"
Team:Washington/Gram Negative/Design
From 2010.igem.org
Designing the Transfer of the Type Six Secretion System into E. coli
Using a fosmid to transfer the T6SS genes into E. coli
The T6SS is comprised of 23 genes across several operons. Capturing and moving these genes via standard restriction digest cloning was determined to be impractical. We discovered that the sequence of the P. aeruginosa strain (PAO1) we were using was solved using fosmids (essentially large plasmids). We were able to locate these fosmids and were very excited to find that one of the fosmids contained all of the necessary T6SS genes organized nicely in two divergent operons. We successfully transferred the fosmid into E. coli. It was not clear, however, whether or not the genes would be expressed in E. coli, since the promoters that controlled the expression of the T6SS genes on the fosmid were P. aeruginosa' genes. In order to verify expression of the T6SS genes we performed a Western blot using antibodies against Fha1, which is a critical protein of the secretion system and a reporter for T6SS activity.
Testing the Native Pseudomonas aeruginosa Promoter-regulated Type 6 Secretion System in E. coli
To determine whether the T6SS genes from the fosmid were being expressed from the native P. aeruginosa promoter, the fosmid was tranferred into E. coli, and a Western blot was performed on cell extracts for Fha1, one of the proteins critical for T6SS activity. As expected, the Western blot showed a band for Fha1 in the P. aeruginosa cell extract sample, but no bands were seen in the E. coli cell extract samples (shown below), indicating that E. coli was probably not transcribing the T6SS units from the native P. aeruginosa promoter.
Strategy to Improve Type 6 Secretion System Expression in E. coli
To allow expression of these genes in E. coli, we designed a promoter system that would allow the same E. coli - recognized promoter to drive expression of both divergent operons. This promoter system would replace the native P. aeruginosa promoter system. We chose a bidirectional T7 promoter, which would promote transcription in both the 5' and 3' direction. T7 promoters are well characterized, and known to be highly robust for expression in E. coli.
Designing Regulation of the Toxin/ Antitoxin System
Separating the Regulation of the Toxin/Antitoxin from the Type 6 Secretion System
We chose to separate the toxin/antitoxin (Tse2/Tsi2) regulation from the regulation of the T6SS, since controlling all of these components would be limited by the complexity of the T6SS, and also the massive amount of protein production. The purpose of generating novel Tse2/Tsi2 regulatory circuits is to activate the killing activity of our E. coli antibiotic only when necessary. If our probiotic system were constitutively producing Tse2, this would adversely affect natural gut flora. In addition, natural gut flora might develop resistance to Tse2 and pass this resistance to potential Gram-negative pathogens. As a BioBrick, the Tse2Tsi2 circuit is modular, and therefore promoters and other regulatory components can be swapped out. For example, one could ingest the probiotic, have it exist in the gut, but only induce its killing behavior by ingesting some user-defined signal, such as arabinose, which would activate expression of the toxin, which would then travel through the already-present T6SS into Gram-negative targets. In addition, one could envision a scenario in which it would be advantageous to separately regulate Tsi2, to kill the probiotic when it is no longer useful by preventing Tsi2 expression, causing cell suicide due to the production of Tse2. For our purpose in this project, we decided to make a probiotic that produced the Tse2 toxin only when the probiotic detected the presence of a pathogen.
Matt's new image goes here
Inducing Toxin Expression Upon Detection of Pathogen: Proof of Concept
In order to activate Tse2 production in response to a pathogen, we needed a promoter that is inducible by some molecular stimulus unique to a specific pathogen. In addition, the expression of Tsi2 would need to be either constitutive or induced by the same stimulus that induces Tse2 expression. As a proof-of-concept, this project uses the LuxR-pLux transcription factor - promoter system from Vibrio fischeri to regulate expression of the Tse2-Tsi2 locus. V. fischeri excretes 3OC6HSL, a small membrane permeable molecule (hereafter referred to as HSL). HSL binds to the transcription factor LuxR, thereby inducing its DNA transcriptional activity. Thus, expression from the pLux promoter is linked to cell density. This is referred to as quorum sensing. Quorum sensing is found in many bacterial species including pathogenic species, making the use of the pLux-LuxR system a good proof-of concept for induction of toxin production when the probiotic detects the presence of a pathogen. When our probiotic detects a gram-negative pathogen-specific molecule (modeled by HSL), transcription is induced by an inducible promoter (modeled by pLux). This leads to expression of Tse2 (a toxic protein) and Tsi2 (its antitoxin). The T6SS then attacks the pathogen, puncturing the cell wall. Tse2 is then secreted into the gram negative pathogen, killing the pathogen. This system could easily be modified to target a wide range of gram-negative pathogens by just changing the regulation of the Tse2/Tsi2 locus.
Diagram of the Tse2/Tsi2 HSL inducible circuit
The Tse2/Tsi2 system has a relatively simple circuit design. Tse2 and Tsi2 are present in one operon (as in Pseudomonas aeruginosa) and are regulated by the pLux promoter. For the pLux promoter, we used the well-characterized BioBrick [http://partsregistry.org/Part:BBa_F2620 F2620]. The LuxR transcription factor is constituitively expressed because no tetR is present to repress the production of LuxR. When HSL is present it binds to LuxR resulting in the induction of Tse2 and Tsi2 production. This BioBrick is part [http://partsregistry.org/Part:BBa_K314203 K314203].
