Team:Warsaw/Calendar-Main/22 September 2008

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<h3>MutD<sub>5</sub> testing</h3>
<h3>MutD<sub>5</sub> testing</h3>
<h4>Piotr</h4>
<h4>Piotr</h4>
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Inoculation MutD<sub>5</sub> carrying: OmpA_Z_alpha, OmpA_Z_omega, Omp_A_omega and OmpA_omega_A + induction using 0.25mM IPTG.
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<p>Inoculation MutD<sub>5</sub> carrying: OmpA_Z_alpha, OmpA_Z_omega, Omp_A_omega and OmpA_omega_A + induction using 0.25mM IPTG.</p>

Revision as of 13:43, 25 October 2008

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MutD5 testing

Piotr

Inoculation MutD5 carrying: OmpA_Z_alpha, OmpA_Z_omega, Omp_A_omega and OmpA_omega_A + induction using 0.25mM IPTG.

'Hunter and prey' system tests: Competition tests

Weronika

  1. Plasmid isolation from 19 September cultures.
  2. Digest with SacI and BamHI.
  3. Electrophoresis.

[photo of the gel is to be placed here]

Conclusion: cells with interracting protein survive competition!

Mutagenesis of protein A

Paweł

Mutagenesis of protein A was performed using 2 pairs of primers: ADelL+KpnI and ADelP (deletion of aminoacids involved in interaction with protein Z) and AMutL+KpnI and AMutP (changing of few aminoacids involved in interaction with protein Z).

Mutagenesis were performed on 3 vectors: pACYClac+ompA-A-omega, pACYClac+ompa-A-alpha and pACYClac+ ompa-alpha-A.

Each mutagenesis was performed using each primer at final concentration 0.1 μM, dNTPs at final concentration 0.25 μM and Walk (Pwo) polymerase (shipped by A&A Biotechnology), with 100 ng of DNA template.


PCR program (15 cycles):

94°C 5 min

94°C 30 s
55°C 30 s
72°C 10 min

72°C 8 min

4°C hold

Preparation of BioBricks

Michał K.

Inoculation of only one colony which grown from transformation (19 September) - RFP(??????)+deltaA plasmid into liquid LB + ampicillin.