BIOLOGY Chapter 3: 10th Edition The Chemistry of Organic ......Saturated - no double bonds between...
Transcript of BIOLOGY Chapter 3: 10th Edition The Chemistry of Organic ......Saturated - no double bonds between...
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Sylv
ia S
. Ma
der
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PowerPoint® Lecture Slides are prepared by Dr. Isaac Barjis, Biology Instructor
BIOLOGY 10th Edition
1
The Chemistry of Organic Molecules
Chapter 3: pp. 37-58
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© The McGraw Hill Companies, Inc./John Thoeming, photographer
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Outline
Organic vs Inorganic
Functional Groups and Isomers
Macromolecules
Carbohydrates
Lipids
Proteins
Nucleic Acids
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Organic Molecules
Organic molecules contain carbon and
hydrogen atoms bonded to other atoms
Organic molecules are a diverse group
Four types of organic molecules
(biomolecules) exist in organisms: Carbohydrates
Lipids
Proteins
Nucleic Acids
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Organic versus Inorganic Molecules
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5
Carbohydrates as Structural Materials
Plants cell wall
consist of
cellulose
Cell wall of fungi
and shell of crab
contain chitin
Bacterial cell wall
contain
peptidoglycan c. Cell walls contain peptidoglycan.
b. Shell contains chitin.
a. Cell walls contain cellulose.
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
a: © Brand X Pictures/PunchStock; b: © Ingram Publishing/Alamy; c: © H. Pol/CNRI/SPL/Photo
Researchers, Inc.
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Carbon Atom
Carbon atoms:
Contain a total of 6 electrons
Only four electrons in the outer shell
Very diverse as one atom can bond with up to four
other atoms
Often bonds with other carbon atoms to make
hydrocarbons
Can produce long carbon chains like octane
Can produce ring forms like cyclohexane
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Octane & Cyclohexane
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octane
cyclohexane
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Functional Groups
Functional groups are clusters of specific atoms bonded to the carbon skeleton with characteristic structure and functions
Always react in the same manner, regardless of where attached
Determine activity and polarity of large organic molecules
Many functional groups, but only a few are of major biological importance
Depending on its functional groups, an organic molecule may be both acidic and hydrophilic
Nonpolar organic molecules are hydrophobic (cannot dissolve in water) unless they contain a polar functional group
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Biologically Important Functional Groups
Hydroxyl Alcohol
as in
ethanol
Ketone
as in
acetone
Carboxyl
(acidic)
Carboxylic acid
as in
acetic acid
Amino
R = remainder of molecule
Amine
as in tryptophan
Sulfhydryl Thiol
as in ethanethiol
Carbonyl Aldehyde
as in
formaldehyde
Phosphate Organic
phosphate
as in
phosphorylated
molecules
Structure
Functional Groups
Compound
Polar, forms
hydrogen bond
Present in sugars,
some amino acids
Polar
Present in sugars
Polar, acidic
Present in fatty
acids, amino acids
Polar, basic, forms
hydrogen bonds
Present in amino acids
Forms disulfide bonds
Present in some
amino acids
Polar
Present in sugars
Polar, acidic
Present in
nucleotides,
phospholipids
Significance Group
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
R OH
R
R R
R
R
R
R
SH
C
O
H
C
O
C OH
O
N
H
H
O P
O
OH
OH
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Isomers
Isomers - organic molecules that have:
Identical molecular formulas, but
Differing internal arrangement of atoms Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
glyceraldehyde dihydroxyacetone
OH OH
H H
H C C C H
O
OH OH
H O
H C C C H
H
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Macromolecules
Carbohydrates, lipids, proteins, and nucleic acids are called macromolecules because of their large size. Usually consist of many repeating units
Resulting molecule is a polymer (many parts) Repeating units are called monomers E.g. amino acids (monomer) are linked to form a protein
(polymer)
Some examples:
NNuucclleeoottiiddee DDNNAA,, RRNNAA NNuucclleeiicc AAcciiddss
