UNIT 3: Cell Membrane
Electrogenic pump
-50 to -200 mv
Inside is negative, outside is positive
voltage difference across membranes
Cations move into cell through gated channels
Sodium Potassium pump
2 K+ in and 3 Na+ out
K+ likes to go down its concentration gradient
K+ goes out
K+ comes back in (when less negative)
Affected by chemical force
Hydrogen Pump
protons pumped against concentration gradient
direction of the pathway depends on placement of protons
Sucrose H+ cotransporter
Helps H+ come back into the cell
Facilitated diffusion
Sucrose moves against concentration gradient
No energy needed to bring it back
Comes in with H+ when enters cell
Energy us coming from proton gradient
Ion channels
Gated channels
stretch gated - mechanical stimulus
Voltage gated
Charge of electrical voltage in cell
Growth Factor
Cell starts growing and dividing
Gene is turned on or off
Cytokines
Cell moves (chemotaxis)
Differentiation
Proliferation (mitosis)
Metabolic activation
Apoptosis (kill itself)
Inhibit proliferation
Hormones
Death Factors
Survival factors
Development
Action Potential
Depolarization
Na+ comes into cell
Cell gets less -
Happens until threshold reaches (+62 mv)
Hyperpolarization
Inside is more negative
More K+ in cell
Na+ and K+ is used to reach threshold
Cell Signaling and Transduction
Physical contact
Gap Junctions
plasmodesmata in plant
Desmosomes Junctions
signal receptors
Subtopic
Eukaryotes
Yeast
signals for cells to combine to one
Local signaling
short distance, have the receptor, target cell is close by
Long distance signaling
Cell signaling helps to bring activators
Combinatorial Gene expression
Signal molecule
Hydrophobic
receptor is inside cell
Hydrophilic
Tyrosine Kinase Receptors
Phosphorlyzes from ATP
Adds phosphate groups to tyrosine
Signal molecule binds together to form dimer
Kinase is activated and phosphorylation behinds
Relay proteins attach to the phosphate groups of the tyrosine to begin transduction
receptor is outside along membrane, receptor is polar
Channel Receptors
Testosterone Signal
Binds to receptor to make transcription factor
The factor binds to promoter to start transcription
Goes through phospholipid bilayer
Helps initiate proteins to be made for male sexual traits
Stages of Signaling
Reception
G protein Coupled Receptor
Alpha, Beta, Gamma Subunits
Binds GDP to GTP
ligand binds to receptor protein
receptor activates and GDP is converted to GTP
Alpha G protein diffuses from the receptor and finds an enzyme
Once enzyme is activated, G protein goes back to GDP
G protein uses the enzyme, Phosphatase to remove the phosphate group from GTP to GDP
Transduction
relate molecules to a signal transduction pathway
Inactive G protein is activated carrying GTP
G protein binds to adenyl cyclase going back to GDP
Active Adenyl cyclase make cyclic AMP (second messenger) from ATP
CAMP starts transduction and then inactivate
Phosphodiesterase removes the cyclic component of CAMP through hydrolytic reactions
CAMP becomes inactive to AMP
Phosphorylate cascade
Adds a phosphate group from ATP to another protein kinase
the other kinase does same to another
Amplifies message until it reaches its target
phosphatase hydrolyzes the phosphate group to turn off kinase
Cell Response
cell responds to the signal
Neuron Communication
Electrical Synapse
Electrical current flows from one cell to another through gap junctions
Subtopic
Chemical Synapse
Communication occurs through a neurotransmitter
The spaces between the presynaptic membrane of axon and post synaptic membrane of dendrite of the synaptic cleft
