Difference between revisions of "Part:BBa K2324011"

Revision as of 17:24, 1 November 2017

T7_FimH_225sfGFP

This part synthesises a FimH adhesin protein fused with sfGFP at its 225th amino acid residue. The coding sequence is under the control of an IPTG-inducible, T7 promoter, with a B0034 RBS and a B0015 terminator. The part, when induced, produces a fluorescent FimH protein that should involve itself in pilus biosynthesis when co-transformed with a plasmid containing the fim operon.The T7 promoter would give very strong expression and sfGFP would both give a visual indication of successful expression and folding. As a large protein, sfGFP would push the chaperone-usher pathway to its steric limits.

<img class="rounded mx-auto d-block w-5" src="" align="right"> <figcaption>Figure 4 These data from a flow cytometer show the fluorescence profile for wild-type (left) BL21(DE3) and BL21(DE3) with T7_FimH_225sfGFP (right).The wild type demonstrates no significant fluorescence, while same cell with the single plasmid insert shows a strong fluorescent signal in the highlighted portion of cells.</figcaption> </figure>

We have tested this construct in BL21(DE3) using a flow cytometer to determine the fluorescence of the sample, compared to the wild type. These results show that a number of cells in the overall culture produced strong fluorescence. This fluorescence suggests successful folding of the sfGFP which can be taken as evidence by proxy of FimH folding. The result also suggests that sfGFP is able to move through the pore formed during pilus biosynthesis.

Sequence and Features