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CAMPBELL
BIOLOGY Reece • Urry • Cain • Wasserman • Minorsky • Jackson
© 2014 Pearson Education, Inc.
TENTH
EDITION
CAMPBELL
BIOLOGY Reece • Urry • Cain • Wasserman • Minorsky • Jackson
TENTH
EDITION
4 Carbon and
the Molecular
Diversity of
Life
Lecture Presentation by
Nicole Tunbridge and
Kathleen Fitzpatrick
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© 2014 Pearson Education, Inc.
Carbon: The Backbone of Life
Living organisms consist mostly of carbon-based
compounds
Carbon is unparalleled in its ability to form large,
complex, and varied molecules
Proteins, DNA, carbohydrates, and other
molecules that distinguish living matter are all
composed of carbon compounds
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Figure 4.1
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Figure 4.1a
Carbon can bond to four other atoms or
groups of atoms, making a large variety of
molecules possible.
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Concept 4.1: Organic chemistry is the study of carbon compounds
Organic chemistry is the study of compounds
that contain carbon
Organic compounds range from simple molecules
to colossal ones
Most organic compounds contain hydrogen atoms
in addition to carbon atoms
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Vitalism was the belief in a life force outside the
jurisdiction of physical and chemical laws
It was thought that organic compounds could only
be produced in living organisms
Vitalism was disproved when chemists were able
to synthesize organic compounds
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Organic Molecules and the Origin of Life on Earth
Stanley Miller’s classic experiment demonstrated
the abiotic synthesis of organic compounds
Experiments support the idea that abiotic
synthesis of organic compounds, perhaps near
volcanoes, could have been a stage in the origin
of life
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Figure 4.2
Water vapor
Cooled “rain”
containing
organic
molecules
Sample for
chemical analysis
Cold
water
Condenser
Electrode
“Atmosphere”
CH4
H2O
“sea
”
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Pioneers of organic chemistry helped shift the
mainstream of biological thought from vitalism
to mechanism
Mechanism is the view that physical and chemical
laws govern all natural phenomena
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Concept 4.2: Carbon atoms can form diverse molecules by bonding to four other atoms
Electron configuration is the key to an atom’s
characteristics
Electron configuration determines the kinds and
number of bonds an atom will form with other
atoms
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The Formation of Bonds with Carbon
With four valence electrons, carbon can form four
covalent bonds with a variety of atoms
This ability makes large, complex molecules
possible
In molecules with multiple carbons, each carbon
bonded to four other atoms has a tetrahedral
shape
However, when two carbon atoms are joined by a
double bond, the atoms joined to the carbons are
in the same plane as the carbons
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Figure 4.3
Molecule
(a) Methane
(b) Ethane
(c) Ethene
(ethylene)
Molecular
Formula
Structural
Formula Ball-and-Stick Model
Space-Filling
Model
CH4
C2H6
C2H4
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The electron configuration of carbon gives it
covalent compatibility with many different
elements
The valences of carbon and its most frequent
partners (hydrogen, oxygen, and nitrogen)
are the building code for the architecture of
living molecules
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Figure 4.4
Hydrogen
(valence = 1)
Oxygen
(valence = 2)
Nitrogen
(valence = 3)
Carbon
(valence = 4)
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Carbon atoms can partner with atoms other than
hydrogen; for example:
Carbon dioxide: CO2
Urea: CO(NH2)2
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Figure 4.UN02
Urea
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Molecular Diversity Arising from Variation in Carbon Skeletons
Carbon chains form the skeletons of most organic
molecules
Carbon chains vary in length and shape
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Figure 4.5
(a) Length
(b) Branching (d) Presence of rings
(c) Double bond position
Ethane Propane 1-Butene 2-Butene
Butane 2-Methylpropane
(isobutane) Cyclohexane Benzene
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Animation: Carbon Skeletons
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Figure 4.5a
(a) Length
Ethane Propane
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Figure 4.5b
(b) Branching
Butane 2-Methylpropane
(isobutane)
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Figure 4.5c
(c) Double bond position
1-Butene 2-Butene
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Figure 4.5d
(d) Presence of rings
Cyclohexane Benzene
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Hydrocarbons
Hydrocarbons are organic molecules consisting
of only carbon and hydrogen
Many organic molecules, such as fats, have
hydrocarbon components
Hydrocarbons can undergo reactions that release
a large amount of energy
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Figure 4.6
Nucleus
Fat droplets
(b) A fat molecule (a) Part of a human adipose cell
10 μm
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Figure 4.6a
Nucleus
Fat droplets
(a) Part of a human adipose cell 10 μm
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Isomers
Isomers are compounds with the same molecular
formula but different structures and properties
Structural isomers have different covalent
arrangements of their atoms
Cis-trans isomers have the same covalent bonds
but differ in spatial arrangements
Enantiomers are isomers that are mirror images
of each other
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Figure 4.7 (a) Structural isomers
(b) Cis-trans isomers
Pentane
cis isomer: The two Xs are
on the same side.
2-methyl butane
trans isomer: The two Xs are
on opposite sides.
(c) Enantiomers
L isomer D isomer
CO2H CO2H
H
CH3 CH3
H NH2 NH2
C C
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Animation: Isomers
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Figure 4.7a
(a) Structural isomers
Pentane 2-methyl butane
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Figure 4.7b
(b) Cis-trans isomers
cis isomer: The two Xs are
on the same side.
trans isomer: The two Xs are
on opposite sides.
