Keywords: Nucleic Acids, Dische Test, Murexide Test, Phosphate Test, Wheeler-Johnson Test1. IntroductionThe experiment solely revolved on the identification of the different structural features that make up the complex structure of nucleic acids as well as its characterization through specific chemical tests namely Dische Test, Murexide Test, Wheeler-Johnson Test and Phosphate Test. Upon performance of the tests mentioned, the principles involved were identified and stated based on the results obtained from the experiment.
2. MethodologyMaterials such as water bath, test tubes, evaporating dish, test compounds and reagents were gathered and prepared.
In Dische Test, ten (10) drops of test compound and Diphenylamine wasplaced in a test tube and heated in boiling water bath for ten minutes. Color change on the solution was noted.
In Murexide Test, ten(10) drops of Guanidine was placed in a test tube. Concentrated Nitric Acid(HNO3) was added to the test compound and then brought to water bath to dry until a solid mixture is obtained. Once the mixture dried up, ten(10) drops of Potassium Hydroxide(KOH) was used to wet the reagent and then later on put to boiling water bath again to dry. After addition of KOH, color change was noted and this time, water was added to wet the mixture and put to boiling water bath again to dry. Any color change to the precipitate was noted.
For Wheeler-Johnson Test, ten(10) drops of Barium Hyrdroxide[Ba(OH)2] and Bromine Water placed in a test tube and once the mixture turned red, it was brought to boiling water bath to expel excess Bromine. More than ten(10) drops of Barium Hyrdroxide[Ba(OH)2] was added in excess and color change of the precipitate was noted.
In Phosphate Test, twenty(20) drops of test compounds were placed in a porcelain crucible and two(2) drops of Potassium Nitrate(KNO3) plus ½ spatula fusion mixture of Sodium Carbonate(NA2CO3) was added to the test compound. Mixture was heated using a Bunsen burner until the mixture turned into gray or white. After cooling the mixture, 5 mL of distilled water was added to the reagent and was transferred to a test tube acidified by ten(10) drops of concentrated Nitric Acid(HNO3). Litmus paper was then used to check for acidity and twenty(20) drops of ammonium molybdate solution was added to the reagent & warmed in water bath. Once warmed, the mixture was allowed to stand for ten minutes and formation as well as color of the precipitate was noted.
After performing all the tests needed, results were tabulated and analyzed accordingly.
3. Results and DiscussionTabulation of ResultsDische TestMurexide TestWheeler-Johnson TestPhosphate TestRibose (RNA)1 minute & 30 seconds:Light blue violet solutionDeoxyribose (DNA)Dark Violet precipitateGuanidineYellow with red mixture+10 drops:Light yellow and orange precipitateCytosineVioletH3PO4YellowThe table above contains the data gathered from the experiments performed. All of which garnered a correct output based on expected results.
Dische Test clearly indicates that DNA can be identified chemically with the Dische diphenylamine test. DNA (deoxyribonucleic acid) and RNA (ribonucleic acid) are aldehydes, which reacts with the compound, diphenylamine, to produce a blue-colored compound. A positive test for DNA is indicated by a blue color change. This procedure involves chemical hydrolysis of DNA: when heated in acid, the reaction requires a deoxyribose sugar and therefore is specific for DNA. Under these conditions, the 2-deoxyribose is converted to w-hydroxylevulinyl. This resulted to a blue solution indicating the presence of protein in DNA.
Murexide Test on the other hand gave out a yellow precipitate which indicates the presence of uric acid visible in the Guanine samples. It is a double-ringed, crystalline organic base, C5H4N4, not known to occur naturally, and is a form of uric acid heterocyclic in nature.
In the Wheeler-Johnson Test, the evidence for a positive result is a violet solution and this clearly shows the concise result of the experiment performed. Cytosine was used in the test which is a Pyrimidine derivative heterocyclic in nature.
Phosphate Test gave out a yellow result for the precipitate which simply means that a phosphodiester bond exists between DNA and RNA between the 3 ' Carbon atom and the 5 ' Carbon of the ribose sugar.
4. ConclusionFrom the experiment, it is therefore meant that through specific tests, it is possible to characterize structural features of nucleic acid whether it be a helix, string loop or miniband. That certain compound complements the test to be performed and will result to a concise data if performed correctly. That DNA differs from RNA in the sense that only Uracil is found in RNA and Thymine is exclusively located in the DNA though Adenine, Guanine, and Cytosine are both found on DNA & RNA..
5. ReferencesPratt, Charlotte W. Title Essential biochemistry / Charlotte W. Pratt. Publication info. New York: Wiley, 2004.
