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    Economic and easy bacterial and yeast colony PCR with 2x premix Gotaq-Green (Promega) or DreamTaq-Green (Thermo Fisher)

    Dariusz Abramczyk

    Published: 2023-03-18 DOI: 10.17504/protocols.io.eq2ly74jqlx9/v1
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    Abstract

    Slightly modified method Gotaq Promega or DreamTaq (Thermo), economical, quick and ready-to-load. Perfect for yeast genotyping and screening

    Steps

    1.

    Bacterial colony PCR

    PCR reactions using ProFlex PCR system, Applied Biosystems. Thermal Cycler

    1.1.
    ABC
    Reagent NameInitial Conc.Volume (μL)
    gotaq green 2x2X5
    oligo 110uM0.6
    oligo 210 uM0.6
    cell suspension in watercells suspension0.8
    ddH2ON/A3
    TOTAL Volume:10 uL
    ABCD
    Number of CyclesStep NameTemperatureDuration
    1Initial Denaturation98oC10min
    30Denaturation98oC10 sec
    Annealing50-55oC30 sec
    1min  (depends on the length)72oC1min per 1kb
    1Hold4-10oChold

    Note
    Maximum (good quality) PCR product up to ~3kb. The best yield is 0.2kb-2kb

    Note
    pick a colony from agar plate and swirl in sterile water 50-100µL . From liquid culture, dilute saturated culture5-10µL in sterile 50-100µL water.This is a source for reaction (taking 0.8µL ).Keep the rest in ice, for re-culture of positively verified clones.

    1.2.

    Load on 1-1.2% agarose gel 8-10µL and visualise under GelDoc or another UV source.

    2.

    Yeast colony PCR (S.cerevisiae, Pichia, Candida)

    2.1.

    Alkaline yeast cells lysis treatment. Pick a yeast colony from agar plate and swirl in sterile 20mM NaOH 50-100µL .

    Optionally, a liquid culture or a agar-plate pick colony resusupend in the sterile water or YPD, take small volume (~20uL) and mix with the same volume of 40mM NaOH.

    20mM NaOH-cells resuspension incubate 95°C 0h 10m 0s and immediately transfer to ice/4°C for at least 0h 5m 0s

    2.2.
    ABC
    Reagent NameInitial Conc.Volume (μL)
    gotaq green 2x2X5
    oligo 110uM0.6
    oligo 210 uM0.6
    cell suspension in 20mMyeast suspension0.8
    ddH2ON/A3
    TOTAL Volume:10 uL
    ABCD
    ABCD
    Number of CyclesStep NameTemperatureDuration
    1Initial Denaturation98oC2min
    30-33Denaturation98oC10 sec
    Annealing52-55oC1min 30sec
    1min (depends on the length)72oC1min per 1kb
    1Hold4-10oChold

    Note
    Maximum PCR product up to ~3kb. The best yield is 0.2kb-2kb

    Note
    Important - annealing 1min30sec

    2.3.

    Load on 1-1.2% agarose gel 8-10µL and visualise under GelDoc or another UV source.

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