Difference between revisions of "Part:BBa K4907108"
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<center><html><imgsrc="https://static.igem.wiki/teams/4907/wiki/parts/jincheng/biaozhen/109-1.png" width="400px"></html></center> | <center><html><imgsrc="https://static.igem.wiki/teams/4907/wiki/parts/jincheng/biaozhen/109-1.png" width="400px"></html></center> | ||
<center><html><B>Fig. 1 Gene circuit of <partinfo>BBa_K4907122</partinfo>_pSB3K3 </B></html></center> | <center><html><B>Fig. 1 Gene circuit of <partinfo>BBa_K4907122</partinfo>_pSB3K3 </B></html></center> | ||
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===Characterization=== | ===Characterization=== | ||
====Agarose gel electrophoresis (AGE)==== | ====Agarose gel electrophoresis (AGE)==== |
Revision as of 17:40, 10 October 2023
pVSW-3 (18)-B0034-rfp-B0015
Biology
pVSW-3(18)
Some RNA polymerases of eukaryotes and viruses have domains that specifically recognize DNA base sequences, and they are specifically matched with their corresponding promoters.(1) VSW-3 RNAP is encoded by the chillophilic phage VSW-3 in plateau lakes and has low temperature specificity(2). Hengxia et al. characterized pVSW-3 series promoters for the first time and pVSW-3(18) is one of them.
Usage and design
XMU-China has developed a novel RNA polymerase, VSW-3 RNAP and we characterized its potentially useful promoters in order to construct a matching expression system. pVSW-3(18) is one of the more efficient promoters in the series. BBa_K4907109_pSB3K3 was constructed as a reporting circuit, for comparing with pVSW-3(GGG) and pVSW-3(genome). By characterizing these three promoters, we hope to determine the effect of the 3' terminal structure of the promoter for VSW-3 RNAP on its efficiency, and to identify a VSW-3 expression system that can effectively function in <r>E. coli</r>.
Characterization
Agarose gel electrophoresis (AGE)
When we were building this circuit, colony PCR was used to certify the plasmid was correct. We got the target fragment-1220bp (lane K4907109).
Comparison of series promoters: pVSW-3(GGG), pVSW-3(genome)
In order to find a promoter that can function efficiently in Escherichia coli, we constructed BBa_K4907109_pSB3K3(pVSW-3(18)), BBa_K4907112_pSB3K3(pVSW-3(GGG)) and BBa_K4907122_pSB3K3(pVSW-3(genome)) to explore the effect of the structure of the 3' terminal of the promoter on its efficiency. The results are shown in the figure, with BBa_K4907109_pSB3K3 showing the highest efficiency.
Reference
1.S. Borukhov, E. Nudler, RNA polymerase: the vehicle of transcription. Trends in Microbiology 16, 126-134 (2008).
2. H. Xia et al., Psychrophilic phage VSW-3 RNA polymerase reduces both terminal and full-length dsRNA byproducts in in vitro transcription. RNA Biology 19, 1130-1142 (2022).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 474
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 596
- 1000COMPATIBLE WITH RFC[1000]