Neurotransmitter binds to post synaptic membrane receptor (ligand gated)
Ca2+ can go in
Ions go through membrane depolarization
Neurotransmitter ligands
Breaks down through hydrolytic reaction
Taken up by pre synaptic membrane
Does not enter post synaptic membrane
DNA Packaging
Beads on string
Histones are proteins, in which DNA wind around twice
Nucleosome- Histone + DNA
Histone Core
H2A, H2B, H3, H4 [no H1]
2 molecules of each histone
Forms a histone octamer
H1 is found outside nucleosome
Brings nucleosomes together
Helps form tight helical fiber (the next level)
Linker DNA is the strand of DNA not winded by histones
The tight helical fiber is formed into loops, which are held together by a protein scaffolds at the bottom
The loop domain then coils to form a metaphase chromosomes
Regulation of Gene Expression
All cells have the same genes
About 20% genes are expressed
Heterochromatin
Highly compacted
No genes expressed
Euchromatin
Less compacted
Genes expressed
Chromatin
Condensation silences gene expression
Proximal Control Element
gene are lowly expressed (basal)
Close sequences in DNA to the gene
General transcription factors bind to the site
Distal Control Element
Far sequences in DNA to the gene
Example: enhancers
May even be located in an intron
Specific transcription factors
High level expression
lens cell in eye
Activators
increase expression
Activators help to initiate high level transcription
Repressors
inhibits expression
Combinatorial Gene expression
Incorporation activates and enhancers for gene expression
Continuous/ Constituted Expression
High level expression
Expression ALWAYS ON
Regulated expression
Basal low level expression
Prokaryotic Gene Expression
Activators
Help increase expression above basal level
Repressors
Proteins help decrease expression
Operators
Activators binds to this sequence to start high level expression
Induced expression
Repressors does the opposite
Basal level expression
On or off switch of transcription
Terminator Sequence
The end sequence in which transcription ceases
Operons
Activators, repressors [operator, promoter & terminator]
Positive Regulation
Activators help with transription
The lac operon - both positive and negative
Negative Regulation
Repressor proteins inhibit transcription
The trp operon
The Lac Operon
Both + and - regulation
Found in prokaryotes like Ecoli
Gene Z
Glucose and galactose
Uses Enzyme B Galactose
Made by Gene Z
They breakdown lactose
Gene Y
the lactose goes through the transmembrane
The gene Y codes for permease
Gene Z
make transacetylase
Adds acetyl groups to lactose to make it easier for B GALACTIDASE to break down lactose
When lactose is available
Repressor is suppressed with allolactose
Contribute activator proetin (CAP) binds to operator
When there is high levels of camp
No presence of glucose
The trp operon
Tryptophan is synthesized
Operon is off when there is tryp
Operon is on when there is no tryp
Negative Regulation
Tryptophan functions as a corepressor
Binds to repressor protein
Repressor protein binds to operon
Operon is turned off
Cell Cycle (Mitosis)
G1
Cell grows nearly to its full size
Synthesis phase
DNA is replicated
cell finishes growing
S
most of the life of the cell is spend here (interphase)
Subtopic
G2
cell finishes growing
more growth
Mitosis
prophase
Condensation of chromosome
Nucleolus disappear
DNA condenses
Chromosome structure appears
Microtubules appears from centrosomes in animals
Prometaphase
microtubules appear and attaches to kinetchore
