Team:Wisconsin-Madison/results

Encapsulation

Our goals is to have each cell be surrounded by a protective 'capsule' to allow them to safely travel through the harsh acidic environment of the stomach to arrive in the small intestine for their main purpose. Imperial 2009 used Transcription Factor RcsB to stimulate a the production of Colonic Acid from the capsule synthesis pathway of E.coli. Colonic Acid s a polysaccharide containing a repeat unit with D-glucose, L-fucose, D-galactose, and D-glucuronate. Colonic Acid has been shown to increase cell survivability in acidic conditions. RcsA and RcsB are transcription factors that are know to be positive regulators of capsular polysaccharides synthesis. We placed RcsA, RcsB, and a combination of the two under a IPTG inducible promoter to test both quantity of colonic acid produced and cell survivability. These two transcription factors form a heterodimer that is know to activate around 19 genes related to colonic acid synthesis. RcsB is also know to form a homodimmer and positively regulate cell division. RcsA and RcsB belong to the multicomponent RcsF/RcsC/RcsD/RcsA-RcsB phosphorelay system.

Colonic Acid Quantification

Background

Colonic Acid is a polysaccharide containing a repeat unit with D-glucose, L-fucose, D-galactose, and D-glucuronate. Biological extracts often contain compounds, which under heating with H2SO4 yield brown products absorbing between 396 nm and 427 nm. Colonic acid can be estimated by measuring L-fucose content.

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Results

Conclusion

Cell Survivability in Low pH

Background

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Results

Conclusion

The cells survivability testing is done in three different pH conditions, pH=2, 4, and 7, for 3 samples and one controls. We use identical cells, which is MG1655, to generate the experimental data. After four hour exposure in the acidic medium, we observed that there are no survivals under the pH=2 condition. However, there is an significant improvement at pH 4 in the experimental strains. Moreover, from the experiments, we observed that the combination of having RcsA and RcsB both presented enhanced the survivability of the experimental straints. Our result from this testing quantified can confirmed the cells survivability at low pH levels.

Timed Lysis

Background

gadAp: A pH Sensitive Promoter Based on available literature (see Project Page), we expected an increase in expression from gadAp (BBa_K318512) under both acidic pH conditions (from pH 5 to 3) and in the stationary phase (after an OD of 1 or 2). As most previous studies of gadAp had focused on gadA mRNA production, we wanted to instead explore the viability of gadAp for use in expression of protein. Given the stressful conditions under which it acts and its complex regulation, the possibility that mRNA-level regulation or an inability of acid-stressed cells to produce large quantities of protein may exist could not be discounted. As such, we combined the gadA promoter with a RFP gene (BBa_K318513) to directly test its ability to produce protein under stationary phase and acid stress conditions.

Low pH/Stationary Phase Induction

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Conclusion

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Enccryption

Unfortunately, we never got to testing our systems. We managed to clone a two component encryption system (as depicted above). Rigorous testing of our system never occurred due to time constraints of the competition. Our enzyme delivery took precedence as the competition drew near and our financial resources became more and more strained.