Mutagenesis of protein A

Paweł

Results of sequencing: unfortunately all sequences were wild-type.

Preparation of vectors for Biobricks

Michał K.

1. Isolation of pSB2K3 and BBa_I739204 (pACYC177 converted into BioBrick vector) plasmids.
2. Digest of isolated plasmids with EcoRI and BcuI (BamHI buffer) Fig. 1.

1. Digest of pACYC177+OmpA_omega_deltaA_alpha with BamHI and PstI (BamHI buffer) Fig. 2.
2. Dephosphorylation (CIAP) of plasmids.
3. Gel elctrophoresis and gel-out of proper band: ??????.
4. Digest of omega_link fragment (PCR from previous day) with EcoRI and BcuI (BamHI buffer)
5. Digest of OmpA_omega with BglII and PstI (Orange buffer).
6. Clean-up of above digest reactions.
7. Overnight digest of purified pLac_OmpA_omega fragment (from previous day) with EcoRI (EcoRI buffer). DNA ends blunting with Klenow fragment.

Piotr

1. E. coli TOP10 transformation with overnight ligations pSB1A3 + Z(BBa_K103004) and pSB1A3 + OmpA_link).
2. Plating on LB + ampicillin.
3. Inoculation of bacteria received from iGEM HQs, carrying pSB2K3 and BBa_I739204 (pACYC177 converted into BioBrick vector) plasmids.