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Disaccharides
IUG, Fall 2012
Dr. Tarek Zaida
1
A disaccharide consists of two sugars joined by
an O-glycosidic bond.
The three common Disaccharides are:
• Maltose
• Lactose
• Sucrose
2
1. Maltose
• Maltose comes from the
hydrolysis of large polymeric
oligosaccharides such as
starch and glycogen and is in
turn hydrolyzed to glucose by
.
• Sucrase, lactase, and maltase
are located on the outer
surfaces of epithelial cells
lining the small intestine
3
• Cellobiose is an isomer of maltose.
• It differs from maltose only in having the β
configuration at C-1 of the left glucose unit.
Otherwise, all other structural features are
identical, including a link from C-1 of the left unit
to the hydroxyl group at C-4 in the right unit.
4
2. Lactose
• Lactose, the disaccharide of milk,
consists of galactose joined to
glucose by glycosidic linkage.
• Lactose is hydrolyzed to these
monosaccharides by in
human beings and by
in bacteria.
 Lactose is formed in the urine of
pregnant women, and it gives a
positive test with Cu2+ containing
reagents since it is a reducing
sugar
5
3. Sucrose
• Sucrose is the common table
sugar
• Is obtained commercially from
sugar cane or sugar beets.
• The anomeric carbon atoms of a
glucose unit and a fructose unit
are joined in this disaccharide;
• The configuration of this
glycosidic linkage is for
glucose and for fructose.
• Sucrose can be cleaved into its
component monosaccharides
by the enzyme .
6
Reducing Properties
• Disaccharides with 1,4 linkage are reducing
because they have a free aldehyde group in
one of the two monosaccharides.
• Lactose & maltose are reducing sugars.
• Sucrose with 1,2 linkage, no aldehyde or
ketone group is free, therefore sucrose is a
nonreducing sugar
7
Fermentation
• Sucrose & maltose will ferment in the
presence of yeast, because yeast does contain
& .
• Lacotse on the other hand will not ferment
when yeast is added, because it does not
contain .
8
Sweetness and Sweeteners (Sugar Substitutes)
• Sweetness is literally a matter of taste.
• Although individuals vary greatly in their sensory
perceptions, it is possible to make some quantitative
comparisons of sweetness.
• For example, we can take some standard sugar solution
(say 10% sucrose in water) and compare its sweetness
with that of solutions containing other sugars or
sweetening agents.
• If a 1% solution of some compound tastes as sweet as
the 10% sucrose solution, we can say that the
compound is 10 times sweeter than sucrose.
9
• D-Fructose is the sweetest of the simple
sugars—almost twice as sweet as sucrose.
• D-Glucose is almost as sweet as sucrose.
• On the other hand, sugars like lactose and
galactose have less than 1% of the sweetness
of sucrose.
10
Many synthetic sweeteners are known
• The most common sugar
substitutes are:
1. Saccharin is made
commercially from
toluene.
2. Cyclamates: they are not
used anymore because
they might cause cancer.
11
3. Aspartame became the first new sweetener to
be approved by the U.S. Food and Drug
Administration (FDA) 25 years ago.
• It is about 160 times sweeter than sucrose.
• Structurally, aspartame is the methyl ester of a
dipeptide of two amino acids that occur
naturally in proteins— acid and
—and is sold under the trade
name
12

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0Tanushree Saha..ppt

  • 2. A disaccharide consists of two sugars joined by an O-glycosidic bond. The three common Disaccharides are: • Maltose • Lactose • Sucrose 2
  • 3. 1. Maltose • Maltose comes from the hydrolysis of large polymeric oligosaccharides such as starch and glycogen and is in turn hydrolyzed to glucose by . • Sucrase, lactase, and maltase are located on the outer surfaces of epithelial cells lining the small intestine 3
  • 4. • Cellobiose is an isomer of maltose. • It differs from maltose only in having the β configuration at C-1 of the left glucose unit. Otherwise, all other structural features are identical, including a link from C-1 of the left unit to the hydroxyl group at C-4 in the right unit. 4
  • 5. 2. Lactose • Lactose, the disaccharide of milk, consists of galactose joined to glucose by glycosidic linkage. • Lactose is hydrolyzed to these monosaccharides by in human beings and by in bacteria.  Lactose is formed in the urine of pregnant women, and it gives a positive test with Cu2+ containing reagents since it is a reducing sugar 5
  • 6. 3. Sucrose • Sucrose is the common table sugar • Is obtained commercially from sugar cane or sugar beets. • The anomeric carbon atoms of a glucose unit and a fructose unit are joined in this disaccharide; • The configuration of this glycosidic linkage is for glucose and for fructose. • Sucrose can be cleaved into its component monosaccharides by the enzyme . 6
  • 7. Reducing Properties • Disaccharides with 1,4 linkage are reducing because they have a free aldehyde group in one of the two monosaccharides. • Lactose & maltose are reducing sugars. • Sucrose with 1,2 linkage, no aldehyde or ketone group is free, therefore sucrose is a nonreducing sugar 7
  • 8. Fermentation • Sucrose & maltose will ferment in the presence of yeast, because yeast does contain & . • Lacotse on the other hand will not ferment when yeast is added, because it does not contain . 8
  • 9. Sweetness and Sweeteners (Sugar Substitutes) • Sweetness is literally a matter of taste. • Although individuals vary greatly in their sensory perceptions, it is possible to make some quantitative comparisons of sweetness. • For example, we can take some standard sugar solution (say 10% sucrose in water) and compare its sweetness with that of solutions containing other sugars or sweetening agents. • If a 1% solution of some compound tastes as sweet as the 10% sucrose solution, we can say that the compound is 10 times sweeter than sucrose. 9
  • 10. • D-Fructose is the sweetest of the simple sugars—almost twice as sweet as sucrose. • D-Glucose is almost as sweet as sucrose. • On the other hand, sugars like lactose and galactose have less than 1% of the sweetness of sucrose. 10
  • 11. Many synthetic sweeteners are known • The most common sugar substitutes are: 1. Saccharin is made commercially from toluene. 2. Cyclamates: they are not used anymore because they might cause cancer. 11
  • 12. 3. Aspartame became the first new sweetener to be approved by the U.S. Food and Drug Administration (FDA) 25 years ago. • It is about 160 times sweeter than sucrose. • Structurally, aspartame is the methyl ester of a dipeptide of two amino acids that occur naturally in proteins— acid and —and is sold under the trade name 12