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How do enzymes work essay
How do enzymes work essay
How do enzymes work essay
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By using spectrophotometer, the effect of enzyme and substrate concentrations were predicted. The experimental design was to observe the effect of particular substrate concentrations on tyrosinase enzyme activity. Any changes in amount of product formed over a time, depended upon the level of enzyme present. Likewise, an enzyme is very specific meaning that, it can recognize its substrate from even closely related isomers. The specificity of tyrosinase for the substrate tyrosine is not high. In fact, it reacts with a variety of ring structures and one of them is Catechol. Sucrose is not affected by the tyrosinase enzyme. So it was hypothesized that there will be no brown color as production when sucrose will be involved. On the other hand,
The purpose of this study is to analyze the activity of the enzyme, catalase, through our understanding
Catecholase is an enzyme formed by catechol and oxygen used to interlock oxygen at relative settings, and it is present in plants and crustaceans (Sanyal et. al, 2014). For example, in most fruits and vegetables, the bruised or exposed area of the pant becomes brown due to the reaction of catechol becoming oxidized and oxygen becoming reduced by gaining hydrogen to form water, which then creates a chain that is is the structural backbone of dark melanoid pigments (Helms et al., 1998). However, not all fruits and plants darken at the same rate. This leads to question the enzymatic strength of catecholase and how nearby surroundings affect its activity. The catecholase enzyme has an optimal temperature of approximately 40°C (Helms et al., 1998). Anything above that level would denature the tertiary or primary structure of the protein and cause it to be inoperable. At low temperatures, enzymes have a slower catalyzing rate. Enzymes also function under optimal pH level or else they will also denature, so an average quantity of ions, not too high or low, present within a solution could determine the efficiency of an enzyme (Helms et al., 1998). Also, if more enzymes were added to the concentration, the solution would have a more active sites available for substrates and allow the reaction rate to increase if excess substrate is present (Helms et al., 1998). However, if more
Abstract: Enzymes are catalysts therefore we can state that they work to start a reaction or speed it up. The chemical transformed due to the enzyme (catalase) is known as the substrate. In this lab the chemical used was hydrogen peroxide because it can be broken down by catalase. The substrate in this lab would be hydrogen peroxide and the enzymes used will be catalase which is found in both potatoes and liver. This substrate will fill the active sites on the enzyme and the reaction will vary based on the concentration of both and the different factors in the experiment. Students placed either liver or potatoes in test tubes with the substrate and observed them at different temperatures as well as with different concentrations of the substrate. Upon reviewing observations, it can be concluded that liver contains the greater amount of catalase as its rates of reaction were greater than that of the potato.
The independent variable for this experiment is the enzyme concentration, and the range chosen is from 1% to 5% with the measurements of 1, 2, 4, and 5%. The dependant variable to be measured is the absorbance of the absorbance of the solution within a colorimeter, Equipments: Iodine solution: used to test for present of starch - Amylase solution - 1% starch solution - 1 pipette - 3 syringes - 8 test tubes – Stop clock - Water bath at 37oc - Distilled water- colorimeter Method: = == ==
Investigating the Effect of Substrate Concentration on Catalase Reaction. Planning -Aim : The aim of the experiment is to examine how the concentration of the substrate (Hydrogen Peroxide, H2O2) affects the rate of reaction. the enzyme (catalase).
In this experiment as a whole, there were three individual experiments conducted, each with an individualized hypothesis. For the effect of temperature on enzyme activity, catalase activity will be decreased when catalase is exposed to temperatures greater than or less approximately 23 degrees Celsius. For the effect of enzyme concentration on enzyme activity, a concentration of greater or less than approximately 50% enzymes, the less active catalase will be. Lastly, the more the pH buffer deviates from a basic pH of 7, the less active catalase will be.
The Effects of Concentration of Sugar on the Respiration Rate of Yeast Investigating the effect of concentration of sugar on the respiration rate of yeast We did an investigation to find how different concentrations of sugar effect the respiration rate of yeast and which type of concentration works best. Respiration is not breathing in and out; it is the breakdown of glucose to make energy using oxygen. Every living cell in every living organism uses respiration to make energy all the time. Plants respire (as well as photosynthesise) to release energy for growth, active uptake, etc…. They can also respire anaerobically (without oxygen) to produce ethanol and carbon dioxide as by-products.
