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Chapter 1 Biological Molecules

,Chapter 1 Biological Molecules
Testing For Reducing Sugars
●​ all monosaccharides and some disaccharides, e.g. maltose are
1.1 Introduction To Biological Molecules reducing sugars
●​ Benedict’s reagent is an alkaline solution of copper(II) sulfate
Bonding And The Formation Of Molecules
(CuSO4)
●​ covalent bonding
1.​ Add Benedict’s solution into the tested food sample.
●​ ionic bonding
2.​ Heat the mixture gently in a boiling H2O bath.
●​ hydrogen (H) bonding
●​ + result: solution turns from blue to brick red

Polymerisation And The Formation Of Macromolecules
●​ monomers link together to form polymers by polymerisation
1.3 Carbohydrates – Disaccharides And
Condensation And Hydrolysis Reactions Polysaccharides
Disaccharides
condensation reactions hydrolysis reactions
●​ glucose + glucose → maltose
●​ glucose + fructose → sucrose
Condensation reaction – Hydrolysis reaction –
●​ glucose + galactose → lactose
Joining of two molecules Breaking a chemical bond
together with the formation between two molecules Disaccharide – Molecules formed by the condensation of two
of a chemical bond involving involving the use of a water monosaccharides.
the elimination of a molecule molecule. ●​ monosaccharides bond together by glycosidic bond during
of water. condensation reactions
●​ e.g. amino acids → a ●​ maltose, sucrose and lactose have a formula of C12H22O11
polypeptide,
monosaccharide C6H12O6
→ polysaccharide starch Test For Non-reducing Sugars
●​ other disaccharides, e.g. sucrose and all polysaccharides are
non-reducing sugars
●​ non-reducing sugar must be hydrolysed into its
monosaccharide components to be tested
1.​ Carry out Benedict’s test with the tested food sample and
observe if the mixture stays blue.
2.​ Boil the mixture with acid and then neutralise with alkali.
●​ addition of acid hydrolyses any glycosidic bonds present in any
carbohydrate molecules
Metabolism
3.​ Heat the mixture with Benedict’s solution gently in a boiling
Metabolism – All the chemical processes that take place in living
H2O bath.
organisms.
●​ + result: solution turns from blue to brick red
Polysaccharides
Polysaccharide – Molecules formed by the condensation of
1.2 Carbohydrates – Monosaccharides many monosaccharides.

Life Based On Carbon ●​ polysaccharides are very large molecules
○​ make it insoluble and suitable for storage
●​ C atoms are ready to form bonds with other C atoms
Test For Starch
○​ allows a sequence of C of various lengths to be built up
●​ test is carried out at room temp.
■​ a backbone is formed
1.​ Add iodine solution to the tested food sample.
●​ + result: solution turns from yellow to blue-black
The Making Of Large Molecules
Monomers – The smaller units from which larger molecules are
made.
●​ e.g. monosaccharides, amino acids and nucleotides 1.4 Starch, Glycogen And Cellulose
Polymers – Molecules made from a large number of monomers Starch
joined together. Starch – A polysaccharide made of alpha glucose monomers that
●​ basic monomer unit in carbohydrates is sugar is used as the main storage of energy in plants.
○​ monosaccharide: a single monomer of carbohydrate
○​ disaccharide: a pair of combined monosaccharides starch
○​ polysaccharides: large numbers of combined
monomers ●​ α-glucose
monosaccharides
Monosaccharides
bond between ●​ 1-4 glycosidic bonds in amylose
Monosaccharide – The individual sugar monomers
monomers
from which larger carbohydrates are made.
●​ general formula (CH2O)n, e.g. glucose, galactose
and fructose
●​ C6H12O6 is the main substrate for respiration and
has two isomers (α-glucose and β-glucose)

, ●​ 1-4 and 1-6 glycosidic bonds in function ●​ major carbohydrate storage product
amylopectin of animals

●​ insoluble
○​ no osmotic effect
■​ does not draw H2O into the
cells by osmosis
●​ coiled
○​ makes molecule compact
■​ a lot of glucose can be stored
location ●​ found in starch grains inside plant
in a small space
cells
properties to ●​ branched form has many ends
functions ○​ enzymes can act on
●​ made of 2 polymers simultaneously
○​ amylose: an unbranched helix ○​ have a higher metabolic rate and
structure chain respiratory rate than plants
○​ amylopectin: a branched ■​ more active
molecule
●​ never found in plant cells
●​ forms an important component of
function food Cellulose
●​ is the major energy source in most Cellulose – A polysaccharide made of β-glucose monomers that is
diets
used as a structural polysaccharide which provides strength to
plant cell walls.
●​ insoluble
○​ no osmotic effect cellulose
■​ does not draw H2O into the
cells by osmosis
monomers ●​ β-glucose
●​ large molecule
○​ does not leave the cell
○​ contains large no. of glucose bond between ●​ 1-4 glycosidic bonds
units monomers
●​ coiled
properties to ○​ makes molecule compact
function ■​ a lot of glucose can be stored
in a small space
●​ forms α-glucose when hydrolysed
○​ provides glucose readily used in
respiration location ●​ found in cell wall of plant cells
●​ branched form has many ends
○​ enzymes can act on ●​ long, straight chains running parallel
simultaneously to one another
■​ glucose monomers are structure ○​ allows H bonds to form
released rapidly cross-linkages between adjacent
●​ never found in animal cells chains

