campbellessentialbiology4th ch.notes
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1. Order - order and organization
2. Regulation - within appropriate limits
3. Growth & Development - genes; instructions
4. Energy Utilization
5. Response to environment
6. Reproduction7. Evolution
Biosphere - all the environments on earth that support life; Earth.
- the whole is greater than the sum of its parts
Biosphere:
1. Biosphere
2. Ecosystem
3. Communities
4. Populations
5. Organisms
6. Organ systems & organs
7. Tissues
8. Cells
9. Organelles
10. Molecules & Atoms
Ecosystems - interaction between organisms & their environment
a. Process 1 - cycling of nutrients
b. Process 2 - gains and looses energy constantly
Cells and DNA:
Cells are the level which properties of life emerge
All organisms are composed of cells
2 types of cells
Prokaryotic - simpler and smaller, i.e. - bactieria
Eukaryotic - Plants, Animals, Fungi and protists. DNA holding nuclear
membrane.
DNA - composed of 4 different molecules (A, G, C, T)
human cell DNA is 3 billion chemical letters long
Biodiversity:
290,000 types of plants
52,000 types of vertebrates
Three domains:
1. Bacteria - or Eubateria; all true bacteria
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2. Archaea - Least evolved forms of life on earth, very similar to bateria
3. Eukarya - Animals, Plants, Fungi and Protists.
Bacteria & Archaea areprokeryotic
Evolution:
Charles Darwin 1859 - Origin of Species decent with modification
Natural Selection:
Darwins Observations:
1. Overproduction & competition
2. Individual variation
3. Unequal reproductive success
Steps of Natural Selection:
1. Population with varied inherited traits
2. Elimination of individuals
3. Reproduction of Survivors
4. Increasing frequency of traits of survivors
Scientific Method:
1. Observation
2. Question
3. Hypothesis
4. Prediction
5. Experiment
6. Result / Predicted result
Discovery Science: Observation and measurements are the data of discovery science
A Controlled Experiment has two groups:
Experimental group
Control group - the group which the experimental group is compared.
Theory is bigger in scope from hypothesis. Theory describes a general behavior and is
widely accepted
Culture in Science:
1. Dependence on observations & measurements others can varify
2. Requires that ideas are testable & repeatable.
Scientists build on each other byremaining scepticaland byseeking reproducible
evidence.
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Chapter 2 matter - anything that occupies space and has mass
elements - substances that cannot be broken down into other substances
92 naturally occurring elements
25 essential to life
O, C, H, P, K, S, Na, Cl, Mg, Ca
Trace: B, Cr, Co, Cu, F, I, Fe, Mn, Mo, Se, Si, Sn, V, Zn
Atomic # = number of protons
Mass # = sum of protons and neutrons in nucleus
Isotopes - have different number of protons and neutrons, differ in mass (ex:
Carbon 13; 6 protons, 7 neutrons)
Radioactive Isotope - isotope whos nucleus is decaying and giving off energy
due to instability (ex Carbon 14; 6 protons, 8 neutrons) compounds - substances containing 2 or more elements
atom - smallest unit of matter
Composed of Proton (+), Electron (-), and Neutron (neutral)
ion - electrically charged atom
ionic bond - bond formed from two oppositely charges ions
covalent bond - 2 or more atoms sharing outer shell electrons (e-) to form molecule to
better fulfill the octet rule.
hydrogen bond - weak attraction in polar molecules
Water
The polarity of water molecules and hydrogen bonding that results explain most
of waters life-supporting properties
cohesion - tendency for molecules to stick together. Responsible forsurface
tension and capillary action.
ice floats - crystal stucture of ice is less dense than liquid water.
Water is a solvent - solution = solvent + solute (aqueous solution)
evaporative cooling - loss of heat through evaporation of water.
water regulates the temperature of the biosphere.
Heat - amount of energy associated with the movement of the atoms and molecules in a
body of matter.
Temperature - measure of heat Acids & Bases & pH
Acids - release H+ in to solution
Base - release OH- (hydroxide ion) into solution
pH scale - logarithmic scale of the concentration of H+ ions. 0(acid) - 14(base); 7
neutral
Slight changes in pH can be very harmful to an organism
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Buffers - substances in biological fluids that prevent harmful changes in pH by
accepting or donating H+ when there is and excess or depletion of H+ ions
CO2 is absorbed by oceans when it combines with seawater which produces an
acid.
Chapter 3 Lactose - milk sugar (many people have a lack of lactase enzyme)
Organic Compounds organic compound - carbon based molecules
hydrogen, oxygen, and nitrogen are commonly found in organic compounds
hydrocarbons: carbon-hydrogen molecules
methane (CH4) is the simplest hydrocarbon
Functional Groups - groups of atoms that perform chemical reactions
hydroxyl group (-OH)
carboxyl group (-COOH)
polymers - large moleculesmade by stringing together smaller molecules called
monomers
dehydration reaction - chemical reactionthat removes a molecule of H2O
Hydrolysis - to break with water ; reverse of dehydration reaction
Carbohydrates - sugars or sugar polymers
monosaccarides - simple sugars that cannot be broken down by
hydrolysis (ex: glucose, fructose) [Glucose = C6H12O6 (fructose has same
chemical formula)]
isomers - molecules that have same molecular formula but different
structure (like glucose and fructose)
The shape of molecular structure is important
monosaccharides - the main fuel for cellular work
dextrose - aqueous solution of glucose
disaccharide - double sugar, contructed from 2 monosaccharides through
dehydration reaction (ie - lactose, maltose, sucrose)
sucrose - disaccharide; table sugar (glucose+fructose)
polysaccharide - long chains of sugar units. Polymers ofmonosaccharides.
glyocogen - animal polysaccharide, more extensively branched than
starch
cellulose - ploysaccharide used by plants for structure (animals this plant
fiber for dietary fiber or roughage)
Lipids - hydrophobic organic molecule; neither
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macromolecules nor polymers
fat - glycerol molecule + 3 fatty acid molecules via dehydration reaction
forming triglycerides
hydrocarbons (fatty acid) store a lot of energy
Omega 3 has double bond in certain spot.
stored in adipose cells
unsturated - do not contain maximum # of hydrogen atoms;
unstarurated fats tend to be solid at room tempurature. One fatty
acid is bent due to double bond.
atherosclerosis - lipid containing deposits in blood vessels.
hydrogenation - adding hydrogen, causes trans fats
steroids - hydrophobic molecules that behave like hormones like
testosterone and estrogen
Cholesterol Testosterone & type of estrogen
THG - synthetic steriod
Proteins - polymers of amino acids amino acid - central carbon with 4 covalent partners (monomer)
Amino Group
Carboxyl Group
Side group
Hydrogen
polypeptide - polymer
peptide bond - bond of amino acid
protiens are made up of one or more polypeptides.
leucine - hydrophobicamino acid
styrine - hydrophillicacid
hemoglobin - 146 amino acid chain
Primary Structure
Alpha helix
pleated sheet
Protein Shape
3D shape determines function
denaturation is loss of proper shape
Nucleic Acids
Nucleotides are monomers
Nitrogen base
sugar
phosphate group
DNA & RNA
DNA sugar is deoxyribose nucleic acid
RNA sugar is ribose
DNA - (A,G,C,T)
A - Adenine
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G - Guanine
T - Thynine
C - Cystocine
Adenine partners with Thynine
Guanine partners with Cystine
RNA - (A,G,C,U) U - Uracil
DNA RNA Amino Acid
Inability to make sufficient amounts of Lactase (enzyme that brakes down
lactose) is genetic; one letter change (C to T) causes this.
Chapter 4 - Tour of a Cell Intro
Antibiotics - drugs that disable or kill bacteria (penicillin, 1928)
ribosomes of humans and bacteria are sufficiently different that antibiotics only
bind to bacterial ribosomes
Microscopy
Resolving power- the ability of an optical instrument to show two objects as
separate
resolving power of human eye is about 0.1 millimeter apart
Light Microscopy (LM) - surface features, low resolving power, though much
better then human
Scanning Electron Microscopy (SEM) - surface features, high resolving power
Transmission Electron Microscopy (TEM) - Inner features, high resolving power
Robert Hooke in 1665 first described cells
Prokaryotic Cells - Domains Bacteria and Archaea
prokaryotic cells are said to be older in evolutionary sense (3.5 billion years
ago)
prokaryotic cells are generally much smaller then eukaryotic cells; about 1/10th
the length.
