divalent cation[4].

Figure 2: Material eluted, acetone precipitated and reapplied to an SDS-20% polyacrylamide gel and then silver stained. Slice numbers are the same as in A. E is whole cell extract used as starting material for protein elution. Arrow shows the estimated position of MazF migration. Ref: Pellegrini O, Mathy N, Gogos A, Shapiro L, Condon C. The Bacillus subtilis ydcDE operon encodes an endoribonuclease of the MazF/PemK family and its inhibitor. Mol Microbiol. 2005 Jun;56(5):1139-48. doi: 10.1111/j.1365-2958.2005.04606.x. PMID: 15882409.

In the figure, the bacteria in this plate contained plasmids of pBAD-MazF. Three of 6-1 groups were the control group without arabinose induction, and three of 6-4 groups were the experimental group with 1.5 M/L arabinose induction. Where, the dilution factor of the group with * is 10^4, and the dilution factor of the group without * is 10^6.

Result: The bacteria without arabinose induction grow normally, while with arabinose induction, the bacteria suicide.

Figure 3: Experimental medium. 6-1 is blank control ,6-4 is experimental group.

Reference

[1]Park, Jung-Ho, Yamaguchi, Yoshihiro and Inouye, Masayori(2011), Bacillus subtilis MazF‐bs (EndoA) is a UACAU‐specific mRNA interferase, FEBS Letters, 585, doi: 10.1016/j.febslet.2011.07.008 [2]Dhirendra K. Simanshu, Yoshihiro Yamaguchi, Jung-Ho Park, et al. Structural Basis of mRNA Recognition and Cleavage by Toxin MazF and Its Regulation by Antitoxin MazE in Bacillus subtilis. 2013, 52(3):447-458 [3]Stein T. Bacillus subtilis antibiotics: structures, syntheses and specific functions. Mol. Microbiol. 2005; 56:845–857. [PubMed: 15853875] [4] Pellegrini O, Mathy N, Gogos A, Shapiro L, Condon C. The Bacillus subtilis ydcDE operon encodes an endoribonuclease of the MazF/PemK family and its inhibitor. Mol Microbiol. 2005 Jun;56(5):1139-48. doi: 10.1111/j.1365-2958.2005.04606.x. PMID: 15882409.

Contribution & Improvement from XJTU-China 2022

Profile

Name

Lysis-phi X174

Base Pairs

273

Design Notes

The gene was optimized by E. coli codon

Source

Shigella flexneri 2a str. 301 (strain: 301, serotype: 2a)

Usage&Biology

Source and Principle

Biosafety is an important consideration when designing engineered bacteria, and MazF has been commonly used in previously work. Here we develop a novel lysis gene (BBa_K4182007) for the design of controlled suicide circuits for engineering efficiency and biosafety reasons, also can be considered as an alternative of suicide protein MazF.

Figure 1: The temperature-controlled suicide circuit with a novel lysis gene

Figure 2:The principle of temperature-controlled suicide circuit

Figure 2 shows the principle of our temperature-controlled suicide circuit. When bacteria grows at a low temperature(30℃), the CI857 protein binds to the Pλ promoter, and downstream lysis gene are unable to be expressed, allowing the cell growth. While at 42℃, the CI protein will be degraded and lead to the expression of lysis gene and eventually cell death and release of the product.

Codon optimization

The lysis gene is from Enterobacteria phage KleenX174. To better express the lysis gene in engineered bacteria, the codon optimization of the lysis gene was conducted according to the codon preference of Escherichia coli. Figure 3 shows the number of codons we optimized to make our codons more in line with Escherichia coli preference. The modified lysis gene is shown in BBa_K4182007.

Figure 3: Codon Optimization of lysis gene

Optimization of suicide circuit

Initially, we planned to construct our suicide circuit (Plasmid 5) using vector backbone pSB1K3 by Golden Gate assembly, and we can obtain several clones. However, it was found that after colony PCR verification, only weak target bands could be observed (Figure 4), and the plasmids extracted from the recombinant DH5α cells was at very low concentration, and sequencing could not be completed.

Figure 4: Plasmid 5 map based on pSB1K3 and its verification (he target band is approximately 1600bp)

We supposed that due to the low copy number of pSB1K3 vector, it is difficult to extract sufficient plasmid from the engineered bacteria for further validation. Therefore, we replaced the backbone to pSEVA341, a higher-copy-number vector and re-constructed the plasmid (Figure 5). As shown in Figure 5, the obvious target bands were observed, and the plasmid correctness was further confirmed by sequencing.

