Difference between revisions of "Part:BBa K4286103"

Revision as of 13:09, 10 October 2022

Effector device for improved version of timed suicide switch

2022 SZU-China has designed the second generation of timed suicide switch. The following improvements have been made to the second-generation effector: the MazF expression device has been deleted; high efficiency tetR binding sites have been added.

Usage and Biology

The core of the effector is the MazEF toxin-antitoxin system from Bacillus subtilis, which can lead to programmed cell death. The antitoxin MazE is controlled by the Promoter tetR, and the toxin MazF is controlled by the constitutive Promoter PJ23110. MazF is an endonuclease that specifically cleaves UACAU sites on mRNA. MazE combines with MazF at a ratio of 1:1 to occupy its active site and make it lose its toxicity. what's more, the effector2.0 removes the function of periodically expressing MazF and adds the function of binding tetR, acting as a tetR sponge. The effector2.0 is encoded in the high-copy plasmid colE1.

Assembly

The oscillator2.0 and the effector2.0 form a timed suicide switch2.0.

The engineered bacteria with a timed suicide switch were placed in an IPTG-rich medium or in a dormant state before being applied in fields. The purpose of being placed in IPTG is to continuously activate the PlacI and make the oscillator unbalanced and stagnant， in which circumstance MazF does not express.

After being applied to the field, the oscillator is re-activated with the release of IPTG and the resuscitation of the engineering bacteria. The contents of three repressor proteins changed cyclically: lacI inhibited the expression of tetR, tetR inhibited the expression of λ cI, and λ cI inhibited lacI expression. That is, the three promoters PlacI, PtetR, and PλcI were alternately activated.

As for the effector, MazE was constitutively expressed and maintained at a certain concentration in the cytoplasm, while the expression of MazF was inhibited by tetR and showed a fluctuating increase. In a simplified model, MazE and MazF bind at the ratio of 1:1, resulting in toxin inactivation. When the concentration of toxin MazF is higher than that of antitoxin MazE, the extra toxin MazF plays the role of endonuclease to cut mRNA and kill the engineered microorganisms.

modeling

Where $$i=TetR,LacI,cI$$, concentration of $$DNA_i$$ is $$[DNA_i]$$, concentration of $$mRNA_i$$is $$[mRNA_i]$$, concentration of protein expression product is $$[p_i]$$, $$k_1$$is transcription rate of $$mRNA_i$$, $$k_2$$ is translation rate of $$mRNA_i$$, $$d_1$$is the rate of $$mRNA_i$$ decay, and $$d_2$$ is the rate of $$p_i$$ decay.

Sequencing

Sequence and Features