Eukaryotic Cells - Domains Protists, Plants, Fungi, andAnimals
eukaryotic cells are about 2.5 billion years
have organelles. All cells have:
A plasma membrane - thin outer membrane that regulates traffic of molecules
between the cell and its surroundings
DNA
Ribosomes - tiny structures that build protiens according to the instruction of
DNA
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Eurkaryoticcells have organelles
Nucleus - houses mose of a eukaryotic cells DNA
prokaryotic cells dont have a nucleus, DNA is bunched together in a region
called the nucleoid.
Someprokaryoticcells have a capsule, a sticky outer layer that surrounds the cell wall
some prokaryotes have pili and flagella that allow them to attach to surfacesand propel them through a fluid environment, repectively.
Eukaryotic Cells Organelles:
Mitochondrion
Nucleus
Rough Endoplasmic Reticulum
Smooth Endoplasmic Reticulum
Ribosomes
Golgi Apparatus
Plasma Membrane
Cytoskeleton
Only in Plant cells:
Central Vacuole
Cell Wall
Chloroplast
Only in Animal cells:
Centriole
Lysosome
Flagellum
Plasma Membrane
Composed of lipids and protiens
lipids belong to special category called phospholipids
phospholipids have 2 (hydrophobic) fatty acid tails and one (hydrophilic)
phosphate group head.
phosphate group is electrically charges making it hydrophilic (likes water),
but fatty acids are hydrophobic (fears water) making one end like water
and the other end avoids water
phospholipid bilayer, hydrophilic on outside and hydrophobic on inside
protiens float around phospholipid bilayer creating a fluid mosaic and
protiens regulate traffic across membrane.
Cell Walls
Plants have cell walls made of rigid cellulose fibers.
Animal cells secrete a sticky coat called an extracellular matrix instead of a cell
wall, and most have cell junctions, structures that connect to other cells.
Nucleus and Ribosomes
Structure and Function of Nucleus:
nuclear membrane - double layer membrane encasing nucleus
chromatin - long DNA molecules and associated proteins that form long
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fibers
chromosome - each long organized structure of chromatin fiber (humans
have 46)
nucleolis - where the components of ribosomes are made
Ribosomes
small dots in cell floating in cytoplasm and attached to endoplasmicreticulum.
responsible for protein synthesis
How DNA Directs Protein Production
1. DNA transfers information to mRNA (messenger RNA)
2. mRNA exits nucleus into cytoplasm though pores in nuclear
membrane
3. Ribosome moves along mRNA, generating a protein.
Endomembrane System: Manufacturing and Distributing Cellular
Products
Endoplasmic Reticulum (ER) - labyrinth of tubes and sacs that run throughoutcytoplasm. Rough & Smooth
Rough ER -ribosomes are attached, producing proteins into ER. ER forms
transport vesicles around proteins
Smooth ER - Part of endoplasmic reticulum that is responsible for detoxifying
cell and creates lipids
Transport Vesicles travel along the cytoskeleton, moving protiens to the Golgi
Apparatus
Golgi Apperatus - refinery, warehouse, shipping center
Transport vesicles from the ER come to the receiving side of the Golgi apparatus
and turn into pancake shapes and release proteins. Golgi produces digestive enzymes, waste or secretory proteins, and cell products
that are moved from the Golgi by the Golgi budding around the enzymes, waste,
or products.
Lysosomes - capsules that hold digestive enzymes that bud off golgi
digest macromolecules and old organelles
lysosomes burst in apoptosis releasing digestive enzymes into
cytoplasm causing the cell to digest itself and die.
Vacuoles - storage cells
Bud off the ER, Golgi Apparatus, or Plasma Membrane
Some are contractile to regulate chemistry
Central Vacuole - holds water for plant cells
Transport Vesicles
Also bud from Golgi (not just ER) to transport secretory proteins
out of the cell.
Chloroplasts and Mitochondria
Chloroplasts - where plant cells produce sugars
Inner and outer membrane
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Stroma - thick fluid inside inner membrane
Granum - stacks of thylakoids
Mitochondria - sites of cellular respiration
2 components:
1. Intermembrane Space2. Matrix
Inner membrane has folding called cristea that increase surface area.
Cytoskeleton
Maintains cell shape
Enables cell movement (amoebas, cilia, and flagella)
microtubles - highways of the cell
different types of fibers
Cilia and Flagella
Cilia are shorter and wiggle; little hairs
cilia lining of respitory tract moves mucus
Flagella whip around a bit like a screw, longer and tail-like
Chapter 5 - The Working Cell
Conservation of Energy Potential Energy (Stored) Kinetic Energy (moving working energy) Entropy (S)
amount of disorder always positive (increasing)
Chemical Energy (Potential Energy) Examples; Hydrocarbons
Octane + O2 Heat + Energy + CO2 + H2O (~30% efficiency) Fat + O2 Heat + Energy + CO2 + H2O (~40% efficiency) (Heat is a form of energy)
Calorie 1 calorie = the heat to raise (1 ml) of H2O (1 degree) Celsius. 1 Calorie = 1 kilocalorie
ATP and Cellular Work ATP - adenosine triphosphate
Each phosphate group is negatively charged Crowding of negative charges gives ATP its potential energy Energy is released when last phosphate is released off of the
triphosphatet tail creating ADP (adenosine diphosphate)
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ATP provides energy for three kinds of cell work: Mechanical Work Transport Work (transport molecules across plasma membrane) Chemical Work (making large molecules)
ATP Cycle Renewable resource
ATP ADP + Energy for Cell ADP + cellular respiration + P ATP
Enzymes metabolism - the tota of all the chemical reactions in an organism enzymes - protiens that speed up chemical reactions
enzymes lower activation energy activation energy - energy required to trigger a chemical reaction;
energy barrier
Induced Fit substrate - enzymes ability to recognize a certain reactant molecule; the
molecule that fits in the enzymes active site. (Lactose is the substrate of
Lactase)
active site - region of an enzyme that has the shape and chemistry thatfits a substrate molecule
induced fit - the change in shape of an enzyme slightly, making the fitbetween the substrate and the active site tighter.
Enzymes functions repeatedly, accepting and releasing substrates more thanonce
Many enzymes are named for their substrate with and -ase ending. (i.e. -lactose and lactase) Enzyme Inhibitors - substrate impostors that plug up the active site of andenzyme, disrupting its function
some inhibitors regulate metabolism penicillin and nerve gas are examples of enzyme inhibitors feedback regulation - keeps cell from wasting resources by using
inhibitors
Membrane Function Transport proteins - transport materials in and out of the cell, through the
plasma membrane
Membrane Protein Functions Cell signaling - binding cite of chemical messanger Attachment to cytoskeleton and extracellular matrix to help maintain
shape
Enzymatic activity - active sites that fit substrates; some proteins mayteam up to carry out steps of a pathway
Transport - provide channel for a solute (integral protein) Intercellular joining - proteins that link adjacent cells (integral protein)
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Cell recognition - proteins with chains of sugars serve as identificationtags recognized by other cells. (peripheral protein)
Diffusion - movement of molecules to spread out into available space passive transport - cell does not expend energy to transport materials
with diffision
facilitated diffusion - a type of passive transport concentration gradient - region where the density of a substancechanges. Concentration represented with square brackets [ ] (i.e.-
concentration of hydrogen ions is [H+].
Osmosis and Water Balance osmosis - diffusion of water across a selectively permeable membrane hypertonic - side with higher concentration of solute hypotonic - side with lower concentration of solute (higher H2O
concentration)
Water moves from hypotonic side to hypertonic side. isotonic - equal concentration osmoregulation - regulation of water balance so to not burst (lysis) or
dehydrate.
plasmolysis - when the under hydrated plant cells plasma membranepulls away from its cell wall
Active Transport Active transport - pumping of molecules across membranes; this
requires energy. Pumping a solute against its concentration gradient.
