1/119
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai |
|---|
No analytics yet
Send a link to your students to track their progress
Scale of Life
Eukaryote cells: 10-100um
Prokaryote cells: >5um
Organelles:
-mitochondria: 1-10um
-chloroplasts: 2-5um
Natural Selection
Variation, Inheritance, Selection, Time
Three Domains of Life
Bacteria, Archaea, Eukarya
Building Blocks
Amino acids, nucleobases, simple carbohydrates, lipids
Macromolecules
Proteins, Nucleic acids (DNA and RNA), complex carbohydrates, lipids
Supramolecular asssemblies
Membranes, ribosomes, chromatin
Organelles
Nucleus, mitochondria, Golgi and Endoplasmic reticulum
Levels of Carbohydrates
Monosaccharides, disaccharides, oligosaccharides, polysaccharides
Functions of Carbohydrates
1. Recognition 2. Energy 3. Structure
Lipids
Not polymers, large, bulky and very different
Functions of Lipids
1. Structural 2. Regulatory 3. Energy
Function of Organelles
Provide conditions for specific processes, keep incompatible processes apart, allow formation of concentration gradient, package substances for transport
What stabilises membrane fluidity
Cholesterol
Passive Transport
Diffusion, facilitated diffusion
Diffusion
Membranes permeable to lipid soluble, membrane restricts water molecules and charged molecules (glucose and ions)
Facilitated diffusion
Movement of hydrophilic molecules require membrane proteins, channels and carriers, aid the movement of specific substances
Active transport (energy)
Active transport, co-transport
Active transport
Requires transport proteins
Co-transport
Indirect active transport, The concentration gradient used to power the movement of a second substance against its concentration gradient
Roles of Membrane Proteins
Transporters
Membrane proteins are involved in
Signal transduction, cell recognition, intercellular joining, linking cytoskeleton and extra cellular matrix
Signal transduction
Relays messages from the body into the cell (e.g. Grow, divide etc.)
Cell recognition
Involves glycoproteins
Intercellular joining
Formation of long-lasting connections between cells
Linking cytoskeleton and extracellular matrix
Allows a cell to physically connect with protein structures outside the cell (in the extracellular matrix)
Endomembrane system includes
Nuclear envelope, endoplasmic reticulum, Golgi apparatus, vesicles, lysosomes, vacuoles, plasma membrane
Endomembrane system
A membrane system interconnected by direct physical contact or transfer by vesicles.
Functions of the smooth endoplasmic reticulum
Metabolism of Carbohydrates, lipids synthesis for membranes (make phosphate lipids), detoxification of drugs and poisons, storage of calcium ions, extensive sER in cells active, sER can be increased and decreased to meet demands
`Functions of the rough endoplasmic reticulum
Protein synthesis (ribosomes), secreted and membrane-bound proteins enter the lumen (interior) of the rER, processed by rER and the endomembrane system for release from the cell or retention on cell membrane.
Function of the Golgi complex
Receives, modifies, sorts and ships proteins arriving from the rE, has polarity (cis and trans), vesicles arrive at the cis face leave at the trans face, Glycosylation, sorting proteins, directing vesicle trafficking
Glycosylaction
Additions/ modification of carbohydrates to proteins (important for secreted or cell surface proteins), Golgi produce many polysaccharides that may need to be secreted from the cell
Sorting proteins
Adds molecular makers to direct proteins to the correct vesicles
Directing vesicle trafficking
Adds molecular 'tags' to vesicles leaving the Golgi to direct them to the correct targets, short proteins exposed on the vesicle surface, acts as docking site, vesicles travel to lysosomes as well we secretory pathways, important for release and surface expression.
Bulk transport across the plasma membrane
Moving things out of the cell: Exocytosis, constitutive exoocytosis, regulated exocytosis
Moving things into the cell: Endocytosis, Phagocytosis, Pinocytosis, Receptor-medicated endocytosis
Exocytosis
Transports material (glycoproteins) out of the cell or delivers it the the cell surface
Constitutive exocytosis
Release extracellular matrix proteins
Regulated exocytosis
Releases hormones and eurotransmitters
Endocytosis
The cell takes in molecules and particulate matter at the plasma membrane
Phagocytosis
Cell 'eating', uptake of 'food' particles, forms a phagocytic vacuole which is 'digested' by the lysosomes
Pinocytosis
Cell 'drinking', up-take of extracellular fluid containing various solutes such as protein and sugars, up-take vesicle is formed with the aid of a coat protein, up-take is non-selective
Receptor-medicated endocytosis
Specialised form of Pinocytosis (looks for specific molecules that a receptor is attached to), allows the cell to take up bulk quantities of specific substances which may be present at only low concentrations in the extracellular fluid, receptor proteins are used to selectively capture the required solute
Lysosomes
Degrade proteins, lipids, carbohydrates and nucleic acids and release breakdown products into the cell, digest and recycle unwanted cellular material called autophagy, interior acidic for enzymes to be activated, phagocytic vacuoles fuse with lysosomes containing hydrolysis enzymes.
