"
Team:Gaston Day/Notebook
From 2010.igem.org
| Home | The Team | The Project | Notebook | Sponsors |
|---|
Contents |
Procedures
Plasmid Prep
SOLUTIONS: TENS (make fresh each time) To 4.5 ml TE add: 250 ul 10% SDS 250 ul 2N NaOH Sodium Acetate 3.0M; pH 5.5 TE with 10 ug/ml of RNAse A
PROCEDURE: 1. Spin 1.5 ml of overnight culture for 30 sec in microfuge
2. Aspirate off all but 100 ul of the supernatant and resuspend the pellet by vortexting
3. Add 300 ul of TENS and mix by inversion. The solution should become viscous.
4. Add 150 ul of sodium acetate and votex. A fine white precipitate should form.
5. Centrifuge for 2.5 minutes at 10K.
6. TRANSFER the supernatant to a clean tube and add 2 volumes (1 ml) of room temperature EtOH.
7. Vortex and pellet DNA by centrifugation for 2-5 minutes at 10K.
8. Wash pellet with 70% ethanol and allow the pellet to dry.
9. Resuspend the pellet in TE with RNAseA.
10. Digest 5-10 ul as usual.
Digest
Ligation
1. Remove the 10X T4 DNA Ligase Reaction Buffer* from the freezer to thaw. You can remove the T4 DNA Ligase enzyme from the freezer at this point but leave the ligase in a cold box to keep it close to -20○ C. Thawing is fast if the buffer tube is immersed in room temperature water. Once thawed, agitate the 10X T4 DNA Ligase Reaction Buffer until all precipitate goes into solution.
2. Add 11ul of H2O to a 200ul PCR tube.
3. Add 2ul from each of the digest to the tube.**
4. Add 2ul of 10X T4 DNA Ligase Reaction Buffer to the tube.
5. Add 1ul of the T4 DNA Ligase to the tube.
6. The total volume in each tube should now be 20ul. Ensue the ligation is well mixed by flicking the tube. You can spin the tube in a microcentrifuge for a few seconds to collect the liquid in the bottom of the tube again.
*Repeated freeze-thaw cycles of the buffer can degrade the ATP in the buffer thereby making the ligation reaction less efficient. It is wise to aliquot the buffer into 10ul aliquots prior to freezing
**There is no need to purify the restriction digests via gel electrophoresis in any other method.
Transformation
1. Thaw tube of NEB 10-beta Competent E. coli cells on ice for 10 minutes.
2. Add 1-5ul containing 1 pg-100 ng of plasmid DNA to the cell mixture. Carefully flick the tube 4-5 times to mix cells and DNA. DO NOT VORTEX.
3. Place the mixture on ice for 30 minutes. Do not mix.
4. Heat shock at exactly 42○ C for exactly 30 seconds. Do not mix.
5. Place on ice for 5 minutes. Do not mix.
6. Pipette 950ul of room temperature SOC into the mixture.
7. Place at 37○ C for 60 minutes. Shave vigorously (250 rpm) or rotate.
8. Warm selection plates to 37○ C.
9. Mix the cells thoroughly by flicking the tube and inverting then perform several 10-fol serial dilutions in SOC.
10. Spread 50-100ul of each dilution onto a selection plate and incubate overnight at 37○ C for 24-36 hours of 25○ C for 48 hours.
March
March 2
Start cultures of:
I 765000 (Fe promoter, amp broth) LARGE FLASKS
E 1010 (RFP gene only, Kan broth) LARGE FLASKS
J 04450, amp SMALL
J 04450 kan SMALL
-Add .5 ml amp and kan to 50 ml bottle LB broth
March 3
All grew well
March 5 Make fresh TENS from plasmid preps
Miniprep Fe promoter + RFP
Teaching plasmid preps (Fe Prom, RFP gene, cRFP-A, cRFP-K) to Augustine E., Taylor G., Spencer J., Joey S., and Al Hall.
April
April 1
Restriction digest of Fe promoter (pSEX), cRFP, RFP gene
10x plasmid
2x 10x buffer 2(NEB)
1x Xba
1x Spe
6x dH20
20x
O/N 37o
April 2
5x loading buffer to each
Gel:
1 ladder – bands present
2 cRFP
3 Fe – bands present
4 RFP gene – bands present
Made TENS
Plated competent cells on plain LB
Plated pNICE on plain LB
Plasmid prep
April 3
Digest w/ spe/xba
5x DNA
1x Xba
1x Spe
2x dH2o
1x buffer 2
10x
April 5
Plasmid Preps of Fe, cRFP, and old Fe
Prepare cometent cells
Spin 5ml cells 30”
Drain sup
Resusp. In 300x CaCl2
Add 1x, 2x, 3x, 4x 50ng/ml plasmid pNICE
Plated on LB o/n
April 7
Selected colonies to grow on Kan. Grow o/n
April 14
Digest w/ Xba, pNICE, new Fe, old Fe, cRFP
Mix 37o @ 10
DNA 10x
Buffer 2x
Xba 1x
dH20 7x
20x
May
May 13
Start cRFP (K) growing
Start Fe pSEX
Cut w/ Xba, Spe, Xba/Spe
FepSEX
DNA 10x 10x 10x
Buffer 2x 2x 2x
Xba 1x Spe 1x Spe 1x
dH20 7x dH20 7x Xba 1x
H20 6x
20x 20x 20x
May 14
Ran 1% gel
1 ladder – 1KG
2 Spe
3 Xba
4 S/x ~1KG band present
Picture on digital camera
Repeat digest w/ new Fe
INSERT ALL OTHER 'JUNK' TILL AUGUST HERE....
August 9
Spec. extraction
Notes: BBa_ k274110 produces red pigment under constitutive promoter (plain coding is K274100)
BBa_k274210 produces orange color under constitutive promoter (plain coding is K274200)
K274002 – purple
K274003 – dark green
K274004 – light green
-all under repressible promoter.
August 10
Made 2 2ml amp liquid cultures for K274100
(-100) and K274200 (-200)
August 13
Miniprep for -100 and -200
Digest of -100 and -200
10ul DNA
5ul Buffer 2
1ul Pst 1
1ul xba
6ul dH20
20ul
.5ul BSA
26.5ul dH20
50ul
Made 2, 3ml amp liquid cultures for -100 and -200
