Difference between revisions of "Part:BBa K1323012"
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<h3>Characterization</h3> | <h3>Characterization</h3> | ||
− | <p><a href="https://2021.igem.org/Team:Toulouse_INSA-UPS">Toulouse_INSA_UPS_2021</a>contributed to the characterization of this part. The <i> | + | <p><a href="https://2021.igem.org/Team:Toulouse_INSA-UPS">Toulouse_INSA_UPS_2021</a>contributed to the characterization of this part. The <i>neoR</i> gene had not been characterized before, but the team showed this year that it is functional for a transformant selection in <i>S. elongatus</i> cyanobacteria. Check the part of the full construction <a href="https://parts.igem.org/Part:BBa_K3930002" class="pr-0" target="_blank">(BBa_K3930002)</a> for more result details.</p> |
<p>Author = ThomasG </p> | <p>Author = ThomasG </p> | ||
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Revision as of 17:03, 17 October 2021
Spc - Spectinomycin Resistance Gene Coding Sequence
This coding sequence is for the antibiotic spectinomycin. The sequence of this gene is obtained from pSPC vector developed by Dr. Jeffery Bose (KUMC) and Dr. Kenneth Bayles (NUMC) (Bose et al., 2013). The 618 bp of the CDS was changed from T to A to eliminate illegal pst1 site. The working concentration of spectinomycin of 1000 µg/mL in S.aureus/S.epidermidis hosts (Bose et al., 2013).
Characterization
Toulouse_INSA_UPS_2021contributed to the characterization of this part. The neoR gene had not been characterized before, but the team showed this year that it is functional for a transformant selection in S. elongatus cyanobacteria. Check the part of the full construction (BBa_K3930002) for more result details.
Author = ThomasG
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 488
References
Bose, J. L., Fey, P. D., and Bayles, K. W. (2013). Genetic Tools to Enhance the Study of Gene Function and Regulation in Staphylococcus aureus. Applied and Environmental Microbiology. 79 (7): 2218-2224.