Difference between revisions of "Part:BBa I739021"
Stefan Luzi (Talk | contribs) (→Purpose) |
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===Part Structure=== | ===Part Structure=== | ||
− | <p>The Biobrick encodes [https://parts.igem.org/wiki/index.php/Help:Tag LVA]-tagged P22 cII ([https://parts.igem.org/wiki/index.php/Part:BBa_C0053 BBa_C0053]) and [https://parts.igem.org/wiki/index.php/Help:Tag LVA]-tagged EYFP ([https://parts.igem.org/wiki/index.php/Part:BBa_E0032 BBa_E0032]) under control of the double promoter [https://parts.igem.org/wiki/index.php/Part:BBa_I739101 BBa_I739101] | + | <p>The Biobrick encodes [https://parts.igem.org/wiki/index.php/Help:Tag LVA]-tagged P22 cII ([https://parts.igem.org/wiki/index.php/Part:BBa_C0053 BBa_C0053]) and [https://parts.igem.org/wiki/index.php/Help:Tag LVA]-tagged EYFP ([https://parts.igem.org/wiki/index.php/Part:BBa_E0032 BBa_E0032]) under control of the double promoter [https://parts.igem.org/wiki/index.php/Part:BBa_I739101 BBa_I739101]. The ribosome binding sites [https://parts.igem.org/wiki/index.php/Part:BBa_B0034 BBa_B0034] are located upstream of each coding region. The transcription of P22 cII and EYFP is terminated by the double terminator [https://parts.igem.org/wiki/index.php/Part:BBa_B0015 BBa_B0015].</p> |
===Mode of Action=== | ===Mode of Action=== | ||
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===Purpose=== | ===Purpose=== | ||
− | <p>This Biobrick was designed for the [http:// | + | <p>This Biobrick was designed for the [http://2007.igem.org/ETHZ ETHZ iGEM 2007 project] and is a composite biobrick including a first generation double promoter. The goal is to show the applicability of such kind of double promoters. In the project description, this part is a composite of the [https://parts.igem.org/wiki/index.php/Part:BBa_I739014 ''PoC intermediate''] and [https://parts.igem.org/wiki/index.php/Part:BBa_I739005 ''Part 5''] and is cloned into plasmid [https://parts.igem.org/wiki/index.php/Part:BBa_I739202 pCK01BB1].</p> |
===Testing=== | ===Testing=== |
Latest revision as of 10:16, 23 October 2007
Single regulated polycistronic P22 cII +LVA / EYFP +LVA expression cassette
Part Structure
The Biobrick encodes LVA-tagged P22 cII (BBa_C0053) and LVA-tagged EYFP (BBa_E0032) under control of the double promoter BBa_I739101. The ribosome binding sites BBa_B0034 are located upstream of each coding region. The transcription of P22 cII and EYFP is terminated by the double terminator BBa_B0015.
Mode of Action
P22 cII and EYFP production can be repressed by TetR. If the inducer [http://openwetware.org/wiki/ATc anhydrotetracycline (ATc)] is added, TetR action is inhibited and the promoter gets derepressed.
Purpose
This Biobrick was designed for the [http://2007.igem.org/ETHZ ETHZ iGEM 2007 project] and is a composite biobrick including a first generation double promoter. The goal is to show the applicability of such kind of double promoters. In the project description, this part is a composite of the PoC intermediate and Part 5 and is cloned into plasmid pCK01BB1.
Testing
Checked for uniqueness of restriction enzyme cleavage sites:
Eco: ok
Xba: ok
Spe: ok
Pst: ok
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 275