What 3 components are in plants cells, but NOT animal cells?
PermanentVacuole
CellWall
Chloroplasts
Cell Surface Membrane:~ Structure
Found in all cells
Phospholipidbilayer - molecules embed within and attached on the outside - fluidmosaic model (proteins, cholesterol, carbohydrates)
Cell Surface Membrane:~ Function
Controls the entrance and exit of molecules
Nucleus:~ Structure
Nuclear Envelope - double membrane with nuclearpores
Nucleoplasm - jelly like material
Chromatin - linear, protein-bound DNA
Nucleolus - smaller sphere inside which is the site of rRNA production and makes ribosomes
Nucleus:~ Function
Site of DNAreplication and transcription (making mRNA)
Contains the geneticcode for each cell
Mitochondria:~ Structure
Double membrane with an inner membrane (cristae)
MitochondrialMatrix - Fluid centre
Loop of mitochondrial DNA
Mitochondria:~ Function
Site of aerobicrespiration
Golgi Apparatus/Vesicles:~ Structure
Folded membranes making cisternae
Golgi Apparatus/Vesicles:~ Function
Adds carbohydrates to proteins to form glycoproteins
Produces secretory enzymes
Secretes carbohydrates
Transport, modify & storelipids, and forms lysosomes
Molecules are 'labelled' with their destination
Lysosomes:~ Structure
Bags of digestiveenzymes (lysozymes)
Lysosomes:~ Function
Hydrolyse phagocytic cells and completely breaks down dead cells (autolysis)
Exocytosis - release enzymes outside the cell to destroy the material
Digest worn-out organelles for reuse of materials
Ribosomes:~ Structure
Made up of 2 sub-units of protein and rRNA
80s found in eukaryotic cells
70s found in prokaryotic cells, mitochondria & chloroplasts
Ribosomes:~ Function
Site of proteinsynthesis
RER & SER:~ Structure
Both have folded membranes (cisternae)
RER have ribosomes on the cisternae
RER & SER:~ Function
RER - Proteinsynthesis
SER - Synthesis and store lipids/carbohydrates
Cell Wall:~ Structure
In plants and fungi cells
Plants - made of microfibrils of cellulose
Fungi - made of chitin, a nitrogenouspolysaccharide
Cell Wall:~ Function
Provides structuralstrength to the cell
Cell Vacuole:~ Structure
Filled with fluid surrounded by a single membrane (tonoplast)
Cell Vacuole:~ Function
Makes cell turgid, providing support
Temporary store of sugars and aminoacids
Pigment may attract pollinators
What are the 5 key differences between prokaryotic and eukaryotic cells?
Prokaryotic cells:
are smaller
have smaller ribosomes (70s)
have no nucleus
have no membrane-boundorganelles
have cell walls made of murein
What are 3 additional organelles that some prokaryotic organisms have?
Plasmid
Capsule
Flagella
Viruses:
Viruses are non-living and acellular. They are even smaller than bacteria and only contain geneticmaterial, a capsid, and an attachmentprotein.
HIV is surrounded by a further lipidenvelope that has attachmentproteins on the outside. This is to enable the virus to identify the host cells to enter.
What are the 3 key types of microscopes?
Optical (light)
Scanning electron
Transmission electron
What is magnification?
How many times larger the image is compared to the object.
What is resolution?
The minimum distance between two objects in which they can still be viewed as separate.
The resolution in an optical microscope is determined by the wavelength of light, and the wavelength of the beam of electrons determines the resolution of an electronmicroscope
Why do light microscopes have a poor resolution?
Light microscopes have a poor resolution due to the longwavelength of light.
Why are small organelles in a cell are not visible using an optical microscope?
They are too small to be visible due to the wavelength of light limiting the resolution and have a lower magnification too.
What's the formula for magnification?
Image size = Actual size x Magnification
Optical Microscopes:~
What creates the image? - beam of light
Condenser - glass lens
Resolution - poor
Magnification - lower
Colour - colour
Types of samples - can view living samples
Electron microscopes:~
What creates the image? - beam of electrons
Condenser - electromagnets
Resolution - high
Magnification - higher
Colour - black & white
Types of samples - samples must be viewed in a vacuum so cannot be living
What are the stages of cell fractionation?
Cells are broken down so that organelles are free to be separated
This is done using a homogeniser, a blender
Once the cell has been broken open, the solution must be filtered to remove larger pieces of debris
The solution in cell fractionation must be:
isotonic
pHbuffered
icecold
Why must the solution be isotonic in cell fractionation?
to prevent any movement of water by osmosis resulting in organelles shrivelling (hypertonic) or bursting (hypotonic)
Why must the solution be pH buffered in cell fractionation?
to prevent pHchanges, therefore not damaging the organelles/enzymes
Why must the solution be ice cold in cell fractionation?
to reduce enzymeactivity to prevent the breakdown of cell components
What is ultracentrifugation?
Once filtered, the homogenate solution is ready to be centrifuged. The solution is placed into a centrifuge which spins at different speeds to separate organelles depending on their density due to the centrifugal force
What are the stages of ultracentrifugation to separate the nuclei, mitochondria/chloroplasts, lysosomes and SER/RER and ribosomes?
Supernatant after the first spin at lowspeed- pellet contains the nuclei.
Supernatant after the second spin at mediumspeed- pellet contains mitochondria and chloroplasts (if a plant cell).
Supernatant after the third spin at highspeed- pellet contains lysosomes and SER/RER.
Supernatant after the fourth spin at veryhighspeed- pellet contains ribosomes
During which stage of the cell cycle does DNA replicate?
interphase/ S phase
During which stage of the cell cycle does the cell divide to produce identical daughter cells?