Nuclear envelope is degraded
Kinetochore attaches to chromosomes in centromeres
Metaphase
Sister chromatids are ready to separate
Chromosome align at the center of cell
anaphase
The cell becomes bigger
Chromosome separate
Sister chromatids separate and move to the ends of the cell
telophase
Nuclear membrane reappear and 2 sets of chromosomes
Spindle fibers are broken up
Chromosomes uncoil and become uncondensed
Cytokinesis
Cell is composed by a contractile ring form microfilament
Cell is divided in nearly equal cells
Cleavage furrow is formed
Organelles are replicated
Meiosis
Gametes are formed through meiosis
Germ line cells produce gametes
2 copies of each chromosome in diploid organelles
Produces gametes
Haploid cells
1 copy of each chromosome
Cells are going through the interphase
DNA in the germ cells are duplicated before meiosis begin
Meiosis 1 (produces 2 diploid cells)
2 unique daughter cells that have the amount of DNA as parent germline cells
Prophase 1
DNA condenses to form chromosomes
Duplicated sister chromatids join together at the centromere
Each pair of homolysis chromosomes undergoes synapses to form a complex
Chromosome material is exchanged by the 2 parts of sister chromatids
Sister chromatids from each chromosomes are no longer identical
No two siblings aside from twin are genetically identical
Nuclear membrane begins to break down
Two centrosomes are present with microtubules -- kinetochores
Metaphase 1
Synapse chromosomes align at the equator
Align randomly
Different combinations
Anaphase 1
Homolysis chromosomes separate and migrate
To 2 poles of the cell
Sister chromatids are attached at centromere
Telophase 1
Cell divides into 2 daughter cells
Nuclear membrane reappears
Meiosis II: similar to mitosis (produces 4 cells)
Prophase II
Chromosomes condense and nuclear envelope breaks down
Centrosomes appear and forms kinetochores
Daughter cells have one copy of each hydrolysis chromosomes
No synapses or recombination
Metaphase II
Chromosomes align at equator of cell
Random alignment
Anaphase II
Sister chromatids are pulled apart
Microtubles shorten and ends of cells are aligned
Telophase II
Nuclear membrane returns
Cytoplasm is divided into 2 haploid cells (gametes) -- cytokinesis
checkpoints G1/G2/M
Failure of CDKs cause cancer
disrupt and inavde issues
accumulation of mutants
no density dependent inhibitioln
oncogenes cause cancer
Tumor suppressor P.53 is mutated it can not do its job
If Ras is hyperactive a signal will continually be
expressed, never turning off
Cell Cycle (Division)
Karyotypes
can be used to diagnose diseases
Down syndrome
Chromosomes 21 has 3 chromosomes instead of 2
Germ Cells
Produce gametes
Meiosis
Produce haploid cells (1N)
Regulators of Cell Division
Cyclins
cyclin dependent kinases ___ to phosphorlyze
They form CDK-cyclin complex
Density dependent inhibitor
Would not grown when mixed cut in environment
Forms single layer
Cancer cells
Doesnt exhibit any growth inhibitions
They propagate mutations
They establish their anchor in different plane
Forms tumor on top of each layer
A disease of signaling cycle
Oncogenes
Cancer causing genes
Proto Oncogenes
Are normal cancer genes
When mutated or muted can cause cancer - become oncogenes
Tumor Suppressor Genes
Suppresses cell division/ cycle
P-53
Pauses cell cycle
Transcription factor
Makes a protein that hurts gene expression
When there is a thymine dimer, p-53 is needed
If p-53 is mutated, there will be continuous cell division
Somatic cells
have autosome (NON SEX) chromosome -