Energy Source: ATP
Exocytosis and Endocytosis - bulk shipment traffic of large molecules (macromolecules) macromolecules are too large to travel through the plasma membrane membrane forms sacs, packaging larger molecules into vesicles Exocytosis - transport vesicles inside cell fuse to plasma membrane,
secreting proteins out of cell (like from Golgi)
Endocytosis - reverse of exocytosis. Takes material into cell withinvesicles that bud inward. 3 types:
pinocytosis - (nonspecific) cellular drinking; gulping fluid droplets phangocytosis - (nonspecific) cellular eating; engulfs particle and
forms food vacuole.
receptor-mediated endocytosis - triggered by certain molecules(specific) binding to the outside of plasma membrane. (like in
neurotransmitters)
Cell signaling signal transduction pathway - passing a signal through relays that turn
into chemical reactions. (i.e. - adrenaline triggers glycogen glucose
without entering cell)
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Chapter 6 - Cellular Respiration Intro
Marathon runners slow-twitch use O2 (aerobic) to make ATP
Sprinters fast-twitch no O2 (anaerobic) to make ATP
Energy Flow and Chemical Cycling Photosythesis - using light to build organic molecules Producers and Consumers
Autotrophes - self-feeders, organisims that make their own orgainicmatter (carbohydrates, lipids, protiens, & nucleic acids) from inorganic
sources (CO2, H2O, minerals). (producers)
Heterotrophs - other-feeders, organisims that cannot make organicmolecules from inorganic ones. Eat organic material (consumers)
Chemical Cycling Between Photosynthesis and Cellular Respiration photosynthesis needs CO2 and H2O
chloroplasts use light energy to rearrange atoms to producesugars (glucose C6H12O6) and other organic molecules
byproduct is O2 Cellular respiration uses O2 and energy extracted from organic sources
(like glucose) to make ATP
production of ATP in plants and animals occurs mainly inorganelles called mitochondria
By product is CO2 and H2O, same as whats needed forphotosynthesis.
Cellular Respiration: Aerobic Harvest of Food Energy
aerobic - requires oxygen The overall equation for cellular respiration
C6H12O6 + 6 O2 6 CO2 + 6 H2O + ATP The main function of cellular respiration is to generate ATP One glucose molecule can produce up to 38 ATP molecules Cellular respiration transfers H atoms from glucose to O, forming H2ORole of Oxygen in Cellular Respiration
During cellular respiration, hydrogen and its bonding electrons change partnersfrom sugar to oxygen, forming water as a byproduct
Redox Reactions
redox reaction - oxidation-reduction reation oxidation - loss of electrons
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reduction - acceptance of electrons (reduce the amount of positive charge) Oxygen is reduced during cellular respiration, accepting election (and oxygen)
lost from glucose
C6H12O6 oxidation 6 CO2 6 O2 reduction 6 H2O
When water is produced in a redox reaction, energy is released (potentialchemical energy is released)
NADH & Electron Transport Chain
1. First carrier of electrons is NAD+ (nicotinide adine dinucleotide)
2. NAD+ is reduced to NADH
3. NADH travels to the electron transport chain eventually forming H2O
Each link in the electron transport chain is a molecule, usually a protein.
Series of redox reaction first accepts then donates electrons
Each transfer releases a small amount of energy used indirectly to form ATP
NADH carries electrons from glucose (and other fuel molecules) and deposits
them at the top of the electron transport chain electrons cascade down the chain, molecule to molecule. Molecule at the bottom
drops the electrons to oxygen forming H2O.
glucose NADH Electron transport chain H2O
The stepwise release of chemical energy in the electron transport chain produces
most of the ATP
Oxygen, the electron grabber makes this all possible. Fuctions as gravity
pulling object downhill.
An overview of Cellular Respiration
1. Glycolysis - molecule of glucose is split into two molecules of pyruvic acid.Enzymes for glycolysis are located in the cytoplasm, outside the mitochondria
2. Citric Acid Cycle - Pyruvic acid enters mitochondria after being split byglycolysis. The Citric Acid Cycle completes the breakdown of glucose all the way
down in to CO2 inside the mitochondria matrix.
3. Eletron Transport Chain - electrons are captured from food (glucose, pyruvicacid, etc.) by NADH formed in the first two stages fall down the Electron
Transport Chain, to oxygen. Electron transport from NADH to oxygen releases
the energy your cells use to make most of their ATP.
The Three Stages of Cellular Respiration
1. Glycolysis - splitting of sugar1. 6-carbon glucose molecule is broken in half forming two 3-carbon
molecules (Pyruvic acid)
2. The 3-carbon molecules donate electrons to NAD+ forming NADH
3. Glycolysis also makes 2 ATP molecules directly when enzymes transfer
phosphate groups from fuel molecules to ADP and two pyruvic acid
molecules.
2. Citric Acid Cycle - pyruvic acid from glycolysis ispreppedfor the Citric AcidCycle forming acetic acid and then down to CO2. This process happens twice
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per glucose molecule (2 Pyruvic acid molecules 2 ATP, 6 NADH, 2 FADH2)
Preparation for Citric Acid Cycle
1. Pyruvic acid loses a carbon forming acetic acid and CO22. Oxidation forms NADH, (NAD+ take two electrons)3. Acetic acid attaches to Co-enzyme A (CoA) to form acetyl CoA.
CoA escorts acetic acid to the Citric Acid Cycle.2. Acetic acid joins 4-carbon acceptor to form 6-carbon citric acid for every
one acetic acid that enters the cycle as fuel
3. Two CO2 molecules exit as waste, citric acid cycle harvests energy from
fuel.
4. Some energy is used to produce ATP directly.
5. NADH is formed 3 NADH
6. FADH2 is formed (flavenoid)
7. All carbons that enter as fuel are accounted for as CO2, and 4-carbon
acceptor molecule is recycled
3. Electron Transport Chain - uses the energy released by the fall of electronsto pump H+ across the inner mitochondrial membrane, then [H+] gradient is
used to produce ATP (square brackets are used to indicate concentration of a
substance, here concentration gradient of H+ ions)
1. NADH transfers 2 electrons to an electron carrier in the first protein
complex, pumping H+ from in the matrix across the inner mitochondrial
membrane
2. FADH2 transfers electrons to a carrierthat transfers H+ to the second
protein complex.
3. Electrons fall through second protein complex pumping out more H+
ions across the inner mitochondrial membrane and a second carrier
moves the electrons from the second protein complex to the third proteincomplex.
4. Oxygen pulls the electron down the chain out of the third protein
complex, combining with H+ in matrix forming H2O, in the process
pumping more H+ across the membrane as well.
5. All of the H+ stored on the outside of the inner wall falls downhill
through the ATP synthase protein. This spins a component of the ATP
synthase.
6. The rotation of the ATP synthase actives part of the synthase molecule
that attach phophate groups to ADP molecules to generate ATP. ATP
synthase produces most of a cells ATP in aerobic cellular respiration (~34
ATP produced)
The Versatility of Cellular Respiration
Cellular respiration can burn many different kinds of molecules, not just
glucose.
Adding up ATP form cellular repiration
Glycolysis and Citric Acid Cycle each directly produce 2 ATP (Totalling 4
ATP)
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ATP synthase produces the rest, to total up to 38 ATP molecules per
glucose molecule.
Fermentation: Anaerobic Harvest of Food Energy
anaerobic - without oxygen fermentation - anaerobic process that cells use for short periods to produce energy
Fermentation in Human Muscle Cells
Blood provides cells with O2
Anaerobic process occurs when body is burning ATP faster than it can deliver O2
for electron transport chain.
Fermentation relies on glycolysis
glycolysis does not require O2, and produces 2 ATP for every molecule
broken down to pyruvic acid.
Cells have to consume more glucose fuel per second, because less ATP per
glucose is being generated NAD+ must be present as an electron acceptor
in aerobic conditions, NAD+ regenerates when NADH drops electron
cargo down electron transport chain
In Anaerobic conditions, NADH disposes electrons by adding them to pyruvic
acid producing a waste product lactic acid.
lactic acid is transported to liver
Fermentation in Microorganisms
2 ATP per glucose is enough energy to sustain many micoorganisms
sharp flavors (like in cheese) are due to lactic acid
Yeast is capable of both cellular respiration and fermentation when forced to be anaerobic, they are forced to fermentation, producing
ethyl alcohol instead of lactic acid. (as well as CO2)
Human heart can use lactic acid as fuel.
Chapter 7 - Photosynthesis: Using Light
to Make Food Intro
biomass - living material
biofuels - fuel from living material
The Basics of Photosynthesis
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Photosynthesis - a process by which plants, algae (protists), and certain bacteria
transform light energy in to chemical energy.
