Team:HokkaidoU Japan/Notebook/aggregation Week 2
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[[image:HokkaidoU2012 120711 pt7-rbs-ag43-dtjpg.jpg|thumb|ligation result]] | [[image:HokkaidoU2012 120711 pt7-rbs-ag43-dtjpg.jpg|thumb|ligation result]] | ||
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===Transformation=== | ===Transformation=== |
Revision as of 00:09, 26 September 2012
Contents |
July 9th
pT7 + RBS (3A Assembly) and Ag43 + dT (standard assembly) ligation products were transformed and incubated. We confirmed ideal insert DNA (pT7 and RBS or Ag43 and dT) were inserted by colony PCR.
Colony PCR
Colony PCR for assembly products.
- Picked up colony from LB plates by Autoclaved toothpicks.
- re-suspension into 10 ul DW in 1.5 ml eppendorf tubes.
- 4 ul was added in PCR reaction solution, and 6 ul was mixed with 200 ul LB.
- Ran PCR machine in recipe below.
DNA solution | 4 ul |
KapaTaq ready mix | 5 ul |
BioBrick prefix forward primer | 0.5 ul |
BioBrick suffix reverse primer | 0.5 ul |
Total | 10 ul |
PCR recipe
(pT7 + RBS)
Number | Degree | Second |
1 | 94 | 120 |
2 | 94 | 30 |
3 | 68 | 60 |
4 | 4 | HOLD |
Cycle:2~3 x 40
(Ag43 + dT)
Ag43 + dT (+ Biobrick prefis & suffix) is about 3290bp.
Number | Degree | Second |
1 | 94 | 120 |
2 | 94 | 30 |
3 | 68 | 180 |
4 | 4 | HOLD |
Cycle:2~3 x 35
Electrophoresis results
Electrophoresis for (pT7 + RBS) by 2% agarose gel and (Ag43 + dT) by 1% agarose gel.
pT7 + RBS on pSB1K3
bbp-Insert-bbs:86bp
Ag43 + dT on pSB1AK3
bbp-Insert-bbs:3290bp
We couldn't confirm insert DNA were really ligated with Vector or not.
Next step, we tried confirmation of insert DNA by Electrophoresis of mini-prep products.
For mini-prep, we needed do liquid culture.
Incubate for mini-prep
- Prepared 1800 ul LB solutions.
- Mixed 200 ul of cultures (suspention were incubated for 2 hrs) and antibiotics(Km (pT7-rbs on pSB1K3), Amp(Ag43-dT on pSB1AK3)).
- Incubated for 15 hrs and 30 min.
July 10th
Mini-prep
Mini-prep for some colonies (we selected colonies which showed more correct bands than other colonies, pT7+RBS were No. 4, 5, 9, 10 colonies and Ag43 + dT were No. 1, 2, 3, 4 colonies)cultivated in LBA(Ag43 + dT) and LBK(pT7 + RBS) in 15 hrs and 30 min.
- Mini-prep for LB culturing products along the protocol of FastGene Plasmid Mini kit(Nippon Genetics).
- Electrophoresis (Used pre-migrated 1% agarose gels with 5 ul EtBr)in 30 min.
pT7 + RBS on pSB1K3(Total 2247bp)
Ag43 + dT on pSB1AK3(Total 6444bp)
To confirm more about insert DNA, we tried to digest these DNA with EcoRI and PstI.
Digestion
Digestion for confirmation of insert DNA. Each DNA mini-prep products were digested with E & P. Digestion recipe pT7-RBS
pT7-RBS | 1.5 ul |
EcoRI | 1 ul |
PstI | 1 ul |
10xH buffer | 2 ul |
DW | 14.5 ul |
Total | 20 ul |
Digestion recipe
Ag43-dT
Ag43-dT | 4 ul |
EcoRI | 1 ul |
PstI | 1 ul |
10xH buffer | 2 ul |
DW | 12 ul |
Total | 20 ul |
Digestioned at 37c in 2 hrs.
Insert DNA were correct we thought. We tried digestion for 3A Assembly[pT7-RBS + Ag43-dT + pSB1C3]
Digestion
Digestion for 3A Assembly. pT7-RBS
DNA | 17 ul |
EcoRI | 1 ul |
SpeI | 1 ul |
10xH buffer | 3 ul |
DW | 8 ul |
Total | 30 ul |
Ag43-dT
DNA | 12.5 ul |
XbaI | 1 ul |
PstI | 1 ul |
10xH buffer | 2 ul |
DW | 3.5 ul |
Total | 20 ul |
pSB1C3
DNA | 20 ul |
EcoRI | 1 ul |
PstI | 1 ul |
10xH buffer | 3 ul |
DW | 5 ul |
Total | 30 ul |
Reacted in 2 hrs at 37c.
July 11th
Ligation
Ligation of pT7-RBS + Ag43-dT + pSB1C3(3A Assembly) Ligation recipe
pT7-RBS | 2 ul |
Ag43-dT | 2 ul |
pSB1C3 | 3 ul |
Ligation Mighty Mix(TAKARA) | 8 ul |
Total | 16 ul |
Ligation reaction time was written below.
Degree | Minute |
16 | 30 |
65 | 10 |
4 | Hold |
Transformation
Transformation for pT7-RBS + Ag43-dT + pSB1C3 into BL21(DE3)(E.coli which have T7 polymerase coadin site in their genomic DNA).
- Added DNA soltions (Ligation products) 1 ul to BL21(DE3) compitent cell.
- Stood on ice in 30 min.
- Heatshock for 1min at 42c.
