* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download Hydrolysis of Aspartame
Fatty acid metabolism wikipedia , lookup
Metalloprotein wikipedia , lookup
Butyric acid wikipedia , lookup
Nucleic acid analogue wikipedia , lookup
Fatty acid synthesis wikipedia , lookup
Peptide synthesis wikipedia , lookup
Protein structure prediction wikipedia , lookup
Genetic code wikipedia , lookup
Amino acid synthesis wikipedia , lookup
Proteolysis wikipedia , lookup
Biosynthesis wikipedia , lookup
Biochemistry wikipedia , lookup
Salter’s A2 Engineering Proteins Hydrolysis of Aspartame Aspartame contains two amino acids joined together by an amide (peptide) bond. In this experiment you are going to hydrolyse aspartame to break the linkage and then separate and identify the amino acids by chromatography. Requirements: 0.5 % aqueous aspartame solution heating apparatus and test tube holders 0.2 % aqueous solutions of glycine, 500 ml beakers aspartic acid and phenylalanine 6 M HCl (aq) hairdryers pipettes and teats ninhydrin in butan-1-ol spray small test tube gloves capillary tubes for spotting Eluent chromatography paper, pencil and ruler Foil to cover beakers To Prepare Eluent of butan-1-ol (CARE harmful and flammable): glacial ethanoic acid (CARE Corrosive; avoid inhaling the vapour): distilled water in a 5:1:4 ratio. Prepare by shaking together in a separating funnel and keeping the top layer for use as the eluent. Method: Salter’s A2 Engineering Proteins Place 4 drops of 0.5 % aspartame solution and 4 drops of 6M HCl (aq) in a small test tube. Cautiously heat the tube, boiling it gently for about 90 seconds. Allow the contents to cool and label it hydrolysed aspartame. For the chromatography: With a pencil lightly draw a line along one end of the chromatography paper. Number each column, and write your name on the top. Using gloves carefully spot the following solutions on the relevant column: 1 hydrolysed aspartame 2 0.5 % aspartame solution 3 0.2 % glycine solution 4 0.2 % aspartic acid solution 5 0.2 % phenylalanine solution Set the chromatogram to run in a large beaker in a mixture of 5:1:4 butan-1ol:ethanoic acid:distilled water (prepared as instructions). This solvent is known as the eluent. Make sure the bottom of the paper is in the eluent but the spots are not. Cover the beaker with foil to prevent evaporation. Remove from the beaker when the solvent front is just at the top of the columns. Mark this point with a pencil line. Dry the chromatograms with a hair dryer and spray them with ninhydrin until they are wet but not dripping. Dry with a hairdryer again. Circle the spots that appear. Analyse your results to decide what amino acids are present in aspartame. Key Words: Chromatography Chromatogram Stationary phase Mobile phase Eluent Solvent front Ninhydrin Salter’s A2 Engineering Proteins