Figure 5: The new plasmid 5 with pSEVA341 backbone and its verification

The verification of heat triggered cell lysis and suicide

The engineered cell harboring plasmid 5 and blank vector respectively, were culture at 30℃ overnight, and then the temperature was shift to 42℃. The OD600 of each group was detected every 1 h, and the growth curve of these strains were determined as follows. The results clearly demonstrated the cell growth was significantly inhibited after heat at 42℃ compared to the strain without lysis gene. And about 9% of whole cell population was retained after heat. Compared to the commonly used suicide protein MazF (BBa_K302033), the lysis protein in our study is also efficient but shorter and easy to be manipulated, which can be used as an alternative and update for MazF.

Figure 6: The cell growth of strains with suicide plasmid 5 and blank vector

References

1. Din, M.O., et al., Synchronized cycles of bacterial lysis for in vivo delivery. Nature, 2016. 536(7614): p. 81-85.

2. Saeidi, N., et al., Engineering microbes to sense and eradicate Pseudomonas aeruginosa, a human pathogen. Mol Syst Biol, 2011. 7: p. 521.

3. Restrepo-Pineda, S., et al., Thermoinducible expression system for producing recombinant proteins in Escherichia coli: advances and insights. FEMS Microbiol Rev, 2021. 45(6).

4. Aparicio, T., V. de Lorenzo, and E. Martínez-García, Improved Thermotolerance of Genome-Reduced Pseudomonas putida EM42 Enables Effective Functioning of the PL/cI857 System. Biotechnology Journal, 2019. 14(1): p. 1800483.

Characterized by BNUZH-China 2022

In this module, we replaced GOI with MazF. We hoped that when illuminated with the 660 nm light, MazF can be transcription and translation. Then MazF works, killing the engineered cells. Figure 1 illustrates the detailed design of the whole device.


Figure 1: Construct design and the principle of the REDMAP-MazF. 5×UAS-P(hCMVmin) was fused to MazF. Gal4 was linked via a linker to PhyA. At the same time, PCB was combined with PhyA. PhyA turned to ΔPhyA. VP64 was linked with FHY1. When 660 nm light illuminating, ΔPhyA combines with VP64. Then, Gal4-ΔPhyA is transported into the nucleus by VP64-FHY1. After that, Gal4 will combine with 5×UAS-P(hCMVmin), activating the transcription of the downstream target gene: MazF. Then MazF works, killing the engineered cells.

Usage and Biology

We planned to use it to activate the transcription of MazF (BBa_K302033) to cause the engineered cells to commit suicide.

Experimental approach

For testing this device, we used HEK293T cells, which were seeded in 25cm2 flask. The PLVX vector was transiently transfected into HEK293T cells by Lipo8000™ transfection system and incubated for 43 h to ensure normal cell status. Then, phycocyanobilin (PCB) with a final concentration of 5 μM was added to the system, and the system was illuminated with red light (660 nm) for 3 h. After illumination, the cells were observed and the cell lysates were analyzed by SDS-PAGE and Western Blot.


Figure 2: (a) REDMAP SDS-PAGE results. The VP64 strip is in the red box, and the MazF strip is in the green box. CG-C was the cell lysate of the control group, and EG-C was the cell lysate of the experimental group. (b) VP64 Western Blot diagram. CG-C was the cell lysate of the control group, EG-C was the cell lysate of the experimental group, and the theoretical size of VP64 was 30 kDa. (c) MazF Western Blot. CG-C was the cell lysate of the control group, EG-C was the cell lysate of the experimental group, and the theoretical MazF size was 13 kDa.


Figure 3: Morphology of control and experimental cells after red light verification. The control group was HEK293T cells without transient transfection, and the experimental group was HEK293T cells with transient transfection. 10×20 refer to the multiple of the eyepiece × the objective.

