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LiAc/SS-DNA/PEG method Page

The TRAFO Page

 

HIGH EFFICIENCY TRANSFORMATION

Reference: Gietz, R.D. and R.A. Woods. (2002) TRANSFORMATION OF YEAST BY THE Liac/SS CARRIER DNA/PEG METHOD. Methods in Enzymology 350: 87-96.

All Solutions for the LiAc/SS-DNA/PEG TRAFO Protocol are listed in the TRAFO Solutions Page.



High Efficiency Transformation Protocol


This protocol can be used to generate sufficient transformants in a single reaction to screen multiple yeast genome equivalents for plasmids that complement a specific mutation. It can also be used to transform integrating plasmids, DNA fragments and oligonucleotides for yeast genome manipulation. Finally, it is used to optimise the conditions for transformation of a particular yeast strain, for example, the transformation of a plasmid library into a two-hybrid yeast strain transformed with a bait plasmid by the Rapid Transformation Protocol. The High Efficiency Protocol can also be employed to transform a yeast strain simultaneously with two different plasmids, such as the two-hybrid bait and prey plasmids.


Day 1


Inoculate the yeast strain into 5 ml of liquid medium (2x YPAD or SC selection medium) and incubate overnight on a rotary shaker at 200 rpm and 30°C. Place a bottle of double strength YPAD broth (2x YPAD) and a 250 ml culture flask in the incubator as well.


Day 2


1. Determine the titer of the yeast culture by pipetting 10 ml of cells into 1.0 ml of water in a spectrophotometer cuvette and measuring the OD at 600 nm. For many yeast strains a suspension containing 1 x 10
6 cells/ml will give an OD600 of 1.0. Alternatively, titer the culture using a hemocytometer. see note:


    Note:



2.
Transfer 50 ml of the pre-warmed 2x YPAD to the pre-warmed culture flask and add 2.5 x 108 cells to give 5 x 106 cells/ml.


3. Incubate the flask on a rotary or reciprocating shaker at 30°C and 200 rpm.

 

4. When the cell titer is at least 2 x 107 cells/ml, which should take about 4 hours, harvest the cells by centrifugation at 3000 g for 5 min, wash the cells in 25 ml of sterile water and resuspend in 1 ml of sterile water.


5. Boil a 1.0 ml sample of carrier DNA for 5 min and chill in an ice/water bath while harvesting the cells.

**** It is not necessary or desirable to boil the carrier DNA every time. Keep a small aliquot in your own freezer box and boil after 3-4 freeze-thaws. But keep on ice when out.****


6. Transfer the cell suspension to a 1.5 ml microcentrifuge tube, centrifuge for 30 sec and discard the supernatant.


7. Add water to a final volume of 1.0 ml and vortex mix vigorously to resuspend the cells.


8. Pipette 100 µl samples (ca. 10
8 cells) into 1.5 ml microfuge tubes, one for each transformation, centrifuge at top speed for 30 sec and remove the supernatant.


9. Make up sufficient Transformation Mix for the planned number of transformations plus one extra. Keep the Transformation Mix in ice/water.

  Number of Transformations

 Reagents

  1

5 (6X)

10 (11X)
PEG 3500 50% w/v

 240 µl

 1440 µl 2640 µl
 LiAc 1.0 M

 36 µl

216 µl 396 µl
 Boiled SS-carrier DNA

 50 µl

300 µl  550 µl
 Plasmid DNA plus Water

 34 µl

204 µl 374 µl

 Total

 360 µl

2160 µl 3960 µl



10. Add 360 µl of Transformation Mix to each transformation tube and resuspend the cells by vortex mixing vigorously.


11. Incubate the tubes in a 42°C water bath for 40 min.


12. Microcentrifuge at top speed for 30 sec and remove the Transformation Mix with a micropipettor.


13. Pipette 1.0 ml of sterile water into each tube; stir the pellet by with a micropipette tip and vortex .


14. Plate appropriate dilutions of the cell suspension onto SC selection medium. For transformation with an integrating plasmid (YIp), linear construct or oligonucleotide, plate 200 µl onto each of 5 plates; for a YEp, YRp or YCp library plasmid dilute 10 µl of the suspension into 1.0 µl of water and plate 10 and 100 µl samples onto two plates each. The 10 µl samples should be pipetted directly into 100 µl puddles of sterile water on the SC selection medium.


15. Incubate the plates at 30°C for 3 to 4 days and count the number of transformants.
The transformation efficiency (transformants/1 mg plasmid/10
8 cells) can be determined by calculating the number of transformants in 1.0 ml of resuspended cells per 1.0 microgram plasmid per 108 cells. For example, if the transformation of 1.0 x 108 cells with 100 ng plasmid resulted in 500 colonies on a plate of SC dropout medium spread with 1 ml of suspension:
Transformation Efficiency = 500 x 1000 (plating factor) x 10 (plasmid factor) x 1 (cells/transformation x 10
8).
Transformation Efficiency = 5 x 10
6 transformants/1.0 mg plasmid/108 cells.
Transformation efficiency declines as plasmid concentration is increased (Gietz et al. 1995) but the actual yield of transformants per transformation increases. For example, 100 ng of plasmid in a transformation might give a Transformation Efficiency of 5 x 10
6 and a yield of 5 x 105 transformants whereas with 1 µg of plasmid the Transformation Efficiency might be 2 x 106 and the yield 2 x 106 per transformation. In order to obtain 5 x 106 transformants it is simpler to set up two or three transformations with 1 µg of plasmid DNA, or a single 3 fold scaled up transformation, than to carry out 10 reactions with 100 ng of plasmid in each.

    Note: Two plasmids, such as an expression plasmid and a library plasmid pool, can be co-transformed into a single cell by including both plasmids in the same transformation reaction. The efficiency is reduced, however, because only about 30-40 % of all transformed cells take up more than one plasmid molecule. An alternative approach, which has a higher efficiency is to transform in the expression plasmid first, using this or the Quick and Easy protocol, and then use the protocol found on the 2 Hybrid System TRAFO Page to transform in the library plasmid pool.



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