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Chapter 3 Biochemistry

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Title: Chapter 3 Biochemistry


1
Chapter 3 Biochemistry
AC
  • Here- Bio molecule art by
  • David Goodsell, creates
  • hyperrealist paintings
  • the molecular world
  • Here,a depiction of HIV
  • shown in cross-section- the
  • structural biology electron
  • microscopy gives a much
  • -maligned pathogen a unique
  • artistic quality.

2
Examples of bio molecules Hemoglobin
  • the oxygen-carrying molecule of erythrocytes,
    formed by developing erythrocytes in the bone
    marrow
  • a protein made up
  • of 4 polypeptide
  • chains that contain
  • 141 - 146 amino
  • acids each.

3
Examples of biological molecules
  • The Helicase enzyme unzips the DNA molecule, to
    expose the nitrogenous bases so we can read the
    genetic code do everything that is in the
    instructions for life.

4
Inside leaves, solar energy is transferred to the
chemical bonds in biological molecules like
GLUCOSE food.
5
Examples Biological molecules
  • Hormones are chemical messengers that regulate
    imperative bodily functions in living organisms.
  • For example pheromones are hormones used by ants
    other insects as a
  • communication system to
  • send messages among one
  • another or to attract the
  • opposite sex.

http//www.reciprocalnet.org/edumodules/commonmole
cules/biochemical/index.html
6
Examples biological molecules
  • Other examples of biomolecules are poisons found
    in animals. Batrachotoxin, a poison at the skin
    of the golden poison frog
  • Phyllobates terribilis is considered
  • to be one of the most deadly poisons to humans,
    however it is harmless to predator,
  • the snake Liophis epinephelus .

bio.davidson.edu
7
  • Before you can study any of these complex
    systems, you must understand the molecules that
    are behind all the wonder..

8
Remember!
CHNOPS the 6 most common elements in living
things
  • Biological molecules, are built by joining atoms
    through covalent bonds.
  • Although more than 25 types of elements can be
    found in biomolecules, 6 elements are most
    common. These are called the CHNOPS

9
All compounds can be classified into 2 broad
categories
  • Organic compounds
  • made primarily of carbon atoms.
  • Most matter in living organisms that is not water
    is made of organic compounds.
  • Inorganic compounds
  • Compounds that, with a few exceptions, do not
    contain carbon atoms. (an exception is CO2- not
    organic!) water is ex. of an inorganic compound.

10
What do people think organic means?
  • A survey showed most people think organic
    refers to organic foods (limited use of synthetic
    materials during growth production), and only a
    few science majors said carbon compounds.
  • Organic chemistry is - the study of the
    structure, properties, and reactions of carbon
    compounds.

11
I. What is an Organic Compound?
  • Contains carbon atoms
  • Even though organic chemistry focuses on carbon,
    many organic compounds also contain hydrogen (H),
    nitrogen (N)-, oxygen (O), phosphorous (P) or
    other elements.
  • Carbon molecules make up the bodies of all living
    things and have many different functions
  • They are also commonly used in medicine, food,
    paints, and gasoline.

12
Where is Carbon on the Periodic Table?
It forms 4 covalent bonds
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14
Carbon has 4 electrons in its outmost electron
shell. (It has a valence of 4)
  • it forms 4 covalent bonds

15
A. Carbon Bonding C atoms form many different
shaped molecules
  • It can form straight chains, branched chains with
    a single bond.
  • A carbon atom can also share two or even three
    pairs of electrons with another atom.

16
Carbon bonds Chains, Branched, RingsEach line
represents a single covalent bond
17
Carbon also forms double triple bonds
A good site for more explanation
www.biologyjunction.com
18
Examples carbon bonding in molecules
19
B. Functional Groups - A specific group of atoms
that gives a known type of behavior to molecules
changes the characteristics of the compound-
(See page 52 in your textbook for more on
functional groups)
Hydrocarbons - C and H only Alcohols
- OH Acids - COOH Amines
- NH2
An excellent site to look more closely at
functional groups http//www.phschool.com/science
/biology_place/biocoach/biokit/function.html
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21
More Functional groups
22
Example -adding a hydroxyl group makes ethane
into an alcohol-
  • Example - adding an amino group
  • - makes methane or ethane into- an amine

