Background: Many people experience excessive gas, bloating, and discomfort in the intestinal areas. While there are other contributing causes, food is the one variable that mainly causes these problems, such as: broccoli, beans, dairy products, grains, etc. Beans, for example, contain oligosaccharides that makes it hard for the body to digest. These carbohydrate rich foods makes digesting difficult because they all contain high-fiber, starch, lactose, etc. Beano® is a product that helps aid in digestion. One tablet is to be ingested before a meal in order to reduce gas. It contains two enzymes: alpha galactosidase and invertase. Alpha galactosidase (a-galactosidase for short) is an enzyme that helps break down oligosaccharides, or complex carbohydrates, …show more content…
Compare the result to the chart on the back of the urinary pH test strips bottle, and record data. Clean the stirring rod with water before moving on to the next test tube. Repeat this process for each increment (2 mL, 3mL, 4mL) Figure #1: Picture of bean solution mixed Figure #2: Picture of materials needed for the with alpha galactosidase experiment Safety considerations: Be careful with the beakers, glass stirring rod, and test tubes, as they could break easily and can cause cuts in the skin. DCP: A scatter plot will be used to display how the amount of alpha galactosidase (measured in mL) in the bean solution affects the glucose concentration (measured in mg/dL) and error bars to show the standard deviation. A line of best fit will be used to show the relationship between the glucose concentration and the amount of alpha galactosidase. Table 2: Glucose concentration based on the amount of alpha galactosidase in bean solution Amount of a-galactosidase (mL) Glucose concentration (100mg/dL) Average glucose concentration Standard Deviation Trial 1 Trial 2 Trial 3 Trial 4 Trial …show more content…
However, for trials 1 and 2, the glucose concentration barely increased, possibly due to human error. (see table #2) In those first two trials, I mixed the bean solution with the water that rests on top of it, simply because I didn’t know that it would make a difference. After those two trials, I noticed that the results weren’t changing, and only then did I decide to dispose the bean water. Disposing the bean water made a dramatic difference, since the results increased drastically afterwards. (see table #2) The mixture with the bean water caused the solution to not be as concentrated, limiting the amount of oligosaccharides that the alpha galactosidase can break down, therefore resulting in a small amount of glucose concentration. The highest stand standard deviation is at 4 mL of alpha galactosidase, which is 185.742. The lowest standard deviation is at 0 mL and 1 mL of alpha galactosidase, which is 0. Since error bars are not all overlapping, it shows that there was a significant difference (see figure #3). However, the R squared value is 0.929, meaning that it is close to fitting the line of best fit. As the amount of alpha galactosidase increased, the glucose concentration also increased. This resulted in the positive trend of the graph and a steeper slope. When 4 mL of alpha galactosidase was added to the bean solution, the result evened out, and didn’t change as drastically
Bean Beetle Methods draft Writeup Would different beans, other then mug bean make the bean beetles produce less offspring. In this group project we conducted a hypothesis that argues, If using different beans for reproduction other then the mug bean, then they will produce less offspring. the dependent vearable is number of offspring and the independent veraible is the different type of beans. when conducting this experiements we used method of division, replication, and messureing.
The data observed and recorded in this lab shows that the concentration of miracle gro’ does affect the growth rate and germination speed of black eyed peas. The data is shown through two graphs and two data tables. The control group in this experiment is the seeds with a 0% concentration of miracle gro’, therefore the seeds with just water. The experimental groups are different concentrations of miracle gro’ including a 10%, 15%, 20%, 25%, and 30% concentration. The variable in this experiment is the amount/concentration of miracle gro’.
Enzymes are proteins that significantly speed up the rate of chemical reactions that take place within cells. Some enzymes help to break large molecules into smaller pieces that are more easily absorbed by the body. Other enzymes help bind two molecules together to produce a new molecule. Enzymes are selective catalysts, meaning that each enzyme only speeds up a specific reaction. The molecules that an enzyme works with are called substrates.
To begin, one must test for monosaccharides. Glucose is necessary, and is needed to be placed into a test tube at a quantity of 5 mL. 3 mL of Benedict’s solution is then added. The test tube is then placed in a beaker of boiling water for five minutes or until the color changes. If the color changes, then it is known that monosaccharides are present in the solution. Next, one will test for starches.
