Team:Warsaw/Calendar-Main/23 September 2008

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<h3>MutD<sub>5</sub> testing</h3>
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<h4>Piotr</h4>
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<p>Inoculation MutD<sub>5</sub> carrying: <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-Z-alpha>pACYC177+OmpA_Z_alpha</a>, <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-Z-omega>pACYC177+OmpA_Z_omega</a>, <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-A-omega>pACYC177+OmpA_A_omega</a> and <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-omega-deltaA>pACYC177+OmpA_omega_&Delta;A</a> to liquid LB + 0.25mM IPTG + kanamycin + 50 μl/ml + prey:<ul><li>Z_alpha for <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-Z-omega>pACYC177+OmpA_Z_omega</a></li><li> Z_omega for <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-Z-alpha>pACYC177+OmpA_Z_alpha</a> </li><li> A_apha for <a hrefhttps://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-A-omega>pACYC177+OmpA_A_omega</a></li><li>A_alpha for <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-omega-deltaA>pACYC177+OmpA_omega_&Delta;A</a></li></ul>
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<h3>Mutagenesis of protein A</h3><h4>Paweł</h4>
<h3>Mutagenesis of protein A</h3><h4>Paweł</h4>
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<li>T4 ligase inactivated by incubation at 55&deg;C for 20 min, then 5U of DpnI added and incubated at 37&deg;C for 3 hours.</li> <li>After DpnI treatment mutagenesis products transformed into <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#top10">TOP10</a> and plated on LB + kanamycin plates.</li></ol></p>
<li>T4 ligase inactivated by incubation at 55&deg;C for 20 min, then 5U of DpnI added and incubated at 37&deg;C for 3 hours.</li> <li>After DpnI treatment mutagenesis products transformed into <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#top10">TOP10</a> and plated on LB + kanamycin plates.</li></ol></p>
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<h3>Preparation of BioBricks</h3>
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<h3>Preparation of <a href=http://partsregistry.org/wiki/index.php?title=Part:BBa_K103003>&Delta;A (BBa_K103003)</a></h3>
<h4>Michał K.</h4>
<h4>Michał K.</h4>
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<li><a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation>Isolation</a> of plasmids from cultures inoculated on previous day.</li>
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<ol><li><a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation>Isolation</a> of plasmid from culture inoculated on previous day.</li>
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<li>Control <a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest>digest</a> of isolated plasmids with EcoRI and PstI (Orange buffer). No proper colonies found.</li>
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<li>Control <a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest>digest</a> of isolated plasmid with EcoRI and PstI (Orange buffer). No visible band on 250 bp. <a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/23_September_2008#fig1">Fig. 1</a>.</li>
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<li> Repettition of <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#ligation">ligation</a> of isolated DNA fragments of <a href=http://partsregistry.org/wiki/index.php?title=Part:pSB1A3>pSB1A3</a> and <a href=http://partsregistry.org/wiki/index.php?title=Part:BBa_K103003>&Delta;A</a> - overnight. </li>
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<a name="fig1"><img src="https://static.igem.org/mediawiki/2008/f/f7/Traw_23_09.jpg" width=160/></a><var><b>Fig. 1.</b> Control EcoRI/PstIdigest of pSB1A3<br>
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1. Marker<br>
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2. digested pSB1A3<br></var>

Latest revision as of 18:14, 28 October 2008

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MutD5 testing

Piotr

Inoculation MutD5 carrying: pACYC177+OmpA_Z_alpha, pACYC177+OmpA_Z_omega, pACYC177+OmpA_A_omega and pACYC177+OmpA_omega_ΔA to liquid LB + 0.25mM IPTG + kanamycin + 50 μl/ml + prey:

Mutagenesis of protein A

Paweł

  1. PNK phosporylation of mutagenesis products for 30 min at 37°C.
  2. PNK heat-inactivated by incubation at 75°C for 15 min.
  3. T4 ligase added and incubated for 1 h at room temperature.
  4. T4 ligase inactivated by incubation at 55°C for 20 min, then 5U of DpnI added and incubated at 37°C for 3 hours.
  5. After DpnI treatment mutagenesis products transformed into TOP10 and plated on LB + kanamycin plates.

Preparation of ΔA (BBa_K103003)

Michał K.

  1. Isolation of plasmid from culture inoculated on previous day.
  2. Control digest of isolated plasmid with EcoRI and PstI (Orange buffer). No visible band on 250 bp. Fig. 1.
  3. Repettition of ligation of isolated DNA fragments of pSB1A3 and ΔA - overnight.

Fig. 1. Control EcoRI/PstIdigest of pSB1A3
1. Marker
2. digested pSB1A3


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