Types of lipids
Triglycerides, phospholipids, glycolipids, sterols
Simple lipids
fatty acid and an alcohol(usually glycerol)
Compound lipids
fatty acid + an alcohol + other groups
Structure of triglyceride + properties of the components
triglyceride=fats
Glycerol - CβHβOβ
- polar due to -OH group
- soluble in water
3 fatty acid/long hydrocarbon chain - carboxyl group(-COOH) and an attached hydrocarbon group
- insoluble in water/hydrophobic due to abundance of non-polar C-H bonds
- Saturated: no double bonds, maximal number of hydrogen bonds bonded per C atom
- Unsaturated: double bonds and kink occurs at every double bond
- Acidic in water: presence of carboxyl group, leading to formation of H+ ions in water
βfatty acid chain
βfatty acid
Process of formation of triglyceride
one glycerol + three fatty acid = triglyceride Hydrolysis of triglyceride
Properties of triglycerides
non-polar/insoluble in water/hydrophobic: abundance of non-polar C-H bonds in hydrocarbon tail
melting point increases as hydrocarbon chain length increases:
- increase length, hydrophobic interactions become more extensive between chains
- more thermal energy required to break enough hydrophobic interactions to liquefy the triglyceride
- melting point increases
Melting point decreases as degree of unsaturation increases/as number of double bonds in fatty acid increases
- kinks in double bonds prevent molecules from packing closely
- less closely packed, hydrophobic interactions less extensive
- less thermal energy required to break enough hydrophobic interactions to liquefy the triglyceride
- melting point decreases
Adaptations of triglycerides
higher proportion of C and H atoms to O atoms/greater number of carbon atoms per unit mass: release a larger amount of energy upon oxidation, more efficient energy stores
1. highly reduced molecules: release more metabolic water when oxidised, crucial for desert animals
C-H bonds non-polar and hence triglycerides are hydrophobic, no associated water molecules stored along with triglyceride
1. no extra water weight due to water of hydration
2. does not affect water potential of cells when stored in large amounts
3. fulfils requirement for an animal’s body mass to be kept to a minimum to facilitate locomotion
Good thermal insulators
1. layer of fat(subcutaneous fat) beneath skin insulates the body
Hydrocarbon tails are non-polar, weak hydrophobic interactions between triglyceride molecules
1. can slide under pressure
2. adipose tissue containing fats around vital organs can help cushion and protect vital organs against physical impacts
Lower molecular weight than water**(less dense than water) **
1. aid buoyancy of aquatic animals
Highly reduced molecule: a molecule that has a lot of hydrogen atoms compared to oxygen atoms, or that has many carbon-hydrogen bonds/low oxidation state -> reducation is gain of hydrogen
Main functions of triglycerides
Structure of a phospholipid(a COMPOUND lipid)
one glycerol + 2 fatty acids + negatively charged phosphate group:
1. 2 OH groups joined to one fatty acid each by ester linkage
2. 1 OH group joined to negatively charged phosphate group by phosphoester linkage
Properties of phospholipids
Ambivalent behaviour towards water/amphiatic
1. two fatty acids that comprise the hydrocarbon tails are non-polar and hence hydrophobic, form bond with hydrophobic molecule or among themselves
2. phosphate group and its attachment form a polar/charged hydrophilic head that has affinity for water
Three types of lipid aggregates:
1. Micelle
2. Bilater
3. Liposome/vesicle
Structure and function of phospholipids
Amphiatic molecules
1. Form a selectively permeable cell surface membrane, forming an effective barrier/boundary between cell and external environment
* phosphate head face outwards towards aqueous environment
* hydrophibic hydrocarbon tails face inwards away from aqueous environment
2. Form liposomes which are used as vesicles for storage and transport of cellular products, digestion of waste, drug delivery
3. Form micelles for transport of fats between gut and body tissue
Hydrophobic interactions exits between fatty acids tails
1. large number of interactions allows maintenance of intergrity of membrane bilayer
2. individual interactions are weak, permitting lateral movement of phospholipids, allowing for membrane fluidity
Most phospholipids contain choline
1. represent a large proportion of body’s store of choline
2. choline is important for the synthesis of acetylcholine, a neurotransmitter
Structure + function of glycolipids
2 hydrophobic hydrocarbon tails + + glycerol + a polar, short carbohydrate chain with no phosphate
short carbohydrate joined to glycerol’s -OH group by glycosidic bond, which is a covalent bond
1. found at cell surface membrane facing exterior environment
2. marker that distinguishes one cell from another in cell-cell recognition. cells recognise other cells by binding to these carbohydrate chains
hydrophobic interactions exist between fatty acids tails
1. anchors entire glycolipids at cell surface membrane
Cholestrol
- components
- function
Components: three fused six-membered and one five membered ring
Function:
- regulate membrane fluidity:
1. rigid steroid rings interferes with motions of hydrocarbon chains of phospholipids due to van de Waals interactions, enhances mechnical stability of cell surface membrane
2. at high temperatures, cholestrol restricts movement of phospholipids by distrupting motions of the hydrocarbon chains, leading to decreased membrane fluidity
3. at low temperatures, cholestrol prevent the hydrocarbon chains from packing too closely together, decreasing the tendency of the membrane to solidify, leading to decreased membrane fluidity
- precursor for synthesis of bile acids, steroid hormone and vitamin D
Emulsion test - test for lipids
Method:
1. Add 2cm3 of absolute ethanol to sample and mix well - lipids solube in organic solvents
2. decant ethanol into another test tube containing an equal volume of water
Interpretation of results:
- Present: lipid dissolves in ethanol to form clear solution which forms emulsion with water
- Absent: clear solution still formed with ethanol, reamins clear when added to water