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💦Biology Unit 1 Biological Molecules
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Organic compounds


Contain
carbon-carbon
bonds
Inorganic
compounds

Do not contain
carbon-carbon
bonds
Three important types of chemical bonds in biochemistry
Covalent
bonds
Ionic
bonds
Hydrogen
bonds
Covalent bonds


Strong, main bonds holding atoms together in
organic
molecules, always made/broken by
enzymes
Ionic bonds


Fairly strong, formed between
positive
and negative ions,
not
common in biology
Hydrogen bonds


Much
weaker
, can break and form spontaneously at biological temperatures
Water molecules


Charged
dipole
, with oxygen slightly
negative
and hydrogen slightly
positive,
forming
hydrogen
bonds
Properties of water due to its
dipole nature

Good solvent
High specific heat
High latent heat
Cohesive and adhesive
Most dense at 4°C
Incompressible
Hydrophilic


Charged
or polar molecules that dissolve readily in water
Hydrophobic


Uncharged
or non-polar molecules that do not dissolve well in water
Monosaccharides


Smallest units of
carbohydrates
, have formula (CH2O)n where n can be 3-7
Types of monosaccharides


Hexose
sugars (C6H12O6, e.g. glucose, galactose, fructose)
Pentose
sugars (C5H10O5, e.g. ribose, deoxyribose, ribulose)
Triose
sugars (C3H6O3)
Disaccharides

Formed when two
monosaccharides
are joined by a glycosidic bond, with loss of a
water
molecule
Common disaccharides
Maltose
(
glucose
-
glucose
)
Sucrose
(
glucose
-
fructose
)
Lactose
(
glucose
-
galactose
)
Condensation
reaction

Two molecules combine into one
larger
molecule, with
loss
of water
Hydrolysis
reaction

Large molecule is broken into
smaller
ones by reacting with water
Disaccharides


Formed when two
monosaccharides
are joined together by a
glycosidic
bond (C–O–C)
Disaccharide formation

Involves the formation of a molecule of
water
(H2O)
Disaccharides


Maltose
(
glucose-glucose
)
Sucrose
(
glucose-fructose
)
Lactose
(
galactose-glucose
)
Maltose


Glucose-glucose,
formed on digestion of starch by amylase
Sucrose


Glucose-fructose
, common in plants as it is less reactive than glucose and their main transport sugar
Lactose


Galactose-glucose,
found only in mammalian milk and the main source of energy for infant mammals
Main polysaccharides


Starch
Glycogen
Cellulose
Starch


Insoluble plant storage polysaccharide, mixture of
amylose
and
amylopectin
Amylose is poly-(
1-4
) glucose, long chain that coils into a
helix
Amylopectin is poly
1-4
glucose with some 1-6
branches,
more open structure
Glycogen
Animal storage polysaccharide, similar to amylopectin but with more
branches,
can be
broken
down
quickly
Cellulose


Main component of plant cell walls, poly (
1-4
) glucose with
β-glucose,
forms
straight
rigid
chains
that form
microfibrils
Lipids


Mixed group of hydrophobic compounds composed of
C
,
H
,
O
and sometimes
P
Triglycerides
Fats or oils, made of
glycerol
and
fatty
acids
Triglyceride formation
One
molecule of glycerol joins with
three
fatty acid molecules by
ester
bonds
Triglyceride uses
Used for
energy
storage,
insulation,
waterproofing
Saturated
fatty acids

No
C=C double bonds,
high
melting point, solids (fats)
Unsaturated
fatty acids

Have
C=C double bonds,
low
melting point, liquids (oils)
Phospholipids
Similar to triglycerides but with a phosphate group instead of a fatty acid, have a polar
hydrophilic
head and non-polar
hydrophobic
tails
Functions of proteins
Structure
(e.g. collagen, keratin, actin)
Enzymes
Transport
(e.g. haemoglobin, transferrin)
Pumps (e.g. Na+K+ pump)
Motors (e.g. myosin, kinesin)
Hormones
(e.g. insulin, glucagon)
Receptors (e.g. rhodopsin)
Antibodies
Storage
(e.g. albumins, casein)
Blood
clotting
(e.g. thrombin, fibrin)
Lubrication (e.g. glycoproteins)
Toxins (e.g. cholera toxin)
Antifreeze (e.g. glycoproteins)
Amino acids


Made of
C
,
H
,
O
,
N
,
S
, contain both an amino group and an acid group
Amino
acid structure

Central
carbon
atom with H,
amino
group,
carboxyl
group,
and
variable
R
group
Protein synthesis occurs in
ribosomes
and requires an
RNA
template
Protein structure levels


Primary
(sequence of
amino
acids
)
Secondary
(α-helix, β-sheet)
Tertiary
(overall 3D structure)
Quaternary
(multiple polypeptide chains)
Tertiary
structure is held together by bonds between R-groups, including
hydrogen
bonds,
ionic
bonds, and
disulfide
bridges
β-sheet
The
polypeptide
chain
zig-zags
back and forward forming a sheet of antiparallel strands, held together by hydrogen bonds
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