BACKGROUND

When we first designed our project, it soon came to our mind that we had to ensure the containment of our bacteria from the environment. The best way to do that, apart from the physical containment performed by the porous membrane, was to implement our bacterial interface with a kill-switch.

What is a kill-switch?

A kill-switch is, literally, something that tells a bacterium whether to live or die, depending on specific environmental conditions. With the rapid development of synthetic biology, these switches are of many kinds and have been increasingly used in recent years [1]. They mainly work by introducing in the bacteria gene constructs that block important genes or express toxins when exposed to a specific environmental condition. We realized an educational video destined to explain to the public audience the principle of a kill-switch. This video can be found here.

OUR SOLUTION

Our kill-switch

Our interface is eventually destined to “cohabit” in a human body. We want to make sure that the bacteria we create cannot develop outside of the space we put them in. Thus, our kill-switch makes sure that when the environmental conditions of the inner human body are not met, the bacteria die.

Reviewing the literature led us to come across a very interesting article presenting the cryodeath kill-switch, invented by Finn Stirling in 2017, which is triggered by temperatures under 37°C [2]. For obvious reasons, this kill switch sounded like a perfect fit to our application. Contacting Finn comforted us in that choice, and we had the chance to exchange a lot, not only concerning the kill switch but on our project in general. After reviewing the original sequence, we modified it so that it would become a biobrick, and we removed what was unnecessary to us, leading to the making of our biobrick BBa_K2616002.

The modified cryodeath kill-switch

The kill-switch functions by the means of the toxin/antitoxin couple CcdB/CcdA. The toxin targets and inhibits the GyrA subunit of DNA gyrase, an essential bacterial enzyme that catalyzes the super-coiling of double-stranded closed circular DNA [3].

In the kill-switch, the transcription of CcdB and CcdA are regulated by two different promoters. CcdA is expressed by the constitutive promoter P_lac, which ensures a constant low production of antitoxin [4]. On the contrary, the toxin CcdB is expressed by the promoter PcspA. This promoter was originally discovered upstream of the Cold Shock Protein A in many bacteria, as a way to cope with environmental stress [5]. This promoter ensures a very low transcription rate at 37°C, but it increases drastically below 22°C.

Overall, at 37°C, the quantity of antitoxin CcdA is high enough to cope with the leaky low level of toxin produced. However, if the bacteria happen to be in an environment at a lower temperature, the toxin promoter is not repressed anymore, the quantity of toxin becomes too important, and the bacteria is not able to grow (see figure 1). This allows us to make sure that our genetically modified organisms will not spread out in an open environment.

Figure 1: Functioning of the cryodeath kill-switch at 37°C and at 22°C.

RESULTS

Achievements:

Successfully cloned a part coding for toxin/antitoxin (CcdB/CcdA) system in iGEM plasmid backbone, creating a new basic part Bba_K2616002

Successfully sequenced BBa_K2616002 in pSB1C3 and sent to iGEM registry

Successfully observe survival of our engineered bacteria at 25°C and 37°C and absence of growth at 18°C and 20°C, showing the efficiency of the kill switch

Next steps:

Find a system that kills bacteria when released in the environment rather than just stopping their growth

REFERENCES

“Kill switches limit modified microbes,” Nature, vol. 528, no. 7581, pp. 166–167, Dec. 2015.
F. Stirling et al., “Rational Design of Evolutionarily Stable Microbial Kill Switches,” Mol. Cell, vol. 68, no. 4, p. 686–697.e3, Nov. 2017.
R. J. Reece and A. Maxwell, “DNA Gyrase: Structure and Function,” Crit. Rev. Biochem. Mol. Biol., vol. 26, no. 3–4, pp. 335–375, Jan. 1991.
T. P. Malan and W. R. McClure, “Dual promoter control of the E. coli lactose operon.,” Cell, vol. 39, no. 1, pp. 173–80, Nov. 1984.
R. Keto-Timonen, N. Hietala, E. Palonen, A. Hakakorpi, M. Lindström, and H. Korkeala, “Cold Shock Proteins: A Minireview with Special Emphasis on Csp-family of Enteropathogenic Yersinia,” Front. Microbiol., vol. 7, Jul. 2016.