Difference between revisions of "Part:BBa K3930022"
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<h2>Introduction</h2> | <h2>Introduction</h2> | ||
− | <p>The | + | <p>The sequences to target the locus XII-4 (Chr XII:830227..831248) of <i>S. cerevisiae</i> genome come from the EasyClone-MarkerFree kit (Jessop-Fabre et al., 2016). |
− | This part is flanking the insert in 3' | + | This part is flanking the insert in 3' and must be used with the <a href="https://parts.igem.org/Part:BBa_K3930021" class="pr-0" target="_blank">(BBa_K3930021)</a> XII-4 up part in 5'.</p> |
<h2>Results</h2> | <h2>Results</h2> | ||
− | <h3>Integration of part (BBa_K3930003) into the yeast genome</h3> | + | <h3>Integration of part <a href="https://parts.igem.org/Part:BBa_K3930003" class="pr-0" target="_blank">(BBa_K3930003)</a> into the yeast genome at locus XII-4</h3> |
− | <p> The part (BBa_K3930003) was linearized and transformed into the <i>S.cerevisiae</i> LycoYeast strain according to the Takara yeast transformation protocol, with 5 µg of DNA. The insert is flanked by parts (BBa_K3930021) and (BBa_K3930022). Figure 1 shows the electrophoresis gel of colony PCR to verify integrants genotype.</p> | + | <p> The part <a href="https://parts.igem.org/Part:BBa_K3930003" class="pr-0" target="_blank">(BBa_K3930003)</a> was linearized and transformed into the <i>S. cerevisiae</i> LycoYeast strain according to the Takara yeast transformation protocol, with 5 µg of DNA. The insert is flanked by parts <a href="https://parts.igem.org/Part:BBa_K3930021" class="pr-0" target="_blank">(BBa_K3930021)</a> and (BBa_K3930022). Figure 1 shows the electrophoresis gel of colony PCR to verify integrants genotype (clone 2 is OK).</p> |
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<a href="https://2021.igem.org/wiki/images/a/a9/T--Toulouse_INSA-UPS--2021_fig23.violette.png" class="internal" title="Enlarge"></a> | <a href="https://2021.igem.org/wiki/images/a/a9/T--Toulouse_INSA-UPS--2021_fig23.violette.png" class="internal" title="Enlarge"></a> | ||
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− | <b>Figure 1: </b> <b> Integration of pVIOLETTE insert in the LycoYeast genome</b> | + | <b>Figure 1: </b> <b> Integration of pVIOLETTE insert in the LycoYeast genome at locus XII-4</b> |
− | <p>pVIOLETTE insert integration was | + | <p>pVIOLETTE insert integration at locus XII-4 was checked by PCR and the result was visualized on EtBr stained agarose electrophoresis gel. A theoretical gel is presented on the right (note that a different ladder is presented on the theoretical gel).</p> |
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</div> | </div> | ||
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</div> | </div> | ||
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− | <p><b>The | + | <p><b>The sequence XII-4 down (BBa_K3930022) coupled with the XII-4 up part <a href="https://parts.igem.org/Part:BBa_K3930021" class="pr-0" target="_blank">(BBa_K3930021)</a> is functional to target integration at the XII-4 locus under these experimental conditions.</b><p> |
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<h2>References</h2> | <h2>References</h2> |
Latest revision as of 21:19, 16 October 2021
Down Integrative sequence to target locus XII-4 of Saccharomyces cerevisiae genome
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Introduction
The sequences to target the locus XII-4 (Chr XII:830227..831248) of S. cerevisiae genome come from the EasyClone-MarkerFree kit (Jessop-Fabre et al., 2016). This part is flanking the insert in 3' and must be used with the (BBa_K3930021) XII-4 up part in 5'.
Results
Integration of part (BBa_K3930003) into the yeast genome at locus XII-4
The part (BBa_K3930003) was linearized and transformed into the S. cerevisiae LycoYeast strain according to the Takara yeast transformation protocol, with 5 µg of DNA. The insert is flanked by parts (BBa_K3930021) and (BBa_K3930022). Figure 1 shows the electrophoresis gel of colony PCR to verify integrants genotype (clone 2 is OK).
The sequence XII-4 down (BBa_K3930022) coupled with the XII-4 up part (BBa_K3930021) is functional to target integration at the XII-4 locus under these experimental conditions.
References
- Chen X, Shukal S, Zhang C. 2019. Integrating Enzyme and Metabolic Engineering Tools for Enhanced α-Ionone Production. J Agric Food Chem. 67(49):13451–13459. doi:10.1021/acs.jafc.9b00860.