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WEEK 4: OCTOBER 11 - 16
I. LEARNING OUTCOMES
a. Describe the properties of Polysaccharides.
b. Test food with the presence of polysaccharides.
II. TOPIC/S
Topic: Polysaccharides
● Definition/ Form of sugar
● Importance/ properties
● Source/ deficiency
APCAS Core Value: Integrity
Integration: Discussion of the Topic
III. ACTIVITIES
Laboratory Task 5
Laboratory Task Sheet 5
L - Lecture Reading
Polysaccharides are long chains of monosaccharides linked by glycosidic bonds. They are also known as
glycans. They are the most abundant carbohydrates found in food.
● This carbohydrate can react with water using amylase enzymes as catalyst, which produces
constituent sugars.
When many monomer units are joined together by a condensation reaction, they form a polymer
called polysaccharides. They are involved in the mechanical stability of cells, organs, organisms, and
act as carbohydrate stores in some other organisms.
Functions of a Polysaccharide
Depending on their structure, polysaccharides can have a wide variety of functions in nature. Some
polysaccharides are used for storing energy, some for sending cellular messages, and others for
providing support to cells and tissues.
● Storage of Energy
➢ Many polysaccharides are used to store energy in organisms. While the enzymes that
produce energy only work on the monosaccharides stored in a polysaccharide,
polysaccharides typically fold together and can contain many monosaccharides in a
dense area. Further, as the side chains of the monosaccharides form as many hydrogen
bonds as possible with themselves, water cannot intrude the molecules, making them
hydrophobic. This property allows the molecules to stay together and not dissolve into
the cytosol. This lowers the sugar concentration in a cell, and more sugar can then be
taken in. Not only do polysaccharides store the energy, but they allow for changes in
the concentration gradient, which can influence cellular uptake of nutrients and
water.
● Cellular Communication
➢ Many polysaccharides become glycoconjugates when they become covalently bonded
to proteins or lipids. Glycolipids and glycoproteins can be used to send signals between
and within cells. Proteins headed for a specific organelle may be “tagged” by certain
polysaccharides that help the cell move it to a specific organelle. The polysaccharides
can be identified by special proteins, which then help bind the protein, vesicle, or other
substance to a microtubule. The system of microtubules and associated proteins within
cells can take any substance to its destined location once tagged by specific
polysaccharides. Further, multi-cellular organisms have immune systems driven by the
recognition of glycoproteins on the surface of cells. The cells of a single organism will
produce specific polysaccharides to adorn its cells with. When the immune system
recognizes other polysaccharides and different glycoproteins, it is set into action, and
destroys the invading cells.
● Cellular Support
➢ By far one of the largest roles of polysaccharides is that of support. All plants on Earth
are supported, in part, by the polysaccharide cellulose. Other organisms, like insects and
fungi, use chitin to support the extracellular matrix around their cells. A polysaccharide
can be mixed with any number of other components to create tissues that are more
rigid, less rigid, or even materials with special properties. Between chitin and cellulose,
both polysaccharides made of glucose monosaccharides, hundreds of billions of tons
are created by living organisms every year. Everything from the wood in trees, to the
shells of sea creatures is produced by some form of polysaccharide. Simply by
rearranging the structure, polysaccharides can go from storage molecules to much
stronger fibrous molecules. The ring structure of most monosaccharides aids this
process, as seen below.
Structure of a Polysaccharide
All polysaccharides are formed by the same basic process: monosaccharides are connected via
glycosidic bonds. When in a polysaccharide, individual monosaccharides are known as residues. Seen
below are just some of the many monosaccharides created in nature. Depending on the polysaccharide,
any combination of them can be combined in series.
The structure of the molecules being combined determines the structures and properties of the
resulting polysaccharide. The complex interaction between their hydroxyl groups (OH), other side
groups, the configurations of the molecules, and the enzymes involved all affect the resulting
polysaccharide produced. A polysaccharide used for energy storage will give easy access to the
monosaccharides, while maintaining a compact structure. A polysaccharide used for support is usually
assembled as a long chain of monosaccharides, which acts as a fiber. Many fibers together produce
hydrogen bonds between fibers that strengthen the overall structure of the material, as seen in the
image below.
The glycosidic bonds between monosaccharides consist of an oxygen molecule bridging two carbon
rings. The bond is formed when a Hydroxyl group is lost from the carbon of one molecule, while the
hydrogen is lost by the hydroxyl group of another monosaccharide. The carbon on the first molecule
will substitute the oxygen from the second molecule as its own, and a glycosidic bond is formed.
Because two molecules of hydrogen and one oxygen is expelled, the reaction produced a water
molecule as well. This type of reaction is called a dehydration reaction as water is removed from the
reactants.
Polysaccharides are categorized into two classes based on the type of monosaccharide units they
contain:
1. Homopolysaccharides
➢ They are composed of repeating units of only one type of monomer. The major
homopolysaccharides include cellulose, chitin, starches, and glycogen.
2. Heteropolysaccharides
➢ in which the monosaccharides vary, depending on which monosaccharides are
connected, and which carbons in the monosaccharides connect, polysaccharides take on
a variety of forms.
➢ Some of the heteropolysaccharides include glycosaminoglycans, agarose, and
peptidoglycans. Naturally, most of the heteropolysaccharides are connected with
peptides, proteins, and lipids.
A molecule with a straight chain of monosaccharides is called a linear polysaccharide, while a chain that
has arms and turns is known as a branched polysaccharide.
Three important polysaccharides, starch, glycogen, and cellulose, are composed of glucose. Starch and
glycogen serve as short-term energy stores in plants and animals, respectively. The glucose monomers
are linked by α glycosidic bonds.
