Difference between revisions of "Team:Chalmers-Gothenburg/BioBricks"
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<h2>1. [http://parts.igem.org/Part:BBa_K1603000 BBa_K1603000]: STE2MAM2</h2> | <h2>1. [http://parts.igem.org/Part:BBa_K1603000 BBa_K1603000]: STE2MAM2</h2> | ||
− | <p>Fusion | + | <p>Fusion GPCR of the non-cytoplasmic N-terminal signal peptide from <i>STE2</i> (<i>Saccharomyces cerevisiae</i>) and Pheromone P-factor receptor <i>MAM2</i> (<i>Schizosaccharomyces pombe</i>) without its signaling peptide. Allows in vivo detection of the Pheromone P-factor from <i>S.pombe</i> through the Pheromone pathway in </i>S.cerevisiae</i>.</p> |
<h2>2. [http://parts.igem.org/Part:BBa_K1603001 BBa_K1603001]: pTEF1-pSUC2</h2> | <h2>2. [http://parts.igem.org/Part:BBa_K1603001 BBa_K1603001]: pTEF1-pSUC2</h2> | ||
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<h2>4. [http://parts.igem.org/Part:BBa_K1603003 BBa_K1603003]: RecA</h2> | <h2>4. [http://parts.igem.org/Part:BBa_K1603003 BBa_K1603003]: RecA</h2> | ||
− | <p>Recombinase A from Deinococcus | + | <p>Recombinase A from <i>Deinococcus radiodurans</i>. Used in DNA-repair mechanisms. |
− | Codon optimized for | + | Codon optimized for <i>Saccharomyces cerevisiae</i> and fused with a nuclear localization signal (NLS) for in vivo DNA repair. Also fused with a His-tag, allowing nickel based purification prior in vitro DNA repair.</p> |
<h2>5. [http://parts.igem.org/Part:BBa_K1603004 BBa_K1603004]: SSB</h2> | <h2>5. [http://parts.igem.org/Part:BBa_K1603004 BBa_K1603004]: SSB</h2> | ||
− | <p>Single strand binding protein from Deinococcus | + | <p>Single strand binding protein from <i>Deinococcus radiodurans</i>. Codon optimized for <i>Saccharomyces cerevisiae</i> and fused with a nuclear localization signal (NLS) for in vivo DNA repair. Also fused with a His-tag, allowing nickel based purification prior in vitro DNA repair.</p> |
Revision as of 20:09, 18 September 2015
Contents
- 1 BioBricks
- 1.1 1. [http://parts.igem.org/Part:BBa_K1603000 BBa_K1603000]: STE2MAM2
- 1.2 2. [http://parts.igem.org/Part:BBa_K1603001 BBa_K1603001]: pTEF1-pSUC2
- 1.3 3. [http://parts.igem.org/Part:BBa_K1603002 BBa_K1603002]: pTPI1
- 1.4 4. [http://parts.igem.org/Part:BBa_K1603003 BBa_K1603003]: RecA
- 1.5 5. [http://parts.igem.org/Part:BBa_K1603004 BBa_K1603004]: SSB
BioBricks
1. [http://parts.igem.org/Part:BBa_K1603000 BBa_K1603000]: STE2MAM2
Fusion GPCR of the non-cytoplasmic N-terminal signal peptide from STE2 (Saccharomyces cerevisiae) and Pheromone P-factor receptor MAM2 (Schizosaccharomyces pombe) without its signaling peptide. Allows in vivo detection of the Pheromone P-factor from S.pombe through the Pheromone pathway in </i>S.cerevisiae</i>.
2. [http://parts.igem.org/Part:BBa_K1603001 BBa_K1603001]: pTEF1-pSUC2
The high expression pTEF1 promoter connected to pSUC2 promoter. Allows induced high expression of downstream gene at low ATP levels.
3. [http://parts.igem.org/Part:BBa_K1603002 BBa_K1603002]: pTPI1
Promoter to TPI1.
4. [http://parts.igem.org/Part:BBa_K1603003 BBa_K1603003]: RecA
Recombinase A from Deinococcus radiodurans. Used in DNA-repair mechanisms. Codon optimized for Saccharomyces cerevisiae and fused with a nuclear localization signal (NLS) for in vivo DNA repair. Also fused with a His-tag, allowing nickel based purification prior in vitro DNA repair.
5. [http://parts.igem.org/Part:BBa_K1603004 BBa_K1603004]: SSB
Single strand binding protein from Deinococcus radiodurans. Codon optimized for Saccharomyces cerevisiae and fused with a nuclear localization signal (NLS) for in vivo DNA repair. Also fused with a His-tag, allowing nickel based purification prior in vitro DNA repair.