Vacuoles
Large vesicles derived from the rER and Golgi, important in plants for storage of organic compounds, large central vacuoles absorb water for plant cells to grow without needing more cytoplasm
Th cytoskeleton
Maintains cell shape and position of organelles within cells, rapidly disassembles and reassembles which allows rapid change in cell shape, highly dynamic but still provides stability
Cytoskeleton made up of
Microtubules, microfilaments, intermediate filaments
Microtubules
Composed of tubular subunits (form larger hollow tube), radiate out from centrosome, help maintain cell shape, allow movement, atp-powered motor proteins walk organelles along microtubules, allows vesicles to be transport to specific targets within the cell
Microfilaments
Double chain of actin subunits, form linear strands and 3-dimensional networks (branching proteins), resist tension, cortical network under the plasma membrane makes the region less fluid and maintain cell shape, interactions between actin and motor proteins (myosin) support cell movement, actin-myosin interactions allow muscle contraction, amoeboid movement, cytoplasmic streaming
Intermediate filaments
Various proteins including keratins (hair), lamins (nucleus), supercoiled into cables, less dynamic, form relatively permanent cellular structures, help maintain shape, anchor organelles, remain after the cell has died.
Cell junctions
Tight junction, desmosomes, gap junction
Tight junction
Prevents movement of fluid across cell layers, hold neighbouring cells tightly pressed together
Desmosomes
Anchoring junction, attachments between sheets of cells (muscles)
Gap junction
Cytoplasmic contact between two cells, ions and small molecules can pass from cell to cell, allows rapid cell to cell communication (intercellular)
How are cells joined together?
Extracellular matrix
Extracellular matrix (ECM)
Composed of material secreted by cells, secretion occur by constitutive Exocytosis, proteins are glycoproteins most abundant collagen, collagen fibres have great tensile strength, embedded in a proteoglycan complex matrix, proteoglycans are proteins with extensive added sugar, they trap water in ECM, membrane proteins (integrins) connect the ECM to the cytoskeleton providing a communication link from ECM to the cell interior
Cellulose
Glucose polymer, forms microfibrils, highly organised structures that are strong and form a major component of both primary and secondary cell walls
Cell wall structure
Phase 1: crystalline microfibrillar phase (cellulose) phase 2: noncrystalline matrix, pectic polysaccharides, hemicellulose polysaccharides , plus a network of extension (protein)
No crystalline matrix (hemicellulose and pectin)
Hemicellulose: Long chain with short side chains
Pectin: branched, negatively charged
The Protein extensin
Cross-linking of pectin and cellulose dehydrates the cell wall, reduces extensibility and increased strength, extensibility controlled by cross-linking
Synthesis of the primary cell wall
1. Cellulose microfibrils at plasma membrane 2. Polysaccharides in the Golgi apparatus are transported to the cell wall in vesicles 3. Cell wall proteins from the rough er
The vesicles fuse with the plasma membrane, cellulose-producing rosettes move parallel to the cortical mircotubules
Cell wall functions
Influences cell morphology, provides structural support, prevents excessive water uptake
The secondary cell wall
Produced after cell growth stops, thicker and stronger than primary cell walls, provides more structural support
Secondary cell wall structure
Multiple layers, microfibrils in each layer have different orientations, chemical characteristics : more cellulose, less pectin, lignin
Lignin
Complex lignin, confers strength and rigidity, acts to exclude water
Secondary cell wall structural support
For specific cell types: water transporting cells and the whole plant
Plasmodesmata
Cell communication, intercellular connections, plasma membrane is continuous, prevent organelles movement, free exchange of small molecules
Major energy requirements of the cell
Mechanical work (motor proteins), formation of new material (growth and replacement), transport (molecules across membranes), maintain order
Mitochondria
Contains mitochondria, DNA and ribosomes ( produces some mitochondrial proteins), two membranes, mitochondrial matrix inside inner membrane, inner membrane (cristae), intermembrane space functionally important
Cellular respiration
Harvesting chemical energy from glucose
1. Glycolysis
2. Pyruvate oxidation and citric acid
3. Oxidative phosphorylation
Glycolysis
In the ctyosol, glucose is converted into pyruvate, generates 2 ATP, electrons are transferred to the high energy electron carrier NAD+ making NADH
Pyruvate oxidation and citric acid
In the mitochondrial matrix, pyruvate is converted into Acetyl CoA which enters the citric acid cycle, output of energy carrier ATP and high energy electron carriers NADH and FADH2
Oxidative phosphorylation
Inner membrane of the mitochondrion, electron transport ( electrons from NADH and FADH2 ), chemiosmosis -ATP production
