Team:WashU/Week5

Then, we ran digests of 9, 10, 5 and BBa J22119 using controls, DNA cut with the enzymes as stated in the biobrick assembly protocol(shown with a "c" below), and then DNA cut with enzymes and then treated with phosphatase (shown as P- on the gel). For the YLC project, we ran 1, 2, 3, 4 and 8. [Gels shown below]



Our digests appear to be successful this time. We extracted the DNA for all of the YLC runs except for 4 and also extracted 9 from the first gel, and then purified all of the above bands.

YLC

We finally ordered the primers from Sigma today and they will arrive in a few days.

Wednesday, June 27

YLC/Saffron in a Kan

After our meeting with our mentor Dr. Dantas this morning, we decided to try several ligations. We agreed to proceed with the J23119 promoter for the future constructs.

One ligation was considered to insert the RBS-ORF-TERM into the J23119 plasmid directly without cutting out the J23119 promoter and proceeding with the usual triple ligation. J23119 in its pSB1A2 plasmid was cut with SpeI and PstI to try to open up the plasmid for the insertion of the RBS-ORF-TERM constructs behind the promoter in a double ligation rather than triple ligation. The main problem with this ligation was that both pieces used came from pSB1A2 plasmid backbones carry Amp resistance so the ability to select was greatly reduced. However, the use of only two substrates of comparable size in the ligation was more favorable than the triple ligations with sizes of ~1 kb, ~35 bp, ~2.5 kb. So there was a win-lose element that we wanted to try out.

The other ligation was traditional triple ligation using gel purified samples of the ORF-region. The plasmid and promoter were both not gel purified. We attempted the ligation knowing that it was not very likely given that the NanoDrop results were poor for the post-purification DNA. (This DNA was recovered from a diagnostic gel that looked good so was thus cut. Even though it was not a fully adequate amount of DNA to cut out, we were hopefully and went for it.) Below is a table of our NanoDrop results:

We digested the BB-plasmids with using the familiar BioBrick Assembly protocol for the plasmid part and digested a tube of J23119 with SpeI and PstI using the same procedure but different these enzymes. We then used the BioBrick Assembly to ligate together J23119 cut with SpeI and Pst1 with a sample of gel purified Construct #9 and mRFP1 since mRFP1 had the best gel purification result. The other gel purified DNA samples were ligated to plasmids and digested promoter using a new vial of ligase for fear that the previous were hindered by expired ligase.

The constructs were all cloned in GC5 competent cells from sigma using the transformation protocol. The J23119 cut with SpeI and PstI constructs were plated onto Amp. The Kan and C plasmid constructs were plated onto their respective resistance plate. The plates were incubated overnight at 37°C.

Today, we began a culture of E. coli transformed with plasmid PSL2131.

Thursday, June 28

Saffron in a Kan

We finally received our gene from DNA 2.0!! We streaked out some of the gene, still in its plasmid onto plates with ampicillin.

In addition, we transformed Synechocystis with the plasmid PSL2131 obtained from one of our mentors, Burt.

We picked the E. coli colonies transformed with plasmid PSL2131 today. We miniprepped these colonies and then put them into 6803.

We have started a third wild type liquid culture of Synechocystis.

Friday, June 29

YLC

In the interest of time, we will use existing biobrick constructs with the necessary fluorescent proteins to show to the YLC students, and then we will complete our own constructs at a later date. Thus, today, we plated several biobrick constructs (RFP: I13521, GFP: I13522, YFP: 13604, and CFP: S03475) and will pick colonies to prep.

Saffron in a Kan

We continued to work with our gene construct today.

We made glycerol stocks of GFP, RFP, plasmid 2131, and then three of our construct, CS42S.

We performed a miniprep to extract the DNA PSL2131.

We performed two digestions - see the gel below for results.

Saturday, June 30

Several Small Projects

We miniprepped the potential constructs. We will need to digest them to check if they worked. They will hopefully be the plasmid that we want to place into Synechocystis.
More Amp and Kan LB plates were made.
Four more glycerol stocks of the construct that we ordered were made. 2 mL of the remaining cells were miniprepped. The rest (.25 mL) were used to continue the line of cells in liquid culture with 3 mL of LB+Amp.
Two glycerol stocks one of an RFP plasmid and one of our functioning GFP were made and frozen at -80°C. (For the glycerol stocks done today, no dry ice was used to flash freeze as a the stock room is closed on Saturdays.)