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TRIACYLGLYCEROLS
TRIACYLGLYCEROLS
What is Triacylglycerols?
Triacylglycerols (TAGs) are an important component of the glycerolipid family. Their primary function in
cells is to store excess fatty acids, and they are most commonly seen in lipid droplets.
Triacylglycerol Structure:
Three fatty acids are ester-linked to a single glycerol molecule.
Each fatty acid is linked to glycerol via the ester bond.
Hydrophobic Characteristics:
Nonpolar molecules are triacylglycerols.
They are extremely hydrophobic, which means they repel water.
Water Insolubility:
Triacylglycerols are insoluble in water due to their hydrophobic nature.
They do not dissolve or mix well with aqueous solutions.
Dietary Fats:
Triacylglycerols make up a significant portion of dietary lipids and oils.
Human cells, with the notable exception of nerve cells, store modest amounts of energy-producing
molecules.
Carbohydrate glycogen - The most common energy storage substance found in trace
amounts.
Simple triacylglycerol:
Triester formed from the glycerol esterification with three similar fatty acids molecules of acid
Mixed triacylglycerol:
Triester formed from the glycerol esterification with more than one type molecule of fatty acid
CHEMICAL REACTIONS OF TRIACYLGLYCEROLS
1. Hydrolysis
2. Saponification
4. Oxidation
Products of Oxidation:
This oxidation process causes the C=C bonds in fatty acids to break.
It produces two types of oxidation products:
Aldehyde: Aldehydes are organic compounds with a carbonyl group (C=O) at the
end of a carbon chain that are generated as a result of the reaction.
Carboxylic Acid: Carboxylic acids are also formed as oxidation products and are
distinguished by a carboxyl group (COOH).
Preservation strategies:
Various preservation strategies, such as the use of antioxidants and suitable storage
conditions, such as reducing exposure to air and light, are used to prevent or delay
the oxidation of triacylglycerols