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Reporter: Week 7 June 26-July 1
From 2011.igem.org
Contents |
Sunday, June 26
Insert tev Protease into K3 Vector, Take 7 Day 1
The plates containing the assembly from 6/25 grew colonies that only contained RFP, none of which contained the tev protease. Thus, this assembly must be done again.
The purified tev protease PCR product from 6/4 and the K3 miniprep from 6/25 were digested with XbaI and PstI in buffer 3. The digests were ligated together, then the ligation was transformed into competent Escherichia coli cells and plated onto kanamycin resistant plates.
Monday, June 27
Insert tev Protease into K3 Vector, Take 8 Day 1
The colonies that grew overnight all contained RFP, meaning that the insertion of tev protease into K3 from 6/26 did not work. As a result, we performed the insertion again. We started with the tev protease (K316017) plasmid from the 6/8 miniprep and the K3 vector miniprep.
| Protocol | Part Involved in Protocol | |
|---|---|---|
| Insert PCR | K316017 | |
| Restriction Digest | Insert using XbaI and PstI: | K316017 |
| Vector using XbaI and PstI: | K3 | |
| Ligation | K316017+K3 | |
| Transformation/Plating | The ligation above was transformed into Escherichia coli cells then plated on a kanamycin resistant plate. | |
Cloning of XylE and GFP, Day 1
The purified PCR products of the mutated XylE and GFP were digested with XbaI and AgeI. The Imperial Linker + K3 served as the vector and was digested with XbaI and AgeI. The two digests were ligated together, transformed into Escherichia coli cells and plated onto kanamycin resistant plates.
Catechol Assay, Day 1
Two 5 ml M9 cultures of K316009 stock were grown up at 37°C with shaking.
Tuesday, June 28
Insert tev Protease into K3 Vector, Take 8 Day 2
Only one colony was white on the kanamycin resistant plate, meaning that this colony did not contain RFP. This white colony was amplified through colony PCR. The PCR product was run on an agarose gel, which yielded a band less than 500 base pairs long. The tev Protease should be just under 1000 base pairs, so the cloning attempt did not work. One idea was that the problem existed with the insert PCR products (poor purification or loss of product). The PCR product was run on the gel, and the corresponding (bright) band was just under 1000 base pairs, indication that the PCR products are correct and in ample amount, so the problem lies elsewhere.
Cloning of XylE and GFP, Day 2: Verification
Three colonies of both the XylE + K3 and GFP + K3 and two colonies of RecAI + K3 were amplified through colony PCR. The PCR products were run on an agarose gel, which showed that the constructs contained the correct number of base pairs. The XylE colony B, GFP colony B and RecAI colony A were grown in culture overnight so their plasmids could be extracted for sequencing tomorrow.
