Amino acids join together by condensation reactions. The -OH from the carboxyl group of one amino acid combines with an -H from the amino group of another, and a molecule of water is removed.The covalent bond that forms between the carbon of the carboxyl group and the nitrogen of the amino group is called a peptide bond, -CONH-. Two amino acids joined in this way form a dipeptide.Further condensation reactions add more amino acids to form a polypeptide. In cells this happens on ribosomes during translation. A polypeptide always has a free amino group at one end (the N-terminal) and a free carboxyl group at the other end (the C-terminal).Because the order matters, two different dipeptides can be made from the same two amino acids. For example, gly-ala and ala-gly are different molecules.Peptide bonds can be broken by hydrolysis, which adds a water molecule back. In the body this is catalysed by protease enzymes.
Peptide Bond Formation
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Specification: AQA Biology (7401), AS-level, 3.1.4.1 General properties of proteins. Topic: Biological Molecules.
Key terms in this lesson
- condensation reaction
- A reaction that joins two molecules together with a covalent bond, with the elimination of a water molecule.
- hydrolysis
- The breaking of a covalent bond within a molecule using a water molecule.
More in Biological Molecules
- Phospholipids
- Properties of Phospholipids
- Test for Lipids
- Amino-Acids
- Primary Structure
- Secondary Structure
- Tertiary Structure
- Quaternary Structure
All 29 lessons in Biological Molecules · All AQA AS-level Biology topics