AAmmiinnoo aacciidd PPoollyyppeeppttiiddee PPrrootteeiinnss
MMoonnoossaacccchhaarriiddee PPoollyyssaacccchhaarriiddee CCaarrbboohhyyddrraatteess
GGllyycceerrooll && ffaattttyy aacciiddss FFaatt LLiippiiddss
SSuubbuunniitt((ss)) EExxaammppllee CCaatteeggoorryy
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Common Foods
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Animation
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Dehydration and Hydrolysis
Dehydration - Removal of water molecule Used to connect monomers together to make polymers
Polymerization of glucose monomers to make starch
Hydrolysis - Addition of water molecule Used to disassemble polymers into monomer parts
Digestion of starch into glucose monomers
Specific enzymes required for each reaction Accelerate reaction
Are not used in the reaction
Are not changed by the reaction
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Biomolecules
Biomolecules
Category Example Subunit(s)
Lipids Fat Glycerol and fatty acids
Carbohydrates* Polysaccharide Monosaccharide
Proteins* Polypeptide Amino acids
Nucleic acids* DNA, RNA Nucleotide
*Polymers
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Synthesis and Degradation of Polymers
monomer monomer
monomer monomer
dehydration
reaction
monomer monomer
hydrolysis
reaction
H2O
OH H
OH H
b. Degradation of a biomolecule
a. Synthesis of a biomolecule
H2O
monomer monomer
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Carbohydrates
Monosaccharides:
Are a single sugar molecule such as glucose, ribose, deoxyribose
Are with a backbone of 3 to 7 carbon atoms (most have 6 carbon).
Disaccharides:
Contain two monosaccharides joined by dehydration reaction
Lactose is composed of galactose and glucose and is found in milk.
Sucrose (table sugar) is composed of glucose and fructose
Polysaccharides - Are polymers of monosaccharides
Polysaccharides as Energy Storage Molecules
Starch, Glycogen
Polysaccharides as Structural Molecules
Cellulose, Chitin
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Popular Models for Representing
Glucose Molecules
C6H12O6
a. b.
c. d.
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© Steve Bloom/Taxi/Getty
CH2OH
C
C
H
C HO
O
C
H
OH C
H OH H
H OH
CH2OH
H
HO
H
OH OH H
H OH
O
O O
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Synthesis and Degradation
of Maltose, a Disaccharide
glucose C6H12O6 water
monosaccharide disaccharide water
glucose C6H12O6
monosaccharide + +
dehydration reaction
hydrolysis reaction
maltose C12H22O11
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CH2OH
O O
CH2OH
H
OH
H
HO
CH2OH
O
O
O
CH2OH
H2O
O
O glucose fructose
sucrose
O
CH2OH CH2OH
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
CH2OH
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Carbohydrates: Monosaccharides
Single sugar molecules
Quite soluble and sweet to taste
Examples
Glucose (blood), fructose (fruit) and galactose
Hexoses - Six carbon atoms
Isomers of C6H12O6
Ribose and deoxyribose (in nucleotides)
Pentoses – Five carbon atoms
C5H10O5 & C5H10O4
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Carbohydrates: Disaccharides
Contain two monosaccharides joined by dehydration reaction
Soluble and sweet to taste
Examples
Lactose is composed of galactose and glucose and is found in milk
Sucrose (table sugar) is composed of glucose and fructose
Maltose is composed of two glucose molecules
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Carbohydrates: Polysaccharides
Polymers of monosaccharides
Low solubility; not sweet to taste
Polysaccharides as Energy Storage Molecules Starch found in plant
Polymer of glucose
Few side branches
Used for short-term energy storage
Amylose and amylopectin are the two forms of starch found in
plants
Glycogen is the storage form of glucose in animals. Highly branched polymer of glucose with many side branches
Glycogen in liver and muscles
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Carbohydrates: Polysaccharides
Polysaccharides as Structural Molecules
Cellulose is a polymer of glucose which forms
microfibrils
Primary constituent of plant cell walls
Main component of wood and many natural fibers
Indigestible by most animals
Chitin is a polymer of glucose with an amino
group attached to each glucose
Very resistant to wear and digestion
Primary constituent of arthropod exoskeletons (e.g.
