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Disaccharide - Sucrose is a non-reducing sugar

– A carbohydrate in which two Note : Non reducing sugar is wala nay –OH
monosaccharide are bonded together. group sa iyang carbon1 (or anomeric carbon).
Non reducing sugars can no longer react
Glycosidic Linkage whereas the reducing sugar can still react
- is the bond in a disaccharide resulting because it still has –OH group in the anomeric
from the reaction between the hemiacetal carbon. Using Benedict’s Reagent you can
carbon (anomeric carbon) atom. The –OH group identify if a chemical is a reducing or non-
of one monosaccharide and an –OH group on reducing sugar. If the solution turns blue then it
the other monosaccharide. is a non reducing sugar if it turns red or orange
then it is a reducing sugar.
- Basis for the formation of
oligosaccharide and polysaccharides because Sucrose Metabolism to ATP
the oligosaccharides and polysaccharide’s
Fructose
nature depend on which monosaccharides are Sucrose Enzyme Sucrase

linked together and on the particular glycosidic


bond formed.
Pyruvate Glucose
Glyceraldehyde
- the glycosidic bond can either be
alpha or beta glycosidic bond.
ATP
Dehydroxyacetone
- a (1 – 4), a (1-6)

- B, B (1 -1)
-Excess consumption of sucrose can
- the glycosidic bond can either be
contribute to health problems.
linear or branched- chain.
10 Ways Sugars can Harm your Health
Important Disaccharides
1.) Causes blood glucose to spike and
- Maltose
plummet
- Lactose
2.) Increases the risk of obesity,
- Sucrose diabetes and heart disease.

Sucrose 3.) Interferes with immune function

- From sugarcane and sugar beets. 4.) A high sugar diet often results in
chromium deficiency
- composed of a-d –glucose and b-d –
fructose 5.) Accelerates Aging.

6.) Causes tooth decay


7.) Can cause gum disease which can Aspartame
lead to heart disease
-Suspected to cause neurological
8.) Affects behavior and cognition in problems especially in individuals whose
children. metabolism cannot tolerate phenylalanine

9.) Increases stress. - Artifical sweetener which is derivative


of sucrose.
10.) Takes the place of important
nutrients. Sucralose

Use of Sucrose - also known as Splenda.

- Sweetener and increase of energy - Differ in sucrose in 2 ways


levels
1.) Three of the –OH groups have been
Alternative Sweeteners replaced with 3 chlorine (C1 and 6 of the
fructose moiety and C4 of the galactose moiety)
- Splenda, High fructose corn syrup,
Saccharin. 2.) Configuration at C4 of the 6-
membered pyranose ring of glucose, producing
Fructose galactose derivative.
- Sweeter than Sucrose - Sucralose is not metabolized by the
- Can produce the same sweetening body.
effect with fewer calories.
- Does not provide calories.
- High Fructose Corn Syrup is frequently
- It is a safe sugar substitute.
used in food processing.
Lactose
- Presence of fructose changes the
texture of food. -Made up of B-D- galactose and D-
Glucose.
- Artificial Sweeteners produced in the
laboratory (suspected to have harmful side - Glycosidic Linkage B(1-4) between the
effects ) anomeric carbon 1 of B-D-galactose and Carbon
4 of D-glucose.
Saccharine
Lactose Intolerance
- Has been found to cause cancer in
laboratory animals. -People who are lactose intolerant
doesn’t have the enzyme lactase in their body.
- Contains cyclamates. Cyclamate is a Lactase (found in small intestine) breaks down
synthetic artificial sweetener that is 30 to 50 lactose into two molecules: Galactose and
times sweeter than sugar. Glucose and they are then used by the body.
Whereas a lactose intolerant person who
doesn’t have the enzyme lactase cannot break it Polysaccharide
down into galactose and glucose. What will
happen is that the bacteria in large intestine will -Made up of many monosaccharides
be the one to break down the lactose but they unit.
will not produce glucose and galactose instead -Can be classified as
they will produce hydrogen gas, carbon dioxide homopolysaccharide and heteropolysaccharide.
and lactic acid and that will cause flatulence and
abdominal pain. - Homopolysaccharide - are
polysaccharides composed of a single type of
-Symptoms of Lactose Intolerance are sugar monomer. For example, cellulose is an
Pain, Bloating and Rumbling of stomach. linear homopolysaccharide made up of glucose
-Solutions to avoid spending time in the monomers.
bathroom: No eating of Dairy Food, Lactose- - Heteropolysaccharide –
Free foods, and intaking lactacid pills before polysaccharides that contain two or more
eating. different monosaccharide units. For example,
- Pharmaceutical use of Lactose : widely Hyaluronic acid, formed by thousands of
used as a filler or diluents in tablets and alternative units of N-acetyl glucosamine and
capsule. glucuronic acid.

