Difference between revisions of "Part:BBa K4765126"
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| '''Figure 1. Agarose gel electrophoresis of PCR products, amplified from bacterial colonies/cultures. | | '''Figure 1. Agarose gel electrophoresis of PCR products, amplified from bacterial colonies/cultures. | ||
− | From left lane(1) to right lane(3) indicate the successful construction of H. ex mtSSB, H. ex mtSSB + SAHS 33020, and H. ex mtSSB + SAHS 33020 + AnAFP. ''' | + | From left lane(1) to right lane(3) indicate the successful construction of ''H. ex'' mtSSB, ''H. ex'' mtSSB + SAHS 33020, and ''H. ex'' mtSSB + SAHS 33020 + AnAFP. ''' |
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====Desiccation Survival Assay==== | ====Desiccation Survival Assay==== | ||
We constructed ''H. ex'' mtSSB, SAHS 33020, and AnAFP into this part using pRAP. Within [https://parts.igem.org/Part:BBa_K4765127 BBa_K4765127], we rearranged the positions of these three proteins. | We constructed ''H. ex'' mtSSB, SAHS 33020, and AnAFP into this part using pRAP. Within [https://parts.igem.org/Part:BBa_K4765127 BBa_K4765127], we rearranged the positions of these three proteins. |
Revision as of 13:01, 12 October 2023
ribozyme connected: H. ex mtSSB + SAHS 33020 + AnAFP
Contents
Introduction
This composite part combines BBa_K4765016(H. ex mtSSB),BBa_K2306003(SAHS 33020)and BBa_K4765015(AnAFP) in our ribozyme-assisted polycistronic co-expression system:pRAP.
AnAFP is an antifreeze protein which endows E. coli with antifreeze capibility. SAHS 33020 is a heat soluble protein found in the tardigrades which increase E. coli 's stability against desiccation. H. ex mtSSB is a type of mitochondrial single-stranded DNA binding protein which improves E. coli 's resistance to desiccation and UV radiation.
Characterization
Agarose gel electrophoresis
Figure 1. Agarose gel electrophoresis of PCR products, amplified from bacterial colonies/cultures.
From left lane(1) to right lane(3) indicate the successful construction of H. ex mtSSB, H. ex mtSSB + SAHS 33020, and H. ex mtSSB + SAHS 33020 + AnAFP. |
Desiccation Survival Assay
We constructed H. ex mtSSB, SAHS 33020, and AnAFP into this part using pRAP. Within BBa_K4765127, we rearranged the positions of these three proteins.
Figure 2. Workflow of Desiccation Survival Assay |
We've designed an experimental group with E. coli expressing H. ex mtSSB , SAHS 33020 and AnAFP, and used E. coli transformed with the empty pET28a vector as a control. All proteins are expressed via leakage in E. coli BL21 DE3. All the groups are incubated overnight. After reaching an OD600 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 weighed and resuspended in LB medium and dilute 10^5-fold for CFU counting.
Through experiments, we observed that when both H. ex mtSSB and SAHS 33020 are co-expressed, E. coli exhibits a higher survival rate under desiccation compared to E. coli expressing these two proteins individually. Furthermore, altering the order of these three proteins in pRAP does not affect the survival rate of E. coli, indicating that pRAP can correctly express these proteins, regardless of their position.
Figure 3. The dry weight of all the gourps 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 4. CFU colony count of all the groups after drying
The E. coli expressing H. ex mtSSB, SAHS 33020 and AnAFP together showed higher CFU counts after drying compared to E.coli expresssing H. ex mtSSB and SAHS33020 individually. Futhermore there's no significant difference between the two E. colis with rearranged CDS positions. Mean values from three rounds of indepdent experiments are shown. Huge error bars suggest variations between rounds of experiments. |
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 247
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 880
Illegal BsaI.rc site found at 515
Illegal BsaI.rc site found at 596
Illegal SapI site found at 409
Illegal SapI.rc site found at 1804