enzyme is determined by the sequence of amino acids. The secondary structure is based on the folding of the primary structure. Lastly, the tertiary structure is based on the folding of the secondary structure and its interactions of the side chains. The purpose of an enzyme is to speed up chemical reactions in a cell. Temperature is a factor that affects enzyme activity because as temperature increases the enzyme reaction increases too. Also, pH levels also play a role in affecting enzyme activity. Very high or very low pH levels can result in the loss of enzyme activity. For an enzyme to maintain activity it needs to be
The purpose of this lab report is to investigate the effect of substrate concentration on enzyme activity as tested with the enzyme catalase and the substrate hydrogen peroxide at several concentrations to produce oxygen. It was assumed that an increase in hydrogen peroxide concentration would decrease the amount of time the paper circle with the enzyme catalase present on it, sowing an increase in enzyme activity. Therefore it can be hypothesised that there would be an effect on catalase activity from the increase in hydrogen peroxide concentration measured in time for the paper circle to ride to the top of the solution.
To find the effect of temperature on the activity of an enzyme, the experiment deals with the steps as follows. First, 3 mL if pH 7 phosphate buffer was used to fill three different test tubes that were labeled 10, 24, and 50. These three test tubes were set in three different temperature settings. The first test tube was placed in an ice-water bath for ten minutes until it reached a temperature of 2° C or less. The second tube’s temperature setting was at room temperature until a temperature of 21°C was reached. The third tube was placed in a beaker of warm-water until the contents of the beaker reached a temperature setting of 60° C. There were four more test tubes that were included in the procedure. Two of the test tubes contained potato juice were one was put in ice and the other was placed in warm-water. The other two test tubes contained catechol. One test tube was put in ice and the other in warm water. After