Maltose Complete Characterization of Polysaccharide

- Product of starch hydrolysis - Specification of monomers

-Can be digest by mammals. - Sequence of monomers

- Common ingredient in baby foods. - Type of glycosidic Linkage (Note:


Nature of linkage determines the
-Found in malted milk polysaccharide function)

- Yeast (brewer’s yeast) contains Cellulose


enzymes that hydrolyze the starch in sprouted
barley (barley malt) first to maltose then to - Linear homopolysaccharide of b-d-
glucose, which is fermented in the brewing of glucose
beer. -Linked in B(1-4)

-Polysaccharide Chain are hydrogen


bonded

- Hydrolyzed by cellulase to two glucose


unit

-Animals lack the enzyme cellulase in


order to break down cellulose that’s why they
can’t eat nor digest tree barks for energy.
-Cellulase attack the B-linkage between hydrolyze a glycosidic linkage anywhere along
glucoses. the chain to produce glucose and maltose.

- B-linkage common to structural - Amylose can be completely degraded


polymers. to glucose and amylase by two amylases.

-Cellulase is found in certain bacteria -Amylopectin is not completely


(inhabit the digestive tracts of insects such as degraded because of the branching linkages are
termites and grazing animals such as cattle and not attacked.
horses)
-Iodine Molecule can form a starch-
Starch iodine complex (dark-blue color): well known
test for the presence of starch amylase.
-Can be classififed into two: Amylose
and Amylopectin. Glycogen

- Amylose is a linear polysaccharide. It’s -It is energy storage. It has a capacity to


glycosidic linkage is a-(1-4). store 2000 calories.

-Amylopectin is a branched-chain -Branched chain polymer of a d-glucose.


polysaccharide. Its glycosidic linkage in its main It is branched every 10 residues.
linear body is a-(1-4) whereas the glycosidic
bond for its branched body is a-(1-6). -Average chain length is 13 glucose
Amylopectin is branched every 25 residues. residues, and there are 12 layers of branching.

-At the heart of every glycogen


molecule is a protein called glycogenin.
-Two enzymes hydrolyzes starches : a-
amylase and b-amylase. Attacks a(1-4) - Found in animal cells in granules
glycosidic linkages similar to the starch granules in plant cells.
-B-amylase: Exoglycosidase (they only - Glycogen granules found in well-fed
attack at the outer part of the chain). They liver and muscles but not seen in brain and
cleave from the non reducing end of the heart cells in normal condition.
polymer. Maltose is the product of reaction
- Glycogen (if broken down) becomes
-A-amylase: Endoglycosidase (attacks Glucose then becomes Energy
only at the inner part of the chain). They
-Significance of branching:

1.) More branched polysaccharide is


more water soluble.

2.) When an organism needs energy


quickly, the glycogen phosporylase has more
potential targets if there are more branches
allowing a quicker mobilization of glucose.

Chitin

- A polysaccharide that is similar to


cellulose in both structure and function.

-Linear homopolysaccharide.

- All the residues linked in B(1-4)


glycosidic bonds.

-Chitin differs from cellulose in the


nature of the monosaccharide unit: In cellulose
the monomer is B-D-Glucose whereas in chitin
the monomer is N-acetyl-B-D-glucosamine

- Plays a structural role and has a fair


amount of mechanical strength because the
individual strands are held together by
hydrogen bonds

-It is the major structural component of


the exoskeletons of invertebrates such as
insects and crustaceans cell walls of algae, fungi
and yeasts.

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