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Screening bacterial colonies by PCR
methodbook.net
NameInstitutione-mail (optional)
Matt LewisDepartment of Pathology
University of Liverpool
m.lewis@liv.ac.uk

Colony screening by PCR

Notes

This is the fastest way to screen bacterial colonies. Our PCR machine takes 24 tubes so I routinely screen 22 colonies + 1 negative + 1 positive control.

Choosing the primers

Ideally you want a primer pair that can only work if the correct construct is present eg. a vector flanking primer and a gene specific primer. However, this may not allow you a positive control (essential) so you might have to use both vector flanking primers instead. If you have enough space in your PCR machine you could do both.

Typical Protocol

Set up 24 PCR tubes each containing 5ml H2O.

Touch a fresh toothpick (or yellow tip) onto a colony, dip it into a PCR tube, then streak it onto a fresh replicate agar plate using a numbered template.

I don't label the PCR tubes. I can tell what number they are and also whether they have been 'dipped' by their position in the rack/block.

Repeat this for the 22 (or whatever) colonies

for tube 23 (-ve control) use a colony that is negative (or use nothing).
for tube 24 (+ve control) use a colony that will yield a product with your primers.
If you don't have a +ve colony then use a tiny amount of plasmid DNA

Incubate the replicate agar plate at 37C.

These streaked colonies will be visible within 6-8 hours so you can set up overnight miniprep cultures on the same day.

Set up a 25 x PCR pre-mix as follows;

1 x pre-mix_25 x pre-mix
2ml
0.6ml
0.1ml
0.1ml
5ml
12ml
0.2ml
10 x PCR buffer
MgCl2 (50mM)
primer 1 (100mM)
primer 2 (100mM)
Template
H2O
cheap Taq
50ml
15ml
2.5ml
2.5ml
- ml
300ml
5ml

Add 15ml of pre-mix to each PCR tube.

PCR program

CyclesTemperatureDuration
194C60 seconds
2594C30 seconds
55C30 seconds
72C1 minute

This PCR should take less than 2 hours. While the PCR is running prepare the agarose gel ready to analyze the PCR products.

When you have the result you can go to the replica agar plate on the same day and set up miniprep cultures of the likely candidate colonies.

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