Electron transport chain: electrons move through protein complexes embedded in the inner membrane, protons pumped across the membrane accumulate in the intermembrane space, accumulation of protons is crucial for chemiosmosis
Chemiosmosis: ATP synthase spans fro the intermembrane space to the mitochondria matrix, protein gradient powers ATP synthase
Adenosine triphosphate (ATP)
Enables controlled release of energy, cell continuously uses and regenerates ATP
Photosynthesis
Light reactions occur in the thylakoid membrane, carbon fixation occurs in the stroma
The light reactions
1. Photosystems are protein complexes that contain the chlorophyll 2. Chlorophyll absorbs light energy 3. Light energy absorbed by chlorophyll produces high energy electrons 4. High energy electrons travel through the photosynthetic electron transport chain
Chloroplast
Contain DNA, ribosomes and are able to make their own proteins
The nuclear pore complex
Controls movement of molecules out of or into the nucleus
Out: mRNA, tRNA and ribosomes
In: control signals, building materials and energy
Within the nucleus
Inner surface of nuclear envelope lined by nuclear lamina, composed of intermediate filaments, maintain nucleus shape, organise the packing of the DNA
Nucleolus
Prominent nuclear structure with non-diving cells, two or more nucleoli per cell, responsible for making ribosomal RNA which combines with proteins to produce ribosomes
DNA organisation within the nucleus
DNA a nucleotide polymer, DNA double helix, helix interacts between the specific proteins histones, DNA strand coiled to form fibre, coil again in cell division to form metaphase chromosomes (karyotype)
Euchromatin and Heterochromatin
Euchromatin: less dense, contains genes being used by that cell
Heterochromatin: more dense, contains genes not being used by that cell
Dynamic relationship
Chargaff discovery
Significant DNA variation between species thus DNA could be the genetic material.
Chargoff' Rules
First rule: A = T and G = C
Second rule: the composition of DNA varies between species
DNA structure
Double stranded helical molecule with particular features
X-ray diffraction patter of DNA
Bases perpendicular to the length of the DNA molecule
Formation of the Phosphodiester Bond
The hydroxyl group (OH) on the 3rd carbon of one nucleotide reacts with the phosphate group attached to the 5th carbon on another nucleotide
Each strand has a direction, the two strands are antiparallel
The Watson-Crick model of DNA structure
Sugar phosphate backbone is on the outside, bases on the inside, stabilised by hydrogen bonds, two polynucleotide strands are oriented in opposite directions
Watson-Crick model provides
A stimulus for deciphering the genetic code, possible mechanism for the replication of DNA
Eukaryotic DNA replication
Multiple large linear chromosomes (23)' multiple origins of replication, bidirectional
Direction of DNA synthesis
DNA always synthesised in the 5' -> 3' direction, parental template strands are run in the 3' -> 5' direction
What is needed to make a DNA copy
Progressive addition of new nucleotides (DNA polymerase III), a starting point for nucleotide addition (Primase enzyme makes RNA primer), unwinding of the helical double-stranded DNA to give two parental templates ( helicase), release of tension generated by unwinding the DNA helix (topoiaomerase nicks and rejoins DNA strands), prevention of unwound double-stranded helical DNA ( single-stranded DNA binding protein, DNA polymerase I removes RNA primer and fills the gap with DNA nucleotides), joining of ends of newly synthesised fragments together (DNA ligase)
Replication of semi-discontinuous
Leading strand: continuously synthesised in its 5' -> 3' direction
Lagging strand: discontinuously synthesised in its 5' -> 3' direction as Okazaki fragments
Primase
Enzyme (type of RNA polymerase) makes aRNA primer = starting point for DNA polymerisation
DNA polymerase III (Pol III)
Needs an OH group which the phosphate group of the incoming nucleotide can be attached to, only makes 5' to 3' DNA synthesising a new DNA strand complementary to the parental template strands, cannot bind to single stranded DNA
DNA polymerase I
Removes RNA primers (RNase H) and fils the gap with DNA nucleotides
DNA Ligase
Joins the new synthesised Okazaki fragments together (creates phophodiester bonds)
DNA Pol I arrives out two activites
1. RNase activity: endonuclear enzyme that recognises DNA : RNA hybrids and degrades the RNA part
2. DNA polymerase activity: synthesises DNA by adding nucleotides (complementary to the parental DNA template of the lagging strand)
Repair of DNA errors
1. During replication : exonuclease
2. After replication : endonuclease
Durning replication
High accuracy, DNA pol III has a proofreading mechanism, check the newly inserted nucleotide bases against the template
After DNA replication
Variety things can cause damage and errors
Incorrectly inserted bases not corrected by Pol III, radiation damage, chemical modification of bases
Importance I'd correcting DNA errors
If not corrected the error becomes part of the DNA template, permanent change, mutation