Categorías: Todo - regulation - glycolysis - enzymes - respiration

por Thanh-Tri Nguyen hace 1 día

106

Final Map Christiana O., Marianna T., Thanh-Tri N.

Biological processes are highly regulated, ensuring that enzymes function efficiently to maintain homeostasis. Enzymes are proteins that act as catalysts in biochemical reactions, and their activity can be modulated through various mechanisms.

Final Map Christiana O., Marianna T., Thanh-Tri N.

Concept Map 3

DNA structure (experiments)

Mutations

Silent
no change in the amino acid
Nonsense
introduces a stop codon
Missense
changes the amino acid
Frameshift
when inserting or deleting 1 or 2 nucleotides causes a shift in the reading frame

Gene Expression (prokaryotic)

Operon: genes that work together controlled by an on/off switch
Lac Operon

Components: Regulatory gene Lac I, Strugtural genes lac z, lac y, lac A, promoters and an operator

Lactose

Beta-Galactosidase: breaks down lactose to galactose and glucose

When glucose is present

production of cAMP is blocked. The operon is off

When lactose is present:

lactose repressor binds to it, which allows CAP activator to bind to it and facillitate transcription

Translation

Termination
The stop codon is found in the mRNA. Then a release factor binds to the A site of the ribosome complex

A release factor binds to the A site of the ribosome complex and the growing polypeptide chain is free

The traslation initiation complex in the ribosomes dissociates using GTP.

Elongation
Ribosomes move along the mRna.

Translocation in the E site: the tRna in the P site is moved to the E site

Peptide Bond Formation (P site): forms between the carboxyl end of polypeptide chain in P-site and the amino group of the A site. Pep bond catalyzed by peptidyl transferase

Codon recognition in the A site: anticodon of tRna pairs up with mRna in the A site

Initiation
Large ribosomal subunit binds with the help of tRna in the P site
Small ribosoman subunit binds to mRna. The initiator tRna binds to the start codon (AUG).

Eukaryotes amino acid is Met

Prokaryotes amino acid is Formal Met

DNA experiments/ Structure

Franklin, Watson, Crick
Discovered DNA was double stranded and helical
Messleson &Stahl
Cultivated DNA in N15 and mixed it with N14, allowed the DNA to replicate and observed the relative density of the solution created

Three models hypothesized: conservative (parental strands reassociate after replication), semi-conservative (strands separate and act as templates for complementary strands), Dispersive (part of the parent strand is mixed in the daughter strands)

Experiment found the solution had an intermediate strip and low density strip

confirmed semiconservative model.

Griffith
Injected mice with pneumonia, S (deadly), R (safe), Heat killed S, heat killed S with R, and found that heat killed S with living R killed mice

Found that something (genetic material) was transferred from the dead S strain to the living R strain.

Hershey & Chase
labeled DNA with P32 and protein with S35 in bacteriophages, blended and centrifuged infected bacteria, and found DNA in the pellet

Discovered DNA carried genetic material

Chargaffs Rule
A=T G=C nucleotide bases come in proportionally equal amount

Gene Expression (Eukaryotic)

Enhancer Sequence
Activator Proteins bind to enhancer sequences (3 distal control elements)
DNA bending protein

DNA bending protein brings the activators closer to the promoter and TATA box.

General and Mediator transcription factors

General transcription factors and mediator proteins bind the activators.

RNA Polymerase II

RNA polymerase II binds the promoter and the gene has Increased Expression.

DNA Replication

Origin of replication (ORI): start point of replication in a strand of DNA, here two forks are formed creating the directions DNA are replicated
DNA Polymerase

adds bases to daughter strand in the 5' to 3' direction

DNA Polymerase I

kicks off primers from the RNA

Ligase: final step/ enzyme connects okazaki fragments (lagging strands)

DNA Polymerase III

adds nucleotides to the 3' end on the leading stand and the RNA primers on the lagging strand

Initiation Enzyme/Protein

Primase: creates RNA primers that attach to DNA

helicase: separates the two strands of DNA (breaks H bond)

Topoisomerase: ensures that the DNA strand is not strained and knotted.

