Differential centrifugation is a technique used to separate cell organelles based on their densities. It involves homogenizing tissue to break open cells and mix organelle contents. The homogenate is then centrifuged at increasing speeds, causing organelles like mitochondria and lysosomes to pellet out after centrifuging at 1000g for 15 minutes. Repeating this process with the supernatant at higher speeds allows separation of organelles into fractions based on their sedimentation rates in a centrifugal field. While convenient and economical, differential centrifugation yields impure preparations and poor recovery of organelles.
Differential centrifugation is a preparative technique in microbiology and cytology to separate cell organelles from tissues. Tissue is homogenised to mix cellular contents.
Homogenate particles are separated based on density or size by varying centrifugal fields. Specific times for sedimentation of organelles like mitochondria are noted.
Pellets obtained are not pure and contain contaminants. Multiple washes are necessary to reduce unwanted particles.
This method is favored for its convenience and economy but often results in poor yield and impure preparations.
Differential centrifugationis a type of ultra centrifugation
technique which comes under preparative ultra
centrifugation.
This technique is a common procedure in microbiology &
cytology.
The main essence of this centrifugation is to separate
certain cell organells from a cell to study & analyse the
specific parts of the cell.
In this process, a tissue sample is first homogenised to
break the cell membrane and mix up the cellular contents.
3.
Mixture ofhomogenate particles can be separated by
centrifugation on the basis of their densities or size.
This can be achieved either by knowing the time required
for their complete sedimentation in a fixed centrifugal field
or the extent of their sedimentation after a given time in a
fixed centrifugal field.
In the same manner we can vary the value of centrifugal
field applied for the each intracellular organelle and again
find out the time required for each of them to sediment
completely under various centrifugal fields.
For example- upon subjecting a homogenate mixture of
cell organelles for centrifugation for 15minutes at 1000g,
the cell organelles like mitochondria and lysosomes will
pellet out.
4.
The beststratagy that we can adapt now to separate
the tissue homogenate into various cell organelles is
to centrifugally divide the homogenate into number of
fractions by increasing the centrifugal field at each
step.
Centrifugal field should be choosed in a manner by
knowing that a particular organelle will sediment at a
known time to give a pellet.
The pellet and supernatent will be seperated in each
step and the supernatent is recentrifugated to
sediment another light intra cellular organells.
5.
Every pellethas to be washed several times
because the pellet obtained is never pure.
That means the pellet will contain contamination
from other particles contained in the
homogenate apart form the desired.
6.
ADVANTAGES
This method however
remainsmost common
method for the isolation
of intracellular organelles
form tissue homogenate
This method is most
common because of
its conveniece
&economy
DISADVANTAGES
Poor yield and
the fact that
preparations
obtained are
never pure
Advantages and Disadvantages of Differential
centrifugation
For certain experiments which
require absolute purity density
gradients methods can be used