Transformation
Transformation
Introduction
The purpose of the lab is to calculate the transformation efficiency of bacteria exposed to plasmid conferring antibiotic Ampicillin resistance and bioluminescence.
Transformation is the uptake of foreign DNA by competent cells to express a foreign gene. In order to be competent, the cell must be in logarithmic growth. It also must have a weak cell wall and plasma membrane. The cell then should undergo rapid binary fission. The foreign DNA is transferred to the competent cell via a vector. The primary vector used is the plasmid. Plasmids are extra chromosomal and contain the gene of interest, in this case bioluminescence. The R plasmid, which causes the resistance to Ampicillin, confirms antibiotic resistance. It makes it able to identify which cells under went transformation. Restriction endonucleases can be used to cut and insert pieces of foreign DNA into the plasmid. Once the bacteria or competent cell takes up the plasmid, the restriction enzymes in the host cell immediately begin cutting up the foreign DNA. The DNA can then fit in the host DNA due to sticky ends. Once the host cell accepts the plasmid, it has been transformed. The transformation efficiency can then be calculated by the following calculation:
Number of transformants * final volume at recovery (ml) = number of mg of DNA volume plated (ml) transformants per mg
Those cells that accept the plasmid will be identified by growing on an Ampicillin positive plate and glow in the dark.
If the exposure of bacteria to plasmid pAMP/pBlu is increased, then the transformation efficiency will increase.
The dependent variable is the rate of transformation efficiency as measured by number of colonies glowing.
The independent variable is the amount of exposure to pAMP/pBlu plasmid as defined by 10 ml of plasmid.
The control is the rate of transformation efficiency of bacteria without exposure to plasmids pAMP/pBlu.
Procedure
Materials
2- 15 ml tubes
2- micropipettes
500 ml- CaCl2
2- cotton swabs
10 ml- pAMP solution (.005mg/ml)
1- 500 ml beaker
250 ml- ice cold water
10- ice cubes
1- clock
1- LB agar plate
1- LB agar plate with Ampicillin
1- permanent marker
1- hear shock bath with water at 42 Celsius
1- thermometer
500 ml- Luria
1- cell spreader
1- Bunsen burner
1- 250 ml beaker
50 ml- alcohol
Experimental Design
For experiment procedure, refer to pages 66-67 of the lab packet with the following modifications:
Instead of using a sample of e-coli from a starter plate, take a sample from one’s self using a cotton throat swab.
Open sterile cotton swab and place down throat.
Rub the cotton swab for optimal transfer.
Swirl the cotton swab in the solution to dislodge the cells.
Instead of using three control agar plates, only use one (LB agar).
While the tubes are on ice, obtain one LB agar plate and one LB/Amp agar plate. Label each plate on the bottom as follows: one LB agar plate as “LB+” and label the Lb/Amp plate “LB/AMP+”
Instead of placing 100ml of “+” cells on to the agar plate labeled “LB/Amp +” and placing 100ml of “-“ cells on the “LB” plate, place all of the cells in the test tube.
Place all of the “+” cells on the “LB/Amp +” plate. Place all of the “-“ cells on the “LB-“ plate.
Instead