Team:Warsaw/Calendar-Main/10 July 2008

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<h3>Preparation of constructs with OmpA protein fusions</h3>
<h3>Preparation of constructs with OmpA protein fusions</h3>
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<h4> Michał K.</h4><p><ol>
<li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation">Isolation of plasmids</a> from cultures inocluated on previous day. </li>
<li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation">Isolation of plasmids</a> from cultures inocluated on previous day. </li>
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<li> Control <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#digest">digest</a> of isolated plasmids with BamHI and NotI (we confirmed pCACYC177 + OmpA_omega). We didn't obtain pCACYC177 + OmpA_alpha probably because of a mistake in plating. </li>
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<li> Control <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#digest">digest</a> of isolated plasmids with BamHI and NotI (BamHI buffer) - we confirmed pCACYC177 + OmpA_omega. We didn't obtain pCACYC177 + OmpA_alpha probably because of a mistake in plating. </li>
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<li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#ligation">Ligation</a> of pACYC177 and OmpA_alpha (1 hr)</li>
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<li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#ligation">Ligation</a> of pACYC177 and OmpA_alpha (1 hr).</li>
<li> Transformation of <i>E. coli</i> <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#top10">TOP10</a> strain with ligation products: pACYC177 and OmpA_alpha.</li>
<li> Transformation of <i>E. coli</i> <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#top10">TOP10</a> strain with ligation products: pACYC177 and OmpA_alpha.</li>
<li> Transformants plating on LB + kanamycin.</li>
<li> Transformants plating on LB + kanamycin.</li>
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<h3>Preparation of construct pKS with A protein<br>
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<h3>Preparation of construct pKS with A protein</h3>
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Michał L., Marcin:</h3>
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<h4>Michał L., Marcin:</h4>
<p><ol>
<p><ol>
<li> Inactivation of digestion enzymes and CIAP.</li>
<li> Inactivation of digestion enzymes and CIAP.</li>

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Preparation of constructs with OmpA protein fusions

Michał K.

  1. Isolation of plasmids from cultures inocluated on previous day.
  2. Control digest of isolated plasmids with BamHI and NotI (BamHI buffer) - we confirmed pCACYC177 + OmpA_omega. We didn't obtain pCACYC177 + OmpA_alpha probably because of a mistake in plating.
  3. Ligation of pACYC177 and OmpA_alpha (1 hr).
  4. Transformation of E. coli TOP10 strain with ligation products: pACYC177 and OmpA_alpha.
  5. Transformants plating on LB + kanamycin.

Preparation of construct pKS with A protein

Michał L., Marcin:

  1. Inactivation of digestion enzymes and CIAP.
  2. Ligation of digested PCR product and pKS 2h at room temperature.
  3. Transformation of E. coli TOP10 strain with 7 µl of ligation mix.
  4. Transformants plating on LB + ampicillin + X-gal + IPTG.