Difference between revisions of "Team:UIUC Illinois/Composite Part"
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− | <h2> | + | <h2> Part Documentation</h2> |
+ | <hr /> | ||
− | < | + | <ul> |
− | < | + | <img src="https://static.igem.org/mediawiki/2015/thumb/0/00/UIUC_Illinois_PartB_Updated.png/797px-UIUC_Illinois_PartB_Updated.png"> |
− | + | <li>Part: K1681000</li> | |
− | </ | + | <li>Part Name: PL lac O-1 SCRIBE(kanR)ON</li> |
+ | <li>Part Type: n/a</li> | ||
+ | <li>Creator: UIUC_Illinois_2015</li> | ||
+ | <li>Short Description: IPTG-inducible kanamycin resistance SCRIBE cassette</li> | ||
+ | <li>Long Description: | ||
+ | SCRIBE(kanR)ON is a cassette coding for the RNA and proteins needed to restore kanamycin resistance by synthesizing multicopy single-stranded DNA (msDNA) for site-specific recombination. The part consists of the IPTG-inducible promoter PL lac O-1, a retron coding for an untranslated RNA molecule and the open reading frame for reverse transcriptase, a RBS, the open reading frame for beta recombinase, and a terminator. The reverse transcriptase uses the msDNA (msd) region of the RNA molecule as a template and the msd RNA (msr) region of the RNA molecule as a primer to synthesize the msDNA. The beta recombinase inserts the kanamycin resistance segment of the msDNA into the host’s genome during DNA replication as an Okazaki fragment.</li> | ||
− | < | + | <li>Design Considerations: |
− | + | This part was designed to be used as a positive control for testing SCRIBE cassettes with different promoters and/ or custom DNA segments for site-specific recombination.</li> | |
− | </ | + | </ul> |
− | < | + | <hr /> |
+ | <ul> | ||
+ | <img src="https://static.igem.org/mediawiki/2015/thumb/f/f3/UIUC_Illinois_PartA_Updated.png/800px-UIUC_Illinois_PartA_Updated.png"> | ||
+ | <li>Part: K1681001</li> | ||
+ | <li>Part Name: SCRIBE(BsaI)</li> | ||
+ | <li>Part Type: n/a</li> | ||
+ | <li>Creator: UIUC_Illinois_2015</li> | ||
+ | <li>Short Description: SCRIBE cassette with BsaI sites for Golden Gate assembly</li> | ||
+ | <li>Long Description: | ||
+ | SCRIBE(BsaI) is a SCRIBE cassette including two restriction sites of the Type-II restriction enzyme BsaI in the msd region of the retron. This part is compatible with Golden Gate assembly.</li> | ||
− | </ | + | <li>Design Considerations: |
+ | This part was designed as a modular assembly part for future users to add custom DNA segments into the msd region for site-specific recombination via Golden Gate assembly and to add promoters of their choice via Standard or 3A assembly. | ||
+ | See Bba_K1681000 for a more detailed description as to how such custom DNA segments would be inserted into the host’s genome.</li> | ||
+ | </ul> | ||
+ | <hr /> | ||
+ | |||
+ | <ul> | ||
+ | <img src="https://static.igem.org/mediawiki/2015/thumb/9/95/UIUC_Illinois_PartD_Updated.png/800px-UIUC_Illinois_PartD_Updated.png"> | ||
+ | <li>K1681002</li> | ||
+ | <li>Part Name: PL lac O-1 SCRIBE(BsaI)</li> | ||
+ | <li>Part Type: n/a</li> | ||
+ | <li>Creator: UIUC_Illinois_2015</li> | ||
+ | <li>Short Description: IPTG-inducible promoter and BsaI SCRIBE cassette</li> | ||
+ | <li>Long Description: | ||
+ | This part is the IPTG-inducible promoter PL lac O-1 immediately upstream of SCRIBE(BsaI), with no scar site in between.</li> | ||
+ | |||
+ | <li>Design Considerations: | ||
+ | This part was designed to be used as a positive control for testing SCRIBE cassettes with different promoters after using Golden Gate assembly to add custom DNA segments into the msd region for site-specific recombination. | ||
+ | See Bba_K1681000 for a more detailed description as to how such custom DNA segments would be inserted into the host’s genome.</li> | ||
+ | </ul> | ||
</html> | </html> |
Latest revision as of 03:31, 19 September 2015
Part Documentation
- Part: K1681000
- Part Name: PL lac O-1 SCRIBE(kanR)ON
- Part Type: n/a
- Creator: UIUC_Illinois_2015
- Short Description: IPTG-inducible kanamycin resistance SCRIBE cassette
- Long Description: SCRIBE(kanR)ON is a cassette coding for the RNA and proteins needed to restore kanamycin resistance by synthesizing multicopy single-stranded DNA (msDNA) for site-specific recombination. The part consists of the IPTG-inducible promoter PL lac O-1, a retron coding for an untranslated RNA molecule and the open reading frame for reverse transcriptase, a RBS, the open reading frame for beta recombinase, and a terminator. The reverse transcriptase uses the msDNA (msd) region of the RNA molecule as a template and the msd RNA (msr) region of the RNA molecule as a primer to synthesize the msDNA. The beta recombinase inserts the kanamycin resistance segment of the msDNA into the host’s genome during DNA replication as an Okazaki fragment.
- Design Considerations: This part was designed to be used as a positive control for testing SCRIBE cassettes with different promoters and/ or custom DNA segments for site-specific recombination.
- Part: K1681001
- Part Name: SCRIBE(BsaI)
- Part Type: n/a
- Creator: UIUC_Illinois_2015
- Short Description: SCRIBE cassette with BsaI sites for Golden Gate assembly
- Long Description: SCRIBE(BsaI) is a SCRIBE cassette including two restriction sites of the Type-II restriction enzyme BsaI in the msd region of the retron. This part is compatible with Golden Gate assembly.
- Design Considerations: This part was designed as a modular assembly part for future users to add custom DNA segments into the msd region for site-specific recombination via Golden Gate assembly and to add promoters of their choice via Standard or 3A assembly. See Bba_K1681000 for a more detailed description as to how such custom DNA segments would be inserted into the host’s genome.
- K1681002
- Part Name: PL lac O-1 SCRIBE(BsaI)
- Part Type: n/a
- Creator: UIUC_Illinois_2015
- Short Description: IPTG-inducible promoter and BsaI SCRIBE cassette
- Long Description: This part is the IPTG-inducible promoter PL lac O-1 immediately upstream of SCRIBE(BsaI), with no scar site in between.
- Design Considerations: This part was designed to be used as a positive control for testing SCRIBE cassettes with different promoters after using Golden Gate assembly to add custom DNA segments into the msd region for site-specific recombination. See Bba_K1681000 for a more detailed description as to how such custom DNA segments would be inserted into the host’s genome.