How the Concentration of the Substrate Affects the Reaction in the Catalase Inside Potato Cells
Investigating the Effect of Enzyme Concentration on the Hydrolysis of Starch with Amylase Aim: Investigate the effect of enzyme concentration on the rate of an enzyme-controlled reaction. Using amylase and starch as my example. Introduction: I am investigating the effect of the concentration of the enzyme, amylase on the time taken for the enzyme to fully breakdown the substrate, starch to a sugar solution. The varied variable will be the concentration and all other variables are going to be fixed. The different concentrations will be: 0.5% 0.75% 1.0% 1.5% 2% An enzyme is a class of protein, which acts as a biological catalyst to speed up the rate of reaction with its substrates.
By taking a Carbon Dioxide, rich substance and mixing it with a yeast, solution fermentation will occur, and then it could be determined if it is a good energy-producer. In this study glacatose, sucrose, glycine, glucose, and water were used to indicate how fast fermentation occurred. The overall result shows that monosaccharides in particular galactose and glucose were the best energy source for a cell.
and a fall in temperature will slow them down. In many cases a rise in
The Effect of pH on Enzyme Activity. pH is a measure of the concentration of hydrogen ions in a solution. The higher the hydrogen ion concentration, the lower the pH. Most enzymes function efficiently over a narrow pH range. A change in pH above or below this range reduces the rate of enzyme reaction. considerably.
...his step, syrup preparations are crystallized to form table sugar. Successive "crops" of sucrose crystals are "harvested," and the later ones are known as brown sugar. The residual syrupy material is called either cane final molasses or blackstrap molasses; both are used in the preparation of antibiotics, as sweetening agents, and in the production of alcohol by yeast fermentation.Sucrose is formed following photosynthesis in plants by a reaction in which sucrose phosphate first is formed.The disaccharide trehalose is similar in many respects to sucrose but is much less widely distributed. It is composed of two molecules of -D-glucose and is also a nonreducing sugar. Trehalose is present in young mushrooms and in the resurrection plant (Selaginella); it is of considerable biological interest because it is also found in the circulating fluid (hemolymph) of many insects. Since trehalose can be converted to a glucose phosphate compound by an enzyme-catalyzed reaction that does not require energy, its function in hemolymph may be to provide an immediate energy source, a role similar to that of the carbohydrate storage forms (i.e., glycogen) found in higher animals.
The phenol-sulfuric acid method is a simple and rapid colorimetric method to determine total sugar in a sample. The method detects virtually all classes of carbohydrates, including mono-, di-, oligo-, and polysaccharides. It is one of the most versatile, relatively easy and cheap approaches for determination of carbohydrate concentrations is the colorimetric method based on reaction between hydrolysed carbohydrate solution and a colouring reagent that develops colour that is detectible in the visible range of the electromagnetic spectrum. Reagents used for colorimetric detection include phenol and concentrated sulphuric acid. The furfural is allowed to develop colour by reaction with phenol and its concentration is detected by visible light absorption.
Reducing sugar is the monosaccharide of carbohydrate which is form in aldehyde in the presence an alkaline solution. Examples of reducing sugar are glucose, lactose and glyceraldehyde. The reducing sugars that contain aldehyde group act as reducing agent during oxidation because it will oxidize to carboxylic acid. Benedict solution is used to test the presence of the reducing sugar in the solutions. Benedict solution is made from anhydrous sodium carbonate, sodium citrate and copper (ii) sulphate. In this experiment glucose solution is poured into the Benedict solution and let them in the water bath about maximum 2 minutes. From the experiment, we can observe that the blue color solution turn to green and red or dark brown. This change of color refers to the level of the sugar inside the solutions. If there is no reducing sugar inside, the color of the solution remain blue. If there has a little sugar inside, the color changes from blue to green. If there is a lot of reducing sugar, so that the color of the solution changes from blue to red or dark brown. How the color of...