We want to make two plasmids:
Plasmid #1 - A constitutive promoter with LacZ and LacY.
Plasmid #2 - A lactose inducible promoter with lysozyme and holin.
The general idea is to overexpress LacY (Lactose transporter) with LacZ (Beta-Galactosidase). When lactose is present, the cell will uptake lactose and will flip on the Lac promoter repressed by lacI when enough lactose is present. We then express lysozyme and holin which will lyse the cell releasing beta-gal cleaving lactose into glucose and galactose. Hopefully, glucose and galactose will be taken up by the host in the colon.
We have decided to use the I732017 LacZ (1009/11H) because we could not transform I732005 LacZ (1018/6F).
To double check, we will plate our transformed I732005 LacZ with 100μL onto a kan plate, and the rest on an Amp plate.
We ordered primers for LacY, and we will need to PCR out LacY. We then need to run site directed mutagenesis on LacY by added 2H to prevent EIIA(GLUC) binding.
For our constitutive promoter, we will use various strengths to test our beta-gal concentrations.
Low expression - J23113
Medium expression - J23106
High expression - J23100
We need to cut out mRFP, which is originally in the promoter plasmid family of J23100, by doing a digest with SpeI and PstI. We will paste in LacZ and LacY, and add a double TT.
Colonies grew from I732017 LacZ transformation. They will be cultured Sunday afternoon.
LacY, LacY +H, and LacY +2H has been inputted into the registry of parts. Primers for LacY site directed mutagenesis were designed.
When primers for LacY arrive, need to PCR LacY out of E. coli genomic DNA.
After LacZ culture is grown, mini prep DNA.
Set up o/n cultures.
1. LacZ in Amp
2. pSB2K3 in Km
3. p1005 in Amp
4. p1005 in Amp + Tet (Just to test the strain is both Tet and Amp resistance)
Mini prep'd LacZ and pSB2K3, eluted in 50 μL.
LacZ conc. = 115.4 ng/μL
pSB2K3 conc. = 427.4 ng/μL
Ran a PCR to amplify LacY out of E. coli genomic DNA (hoping that E. coli genomic DNA has LacY wild type).
1 ul PFU Ultra II, 1 ul E. coli genomic DNA, 2 ul (Primer FWD), 2 ul (Primer RVS), 10 ul 10x PFU Buffer, 2 ul dNTP's, and 82 ul dH20.
PCR's did not work first time. Ran another PCR in 50 ul with 5 ul of template as the biggest revision. Annealing temp's were lowered by 4°C, and extensions were lengthened another 15 seconds.
Transformed 2 RBS's (Weak and weaker) b0031 and b0033, and LacY J22101. Will check tomorrow for grwoth.
Set up digests for LacZ and LacY.
1. Cut LacY XP
2. Cut RBS34 SP
3. Cut RBS32 SP
4. Cut High Copy Plasmid XP
5. Cut LacZ ES
6. Cut TT EX
Transformations of the 2 RBS's B0031 and B0033 was successful. The LacY J22101 did not look so good, so the plate was tossed.
Only 2,3, and 5 worked. Gel extracted them and they were put in the digest box. Concentration was not measured.
Ran another LacY PCR with template from previous LacY purification.
The gel from the PCR looked OK, so digested LacY, pSB1A2, and TT again.
Treated digest backbones with CIP, and heat inactivated.
Miniprep'd transformations from last night, B0031 and B0033 (Weak RBS's).
B0031: 113 ng/ul
B0033: 120 ng/ul
Ran last nights digests on a gel and gel extracted them.
Set up 6 ligations and transformed them.
1. LacY + RBS34
2. LacY + RBS32
3. LacY + pSB1A2
4. Control: RBS34
5. Control: RBS32
6. Control: pSB1A2
Also transformed a Control for the NEW LB+Amp plates with just D10HB. The Amp will kill off the cells if the plates were poured correctly.
The transformed plates didn't look good. On the experiment plates 1-3, there were MANY colonies on the edges of the plates, but the middle of the plate had streakyness of something. On control plates 4-6, there were no colonies, but there was the same streakyness all across the plate. A few thing could have gone wrong such as the transformation protocol, the LB + Amp plates, or the HB cells. We will see how the colony PCR turns out for plates 1-3. We took 6 colonies from plates 1 and 2, and 1 colony from plate 3.