Body cells
2N diploid cells (one from dad one from mom)
Normally in G0 phase
UNIT 2: DNA Replication, Transcription, Translation
Oparin Harding theory
Volcanic eruption was the source of molecules
Miller Urey
redid experiment of Oparin Harding
Tried to recreate the environment
Ribozyme oldest organelle
contains RNA and protein
Hydrocarbons, hydrogen cyanide, amino acids
3 domains of life:
Archaea
halophiles
methanophiles
thermophiles
Has introns
Bacteria
Capsule
Petidoglycan - sugar coated cell wall
No nucleus
Plasmid
chromatin/somes
Pili- attachment for reproduction
Cilia - hairlike projections of the exterior of the bacteria, for movement
Flagellum
No introns
Coupled DNA rep and transcription
Has UNBRANCHED lipids, its saturated, because its rigid
Eukarya
Has nucleus- double membrane
Has envelope
Has lamina
intermediate filament,
helps with stability and structure of the nucleus
Chromatid in nucleus
Nuclelous
DNA
Lysosomes
has hydrolase
lysozyme
which helps engulfs and digest bacteria
break down macromolecules
phagocytosis
engulfs outside materials
autophagy
recycles organelles or any cell material
pH acidic
Peroxisomes
Produce Hydrogen Peroxide to form water! H2O2 to H2O
Form water
Vacuoles
contractile vacuoles
rigid, moving excess water out of the cell
prevents lysine when cell self-destructs
food vacuole (vesicle)
carries things for transportation
Central vacuole
found in plants, rigid
Mitochondria
Produces ATP
Cellular respiration
DNA and protein
Has a double membrane
Cristae
where atp and cellular respiration happens
Rough ER
Double membrane
Nucleus
Protein modifications
Glycoproteins
sugars in the rough ER
Smooth ER
Double membrane
Iipid synthesis
Detoxification
Golgi
Helps package proteins
Sends them out
Synthesis
Modification
Chaperones
2nd tag of protein
helps in modification and folding
Ribosomes
Free bound
Two components
rRNA and proteins
Translation
Cytoskeleton
Microfilaments
Transport/motor protein
myosin
Amoeba
Actin Monomer
muscle contraction
movement
Microtubules
monomer: tubulin
Alpha
Beta
movement
structure
cell division
Motor protein
kinesin
Found in flagella
Intermediate filaments
Nuclear lamina, keratin
Structure and maintenance, stability
fibers
Progeria
Junctions
Tight
No passage of the free nucleus
Intestines and skin
Rat = poison by opening the gap junctions
Gap/ Plasmodesmata
Allows everything to pass through
Desmosomes
Selected passage
Intermediate filaments found in here
Signaling
ECM
plasma membrane
-peripheral proteins - sodium, potassium ion channels
collagen
Griffith
Bacteriologist
Looking for a vaccine for pnemonia
Streptococcus pneumonia
Four trials
S- dead rat
R- alive rat
Heat S - alive
Heat S & R- dead rat
There was a transforming principle!
Mckay & Mcleoud (M&M)
redid griffith’s 4th trial
reinforced the transforming principle
test tube
didn’t prove anything
Hershey and Chase
Used radioactive phosphorus and sulfur
RNA is not genetic material because it is unstable
this is due to the OH group in the ribosugar
Chargraff’s Rule
PURE AS GOLD
Pyramidines - C and T
Number of purines = number of pyramidines
15% A, 15% T….. 35% G, 35% C
Always have to be 50% 50%. A& C= 50%... G&T= 50%
Watson and Crick
Watson and Crick
Made 3D replica of the dna
Discovered that DNA was a double helix
Messelson and Stahl
semi-conservative
PCR
polymerase chain reaction, all happens in the test tube!
Makes a lot of dna
artificial
Denaturation
Temp is increased so that hydrogen bonds can break and strands can separate
Hydrogen bond is broken
Both strands separate