Dependent Variable amount of product (glucose and fructose) produced 2. Independent Variable temperature 3. Controlled Variables pH, amount of substrate (sucrose) present, sucrase + sucrose incubation time Effect of Substrate Concentration on Enzyme Activity 1. Dependent Variable amount of product (glucose and fructose) produced 2.
The starch-iodide complex forms because of the transfer of charge between the starch and iodide ion and results in spacing between the energy levels. This allows the complex to absorb light at different wavelengths resulting in a dark blue colour (Travers et al., 2002). A blue colour would indicate a positive test while a yellow colour would show a negative test. The Benedict’s test is useful for reducing sugars.
55 degrees celcius Table 6: Effect of Sucrose Concentration on Sucrase Activity Optical Density 35 g/L 30 g/L 25 g/L 20 g/L 15 g/L 10 g/L 5 g/L 0 g/L 1 1.007 0.974 0.950 0.926 0.849 0.734 0.515 0.003 2 1.002 1.011 0.947 0.937 0.834 0.766 0.496 0.002 3 0.980 0.998 0.944 0.932 0.838 0.754 0.495 0.001 average 0.996 0.994 0.947 0.932 0.840 0.751 0.502 0.002 Effect of Sucrose Concentration on Sucrase Activity 5. State how sucrase activity changes with increasing sucrose concentration. First sucrase activity increases greatly. After 10 g/l sucrase activity continues to increase but at a slow rate until it reaches 30 g/l. At 30 g/l to 35 g/l sucrase activities mostly stayed the same
Figure 1, 2, and 3 shows the slope of the line of best fit, which describes the cellular respiration. Lactose not only had the lowest average
Uncontrolled Environmental conditions Atmospheric conditions The controlled variable Concentration of amylase was kept under control by measuring the amount of amylase used and also it was made sure the percentage of amylase used was 1%. The Amount of amylase/starch used were kept to 5cm3 at all times. Materials needed Beakers Bunsen burner Test tube Thermometer Stopwatch Test plate Glass rod Starch Amylase solution Water bath Iodine solution. Test tube holder Labels Marker Procedure First 5 test tubes were taken and labeled with numbers from 1 to
References: Wang, B. B., Xu, Y. K., Ng, W. G., & Wong, L. J. C. (1998). Molecular and biochemical basis of galactosemia. Molecular genetics and metabolism, 63(4), 263-269. McCorvie, T. J., & Timson, D. J. (2011).
Next, weigh out 5 grams of sugar and 1 gram of yeast. Once in proportions, add it to test tube A. Thoroughly mix around the sugar, yeast, and tap water. You can do this by shaking the test tube gently. Make sure you do not turn it upside down. Then, cover the top of the test tube with a balloon and gently place it into a 400mL beaker filled up about half way (about 250mL) with water.
The genetic changes completely eradicate the activity of the enzyme created from the GALT gene, thus forestalling the normal processing of galactose. This creates severe signs and symptoms of this disorder (2,5). Furthermore, another GALT gene, known as the Duarte variant, is not as an aggressive gene, as it reduces but does not eradicate the activity of the enzyme. Individual who are diagnosed with Duarte variant are more likely to have much slighter characteristics of Galactosemia (4,5,6). Galactosemia deficiently (type II), is a direct result from the mutations in the GALK1 gene.
The 3 concentrations of enzymes were 0.5 ml, 1.0 ml, and 2.0 ml of turnip extract, while the substrate consisted of 0.1ml, 0.2 ml, and 0.4 ml of hydrogen peroxide. In a separate tube, the control was made up of turnip extract and guaiacol, known as the color reagent. This was recorded the absorbance every 20 seconds for 3 minutes.
This table presents the information in colony factoring units per gram, or CFU/G. To obtain this number, a series of calculations were conducted. Beginning with the total number of colonies in each dilution, this number was divided by 0.1. Then the number found from the division explained previously was then multiplied by 10 to the power of n, where n was the number in the dilution set. For example: dilution 4 would solved using the answer to the division problem and multiplying by 10 to the 4th power.
At 10-minute intervals, we would take them out and weigh them again for 30 minutes. We repeated this experiment using another five set of cups that contained 50 mL of 1M sodium chloride. After gathering the data, we calculated the change in weight of the yam cores, performed a t test and constructed graphs. After performing a t test, I found the p value