●​ provides rigidity to the plant cell
Glycogen
○​ provides the maximum SA for
Glycogen – A highly branched polysaccharide made of alpha photosynthesis
glucose monomers that is used as the main storage of energy in ●​ prevents cell from bursting as H2O
humans and animals. function enters it by osmosis
○​ is done by exerting an inward
glycogen pressure that stops any further
influx of H2O
monomers ●​ α-glucose
●​ made up of β-glucose
bond between ●​ 1-4 and 1-6 glycosidic bonds ○​ forms long, straight and
monomers unbranched chains
■​ provides support and rigidity
properties to ●​ parallel chains crossed linked by H
function bonds
○​ adds collective strength
●​ grouped molecules
○​ form microfibrils to provide more
location ●​ found in muscles and liver cells in strength
animals

structure ●​ has shorter chains than starch
●​ more highly branched than starch
1.5 Lipids
●​ main groups of lipids are triglycerides and phospholipids

, ●​ a phospholipid is made up of 2 parts
Roles Of Lipids ○​ hydrophilic head (phosphate) interacts with H2O but not
●​ phospholipids contribute to the flexibility of membranes and with fat
the transfer of lipid-soluble substances across them ○​ hydrophobic tail (two fatty acids) orients itself away from
●​ source of energy H2O but mixes readily with fat
○​ provide more than twice the energy as the same mass of ●​ molecules that have two ends behaving differently are said to
carbohydrate when oxidised be polar
○​ release valuable H2O when oxidised ○​ polar molecules position themselves when placed in H2O
●​ waterproofing ○​ hydrophilic heads are as close to the H2O as possible
○​ insoluble in H2O ○​ hydrophobic tails are as far away from H2O as possible
○​ plants and insects have waxy, lipid cuticles that conserve The Related Properties To Functions Of Phospholipids
H2O ●​ polar molecules that have a
○​ mammals produce an oily secretion from the sebaceous hydrophilic head and a hydrophobic
glands in the skin tail of two fatty acids
●​ insulation ○​ hydrophobic barrier is formed
○​ fats are slow conductors of heat between the inside and outside
○​ help retain body heat of a cell
○​ act as electrical insulators in the myelin sheath around ○​ form a bilayer within cell-surface membranes in an
nerve cells aqueous membrane
●​ protection ●​ hydrophilic phosphate heads of phospholipid molecules
○​ often stored around delicate organs, e.g. kidney ○​ help to hold hydrophilic PO43- heads at the surface of
the cell-surface membrane
Triglycerides ●​ phospholipid structure

Triglyceride – A type of lipid formed by ○​ allows them to form glycolipids by combining with

the condensation of one molecule of carbohydrates within the cell-surface membrane

glycerol and three molecules of fatty ○​ important in cell recognition

acid.
●​ an ester bond forms when a Test For Lipids
hydroxyl (OH) group on glycerol 1.​ Add ethanol then add H2O and shake.
bonds with the carboxyl (COOH) ●​ + result: cloudy-white emulsion
group of the fatty acid ○​ light passing through the emulsion is refracted as it
●​ fatty acid is described as saturated passes from oil droplets to H2O droplets
if the hydrocarbon chain has no
C=C bond
●​ fatty acid is described as 1.6 Proteins
mono-unsaturated if there is a
single C=C bond
Structure Of An Amino Acid
●​ fatty acid is described as polyunsaturated if more than one Amino acid – The monomers containing an amino group (NH2), a

C=C bond is present carboxyl group (COOH), a H atom and a variable R group that

The Related Properties To Functions Of Triglycerides make up protein.

●​ long hydrocarbon chains contain many C-H bonds with ●​ basic monomer units which combine

little O to make up polypeptide that can be

○​ C-H bonds break when oxidised during cellular combined to form proteins

respiration
○​ release an excellent source of energy used to produce The Formation Of A Peptide Bond
ATP ●​ amino acid monomers combine
●​ low mass to energy ratio together by a peptide bond to
○​ much energy can be stored in a small vol. form a dipeptide in
○​ good storage molecules condensation reaction
○​ reduces the mass animals have to carry as they move ●​ a hydroxyl (OH) is lost from the COOH and a H atom is lost
around from the NH2 group of another amino acid
●​ large, non-polar molecules
○​ allows their storage to not affect osmosis in cells or the The Primary Structure Of Proteins – Polypeptides
H2O potential of them Primary structure – The individual sequence
○​ insoluble in H2O of amino acids bonded by covalent peptide
●​ high ratio of H to O atoms bonds in a polypeptide.
○​ release H2O when oxidised ●​ the sequence of amino acids in a
○​ important source of H2O polypeptide chain is determined by DNA
○​ important for determining the final
Phospholipids 3D shape of a protein molecule
Phospholipid – A type of lipid formed by the condensation of one ●​ determines its ultimate shape and function
molecule of glycerol, two molecules of fatty acid and a phosphate ○​ change in an amino acid in the primary sequence can lead
group. to a change in the shape of the protein
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