Macromolecules
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Transcript Macromolecules
Chapter 5:
The Structure and Function of
Macromolecules
Macromolecules
Large molecules formed by joining many
subunits together.
Also known as “polymers”.
Monomer
A building block of a polymer.
Condensation Synthesis or
Dehydration Synthesis
The chemical reaction that joins monomers
into polymers.
Covalent bonds are formed by the removal of
a water molecule between the monomers.
Hydrolysis
Reverse of condensation synthesis.
Hydro- water
Lysis - to split
Breaks polymers into monomers by adding
water.
4 Main Types Of Macromolecules
Carbohydrates
Lipids
Protein
Nucleic acids
Carbohydrates
Used for fuel, building materials, and
receptors.
Made of C,H,O
General formula is CH2O
C:O ratio is 1:1
Types Of Carbohydrates
Monosaccharides
Disaccharides
Oligosaccharides
Polysaccharides
Monosaccharides
Mono - single
Saccharide - sugar
Simple sugars.
3 to 7 carbons.
Can be in linear or ring forms.
Can be “Aldoses” or “Ketoses” depending on
the location of the carbonyl group.
Examples
Glucose
Galactose
Ribose
Fructose
- OSE
Word ending common for many
carbohydrates.
Disaccharides
Sugar formed by joining two
monosaccharides through a “glycosidic
linkage”.
Examples
Maltose = glucose + glucose
Lactose = glucose + galactose
Sucrose = glucose + fructose
Oligosaccharides
2 - 10 joined simple sugars.
Used in cell membranes.
Polysaccharides
Many joined simple sugars.
Used for storage or structure.
Examples:
Starch
Cellulose
Glycogen
a glucose and b glucose
Starch
Made of 1-4 linkages of a glucose.
Linkage makes the molecule form a helix.
Fuel storage in plants.
a glucose
Cellulose
Made of 1-4 linkages of b glucose.
Linkage makes the molecule form a straight
line.
Used for structure in plant cell walls.
b glucose
Comment
Most organisms can digest starch (1- 4 a
linkage), but very few can digest cellulose (14 b linkage).
Another example of the link between
structure and function.
Glycogen
“Animal starch”
Similar to starch, but has more 1-6 linkages
or branches.
Found in the liver and muscle cells.
Starch
Glycogen
Lipids
Diverse hydrophobic molecules.
Made of C,H,O
No general formula.
C:O ratio is very high in C.
Fats and Oils
Fats - solid at room temperature.
Oils - liquid at room temperature.
Fats and Oils
Made of two kinds of smaller molecules.
Fatty Acids
Glycerol
Fatty Acids
A long carbon chain (12-18 C) with a -COOH
(acid) on one end and a -CH3 (fat) at the
other.
Acid
Fat
Neutral Fats or Triacylglycerols
Three fatty acids joined to one glycerol.
Joined by an “ester” linkage between the -
COOH of the fatty acid and the -OH of the
alcohol.
Saturated Fats/Unsaturated Fats
Saturated - no double bonds.
Unsaturated - one or more C=C bonds. Can
accept more Hydrogens.
Double bonds cause “kinks” in the molecule’s
shape.
Question
Why do fats usually contain saturated fatty acids and
oils usually contain unsaturated fatty acids?
The double bond pushes the molecules apart,
lowering the density, which lowers the melting point.
Fats
Differ in which fatty acids are used.
Used for energy storage, cushions for organs,
insulation.
Question ?
Which has more energy, a kg of fat or a kg of
starch?
Fat - there are more C-H bonds which
provide more energy per mass.
Phospholipids
Similar to fats, but have only two fatty acids.
The third -OH of glycerol is joined to a
phosphate containing molecule.
Result
Phospholipids have a hydrophobic tail, but a
hydrophilic head.
Self-assembles into micells or bilayers, an
important part of cell membranes.
Steroids
Lipids with four fused rings.
Differ in the functional groups attached to the
rings.
Examples:
cholesterol
sex hormones
Proteins
The molecular tools of the cell.
Made of C,H,O,N, and sometimes S.
No general formula.
Uses Of Proteins
Structure
Enzymes
Antibodies
Transport
Movement
Receptors
Hormones
Movie
Proteins
Polypeptide chains of Amino Acids linked by
peptide bonds.
Amino Acids
All have a Carbon with four attachments:
-COOH (acid)
-NH2 (amine)
-H
-R (some other side group)
R groups
20 different kinds:
Nonpolar - 9 AA
Polar - 6 AA
Electrically Charged
Acidic - 2 AA
Basic - 3 AA
Amino Acids
Amino Acids
R groups
Contain the S when present in a protein.
Cysteine or Cys
Methionine or Met
The properties of the R groups determine the
properties of the protein.
Polypeptide Chains
Formed by dehydration synthesis between
the carboxyl group of one AA and the amino
group of the second AA.
Produce an backbone of: (N-C-C)X
Levels Of Protein Structure
Organizing the polypeptide into its 3-D
functional shape.
Primary
Secondary
Tertiary
Quaternary
Primary
Sequence of amino acids in the
polypeptide chain.
Many different sequences are
possible with 20 AAs.
Secondary
3-D structure formed by hydrogen bonding between the
R groups.
Two main secondary structures:
a helix
pleated sheets
Tertiary
Bonding between the R groups.
Examples:
hydrophobic
ionic bonding
Disulfide bridges
interactions
(covalent bond)
Quaternary
When two or more polypeptides unite to
form a functional protein.
Example: hemoglobin
Is Protein Structure Important?
Denaturing Of A Protein
Events that cause a protein to lose structure (and
function).
Example:
pH shifts
high salt concentrations
heat
Nucleic Acids
Informational polymers
Made of C,H,O,N and P
No general formula
Examples: DNA and RNA
Nucleic Acids
Polymers of nucleotides
Nucleotides have three parts:
nitrogenous base
pentose sugar
phosphate
Nitrogenous Bases
Rings of C and N
The N atoms tend to take up H+ (base).
Two types:
Pyrimidines (single ring)
Purines (double rings)
Pentose Sugar
5-C sugar
Ribose - RNA
Deoxyribose – DNA
RNA and DNA differ in a –OH group on the
3rd carbon.
Nucleosides and Nucleotides
Nucleoside = base + sugar
Nucleotide = base + sugar + Pi
DNA
Deoxyribonucleic Acid.
Makes up genes.
Genetic information source
for most life.
RNA
Ribonucleic Acid.
Structure and protein synthesis.
Genetic information for a few viruses only.
Summary
For each macromolecule, know the following:
Elements and monomers
Structures
Functions