Western blotting for proper Tse2 expression

In order to detgermine that Tse2 and Tsi2 were only being produced in the presence of 3OC6HSL, E. coli MG1655 containing the F2620-Tse2-Tsi2 construct was cultured in liquid LB containing either 10,000nM 3OC6HSL, or no HSL. the cultures were pelleted, and western blotted for Tse2. The cultures grown in 3OC6HSL+ media showed bands on the western blot (figure x) indicative of Tse2 being produced when 3OC6HSl is present. The cultures grown in media without 3OC6HSL showed no bands ( figure X), meaning that Tse2 is not being produced unless HSL is present. This is exactly the behavior that was expected if the Tse2/tsi2 system was working properly. The survival of cells in the HSL+ media despite the production of Tse2, combined with the sequence confirmation of Tse2 in the construct implies that tsi2 is working as an antitoxin.

PCR testing for insertion

We want to test for gene insertions and recombinations at several steps of our project. PCR is the easiest and fastest way to determine the success of Recombineering.

galK insertion

Using a set of primers flanking the galK cassette, we tested the insertion on our recombinants. galK is around 1200 base pairs in size, so we would expect the recombinant PCR to be about 1200 bp larger than the non-recombinant. Indeed, this is exactly what we saw.

SDS-PAGE Protein Array

Hcp secretion is the hallmark of a working T6SS. We plan to use SDS-PAGE to confirm our promoters.

Competition Arrays

Once we have a working T6SS in E. Coli, we can use GFP-labelled organisms to test the competitive advantage of our T6SS strain vs. non-T6SS organisms.