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Sbl-Report3 Protein
Sbl-Report3 Protein
INTRODUCTION
Protein is one of classes of food that very important in our body. To know how
much protein needed to our body, there are many ways to measure the concentration
of protein. To measure the concentration of protein is also known as quantitative
analysis. There are five ways to determine the concentration of protein such as Biuret
test, Lowry (Folin) protein assay, Bradford protein assay, Spectrophotometry based
on UV light absorption and BCA assay. For this experiment, spectrophotometry was
chosen because this method is very quick and easy. This is because this method has
no chemical reaction to be carried out. This method[1] can measure how much a
chemical substance absorbs light by measuring the intensity of light as a beam of light
passes through sample solution. The main principle is each solution absorbs or
transmits light over a certain range of wavelength.
Other method that have to be applied in this experiment is Biuret protein assay.
This is because biuret reagent can be detect the presence of peptide bond. When
peptide bond present in an alkaline solution, the protein reacts with copper (II) ions to
form a violet coloured complex that called as biuret. Nitrogen atoms of peptide bond
will form coordination with copper (II) ions. Therefore, protein intensity affects the
intensity of the colour which means that, the colour will be more intense with higher
concentration of protein.
OBJECTIVE
To determine the protein concentration of sample A (fresh milk) and sample B
(chocolate milk).
METHODOLOGY
1. Nine test tube are prepared and labelled. Every test tube are added with
different volume of Gelatin, and water except for test tube eight and nine. Table
1.0 below shows that the volume of Gelatin and water needed for every test
tube.
Table 1.0
1 0 1.0 0
2 0.1 0.9 1
3 0.2 0.8 2
4 0.3 0.7 3
2 mL of 15 minutes
5 0.4 0.6 4 Biuret incubation
6 0.5 0.5 5
7 0.6 0.4 6
8 1 mL of sample A X2
9 1 mL of sample B X1
2. Sample A and sample B are prepared for test tube eight and nine.
3. Both samples are prepared by adding 5 mL of distilled water and the volume of
both type of milks are taken for 10L by using micropipette.
4. Sample A for test tube eight and sample B for test tube nine. 1 mL of every
sample are taken to be tested.
5. All test tubes are added with 2 mL of Biuret and incubated for 15 minutes.
6. The spectrophotometer is switched on and adjusted the wavelength to 550nm.
7. 1 mL of solution from every test tube are transferred into cuvette and gently the
cuvette wiped with tissue to remove fingerprint and dust.
8. The absorbance is set to zero by using solution from test tube 1. It served as
blank.
9. The absorbance of every test tube are measured and recorded by using
spectrophotometer without blank the instrument again.
10. A graph of standard curve is plotted by using the absorbance value of protein
standards and interpolate the absorbance values of the protein samples.
RESULTS
1 0 1.0 0 0.000
8 1 mL of sample A X2 0.209
9 1 mL of sample B X1 0.052
Diagram 2.0
The diagram 2.0 shows that solution for every test tube after added with biuret
reagent.
Diagram 3.0
The diagram 3.0 shows that 1 mL solution of every test tube are transferred into
cuvette to measure the absorbance by using spectrophotometer. From left is taken
form test tube 1 and so on.
Graph 1.0
0.35 0.347
Absorbance at 550 nm
0.3
0.286
0.25
0.2
0.161
0.15
0.1 0.104
0.05 0.049
0
1 X1 2 3 X2 4 5 6
Graph 1.0 shows that the concentration for sample A, X2 and sample B X1 can be
determine by using graph.
2.
3. Lecture note, Protein (The Analysis)
4. Laboratory Manual SBL1023