- Added 200 ul of LB to transformed BL21(DE3) solution.
- Pre-cultivate in 2 hrs
- Splead 200 ul of LB&BL21(DE3) solution supernant to LBC.
- 50ul of LB&BL21(DE3) solution were added to 200ul LB solution then spread 200 ul to LBC plate.
- Cultivated.
</p>
July 12th
Colony PCR
Colony PCR for ligation product.Each products were reacted in recipes written below.
- picked up each 16 colonies from LB plates by Autoclaved toothpicks.
- Dipped into 10 ul DW in 1.5 ml eppendorf tubes.
- from 10 ul DW, 4 ul was added in PCR reaction solution (below), 6 ul was mixed with 200 ul LB.
- Ran PCR machine in recipe below.
- Electrophoresis for confirmation of PCR results.
DNA solution | 4 ul |
KapaTaq ready mix | 5 ul |
BioBrick prefix forward primer | 0.5 ul |
BioBrick suffix reverse primer | 0.5 ul |
Total | 10 ul |
PCR recipe
(pT7 + RBS)
Number | Degree | Second |
1 | 94 | 120 |
2 | 94 | 30 |
3 | 68 | 90 |
4 | 4 | HOLD |
Cycle:2~3 x 40
Liquid culturing
Liquid culture for some colonies used in colony PCR.
- Prepared 200 ul LB solutions.
- To these LB solutions, added 6 ul of LB solutions (colony PCR solutions were pre-cultivated in about 3 hrs) and added 2 ml LB and antibiotic(Cp).
- Cultivated 18 hrs and 30 min.
July 13th
July 14th
Ligation
Ligation for digestion fragments written above. Ligation recipe Each DNA fragments (pT7-RBS + pSB1C3 and Ag43-dT + pSB1T3) were reacted in recipe written below.
Insert | 5 ul |
Vector | 1 ul |
Ligation Mighty Mix(TAKARA) | 6 ul |
Total | 12 ul |
Degree | Minute |
16 | 30 |
65 | 10 |
4 | Hold |
Ligation result with colony no. 1 (see colony pcr result in 9th)
Transformation
Transformation for ligation products written above.
- Added DNA soltions (Ligation products) 1 ul to DH5α compitent cell.
- Stood on ice in 30 min.
- Added 600 ul of LB to transformed DH5α solution.
- Pre-cultivate in 2 hrs
- Splead 300 ul of LB&DH5α solution to LBC and LBT , 100 ul added into 900 ul of LB.
- Splead 300 ul of LB&DH5α solution from 1000 ul LB (100 ul added into 900 ul) to LBC and LBT.
- Cultivated in 21 hrs.
Liquid culture
Liquid culture for Ag43(BBa_K346007)
- Picked up one colony from single colony isolated plate.
- Dipped into LBC.
- cultivated.
July 15th
Gel extraction
We used Gel Extraction Kit (FastGene Gel/PCR extraction kit:NipponGenetics) to purify digestion products (see 14th).
Digestion
Digestion to confirm what kind of restriction enzyme cutting sites these DNA (colony 1 and 6) have. EcoRI
DNA solution | 6 ul |
EcoRI | 1 ul |
10xH buffer | 1 ul |
DW | 2 ul |
Total | 10 ul |
XbaI
DNA solution | 6 ul |
XbaI | 1 ul |
10xM buffer | 1 ul |
BSA | 1 ul |
DW | 1 ul |
Total | 10 ul |
PstI
DNA solution | 6 ul |
PstI | 1 ul |
10xH buffer | 1 ul |
DW | 2 ul |
Total | 10 ul |
SpeI
DNA solution | 6 ul |
SpeI | 1 ul |
10xM buffer | 1 ul |
DW | 2 ul |
Total | 10 ul |
EcoRI + PstI
DNA solution | 6 ul |
EcoRI | 1 ul |
PstI | 1 ul |
10xH buffer | 1 ul |
DW | 11 ul |
Total | 20 ul |
XbaI + SpeI
DNA solution | 6 ul |
XbaI | 1 ul |
SpeI | 1 ul |
10xM buffer | 1 ul |
DW | 11 ul |
Total | 20 ul |
Ethanol precipitation
Ethanol precipitation for digestion products.
- Added 2 ul of NaoAc, 1.5 ul of glycogen and 50 ul of 100% ethanol.
- Centrifuged in 15000 rpm, 10 min at 4C.
- Remove supernatant and added 220 ul of 70% ethanol.
- Centrifuged in 15000 rpm, 5 min at 4C.
- Remove supernatant and air drying in room temperature then added 5 ul of DW.
Electrophoresis
Electrophoresis for digest-ethanol precipitation products.
- added 5 ul of EtBr.
- Migrated in 30 min.
Single colony isolation
Single colony isolation for Transformation products synthesized yesterday.
- one colony picked up from cultivated LBC and LBT plate.
- Spread on LBC and LBT.
- Cultivated.
Digestion
Digestion of Ag43(with S,P), dT(With X,P) and pT7-RBS(With E). Ag43
DNA solution | 9 ul |
SpeI | 1 ul |
PstI | 1 ul |
10xH buffer | 2 ul |
DW | 7 ul |
Total | 20 ul |
dT
DNA solution | 1.1 ul |
XbaI | 1 ul |
PstI | 1 ul |
10xM buffer | 2 ul |
DW | 14.9 ul |
Total | 20 ul |
pT7-RBS
DNA solution | 6 ul |
EcoRI | 1 ul |
10xH buffer | 2 ul |
DW | 11 ul |
Total | 20 ul |