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Figure 4.7c
(c) Enantiomers
L isomer D isomer
CO2H
H
CH3
H NH2
CO2H
NH2
CH3
C C
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Enantiomers are important in the pharmaceutical
industry
Two enantiomers of a drug may have different
effects
Usually only one isomer is biologically active
Differing effects of enantiomers demonstrate that
organisms are sensitive to even subtle variations
in molecules
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Figure 4.8
Drug Effects Effective
Enantiomer
Ineffective
Enantiomer
Ibuprofen
Albuterol
Reduces
inflammation
and pain
Relaxes bronchial
(airway) muscles,
improving airflow
in asthma
patients
S-Ibuprofen
R-AIbuterol S-AIbuterol
R-Ibuprofen
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Animation: L-Dopa
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Concept 4.3: A few chemical groups are key to molecular function
Distinctive properties of organic molecules depend
on the carbon skeleton and on the chemical
groups attached to it
A number of characteristic groups can replace
the hydrogens attached to skeletons of organic
molecules
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The Chemical Groups Most Important in the Processes of Life
Estradiol and testosterone are both steroids with
a common carbon skeleton, in the form of four
fused rings
These sex hormones differ only in the chemical
groups attached to the rings of the carbon
skeleton
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Figure 4.UN03
Estradiol Testosterone
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Functional groups are the components of
organic molecules that are most commonly
involved in chemical reactions
The number and arrangement of functional groups
give each molecule its unique properties
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The seven functional groups that are most
important in the chemistry of life
Hydroxyl group
Carbonyl group
Carboxyl group
Amino group
Sulfhydryl group
Phosphate group
Methyl group
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Figure 4.9 Chemical Group Compound Name Examples
Ethanol
Propanal Acetone
Acetic acid
Glycine
Cysteine
Glycerol phosphate
Organic
phosphate
Thiol
Amine
Carboxylic acid, or
organic acid
Ketone
Aldehyde
Alcohol Hydroxyl group (—OH)
Carboxyl group (—COOH)
Amino group (—NH2)
Sulfhydryl group (—SH)
Phosphate group (—OPO32−)
Methyl group (—CH3) Methylated
compound
5-Methyl cytosine
Carbonyl group ( C=O)
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Figure 4.9a
Chemical Group Compound Name Examples
Ethanol
Propanal Acetone
Acetic acid
Glycine
Amine
Carboxylic acid, or
organic acid
Ketone
Aldehyde
Alcohol Hydroxyl group (—OH)
Carboxyl group (—COOH)
Amino group (—NH2)
Carbonyl group ( C=O)
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Figure 4.9aa
Ethanol, the alcohol
present
in alcoholic
beverages
Polar due to electronegative oxygen. Forms hydrogen bonds with water.
Compound name: Alcohol
Hydroxyl group (—OH)
(may be written HO—)
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Figure 4.9ab
Propanal,
an aldehyde Acetone,
the simplest ketone
Sugars with ketone groups are called ketoses; those with aldehydes
are called aldoses.
Compound name: Ketone or aldehyde
Carbonyl group ( C=O)
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Figure 4.9ac
Acetic acid, which
gives vinegar its
sour taste
Acts as an acid.
Compound name: Carboxylic acid, or organic acid
Carboxyl group (—COOH)
Ionized form of —COOH
(carboxylate ion),
found in cells
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Figure 4.9ad
Glycine, an amino acid
(note its carboxyl group)
Acts as a base.
Compound name: Amine
Amino group (—NH2)
Ionized form
of —NH2,
found in cells
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Figure 4.9b
Cysteine
Glycerol phosphate
Organic
phosphate
Thiol Sulfhydryl group (—SH)
Phosphate group (—OPO32−)
Methyl group (—CH3) Methylated
compound
5-Methyl cytosine
Chemical Group Compound Name Examples
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Figure 4.9ba
Cysteine, a sulfur-
containing amino acid
Two —SH groups can react, forming a “cross-link” that helps stabilize
protein structure.
Compound name: Thiol
Sulfhydryl group (—SH)
(may be written HS—)
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Figure 4.9bb
Glycerol phosphate,
which takes part in
many important
chemical reactions in
cells
Contributes negative charge. When attached, confers on a molecule the ability
to react with water, releasing energy.
Compound name: Organic phosphate
Phosphate group (—OPO32−)
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Figure 4.9bc
Methyl group (—CH3)
Affects the expression of genes. Affects the shape and function of
sex hormones.
Compound name: Methylated compound
5-Methyl cytosine, a
component of DNA
that has been modified
by addition of a methyl
group
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ATP: An Important Source of Energy for Cellular Processes
An important organic phosphate is adenosine
triphosphate (ATP)
ATP consists of an organic molecule called
adenosine attached to a string of three phosphate
groups
ATP stores the potential to react with water,
a reaction that releases energy to be used by
the cell
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Figure 4.UN04
Adenosine
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Figure 4.UN05
Reacts
with H2O
Inorganic
phosphate
ADP
Energy Adenosine Adenosine
ATP
P P P P P P i
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The Chemical Elements of Life: A Review
The versatility of carbon makes possible the great
diversity of organic molecules
Variation at the molecular level lies at the
foundation of all biological diversity
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Figure 4.UN01a
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Figure 4.UN01b
Some of Stanley Miller’s notes from his
1958 hydrogen sulfide (H2S) experiment
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Figure 4.UN01c
Some of Stanley Miller’s
original vials from his
1958 hydrogen sulfide
(H2S) experiment
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Figure 4.UN06
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Figure 4.UN07
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Figure 4.UN08
a b c d e
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Figure 4.UN09
L-dopa D-dopa
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Figure 4.UN10