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Team:University College London/LabBook/Week14
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Revision as of 01:03, 27 September 2012
Contents |
Monday 10.09.12
Aim: Day 2 of Generating competent cells. The aim is to incubate cells in the presence of CaCl2 to prepare the cell wall, allowing it to become permeable to DNA for transformation.
Method:
Step 1 -Creating culture media: In a sterile environment, set up a falcons, with 5mls of Lysogeny Broth and 100ul 1M MgS04.
Step 2 – Selecting a Colony: Select a clear, isolated colony and using an inoculation hoop, scoop up a colony onto the tip. Deposit in the falcon tube
Step 3 - Cell culture: Culture your falcon tubes overnight at a temperature of 37 oC. Leave for no longer than 16 hours.
Tuesday 11.09.12
Aim: Day 3 of Generating competent cells
Method:
Step 1 – Innoculation: Inoculate 100mls of Lysogeny Broth in pre-warmed conical with 1ml of the overnight culture from Day 2
Step 2 – Incubation: Incubate for two hours in a 37oC shaker until the cells are at the early log phase of the growth curve. Measure absorbance on a spectrometer until A6000 is approximately 0.3.
Step 3 – Incubation: Transfer to a chilled sterile 50ml Falcon tube and incubate on ice for 10 minutes Step 4 – Centrifuge:
-Time: 5 mins -G – 3300 -Temperature: 180C
Step 5 – Incubate: Resus in 10ml of ice cold 0.1M CaCl2 in 15% glycerol and incubate on ice for 30 minutes.
Step 6 – Centrifuge: -Time: 5 mins -G – 3300 -Temperature: 180C
Step 7 – Transfer: Resus in 1ml of ice cold 0.1M CaCl2 in 15% glycerol. Transfer 100ul aliquots to pre-chilled, pre-labelled eppendorf tubes. Store at -70oC
Step 8 – Centrifuge -Time: 5 mins -G – 3300 -Temperature: 180C
Step 9 - Storage: Store cells at -80oC
Wednesday 12.09.12
Aim: To carry out a transformation using the 3A ligation products in order to be able to analyse whether ligation was successful.
Method: https://2012.igem.org/Team:University_College_London/Protocols/Transformation1
Thursday 13.09.12
Aim:
Picking of colonies from the ligation transformation plates
Friday 14.09.12
Aim:
To check whether the 3A assembly ligation has been successful by purifying the overnight culture from the previous day, carrying out an analytical digest and analysing results on a gel.
Methods:
A mini-prep was carried out as per the following protocol:
https://2012.igem.org/Team:University_College_London/Protocols/Miniprep2
This was followed by a 10ul analytical digest as per the following:
https://2012.igem.org/Team:University_College_London/Protocols/EnzDig2
Finally, results of the figest were run on a gel as follows:
https://2012.igem.org/Team:University_College_London/Protocols/Electrophoresis
Results:
The following digram shows results of the analytical digest, with each purified DNA being cut once and twice in order to confirm identity:
| BioBricks | BioBrick Size (bp) | Ligation size (bp) | Plasmid Backbone | Plasmid Expected Size (bp) | Combined Size |
|---|---|---|---|---|---|
| BBa_K729001 & BBA_J23100 | 933 & 35 | 968 | pSB1C3 | 2070 | 3038 |
| BBa_K729001 & BBa_J23119 & BBa_B0034 | 933 & 35 & 12 | 980 | pSB1C3 | 2070 | 3050 |
| BBa_K729002 & BBa_J23119 & BBa_B0034 | 484 & 35 & 12 | 531 | pSB1C3 | 2070 | 2601 |
Conclusion:
The bands on the gel indicate are not as expected. Hence, it is concluded that the ligation was unsuccessful.
Tuesday 11.09.12
Step 1 - Aim:
To generate enough plasmid backbone (pSB1C3) to be used in a 3A ligation. This is followed by a PCR clean-up.
Methods:
https://2012.igem.org/Team:University_College_London/LabBook/Protocols/PCR#Transformation_Protocol_2
Step 2 - Aim:
To check whether PCR is successful. After the PCR reaction, we can detect the presence of the correct products by running a 1% gel electrophoresis.
Methods:
https://2012.igem.org/Team:University_College_London/Protocols/Electrophoresis
Results:
The following gel results indicate whether PCR was successful.
Conclusion:
Since band sizes were as expected, the PCR was considered to be successful. Hence, the backbone was purified and used in the 3A ligation.
Thursday 13.09.12
Aim:
To generate enough linker (BBa_J23119 + BBa_B0034) to be used in a 3A ligation. This is followed by a PCR clean-up.
Methods: https://2012.igem.org/Team:University_College_London/LabBook/Protocols/PCR#Transformation_Protocol_2
Step 2 - Aim:
To check whether PCR is successful. After the PCR reaction, we can detect the presence of the correct products by running a 1% gel electrophoresis.
Methods:
https://2012.igem.org/Team:University_College_London/Protocols/Electrophoresis
Results:
The following gel results indicate whether PCR was successful.
Conclusion:
Since we obtained the expected bands in the gel, the PCR was considered successful and the purified DNA used in the 3A ligation.
Friday 14.09.13
Aim: To characterise nuclease activity BL21 cells
Method:
To add protocol
Results:
The following table shows readings of the diameters and OD at different time points:
| Date | Time | Colony diameter/mm | Halo diameter/mm | Absorbance at 600 OD |
|---|---|---|---|---|
| Friday | 12.30 | 0 | 0 | 0 |
| Friday | 16.30 | 0 | 0 | 0 |
| Friday | 19.30 | 0 | 0 | 0 |
| Friday | 22.30 | 0 | 0 | 0 |
| Saturday | 01.30 | 0.5 | 1.5 | 0.068 |
| Saturday | 04.30 | 1 | 2 | 0.098 |
| Saturday | 07.30 | 1.5 | 3 | 0.159 |
| Saturday | 10.30 | 1.5 | 3.5 | 0.192 |
| Saturday | 12.30pm | 2 | 4 | 0.203 |
| Saturday | 14.30 | 2 | 4 | 0.209 |
| Saturday | 16.30 | 2.5 | 5 | 0.215 |
The average depth of the colonies was noted to be 0.5 - 1mm
Conclusion:
It can be seen that nuclease works as expected in BL21 cells. However, nuclease activity is less efficient when compared to nuclease activity in WNu cells. This is in line with expectations, since nuclease is found naturally in WNu cells but not in BL21 cells.
