Difference between revisions of "Part:BBa K3838777"
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[[File:T--SZU-China--resultfigure1B.png|300px|center]]
 
[[File:T--SZU-China--resultfigure1B.png|300px|center]]
 
[[File:T--SZU-China--resultfigure1C.png|300px|center]]
 
[[File:T--SZU-China--resultfigure1C.png|300px|center]]
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<center>Fig1. Plasmid vector diagram</center>
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<center>Fig.1 Plasmid vector diagram</center>
 
As can be seen from the figure 1, the sample band was larger than 5000 bp, which was consistent with our plasmid vector 5939 bp, indicating that our plasmid transformation was successful.
 
As can be seen from the figure 1, the sample band was larger than 5000 bp, which was consistent with our plasmid vector 5939 bp, indicating that our plasmid transformation was successful.
  
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We then verified the engineering bacteria at the protein level. The experimental group was DH5α strain with PJSG plasmid, and the control group was DH5α empty vector. As can be seen from figure 2, only DJSG protein was expressed near 14.4 kDa, which was consistent with our target protein band of 16 kDa, indicating that the engineering bacteria successfully expressed HSP protein.
 
We then verified the engineering bacteria at the protein level. The experimental group was DH5α strain with PJSG plasmid, and the control group was DH5α empty vector. As can be seen from figure 2, only DJSG protein was expressed near 14.4 kDa, which was consistent with our target protein band of 16 kDa, indicating that the engineering bacteria successfully expressed HSP protein.
 
[[File:T--SZU-China--BBa K3838111-JSHSP2.png|500px|center]]
 
[[File:T--SZU-China--BBa K3838111-JSHSP2.png|500px|center]]
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<center>Figure 2.SDS-PAGE was performed for DH5α (DJSG) intracellular protein containing PJSG plasmid. Untransformed DH5α was used as blank control group. The target protein size was 16 kDa.</center>
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<center>Fig.2 SDS-PAGE was performed for DH5α (DJSG) intracellular protein containing PJSG plasmid. Untransformed DH5α was used as blank control group. The target protein size was 16 kDa.</center>
  
 
3. Functional representation
 
3. Functional representation
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[[File:T--SZU-China--BBa K3838111-JSHSP3E.png|400px|center]]
 
[[File:T--SZU-China--BBa K3838111-JSHSP3E.png|400px|center]]
 
[[File:T--SZU-China--BBa K3838111-JSHSP3F.png|400px|center]]
 
[[File:T--SZU-China--BBa K3838111-JSHSP3F.png|400px|center]]
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<center>Figure 3 A. Survival rate determined by 0.5 mM hydrogen peroxide stress culture B. Survival rate determined by ethanol (10%) stress culture C-F. Survival rate was determined by stress culture at different temperatures</center>
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<center>Fig.3 A Survival rate determined by 0.5 mM hydrogen peroxide stress culture. B Survival rate determined by ethanol (10%) stress culture C-F. Survival rate was determined by stress culture at different temperatures.</center>
  
 
===References===
 
===References===
 
Tian H, Tan J, Zhang L, et al. Increase of stress resistance in Lactococcus lactis via a novel food-grade vector expressing a shsp gene from Streptococcus thermophilus. Braz J Microbiol. 2012;43(3):1157-1164. doi:10.1590/S1517-838220120003000043
 
Tian H, Tan J, Zhang L, et al. Increase of stress resistance in Lactococcus lactis via a novel food-grade vector expressing a shsp gene from Streptococcus thermophilus. Braz J Microbiol. 2012;43(3):1157-1164. doi:10.1590/S1517-838220120003000043

