Water is arguably the most important biochemical of all. Without water life would not exist on this
planet. It is important for two reasons. First it is a major component of cells, typically forming between
70% and 95% of the mass of the cell. Human is about 60% water, jellyfish is about 98% water. Second, it
provides an environment for those organisms that live in water. Three-quarters of the planet is covered
in water.
The water molecule is formed from two hydrogen atoms and one oxygen atom. The bonding angle
between these atoms is 104.5˚. This causes water to have dipolar properties which means it has both
positive and negative sides. The dipolar property allows the formation of hydrogen bond between
adjacent molecules. Along with this, there is a weak intermolecular force of electrostatic between the
molecules which known as Van der Waals force. These two types of bond cause the water molecules to
act as larger units rather than the individual molecules. It explains the reason why such small molecules
are able to stay in the liquid form at normal earth temperatures.
The hydrogen bonding of water molecules makes the molecules more difficult to separate and
affects the physical properties of water. For example the energy needed to break the hydrogen bonds
makes it more difficult to convert water from liquid to gas than to convert similar compounds which lack
hydrogen bonds such as hydrogen sulfide (H2S), which is gas at normal air temperature.
As the essential molecule for the continuity of life, water has some unique characteristics. Some of
them are:
Carbohydrate
All carbohydrates contain the element carbon, hydrogen, and oxygen. The ‘hydrate’ part of the
name comes from the fact that hydrogen and oxygen atoms are present in the ratio of 2:1, as they are in
water (hydrate refers to water). The general formula of carbohydrate can be written as Cx(H2O)y.
Carbohydrates are divided into three main groups, monosaccharides, disaccharides, and
polysaccharides. The word ‘saccharide’ refers to a sugar or sweet substance.
A. Monosaccharides
Monosaccharides are sugars. Sugars dissolve easily in water to form sweet tasting solutions.
Monosaccharides have the general formula (CH2O)n. and consist of a single sugar molecule (mono =
one). According to the number of carbon atom present in each molecule, are trioses (3C), pentose
(5C), and hexoses (6C). The names of all sugars end with –ose.
(Attach the structural formula of glucose; show the hydroxyl and carboxyl group)
Ring structures
One important aspect of the structure of pentoses and hexoses is that the chain is long
enough to close up on itself and form a more stable ring structure. When glucose forms a ring,
carbon atom number 1 joins to the oxygen in carboxyl group attached to the carbon atom number
5. The ring therefore contains oxygen, and carbon atom number 6 is not part of the ring.
In the glucose molecule there are two important group which are the hydroxyl group (-OH)
and aldehyde group (-COH). The position of the hydroxyl group attached to the first carbon
determines whether the glucose is in α or β form. The form of glucose where it is below the ring is
known as α-glucose and the form where it is above the ring is β-glucose. The same molecule can
switch between these two forms. Alpha and beta glucose are each other’s isomer. An isomer is the
molecule which has the same number of atoms of each element but has different arrangement of
the atoms. The extra variety provided by the different arrangement of the hydroxyl group has
important biological consequences as we could see in the structures of starch, glycogen, and
cellulose.
B. Disaccharides
Disaccharides formed by two monosaccharides joining together. The three most common
disaccharides are maltose, sucrose, and lactose. Sucrose is the transport sugar in plant and
commonly bought sugar in store. Lactose is the sugar found in milk and is therefore an important
constituent of the diet of young mammal.
Types of disaccharides Forming unit
Maltose Glucose + glucose (making α-glycosidic bond)
Sucrose Glucose + fructose
Lactose Glucose + galactose
Cellobiose Glucose + glucose (making β-gycosidic bond)
The joining of two monosaccharides takes place by a process known as condensation. For each
condensation reaction, two hydroxyl (-OH) groups line up alongside each other. One combines with
hydrogen atom from the other to form a water molecule. This allows an oxygen bridge to form
between the two molecules, holding them together and forming a disaccharide. The bridge is called
a glycosidic bond.
Theoretically, any two hydroxyl group can line up and since monosaccharide has many
hydroxyl groups there are large numbers of possible disaccharides. The shape of enzyme controlling
the reaction determines which hydroxyl groups come alongside with each other. Only few of
disaccharides are common in nature.
The reverse reaction of condensation is hydrolysis. Hydrolysis is chemical decomposition in
which a compound is split into another compound (simpler compound) by reacting with water. This
takes place during the digestion of disaccharides and polysaccharides when they are broken into
monosaccharide.
Reducing sugar
The reducing sugar is a group of sugars that can carry out reduction reaction which in the process
they are oxidized. The reducing sugar characterized by the open chain of aldehyde group which
tends to oxidize forming carboxylic acid.
The reducing sugar gives positive result in Benedict, Fehling, and Tollen’s test.
C. Polysaccharide
Polysaccharides are polymers whose subunit (monomers) are monosaccharides. They are
made by joining many monosaccharides molecule by condensation reaction. Each monosaccharide
comes together by making glycosidic bond among them. The final molecule may be several
thousand monosaccharide units long, forming macromolecule. The most important polysaccharides
are starch, glycogen, and cellulose, all of which polymers of glucose. Polysaccharides are not sugar
therefore they are not sweet.
Since glucose is the main source of energy for cells, it is important for living organisms to store
it in the appropriate form. If glucose accumulates in cells, it would dissolve and make the content of
the cell too concentrated which would affect its osmotic properties. In addition glucose is also a very
reactive molecule and would interfere with the cell chemistry. This problem is avoided by converting
glucose by condensation reaction into polysaccharide which is convenient, compact, inert
(unreactive), and insoluble molecule. The storage polysaccharide form is starch in plants and
glycogen in animals. Glucose can be made available again quickly by an enzyme-controlled reaction.
Cellulose
Cellulose is the most abundant organic molecule on the planet, due to its presence in plant cell walls
and its slow rate of breakdown in nature. Unlike starch and glycogen it is a strong molecule.
However, the only difference between cellulose, starch, and glycogen is that cellulose is a polymer
of β-glucose, not α-glucose.
In the ring structure of β-glucose the –OH group attached to the first carbon facing upwards thus in
order to make glycosidic bond the second glucose should rotate 180˚. This arrangement of β-glucose
molecule results in a strong molecule because the hydrogen atoms of –OH groups are weakly
attracted to oxygen atoms in the same cellulose molecule.