SSB: ensures that the single strands do not recombine

Transcription/ Processing

Termination: a nucleotide sequence, AAUAA, is read by the RNAP which tells it when to cleave the RNA strand.
Eukaryotes

Pre-mRNA is formed: we get a poly-A tail which helps with the RNA's stability and we have a 5' cap which helps us with Translation later on.

Spliceosomes help remove introns leaving exons.

Alternate splicing: allows the expression of certain proteins over others.

exons: the coding nucleotides that will be expressed (different ways of splicing = different proteins)

introns: separate the coding nucleotides that will be expressed.

Prokaryotes

The process is done at this point RNA is made w/out processing

Elongation: the template strand is read from the 3' to 5' end and nucleotides are added to the 3' end of the RNA strand
Initiation: RNA polymerase starts this process by binding to the promoter: no primers or helicases needed.
Promoter: a sequence that allows RNAP to bind to the DNA strand
Pro: RNAP
Eukaryotes: RNAP II, transcription factors (proteins that help RNAP II to bind).

Concept Map 2

Photosynthesis

Calvin Cycle (C3)
3x CO2

Rubisco

3x Short-lived intermediate

6x 3-phosphoglycerate

6x 1,3 bisphosphoglycerate

6x Glyceraldehyde 3 Phosphate (G3P),

3x Ribulose bisphosphate

1 G3P

Light Reactions
Non-cyclic/ Linear flow

Photosystem II

These electrons get sent to the electron transport chain.

Electron Transport Chain

Photosystem I

ferredoxin (Fd)

NADP+ reductase

NADPH+

Light (photons) hit the chlorophyll in the light harvesting complex.

This excites the photons and then they return to ground state and the energy jumps between them until they reach the main chlorophyll a in the reaction center complex.

These main chlorophyll a get excited but instead of returning to ground state, these are captured by the primary electron acceptor.

These electrons are sent outside of photosystem I to Fd

Plastoquinone (Pq),

Cytochrome Complex

Plastocyanin (Pc)

ATP Synthase

ATP

Metabolism

Catabolic
pathway that releases energy by breaking down complex molecules to simple molecules

Subtopic

Anabolic
pathway that consumes energy to build larger complex molecules

Endergonic: energy is required, energy is absorbed

Spontaneous reaction: free energy is negative

Cell Signaling

Aldosterone Pathway
Signal moves through the membrane

Signal binds to the receptor, changes its shape and activates the receptor

Active Receptor travels into the nucleus and binds to DNA

Transcription occurs which produces mRNA

mRNA leaves the nucleus, ribosomes bind and translation occurs, producing a protein.

G Protein signaling pathway
Signal binds to the GPCR which changes its shape and activates it

GCPR binds to G protein, bound by GTP, which activates the G protein

Activated G protein binds to the adenylyl cyclase. GTP hydrolyzes which activates adenylyl cyclase and changes its shape.

Adenylyl cyclase converts ATP to cAMP

cAMP activates pka which leads to cell response

Enzymes

Feedback Inhibition
The end product of a metabolic pathway shuts down the pathway by going back to the first enyme and binding to its allopsteric site.
Cooperativity
The binding of one substrate molecule to the active site of one subunit locks all other subunits into the active shape.
Allosteric Regulation
Allosteric activator

A regulatory molecule binds to the allosteric site of an enzyme an locks it in its active form. Substrates can bind.

Allosteric inhibitor

A regulatory molecule binds to the allosteric site of an enzyme an locks it in its in-active form. Substrates can't bind.

Inhibition
Non-competitive Inhibition

An inhibitor binds to a site other than the allosteric site, and changes teh enzyme's shape. Even if the substrate binds the active site, the ezyme no longer works.

Competitive Inhibition

An inhibitor binds to the active site of an enzyme. This doesn't allow for the substrate to bind and it stops the enzyme for functioning.

Cellular Respiration

Glycolysis
Without O2

Lactic Acid Fermentation

Outputs: Lactate, NAD+

Alchohol Fermentation

Inputs: 2 Pyruvate, NADH

Outputs: Ethanol NAD+

with O2

Inputs: 1 glucose, 2 ATP

Step 1: glucose binds to hexokinase and with ATP becomes G6P.

