Model Procedure for Assembling Parts: Classic Ligation for Beginners
or, Cloning Sensei's Guide For the Aspiring Cloning Ninja
Day 1*: Pick and amplify the desired plasmid DNA by growing transformed DH5α Turbo bacteria.
Make streaks from glycerol stocks 6 hours
- Warm an agar plate at 37°C for at least 20 min.
- Label the plate with the bacterial strain name (e.g., DH5α), the antibiotic, the BioBrick part(s) name, your initials, and the date.
- Locate the desired -80°C glycerol stock. Use a sterile wooden toothpick to scrape up a tiny bit of the frozen bacteria and streak the plate.
- Incubate the plate at 37°C for 6 hours to grow the bacteria.
Grow liquid cultures
- Label 15 ml sterile culture tube(s) appropriately. Fill each tube with 2 ml of LB growth medium + appropriate antibiotic (e.g., 100 μg/ml ampicillin).
- Using a sterile pipette tip, touch the bacterial streak (or pick up a single colony) and put the tip into the LB medium (bacterial end down).
- Grow the cultures overnight in a shaking 37°C incubator.
Day 2: Extract the plasmids. Digest (cut), purify, and ligate (paste) the BioBricks. Put the assembled plasmid into bacteria
Extract the plasmid DNA: Qiagen Miniprep Kit 1.5 hours
To extract the plasmid DNA from the bacteria, perform a mini prep (refer to the Qiagen miniprep protocol). 2 ml of culture usually gives a yield of about 200 ng/μl (elution vol. = 75 μl).
Digest (cut) the DNA with restriction enzymes 30 minutes
- First, write out a brief assembly strategy:
New Construct Name: BioBrick Insert Name, size (bp), cut sites + BioBrick Vector Name, size+backbone (bp), cut sites
- Set up your digest reaction(s) as shown below:
|Plasmid DNA||15.0 μl*|
|Fermentas FastDigest enzyme 1||1.0 μl|
|Fermentas FastDigest enzyme 2||1.0 μl|
|10x FastDigest buffer + green loading dye||3.0 μl|
|30.0 μl total|
| *For low yield DNA, use up to 25 μL and decrease dH2O accordingly.|
Mix the reaction(s) thoroughly by flicking the tube.
Incubate at 37°C for 10 minutes.
Separate the fragments via gel electrophoresis and purify the fragments 2 hours
- Make a 0.8% gel: add 0.48 g agarose to ~60 ml 1x TAE buffer in a glass flask.
- Mix by swirling and microwave for 40 seconds. Mix by swirling again (to eliminate air pockets and prevent boiling-over) and microwave for 40 seconds.
- Set up a gel mold and comb. Make sure the teeth are the right size to hold 30 μL of sample.
- Add 5 μl of 10 mg/ml ethidium bromide (etBr) to the agarose for a final concentration of ~0.8 μg/mL etBr. Mix by swirling (avoid making bubbles).
- Pour the gel into the gel mold. Allow it to cool until it becomes opaque.
- Fill a gel electrophoresis chamber with 1x TAE.
- Remove the comb from the gel and carefully submerge the gel into the filled electrophoresis chamber.
- Carefully pipette 15 μL pre-made 1 kb ladder mix into the first empty well and the DNA samples into the other empty wells.
- Connect the electrical leads so that the positive end is at the bottom (DNA migrates to the positive end). Run the gel at 100 V.
- Stop the gel when the yellow dye (Orange G) reaches the desired place on the gel (~1 hr.).
- Remove the gel from the chamber and photograph under UV light.
- Use a scalpel to cut the appropriate sized band(s) from the gel, place each gel slice in a 1.5 mL tube, and purify the DNA (refer to the Qiagen gel purification protocol; elute with 30 μL EB buffer).
- Measure the concentration of the purified fragment samples with a Nanodrop Spectrophotometer.
- Record the absorbance (A260), purity (A260/A280), and concentration (ng/μl) for each sample.
Ligate (paste) the DNA fragments together
- Calculate how many ng of insert you need to get a 2:1 ratio of insert molecules to 50 ng vector molecules
X ng insert = (bp insert / bp vector) x 2 x 50 ng vector
- Calculate how many μL of insert and vector you will need for each ligation:
X μL insert = desired ng insert ÷ insert concentration ng/μL (do the same for vector)
- Set up your ligation reaction(s) in sterile 0.5 mL tubes as shown below:
|Ligation||Negative Control||Insert DNA (X ng)||___ μL||none|
|Vector DNA (50 ng)||___ μL||same|
|2x Roche Rapid Ligation buffer||5.0 μl||same|
|NEB T4 ligase||1.0 μl||same|
|dH2O||___ μL||___ μL + insert volume|
|10.0 μL total|
| Mix the reaction(s) thoroughly by flicking the tube.|
Incubate at room temperature for 10 minutes.
Transform bacteria with the ligated plasmids 30 minutes
- Warm selection agar plates at 37°C.
- Incubate DH5α Turbo competent cells on ice just until thawed. Use 30 μL per ligation.
- Add 30 μL thawed cells to the ligation reaction. Immediately place on ice and incubate for 10 min. (Do not heat shock; No 30 min. recovery is required for Amp resistance)
- Label the pre-warmed plates with the antibiotic name, strain name, ligation (e.g., "BB part A insert + BB part B vector"), your initials, and the date.
- Pipette the total volume of cells + ligation onto the agar; speared using sterile glass beads.
- Incubate overnight at 37°C to get colonies
Note: The negative control will show you the number of “background” colonies so that you can determine whether your transformation worked, or is just the result of vector self-ligation or selection failure.