Cell structure part 2 Flashcards
What is the object?
The material put under the microscope.
What is the image?
The appearance of the object when viewed under the microscope.
What is magnification?
How many times bigger the image is when compared to the object.
What is the equation for magnification?
Magnification = size of image / size of real object
Convert the units of kilometres, metres, millimetres, micrometres and nanometres.
Km = 10^3m
m = 1m
mm = 10^-3
μm = 10^-6
nm = 10^-9
x 1000 to get smaller units (e.g. μm to nm, /1000 to go bigger).
What is resolution?
The minimum distance apart two objects can be in order for them to appear as separate items.
It depends on the wavelength or form of radiation used.
What is cell fractionation?
The process where cells are broken up and the organelles separated out.
What happens before cell fractionation?
The tissue is placed in a cold, buffered solution of the same water potential as the tissue.
Why is the solution cold?
To reduce enzyme activity that might break down the organelles.
Why is the solution the same water potential?
To prevent organelles bursting or shrinking as a result of osmotic gain or loss of water.
Why is the solution buffered?
So that the pH does not fluctuate.
Any change in pH could alter the structure of the organelles or affect the functioning of enzymes.
What is the first stage of cell fractionation?
Homogenation - cells are broken up by a homogeniser.
This releases the organelles from the cell.
The resultant fluid, homogenate, is then filtered to remove any complete cells and large pieces of debris.
What is the second stage of cell fractionation?
Ultracentrifugation - the process that separates the fragments of the homogenate in a centrifuge.
This spins the tubes of homogenate at very high speed to create a centrifugal force.
What is the process of ultracentrifugation?
The tube of filtrate is placed in the centrifuge and spun at a slow speed.
The heaviest organelles, the nuclei, are forced to the bottom of the tube, where they form a thin sediment or pellet.
The fluid at the top, supernatant, is removed and transferred to another tube and spun at a faster speed than before.
The next heaviest organelles, the mitochondria, are forced to the bottom.
The process is continued, with increased speed, so the next heaviest organelles are sedimented and separated out.
What is the speed of centrifugation for each organelle?
Nuclei - 1000 revolutions per minute.
Chloroplasts
Mitochondria - 3500
Lysosomes - 16500.
Endoplasmic reticulum
Ribosomes
What are the advantages of an electron microscope?
The electron beam has a very short wavelength so it can resolve objects very well.
Electrons are negatively charged so the beam can be focused using electromagnets.
What is the resolving power of the best electron microscopes?
Resolves objects that are only 0.1nm apart - 2000 times better than a light microscope.
Why do electron microscopes use vacuums?
Electrons would be absorbed or deflected by molecules in the air otherwise.
What are the disadvantages of electron microscopes?
Living specimens can’t be observed because there is no air in a vacuum.
What are the two types of electron microscope?
The transmission electron microscope (TEM)
The Scanning electron microscope (SEM).
How does the TEM work?
It consists of an electron gun that produces a beam of electrons that is focused onto the specimen by a condenser electromagnet.
The beam passes through a thin section of the specimen.
Parts of the specimen absorb electrons and appear dark.
Other parts of the specimen allow electrons through and so appear bright.
An image appears on the screen and can be photographed to give a photomicrograph.