Identifying Macromolecules by Means of Colour Change

Identifying Macromolecules by Means of Colour ChangeBy Marike CoetzeeB Dietetics II1. Introduction1.1 AimThe purpose of this lab was to honour the glossary win overs (due to chemical reactions) indicants had on diametrical macromolecules in food1 such as starch, proteins and lipides and then to identify the macromolecules found in an unfamiliar modeltlement.These cognize resultant roles contained diverse types of macromolecules which distributively reacted with at least one indication solution in a unique way, which allowed us to identify the macromolecule based upon the presence or absence of a colour change. piddle was also used as a control solution, as it showed a negative reaction with the forefinger solutions.2This experiment produced results which provided a clear brain of the colour change that occurred when each cognize solution reacted with each index finger solution. When the colour changes associated with the terra incognita solution were comp ard with those of the known solutions, it is possible to deduce which macromolecules argon present in the Unknown solution1.2 General backgroundThe four types of macromolecules (organic compounds) found in all living organisms and substances are lipids, carbohydrates, proteins, and nucleic acids. Foods and nutrients, which consist of plants, animals or derivatives thereof are a combination of these macromolecules.3 It is important to determine which macromolecules are found in food as macromolecules play an important section in nutrition.The basis of this experiment is that the four types of macromolecules consist of different segments and atom arrangements. Protein for example contains an NH group while carbohydrates contain a CHO group. This disagreement leave behind cause the molecules to react otherwise with substances and enabling us to determine the compositions of different trys.4ProteinCarbohydrate1.3 Focussed backgroundNegative and positive results for each indicator1*The in tensity of the work is an indication of the amount of the respective macromolecules found in the samples.Water, protein, starch, lipid, vitamin C and an unsung sample were each treated with the different indicators solutions ( iodine, Sudan triplet and Biuret cop sulphate) to determine how that sample solution (and that type of macromolecule) would react with each specific indicator. The individualism of the unknown solution can then be determined by comparing the reactions of the unknown solution with the reactions of the five known solutions.2. Method and Materials2.1 Materials/ ReagentsApparatus usedWhite paper10ml test tubes pipetteReagentsWaterAscorbic Acid unity solutionProteinGlucoseSudan IIILipidUnknownBiuret copper solution2.2 ProcedureSet up three sets of seven clear, clean, 10ml test tubes and mark each set with the spare-time activity water, protein, starch, lipid, vitamin C and an unknown sample.Place 5 ml of each solution into each tube.Add one drop iodine to the first set of seven tubes, Sudan III to the second set and Biuret copper sulphate to the resist set of tubes.Place a white paper behind the tubes so any colour change can be easily observeRecord the colour changes in the table below.3. Results4. DiscussionInterpretation of resultsTo fashion a control group, the different indicator solutions was added to water and used as a colour standard for a negative result. Any colour variation from the control group means a positive result.The indicator solution that could best be used to show the presence of different starch molecules was Iodine as it turned from yellow to a naughty/ purple black in the presence of starch.Sudan III is the best indicator of lipids, since this solution turned orange, which is different than the controls red colour, and also only reacts with lipids and none of the other macromolecules.To test for protein a biuret copper sulphate solution was used, since protein reacted with the biuret copper sulphate to form a dark purple solution. This is considered a change since this solution (purple) is a different colour than the control solution (light blue).Vitamin C has two indicator solutions that can be used to determine its identity iodine and biuret copper sulphate. The iodine indicator reacted with the vitamin C to produce a colourless solution, which can be contrasted with the yellow control, while the biuret and copper sulphate produced a yellow solution that differed from the light blue control.Broader implication of resultsThe Iodine solution turned yellow to colourless in the presence of dim-witted carbohydrates (starch and Vitamin C) but it turned dark purple/black when it was added to the Unknown solution. From the focused background information, it can be deduced that the Unknown sample contained a labyrinthine carbohydrate.The Sudan III tested positive (changed from light red to orange) when added to a lipid but no colour change occurred when the indicator was added to th e unknown. Therefore the unknown sample does not contain any lipidsAlthough the Biuret and Copper solution reacted differently for each of the protein, lipid and vitamin C the solution stayed light blue when added to the starch and unknown. This proves again that the Unknown is a carbohydrate.ConclutionDue to the colour changes observed when the Unknown sample was treated with the different indicators, it can be deduced that the Unknown sample contained a complex carbohydrate, and none lipids or proteins.The unknown solution, labelled Unknown, reacted with the iodine indicator to form a purple black solution. The only known solution which reacted with iodine to form a black solution was starch. Although these colours dont match up perfectly, they are the closest match.The difference in colour between the starch solution and the Unknown solution could be explained by a difference in concentration between the two solutions or by the difference in degree of complexness of the different starches. A factor that could have influence the difference in concentration is if the solutions werent both well shaken, since starch can placate out of solution.5. ReferencesYourscienceteacher.net Internet. Identifying macromolecules and Nutrients Lab background. Your Science teacher. updated 2010 cited 2014-10-09. in stock(predicate) from http//www.cpet.ufl.edu/wp-content/uploads/2013/03/Identifying-Macromolecules-Lab.pdfInky, EFA Internet. Identification of Macromolecules. Study Mode. updated 2011-10-23 cited 2014-10-09. Available from http//www.studymode.com/essays/Identification-Of-Macromolecules-Lab-Report-810104.htmlnesscityschools.org Internet. Identifying macromolecules. Nesscity Schools updated 2013 cited 2014-10-09. Available from http//www.nesscityschools.org/vimages/shared/vnews/stories/53f3996a455d1/Macromolecules%20Lab.pdfSmith JK Internet. Identifying macromolecules and proteins. Osborne Highschool updated 2013 cited 2014-10-09. Available from http//osbornehighsc hool.typepad.com/files/biochemistry-lab-identifying-macromolecules2013s-with-post-lab-questions.doc