References

[1] Park, J. H., Yamaguchi, Y. & Inouye, M. Bacillus subtilis MazF-bs (EndoA) is a UACAU-specific mRNA interferase. FEBS Lett 585, 2526-2532 (2011). https://doi.org:10.1016/j.febslet.2011.07.008
[2] Zhou, Y., Kong, D., Wang, X. et al. A small and highly sensitive red/far-red optogenetic switch for applications in mammals. Nat Biotechnol 40, 262–272 (2022). https://doi.org/10.1038/s41587-021-01036-w
[3] Simanshu, D. K., Yamaguchi, Y., Park, J. H., Inouye, M. & Patel, D. J. Structural basis of mRNA recognition and cleavage by toxin MazF and its regulation by antitoxin MazE in Bacillus subtilis. Mol Cell 52, 447-458 (2013). https://doi.org:10.1016/j.molcel.2013.09.006
[4] Stein, T. Bacillus subtilis antibiotics: structures, syntheses and specific functions. Mol Microbiol 56, 845-857 (2005). https://doi.org:10.1111/j.1365-2958.2005.04587.x
[5] Pellegrini, O., Mathy, N., Gogos, A., Shapiro, L. & Condon, C. The Bacillus subtilis ydcDE operon encodes an endoribonuclease of the MazF/PemK family and its inhibitor. Mol Microbiol 56, 1139-1148 (2005). https://doi.org:10.1111/j.1365-2958.2005.04606.x

Improvement by 2022 Canton_HS

Autism Spectrum Disorder (ASD) is a neuro-developmental disorder characterized by social communication disorders. Our research aims at early diagnosis and accurately diagnosing and treatment. In order to carry forward the spirit of iGEM, we specially searched the iGEM Biological Parts library for related projects and picked BBa_K302033, MazF. This is a biological part submitted by iGEM10_Newcastle in 2010, they developed an ASD diagnosis and treatment method, but didn’t totally achieve ASD treatment through the brain-gut-axis. So that it is really important to provide another candidate protein for ASD treatment. In this project, our team carried out a related protein SLC7A4 for this part in the laboratory. The SLC7A5 transports the so-called branched-chain amino acids (BCAA) into the brain. Mutation in this gene reduces branched-chain amino acid levels in the brain and interferes with neural cell protein synthesis which reduced social interactions and other changes. Improving the SLC7A5 levels by building engineered probiotics may achieve the treatment of autism. In order to verify if the new part SLC7A5 we developed worked well, we transformed the recombinant plasmid into E. coli BL21(DE3) to verify the protein expression level by SDS-PAGE. This protein may could be used in future research.

Profile

Name: SLC7A5

Base Pairs: 1524 bp

Origin: Homo sapiens, genome

Properties: amino acid transporter

Usage and biology

Solute carrier transporter 7a5 (SLC7A5), also known as LAT1, belongs to the APC (amino acid, polyamine, choline) superfamily. The heterodimer SLC7A5 and glycoprotein CD98 linked through a conserved disulfide is responsible for the uptake of essential amino acids in crucial body districts such as the placenta and blood-brain barrier. The SLC7A5 transports the so-called branched-chain amino acids (BCAA) into the brain. Mutation in this gene reduces branched-chain amino acid levels in the brain and interferes with neural cell protein synthesis which shows reduced social interactions and other changes. There are many different genetic mutations causing autism, and this heterogeneity makes it difficult to develop effective treatments.

Construct design

SLC7A5 transporter is expressed under the promoter T7. The gene fragment was inserted into pET28a.

Figure 1. The map of pET28a-SLC7A5

Experimental approach

1.1 Construction of biosensor expression plasmids

In order to build our plasmids, we let the synthetic company synthesize the SLC7A5 DNA sequence and inserted it into the pUC57 vector. We amplified the SLC7A5 from the plasmid by PCR (Figure 2) and inserted it into the EcoRI and XhoI sites of the pET28a vector. We transformed it into E. coli Top10 competent cells.

Figure 2. SLC7A5 amplification electrophoresis result.

1.2 Colony PCR of pET28a-SLC7A5

We selected the 8 colonies to perform by colony-PCR (Figure 3). The electrophoresis result showed that No. 1, 2, and 7 has correct bands.

Figure 3. colony PCR electrophoresis result.

1.2 Sanger sequencing of recombinant plasmid

We inoculated the correct colonies in LB (Kan+) liquid medium and extracted the plasmids and sent them to the company for Sanger sequencing. The returned sequencing data showed that there were no mutations in the gene region which means we successfully constructed the recombinant plasmid.

Figure 4. Sanger sequencing.

Proof of function

SLC7A5 purification

In order to verify if SLC7A5 expression in the E. coli host strain, we transformed the recombinant plasmids into E. coli BL21(DE3), inoculated the recombinants and added IPTG to induce protein expression when the OD600 reached 0.6. After overnight induce and culture, we collected the cells and ultrasonic fragmentation of cells to release the intracellular proteins. Next, we verified the expression level of the target protein by SDS-PAGE (Figure 5). As a result, the recombinants successfully expressed our target protein.

Figure 5. SDS-page of SLC7A5 purification.