Annealing
Temperature is reduced
DNA primers are added to parent strands through hydrogen bonds
Elongation
Temp is slightly increased
Tag polymerase (from archea) elongate synthetic DNA primers
dnTP
energy used in PCR TO KEEP ELONGATION MOVING
DNA
Oparin Harding theory
Volcanic eruption was the source of molecules
Miller Urey
redid experiment of Oparin Harding
Tried to recreate the environment
Ribozyme oldest organelle
contains RNA and protein
Hydrocarbons, hydrogen cyanide, amino acids
3 domains of life:
Archaea
halophiles
methanophiles
thermophiles
Has introns
Bacteria
Capsule
Petidoglycan - sugar coated cell wall
No nucleus
Plasmid
chromatin/somes
Pili- attachment for reproduction
Cilia - hairlike projections of the exterior of the bacteria, for movement
Flagellum
No introns
Coupled DNA rep and transcription
Has UNBRANCHED lipids, its saturated, because its rigid
Eukarya
Has nucleus- double membrane
Has envelope
Has lamina
intermediate filament,
helps with stability and structure of the nucleus
Chromatid in nucleus
Nuclelous
DNA
Lysosomes
has hydrolase
lysozyme
which helps engulfs and digest bacteria
break down macromolecules
phagocytosis
engulfs outside materials
autophagy
recycles organelles or any cell material
pH acidic
Peroxisomes
Produce Hydrogen Peroxide to form water! H2O2 to H2O
Form water
Vacuoles
contractile vacuoles
rigid, moving excess water out of the cell
prevents lysine when cell self-destructs
food vacuole (vesicle)
carries things for transportation
Central vacuole
found in plants, rigid
Mitochondria
Produces ATP
Cellular respiration
DNA and protein
Has a double membrane
Cristae
where atp and cellular respiration happens
Rough ER
Double membrane
Nucleus
Protein modifications
Glycoproteins
sugars in the rough ER
Smooth ER
Double membrane
Iipid synthesis
Detoxification
Golgi
Helps package proteins
Sends them out
Synthesis
Modification
B cells
secrete antibodies
carries golgi bodies
Chaperones
2nd tag of protein
helps in modification and folding
Ribosomes
Free bound
Two components
rRNA and proteins
Translation
Cytoskeleton
Microfilaments
Transport/motor protein
myosin
Amoeba
Actin Monomer
muscle contraction
movement
Microtubules
monomer: tubulin
Alpha
Beta
movement
structure
cell division
Motor protein
kinesin
Found in flagella
Intermediate filaments
Nuclear lamina, keratin
Structure and maintenance, stability
fibers
Progeria
Junctions
Tight
No passage of the free nucleus
Intestines and skin
Rat = poison by opening the gap junctions
Gap/ Plasmodesmata
Allows everything to pass through
Desmosomes
Selected passage
Intermediate filaments found in here
Signaling
ECM
plasma membrane
-peripheral proteins - sodium, potassium ion channels
collagen
Griffith
Bacteriologist
Looking for a vaccine for pnemonia
Streptococcus pneumonia
Four trials
S- dead rat
R- alive rat
Heat S - alive
Heat S & R- dead rat
There was a transforming principle!
Mckay & Mcleoud (M&M)
redid griffith’s 4th trial
reinforced the transforming principle
test tube
didn’t prove anything
Hershey and Chase
Used radioactive phosphorus and sulfur
RNA is not genetic material because it is unstable
this is due to the OH group in the ribosugar
Chargraff’s Rule
PURE AS GOLD
Pyramidines - C and T
Number of purines = number of pyramidines
15% A, 15% T….. 35% G, 35% C
Always have to be 50% 50%. A& C= 50%... G&T= 50%
Watson and Crick
Watson and Crick
Made 3D replica of the dna
Discovered that DNA was a double helix
Messelson and Stahl
semi-conservative
PCR
polymerase chain reaction, all happens in the test tube!