Crab) and cell walls of fungi
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Starch Structure and Function
a. Starch
starch
granule
250mm
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© Jeremy Burgess/SPL/Photo Researchers, Inc.
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Glycogen Structure and Function
b . Glycogen
glycogen
granule
150 nm
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
© Don W. Fawcett/Photo Researchers, Inc.
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Cellulose Structure and Function
cellulose fiber
cellulose fibers
Plant
cell wall
microfibrils
glucose molecules
5,000 m
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© Science Source/J.D. Litvay/Visuals Unlimited
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Lipids
Lipids are varied in structure
Insoluble in water Long chains of repeating CH2 units
Renders molecule nonpolar
Lack polar groups
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Lipids
Fat provides insulation
and energy storage in
animals
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
© Paul Nicklen/National Geographic/Getty
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Types of Lipids
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Types of Lipids: Triglycerides
Fats and oils contain two molecular units:
glycerol and fatty acids.
Dehydration Synthesis of Triglyceride from
Glycerol and Three Fatty Acids Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
+
C OH H
H
C OH H
C
C
OH H
H
H
H
C O H
H
C O H
C O H
H
C
H
C O
C
H O
H
C
H
C
C
O
C
H
H H H
C
H
C
H
C
H
H
C O
HO
C
H
H
C
H
H
H C
H
H H H
C
H
C
H
C
H
H
C
O
C
H
H
C
H
H
H
C
H
H H H
C
H
C
H
C
H
H
C O
H C
H
H H H
C
H
C
H
C
H
H
H
HO
HO
+
a. Formation of a fat
3 H2O
glycerol 3 fatty acids fat molecule 3 water
molecules
dehydration reaction
kink kink
hydrolysis reaction
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Types of Lipids: Triglycerides
C
H
H H H
C
H
C
H
C
H
H
C O
HO C
H
H
C
H
H
C
H
H
C
H
C
H
C
H
H
C
H
C
H
C
H
H
C
H
C
H
C
H
H
C
H
H
H
C
H
H
H C
H
H H H
C
H
C
H
C
H
H
C O
HO
C
H
H
C
H
H
C
H
H
C
H
H H H
C
H
C
H
C
H
H
C
H
H
C
H
H
C
H
H
unsaturated fatty acid with double bonds (yellow)
corn corn oil
milk butter
unsaturated fat
saturated fatty acid with no double bonds saturated fat
b. T ypes of fatty acids c. T ypes of fats
C
H
H
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Types of Lipids: Triglycerides
Triglycerides (Fats) Long-term energy storage
Consist of a backbone of one glycerol molecule Glycerol is a water-soluble compound with three hydroxyl
groups.
Three fatty acids attached to each glycerol molecule Long hydrocarbon chain
Saturated - no double bonds between carbons e.g. in fats (butter)
Unsaturated - 1 or more than1 double bonds between carbons e.g. in oils
Carboxylic acid at one end
Carboxylic acid connects to –OH on glycerol in dehydration reaction
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Types of Lipids: Phospholipids
Phospholipids
Derived from triglycerides
Glycerol backbone
Two fatty acids attached instead of three
Third fatty acid replaced by phosphate group
The fatty acids are nonpolar and hydrophobic
The phosphate group is polar and hydrophilic
Molecules self arrange when placed in water
Polar phosphate “heads” next to water
Nonpolar fatty acid “tails” overlap and exclude water
Spontaneously form double layer & a sphere
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Types of Lipids: Phospholipids
Phospholipids Form Membranes Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
b. Plasma membrane of a cell
ins
ide
ce
ll
ou
tsid
e c
ell
Polar Head
phosphate
a. Phospholipid structure
fatty acids
glycerol
Nonpolar Tails
1CH2 O
2CH O –O
O P O 3CH2 R
O
O
O
CH2 CH2 CH2 CH2 CH2 CH2 CH2 CH2 CH3
O
CH2 CH2 CH2 CH2 CH2 CH2 CH2 CH =
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Types of Lipids: Steroids & Waxes
Steroids
Cholesterol, testosterone, estrogen
Skeletons of four fused carbon rings
Waxes
Long-chain fatty acid bonded to a long-chain alcohol
High melting point
Waterproof
Resistant to degradation
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Steroid Diversity
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
© Ernest A. Janes/Bruce Coleman, Inc.
