Experiment No 3

Date 27-28 May 2008 
Start Time 1530						
End Time 1800

Personnel:

Choon Kit, Hung, Dr Tan TL

Title of Experiment:

The experiment could be classified in 3 phases

1.	Amplification of transformed colonies (for 2 samples)
2.	LacI Plasmid Extraction using Qiagen MiniPrep Kit
3.	Plasmid analysis by Gel Electrophoresis

Materials:

Phase I:
2 x 15ml centrifuge tubes
Marker
LB broth with amipicllin resistance
2 x inoculating loops
Agar plate containing transformed colonies

Phase II:
Qiagen MiniPrep Kit
Mega Centrifuge
Small Centrifuge
Pipette with pipette tips
2 x 1.5ml centrifuge tubes
2 x 2.0ml centrifuge tubes 

Phase III:
PstI and EcoRI in icebox
BSA and EcoRI buffer 
DI water
2 x PCR tubes
Pipette with pipette tips
DNA marker (10kb)
Blue loading dye
Gel Electrophoresis setup

Protocols/Procedures:

Phase I:(done in 27 May)

1. Label the 2 tubes with LacI(1) and LacI(2) on cover and sides.
2. Sterilized LB Bottle before bringing into the fume hood with 70% ethanol solution. Transfer approximately 20 ml of LB broth into one cryotube and cover the LB Bottle. Transfer another 10 ml of LB broth from one cryotube to the other.
3. Select 1 colony using inoculating loop by gently touching the tip with the Agar so that the colony just sticks to the tip of the loop.
4. Carefully insert the tip of the loop into the tube with LB and mix uniformly by rubbing the tip of the loop with the tube’s bottom.
5. Incubate at 37oC overnight with vigorous shaking.

Phase II:

1. Pipette 5ul of TE buffer to 50oC in PCR Eppendorf tubes. Warm a water bath to 42oC
2. Using the cutting mat as a backing, a sample of plasmid is punched off the edge of the spot using the puncher by pressing firmly down and rotating the punch tool. (Do not press the ejection button)
3. Eject the punched paper spot into the PCR tube by pressing the ejection button
4. Clean punch tool to prevent cross contamination as mentioned in phase I

Phase III:

1. Soak the spots in 5ul of warmed TE for 20 minutes. Also, thaw the competent cells on wet crushed ice.
2. Chill labeled 2ml concial bottom tubes on wet ice. Add 2ul of DNA in TE and 50ulof thawed competent cells to the tubes. Extra eluted DNA can be kept frozen at -80oC for several weeks.
3. Also, do a control transformation using pUC18 plasmid DNA.
4. Hold the DNA and competent cells on ice for 30 minutes to increase transformation efficiency.
5. Heat shock the cells by immersion in a pre-heated water bath at 42oC for 1 minute. This is to improve heat transfer to the cells.
6. Incubate the whole floating tray of conical tubes on ice for 2 minutes.
7. Add 200ul of LB broth. (no antibiotic, check that broth is not turbid, which indicates contamination and bacterial growth)
8. Incubate the cells at 37oC for 1-2 hours. 2 hours is optimal for plasmids with other antibiotic resistance other than amipicillin.
9. Label an LB agar plate with amipicillin with the date, project name, and plasmid e.g. LBA – 26May08 – iGEM – Fe promoter, LBA – 26May08 – iGEM – LacI, LBA – 26May08 – iGEM – pUC18.
10. Plate 250ul of the incubated cell culture on the plate
11. Incubate the plate at 37oC overnight or 12-14 hours. Do not incubate too long as the antibiotic may break down, resulting in growth of untransformed cells.

Observations:

2 colonies observed in LacI LB plate, 0 colony in Fe2+ LB plate, positive control pUC-18 showed many colonies.

Conclusion:

Fe2+ not successfully transformed in home-made competent cells. LacI and pUC-18 transformation were successful.

Notes:

Refer to video clip 26 May 08 for details.

To be follow up:

1. Repeat whole transformation of Fe2+ plasmid using commercially competent cells.
2. Pick out 2 colonies from LacI LB plate into LB broth with ampicillin overnight.