Revision as of 11:11, 19 October 2021


SHSP

SHSP is a stress protein, also known as heat shock protein, which is a group of proteins preferentially synthesized by cells. Compared with the mutant strains without the plasmid encoding SHSP, the parental strains with the plasmid encoding SHSP were significantly more resistant to temperature changes from 42℃ to 62℃, and there was a significant difference in cell survival rate between the SHSP plasmid carrying streptococcus thermophilus strain and the SHSP elimination plasmid under heat shock condition. The cloned SHSP gene was transformed into streptococcus thermophilus strains lacking plasmid encoding SHSP, resulting in increased resistance at 60℃ or pH 3.5, and increased growth ability at 52℃. Meanwhile, the presence of PET-SHSP and the overexpression of SHSP gene demonstrated its ability to protect E. coli cells from ethanol stress. Results from the literature showed that escherichia coli cells overexpressing SHSP gene of the smaller plasmid pQC2 of Streptococcus thermophilus ST-QC significantly increased their resistance to heat, acid and ethanol stress. Therefore, we chose HSP as a non-antibiotic E. coli screening method.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 79
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]



Data:SZU-China 2021 TEAM

1. The DNA level

We added the HSP gene to the plasmid construction of each of the target genes to express heat shock proteins. On the plasmid level verification, we chose DH5a strain with PJSG plasmid and Nissle 1917 to experiment. Due to the resistance of heat shock protein expression element and triclosan protein expression components on the same plasmid, the results can be seen in figure 1.

T--SZU-China--resultfigure1A.png
T--SZU-China--resultfigure1B.png
T--SZU-China--resultfigure1C.png
Fig.1 Plasmid vector diagram

As can be seen from the figure 1, the sample band was larger than 5000 bp, which was consistent with our plasmid vector 5939 bp, indicating that our plasmid transformation was successful.

2. Protein level

We then verified the engineering bacteria at the protein level. The experimental group was DH5α strain with PJSG plasmid, and the control group was DH5α empty vector. As can be seen from figure 2, only DJSG protein was expressed near 14.4 kDa, which was consistent with our target protein band of 16 kDa, indicating that the engineering bacteria successfully expressed HSP protein.

T--SZU-China--BBa K3838111-JSHSP2.png
Fig.2 SDS-PAGE was performed for DH5α (DJSG) intracellular protein containing PJSG plasmid. Untransformed DH5α was used as blank control group. The target protein size was 16 kDa.

3. Functional representation

We inoculated BL21 strain (BJSG) transformed into PJSG plasmid and BL21 (BPUC) transformed into empty vector pUC18 into 15 tubes of 5 mL LB medium, which were divided into 5 groups with 3 tubes per group. Each group was placed at 37℃ for 5h, and OD value was about 1.0. Then, each group was cultured at 37℃, 42℃, 47℃, 52℃ and 57℃, and under 0.5mM hydrogen peroxide stress and ethanol stress, respectively. The OD600 of bacterial solution was measured per hour for 8h. The survival rate was calculated by taking the first OD600 as 100%, and the result was shown in figure 3. It can be seen that the survival rate of BJSG under hydrogen peroxide and ethanol stress is higher than that of the untransformed blank bacteria, indicating that the engineered bacteria have acquired such stress resistance, and this gene has the potential to be used as a screening gene. In addition, hydrogen peroxide and ethanol mimicked two states common in the human gut: excess reactive oxygen species and the drunk gut. This means that HSP can also effectively help engineered bacteria colonize IBD patients with abnormal ROS levels.

T--SZU-China--BBa K3838111-JSHSP3A.png
T--SZU-China--BBa K3838111-JSHSP3B.png
T--SZU-China--BBa K3838111-JSHSP3C.png
T--SZU-China--BBa K3838111-JSHSP3D.png
T--SZU-China--BBa K3838111-JSHSP3E.png
T--SZU-China--BBa K3838111-JSHSP3F.png
Fig.3 A Survival rate determined by 0.5 mM hydrogen peroxide stress culture. B Survival rate determined by ethanol (10%) stress culture C-F. Survival rate was determined by stress culture at different temperatures.

References

Tian H, Tan J, Zhang L, et al. Increase of stress resistance in Lactococcus lactis via a novel food-grade vector expressing a shsp gene from Streptococcus thermophilus. Braz J Microbiol. 2012;43(3):1157-1164. doi:10.1590/S1517-838220120003000043