Pharm-D Biochemistry, Lipids
Pharm-D Biochemistry, Lipids
Pharm-D Biochemistry, Lipids
Bloor has proposed the following classification of lipids based on their chemical
composition.
1. Simple lipids: These are esters of fatty acids with various alcohols.
a) Neutral Fats (Triacylglycerol,TAG):
These are esters of fatty acids with trihydroxy alcohol, glycerol. Oils are fats in the
liquid state.
b) Waxes:
These are esters of fatty acids with higher molecular weight monohydric alcohols.
CLASSIFICATION OF LIPIDS
2. Compound lipids: These are esters of fatty acids with alcohol and possess
additional group(s) also.
a) Phospholipids:
These are lipids containing, in addition to fatty acids and glycerol, a phosphoric acid,
a nitrogen base and other substituents. For example, in glycerophospholipids the
alcohol is glycerol and in sphingophospholipids, the alcohol is sphingosine.
b) Glycolipids:
These are lipids containing a fatty acid, sphingosine, and carbohydrate.
CLASSIFICATION OF LIPIDS
Lipids are grouped into two main classes in the chemical reaction (saponification)
classification system:
1) Saponifiable lipids
2) Nonsaponifiable lipids.
Fatty acids are long, unbranched hydrocarbon chains with a carboxylic acid group at
one end.
It is represented by a chemical formula R-COOH, where R stands for hydrocarbon
chain.
Fatty acids are amphipathic compounds because the carboxyl group is hydrophilic
and the hydrocarbon tail is hydrophobic.
The carboxyl group can ionize as the carboxylate anion (–COO- ) under the proper
conditions of physiological pH.
FIGURE: The molecular structure of fatty acid. A. Lauric acid and B. a simplified
diagram of a fatty acid with a nonpolar tail and a polar head.
FATTY ACIDS
The fatty acids found in natural lipids have several characteristics in common:
1. They are usually straight-chain carboxylic acids (no branching).
2. The sizes of most common fatty acids range from 10 to 20 carbons.
3. Fatty acids usually have an even number of carbon atoms (including the carboxyl
group carbon).
4. Fatty acids can be saturated (containing no double bonds between carbons) or
unsaturated (containing one or more double bonds between carbons).
FATTY ACIDS
The hydrocarbon chain of a fatty acid may or may not contain carbon–carbon double
bonds.
On the basis of this consideration, fatty acids are classified as:
1. Saturated fatty acids (SFAs),
2. Unsaturated Fatty Acids
3. Monounsaturated fatty acids (MUFAs), and
4. Polyunsaturated fatty acids (PUFAs).
CLASSIFICATION OF FATTY ACIDS
The systematic nomenclature of the fatty acids is based on the Genevan system.
According to this system, the fatty acid is named after the hydrocarbon with the
same number of carbon atoms.
The suffix -oic is written in place of the final letter e in the name of the hydrocarbon.
The names of saturated fatty acids end with the suffix –anoic e.g., Octadecanoic
acid.
The names of unsaturated fatty acids end with the suffix –enoic e.g.,
Octadecenoic acid (Oleic acid).
NOMENCLATURE OF FATTY ACIDS
The notation most commonly used for fatty acids indicates the:
• Number of carbon atoms, and
• Number of double bonds.
The notation 18:0 denotes an C18 fatty acid with no double bonds, while 18:1
signifies an C18 fatty acid with one double bond.
NOMENCLATURE OF FATTY ACIDS
The unsaturated fatty acids exhibit geometric (or cis-trans) isomerism at the double
bonds.
In biochemically important MUFAs, the configuration about the double bond is nearly
always cis rather than trans.
‘Cis’ form is comparatively unstable and is more reactive.
For example, Oleic acid can exist in two forms: cis-oleic acid and trans-oleic acid which is
also called elaidic acid.
ISOMERISM IN FATTY ACIDS
ISOMERISM IN FATTY ACIDS
Essential fatty acids are those polyunsaturated fatty acids that cannot be synthesized
by our cells and we should obtain them from plants through diet.
Linoleic acid and linolenic acid are the only essential fatty acids for animals.
Other polyunsaturated fatty acids can be synthesized from these essential fatty acids.
For example, arachidonic acid can be synthesized only from linoleic acid.
Therefore, in deficiency of linoleic acid, arachidonic acid also becomes an essential
fatty acids.
IMPORTANCE OF ESSENTIAL FATTY ACIDS
Linoleic acid is the starting material for the biosynthesis of arachidonic acid.
Arachidonic acid is the major starting material for eicosanoids, substances that help
regulate blood pressure, clotting, and several other important body functions.
Linolenic acid is the starting material for the biosynthesis of two additional omega-3
fatty acids.
Linolenic acid (18:3) → EPA (20:5) → DHA (22:6)
IMPORTANCE OF ESSENTIAL FATTY ACIDS