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DISACCHARIDES
They are formed when two monosaccharides, usually hexoses, combine by means of a
chemical reaction known as condensation.
The monosaccharide units are called residues once they have been linked.
Example: maltose molecule contains two glucose residues.
(a)Maltose
Maltose occurs mainly as a breakdown product during digestion of starch by enzyme
called amylase. This commonly occurs in animals and in germinating seeds.
(b) Lactose
Lactose or milk sugar is found exclusively in milk and is an important energy source for
young mammals. It can only be digested slowly, so gives a slow steady release of energy.
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(c) Sucrose
Sucrose or cane sugar is the most abundant disaccharide in nature. It is most commonly
found in plants, where it is transported in large quantities through phloem tissue.
POLYSACCHARIDES
They function chiefly as food and energy storage (for example starch and glycogen) and
as structural materials (for example cellulose).
Starch
Starch is a polymer of α-glucose. It is a major fuel store in plants, but is absent in
animals where the equivalent is glycogen.
Amylose has a straight chain structure consisting of several thousand glucose residues
joined by 1,4-bonds. These bonds cause the chain to coil helically into a more compact
shape. (Amylose chain held by hydrogen bonds formed between hydroxyl groups)
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Amylopectin is also compact as it has many branches, formed by 1,6-glycosidic bonds. It
has up to twice as many glucose residues as amylose. The linear chain of α-glucose
residues are held together by α-1,4-glycosidic bonds. Branches occur at intervals of
approximately 25 to 30 where α-1,6-glycosidic bonds occur.
The amylose helices are entangled in the branches of amylopectin to form a complex
compact three dimensional starch molecule.
Cellulose
Cellulose is a polymer of β-glucose.
When two molecules of β-glucose line up, the –OH group on carbon atom 1 can only line
up alongside the –OH group on carbon atom 4 if one of the molecule is rotated at 180 to
the other.
This is because the –OH group in carbon atom 1 projects below the ring and the –OH
group on carbon atom 4 projects above the ring. This rotation of successive residues is
the underlying reason why cellulose has a different structure to starch.
It consists of long chain of glucose residues with about 10000 residues per chain. The
β-1,4 linkages make the chain straight.
Hydroxyl group (-OH) projected outwards from each chain in all directions and form
hydrogen bonds with neighbouring chains.
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The chains associate in group of about 60 to 70 to form microfibrils, which are arranged
in larger bundles to form macrofibrils.
The statement in the table below refers to the three polysaccharides molecules. Place a tick (√) in
the appropriate box if the statement is correct and a cross (Х) if the statement is incorrect.
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OBJECTIVES QUESTIONS
1. Lactose is a reducing sugar because
(a) It contains a glucose and a galactose
(b) It has a hydroxyl group
(c) It contains aldehydes group
(d) It cannot be crystallised in Benedict’s solution
2. Which of the following statements is true about the polysaccharides in living organisms?
Form storage compound Form supporting structures Provides energy
A. No Yes No
B. No Yes Yes
C. Yes Yes Yes
D. Yes No Yes
Which of the following polymers can be formed from the condensation of the molecules shown
above?
I. Glycogen
II. Amylose
III. Amylopectin
IV. Starch
A. II and III
B. I, II and III
C. II, III and IV
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D. I, II, III and IV
7. The diagram below shows a type of monosaccharide.
Which of the following polymers can be formed from the condensation of the molecule shown
above?
I. Cellulose
II. Amylose
III. Amylopectin
IV. Starch
A. I only
B. I, II and III
C. II, III and IV
D. I, II, III and IV
Question 8 and 9 are based on the diagram below, which shows a type of disaccharide.
8. Which of the following statements are true about the molecule shown above?
I. Has α-1,2 glycosidic bond
II. Has α-1,4 glycosidic bond
III. Formed from the condensation of two aldose sugars
IV. Formed from the condensation of one ketone and one aldose sugar.
A. I and III
B. I and IV
C. II and III
D. II and IV
9. Which combination of statements below is correct for the molecule shown above?
A. Reducing sugar soluble in water
B. Non reducing sugar soluble in water
C. Reducing sugar Insoluble in water
D. Non reducing sugar Insoluble in water
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Question 10 and 11 are based on the diagram below which shows a type of carbohydrate.
10. Which statements about the carbohydrate shown above are true?
I. Polymer made up of α-glucose units
II. Polymer made up of β-glucose units
III. Storage polysaccharide
IV. Structural component of cell
A. I and III
B. I and IV
C. II and III
D. II and IV
11. Which of the following statements about the carbohydrate shown above are correct?
I. Impermeable to water
II. Unbranched linear chains
III. Forms microfibrils
IV. Linked by β-1,4 glycosidic bonds
A. I and II
B. II and III
C. II, III and IV
D. I, II, III and IV
ESSAY QUESTIONS
Describe the structure of starch and cellulose. Explain how the structures of these molecules are related to
their functions.
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