23
C. Naming Hydrocarbons
The simplest organic compounds are hydrocarbons.
Hydrocarbons are compounds that consist of
hydrogen and carbon atoms. When naming
hydrocarbons, the prefixes vary depending on the
number of carbons in a compound, the prefixes are
Number of Carbon(s) Prefix Number of Carbon(s) Prefix
1 Met- 6 Hex-
2 Eth- 7 Hept-
3 Prop- 8 Oct-
4 But- 9 Non-
5 Pent- 10 Dec-
http//chemwiki.ucdavis.edu/index.php?titleOrgani
c_Chemistry/Case_Studies/What_is_Organic3FCarbon
-containing_Compounds
24
Methane - the simplest carbon compound- 1
Carbon 4 hydrogen atoms
25
Other simple organic molecules
  • Butane cyclohexane

26
D. Drawing Molecules ways that a molecule can be
drawn
  • 1. Skeletal Structure (Kekulé Structure)
  • In this form of representation, atoms are placed
    on a plane and lines are drawn between atoms to
    represent bonding electrons.

27
  • 2. Condensed Structure
  • A simplified version
  • of the bond-line structure that omits the lines.
    When there are 2 or more of the same kinds of
    atoms attached to a central atom, a subscript is
    used to indicate how many of these atoms are
    attached.
  • 3. Lewis Structure
  • valence electrons are represented
  • as dots. This structure shows what
  • atoms are bonded together, which electrons are
    involved in bonding, lone pairs, any formal
    charges.

28
E. Isomers- same chemical formula, different
structure!
  • Organic molecules are three-dimensional
  • the same set of atoms can be put together in
    different ways, resulting in isomers
  • Example The atoms found in a simple sugar, with
    the structural formula C6H12O6, can be arranged
    in over a dozen different ways.

sonefe.org
29
F. Polarity Unequal electron sharing
  • In covalent bonds e sharing is not always equal.
  • Example Water - oxygen contains a higher
    negative charge density than hydrogen. So
    electron distribution is asymmetric, or polar,
    and the oxygen atom is said to be
    electronegative.
  • This asymmetry results in regions
  • of slight negative positive
  • charge in different regions of the
  • molecule, denoted by the Greek
  • symbol d (delta), for "partial" charge.

30
Electronegativity is a measure of the tendency of
an atom to attract a bonding pair of electrons
  • Oxygen is a very electronegative atom pulls
    electrons to itself.
  • That would leave the oxygen side of a molecule
    fairly negative and the carbon fairly positive.

http//www.chemguide.co.uk/basicorg/bonding/eneg.h
tml
31
G. Sizes of Molecules
  • 1. Monomers- small simple molecules
  • 2. Polymers- big molecules formed when monomers
    bonded to each other

32
3. Reactions to build or break down molecules
  • Condensation Reaction
  • 2 monomers join together- a water is released
  • (an H from 1 end and an OH from the other
  • end are cut loose when the monomers join.)
  • Hydrolysis Reaction
  • polymers are broken back down- they need a water
    added.

33
Hydrolysis of sucrose
34
Condensation Reactions (also called dehydration
synthesis) -builds monomers into polymers
http//nhscience.lonestar.edu/biol/dehydrat/dehydr
at.html
35
Hydrolysis Reactions- break down polymers into
monomers by adding water
36
H. Energy from ATP
  • Life needs a constant supply of energy
  • Chemical bonds store energy.
  • One molecule that living things use to store
    energy is in the bonds of the ATP molecule
  • Adenosine Triphosphate

37
Adenosine Triphosphate
                                             
       
Blue ribose (a 5-carbon sugar)
Green adenine (a nitrogenous base)
Yellow phosphate groups Energy is stored in
bonds joining the phosphate groups
38
ATP-ADP Cycle.
The energy is released when the last P is taken
off
Energy is stored in ATP (ADP P) Energy is used
as needed ATP is converted back to ADP
phosphate.
39
ATP further explained
  • A nitrogen-containing compound, adenine, is
    represented by the two rings The three linked
    phosphate groups, -PO4- are represented by the
    small circles with a P.
  • Because the phosphate groups are close together
    and have negative charges. When a bond between
    the phosphate groups is broken, energy is
    released.
  • This hydrolysis of ATP is used by the cell to
    provide the energy needed to drive the chemical
    reactions in an organism

40
II. Four Classes of Organic Molecules
  • Much of biochemistry deals with the structures,
    functions and interactions of cellular
    components, basically
  • Carbohydrates
  • Proteins,
  • Lipids
  • Nucleic Acids

41
Monomers Polymers
  • Each group has small molecules (monomers)
  • linked to form larger macromolecules
  • (polymers) three to millions of subunits.

