Revision as of 13:05, 11 September 2019

f1-AraC-Pbad-lysis-f2

We put AraC-Ara Promoter in front of the lysin gene from phage, and then we use CRISPR/Cas9 technology to turn the construction of AraC-Ara Promoter-Lysis into the genome of E.coli MG1655 wild strain. This part consists of fragments from the E.coli MG1655 genome, AraC-AraPromoter and lysin genes from phages.

Usage and Biology

In order to achieve cell lysis, we usually express the lysin gene. Then we find the part BBa_K2277000, which constructed by 2017 iGEM team ZJUT-China. They construct the lysinene in the plasmid. But in most cases, resistance genes will be added to plasmids in order to screen transformants. So we choose to construct the lysingene directly into the genome,for two advantages. First, it can reduce the number of plasmids that need to be transformed in the engineering bacteria, which can reduce the additional metabolic pressure. Second, it can avoid the addition of new resistance. We added the E.coligenome homology arm to both ends of this part. The genomic homology arms at both ends of our part allow us to insert this part into the non-metabolic pathway on the E.coli genome.

Characterize

We first built this part on plasmid T vector. To verify whether the expressed lysin protein has the function of cell lysis, we used E.coli MG1655 as a chassis. we transformed this plasmid into MG1655 and characterized the function of the lysin gene based on the growth curve of the bacteria. 

When the function of lysin protein was verified, we started to construct this part in the genome of E.coil MG1655 by using CRISPR/Cas9 system.

Experimental Results

Before genome editing, we first tested the cleavage function of the part containing the genomic homology arm on the plasmid. Our part is built on the T vector. The result is shown in Fig 1:

Fig.1 Growth curve

Our results show that when we added arabinose(the concentration is 10mM) to inducelysin gene expression, the OD₆₀₀ value of the bacterial culture was significantly lower than that of the control group without arabinose induction. And comparing with adding arabinose after 4.5 h of culture, when we added arabinose at the beginning, the OD₆₀₀ is lower.
Our vector experiments have initially confirmed that the expression of the lysin gene is effective for cell lysis. Based on the results of this experiment, we inserted the lysis part into the E.coli genome by CRISPR/Cas technology. In order to obtain a transformant that was successfully inserted the part into genome, we screened by plate streaking, and the experimental results are shown in Fig 2:

Fig.2 Result of plate streaking

We selected 34 transformants for plate streaking, and 5 of them showed lysis effects on arabinose containing plates. They were probably the strain we have insert lysis part into genome. And finally we got a strain with a significant lysis effect after arabinose induction, and we named it E.coli MG1655-Lysis. You can see the result in Fig. 3.

Fig.3 E.coli MG1655-Lysis cultured in tubes

Sequence and Features

Contribution

• Group: [http://2019.igem.org/Team:UESTC-China iGEM Team UESTC-China 2019]
• Author: Jing Yao, Yingying Cao
• Summary: Characterization of the effect of lysin on the growth of Escherichia coli DH5α and BL21(DE3) strains by growth curve

Characterization from iGEM19-UESTC-China

We obtained the plasmid vector containing this part from 2019 iGEM team ZJUT-China. We transformed this plasmid into DH5α and BL21 (DE3) and mapped the corresponding growth curves to characterize the function of this part.

Growth curves

Our results show that when the addition of arabinose inducer (at the beginning and 4h later, concentration of 10 mM) to induce lysin gene expression. Both the DH5α and the BL21 (DE3) were significantly inhibited, their Abs600 values decreased significantly, proving that this part can exert a cleavage effect against DH5α and BL21 (DE3). However, it is worth noting that the Abs600 value of BL21(DE3) increases rapidly after about three hours of lysin expression, suggesting that the lysin in this part may not be sufficient to inhibit BL21(DE3) growth.

Reference

[1]Jiang W, Bikard D, Cox D, et al. CRISPR-assisted editing of bacterial genomes[J]. Nature Biotechnology, 2013, 31(3):233-239.
[2]Doench J G, Fusi N, Sullender M, et al. Optimized sgRNA design to maximize activity and minimize off-target effects of CRISPR-Cas9[J]. Nature Biotechnology, 2016, 34(2):184-191.
[3]Wang G, Lu X, Zhu Y, et al. A light-controlled cell lysis system in bacteria.[J]. Journal of Industrial Microbiology & Biotechnology, 2018:1-4.
[4]Park T, Struck D K, Dankenbring C A, et al. The Pinholin of Lambdoid Phage 21: Control of Lysis by Membrane Depolarization[J]. Journal of Bacteriology, 2007, 189(24):9135.

Functional Parameters