Difference between revisions of "Part:BBa K4765016"
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====Desiccation Survival Assay==== | ====Desiccation Survival Assay==== | ||
We attempt to compare the anti-desiccation capabilities of ''H. ex'' mtSSB and the pre-existing protein SAHS 33020[https://parts.igem.org/Part:BBa_K2306003 BBa_K2306003] in order to identify a suitable desiccation-resistant protein for B-HOME. Through the experiments, we found that H. ex mtSSB exhibits desiccation resistance comparable to SAHS. | We attempt to compare the anti-desiccation capabilities of ''H. ex'' mtSSB and the pre-existing protein SAHS 33020[https://parts.igem.org/Part:BBa_K2306003 BBa_K2306003] in order to identify a suitable desiccation-resistant protein for B-HOME. Through the experiments, we found that H. ex mtSSB exhibits desiccation resistance comparable to SAHS. | ||
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+ | | <html><img style="width:400px" src="https://static.igem.wiki/teams/4765/wiki/zsl/anti-desiccation-protocol.png" alt="contributed by Fudan iGEM 2023"></html> | ||
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+ | | '''Figure 2. Workflow of Desiccation Survival Assay''' | ||
+ | There is no statistically significant difference in the dry weights among the experimental groups, indicating that the number of ''E. coli'' is consistent between the bacterial tubes. | ||
+ | |} | ||
We've designed an experimental group with H. ex mtSSB and SAHS 33020, and used ''E. coli'' transformed with the empty PET28 vector as a control. All proteins are expressed via leakage in ''E. coli'' BL21 DE3. All the groups are incubated overnight. After reaching an OD value of 1.0, liquid culture is centrifuged, and the supernatant is removed. Pellets are dried for 6.5 hr in SpeedVac (Savant SpeedVac SC100) under 4 0 °C .Finally, the pellets are resuspended in LB medium and dilute 10^5-fold for CFU counting. | We've designed an experimental group with H. ex mtSSB and SAHS 33020, and used ''E. coli'' transformed with the empty PET28 vector as a control. All proteins are expressed via leakage in ''E. coli'' BL21 DE3. All the groups are incubated overnight. After reaching an OD value of 1.0, liquid culture is centrifuged, and the supernatant is removed. Pellets are dried for 6.5 hr in SpeedVac (Savant SpeedVac SC100) under 4 0 °C .Finally, the pellets are resuspended in LB medium and dilute 10^5-fold for CFU counting. |
Revision as of 09:30, 11 October 2023
Hypsibius exemplaris mitochondrial single-stranded DNA binding protein (H. ex mtSSB)
Contents
Introduction
H. ex mtSSB is a type of mitochondrial single-stranded DNA binding protein derived from Hypsibius exemplaris . H. ex mtSSB is non-specific in binding single-stranded DNA. ssDNA is exposed by normal cellular functions like replication and transcription, as well as during genotoxic stress. DNA wrapped around H. ex mtSSB could be physically buffered against DNA damage and ensuing lethality. Under harsh conditions like desiccation heat, and radiation, H. ex mtSSB can maintain the stability of DNA through the above mentioned mechanism, thus enhance the survival rate of organisms in harsh environments[1].
Usage and Biology
We heterologously expressed H. ex mtSSB in E. coli, conferring improved resistance to desiccation and UV radiation. We also compared its desiccation resistance with that of SAHS 33020(BBa_K2306003) and tested the combined desiccation resistance of both proteins in BBa_K4765117
Characterization
Sequencing map
Figure 1. Sequencing map of H. ex mtSSB
Sequencing starts from the T7 terminator, with the primer 5-GCTAGTTATTGCTCAGCGG-3. |
Desiccation Survival Assay
We attempt to compare the anti-desiccation capabilities of H. ex mtSSB and the pre-existing protein SAHS 33020BBa_K2306003 in order to identify a suitable desiccation-resistant protein for B-HOME. Through the experiments, we found that H. ex mtSSB exhibits desiccation resistance comparable to SAHS. | | |- | Figure 2. Workflow of Desiccation Survival Assay There is no statistically significant difference in the dry weights among the experimental groups, indicating that the number of E. coli is consistent between the bacterial tubes. |}
We've designed an experimental group with H. ex mtSSB and SAHS 33020, and used E. coli transformed with the empty PET28 vector as a control. All proteins are expressed via leakage in E. coli BL21 DE3. All the groups are incubated overnight. After reaching an OD value of 1.0, liquid culture is centrifuged, and the supernatant is removed. Pellets are dried for 6.5 hr in SpeedVac (Savant SpeedVac SC100) under 4 0 °C .Finally, the pellets are resuspended in LB medium and dilute 10^5-fold for CFU counting.
Figure 2. The dry weight of H.ex mtSSB, TDP, and control after drying
There is no statistically significant difference in the dry weights among the experimental groups, indicating that the number of E. coli is consistent between the bacterial tubes. |
Figure 3. CFU colony count of H.ex mtSSB, TDP, and control after drying
Colonies (CFU/mL)= CFU count*10^6= CFU count*10^6 The E. coli expressing H.ex mtSSB and SAHS showed higher CFU counts after drying compared to the control group, indicating their desiccation resistance abilities. |
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 186
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 454
Illegal BsaI.rc site found at 535
Illegal SapI site found at 348
Reference
- ↑ Hibshman, J. D., Clark-Hachtel, C. M., Bloom, K. S., & Goldstein, B. (2023). A bacterial expression cloning screen reveals tardigrade single-stranded DNA-binding proteins as potent desicco-protectants (2023.08.21.554171). bioRxiv. https://doi.org/10.1101/2023.08.21.554171