42
  • Carbohydrates
  • the most important energy source for cells
  • short-term energy storage (sugar)
  • intermediate-term energy storage
  • starch for plants
  • glycogen for animals
  • as structural components in cells
  • cellulose cell walls of plants
  • chitin -exoskeleton of insects

43
Monomers Polymers
1.   Monosaccharides - single sugar units
glucose 2.   Disaccharides - two
monosaccharides. Lactose, maltose    3.   Polysacc
harides - linking many sugar units
together Examples starch, glycogen,
cellulose
44
Carbohydrates
  • General formula CH2On
  • where n is a number between 3 and 6.
  • Ex- glucose C6H12O6

45
Maltose Lactose are examples of disaccharides
What does it mean to be lactose intolerant?
46
Got Milk?- milks sugar is lactose
  • Infant mammals are fed on milk from mom
  • Enzyme lactase digests
  • the molecule into its two
  • subunits for absorption.
  • in most species, including humans,
  • the production of lactase gradually
  • ceases with maturity, they are
  • then unable to metabolize lactose
  • becoming Lactose intolerant

47
A Polysaccharide
Lots of monomers linked together
48
B. Proteins
  • Important as control and structural elements.
  • Control enzymes, hormones.
  • Structural -cell membrane, muscle tissue, etc.
  • Amino acids are the
  • building block of proteins
  • All living things (and even viruses) use various
    combinations of the same 20 amino acids.

49
1. An Amino Acid
an amino end (NH2) a carboxyl end (COOH).
R is the variable (R-group) of each amino acid.
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Amino acids are linked together by joining the
amino end of one molecule to the carboxyl end of
another. Removal of water (condensation
reaction) links amino acids with a peptide bond.
52
2. PEPTIDE BONDS
53
Condensation reaction- (also called dehydration
synthesis) To build a peptide chain- add
monomers lose a water! Makes a peptide bond!
http//nhscience.lonestar.edu/biol/dehydrat/dehydr
at.html
54
  • your amino acid pun for the day The cysteine
    chapel.

http//popperfont.net/tag/biochemistry/
55
Some examples of proteins
  • Antibodies they recognize molecules of invading
    organisms.
  • Receptors part of the cell membrane, they
    recognize other proteins, or chemicals, and
    inform the cell... 'The Door Bell'.
  • Enzymes assemble or digest.
  • Neurotransmitters and some hormones Trigger the
    receptors... (the finger on the door bell...)
  • Channels, and pores holes in the cell membrane
    (with or without a gate). Usually, filter the
    flow...

56
3. Enzymes-
  • Organic molecules that act as catalysts
  • Enzymes substrates (the reactants) fit
    together like a lock key
  • This fit weaken bonds so that less energy is
    needed for reaction.

57
Enzymes- really important little guys!
  • protein molecules, (or RNA molecules) can act as
    biological catalysts -are essential for the
    functioning of any cell.
  • Enzyme reactions depend on a physical fit between
    the enzyme, at its active site on a specific
    substrate.
  • the substrate and enzyme link together, it causes
    a slight change in the enzymes shape, which
    weakens some chemical bonds in the substrate,
    that reduce the amount of activation energy
    needed.

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How Enzymes Work
  • How Enzymes Work
  • Most reactions in a cell require very high
    temperatures to get going, which would destroy
    the cell. Enzymes work by lowering the Activation
    Energy of a reaction.

http//alevelnotes.com/Enzymes/144
  • Most reactions in a cell require high
    temperatures to start, which would destroy the
    cell. Enzymes work by lowering the Activation
    Energy of a reaction.

60
Examples
  • Enzymes like DNA polymerase make important
    molecules (like DNA) in cells.
  • Enzymes are used for a wide variety of purposes,
    such as Pepsin Trypsin in digestion.
  • Enzymes are also used to destroy invading
    Microorgansims. Phagocyte cells engulf pathogens
    and the endocytosed
  • vesicle then fuses with Lysosomes
  • which contain enzymes that destroy
  • the pathogen's cell membrane.

61
tutorvista.com
62
Enzymes Need Optimal Temperatures -Unwind if too
hot, dont work if too cool.
  • At high temperatures, enzymes denature (unwind)
    and lose their catalytic properties.
  • at low temperatures, the reaction rate decreases.

63
Enzymes also need optimal pH!
  • The pH at which enzymatic activity is maximal is
    known as the optimum pH.
  • Within limits, enzymatic activity increases as
    substrate concentration increases.

http//classes.midlandstech.com/carterp/Courses/bi
o225/chap05/ss2.htm
64
C. Lipids
  • Functions
  • Long-term energy storage.
  • -Generally insoluble in polar substances (water)
  • phospholipids are the major building block in
    cell membranes
  • hormones ("messengers") play roles in
    communications within and between cells.