Makes a lot of dna
artificial
Denaturation
Temp is increased so that hydrogen bonds can break and strands can separate
Hydrogen bond is broken
Both strands separate
Annealing
Temperature is reduced
DNA primers are added to parent strands through hydrogen bonds
Elongation
Temp is slightly increased
Tag polymerase (from archea) elongate synthetic DNA primers
dnTP
energy used in PCR TO KEEP ELONGATION MOVING
DNA Replication
e use both strands
In euk- 2 ORI
In pro - 1 ORI
DNA III - extends and proofreads
DNA transcription
happens downstream
uses the template strand
Promoter
located upstream
TATA box
found in promoter
contains transcription factor which contains protein
RNA pol II binds because it needs transcription factor to bind
+1 sequence -
Poly A
signals the nuclease to make a cut at the mRNA strand
Ribonuclease
cuts the sequence at the poly A
Poly A polymerase
brings a bunch of As to stabilize
Splicesosomes
cuts out the introns
RNA splicing occurs before the cap is added
DNA Translation
Initation
Small subunit ribosome
scans where it starts
Trna comes with anticodon, happens at P site
Large subunit ribosome attaches to the TRNA
Elongation
another trna comes in and puts another anticodon at the a site
Amino acid
synthases
connects the tRNA to the correct amino acid, reads it first inorder to use the enzyme
Steps:
small ribosomal subunit attaches
- scans for AUG codon
- tRNA attaches to the codon
- large ribosomal unit attaches to the complex
- this happens in P site
-tRNA comes into A site
release factor comes into this site
-the mRNA shifts in codon to P site then E
-release factor attaches to stop codon on A site
-hydrolysis reaction breaks the ribosomal complex
-translation is finished
Mutations
happens in nucleotides of DNA
silent
1 nucleotide change
- no change in amino acid
Missense
1 or 2 Nucleotides
Change in Amino Acid
Nonsense
Early stop codon that stops translation
Translocation
2 Membranes
Mitochondria
Chloroplast
Nucleus
Endomembrane system
ER- GOLGI- PLASMA MEMBRANE OR GOES BACK TO THE ER
Steps:
Free ribosome bound
Translation is done
Signal sequence is reached for signal peptidase to make a cut
The protein is now in the lumen of ER
The protein is modified to glycoprotein by chaperones
The protein is transported to golgi
The golgi further modifies the protein and packages it
The vesicle is sent to lysosomes, extracellular matrix, plasma membrane
Unit 4: Photosynthesis
Retrieve energy (light reactions)
harvest energy
light reactions gather energy and transfer it to electron carriers (NADPH is an electron carrier) or use energy to make ATP
NADPH & ATP is used to drive calvin cycle
-not make sugars directly
Photosystem
collection of proteins and pigment molecules
a ray of satellite dishes that tries to gather light
Photon hits the photosystem and hits the cholorphyll molecules and ultimately funneled by the reaction center (special chlorophyll molecules)
Reaction center is where the electron will be excited and ultimately lost from the chrolophyll, primary electron acceptor grabs it chlorophyll loses it
Starts on photosystem II in the process: Light Reactions: Part I
Act 1 :
Energy is captured by Photosystem II
H2O split into oxygen and hydrogen
Chlorophylls lost electron is REPLACED BY TAKING AN ELECTRON FROM WATER “splitting water”
O2 IS RELEASED AS A BY-PRODUCT
protons (from water) are released to thylakoid space (lowering pH) , used to drive the synthesis of ATP
Act 2:
Energy is transferred through Electron Transport Chain to Photosystem I
primary e acceptor passes it to ETC, uses energy to move protons against concentration gradient to move it into the thylakoid space
proton gradient is used to make ATP
Act3:
Photosystem transfers electrons, reduces NADP+ to NADPH
electron in that reaction center bounces to a higher state
this electron goes to a shorter ETC, then electron carrier NADP grabs the electron and becomes NADPH
Light reactions:
olar energy is used to make ATP and NADP not for cellular work but for calvin cycle
this is called NON- CYCLIC FLOW
Chemiosmosis
using proton motive force to generate atp
can be used to do work
atp synthases allows protons to move down their concentration gradient to produce ATP from ADP
protons are released from the thylakoid space
pumping of protons from the stroms to the thylakoid space using the energy inherent in the ETC
RESULT: HIGH PROTON CONCENTRATION BUILDING UP IN THE THYLAKOID SPACE
Mitochondria and Chloroplast similarities in Chemiosmosis
both cases, there is inherent energy and electron transport chain pumping protons across the membrane
Subtopic
Subtopic
Subtopic
both respiration and photosynthesis, rely on a proton gradient that is generated by the ETC as electrons move down their electron transport chain
ATP synthase uses proton motive force to phosphorylate ADP to make ATP
ATP is generated in the compartment where its needed
Mitochondria and Chloroplast Differences in Chemiosmosis
proton movement in both organelles.
