Difference between revisions of "Part:BBa K2292002"

Latest revision as of 00:54, 27 October 2020

Toxin-antitoxin mazEF

MazEF is a suicide system in Escherichia coli which consists of a stable toxin mazF and labile antitoxin mazE. MazF causes cell death by cleaving mRNA at a specific site. On the other hand, mazE plays a role of antitoxin which can antagonize the toxin mazF.

In general, continuous generation of mazE can prevent the situation of cell death by antagonizing mazF. However, once mazE ceased to be produced, it would be degraded by the protease ClpAP. Hence, the remaining toxin mazF will cause the cell death by cleaving mRNA.

Figure 1 Mechanism of mazEF kill switch

Figure 2 MazEF function test (OD600 vs. Time)

In the beginning, we add arabinose to the E. coli, and the kill switch start. During the first hour, mazE and mazF are produced. Because of the toxin-antitoxin characteristic, E. coli grows normally in the first hour. After one hour, the mazE and mazF concentrations reach saturation, and then start degrading. Compared with mazF, mazE degrades faster, so mazF cut mRNA for important protein. Finally, E. coli cannot survive. The OD600 value we observe is that it maintains a stable value.

Figure 3 MazEF function test (Plate count method)

Figure 4 MazEF function test (Plate count method)

Following five hours, we test the survival rate every hour (we only see result of negative control and 6 mM arabinose, because kill switch is independent on concentration of arabinose.) By adding different concentration of arabinose, we found the most appropriate arabinose concentration to induce the suicide system. After five hours, almost all E. coli dead.

Adapted Uses

The 2020 CLS_CLSG_UK team has adapted this kill switch so that it can be induced by hypoxic conditions. As well as this we adapted the system by which the kill switch works into a system we believe is more efficient, our system works by having the MazE under the control of the CMV promoter while the MazF expression is under the control of a hypoxia induced promoter that was characterised alongside the CMV promoter. By using the characterisation as well as the strength of various RBS from the literature we were able to construct a system that is more efficient at keeping the E. coli alive over long periods but still acting as an efficient kill switch. While constructing this would create a larger insert and potentially an extra set of digestions and ligations we believe that the advantage it presents on the original system is worth it given that in the original system the negative control still ended up killed the bacteria after a matter of hours, for long term use this would not be efficient. To view the updated version see part:BBa_K3588014.

Sequence and Features