What is DNA? : A biology adventure / written by Transnational College of LEX translated by Alan Gleason. Publication info. Boston: Language Research Foundation, c2003.
http://www.saddleback.edu/faculty/thuntley/bio3a/labs/bio3aLABmolecules.pdfhttp://www.jbc.org/cgi/reprint/181/2/713.pdfhttp://www.medilexicon.com/medicaldictionary.php?t=90918http://www.uni-regensburg.de/Fakultaeten/nat_Fak_IV/Organische_Chemie/Didaktik/Keusch/p31_d_rib-e.htm
References: ratt, Charlotte W. Title Essential biochemistry / Charlotte W. Pratt. Publication info. New York: Wiley, 2004. What is DNA? : A biology adventure / written by Transnational College of LEX translated by Alan Gleason. Publication info. Boston: Language Research Foundation, c2003. http://www.saddleback.edu/faculty/thuntley/bio3a/labs/bio3aLABmolecules.pdfhttp://www.jbc.org/cgi/reprint/181/2/713.pdfhttp://www.medilexicon.com/medicaldictionary.php?t=90918http://www.uni-regensburg.de/Fakultaeten/nat_Fak_IV/Organische_Chemie/Didaktik/Keusch/p31_d_rib-e.htm
You May Also Find These Documents Helpful
-
Procedure: Filled each test tube with substances provided and subjected them to various conditions. These conditions included, heat, cold water, hot water, acid and basic additions and tested on litmus paper. The reactions were observed and documented at each step.…
- 730 Words
- 3 Pages
Good Essays -
The purpose of Module 11A was to test for the presence or absence of a particular set of functional groups through the use of wet chemical tests. In this manner, Unknown A which was a colorless solution, was first tested with 2,4-DNP which after mixing for a few seconds formed a bright yellow precipitate. Although this confirms the presence of either a ketone or aldehyde group, one simple chemical test does not completely specify the presence or absence of other functional groups. Therefore, a second test was made in order to test for the presence of alkyl halides (R-Br or R-I specifically). However, after the addition of alcoholic silver nitrate, AgNO3 (test #2) to a few drops of the unknown, the mixture remained colorless and no precipitate formed. Following this, the third test was performed in…
- 686 Words
- 3 Pages
Good Essays -
7. Put 10 drops of 0.5 M nitric acid and 10 drops of 0.5 M phosphoric acid into separate test tubes. Add 1 drop of phenolphthalein to each test tube. Add drops of dilute (0.5 M) sodium hydroxide solution into each of the test tubes until a permanent color change is observed. (NOTE: Phenolphthalein is an acid-base indicator that is colorless in acidic and neutral solutions, but pink in basic solutions). HINT: When writing your net ionic equations: nitric acid is a strong acid while phosphoric acid is a weak…
- 1383 Words
- 6 Pages
Good Essays -
The aim of this experiment is to investigate the process of Electrophoresis and successfully analyse DNA fragments.…
- 1259 Words
- 6 Pages
Good Essays -
References: Berg J.M, Tymoczko, J.L, Stryer, L Bio Chemistry. 5th edition. New York: W.H Freeman; 2002 Chapter 5, DNA, RNA, and the Flow of Genetic Information retrieved from http://www.ncbi.nlm.gov/books/NBK21171…
- 663 Words
- 3 Pages
Good Essays -
In chapter 11, we learned about DNA and Genes (11.1DNA: The Molecule of Heredity; 11.2From DNA to Protein; 11.3Genetic changes). DNA (deoxyribonucleic acid), which is in a shape called a double helix, developed its name from the simple sugar in DNA (deoxyribose). The phosphate group is composed of one atom of phosphorus surrounded by four oxygen atoms. A nitrogen base is a carbon ring structure that contains one or more atoms of nitrogen. Next to cover is DNA replication in which enzyme breaks the hydrogen bonds with the DNA unzipping. Another enzyme bonds floating nucleotides to the single strands to make two new DNA. Each DNA will have an old strand and a new strand. RNAwhich is a nucleic acid, a nucleotidediffers from DNA in three ways: 1. sugar is ribose; 2. there is a single strand of nucleotides, not two; 3. and uracil instead of thymine. There are three types of RNA: 1. mRNAmessengertakes the message from DNA to the ribosome; 2. rRNAribosomalthe ribosomes are made of RNA; 3. tRNAtransferbrings amino acids to the mRNA, about 80 nucleotides long. There are two different types of processes called transcription, and translation.…
- 512 Words
- 3 Pages
Satisfactory Essays -
λ DNA and puC18 DNA were put into two tubes respectively. Then, EcoRI buffer, EcoRI enzyme and deionized water would be put into both tubes. EcoRI enzyme was the restriction enzyme that cut the DNA at the specific sequence. The EcoRI buffer enhanced the stability of many enzymes and binds contaminants that may be present in DNA preparations. DI water was used to bring the solution into a required volume for gel electrophoresis. The prepared sample was incubated at 37℃ for overnight.…
- 463 Words
- 2 Pages
Good Essays -
- First, obtain seven test tubes and label them from 1 to 7 to make it easy to…
- 1405 Words
- 16 Pages
Better Essays -