Mitochondria
pump protons pump in the inner membrane gradient
Chloroplasts
protons pumped in the thylakoid space, (stacks)
where electrons are coming from that moved down from ETC and established the proton gradient
Photosynthesis
source of the electrons - the excited energy, higher energy state, is coming from chlorophyll molecules as photon hits a cholorphyll molecule that excites a electron and that energy is what is driving the generation of ATP
Respiration
the high energy electrons are coming from food as we break down like glucose that has a high PE which we use to make ATP
Store energy (Calvin cycle) Part 2
CO2 fixation
energy in ATP and NADPH is transferred into sugar, a more stable storage form
products of the light reactions except of o2 are reactants in calvin cycle
we need a source of carbon, so we use co2
carbon fixing reactions are light independent
Act 1:
co2 enters the cycle diffused into the leaf through the stomata and into the chloroplast, and its carbon is snapped onto a pre-existing 5 carbon carboyhdate by the enzyme rubisco
this makes a highly unstable 6 carbon molecule and breaks down immediately due to its 2 phosphate groups
Act 2:
ATP is used to phosphorylate the other side of the 3 carbon molecule, and 3 carbon molecule is reduced by NADPH to form one molecule of G3P
end of 2nd act makes the product
G3P is half a glucose, so far we have spent 6 atp and 6 nadph
need 3 more atp
End of act 2, we have 6 G3P, one will be released to make glucose ultimately and FIVE will continue
ATP becomes ADP
NADPH has been oxidized to form NADP (lost electrons)
ADP and NADP will return to the light reactions and get recharged
Act 3:
5 g3p CONTINUES IN THE CYCLE
basically be rearranged with the help of ATP to form a 5 carbon sugar and becomes a starting point ones again
another carbon from carbon dioxide attaches again, attaches to the carbon ribulose bisphosphate to make unstable 6 carbon intermediate and so on and so forth
TWO g3ps are needed to make 1 glucose(which was released in act 2)
and glucoses will quickly be assembled into starch
Respiration
Use energy (respiration)
glycolysis
Citric acid cycle
Oxidative phosphorylation
Begins with Glucose
1st stage of Cellular Respiration with oxygen
Fermentation occurs when no oxygen is present
Glycolysis
Signal sequence is recognized by signal recognition protein (SRP)
Checkpoints include G1/S, G2/M, and M
Regulators include CDKs
phosphorlation occurs initating chain of events promoting transcrption
hit by photon of light that energy is transferred and funneled to the reaction center
Uses 2 ATP to break up glucose into 2- 3 carbon chains
each 3 carbon has a phosphate atachted to it
2 NAD+ are reduced to NADH with the addition of hydrogen
2 molecules of pyruvate per glucose and 4 ATP, Net 2 ATP are produced
enzyme hexokinase phosphorylates glucose phosphoglucoisomerase converts glucose 6-phosphate into isomer
Uses 2 ATP to break up glucose into 2- 3 carbon chains
2 NAD+ are reduced to NADH with the addition of hydrogen
2 molecules of pyruvate per glucose and 4 ATP, Net 2 ATP are produced
Unit 1
Chemical bonding
Covalent
Polar
Different Electronegativities
Dipole Dipole Interactions
Paritial negative
Partial positive
Hydrophillic
Hydrophilic Heads
Nonpolar
Similar Electronegativies
Hydrophobic Interactions
Cage Away from Water
Hydrophobic Tails
Van Der Waals Interactions
Separation of charges
Metallic
Ionic
Transfer of Electrons
anion
Negative Charge
cation
Positive Charge
Macromolecules
Macromolecules are polymers, built from monomers
Large carbohydrates (polysaccharides), proteins, and nucleic acids are polymers, which are chains of monomers
The components of lipids vary
Monomers form larger molecules by dehydration reactions, in which water molecules are released
Polymers can disassemble by the reverse process, which is hydrolysis
no anchorage dependance
Subtopic
each 3 carbon has a phosphate attached to it
Carbohydrates
