The most predominant and versatile element of life. It possesses a unique property to form infinite number of compounds. This is attributed to the ability of carbon to form stable covalent bonds and C—C chains of unlimited length. It is estimated that about 90% of compounds found in living system invariably contain carbon.
Complex biomolecules
Proteins
Nucleic acids (DNA and RNA)
Polysaccharides
Monomers
Amino acids, nucleotides and monosaccharide's serve as the buildingblocks of complex biomolecules
Lipids are not biopolymers in a strict sense, but majority of them contain fatty acids.
Macromolecules (proteins, lipids, nucleic acids and polysaccharides)
They form supra-molecular assemblies (e.g., membranes) which in turn organize into organelles, cells, tissues, organs and finally the whole organism.
Carbohydrates
The most abundant organic molecules in nature. They are primarily composed of the elements carbon, hydrogen and oxygen. The name carbohydrate literally means 'hydrates of carbon.' Carbohydrates may be defined as polyhydroxy- aldehydes or ketones or compounds which produce them on hydrolysis.
Sugars
Carbohydrates soluble in water and sweet to taste.
Classification of Carbohydrates
Monosaccharide's
Oligosaccharides
Polysaccharides
Monosaccharide's
The simplest group of carbohydrates and are often referred to as simple sugars. They have the general formula Cn(H2O)n, and they cannot be further hydrolysed.
Oligosaccharides
Contain 2-10 monosaccharide molecules which are liberated on hydrolysis.
Polysaccharides
Polymers of monosaccharide units with high molecular weight (up to a million). They are usually tasteless (non-sugars) and form colloids with water.
Types of Polysaccharides
Homopolysaccharides
Heteropolysaccharides
Stereoisomerism
An important character of monosaccharides. Stereoisomers are the compounds that have the same structural formulae but differ in their spatial configuration.
Asymmetric carbon
A carbon is said to be asymmetric when it is attached to four different atoms or groups.
Glyceraldehyde
The simplest monosaccharide with one asymmetric carbon atom. It exists as two stereoisomers, and has been chosen as the reference carbohydrate to represent the structure of all other carbohydrates.
and L-isomers
Mirror images of each other. The special orientation of —H and —OH groups on the carbon atom (C5 for glucose) that is adjacent to the terminal primary alcohol carbon determines whether the sugar is D- or L-isomer.
Optical activity
A characteristic feature of compounds with asymmetric carbon atom. When a beam of polarized light is passed through a solution of an optical isomer, it will be rotated either to the right or left.
Glycosides
Formed when the hemiacetal or hemiketal hydroxyl group (of anomeric carbon) of a carbohydrate reacts with a hydroxyl group of another carbohydrate or a non-carbohydrate (e.g. methyl alcohol, phenol, and glycerol). The bond so formed is known as glycosidic bond and the non- carbohydrate moiety (when present) is referred to as aglycone.
Derivatives of Monosaccharide's
Amino sugars
Deoxysugars
L-Ascorbic acid (vitamin C)
Amino sugars
When one or more hydroxyl groups of the monosaccharide's are replaced by amino groups.
Deoxysugars
Sugars that contain one oxygen less than that present in the parent molecule.
Ascorbic acid (vitamin C)
A water- soluble vitamin, the structure of which closely resembles that of a monosaccharide.
Types of Disaccharides
Reducing disaccharides with free aldehyde or keto group
Non-reducing disaccharides with no free aldehyde or keto group
Homopolysaccharides
On hydrolysis yield only a single type of monosaccharide. They are named based on the nature of the monosaccharide unit.
Heteropolysaccharides
On hydrolysis yield a mixture of a few monosaccharide's or their derivatives.
Starch
The carbohydrate reserve of plants which is the most important dietary source for higher animals, including man. It is a homopolymer composed of D-glucose units held by α glycosidic bonds. It consists of two polysaccharide components-water soluble amylose (15-20%) and a water insoluble amylopectin (80-85%).
Glycogen
The carbohydrate reserve in animals, hence often referred to as animal starch. It is present in high concentration in liver, followed by muscle, brain etc. The structure of glycogen is similar to that of amylopectin with more number of branches.
Cellulose
Occurs exclusively in plants and it is the most abundant organic substance in plant kingdom. It is a predominant constituent of plant cell wall. Cellulose is composed of β-D-glucose units linked by β (1 → 4) glycosidic bonds. Cellulose cannot be digested by mammals—including man—due to lack of the enzyme that cleaves β-glycosidic bonds.
Mucopolysaccharides
Heteroglycans made up of repeating units of sugar derivatives, namely amino sugars and uronic acids. They are more commonly known as glycosaminoglycan's (GAG). Acetylated amino groups, besides sulfate and carboxyl groups are generally present in GAG structure.
Lipids
Of great importance to the body as the chief concentrated storage form of energy.
Polysaccharides
More commonly known as glycosaminoglycans (GAG)
GAG structure
Acetylated amino groups, besides sulfate and carboxyl groups are generally present
Mucoproteins
Combination of mucopolysaccharides and proteins
Mucoproteins may contain up to 95% carbohydrate and 5% protein
Mucopolysaccharides are essential components of tissue structure
Extracellular spaces of tissue
Consist of collagen and elastin fibers embedded in a matrix or ground substance
Ground substance is predominantly composed of GAG
Important mucopolysaccharides
Hyaluronic acid
Chondroitin 4-sulfate
Heparin
Dermatan sulfate
Keratan sulfate
Lipids
Organic substances relatively insoluble in water, soluble in organic solvents (alcohol, ether etc.), actually or potentially related to fatty acids and utilized by the living cells
Unlike the polysaccharides, proteins and nucleic acids, lipids are not polymers