Lenses work more effectively if they
are in a compound light microscope
Light waves a have a relatively long wavelength;
therefore, they can only distinguish between objects
that are at least 0.2 micrometers apart
Beams of electrons have
shorter wavelengths and are
therefore able to distinguish
between objects as close as
0.1 nm apart
Magnification
When viewed under a microscope, the
material seen in called an image
Magnification tells you how many
times bigger the image is in relation
to the actual size of the object
Magnification = size of image/size of object
Resolution
The resolving power of a microscope is the
minimum distance two objects can be
apart in order for them to appear as
separate items
The greater the resolution, the greater the clarity of the image that is produced
Cell fractionation
Cell fractionation is the process where cells
are broken up and the different organelles
they contain are separated out
Before fractionation begins, the cells
are put in a solution that is:
Cold
to reduce enzyme activity that
might break down the organelles.
Isotonic
to prevent organelles
bursting or shrinking as a
result of osmotic gain or loss
of water. An isotonic solution
is one that has the same
water potential as the original
tissue.
Buffered
to maintain a constant pH
Homogenation
Cells are broken up by a
homogeniser that releases the
organelles
The fluid is called a homogenate
It is then filtered to remove complete cells and large
pieces of debris
Ultracentrifugation
Ultracentrifugation is the process by which the homogenate is
separated in a machine called a centrifuge
This spins tubes of the homogenate, creating a centrifugal force that
makes the mixture separate
The tube of filtrate is placed in the ultracentrifuge and spun at a slow speed
The heaviest organelles such as the nucleus are forced to the bottom where they form a thin
sediment
The fluid at the top, called the supernatant is removed, leaving just the sediment of nuclei at the
bottom
The supernatant is then put in another tube where it is spun at an even higher speed than before
The next heaviest organelles (mitochondria) are forced to the bottom and the process continues
until all the organelles are separated
electron microscope
Electrons have a shorter wavelength
than light and so they have a greater
resolving power
As electrons are negatively charged, the beam
can be focused using an electromagnet
Because electrons are absorbed by
molecules in the air, a near vacuum
must be created within the chamber
of an electron microscope for it to
work effectively
Transmission electron microscope
The TEM consists of a gun that fires electrons which are focused onto the specimen by an
electromagnet
Some of the electrons are absorbed by the specimen and appear dark on the image; other parts
allow the electrons through and so appear light. This produces an image of the specimen
The image that appears on screen is called a photomicrograph
Because the process takes place in a vacuum, living specimens cannot be observed
A complex staining process is required and even then the image is only in B&W
The specimen must be extremely thin
Artefacts (structure not present in the organism when it was alive) may appear on the image, these
appear as a result of the way the specimen is prepared
Scanning electron microscope
All the limitations of the TEM apply to the SEM but the
specimen does not have to be extremely thin as the
electrons do not penetrate
The beam of electrons is directed over the surface of the specimen in a regular pattern
The electrons bounce on the contours of the specimen and are scattered
The scattering of the electrons can be analysed and from this an image can be produced using
a computer
The SEM has a lower resolving power than the TEM (20nm) but is still ten times better than
a light microscope