Autotrophs
Chloroplasts: Sites of Photosynthesis
Chloroplasts - light absorbing organelles
Chlorophyll - Light absorbing pigment the chloroplasts (often green) that plays acentral role in converting solar energy to chemical energy
chloroplasts are concentrated on the interior of cells of leaves
Stomata - where CO2 enters the O2 exits; tiny pores
H2O absorbed by plants roots
chloroplasts have double membrane like mitochondria
Stroma - thick fluid that fills the inner membrane of chloroplasts
Thylakoids - interconnected membrane sacs suspended in stroma
Grana - concentrated stacks of thylakoids.
chlorophyll molecules are built into the thylakoid membranes
The Overall Equation of Photosynthesis 6 CO2 + 6 H2O + Light Energy C6H12O6 + 6 O2
Photosynthesis take exhaust from cellular respiration
Electrons are boosted and added to CO2 to produce sugar
Hydrogen moved with electrons to H2O and CO2 in a redox reaction
chloroplasts must split H2O to perform this reaction
A Photosynthesis Road Map
Photosynthesis happens in 2 stages: Light Reaction and Calvin Cycle
Light reaction - chlorophyll in the thylakoid membrane absorbs solar energy,
which is then converted to the chemical energy of ATP and NADPH
NADPH - electron carrier light drives electrons from H2O to NADP+ (oxidized form of carrier) to form
NADPH (reduced form of carrier)
H2O is split providing source of electrons and O2 is released
Calvin Cycle - uses products of light reaction to produce sugar from O2
enzymes for Calvin Cycle stored in stroma
ATP provides energy for sythesis of sugar
NADPH provides electrons for reduction of CO2 to sugar (glucose)
The Light Reactions: Converting Solar Energy to
Chemical Energy
The Nature of Sunlight
radiation energy
Wave and Particle energy
wavelength - distance between crests of 2 adjacent waves
electromagnetic spectrum - full range of radiation. Gamma rays to radio waves,
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visible light is a very small fraction of this spectrum
The wavelengths not absorbed are reflected
green is poorly absorbed by chloroplasts and is reflected and transmitted
toward the observer
Chloroplast Pigments
Chlorophyll-a - absorbs mainly blue-violet and red light; participates directly inlight reactions
Carotenoids - absorbs blue-green light
some energy is passed to chlorophyll-a
carotenoids protect by absorbing and dissipating excessive light that
could damage chlorophyll
Carrots, fall colors
Chlorophyll-b - absorbs blue and orange.
How Photosystems Harvest Light Energy
particle light
Photons - fixed quatities of light energy shorter the wavelength of light, the greater the energy of photon
photon of violet is nearly twice the energy of red photon
When pigment molecule absorbs a photon, the pigments electrons gain energy to
an excited state (higher orbital), which is highly unstable.
Electron falls back to ground state almost immediately releasing heat and
sometimes light (floresence). In photosystems, this excited electron is grabbed
instead of falling back down.
Photosystem - a cluster of a few hundred pigment molecules (chlorophyll-a,
chlorophyll-b, and carotenoids)
photosystems function as a light gathering antennae.
Reaction center - a chlorophyll-a molecule that sits next to aprimary electron
acceptor
Primary Electron Acceptor- traps light-excited electron from chlorophyll-a in
the reaction center
How the Light Reactions Generate ATP and NADPH
1. Photons excite electrons in chlorophyll of water-splitting photosystem. Electrons
are trapped by primary electron acceptor. The H2O splitting photosystem
replaces its light-excited electrons by extracting the electrons form H2O. O2 is
released
2. Energized electrons from H2O splitting photosystem pass down an electron
transport chain to the NADPH-producing photosystem. The chloroplast uses the
energy released by this electron fall to make ATP.
3. The NADPH-producing photosystem transfers its light-excited electrons to
NADP+, reducing it to NADPH
ATP production is very similar to cellular respiration, using [H+] gradient to power
ATP synthase in thykaloid membrane
The Calvin Cycle: Making Sugar from Carbon Dioxide
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Sugar factory within stroma of cholorplasts. Uses ATP and NADPH
Like Citric Acid Cycle, starting material is regenerated (3-carbon sugar)
CO2 + ATP + NADPH G3P
G3P - glyceraldehyde 3-phosphate
G3P is raw material to make glucose and other organic compounds
(cellulose, starch, etc.) CO2 (from air) is added to RuBP (5-carbon sugar)
ATP & NADPH form two 3-carbon sugars ( ADP and NADP+ for electron
transport chain)
Every three CO2 molecules added makes one 3-carbon (G3P) sugar to use (two
3-carbon molecules makes one glucose)
One extra G3P from Calvin cycle is taken to make glucose and other molecules,
the rest is recycled into the Calvin Cycle.
Solar Driven Evolution
C3 Plants - plants that use CO2 directly
When weather is hot, stomata close holding in H2O but also do not allow CO2 in,halting sugar production
C4 Plants orCAM plants - use alternative modes of incorporating carbon
(shuttle cells) from CO2 to allow them to save water without giving up sugar
production. (sugarcane and corn (C4), pineapple and cacti (CAM))
Chapter 8 - Cellular Reproduction: Cells
from Cells (Part A)
What Cell Reproduction Accomplishes
Cell Division - two daughter cells that are genetically identical
chromosomes - structures that contain most of an organisms DNA. Daughter cells
receive identical sets of chromosomes
Millions of cells must divide every second to replace damaged or lost cells in ones body
Cell division is also vital for reproduction of an organism
Asexual Reproduction - does not involve fertilization of and egg by sperm. Reproduceby dividing in half and offspring are genetic replicas of the parent, inheriting all of their
chromosomes from a single parent
Mitosis - the type of cell division that is responsible for asexual reproduction and the
growth and maintenance of multicellular organisms
Sexual Reproduction - requires fertilization of an egg by sperm
Meiosis - special type of cell division which occures on in reproductive organs (such as
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testes and ovaries in humans)
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Sexual organisms require both mitosis for growth and development and meiosis for
reproduction
The Cell Cycle and Mitosis
Almost all Genes of a eukayotic cell - around 21,000 in humans - are located in thechromosomes in the cell nucleus.
Eukaryotic Chromosomes
Each eukaryotic chromosome contains on very long DNA molecule, typically
bearing thousands of genes
Chromatin - combination of DNA and protein molecules that make
chromosomes
protein molecules help organize the chromatin and help the activity of
genes
Most of the time, the chromosomes exist as a diffuse mass of fibers that are
much longer that the nucleus they are stored in. Stretched out, DNA would belonger than a person
As a cell prepares toe divide, its chromatin fiber coil up, forming compact
chromosomes. When the cells are not dividing chromosomes are too thin to be
seen with a Light Micrograph
Histones - found only in eukaryotes, small proteins that help DNA pack into
small packages
Nucleosome - small beads of DNA wrapped around histones; appear as small
beads on a string in an electron micrograph
When preparing to divide, the beaded string packs into a tight helical fiber, this
fiber coils further into a thick supercoil
Looping and folding further compact DNA
Before cell begins division process, the DNA molecules of each chromosome
is copied through a process call DNA replication producing 2 copies call sister
chromatids
Centromere - the narrow waist where two sister chromatids are joined.
Once seperated from its sister, each chromatid is considered a full fledged
chromasome
The Cell Cycle
Cell cycle - the ordered sequence of events that extends from the time a cell is
first formed from a dividing parent cell until it own division into two cells
Interphase - most of the cell cycle; the time when a cell performs its normalfunctions within the organism. Lasts at least 90% of cell cycle.
During interphase, a cell roughly doubles everything in its cytoplasm.
It increases supply of proteins, organelles (such as mitochondria and
ribosomes), and grows in size.
From the standpoint of cell reproduction, the most important event of
interphase is chromosome duplication
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G1 phase - (G for gap) occures before S phase
S phase - (S for DNA synthesis) approximately in the middle of the
interphase, this is the phase when chromosomes duplication occures
G2 phase - occurs after S phase, cell is preparing to divide.
M phase - (Mitotic Phase) part of the cell cycle when the cell actually dividing
Includes two overlapping processes: mitosis and cytokinesis Cytokinesis - cytoplasm is divided in two. Begins before mitosis is
completed
Combination of mitosis and cytokinesis produces 2 genetically identical
daughter cells, each with its own nucleus, organelles, cytoplasm, and
plasma membrane.
Mitosis and Cytokinesis
Mitosis is a continuum divided into 4 main stages (P.M.A.T.):
1. Prophase - chromatin fibers coil and appear as two identical chromatidsjoined at the centromere. Mitotic spindle begins to form
mitotic spindle - football shaped structure of microtubles thatguides the separation of the two sets of daughter chromatids.
Microtubles connect to proteins located at the centromere.
2. Metaphase - mitotic spindle fully formed and centromeres line up onimaginary plate
3. Anaphase - When sister chromatids separate. Each considered a fullfledged (daughter) chromosome.
4. Telephase and Cytokinesis - 2 groups of chromosomes have reachedopposite ends of cell. Telephase opposite of prophase, nuclear envelopes
form and chromosomes uncoil.
cleavage furrow - indentation at equator of cell. A ring of
microfillaments in the cytoplasm contracts just under the plasma
membrane. Used in cytokinesis of animal cells.
cell plate - the beginning of a new cell wall. Used in cytokinesis of
plant cells. Transport vesicles bring material to make cell wall to
equator of cell and release material. The material forms together
to produce a cell plate.
