Everything about Replica Plating totally explained
In
molecular biology and
microbiology,
replica plating is a technique in which one or more secondary
Petri plates containing different solid (
agar-based)
selective growth media (lacking nutrients or containing chemical growth inhibitors such as
antibiotics) are inoculated with the same colonies of
microorganisms from a primary plate (or master dish), reproducing the original spatial pattern of colonies. The technique involves pressing a
velvet-covered disk,
nitrocellulose membrane, or filter paper to a primary plate, and then imprinting secondary plates with cells in colonies removed from the original plate by the material. Generally, large numbers of colonies (roughly 30-300) are replica plated due to the difficulty in
streaking each out individually onto a separate plate.
The purpose of replica plating is to be able to compare the master plate and any secondary plates to
screen for a
selectable phenotype. For example, a colony which appeared on the master plate but failed to appear at the same location on a secondary plate shows that the colony was sensitive to a substance on that particular secondary plate. Common screenable phenotypes include
auxotrophy and
antibiotic resistance.
Replica plating is especially useful for
negative selection. For example, if one wanted to select colonies that were sensitive to
ampicillin, the primary plate could be replica plated on a secondary Amp
+ agar plate . The sensitive colonies on the secondary plate would die but the colonies could still be deduced from the primary plate since the two have the same spatial patterns from ampicillin resistant colonies. The sensitive colonies could then be picked off from the primary plate. While doing this, frequently the last plate will be non-selective, in this example, a nonselective plate will be replica plated after the Amp+ plate, to confirm that the absence of growth on the selective plate is due to the selection itself, and not a problem with transferring cells. Basically, if one sees growth on the third (nonselective) plate but not the second one, this indicates the selective agent is responsible for the lack of growth; if the non-selective plate shows no growth then one can't say whether viable cells were transferred at all and no conclusions can be made about the presence or absence of growth on selective media. This is particularly useful if there are questions about the age or viability of the cells on the original plate.
By increasing the variety of secondary plates with different
selective growth media, it's possible to rapidly screen a large number of individual isolated colonies for as many phenotypes as there are secondary plates.
This technique was first described by
Joshua Lederberg and
Esther Lederberg in
1952.
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