Step 2: G6P becomes F6P

Step 3: F6P binds to the phospho-fructo-kinase enzyme and with ATP becomes fructose 1,6 bi-phosphate

Step 4 + 5: That fructose 1,6 biphosphate becomes 2 G3P

pyruvate oxidation

Inputs: 2 pyruvate

Products: 2 Acetyl CoA, 2 Co2, 2 NADH

Citric Acid Cycle

Inputs: Acetyl CoA

Step 1: Oxaloacitate goes to an enzyme and with Acetyl CoA becomes Citrate.

Step 2: Citrate becomes Isocitrate.

Step 3: Isocitrate becomes alpha ketogluta and NADH is released.

Other Steps: 2 NADH, ATP, FADH are formed.

Products: 1 ATP, 3 NADH, 1 FADH

Oxidative Phosphorelation

Inputs: 10 NADH, 2 FADH

Electron Transport Chain:

Cyt c

Q

Complex I

NADH transfers electrons to complex I

Complex II

FADH2 transfers electrons to complex II

Complex IV

O2 + H+ = H20

Outputs: H2O, about 26 - 28 ATP

Complex III

Chemosmosis

ATP Synthase

Here, H+ in the intermembrane space, go back down their concentration gradient. This energy is used to add an inorganic phosphate to ADP to form ATP

Membranes

Structure
phospholipid bilayer
Fluidity

helps regulated fluidity when too rigid or too fluid

Unsaturated fats

higher diffusion+ fluid

saturated fats

lower diffusion+ rigid

Temperature

lower temp= rigid

high temp= fluid

Transport
Permeability (high to low)

small, nonpolar > small, uncharged polar > large, uncharged polar > ions

Cotransport

when active transport indirectly transport of another

sucrose/H+: H+ drives sucrose in when H+ is pumped out of the cell and a gradient is created

Active

Uses energy to transport solute against its concentration gradient

electrogenic pump

Phases:

Resting State: na and k voltage gated pumps are closed

Depolartization: Na pump opens allowing Na to flow in making it less negative (if this hits a threshold it moves on to the rising phase)

Rising Phase: cell becomes positive while K pumps are still closed until action potential is reached

Falling Phase: Some k pumps open while na pumps close making the cell overall negative

Undershoot: the cell uses na/k pump to help return it to the resting phase.

creates a charge gradience generating voltage across a membrane

Na/K Pump

2 K+ in 3 Na+ out

Cells are slightly - because there are fewer positive charges in the cell

1. 3 Na in the cytoplasm bind to the pump

2. phosphorylation via kinase triggered (PO4 attaches to the pump)

3. Pump changes shape and releases Na+ out

4. 2 K+ outside the cell attach to the pump while removing PO4

5. pump returns to its original shape

6. K+ comes off the pump and the cycle repeats

Proton Pump

Bulk Transport

Use vesicles to transport large molecules. membrane stretches to engulf particles

exocytosis

cell ejects substances

endocytosis

cell takes in substances

receptor mediated

uses receptors and ligands to take in molecules

pinocytosis

takes in fluids

phagocytosis

takes in "food" particles

Facilitated

uses proteins and other channels to aid passive diffusion

Carrier proteins

changes shape to move solute

Channels

channel that allows water/solute to enter (no shape change)

Ion Channels

gated

voltage

opens/ closes when membrane potential changes

ligand

opens/closes when ligand binds to a receptor

stretch

opens/closes when deformed

ungated

constantly openn

Passive

diffusion down a concentration gradient w/out using energy

Tonicity
ability to cause cell to gain/lose water

Hypertonic sol.

relatively higher concentration compared to the cell

Plant: Plasmolyzed animal: shriveled

Isotonic sol.

same concentration as the cells

Plant: Flaccid animal: normal (ideal)

hypotonic sol.

relatively lower concentration compared to the cell

Plants: turgid (ideal) animal: lysed

Osmosis (H2O moves to areas with higher concentration)

Step 6 + 7: The two G3P become 2 pyruvate and 4 ATP, 2 NADH are produced.

x2

Products: 2 ATP, 6 NADH, 2 FADH

Inputs: 2 Acetyl CoA

Products: 2 pyruvate, 4 ATP, 2 NADH

Net Total: 2 pyruvate, 2 ATP, 2 NADH

Payoff Phase

trans & cis

Energy Investment Phase

Examples

Concept Map 1

Biomolecules

Lipids
Steroids

4 fused carbon rings

Hormones

Cholesterol

Low-Density Lipoprotein

deposits extra cholesterol in blood cells which can lead to plaque buildup.