Examples of a Polysaccharide
➢ When a glycogen or starch molecule is broken down, the enzymes responsible start at
the ends furthest from the center. This is important, as you will notice that because of
the extensive branching there are only 2 starting points, but many ends. This means the
monosaccharides can be quickly extracted from the polysaccharide and be utilized for
energy. The only difference between starch and glycogen is the number of branches
that occur per molecule. This is caused by different parts of the monosaccharides
forming bonds, and different enzymes acting on the molecules. In glycogen a branch
occurs every 12 or so residues, while in starch a branch occurs only every 30 residues.
https://www.youtube.com/watch?v=SgDeHXWm8Hk
Reference;
https://www.biologyonline.com/dictionary/polysaccharide
https://conductscience.com/polysaccharides-properties-functions-and-applications/
W - Weekly Assignment
List at least 5 Polysaccharides sources and state the importance of each on the human body.
Quiz #2
What elements make up carbohydrates? (D)
a. Carbon, hydrogen, nitrogen, oxygen
b. sulfur, carbon, hydrogen
c. glucose and fructose
d. carbon, hydrogen, oxygen
A patient has a genetic defect that causes intestinal epithelial cells to produce disaccharidases of much
lower activity than normal. Compared to a normal person, after eating a bowl of milk and oatmeal, this
patient will have higher levels of? (A) 2 PTS
a. maltose, sucrose, and lactose in the stool.
b. starch in the stool.
c. galactose and fructose in the blood.
d. glycogen in the muscles.
The diagrams below show a complex carbohydrate in some of your body cells. Which complex
carbohydrate is it? (D)
a. Cellulose
b. Chitin
c. Glucagon
d. Glycogen
Carbon is the basis for carbohydrates and all other biologically important molecules. All of the following
are reasons why Carbon lends itself to being the basic building block of life on our planet - except for
one. Which statement is incorrect? (B) 2 pts
a. Carbon readily makes four stable bonds, in single, double or triple configurations.
b. Carbon is a very dense & heavy element, giving living things stability.
c. Carbon is the least electronegative non-metal
d. Carbon has a high affinity for Oxygen & Hydrogen, which make bonds easily with C
Disaccharidases are enzymes found in the small intestine that participate in degradation of
disaccharides. Which of the following molecules can be broken down by these enzymes? (D) 2 pts
I. Fructose
II. Sucrose
III. Starch
a. II and III
b. I only
c. I and III
d. II only
Which of the following is true regarding the polysaccharides glycogen and cellulose? © 2 pts
a. Both molecules involve a glycosidic bond between the 1-carbon and the 6-carbon
b. Cellulose can be found as either amylose or amylopectin
c. Only glycogen molecules have branching regions
d. Humans can digest glycogen because it has beta glycosidic bonds
a. Extractions of honey
b. Heating sucrose
c. Converting the glucose in grapes
d. Germinating grains especially barley
What health problems are a consequence of eating too much added sugar? D
a. overweight
b. heart disease
c. diabetes
d. all of the above
Glucose and glycogen are examples of how carbohydrates _______________. (B) 2 pts
a. Are stored and circulated.
b. Circulate and are stored.
c. Are stored in the liver and muscles.
d. Provide energy to the body.
The carbohydrate known as milk sugar is also known by the common name: (C)
a. Sucrose
b. Fructose
c. Lactose
d. Galactose
Glucose is stored in plants as amylopectin granules and in animal tissues as glycogen granules. The two
homopolysaccharides are similar in linkages but differ in the degree of branching and in shapes of the
granules. Amylopectin usually forms large, single grains, while glycogen is usually present as smaller,
clustered granules resembling bunches of grapes. How does this structure of glycogen granules benefit
an animal? © 2 PTS
a. The glycogen granules are more resistant to oxidation
b. The glycogen granules find safety in numbers
c. The glycogen granules have more surface area and can be dissolved faster
d. Animals would actually be better off if their starch were stored as amylopectin because it would
be more resistant to chemical attack
When all the monosaccharides in a polysaccharide are the same type as polysaccharide is called? (C)
a. Starch
b. Glycogen
c. Homoglycan
d. Heteroglycan
Which of these cannot be digested by the enzymes in the human digestive system? (C)
a. Starch
b. Glycogen
c. Cellulose
d. Glucose
When all the monosaccharides in a polysaccharide are of different types, such type is called a? (D)
a. Starch
b. Glycogen
c. Homoglycan
d. Heteroglycan
Which of the following statements is true about the glycosidic bond? (D) 2 PTS
a. Glycosidic bond in maltose is not hydrolyzed in lactose intolerant humans.
b. Glycosidic bond in sucrose is hydrolyzed by bees
c. Glycosidic bond joins glucose and fructose to form sucrose
d. Both b and c
Which of the following statements is TRUE about the structure of Polysaccharides? (B) 2 PTS
a. All polysaccharides are formed by a different basic process: monosaccharides and disaccharides
are connected by glycosidic bonds.
b. All polysaccharides are formed by the same basic process: monosaccharides are connected by
glycosidic bonds.
c. The structure of the molecules being combined determine the function of the resulting
polysaccharide.
d. Both a and b
https://quizlet.com/511142887/biochemistry-carbohydrates-by-mhashi-biochem-ch-8-ch-9-lehninger-
biochem-chapter-10-multiple-choice-chapter-7-biochemistry-biochem-ch-6-old-test-3-june-2010-my-
test-2-quiz-1-cell-componen-flash-cards/