- 1 Growing a Bacterial E. coli Culture
- 2 Plasmid Minipreps: Qiagen Miniprep Kit
- 3 DNA Digests
- 4 DNA Gel Electrophoresis and Fragment Purification
- 5 Measuring DNA Concentration using a Nanodrop Spectrophotometer
- 6 Ligation Reaction
- 7 Transformation of E. coli
- 8 Confirming the Assembly
- 9 Growing Arabidopsis
- 10 Growing an Agrobacterium Culture
- 11 Arabidopsis transformation via Flower Dipping
Growing a Bacterial E. coli Culture
E. coli is a typical bacteria used for molecular cloning. Long-term storage of BioBrick plasmids is in E. coli suspended in glycerol (500ul cells:500ul glycerol) and kept at -80˚C. Growing E. coli is performed at 37˚C, at which temperature they divide every 20 minutes.
- Day1: Making streaks from glycerol stocks
- Warm agar plate at 37˚C for 10 minutes
- Label lid of plate with what you're streaking on it, and your name, and the date
- Locate desired glycerol stock in -80˚C freezer and, using a sterile toothpick, scrape out a tiny bit and streak on plate
- Incubate plate overnite at 37˚C
- Day2: Growing liquid cultures
- Label 15mL falcon tube and add 5mL of LB media + selective antibiotic
- Using 200uL tip w/o filter, touch streak or single colony and put tip in falcon tube
- Grow culture overnite in a shaking 37˚C incubator
Plasmid Minipreps: Qiagen Miniprep Kit
To extract plasmid DNA from bacteria, perform a miniprep using the Qiagen miniprep protocol.
Use appropriate enzyme to cut the BioBrick plasmids or parts to be ligated, taking care as to whether you're performing a "front-end" or "back-end" ligation.
- Write out exactly what you're building, i.e. part names, sizes, etc
- In a 1.5mL centrifuge tube, set up digest reaction as follows:
- Plasmid DNA: ____ uL = ~1000ng
- Enzyme 1: 1.0 uL
- Enzyme 2: 1.0 uL
- Buffer: 2.0 uL
- Water: ____ uL
- Total: 20.0 uL
(Note: Always be sure that the TOTAL enzyme concentration is never >10% of TOTAL volume, i.e. 2uL enzymes/20uL total reaction is 10%.)
- Mix tube well and digest at 37˚C for at least 5 minutes. If you are including a phosphotase enzyme, you need to deactivate it by next incubating the tube at 65˚C for 10 minutes.
- Proceed to gel purification.
DNA Gel Electrophoresis and Fragment Purification
- NOTE: Ethidium Bromide (EtBr) is a mutagen ---- always wear gloves when handling it*****
- Making an agarose gel
- To make a 1% gel, add 1g agarose to 100mL 1x TAE buffer in 200mL flask
- Microwave for 1.5 minutes
- Swirl and check that the agarose is completely dissolved and there are no air bubbles
- Allow gel solution to cool for a bit
- While gel is cooling, tape the ends of gel mold so gel liquid cannot escape. Don't forget the combs!! Sit mold on a flat surface.
- Add 4.5ul of EtBr to 100mL of gel and mix by swirling (avoid making bubbles)
- Pour into taped gel mold and allow to cool until solid