a. Cholesterol
c. Estrogen
b. Testosterone
OH
CH3
HO
HO
(CH2)3
HC CH3
CH3
HC CH3
OH
CH3
CH3
O
CH3
CH3
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Waxes
a. b.
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38
Proteins
Functions
Support proteins
Keratin - makes up hair and nails
Collagen - support many of the body’s structures e.g. tendons, skin
Enzymes – Almost all enzymes are proteins
Acts as organic catalysts to accelerate chemical reactions within cells
Transport – Hemoglobin; membrane proteins
Defense – Antibodies
Hormones are regulatory proteins that influence the metabolism of cells e.g. insulin
Motion – Muscle proteins, microtubules
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40
Protein Subunits: The Amino Acids
Proteins are polymers of amino acids
Each amino acid has a central carbon atom (the alpha carbon) to which are attached a hydrogen atom,
an amino group –NH2,
A carboxylic acid group –COOH,
and one of 20 different types of –R (remainder) groups
There are 20 different amino acids that make up proteins
Amino acids differ according to their particular R group
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42
Structural Formulas for the 20 Amino Acids
proline (Pro) valine (Val) phenylalanine (Phe) methionine (Met) leucine (Leu)
glutamine (Gln)
threonine (Thr) asparagine (Asn)
aspartic acid (Asp) arginine (Arg) histidine (His)
cysteine (Cys) serine (Ser)
tyrosine (Tyr)
glutamic acid (Glu) lysine (Lys)
H
H3N+ C
CH
H3C CH3
C
O
O–
H O
O
C C
(CH2)2
S
CH3
CH2
C
H
H3N+ C
O
O–
H3N+
H
CH
CH3 CH3
H3N+ C
H
O–
H2N+
H
C C
H
O–
CH2
H2C CH2
CH2
H
C
CH2
H3N+ C
O
O–
SH
H3N+ C C
O
O–
H
CH2
OH
O
O–
C
CH2
OH
H3N+
C
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O
O–
C
H
(CH2)2
H3N+
NH2 O
C
O
O–
C
H
C
CH2
H3N+
NH2 O
H O
O–
C C H3N+
OH CH3
CH
H
H3N+ C C
O
O–
CH2
CH2
COO–
H
C
CH2
CH2
CH2
H3N+ C
O
O–
N+H3
H
C
CH2
C
–O O
C
O
O–
H3N+
H
C
(CH2)3
NH
C
NH2
N+H2
H3N+ C
O
O– H3N
+ C C
H
CH2
NH
N+H
O–
O
H
C C C
Sample Amino Acids with Polar (Hydrophilic) R Groups
Sample Amino Acids with Ionized R Groups
Sample Amino Acids with Nonpolar (Hydrophobic) R Groups
C
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43
Proteins: The Polypeptide Backbone
A peptide bond is a covalent bond between two amino acids (AA)
COOH of one AA covalently bonds to the NH2 of the next AA
Two AAs bonded together – Dipeptide
Three AAs bonded together – Tripeptide
Many AAs bonded together – Polypeptide
Characteristics of a protein determined by composition and sequence of AA’s
A protein may contain more than one polypeptide chain
Virtually unlimited number of proteins
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Synthesis and Degradation of a Peptide
dehydration reaction
hydrolysis reaction
water
peptide bond
dipeptide amino acid amino acid
acidic group amino group
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45
Protein: Levels of Structure
Protein shape (3-D structure) determines the function of the protein in the organism
Proteins can have up to four levels of structure Primary:
Literally, the sequence of amino acids
A string of beads (up to 20 different colors)
Secondary: The way the amino acid chain coils or folds
Describing the way a knot is tied
Tertiary: Overall three-dimensional shape of a polypeptide
Describing what a knot looks like from the outside
Quaternary: Consists of more than one polypeptide
Like several completed knots glued together
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46
Levels of Protein Organization
(beta) sheet = pleated sheet
COO –
Primary Structure
Secondary Structure
Tertiary Structure
Quaternary Structure
amino acid peptide bond
disulfide bond
hydrogen bond
hydrogen bond
(alpha) helix
H3N+
This level of structure
is determined by the
sequence of amino
acids that join to form
a polypeptide.
