Amino acid Revision cards for Amino acids section of AQA unit 4 syllabus 2.5 / 5 based on 2 ratings ? ChemistryAcids, bases and saltsAmines and azo dyesA2/A-levelAQA Created by: Kirsty JonesCreated on: 08-06-10 16:03 Amino Acids have acid and base properities General formular H2NCHRCOOH other than glycerine all amino acids are chiral Carboxylic group has a tendency to lose a proton -COOH --(eqm)--> -COO- + H+ amine group has tendency to accept a proton in strongly acidic conditions H+ + -NH2 --(eqm) --> -NH3+ Amino acids can exist and Zwitterion H3NHCRCOO High melting points as they are ionic 1 of 4 Proteins and formation of peptide links Proteins are sequences of amino acids joined by peptide links H2NHCRCOOK + H2NRCHCOOH --> H2NCONHRCHCOOH + H2O the two amino acids are linked by a peptide bond. can react again to form large peptide chains The above reaction is a condensation reaction (H2O eliminated). 2 of 4 Hydrolysis of peptide links produce original amino when a protein or peptide is boiled with HCl acid of conc 6 mol dm-3 for about 24 hours it breaks down to a mixture of amino acids. Acid hydrolises the peptide links H2NRCHCONHRCHCOOH +H2O --(H+ catalyst)--> 2H2NRCHCOOH These amino acid mixtures can be separated by chromatography. allows us to find out which ones are present 3 of 4 Hydrogen bonding in proteins Complex structures in proteins held together by hydrogen bonding Shapes of proteins vital to function (e.g. enzymes and active site!) 4 of 4
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