Lab 7: Picking Your Transformant
In theory, any colony of bacteria growing on your LB+amp plate should contain a plasmid because the plasmid is what confers antibiotic resistance to the bacteria. However, sometimes there is an instance where some of the bacteria either do not have a plasmid or have a plasmid but it annealed back on itself and does not contain your gene of interest. We need a way to find the colonies that do have our plasmid with gene of interest in them.
To achieve this goal we are going to do a "colony PCR". Instead of adding purified DNA to our tubes you can add a TINY little part of a colony to your PCR reaction. During the first heat cycle the cells will burst open and release their DNA into the reaction. We will test 8 colonies per group.
- Obtain a strip of PCR tubes and lids from your instructor. DO NOT separate the tubes!
- Label the side of each tube 1-8
- Find 8 well isolated colonies and circle them and number them 1-8.
- Add 30 ul of master mix to each tube. Your master mix will include: 1X PCR buffer, 10 mM dNTPs, 0.4 uM forward primer, 0.4 uM reverse primer and 2 units/ul Taq.
- After each tube has master mix use a sterile toothpick and gently touch your colony of interest - starting with #1 - and pick up a small amount of the bacteria NOT THE ENTIRE COLONY!!!
- Gently twirl the toothpick in the tube then discard the toothpick
- Repeat until all colonies are picked.
- Snap the lid on the tubes and bring them to your instructor.
| Step || Temperature || Time || Repeat
|| 2 minutes
|| 1 time
|| 30 seconds
|| 30 seconds
|| 1 minutes
|| Steps 2-4 30 times total
|| 10 minutes
|| 1 time
|| end program
Agarose Gel Electrophoresis
While the PCR reaction is running you will pour your own gels to analyze the results of the reactions.
To do on the day before the next lab:
You and your partner will return to the lab to make an overnight broth culture of your selected colony as described below. This process will create a sub-culture of many identical copies of the plasmid carrying the pL4440 plasmid construct to RNAi the gene that you want to study.
- Find your plate in the glass front refrigerator in a rack labeled with your lab day. Make sure you can see the colony you selected last lab period.
- Begin by pouring (DO NOT PUT A PIPET INTO THE STOCK LB!!) 10 ml of sterile LB + tetracycline (12.5 μg/ml) broth from one of the stock containers in the refrigerator into a sterile orange-capped 15ml conical tube. You will use the volumetric marks on the tube for measuring the media rather than using a pipet. Make sure the LB stock does not look cloudy (indicating contamination by a previous user) and take care not to contaminate it yourself.
- Add 10 microliters of the 50mg/ml ampicillin stock (also found in the refrigerator). Calculate the effective concentration of ampicillin that you will have in your LB tube (remember V1 x C1= V2 x C2) and record that information in your lab notebook.
- Replace the cap of your LB +amp broth and invert the tube several times to mix the contents.
- Label two sterile glass culture tubes (found in a rack in the lab) with tape in your team color. Label one with "pL4440 and the gene name" and your initials. Label the other with your initials only.
- Using a 5 or 10 ml sterile disposable pipet, pipet 4 ml of your working solution of LB+ampicillin broth into each of the 2 tubes. Be careful not to touch the tip to anything non-sterile.
- Inoculate the broth with your bacteria by using a sterile toothpick to scrape your candidate colony off the plate. Be sure not to touch the plate with the toothpick except on the desired colony and don’t pick up any satellite colonies. Make sure the toothpick falls into the sterile broth. The second tube of broth labeled with just your initials is a control and should not be inoculated with bacteria as it is your control for contamination.
- Balance the 2 tubes across from each other on the rotating wheel in the incubator at the front of the room when you come in the door and incubate them at 37°C overnight. Do not forget to make sure the wheel is rotating when you leave!
RNAi General Information
Lab 11: RT PCR reactions
Lab 5: Picking your gene to RNAi
Lab 6: Cloning your gene of interest
Lab 8: Plasmid purification and transformation
Lab 9: Induction of bacteria for RNAi
Lab 10: Scoring your worms and RNA purification