65
Structure of Fatty Acids
  • The carboxyl head is polar- therefore it is
    HYDROPHILIC water loving
  • The hydrocarbon CH2 units are HYDROPHOBIC- water
    fearing
  • (not water soluble).

66
Fatty acids
  • Can be saturated (meaning they have as many
    hydrogens bonded to their carbons as possible)
  • Unsaturated (with one or more double bonds
    connecting their carbons, hence fewer hydrogens).
  • A fat is solid at room temperature, while an oil
    is a liquid under the same conditions. The fatty
    acids in oils are mostly unsaturated, while those
    in fats are mostly saturated.

67
2. Triglycerides
  • Triglycerides are composed of three fatty acids
    (usually) covalently bonded to a 3-carbon
    glycerol.

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Fats and oils function in energy storage.
  • Animals convert excess sugars into fats.
  • Most plants store excess sugars as starch,
    although some seeds and fruits have energy stored
    as oils (e.g. corn oil, peanut oil, palm oil,
    canola oil, and sunflower oil).
  • Fats yield 9.3 Kcal/gm, while carbohydrates yield
    3.79 Kcal/gm. Fats store six times as much energy
    as glycogen.

71
Diets Fat Intake
  • Attempts to reduce the amount of fats present in
    specialized cells known as adipose cells that
    accumulate in certain areas of the human body.
  • By restricting the intakes of carbohydrates and
    fats, the body is forced to draw on its own
    stores to makeup the energy debt.
  • The body responds to this by lowering its
    metabolic rate, often resulting in a drop of
    "energy level."
  • Successful diets usually involve three things
    decreasing the amounts of carbohydrates and fats
    exercise and behavior modification

72
3.  Phospholipids
  • One fatty acid is
  • replaced with a
  • phosphate.
  • The negative charge(s) of the phosphate makes the
    head of the phospholipid hydrophilic. The long,
    hydrocarbon tail is non-polar and, therefore,
    hydrophobic.

73
  •     

The water loving edge of the molecule orients
toward water- the inside and outside of the
cell. The water fearing edges of the molecule
orient toward each other to make a lipid
bilayer - the construction of the cell
membrane.
74
4. Cholesterol and steroids
  • Structure is a lipid with 4 carbon rings with
    various functional groups attached
  • Cholesterol has many biological uses, such as its
    occurrence in the cell membranes, and its role in
    forming the sheath of some neurons. Excess
    cholesterol in the blood has been linked to
    atherosclerosis, hardening of the arteries.
  • Steroids are mainly used as hormones in living
    things
  • Structure of four steroids. Image from Purves et
    al., Life The Science of Biology, 4th Edition,
    by Sinauer Associates (www.sinauer.com) and WH
    Freeman (www.whfreeman.com), used with permission.

75
D. Nucleic Acids
  • Function - informational molecules
    heredity/genetic, protein synthesis, and energy
  • A nucleotide is formed from a 5 carbon sugar, a
    phosphate and a nitrogen base.
  • Polymers formed by linking together long chains
    of nucleotide monomers.

76
  • 3 Nucleic Acids
  • DNA-deoxyribonucleic acid
  • Double strand of nucleotides
  • Double Helix shape
  • RNA-ribonucleic acid
  • Single strand nucleotides
  • ATP -Adenosine Triphosphate

77
Structure of DNA Structure of tRNA
-double strand of nucleotides -single
strand of nucleotides
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RNA differs from DNA in the following ways
  • RNA is single stranded while DNA is double
    stranded.
  • RNA has a sugar called ribose while DNA has a
    sugar called deoxyribose.
  • RNA has the base uracil while DNA has the base
    thymine.

80
How DNA RNA work together
  • DNA(deoxyribonucleic acid) is the genetic
    material.
  • It functions by storing information regarding
    the sequence of amino acids in each of the bodys
    proteins.
  • This "list" of amino acid sequences is needed
    when proteins are synthesized.
  • Before protein can be synthesized, the
    instructions in DNA must first be copied to
    another type of nucleic acid called messenger
    RNA.

81
3 types RNA
  • Messenger RNA, or mRNA.
  • carries the code for building a protein from the
    nucleus to the ribosomes in the cytoplasm. It
    acts as a messenger.
  • Transfer RNA or tRNA.
  • picks up specific amino acids in the cytoplasm
    brings them into position on ribosome where they
    are joined together in specific order to make a
    specific protein.
  • Ribosomal RNA or rRNA place for protein synthesis

82
How a protein is built
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