Reporter: Week 7 June 26-July 1

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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

     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.



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