Difference between revisions of "Part:BBa I742151"
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Firstly, we obtained the target gene expression frames (GAP promotor-gene-CYC terminator) by PCR amplification, and agarose gel electrophoresis results showed that we succeeded in obtaining these fragments. Next, we double-digested the target fragment and the vector (containing the <i>S. cerevisiae</i> X-2 integration site genes) and obtained the plasmid by enzymatic ligation. Finally, we transformed the enzyme-ligation product into <i>E. coli</i> DH5α competent cells, and the colony PCR and sequencing results showed that we successfully constructed the plasmid (Figure 2). | Firstly, we obtained the target gene expression frames (GAP promotor-gene-CYC terminator) by PCR amplification, and agarose gel electrophoresis results showed that we succeeded in obtaining these fragments. Next, we double-digested the target fragment and the vector (containing the <i>S. cerevisiae</i> X-2 integration site genes) and obtained the plasmid by enzymatic ligation. Finally, we transformed the enzyme-ligation product into <i>E. coli</i> DH5α competent cells, and the colony PCR and sequencing results showed that we successfully constructed the plasmid (Figure 2). | ||
Revision as of 15:02, 1 October 2024
crtE (geranylgeranyl pyrophosphate synthase) coding sequence.
crtE (geranylgeranyl pyrophosphate synthase) from Pantoea ananatis (formerly Erwinia uredovora) DSMZ 30080 (ATCC 19321). Accession: D90087. Part of the carotenoid biosynthesis parthway.
Usage and Biology
Team Fudan 2022 used BBa I742151 in retinoid biosynthesis by E. coli.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 715
- 1000COMPATIBLE WITH RFC[1000]
Contribution by Team 2024 Foshan-GreatBay
To increase the yield of β-carotene in yeast cells, we constructed a new composite part BBa_K5419000 (pX-2-PaCrtE) with crtE (BBa_I742151) gene fragment. This composited part was used together with other composite parts, BBa_K5419005 (pXII-5-BtCrtI), and BBa_K5419009 (pXI-2-XdCrtYB), for the construction of yeast strains with high β-carotene production.
Construction Design
We constructed the plasmid by placing the gene under the regulation of a strong constitutive GAP promoter and a CYC terminator, respectively. Integration sequence was added upstream and downstream of the expression cassette to integrate the target gene into the genome of S. cerevisiae using the CRISPR/Cas9 system (Figure 1).
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Experimental Approach
Construction of integration plasmids
Firstly, we obtained the target gene expression frames (GAP promotor-gene-CYC terminator) by PCR amplification, and agarose gel electrophoresis results showed that we succeeded in obtaining these fragments. Next, we double-digested the target fragment and the vector (containing the S. cerevisiae X-2 integration site genes) and obtained the plasmid by enzymatic ligation. Finally, we transformed the enzyme-ligation product into E. coli DH5α competent cells, and the colony PCR and sequencing results showed that we successfully constructed the plasmid (Figure 2).
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