Hydrogen bonding
between amino acids
causes the polypeptide
to form an alpha helix
or a pleated sheet.
Due in part to covalent
bonding between R
groups the polypeptide
folds and twists giving
it a characteristic
globular shape.
This level of structure
occurs when two or more
polypeptides join to form
a single protein.
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Animation
47
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48
Examples of Fibrous Proteins
a. b. c.
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50
Protein-folding Diseases
Assembly of AA’s into protein extremely complex
Process overseen by “chaperone” molecules
Inhibit incorrect interactions between R groups as
polypeptide grows
Defects in these chaperones can corrupt the tertiary
structure of proteins
Mad cow disease could be due to mis-folded proteins
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51
Nucleic Acids
Polymers of nucleotides
Very specific cell functions
DNA (deoxyribonucleic acid)
Double-stranded helical spiral (twisted ladder)
Serves as genetic information center
In chromosomes
RNA (ribonucleic acid)
Part single-stranded, part double-stranded
Serves primarily in assembly of proteins
In nucleus and cytoplasm of cell
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52
The Nucleotides of Nucleic Acids
Three components:
A phosphate group,
A pentose sugar (ribose or deoxyribose), and
A nitrogenous base (4 kinds in DNA, 3 kinds in RNA, 3
common to both
Nucleotide subunits connected end-to-end to make
nucleic acid
Sugar of one connected to the phosphate of the next
Sugar-phosphate backbone
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53
Nucleotides
pentose sugar
nitrogen-
containing
base phosphate
deoxyribose (in DNA) ribose (in RNA)
cytosine thymine in DNA uracil in RNA
a. Nucleotide structure
c. Pyrimidines versus purines
b. Deoxyribose versus ribose
adenine guanine
Pyrimidines Purines
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54
DNA Structure
A
T
b. Double helix a. Space-filling model
A
A
T T G
G
C C
G
P
C
Guanine
Thymine
Adenine
Cytosine Sugar
Phosphate
S
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55
RNA Structure
Guanine
Uracil
Adenine
Cytosine Ribose
Phosphate P
S
Backbone
Nitrogen-containing bases S
S
S
S
P
P
P
P
G
C
A
U
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56
Complementary Base Pairing
N
adenine (A)
sugar
sugar
thymine (T)
cytosine (C) guanine (G)
sugar
sugar
c. Complementary base pairing
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57
Comparison of DNA & RNA
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Other Nucleic Acids
ATP (adenosine triphosphate) is composed of
adenine, ribose, and three phosphates
In cells, one phosphate bond is hydrolyzed –
Yields:
The molecule ADP (adenosine diphosphate)
An inorganic phosphate molecule pi
Energy
Other energy sources used to put ADP and pi
back together again
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60
ATP
+ +
adenosine
ATP
triphosphate adenosine diphosphate phosphate
energy
ADP
adenosine triphosphate
H2O
P P P P P P
b.
a. c.
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61
Review
Organic vs Inorganic
Functional Groups and Isomers
Macromolecules
Carbohydrates
Lipids
Proteins
Nucleic Acids
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Sylv
ia S
. Ma
der
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PowerPoint® Lecture Slides are prepared by Dr. Isaac Barjis, Biology Instructor
BIOLOGY 10th Edition
62
The Chemistry of Organic Molecules
Chapter 3: pp. 37-58
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