Cancer Cells: Growing out of control
Cell cycle control system - system of specialized protiens that integrate information
form the environment and form other body cells and sent STOP and go-ahead signalsat certain key points during the cell cycle using transduction pathways
Muscle and brains cells never receive signal to go beyond G1.
What is Cancer?
Disease of cell cycle
Cells divide excessively and can invade other tissues
Cell is transformed because of genetic change (mutation) in one of more genes
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that encode proteins in the cell cycle control system
Tumor- if bodys immune system fails to destroy the cell. (All it takes is one cell)
Benign Tumor- if the abnormal cells remain at the original site. Usually can be
completely removed by surgery
Malignant Tumor- a tumor can spread to neighboring tissues and other parts of
the body through blood stream. Cancer- a disease of an individual with a malignant tumor.
Cancer Treatment
Slash, burn, and poison
Remove tumor slash
Radiation Therapy - burn
side effects nausea, hair loss.
Chemotherapy - drugs that disrupt dell division poison
paclitaxil - from the Pacific Yew tree
Metastasis - The spread of cancer cells beyond their original site.
Cancer Prevention and Survival Not smoking
Excercise
High-fiber diet
Low fat diet
Chapter 10: The Structure and Functionof DNA
Intro
flu vaccine
influenza virus
virus - nucleic acid and protien
DNA: Structure and Replication
molecular biology - study of heredity at the molecular level.
Discovery of DNA led to a race to discover how the structure of this molecule could
account for its role in heredity
DNA and RNA Structure
DNA and RNA are nucleic acids
Nucleotides - monomers of DNA
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Polynucleoties - nucleotide polymer
polynucleotides tend to be very long and can have any sequence of
nucleotides, so a large number of polynucleotide chains are possible
nucleotides are joined together by covalent bonds between the sugar of one
nucleotide and the phosphate of another nucleotide
Sugar-phosphate backbone - repeating pattern of sugar - phosophate - sugar -phosphate that form the backbone of polynucleotides
nitrogenous bases are arranged like ribs that project from the backbone.
Each nucleotide has three components:
a. Phosphate group - with phosphorus atom at center, the source of
the acid in nucleic acid
b. Sugar - 5 carbon atoms, 4 in its ring and one extending above the ring.
(Deoxyribose is missing an oxygen atom that ribose has)
c. Nitrogenous base - Thymine [T], Cytosine [C], Adenine [A], and Guanine
[G]. T and C are single ring structures, and A and G are larger double ring
structures.
RNA had Uracil [U] instead of Thymine [T], and a different sugar call ribose.
Watson and Cricks Discovery of the Double Helix
Cambridge University, x-ray crystallography
X-ray image taken by Rosalind Franklin
Watson concludes x-ray image reveals a double helix
Double helix - spiral shape made of two strands, in DNA the two strands are
polynucleotide strands
Specific base pairing - four kinds of nitrogenous bases pair in a specific way
Each base has chemical side groups that can best form hydrogen bonds wit
hone appropriate partner
Adenine [A] with Thymine [T]
Guanine [G] with Cytocine [C]
(At The Grocery Ctore, A-T G-C)
Double helix looks like a twisted rope ladder
No restriction on the sequence of nucleotides along the length of the DNA
Watson and Cricks discovery published in Nature scientific journal in 1953
Watson, Crick, and Wilkins received Noble Prize in 1962, (Franklin died of
cancer)
DNA Replication
Watson and Crick suggest that DNAs structure serves as a mold, or template, to
guide reproduction of another strand
If one knows the sequence of the nitrogenous bases on one strand of the double
helix, on can very easily determine the sequence of the nitrogenous bases in the
other strand by applying base pairing rules
Enzymes link the nucleotides to form the new DNA strands (2 from 1)
DNA replication is complex and requires the cooperation of more that a dozen
enzymes and other proteins
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DNA polymerase - enzymes that make the covalent bonds between the
nucleotides of a new DNA strand.
The process is both fast and amazingly accurate, DNA replication proceeds at 50
nucleotides per second, with fewer then one in a billion incorrectly paired
DNA polymerase and some of hte associated proteins are also involved in
repairing damaged DNA DNA can be harmed by toxic chemicals and by high-energy radiation
Origins of replication - specific sites on a double helix where DNA replication
begins
DNA replication
DNA replication proceeds in both directions, creating bubbles
Parental DNA opens up (bubbles get bigger) as daughter strands
elongate
Eukaryotic DNA has many origins where replication can start
simultaneously, shortening total time of process
Bubbles merge, yielding two completed double-stranded daughter DNA
molecules
DNA replication ensures that all the bodys cells in a multicellular organism can
carry the same genetic information
It is also the means by which genetic information is passed along to offspring
The Flow of Genetic Information from DNA to RNA to
Protein
How an Organisms Genotype Determines Its Phenotype
Genotype - an organisms genetic makeup; the sequence of nucleotide bases inits DNA.
Phenotype - an organisms physical traits that arise from the actions of a wide
variety of proteins.
Indirectly, DNA carries instructions to build proteins
central dogma [Francis Crick] - chain of command: DNA RNA Protein
Transcription - the transfer of genetic information from DNA to RNA molecules
Translation - the transfer of information from RNA into a protein
Relationship between genes and proteins first proposed by Archibad Garrod in
1909
George Beadle and Edward Tatum in the 1940s, from bread mold, make a
breakthrough and show individual genes dictate the production of specific
enzymes
The function of a gene is to dictate the production of a polypeptide
(polypeptide - amino acid polymer linked by peptide bonds)
From Nucleotides to Amino Acids: An Overview
When a segment of DNA is transcribed, the result is an RNA molecule
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transcription - is called so because the nucleic acid language of DNA has
simply been rewritten (transcribed) a sequence of bases of RNA; the language is
still that of nucleic acid.
RNA is synthesized using the DNA as a template
translation - is the conversion of the nucleic acid laguage to the polypeptide
language polypeptides are the polymers chains consisting of 20 different amino
acid monomers
the sequence of the nucleotides of the RNA molecule dictates the
sequence of amino acids of the polypeptide
triplets of bases are the smallest words (codons) of uniform length that
specify all the individual amino acids
64 possible code words (43); enough triplets to allow more that one
coding fro each of the 20 amino acids.
codons - the 3-base words of nucleic acid chains
1 DNA codon (3 nucleotides) 1 RNA codon (3 nucleotides) one amino acid
The Genetic Code
Genetic code - set of rules relating to nucleotide sequence to amino acid
sequence
AUG sequence of amino acids in RNA has dual function; amino acid methionine
(Met) and signal for the start of the polypeptide chain.
Three codons, UAA, UAG, and UGA, do not designate amino acids and function
as stop codons
The nucleotides making up the codons occur in a linear order in the DNA and
RNA, with no gaps separating the codons
Almost all the genetic code is shared by all organism, from the simplest of
bacteria to the most complex plants and animals.
Because diverse organisms share a common genetic code, it is possible to
program one species to produce a protein from another species by transplanting
DNA. (like transplanting the instructions for the production of GFP, green
florescent protein, from jelly fish to mice to make glowing mice)
Transcription: From DNA to RNA
RNA polymerase - transcription enzyme that lin RNA nucleotides
Three steps:
1. Intiation of Transcription - the attachment of RNA polymerase to promoter
and the start of RNA synthesis
promoter- a nucleotide sequence that provides the starttranscribing signal, a specific place where DNA polymerase
attaches
promoter dictates which of the two DNA strands is to betranscribed
2. RNA Elongation - RNA grows longer
RNA synthesis continues, RNA strand peels away from DNA
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template, allowing DNA strands to come back together within the
RNA polymerase
3. Termination of Transcription - sythesis stops
terminator- special sequence of bases in DNA template thatsignals the end of the gene
RNA polymerase molecule detaches from the RNA molecule andthe gene (section of DNA molecule), and DNA molecule strands
rejoin.
2 other types of RNA are also produced on top of the amino acid sequence that
are involved in building polypeptides
Processing of Eukaryotic RNA
Capping, tailing and splicing
Eukaryotic, unlike prokaryotic cells, modifies (or processes) RNA transcripts
before they move out to the cytoplasm
Cap and tail - additions that protect the RNA form attack by cellular enzymes
and help enzymes recognize RNA as mRNA (messenger RNA) Introns - non-coding sections of nucleotides randomly interspersed in RNA
between exons which are removed before mRNA enters cytoplasm.
Exons - parts of the genes that are expressed.
RNA splicing - the process of joining exons and clipping out introns.
RNA splicing is believed to play a significant role in human cells by allowing our
approximately 25,000 genes to produce many thousands more polypeptides by
varying the exons that are included in the final mRNA
Translation: The Process
Translation is the divided into the same three phases as transcription, Initiation,
Elongation, and Termination.
