The experimental setup began by placing paper under two spot plate and label the short side Temperature (0, 25, 65, 85 Celsius) and the long side Time (0, 2, 4, 6, 8, 10 minutes) for each. Sixteen test tubes was needed to complete the experiment, 4 tubes for each amylase (Fungal and Bacterial) and 8 tubes for the starch component. Four test tubes were labeled BA for Bacterial amylase and corresponding temperatures. The same was done for the Fungal amylase (FA). The other eight test tubes remaining were labeled S with the same corresponding temperatures. 5 mL of 1.5% starch was placed into the tubes labeled FS & BS and 1 mL of bacterial amylase and fungal amylase was deposited into the test tubes that did not contain starch (FA & BA). Next,
As much as 95% of employers favor urine testing as a method for drug testing, and this one piece of statistic may have positively affected the trend and demand for synthetic urine over the years.
The purpose of this lab was to calculate the specific heat of a metal cylinder
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: = == ==
Affect of the Rate of Reaction of Amylase on Starch and How Its Affected by the Concentration of the Substrate
However, the decrease varied depending on the temperature. The lowest temperature, 4 degrees Celsius, experienced a very low decrease of amylose percentage. Temperature at 22 degrees Celsius and 37 degrees Celsius, both had a drastic decrease in amylose percentage. While the highest temperature, 70 degrees Celsius, experienced an increase of amylose percentage. In conclusion, as the temperature increases the percentage of amylose decreases; however, if the temperature gets too high the percentage of amylose will begin to increase. The percentage of amylose increases at high temperatures because there is less enzyme activity at high temperatures. However, when the temperature is lower, more enzyme activity will be present, which results in the decrease of amylose percentage. This is why there is a decrease of amylose percentage in 4, 22, and 37 degrees Celsius. In this experiment the optimal temperature is 37 degrees Celsius, this is because this is the average human body temperature. Therefore, amylase works better at temperatures it is familiar
The Effect of Temperature on the Activity of the Enzyme Catalase Introduction: The catalase is added to hydrogen peroxide (H²0²), a vigorous reaction occurs and oxygen gas is evolved. This experiment investigates the effect of temperature on the rate at which the enzyme works by measuring the amount of oxygen evolved over a period of time. The experiment was carried out varying the temperature and recording the results. It was then repeated but we removed the catalase (potato) and added Lead Nitrate in its place, we again tested this experiment at two different temperatures and recorded the results. Once all the experiments were calculated, comparisons against two other groups were recorded.
at a volume of 4cm3. The preliminary work also proved to me that my basic method worked without any setbacks that may affect my results. Variables:.. The variables involved in the rate of reaction between amylase and starch are. The volume of amylase The volume of starch
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.
Despite of general properties of enzymes, the properties also varies from where it comes from and how it been produced. For instance, the enzymatic saccharification method in lignocellulosic bioethanol is generated by hydrolyzing cellulose and hemicelluloses. This method gets high attention because of its higher theoretical yield compared to other methods (Taneda et al., 2012). Acremonium cellulolyticus with high activities of cellulase, amylase and pectinase enzymes allow it for the easy separation of solids/liquids in potato pulp, resulting in high saccharification efficiency and a high recovery rate of products (Gao et al., 2014). On the other hand, Enzyme-modified carboxymethyl starch (ECMS) is beneficial in enhancing water holding capacity, emulsion stability and improving sensory characteristics of sausages with a declined fat content (Luo and Xu, 2011). Lipases and phospholipases of dormant cotton seeds have stability in heat, various media and nature of the hydrolysis of the lipids properties (Rakhi...
The porpoise of these is to determine the Specific Heat. Also known as Heat Capacity, the specific heat is the amount of the Heat Per Unit mass required to raise the temperature by one degree Celsius. The relationship between heat and temperature changed is usually expected in the form shown. The relationship does not apply if a phase change is encountered because the heat added or removed during a phase change does not change the temperature.
This experiment shows the effect of rising temperature on enzyme amylase activity on converting starch to maltose. The reason for conducting the experiment is to find optimal temperature for enzyme activity. The enzymes that will be comparing are fungal and bacterial amylases. The enzymes were set at 4 temperatures 0-850 Celsius and checked at 4 different times from 0-10. The results showed the enzymes activity increased until 850 Celsius. Then the enzyme shows no hydrolysis. Enzymes denature at high temperature. To sum up, enzymes have optimal temperatures at which they operate. This experiment shows
If I was to do this experiment again I might use a Fungi amylase to
Test Tube B, however, produced a weak positive reaction between the starch and amylase. This was unexpected, as once the tube was subject to the boiling water bath the temperature should have changed enough to denature the enzyme. Test tube C produced another positive reaction, as
Amylase can be found in different types of industry. Detergent is one of the industry that Amylase is used. Amylase is use in detergent industry to breakdown(remove) the variable stain on the cloth from food that includes starch in it. The production of Amylase that contained in detergent is produce from the ‘Bacillus spp’(Bacteria) that produced from others living thing (Human and animal).