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B1
B1.2 Proteins
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Elise Segura
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Cards (87)
Amino acids
Monomers
used to make
proteins
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Proteins
Complex macromolecules
Composed
of
one
or
more chains
of
amino acids
Play an important role in many
biological processes
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Amino acid structure
Amine
Group (
NH2
)
Carboxyl
group (
COOH
)
Alpha Carbon
(C)
R
Group
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Condensation
reactions forming
dipeptides
1.
Amino acids
join together
2.
Peptide bond
formation
3.
Water
molecule released
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Peptide
bond
Formed when the
carboxyl
group of one
amino acid
reacts with the
amino
group of another
amino acid
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Dipeptide
Molecule consisting of
two amino acids
joined by a
single peptide
bond
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Oligopeptide
Molecule
composed of a few (typically
2-20
)
amino acids
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Polypeptide
Longer
chain of
amino acids
, typically longer than
20 residues
, but not yet a fully functional protein
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terminal
Free amino
group not involved in the
peptide
bond
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terminal
Unbound carboxyl
group
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Polypeptide formation
1. Occurs in the
ribosome
2. Can be found in the
cytoplasm
or on the
rough endoplasmic reticulum
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Each time an
amino acid
joins the
growing polypeptide strand
, a
new peptide bond
is formed and a
water molecule
is
released
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Sources of
amino acids
Plant cells
Animal cells
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Essential amino acids
Amino acids
that your body
cannot produce
and must
obtain
from
food
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Non-essential
amino acids
Amino acids
that can be
produced
by the
body
from other
amino
acids or by the
breakdown
of
proteins
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Non-essential
amino acids are
important
to have but
not required
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Vegans need to
consume
a variety of
plant-based foods
to ensure they get all
essential amino acids
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Most plants are
incomplete proteins
, lacking
one
or
more essential amino acids
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Monosaccharides
Simple sugars
classified by the
number
of
carbon
atoms they
contain
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Types of monosaccharides
Pentoses
Hexoses
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Pentoses
Ribose
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Hexoses
Glucose
Galactose
Fructose
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Fructose
A type of
sugar naturally
found in
fruits
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Galactose
A type of
sugar
commonly found in
dairy products
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Glucose
The most
common monosaccharide
found in
nature
and an important source of
energy
for many
organisms
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Properties of glucose
Has
two isomers
Is
soluble
Is
stable
Can be
oxidised
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Formation
of
isomers
Orientation
of
hydroxyl
group
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Alpha-glucose
Isomer
of
glucose
with
–OH
group oriented
downwards
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Beta-glucose
Isomer
of
glucose
with
–OH
group oriented
upwards
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Difference in orientation between alpha-glucose and
beta
-glucose
Plays
a
critical role in the formation of polysaccharides
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Polysaccharides
formed from
glucose
Starch
Glycogen
Cellulose
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Starch
The
primary storage form
of
glucose
in
plants
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Amylose
A
linear
polysaccharide
made up of
glucose monomers
linked through
alpha-1
,
4-glycosidic
bonds
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Amylopectin
A
highly branched
polysaccharide
made up of
glucose
units linked through
alpha-1
,
4-glycosidic
bonds and occasional
alpha-1
,
6-glycosidic
bonds
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Starch
structure
Coiled
structure
Compact
due to
polymerisation
Relatively
insoluble
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Glycogen
The
primary storage form
of
glucose
in
animals
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Glycogen
structure
Branched polymer
Highly compact
Coiled structure
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Cellulose
A
complex polysaccharide
composed of
beta-glucose
molecules, essential for
plant cell walls
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Cellulose
structure
Forms
straight chains
Cross-linked microfibrils
Provides
tensile strength
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Glycoproteins
Proteins
with
one
or
more carbohydrates attached
,
playing roles
in
cell signalling
and
communication
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