1. Initiation - bringing together mRNA, the first amino acid with its tRNA, and
the two subunits of a ribosome
i. An mRNA molecule attaches to a small ribosomal subunit. A
special tRNA initiator binds to the start codon (AUG or methionine)
with anticodon UAC
ii. A large ribosomal subunit binds to the small ribosomal subunit,
creating a functional ribosome. The initiator tRNA fits into the P
site on the ribosome
2. Elongation - amino acids are added one by one to the first amino acid in a
three-step process
i. Codon recognition - anticodon of an incoming tRNA molecule,carrying its amino acid, pairs with the mRNA codon in the A site of
the ribosome.
ii. Peptide bond formation - the polypeptide leaves the tRNA in the
P site and attaches tothe amino acid on the tRNA in the A site.
Ribosome catalyzes bond formation and the chain has one more
amino acid.
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iii. Translocation - the tRNA in the P site leaves the ribosome,
and the remaining tRNA in the A site, carrying the growing
polypeptide, moves to the P site and process is cycled back to
step (2.i), codon recognition.
3. Termination - elongation continues unit a stop codon is reached (UAA,
UAG, and UGA) in the ribosomes A site. The completed polypeptide,typically several hundred amino acids long, is freed, and the ribosome
splits into its subunits.
Review: DNA RNA Protein
In eukaryotic cells, transcription occurs in the nucleus, and RNA is processed
before it enters the cytoplasm
Translation is rapid; a single ribosome can make an average sized polypeptide in
less than a minute
As the polypeptide is being made it coils into its 3-dimentional tertiary structure.
Several polypeptides may come together forming a protein with a quaternary
structure. The overall significance of transcription and translation is that transcription are
processes whereby genes control the structure and the activities of cells - or
more broadly, the way a genotype produces the phenotype.
Genes in DNA dictates complementary sequence of nucleotides in the mRNA
(transcription) mRNA specifies the linear sequence of amino acids in a
polypeptide (translation) these polypeptides determine the appearance and
capabilities ofthe cell and organism
Mutations
Mutation - any change in the nucleotide sequence of DNA
Occasionally, a base substitution leads to an improved protien or one with
new capabilities that enhance the success of the mutant organism and itd
decendants
Types of Mutations: Base substitution, Deletions, and Insertions
1. Base substitution - replacement of one base, or nucleotide, by another.this can result in no change in the protein (base redundancy), and
insignificant change, or a change that might be crucial to the life of the
organism.
silent mutation - base substitution results in a base redundancyand no change in protein product.
missence mutation - when changes of a single nucleotide dochange the amino acid coding, but have little or no effect on theshape or function of the resulting protein.
nonsence mutation - base substitution that results in a changeof an amino acid codon into a stop codon, resulting protein is
incomplete
2. Nucleotide Deletion - when a nucleotide is deleted, all codons from thatpoint on (downstream) are misread. Resulting polypeptide is likely to be
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completely nonfuntional.
3. Nucleotide Insertions - When a nucleotide is inserted. Disrupts allcodons that follow (downstream), most likely producing a nonfuntional
polypeptide
Mutagens
Mutagens - physical and chemical agents that are sources of mutations
Most common mutagen is high-energy radiation such as x-rays and UV light
Chemical mutagens are various types, some are similar to normal DNA bases
which cause incorrect base pairing when incorperated into DNA.
Many mutagens act as carcinogens, agents that cause cancer.
Although mutations are often harmful, they can also be extremely useful in nature
and in the labratory
Mutations are one source of the rich diversity of genes in the living world, a
diversity that makes evolution by natural selection possible.
Mutations are responsible for the different alleles (an alternative version of a
gene) needed for genetic research.
Viruses and Other Noncellular Infectious Agents
Viruses are not considered alive because it is not cellular and cannot reproduce on its
own.
virus - nucleic acid molecule wrapped in a protein coat. genes in a box
viruses survive only by infecting a living cell with genetic material that direct the cells
molecular machinery to make more viruses.
Bacteriophages
Bacteriophages - viruses that attack bacteria. bacteria - eaters, phages forshort
T4 virus infects e. coli, head made of DNA enclosed in an elaborate protein
structure, tail, a hollow structure enclosed in a springlike sheath, and tail fibers
which are the legs that bend and touch the cell surface.
Lytic cycle - after many copies of the phage are produced, the bacterium lyses
releasing phages. Reproductive cycle for most bacteriophages
Lysogenic cycle - viral DNA replication occurs without phage production or
death of the host cell
1. Viral DNA, prophage (viral DNA in host DNA) is inserted into bacterial
chromosome
2. Host cell replicates, reproducing the prophage DNA with the cellular DNA.A single infected bacterium can quickly give rise to a large population of
bacteria that all carry prophages.
3. Something, like an environmental change, triggers the release of the
prophages from the bacterial chromosome, and switches to the lytic
cycle.
Diphtheria (upper respiratory tract illness), botulism, and scarlet fever
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would be harmless to humans if it were not for the prophage genes they
carry.
Plant Viruses
Most plant viruses have RNA rather than DNA as their genetic material.
Viruses must get past the outer protective of plants, which makes plants
damaged by wind, chilling, injury or insects more susceptible to infection that ahealthy plant
No cure for most viral plant diseases.
Animal Viruses
influenza virus is an example of an animal virus
Outer envelope made of phospholipid membrane that allow virus to enter and
leave a cell.
Projecting protein spikes
Many animal viruses have RNA as their genetic material (common cold, measels,
mumps, HIV, and polio are all RNA viruses)
RNA virus reproduction1. Protein spikes attach to receptor proteins on the cells plasma membrane
and the viral membrane fuses with the cells membrane allowing protein
coated RNA to enter the cytoplasm
2. Enzymes remove protein coat.
3. An enzyme that entered the cell as part of the virus, uses the viruss RNA
genome as a template for making complementary strands of RNA which
have two purposes (4 & 5)
4. mRNA for synthesis of proteins
5. Templates for new viral genome DNA
6. The new coat of proteins assemble around the new viral RNA
7. Virus leave the cell by cloaking themselves in the plasma membrane
DNA viruses include hepatitis, chicken pox, and herpes.
Herpesvirus (chickenpox, shingles, cold sores, and genital herpes) enveloped
DNA viruses that reproduce in the cells nucleus, rather than the cytoplasm.
Herpesvirus get envelopes from nuclear membrane, rather than plasma
membrane.
Copies of herpevirus DNA usually remain behind as mini-chromosomes in the
nuclei of certain nerve cells, and remain latent until they are triggered (by stress,
or sunburn, or catching a cold, etc.)
Over 75% of American adults are the thought to carry herpes simplex 1 (cold
sores), and over 20% carry herpes simplex 2 (genital herpes). Viruses that attack non replaceable tissue (like nerve cell poliovirus) are not easy
to recover fully from.
HIV, The AIDS Virus
AIDS - Acquired Immuno-Deficiency Syndrome
HIV - Human Immuno-deficiency Virus, a type of RNA virus which resembles the
influenza and mumps virus, but is a retrovirus
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Retrovirus - An RNA virus that reproduces by means of DNA molecule. Reverse
to the usual DNA RNA synthesis. Retroviruses use reverse transcriptase.
Reverse transcriptase - an enzyme carried by the virus and catalyzes reverse
transcription, the synthesis of DNA on a RNA template.
After the RNA of HIV is uncoated:
1. Reverse transcriptase uses the viral RNA as a template to make a DNAstrand
2. Adds a secondary DNA strand.
3. The double-stranded viral DNA enters the cell nucleus and inserts itself
into the cells chromosomal DNA, becoming a provirus.
4. Occasionally the provirus is transcribed into RNA
5. Occasionally this mRNA is translated into viral protiens
6. Transcribed viral RNA and translated viral proteins, both from inserted
provirus, combine and leave the cell and can then infect other cells.
HIV infects and eventually kills several kinds of white blood cells that are
important to bodies immune system.
Due to the damaged immune system, body is susceptible to other infections that
cause the syndrome (a collection of symptoms) tha eventually kills the AIDS
patients.
HIV was first recognized before 1981
Two types of HIV drugs, one that inhibits the action of the enzymes called
proteases, which help produce final versions of HIV proteins, and a second type
which inhibits reverse transcriptase enzyme of HIV (AZT)
Because AIDS has no cure yet, prevention is the only healthy option.
Viroids and Prions
Very small pathogens, smaller than viruses
Viroids - small circular RNA molecules that infect plants and duplicate
themselves without encoding proteins. Viroids seem to cause disease by
interfering with the regulatory systems that control plant growth.
