"Catalysis" Essays and Research Papers

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    Peroxidase Experiment

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    Abstract Over a two week period of time in the laboratory‚ we experimented and tested the reaction rate of a peroxidase enzyme and the factors that affected it‚ both positively and negatively. The purpose of these experiments was to probe and manipulate the activity of the enzyme peroxidase by varying temperature‚ pH‚ the amount of enzyme compared to the substrate and the effect of hydroxylamine. Peroxidase activity is expressed when the potato extract is subjected to stresses such as low temperature

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    Enzyme Kinetic Lab Report

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    Abstract The main goal of the enzyme kinetics experiment was to see how the phosphatase-catalyzed hydrolysis of p-nitrophenyl produced p-nitrophenol in the presence of phosphate and fluoride ion inhibitors of various concentrations. The calculated Km constant was found to be 0.22 for all reactions. The Vmax values for each inhibition ion were 0.00986 for the phosphate ion and 0.00436 for the fluoride ion. The inhibitor constant‚ Ki‚ was determined to be 0.0967 for the phosphate ion. The inhibitor

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    Abstract The decomposition of hydrogen peroxide (H2O2) in a whole and diced wedges by with The enzyme catalase was observed. The catalase was able to break down the hydrogen peroxide In the diced banana wedge better than the whole banana because after the banana was diced that Increases the surface area allowing the breakdown to flow. The effects of temperature on enzyme In a liver sample were observed under iced‚ boiling‚ 37 degrees‚ and room temperature Conditions. The enzymes became completely

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    Sn1 Reaction Lab Report

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    The effect of temperature on the reaction rate: As the temperature increases it provides more kinetic energy to the molecules allowing them to move faster and with more energy the molecules can overcome the activation energy barrier and therefore the reaction occurs faster. 5. Since the proposed mechanism is a SN1 reaction the reaction got faster as the polarity increased. This is because SN1 reactions work best with polar protic solvents as they stabilize the carbocation. Therefore‚ as seen

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    Ap Bio Enzyme Lab

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    Introduction Enzymes are catalytic proteins. The purpose of a catalyst is to speed up metabolic reactions by lowering the free energy of activation or activation energy. Activation energy is known as the amount of energy needed to push the reactants over an energy barrier‚ so that the downhill part of the reaction can begin (Campbell 151). In an enzyme catalyzed reaction‚ the enzyme binds to its substrate‚ which is the reactant an enzyme acts on. In the reactions‚ the enzymes are very specific

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    Metabolism Before class‚ skim the chapter and fill in the sections in bold italics. Definitions: Metabolism (Concept 8.1) Energy (Concept 8.1) Catalyst (Concept 8.4) I. Energy in a Biological Context: II. Chemical Reactions Review chemical reactions in Ch.2 Concept 2.4. Define: Reactants Products Chemical equilibrium A. Equilibrium B. Energy in chemical reactions: Concept 8.3 C. Making chemical reactions

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    Introduction Have you ever bit into a nice big juicy bacon double cheeseburger and your mouth began to salivate before the food has entered your mouth? The reason why you salivate is because your body wants to release an enzyme called amylase. Amylase is the enzyme found in your saliva. The purpose of this enzyme is to help in the digestion process (McD‚ 2002). Enzymes are biological catalyst that help speed up the reaction by lowering the activation energy. These enzymes allow your food to be digested

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    This study focuses on the effect that temperature has on the enzyme amylase. Enzymes are composed of proteins and acts as a catalyst to speed up the rate of a specific chemical reaction by lowering the activation energy. Reactions do not need enzymes to occur‚ but the human body and other living organisms depend on the use of enzymes in order for biochemical reactions to happen in milliseconds. Each enzyme contains a distinct three dimensional structure which is related to its particular function

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    CFR11-Protease Lab Report

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    The pH is another important factor that influences the enzyme activity‚ as it affects the shape of the enzyme or charge on substrate and ultimately its functionality (Reece et al.‚ 2011; Eed and John‚ 2013). With respect to effect of pH on enzyme activity‚ there was a steady increase in the activity for CFR15-protease‚ i.e. from pH 3.5 to 10.5 and a sudden fall was observed over pH 10.5. The activity was stable in the range of pH 7 to 10.5 and this reveals the alkaline protease nature of the enzyme

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    Enzymes Abstract: The following 2 labs experimented the more enzymes and substrates added to the concentration will effect the reaction rate. Our second lab‚ we tested enzyme and substrate concentrations to determine the increase of temperature and inhibitor. The enzyme source used in both labs was peroxide‚ guaiacol is used as a substrate for peroxide. We used Guaiacol‚ turnip extract‚ peroxide and distilled water for enzyme and substrate concentration. In the second lab we used the same substances

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