Team:WashU/Week11

Monday, August 6

Colony PCR of U construct using four new colonies and the same positive Z control has once again resulted in no successful colonies. However, the PCR has reaffirmed that the control works, which is a good sign.

We also did a PCR of the color constructs in order to form our BioPaint set. [PICTURE BELOW]

Since our T plasmid and Z construct ligations have not been going well, we started over by preparing new cultures of Z and T, running them on a gel, and then gel purifying the results. [SEE PICTURE]

We began 5 ml cultures for the good Z construct with TOPO and for one of the U ligation colonies. We will use the Z culture for a glycerol stock, and digest the U culture to see if our ligations actually succeded.

Tuesday, August 7

Today, we digested the U ligation construct by cutting it, in two tubes, with AgeI-HI and NcoI. A double cutter, the AgeI-HI would excise out the insert, whereas NcoI cuts once. The results, shown below, indicate [PICTURE + FINISH]

We also PCR'd up the Z construct, U construct, and Z+TOPO constructs using KlenTaq.

Wednesday, August 8

This morning, we ran the three PCRs from yesterday on a gel. [RESULTS OF GEL]

We took the Z and U constructs, digested them with EcoRI (E) and PstI (P), and ran them on a gel. We also digested the chloramphenicol plasmid that we plan to use for submission and ran it on the same gel. Afterwards, we gel purified the three pieces of DNA. We finished off by ligating together the Z construct and C plasmid in one tube and the Z construct and C plasmid in another tube. Tomorrow, we will transform E. coli with our ligation results.[PICTURE]

Finally, we started cultures of our Z ligation, control, and a zeaxanthin culture to use tomorrow to test whether our genes are working properly.

Thursday, August 9

We transformed E. coli GC5 cells with the ligation results from yesterday and plated the cells.