Prions - infectious proteins, which somehow convert normal proteins which are
normally present in brain cells, into a misfolded prion version. Responsible for
mad-cow disease and Creutzfeldt-Jakab disease.
Emerging Viruses
Emerging Viruses - viruses that have appeared suddenly or have recently come
to the attention of medical scientists
Avian flu - if this virus evolves so that it can spread easily from person to person,
the potential for outbreak is significant RNA viruses tend to have unusually high rates of mutation because errors
in the replicating their RNA genomes are not subject to certain proof reading
mechanisms
Mutations enable viruses to evolve into new strains that can cause disease in
individuals who have developed resistance to ancestral virus (need for yearly flu
vaccines)
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Joshua Lederberg: We Live in evolutionary competition with microbes. There is
no guarantee that we will be the survivors.
Chapter 8 - Cellular Reproduction: Cells
from Cells (Part B)
Homologous Chromosomes
Individuals of the same sex and species have the same number and types of
chromosomes
Somatic cell - a typical body cell. (in humans, 46 chromosomes, diploid)
Karyotype - a display of the stained chromosomes during metaphase on mitosis, where
chromosomes are arranged in matching pairs.
Homologous chromosomes - two chromosomes of a matching pair; genes controlling
the same inherited characteristics. Nearly identical chromosomes, each of which
consists of two identical sister chromatids after chromosome duplication.
Females, the chromosomes of each pair are essentially identical
Males, the chromosome of one pair do not look alike (single pair of sex chromosomes).
Sex chromosomes - chromosomes that determine a persons sex. Males are XY;
females are XX.
Autosomes - All the chromosomes excluding the pair of sex chromosomes.
Gametes and the Life Cycle of a Sexual Organism
Life cycle - the sequence of stages leading from the adults (of a multicellular organism)of one generation, to the adults of the next generation.
Diploid - cells which contain pairs of homologous chromosomes. Diploid organismsinclude humans and many other animals and plants. Diploid number is represented by
2n.
Gametes - cells which only have a single set of chromosomes (n). Produced by testisor ovary by the process of meiosis. 22 autosomes plus an X or Y sex chromosome.
(haploid) Haploid - a cell with a single chromosome set; only has one member of eachhomologous pair. Haploid number = n. (Humans, n = 23)
Fertilization - In human life cycle, a haploid sperm cell from father fuses with a haploidegg cell from mother.
Zygote - the diploid resulting from the fertilized egg, with two sets of homologouschromosomes, one set from each parent.
Life cycle is completed as a sexually mature adult develops from the zygote.
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Mitotic cell division ensures that all somatic cells of the human body receive a copy ofthe zygotes 46 chromosomes.
All trillions of cells in the body can be traced back to the single zygote produced byfertilization.
All sexual life cycles involve alteration of diploid and haploid stages. Producing haploid gametes by meiosis keeps chromosome number from doubling every
generation
Overview of Meiosis:1. Each of the chromosomes is duplicated during interphase (before mitosis)
2. Meiosis I, the first division segregates two chromosomes from a homologous
pair, packaging them in separate haploid daughter cells. (Each chromosome is
still doubled)
3. Meiosis II, sister chromatids separate, producing 4 haploid daughter cells,
containing one single chromosome from a homologous pair.
The Process of Meiosis Meiosis - the process that produces haploid daughter cells in diploid organisms. Has
two special features. (Lecture: 3 special features)
1. Number of chromosomes is reduced to half.
2. Exchange of genetic material between homologous chromsomes, crossing over
crossing over occurs during the first Prophase (meiosis I)
3. Sister chromatid pairs move toward poles in Anaphase I
Two consecutive divisions, meiosis I and meiosis II, where duplication of chromosomes
is followed by two divisions, resulting in 4 haploid daughter cells
! - Keep in mind the difference between homologous chromosomes and sister
chromatids.
Interphase
chromosomes duplicate producing two identical sister chromatids.
Meiosis I: Homologous Chromosomes Seperate
1. Prophase I - As chromosomes coil up, special proteins cause the homologous
chromosomes to stick together in pairs. Homologous chromosomes cross over
or exchange corresponding segments. Spindle forms.
2. Metaphase I - Homologous pairs are aligned in the middle of the cell. The sister
chromatids of each chromosome are still attached at their centromeres, where
the spindle microtubles are anchored.
3. Anaphase I - The attachment between the homologous chromosomes of eachpair breaks and the chromosomes migrate toward the poles of the cell, separated
not from each other, but from their homologous partners (in mitosis, the sister
chromatids separate).
4. Telophase I & Cytokinesis - Chromosomes arrive at poles of the cell, each pole
now has haploid chromosome set (each chromosome is still in duplicate form).
Cytokinesis occurs and two daughter cells are formed.
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Meiosis II: Sister Chromatids Separate
Essentially the same as mitosis, except meiosis II starts with haploid cells that
has not undergone duplication.
1. Prophase II - Spindle forms and moves chromosomes to middle of cell
2. Metaphase II - chromosomes are aligned with microtubles attached to sister
chromatids of each chromosome.
3. Anaphase II - centromeres of sister chromatids separate, and sister chromatids
of each pair migrate to opposite pols of cell.
4. Telophase II & cytokinesis - nuclei form at cell poles, and cytokinesis occurs,
yielding 4 daughter cells, each with haploid number (n) of single chromosomes.
Review: Comparing Mitosis to Meiosis
Mitosis provides for growth, tissue repair, and asexual reproduction; produces daughter
dells that are genetically identical to parent cell
Meiosis is needed for sexual reproduction, yields genetically unique haploid daughtercells
2 special features (Lecture: 3 special features)
1. Chromosomes reduced by half
2. Exchange of genetic material crossing over
3. Sister chromatid pairs move toward poles in anaphase I
For both mitosis and meiosis, chromosomes duplicate only once in the preceding
Interphase.
Mitosis involves two nuclear and cytoplasmic divisions, yielding 4 haploid cells.
All the events unique to meiosis occur in meiosis I
Meiosis II virtually identical to mitosis, but meiosis II yields haploid daughter cells.
The Origins of Genetic Variation
Another look at meiosis
Independent Assortment of Chromosomes
The arrangement of homologous chromosomes varies. The side-by-side
orientation of each homologous pair of chromosomes (two sister chromatids) is
a matter of chance
Every chromosome pair randomly orients its homologous chromosomes
independently of all others at metaphase I.
Total number of chromosome combinations that can appear in gametes is 2n.
In humans n=23, resulting in about 8 million, or possible chromosome
combinations.
Random Fertilization
Fertilization requires two gamete (haploid) cells to fuse, resulting in
trillioncombinations of chromosomes between two
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parents without accounting for crossing over.
Crossing Over
Crossing over- the exchange of corresponding segments between chromatids
of homologous chromosome pairs during prophase I of meiosis.
Chiama - (plural: chiasmata) sites of crossing over.
Homologous chromatids remain attached to each other at the chiasma untilanaphase I.
The exchange of segments between nonsister chromatids - one maternal
(mother) chromatid and one paternal (father) chromatid of a homologous pair -
adds to the genetic variety resulting from sexual reproduction.
Genetic recombination - gametes that have chromosomes that are part
maternal and part paternal due to crossing over, called recombinant
chromosomes.
When Meiosis Goes Awry
Mistakes that occur during meiosis can result in genetic abnormalities that range from
mild to severe to fatal.
How Accidents During Meiosis Can Alter Chromosome Number
Nondisjunction - when the members of a chromosome pair fail to separate at
anaphase.
Nondisjuntions result in gametes with abnormal numbers of chromosomes.
Nondisjuctions can occur in meiosis I or meiosis II.
Meiosis I - pair of homologous chromosomes fail to separate in anaphase
I (nondisjuction), resulting in incorrect number of chromosomes in haploid
cells at the beginning of meiosis II that results in 4 abnormal gametes.
Meiosis II - nondisjunction of a pair of sister chromatids that occurs during
anaphase II that results in 2 abnormal gametes and 2 healthy gametes.
Down Syndrome: An Extra Chromosome 21
Trisomy 21 - three number 21 chromosomes, yeilding 47 chromsomes in total.
In most cases, a human embryo with an atypical number of chromosomes
develops so abnormally that it is spontaneously aborted (miscarried) long before
birth.
Some aberrations in chromosomes number results in individuals that do survive,
but individuals have a character set of symptoms call a syndrome.
Down syndrome - an individual with trisomy 21. Affects about 1 out of every 700
children.
Trisomy 21, or down syndrome, is the most common serious birth defect
in the U.S.
