The primary structure of a protein refers to the linear sequence of amino acids in the polypeptide chain.
Key molecules required to build structures for organisms to function:
Carbohydrates
Proteins
Lipids
Nucleic Acids
Water
Polymers are molecules made from a large number of monomers joined together in a chain
Monomers are smaller units from which larger molecules are made
Carbohydrates, proteins, lipids, and nucleic acids contain carbon (C) and hydrogen (H) making them organic compounds
Carbon atoms are key to organic compounds because:
Each carbon atom can form four covalent bonds, making the compounds very stable
Carbon atoms can form covalent bonds with oxygen, nitrogen, and sulfur
Carbon atoms can bond to form straight chains, branched chains, or rings
Carbon compounds can form small single subunits (monomers) that bond with many repeating subunits to form large molecules (polymers) through polymerisation
Macromolecules are very large molecules containing 1000 or more atoms, therefore having a high molecular mass
Polymers can be macromolecules, but not all macromolecules are polymers as the subunits of polymers have to be the same repeating units
Three types of carbohydrates:
Monosaccharides
Disaccharides
Polysaccharides
A covalent bond is the sharing of two or more electrons between two atoms
Covalent bonds can be nonpolar (equal sharing) or polar (unequal sharing)
Covalent bonds are very stable and require high energies to break
Multiple pairs of electrons can form double bonds (e.g. unsaturated fats C=C) or triple bonds
Condensation (dehydration synthesis) reaction:
Monomers combine by covalent bonds to form polymers or macromolecules, and water is removed
Hydrolysis:
Involves breaking covalent bonds in polymers when water is added
Reducing sugars can donate electrons, making them the reducing agent
Reducing sugars can be detected using Benedict’s test as they reduce soluble copper sulphate to insoluble brick-red copper oxide
Examples of reducing sugars include: glucose, fructose, and galactose
Fructose and galactose have the same molecular formula as glucose but a different structural formula
Non-reducing sugars cannot donate electrons and therefore cannot be oxidised
Non-reducing sugars must be hydrolysed into monosaccharides before a Benedict’s test can be carried out
Example of a non-reducing sugar: sucrose
Glucose is the most common monosaccharide with the molecular formula C6H12O6
Glucose exists in two structurally different forms: alpha (α) glucose and beta (β) glucose, known as isomers
Different types of monosaccharides are formed from molecules with varying numbers of carbon atoms, such as trioses (3C), pentoses (5C), and hexoses (6C)
Monosaccharides are bonded together to form disaccharides and polysaccharides for transport, storage, and to have less influence on a cell’s osmolarity
Disaccharides and polysaccharides are formed when two hydroxyl (-OH) groups interact to form a glycosidic bond
Each glycosidic bond results in the removal of one water molecule through condensation
Different types of glycosidic bonds form depending on the interacting OH groups, catalysed by specific enzymes (e.g., maltose has an α-1,4 glycosidic bond, and sucrose has an α-1,2 glycosidic bond)
The glycosidic bond is broken when water is added in a hydrolysis reaction
Disaccharides and polysaccharides are broken down in hydrolysis reactions
Hydrolytic reactions are catalyzed by enzymes, different from those present in condensation reactions
Examples of hydrolytic reactions include:
Digestion of food in the alimentary tract
Breakdown of stored carbohydrates in muscle and liver cells for use in cellular respiration
Sucrose is a non-reducing sugar that gives a negative result in a Benedict’s test
When sucrose is heated with hydrochloric acid, it provides the water that hydrolyses the glycosidic bond, resulting in two monosaccharides that will produce a positive Benedict's test