Difference between revisions of "Part:BBa K4304009"
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invA Plasmid | invA Plasmid | ||
+ | ==Contribution== | ||
+ | |||
+ | InvA, which is essential for Salmonella spp. to enter cultured epithelial cells, is a member of a family of proteins involved in either flagellar biosynthesis or the secretion of virulence determinants by a number of plant and mammalian pathogens. | ||
+ | We designed this plasmid by inserting InvA DNA fragment into the plasmid pUC57 with a T7 promoter and terminator in front and after the sequence. This plasmid is used to obtain the gene fragment of Shigella which will bind with sgRNAs and recruit cas12a protein to cleave the DNA fragment of it. | ||
+ | ===Construction of the gene InvA containing plasmids=== | ||
+ | We send the company to synthesize the DNA fragments of InvA, and inserted it into the pUC57 vector, the sequenced data showed that the plasmids which were provided by the company were successfully constructed (Figure 1). The constructed plasmids were contained in E. coli strains, we streak inoculated them on LB solid medium plates containing corresponding antibiotics, and incubate them at 37℃ overnight, then we extracted the plasmids. | ||
+ | [[File:T--YkPaO--BBa K4304009-figure1.png|500px|thumb|center|Figure 1. the sequencing data of InvA DNA fragment.]] | ||
+ | |||
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Revision as of 12:30, 26 September 2022
invA Plasmid
invA Plasmid
Contribution
InvA, which is essential for Salmonella spp. to enter cultured epithelial cells, is a member of a family of proteins involved in either flagellar biosynthesis or the secretion of virulence determinants by a number of plant and mammalian pathogens. We designed this plasmid by inserting InvA DNA fragment into the plasmid pUC57 with a T7 promoter and terminator in front and after the sequence. This plasmid is used to obtain the gene fragment of Shigella which will bind with sgRNAs and recruit cas12a protein to cleave the DNA fragment of it.
Construction of the gene InvA containing plasmids
We send the company to synthesize the DNA fragments of InvA, and inserted it into the pUC57 vector, the sequenced data showed that the plasmids which were provided by the company were successfully constructed (Figure 1). The constructed plasmids were contained in E. coli strains, we streak inoculated them on LB solid medium plates containing corresponding antibiotics, and incubate them at 37℃ overnight, then we extracted the plasmids.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1116
Illegal BglII site found at 1920
Illegal BamHI site found at 1811 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 595
Illegal NgoMIV site found at 1106 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1072
Illegal SapI.rc site found at 1101