Characteristic facial features include fold at the inner corner of eye, a round face,
and flattened nose
Short stature, heart defects, susceptibility to leukemia and Alzheimers, short life
span, and mental retardation.
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Some live to middle age years and function well within society
Incidence of down syndrome has a positive correlation with the age of the
mother. (personal note: appears to be exponential increase after age 35).
Abnormal Numbers of Sex Chromosomes
Nondisjunctions affect autosomes (like chromosome 21) as well as sex
chromosomes (X and Y)
Unusual numbers of sex chromosomes seem to not upset the genetic balance as
much as autosomes.
Some possible reasons as to why sex chromosomes are more forgiving are
that Y chromosomes carry a small amount of information, and mammalian cells
normally operate with only one functioning X chromosome because other copies
become inactivated in each cell.
Klinefelters syndrome - XXY, have male sex organs and normal intelligence,
but the testes are abnormally small, the individual is sterile, and often has
breast enlargement and other feminine body contours. Can occur with multiple
nondisjunctions (more than 3 sex chromosomes XXYY, XXXY, and XXXXY) XYY, tend to be taller than average, no syndrome
XXX, cannot be distinguished from XX females
Turners Syndrome - XO, absence of second sex chromosome which results in
women with short stature, web skin between head and shoulders, sex organs do
not fully mature as adolescence, poor development of breasts and secondary
sex characteristics. Normal intelligence. Only known case where having 45
chromosomes is not fatal.
A single Y chromosome is enough to produce maleness, regardless to the
number of X chromosomes. Absence of Y results in femaleness
SexChromosome
Syndrome Origin Frequency
XXY Klinefelter (male) Meiosis egg or sperm 1/2000
XYY None (male) Meiosis in sperm 1/2000
XXX None (female) Meiosis in egg or sperm 1/1000
XO Turners (female) Meiosis in egg or sperm 1/5000
Advantages of Sex Sex must enhance evolutionary fitness
Varied genetic makeup, quickening adaptation to changing environment
Shuffling of genes might allow a population to rid itself of harmful genes more
rapidly.
Sex is awesome.
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Chapter 9 - Patterns of Inheritance Intro
Dog breeding
Explain inborn traits through genetics.
Generations of inbreeding can bring about serious genetic defects
Certain breeds have behavioral tendencies like herding in boarder collies and
sheep dogs
Heritable Variation and Patterns of Inheritance
Heredity - the transmission of traits from one generation to the next
Genetics - the scientific study of heredity Gregor Mandel, an Augustinian monk, deduced its fundamental principles by breeding
garden peas, and applying the scientific method and mathematics. He published his
findings in 1866, only seven years after Darwins The Origin of Species.
Mendel stressed that the heritable factors (today called genes) retain their individual
identities generation after generation, regardless to how they are mixed up or temporary
masked.
In an Abbey Garden
Mendels experimental model is a pea plant because reproduction can be highly
controlled. (Also easily observable traits, many offspring, short life cycle [gap
between generations is very short]) Charachter- a heritable feature that varies among individuals; flower color, seed
shape, etc.
Trait - a variant of a character; purple or white flower color, wrinkled or round
seed shape, etc.
Mendel manipulated the reproduction of pea plants by controlling pollination
patterns, with known pollen sources. Always sure of parentage.
True-breeding - purebred varieties produced through self-fertilization (in pea
plants) until no variation is observed.
Cross - the action of cross-fertilization.
P generation - parental plants
F1 Generation - hybrid offspring of P generation (F from filial, Latin for sonor daughter). 1 for first generation. F2, second generation.
Seven characteristics of pea plant studied: 1) Flower color, 2) Flower position, 3)
Seed color, 4) Seed shape, 5) Pod shape, 6) Pod color, 7) Stem length.
Mendels Law of Segregation
Monohybrid Crosses - hybrids between two true breeding varieties (true-
breeding purple flowers with true breeding white flowers)
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(like seed color and seed shape)
Mendel crossed homozygous plants having round-yellow seeds (RRYY) and
green-wrinkled seeds (rryy)
F1 generation is all RrYy; round-yellow
F2 generation phenotypic ratio: 9/16 round-yellow, 3/16 Round-green, 3/
16 Wrinkled-green, 1/16 Green-wrinkled (9:3:3:1) Punnet square (4 X 4) with 4 variations (RY, rY, Ry, ry) supports findings.
Law of Independent Assortment - Each pair of allele assorts independently of
the other pairs of alleles during gamete formation. (Inheritance of one factor has
no effect on the inheritance of another)
Using a Testcross to Determine an Unknown Genotype
Testcross - a mating between an individual of dominant phenotype but unknown
genotype, and a homozygous recessive individual.
Rules of Probability
Genetic crosses obey the law of probability
Rule of multiplication - the probability of a dual event is the product of theseperate probabilities of independent events. ( x x ; x = 1/16)
Family Pedigrees
Wild-type traits - phenotypes seen most often in nature; not nessisarily specified
by dominant alleles. (Absence of freckles ins more common than thier presence,
even though freckles are a dominant allele)
Pedigree - the collection of family history and the arrangement into a family tree.
Human Disorders Controlled by a Single Gene
Recessive Disorders
Most human genetic disorders are recessive
Most people who have recessive disorders are born to normal parentswho are both heterozygotes
Carrier- An individual who is heterozygous for a recessive allele for a
genetic disorder
Using Mendels laws, one can predict the fraction of affected offspring
that is likely to result from a marriage between two carriers
In single gene disorders, of the offspring form heterozygote parents will
be homozygous for recessive allele, and will be heterozygous carriers.
Cystic fibrosis - recessive genetic disease that is characterized by an
excessive secretion of very thick mucus form the lungs, pancreas, and
other organs. Affects 1 in 25 people of European ancestry. Inbreeding - mating between close blood relatives, which cause a higher
likelihood of producing offspring which are homozygous for a recessive
trait. (most lines of purebred dogs have known genetic defects.)
Dominant Disorders
Extra fingers of toes and toes which are webbed
Anchondroplasia - a form of dwarfism in which the head and torso
develop normally, but the arms and legs are short. (homozygous
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dominant genotype causes death of embryo; single copy disorder)
99.99% of population are homozygous for achodroplasia recessive trait.
Huntingtons disease - degeneration of the nervous system that usually
does not begin until middle age
A dominant allele is not necessarily better than the corresponding
recessive allele.Genetic Testing
Today there are many tests that can detect the presence of disease
causing allele in an individuals genome.
Amniocentesis; physician uses a needle to extract about 2 tablespoons of
amniotic fluid
Chronic villus sampling; physician inserts a narrow tub through the vagina
to the uterus and removes some placental fluid.
Testing fetal cells or DNA released into the mothers bloodstream
Variations on Mendels Laws Mendels laws stop short at explaining some patterns of genetic inheritance
Incomplete Dominance in Plants and People
Incomplete dominance - An appearance in between the phenotypes of two
parents
Hypercholesterolemia - a condition charachterized by dangerously high levels
of cholesterol in the blood, an example of incomplete dominance.
ABO Blood Groups: An Example of Multiple Alleles and
Codominance
Most gene in more than two forms, known as multiple alleles. ABO bloodgroups - and example of multiple alleles in humans. Red blood cells
may be coated with carbohydrate A, carbohydrate B, both (type AB), or neither
(type O)
Three different alleles: IA, IB, and i(neither A or B). Each person inherits one of
the alleles from each parent.
iiis type O, IAIB is type AB, IBIB or IBiis type B
IAIB exhibit codominance
Codominance - both alleles are expressed in heterozygous individuals.
Pleiotropy and Sickle-Cell Disease
Pleiotropy - the impact of one gene on more than one charachter Sickle-cell disease - a disorder that cuases red blood cells to produce abnormal
hemoglobin protein causing them to form a sickle shape which results in a
diverse set of symptoms.
One allele of sickle-cell results in a healthy individual, but at the molecular level
the two alleles are actually codominant.
Polygenic Inheritance
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Polygenic inheritance - the additive effects of two or more genes on a single
phenotype character.
Skin pigmentation in humans is controlled by 3 genes, AABBCC very dark,
AaBbCc intermediate, aabbcc very light
Role of the Environment
As geneticists learn more and more about out genes, its becoming clear thatmany human characters are influenced by both genes and environment.
Identical twins even have different traits because of effects of environment.
The Chromosomal Basis of Inheritance
The chromosome theory of inheritance is one of biologys most important concepts.
Chromosome theory of inhertance - theory that states that genes are located in
specific positions on chromosomes and that the behaviour of chromosomes during
meiosis and fertilization accounts for inheritance patterns