Group 2

39
ana | Miranda | Dofredo | Rada Ramos | Pama | Perez BMLS 2A (Summer)

Transcript of Group 2

Page 1: Group 2

Pacana | Miranda | Dofredo | Rada

Ramos | Pama | PerezBMLS 2A (Summer)

Page 2: Group 2

Qualitative Test for Proteins (Color Reaction)

Page 3: Group 2

Objectives

Page 4: Group 2

Detect proteins using different tests.

Determine significance of tests to protein hydrolysis.

Determine chemical structures in protein that brings out color change.

Determine positive/negative results.

Know the principles involved in each test.

Objectives

Page 5: Group 2

Tests

Page 6: Group 2

Xanthoproteic Test

1 mL egg albumin

+ 5 drops of conc. HNO3

Heat, then Cool

+ 5 drops NH4OH

Page 7: Group 2

Xanthoproteic Test

Principle:It uses concentrated nitric acid.

The test gives a positive result in those proteins with amino acids carrying aromatic groups, especially in the presence of Tyrosine.

Page 8: Group 2

Xanthoproteic Test

Present:

Proteins with amino acids

carrying aromatic groups,

especially Tyrosine

Page 9: Group 2

Xanthoproteic Test

Color of precipitate:

Dark yellow (+HNO3)

Orange (+NH4OH)

Page 10: Group 2

Hopkins-Cole Test

1 mL egg albumin

+ 1 mL H-C reagent

Incline + 10 drops pure conc. H2SO4

Page 11: Group 2

Hopkins-Cole Test

Principle:When protein mixed with glyoxylic acid and H2SO4, a violet ring will form beneath the protein mixture.

Due to the presence of an indole nucleus in the tryptophan component.

Tryptophan condenses with the aldehyde to form the colored product.

Page 12: Group 2

Hopkins-Cole Test

Present:

Tryptophan (indole group)

Page 13: Group 2
Page 14: Group 2

Hopkins-Cole Test

Color:

Violet ring between two

liquids

Page 15: Group 2

Biuret Test

1 mL egg albumin

+ 1 mL 10% NaOH

1 mL 0.5% CuSO4, drop by drop

Page 16: Group 2

Biuret Test

Principle:Alkaline solution of proteins treated with copper sulfate solution results in the production of a rose-pink to violet color.

This is due to the presence of a peptide linkage.

Page 17: Group 2

Biuret Test

Present:

Peptide bonds

(--C=ONH2)

Page 18: Group 2

Biuret Test

Color:

Purple solution

Page 19: Group 2

Ninhydrin Test

1 mL egg albumin

+ 1 mL 0.1% Ninhydrin(aq)

Heat to boiling

Cool

Page 20: Group 2

Ninhydrin Test

Principle:When protein is boiled with ninhydrin, a blue color is produced.

Due to the presence of the alpha-amino acid.

All proteins are positive except proline.

Page 21: Group 2

alpha-amino acid + 2 ninhydrin ---> CO2 + aldehyde + final complex(BLUE) + 4H2O

alpha-amino acid + ninhydrin ---> reduced ninhydrin + alpha-amino acid + H2O alpha-amino acid + H2O ---> alpha-keto acid +NH3

alpha-keto acid + NH3 ---> aldehyde + CO2

Page 22: Group 2

Ninhydrin Test

Present:

All proteins, peptides,

And amino acids

Except Proline

Page 23: Group 2
Page 24: Group 2

Ninhydrin Test

Color:

Blue solution

Page 25: Group 2

Sakaguchi Test

1 mL test solution

+ 1 mL 10% NaOH

+ 6 drops dilute alcoholic alpha-naphthol solution

Mix

+ 10 drops NaBrO solution

Page 26: Group 2

Sakaguchi Test

Present:

Arginine (guanidinium group)

Page 27: Group 2

Sakaguchi Test

Principle:It is used for the detection of a specific type of protein with the amino acid containing the guanidinium group to form a red color.

Page 28: Group 2
Page 29: Group 2

Sakaguchi Test

Color:

Red solution

Page 30: Group 2

Results

Page 31: Group 2

Test Test SpecificityTheoretical

Result

Experimental Result

Remarks

Result Drawing

1. Xanthoproteic Test

Amino acids with a benzene ring

Yellow precipitate Yellow Precipitate (+)

2. Hopkins-Cole Test TryptophanViolet ring between

the two liquidsCloudy white Precipitate

(-)

3. Biuret Test Peptide Bonds Violet Solution Violet Solution (+)

4. Ninhydrin TestAll proteins, peptide

bonds and amino acids except Proline

Blue Solution Blue Solution (+)

5. Sakaguchi Test Arginine Red Solution Red Solution (+)

ResultsTable 2A – 1 Qualitative Test for Ovalbumin

Page 32: Group 2

Analysis

Page 33: Group 2

The experiment yielded a positive result when a yellow precipitate formed.

Thus, amino acids with benzene rings (Tyosine, Phenylalanine, Tryptohan)

are present.

Xanthoproteic Test - Analysis

Page 34: Group 2

The experiment yielded a negative result when a cloudy precipitate formed instead of a violet ring between the two liquids.

Thus, tryptophan is absent.

We accept this as an experimentl error as ovalbumin generally contains a lot of tryptophan.

Hopkins-Cole Test - Analysis

Page 35: Group 2

The experiment yielded a positive result when the solution turned blue-violet.

Thus, many peptide bonds are present.

Biuret Test - Analysis

Page 36: Group 2

The experiment yielded a positive result when the solution turned blue.

Thus, many proteins, peptide bonds and amino acids are present.

Though it exempts Proline, it is not a guarantee that Proline is not present. It’s just that it cannot detect Proline’s existence.

Ninhydrin Test - Analysis

Page 37: Group 2

The experiment yielded a positive result when the solution turned red.

Thus, the amino acid containing the guanidinium group, Arginine, is present.

Sakaguchi Test - Analysis

Page 38: Group 2

Conclusion

Page 39: Group 2

Conclusion

Ovalbumin in egg white contains many types of amino acids, be it as residues, connected via peptide bonds, or part of long-chain proteins. That is why eggs are important in the human diet, as it provides the essential amino acids required to run our body in the principle of homeostasis.

There are different tests for different types of amino acids and some tests exclude a specific amino acid.

Tryptophan is present in ovalbumin, even if our experimental data showed otherwise. This just means that there are many factors involved in the accuracy of data gathered.