Carbohydrates serve as fuel and building material
Examples of carbohydrates
Monosaccharides
Glucose
Fructose
Disaccharides
Lactose
Sucrose
Serve as fuel and are carbon sources that can be converted to other molecules or combined into polymers
Polysaccharides
Cellulose (plants)
Strengthens plant cell walls
Starch (plants)
Stores glucose for energy
Glycogen (animals)
Stores glucose for energy
Chitin (animals and fungi)
Strengthens exoskeletons and fungal cell walls
Lipids
Lipids are a diverse group of hydrophobic molecules
Components of lipids
Glycerol
Consists of 3 fatty acids
Examples of glycerol
Triacylglycerols
(Fats or oils) -> glycerol + three fatty acids
Important sources of energy
Phospholipids
Consist of a phosphate head and 2 fatty acids
Glycerol + phosphate group + two fatty acids
Are lipid bilayers of membranes
Steroids
Four fused rings with attached chemical groups
Consist of a steroid backbone
Component of cell membranes (cholesterol)
Signaling molecules that travel through the body (hormones)
Proteins
Proteins include a diversity of structures, resulting in a wide range of functions
Consist of R groups (a type of amino acid monomer)
There are 20 types
Examples of proteins
Enzymes
Catalyze chemical reactions
Defensive proteins
Protect against disease
Storage proteins
Store amino acids
Transport proteins
Transport substances
Hormones
Coordinate organismal responses
Receptor proteins
Receive signals from outside cell
Motor proteins
Function in cell movement
Structural proteins
Provide structural support
Nucleic acids
Nucleic acids store, transmit, and help express hereditary information
Consists of a phosphate group, sugar, and nitrogenous base
Examples
DNA
Consists of:
Nitrogenous bases = C, G, A, T
Sugar = deoxyribose
Usually double-stranded
Phosphate group
Stores hereditary information
RNA
Consists of:
Sugar = ribose
Nitrogenous bases = C, G, A, U
Usually single stranded
Phosphate group
Various functions in gene expression, including carrying instructions from DNA to ribosomes
Genomics and Proteomics
Genomes and proteomics have transformed biological inquiry and applications
Recent technological advances in DNA sequencing have given rise to:
Genomics
An approach that analyzes large sets of genes or whole genomes
Biofinformatics
The use of computational tools and computer software to analyze these large data sets
Proteomics
A similar approach for large sets of proteins
The more closely two species are related evolutionarily, the more similar their DNA sequences are
DNA sequence data confirm models of evolution based on fossils and anatomical evidence
Carbon skeletons
Length
Branching
Unbranched
Branched
Double bond position
Presence of Rings
Isomers
compounds with same # of atoms of same elements but different structures and different properties
Structural
Cis-trans
cabons that have covalent bonds to the same atoms but differ in spatial arrangements due to the inflexibility of double bonds
cis isomer
2 x's on same side
trans isomer
2 x's on opposite sides
Enantiomers
L isomer
R isomer
Hydrogen Bonding
Water Molecules
Properties
High Specific Heat
High Heat of Vaporization
High Humidity prevents Evaporation
Denser as solid than
Expand when Heated
Contract when cooled
Solvent of Life
Phospholipid Bilayer
Hydrocarbons
Isomers
Stutural
Different Covalent Arrangements
Geometric
Different Spacial Arrangements
Enantionmers
Mirror Images
Opposite Charges can form Salts
How Salts dissolve in water
hydration shell
Ex: NaCl
Organic Compounds
Functional Groups
Hydroxyl
polar because of electronegative oxygen
forms H bonds with H2O
usually ends with -ol
Carbonyl
sugars w/ ketone groups (ketoses)
sugars w/ aldehydes (aldoses)
Carboxyl
acts as an acid
covalent bond between O-H is very polar
Amino Group
acts as a base
Sulfhydryl
two -sh groups can react forming a "cross-link that help stabilize protein structure
Phosphate
contributes positive charge
Methyl
affects gene expression when on DNA or on proteins bound to DNA