High-Density Lipoprotein

helps remove excess cholesterol by taking it to the liver for excretion

Phospholipids

Function

forms phospholipid bilayers in cell membrane

amphipathic

phosphate group

2 fatty acids

glycogen

Triglycerides (Fats)

fatty acids (3)

Unsaturated

liquid at room temp.

double bonds

Saturated

solid at room temp.

No double bonds

Glycerol

Carbohydrates
Polysaccharides

Structural

Cellulose

linear structure

b (1,4) glycosidic linkages

No branching

Storage

Glycogen (animals)

Extensively Branched

Starch (plants)

Amylopectin

a (1,4), a (1,6) glycosidic linkages

Branched

Amylose

helical structure

a (1,4) glycosidic linkages

Unbranched

Disaccharides

Maltose(glucose+glucose)

Lactose (glucose+galactose)

Sucrose (glucose+fructose)

Monosaccharides

Aldoses

Ketoses

Trioses (3C)

Pentoses (5C)

Hexoses (6C)

Proteins
Structure

Quatenary

multiple tertiary protiens

Tertiary

Disulfide Bonds

R group interactions

Secondary

H-Bonds

Alpha + Beta Structures

Primary

Amino Acids

Peptide Bonds

DNA/RNA
Monomer

Nucleic Acids

Phosphate Group

Nitrogenous Base

RNA

U

DNA

A,T,C,G

Pentane Sugar

Ribose=RNA

Deoxyribose=DNA

Polymer

DNA= 2x strand RNA= 1 strand

Phosphodiester Linkage (5,3)

Eukaryotic/ Prokaryotic Cells

Double Membrane Bounded
Cells in plants and animals

Nucleus

Chromatin

Nucleolus

Nuclear Envelope

Endoplasmic Reticulum

Rough ER

Smooth ER

Cytoskeleton

microtubules

microfilaments

Golgi Apparatus

responsible for the synthesis and secretion of a cells products

Plasma Membrane

Mitochondria

where cellular respiration occurs and ATP is generated

Plant Cells

Cell Wall

maintains cell shape and protects cells from mechanical damage

Central Vacuole

used for storage, breaking down waste & hydrolysis of macromolecules

Plasmodesmata

channels through cell walls that connects the cytoplasm of adjacent cells

Chloroplast

converts energy of sunlight to chemical energy stored in sugar cells

Animal Cells

Lysosomes

Where macromolecules are hydrolized

Centrosome

region where microtubules are initiated

Domains of life
Eukarya
Bacteria

Components

Fimbrae

Cell Wall

Flagellum

Plasma Membranes

Ribosomes

Nucleoid

Archaea

Extremophiles

Extreme Halophiles

methanogens

Extreme thermophiles

Chemical Bonds

Intermolecular Forces (within molecules)
Ionic (electrons transferred from one atom to another creating an electrostatic force)
Covalent (electrons shared)

Electronegativity

<2.5

nonpolar

>2.5

Polar

Water Properties
Structure Based

Hydrophobic/Hydrophilic Interactions

High Surface Tension

Universal Solvent

Temperature Based

High Specific Heat

Expands when Freezing

Denser as a liquid

High Heat of vaporization

Intramolecular Forces (between molecules)
Hydrophobic Interactions

A repulsive interaction between water and non-polar molecules. The non-polar molecules will cluster together and be surrounded by water.

Van der Waals

A weak force that attracts non-polar atoms (this is distant dependent) and LDF's (a form where temporary dipoles form and attract other molecules) is a sub-category

Hydrogen Bonding

A form of Dipole-Dipole interaction between hydrogen and one following from another molecule (F, O, N)

Ion-Dipole

an Ion is attracted to the oppositely charged side of a polar molecule (water's oxygen atom and Na+ ion)

Dipole-Dipole

when 2 polar atoms have polarity and the positive end of one atom is attracted to the negative end of another