What is known as disaccharide? What is the main function of disaccharides?

 DISACCHARIDES

When two monosaccharides are combined together by glycosidic linkage, a

disaccharide is formed.

The important disaccharides are

1. Sucrose

2. Maltose and isomaltose

3. Lactose.

Sucrose

It is the sweetening agent known as cane sugar. It is present in sugarcane and

various fruits.

Sucrose contains glucose and fructose.

Sucrose is not a reducing sugar; and it will not form osazone.

 This is because the linkage involves first carbon of glucose and second

carbon of fructose

 Free reducing groups are not available. So…

When sucrose is hydrolysed, the products have reducing action.

 A sugar solution which is originally nonreducin

 but becomes reducing after hydrolysis, is identified as sucrose (specific

sucrose test)

Sucrose hydrolysis is inversion

 Hydrolysis of sucrose (optical rotation +66.5°) will produce one molecule of

glucose (+52.5°) and one molecule of fructose (–92°).

 Therefore the products will change the dextrorotation to levorotation

 the plane of rotation is inverted.

 Equimolecular mixture of glucose and fructose thus formed is called invert

sugar.

 The enzyme producing hydrolysis of sucrose is called sucrase or invertase.

 Honey contains invert sugar. Invert sugar is sweeter than sucrose.

Lactose

It is the sugar present in milk. It is a reducing disaccharide.

 On hydrolysis lactose produce glucose and galactose Beta glycosidic linkage is present in lactose.

 The anomeric carbon atom of beta-galactose is attached to the 4th

hydroxyl group of glucose through beta-1,4 glycosidic linkage.

 Lactose forms osazone which resemble "badminton ball" or "hedgehog" or

flower of "touch-me-not" plant.

Maltose

Maltose contains two glucose residues.

 There is alpha-1,4 linkage, i.e.1st carbon atom of one glucose is combined

with 4th carbon of another glucose through alpha-glycosidic linkage.

 It is a reducing disaccharide.

 It forms petal shaped crystals of maltose-osazone.

Isomaltose

It contains 2 glucose units combined in alpha -1, 6 linkage.

 Thus first carbon of one glucose residue is attached to the sixth carbon of

another glucose through a glycosidic linkage.

 It is a reducing sugar

 Partial hydrolysis of glycogen and starch produces isomaltose.



POLYSACCHARIDES

These are polymerized products of many monosaccharide units. They may be

1. Homoglycans are composed of single kind of monosaccharides, e.g. starch,

glycogen and cellulose.

2. Heteroglycans are composed of two or more different monosaccharides, e.g.

hyaluronic acid, chondroitin sulphate.

Homopolysaccharides / homoglycanes

1. Starch

A. Structure of Starch

 It is the reserve carbohydrate of plant kingdom.

Sources: Potatoes, tapioca, cereals (rice, wheat) and other food grains.

Starch is composed of amylose and amylopectin When starch is treated with boiling water, 10-20% is solubilized; this part is

called amylose.

 Amylose is made up of glucose units with alpha-1,4 glycosidic linkages

 The insoluble part absorbs water and forms paste like gel; this is called

amylopectin.

 Amylopectin is also made up of glucose units, but is highly branched

 The branching points are made by alpha-1,6 linkage.

B. Hydrolysis of Starch

Starch is non reducing.

 When starch is hydrolysed , It produce smaller and smaller fragments are

produced.

 Thus hydrolysis produces amylodextrin .

 Further hydrolysis produces erythrodextrin ,Than achrodextrins

 Further it produce maltose and then glucose.

Digestion

Salivary amylase and pancreatic amylase are alpha-amylases

 They act on alpha- 1,4 glycosidic bonds to split starch into smaller units

(dextrins), and finally to alpha-maltose.

2. Glycogen

 It is the reserve carbohydrate in animals.

 It is stored in liver and muscle.

 Excess carbohydrates are deposited as glycogen.

 Glycogen is composed of glucose units joined by alpha-1,4 links in the

straight chains.

 It also has alpha-1,6 glycosidic linkages at the branching points

 Glycogen is more branched and more compact than amylopectin.

3. Cellulose

It is the supporting tissues of plants.

 Cellulose is the most abundant organic material in nature.

 It is made up of glucose units combined with beta-1,4 linkages.

It has a straight line structure, with no branching points.

 Beta-1,4 bridges are hydrolysed by the enzyme cellobiase.

 But this enzyme is absent in animal and human digestive system, and hence

 cellulose cannot be digested.

 Herbivorous animals have large caecum, which harbor bacteria.

 These bacteria can hydrolyse cellulose,and the glucose produced is utilized

by the animal.

4. Inulin

It is a long chain homoglycan composed of D-fructose units with repeating beta-

1,2 linkages.

 It is clinically used to find renal clearance value and glomerular filtration

rate.

5. Dextrans

 These are highly branched homopolymers of glucose units with 1-6, 1-4 and

1-3 linkages.

 They are produced by microorganisms.

Since they will not easily go out of vascular compartment,

 They are used for intravenous infusion as plasma volume expander for

treatment of hypovolemic shock

6. Chitin

 It is present in exoskeletons of insects.

 It is composed of units of N-acetylglucosamine with beta-1,4 glycosidic

linkages.


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