My name is Erwin Chargaff and I discovered the structure of DNA. After reading Oswald Avery’s report, in 1944, about how genes were composed of DNA I become motivated to begin work on the chemistry of nucleic acids. I started researching with the belief that DNA from different species are different so I had to come up with an experiment to examine the DNA from different species. It was hard for me because I couldn’t get large amounts of DNA so it took awhile for my experimenting. After about 2 years I was able to come up with a solid procedure containing three steps. First, I had to separate the DNA mixture with chromatography paper. Then I converted the separated components into mercury salts and last but not least I was able to identify the purines and pyrimidines ( the building blocks of nucleic acids) by using their ultraviolet absorption spectra. I tested this method several times and was finally able to use it to examine the DNA of yeast and pancreatic cells. About a month later, I submitted two papers on my findings of the DNA of calf thymus and beef spleen and tubercle bacilli and yeast. My papers were rejected so I decided to improve my procedure and by doing that I was able to examine more species. I summarized what I found on nucleic acids in a review and finally in 1950, my experimenting lead to me discover important facts. I came up with three rules that I named as Chargaff’s rule. The first rule is that the number of Adenine always equals the number of thymine. The second is that the number of guanine always equals the number of cytosine and the last one is that the purines (adenine and guanine) always equal the number of pyrimidines (thymine and cytosine. I was also able to prove that the DNA of various species are different from one another. I did not collaborate with anyone for my experiment but two years later I explained my findings to Watson and Crick who were then later to come up the with DNA structure. I was a bit surprised that I wasn’t…
- 410 Words
- 2 Pages
Satisfactory Essays -
DNA is put in the in the class of compounds known as nucleic acids, which are polymers made out of the monomers. The monomers that make the polymers that construct DNA are called nucleotides. Two types of nucleic acids allow living organisms to copy their own complex components to their offspring through reproduction; deoxyribonucleic acid (DNA) and ribonucleic acid (RNA). Nucleic acids exist as polymers known as polynucleotides that all are made up of nucleotides. Nucleotides have only one phosphate group, and the part of a nucleotide without a phosphate group is known as a nucleoside.…
- 1401 Words
- 6 Pages
Powerful Essays -
Agarose is a polymeric cross-linked polysaccharide extracted from the seaweed agar. Agarose is used widely in gel electrophoresis because it gels at a lower temperature, does not contain the inhibitors of virus growth frequently present in agar, and has more uniform pore size than that of agar. It is also easily poured and does not denature the samples. In agarose gel electrophoresis, DNA or RNA fragments are separated or isolated according to their size and electrical charge.The negatively charged nucleic acid molecules move through the agarose matrix with the assistance of an electric field. The genetic material is negatively charged, and will move towards the anode when current is passed through. The shorter molecules migrate faster than the longer molecules. The use of electrophoresis buffer in the making of the agarose gel is to establish a constant pH and to provide ions to support the conductivity. There are three common buffers used in agarose gel electrophoresis. They are Tris-Acetate-EDTA (TAE), Tris-Borate-EDTA (TBE) and Tris-phosphate. For this experiment, the best choice of buffer to use is TAE. The result of our experiment showed no bands. The reasons can be whether the concentration is either very low or DNA is not present at all. This may occur if students punctured the well while loading their DNA.…
- 1260 Words
- 6 Pages
Better Essays -
Agarose gel electrophoresis is an effective way of sizing the DNA to determine the number of base pairs. The microscopic pores inside of the gel allow molecules to travel through them according to their size and shape such that a smaller molecule will move faster and further through the gel. Restriction sites are generally 4-6 base pairs long and palindromic which allow the DNA strands to always correspond to one another (Biotech, 2008). The objectives of this particular study are to:…
- 827 Words
- 4 Pages
Better Essays -
Kuhn, Thomas. "The Nature and Necessity of Scientific Revolutions." The Structure of Scientific Revolutions (1962): 92-111. Print.…
- 1582 Words
- 7 Pages
Powerful Essays -
For the test of Ammonia, ammonia reacted with salicylate to form 5-aminosalicylate and oxidation of 5-aminosalicylate caused the solution to be green. In the blank solution, it was colourless as no ammonia presence in the solution. In the sample water, concentration of ammonia was 0.27mg/l, the colour observed was dark green.…
- 836 Words
- 4 Pages
Good Essays -
(ii) nucleic acid molecules that are chemically or by other means synthesized or amplified, including those that are chemically or otherwise modified but can base pair with naturally occurring nucleic acid molecules, i.e. synthetic nucleic acids, [...]”…
- 471 Words
- 2 Pages
Satisfactory Essays