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Lipid Def: compounds which are relatively insoluble in water, but freely soluble in non polar organic solvents like benzene, ether, chloforom etc.

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Presentation on theme: "Lipid Def: compounds which are relatively insoluble in water, but freely soluble in non polar organic solvents like benzene, ether, chloforom etc."— Presentation transcript:

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2 Lipid Def: compounds which are relatively insoluble in water, but freely soluble in non polar organic solvents like benzene, ether, chloforom etc.

3 Function 1.Storage form of energy 2.Structure component of biomembranes 3.Insolution 4.Shape and contour of body 5.Protect internal organ 6.Metabolic regulator 7.Electric insulator in neurons 8.Help in absorbtion of fat soluble vitamins 9.Taste and palatability

4 Clinical importance of lipid Obesity Artheroscreloris Fatty liver Lipid storage disorder Lipoproteinimias

5 CLASSIFICATION OF LIPIDS Simple Lipids, exp: fat or oil, wax Compound Lipid – Phospholipid – lechitin – Glycolipids – cerebrosides – Sulpholipids – sulfated cerebrosides Derived lipids – exp. Fatty acids, prostaglandin, steroids, etc. Micellaneous lipids, exp. Carotenoids, squalene, etc.

6 6 Types of Lipids Lipids with fatty acids Waxes Fats and oils (trigycerides) Phospholipids Sphingolipids Lipids without fatty acids Steroids

7 7 Fatty Acids Long-chain carboxylic acids Insoluble in water Typically 12-18 carbon atoms (even number) Some contain double bonds corn oil contains 86% unsaturated fatty acids and 14% saturated fatty acids

8 8 Saturated and Unsaturated Fatty Acids Saturated = C–C bonds Unsaturated = one or more C=C bonds

9 9 Structures Saturated fatty acids Fit closely in regular pattern Unsaturated fatty acids Cis double bonds

10 10 Properties of Saturated Fatty Acids Contain only single C–C bonds Closely packed Strong attractions between chains High melting points Solids at room temperature

11 11 Properties of Unsaturated Fatty Acids Contain one or more double C=C bonds Nonlinear chains do not allow molecules to pack closely Few interactions between chains Low melting points Liquids at room temperature

12 12 Learning Check L1 How would the melting point of stearic acid compare to the melting points of oleic acid and linoleic acid? Assign the melting points of –17°C, 13°C, and 69°C to the correct fatty acid. Explain. stearic acid (18 C) saturated oleic acid (18 C) one double bond linoleic acid (18 C) two double bonds

13 13 Solution L1 Stearic acid is saturated and would have a higher melting point than the unsaturated fatty acids. Because linoleic has two double bonds, it would have a lower mp than oleic acid, which has one double bond. stearic acid mp 69°C oleic acid mp 13°C linoleic acid mp -17°C

14 14 Fats and Oils Formed from glycerol and fatty acids

15 15 Triglycerides (triacylglcerols) Esters of glycerol and fatty acids

16 16 Learning Check L2 What are the fatty acids in the following triglyceride?

17 17 Solutions L2 What are the fatty acids in the following triglyceride? Stearic acid Oleic acid Myristic acid

18 18 Properties of Triglycerides Hydrogenation Unsaturated compounds react with H 2 Ni or Pt catalyst C=C bonds C–Cbonds Hydrolysis Split by water and acid or enzyme catalyst Produce glycerol and 3 fatty acids

19 19 Hydrogenation

20 20 Product of Hydrogenation Hydrogenation converts double bonds in oils to single bonds. The solid products are used to make margarine and other hydrogenated items.

21 21 Hydrolysis Triglycerides split into glycerol and three fatty acids (H + or enzyme catalyst)

22 22 Saponification and Soap Hydrolysis with a strong base Triglycerides split into glycerol and the salts of fatty acids The salts of fatty acids are “soaps” KOH gives softer soaps

23 23 Saponification

24 24 Learning Check L3 What are the products obtained from the complete hydrogenation of glyceryl trioleate? (1) Glycerol and 3 oleic acids (2) Glyceryltristearate (3) Glycerol and 3 stearic acids

25 25 Solution L3 What are the products obtained from the complete hydrogenation of glyceryl trioleate? 2. Glyceryltristearate


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