Notes On Lipids
Notes On Lipids
FUNCTIONS
1. Fuel
Fat – is the most concentrated storage form of
energy
- Yields 9 calories per gram
Ex. Triglyceride (Triacylglycerol, TAG)
- can be hydrolyzed t be used for energy
- Used for storage of excess energy; stored in
adipose tissue
STRUCTURAL DIVERSITY
D. Steroid Lipids – cholesterol, cholesteryl esters, a. Saturated Fatty Acids
cholesterol derivatives (with ring structure - No double bonds between carbons in the
chain
E. Miscellaneous Lipids – aliphatic hydrocarbons, - All carbon atoms are single bonded –
carotenoids, squalene, terpenes, vitamin E and K, filled with hydrogen atoms
glycerol ether, glycosyl glycerols - Solid at room temperature
- Higher melting temperature
ABILITY TO UNDERGO HYDROLYSIS UNDER
Melting temperature – temp at which a
ALKALINE CONDITION substance changes from solid to liquid
state
A. Saponifiable –exposure to alkaline medium will break - Straight chain (mol. are compact)
them down into simpler components
- Can be converted into 2 or more smaller molecules
when hydrolysis occurs
Ex. TAG, Phospholipids, Sphingoglycolipids, - Found in animals, butter, lard, palm
Biological Waxes coconut
- Must have: (at least 1)
o Ester bond
o Glycosidic bond b. Unsaturated Fatty Acids
o Amide bond - Contain 1 or more double bond
- Double bond appears as kinks –
B. Nonsaponifiable – lipids can no longer undergo contributes to the fluidity and permeability
hydrolyzation in an alkaline medium of the membrane, prevents efficient
- Only has 1 building block – does not need packing (mol not as compact)
bonds to link them together - Liquid at room temperature
- No site for hydrolysis to occur - Lower melting temperature
- Does not react with water
Ex. Cholesterol, Bile Acids, Steroid Hormones
FATTY ACIDS
C. Classification
1. Length of the Hydrocarbon Tail Trans configuration
Type of Fatty Acid No. of Carbon - H atoms are on the opposite ends of the
Long chain 12 – 16 carbons
Medium chain 6 – 12 carbons
bond
Short chain < 6 carbons - Linear
*** Range may vary per reference - Behaves much like a saturated fatty acid
2. Degree of unsaturation
3. Source NOMENCLATURE OF FATTY ACIDS
a. Non-essential fatty acids
Carbon Skeleton
- Can be synthesized by the body
Ex. Palmitic acid, and other saturated - No. of Carbon : No. of Double Bond
and monoenoic FA’s - 12:0 = 12 Carbon : 0 double bond
b. Essential fatty acids - ∆ = where double bond is located
- Must be obtained from exogenous - 16:1(∆9) = 12 C : 1 DB (DB at C 9)
sources (diet)
- Plays a role in normal growth and Structure
development - CH2(CH2)10COOH
Ex. Breastmilk - CH3(CH2)5CH=CH(CH2)7COOH
Systematic Name
- n = normal unbranched structure
- 12 = dodeca
- n - Dodecanoic acid
- cis – 9- Hexadecenoic acid
- 9 = where DB is located
- decenoic – one double bond
- Linolenic Acid - Responsible for proper
- dienoic – 2 double bond
membrane structure
- trienoic – 3 double bond
- Serve as anti-inflammatory, prevents heart
disease, reduces risk of heart disease and Common Name
cancer
- Arachidonic Acid – regulate blood pressure, - usually comes from the source
blood clotting, and different body functions - “Lauric acid” – from laurel plant
18 : 2 ( ∆9, 12)
BAD FATS
Saturated Trans 2. Omega ( ω ) Numbering System
Fatty meats, chicken Biscuits, cakes, pastries - Starts with the methyl end (H3C or CH3) or
skin, butter, cream, and doughnuts omega end
cheese, ice cream, deep - Omega ( ω ) ends hydrocarbon will be read as
fried, take away and fast C1
food
- Can increase cardiovascular disease risk
- Trans – produced by partial hydrogenization
of unsaturated fatty acids
Omega System: ω – 6,9