Team:Goettingen/week10-3

V07_02

• Experiment:
  We aim to apply directed evolution to reprogram the bacterial chemoreceptor TAR in order to enable the perception of novel substances. A saturated mutagenesis PCR was performed to mutate five individual amino acid residues in the ligand binding site of TAR. The primers that are utilized are the following:
  
  TARR6973Fw:
  gcgcaGGAAAGGTCTCACTGAGTnnNTCAGCGGTAnnNATGATGATGGATTCCTCCAATCAACAAAG
  TARR6973Rv:
  gcgcaGAGTAGGTCTCATCAGGTTAATGCGCGTTTGCAG
  TARY149F150T154Fw:
  gcgcaGGAAAGGTCTCAGGAGCTnnNnnNGCTCAGCCAnnNCAGGGAATGCAAAATGCAATGGGCGAAG
  TARY149F150T154Rv:
  gcgcaGAGTAGGTCTCACTCCAGTATTGCCATAATCTAGGTAATC
  
  We firstly did a test PCR with both primer pairs to verify the mutagenesis PCR protocol and conditions. As a template we use the vector pSB1C3_TAR_QC_18C isolated from E. coli DH10B since this promoter is the strongest among the promoter constructs we use. After the amplification we have multiple linear vectors that contain every possible mutation.

• Observations & Results:
  According to the agarose gel the PCR worked well. A band of the expected size of 3769 bp was observed for both reactions.

V07_03

• Experiment:
  The saturated mutagenesis PCR was set up in a 50 µL batch according to the established protocol V07_02). The following experiments are performed as "attempt a" 1^st and 2^nd round. Beginning V08_20 "attempt b" was carried out to increase mutant diversity!

• Observations & Results:
  The corresponding gel showed bands of the expected size.

V07_04

• Experiment:
  The clean-up was performed using peqGOLD Cycle-Pure Kit (PeqLab) following the user manual. We modified the protocol by using columns from the peqGOLD Plasmid Miniprep Kit I (PeqLab) because these can bind a higher amount of DNA (30 µg/column). Thus, we lose fewer DNA material in the cleaning steps. 50 µL of elution buffer was used.

• Observations & Results:
  The corresponding gel showed a band of the expected size.

• Experiment:
  The digestion was performed with a total volume of 50 µL according to protocol.

• Experiment:
  The clean-up was performed using peqGOLD Cycle-Pure Kit (PeqLab) modified by using columns from the peqGOLD Plasmid Miniprep Kit I (PeqLab) with an EB volume of 50 µL.

• Observations & Results:
  The corresponding gel showed a band of the expected size.

• Experiment:
  The ligation was set up in a 100 µL batch according to protocol. Incubation over night at 16 °C.

V07_05

• Experiment:
  The ethanol precipitation was performed according to protocol.

• Observations & Results:
  Unfortunately we used the wrong amount of ethanol, so that the subsequent transformation did not work successfully!

• Experiment:
  Electrocompetent cells were prepared according to protocol. We transformed 200 µL of cells with 10 µL of DNA. A detailed protocol for the electroporation can be found here. The transformed cells were transferred to 100 mL liquid LB medium + CM and incubated over night at 37 °C, 180 rpm. We prepared three dilution plates LB+CM (10⁴, 10⁵, 10⁶) for counting colonies to verify whether the desired library diversity is reached. Plates were incubated over night at 37 °C aswell.

• Observations & Results:
  Continuous bug see V07_05_1!

V07_06

• Experiment:
  Plates and liquid culture were checked for successful transformation.

• Observations & Results:
  No bacterial growth on neither plates nor in liquid culture. Continuous bug see V07_05_1!

• Experiment:
  The PCR V07_03 was set up again + 1 backup. The clean-up was performed with the peqGOLD Cycle-Pure Kit (PeqLab). Elution in 50 µL EB.

• Observations & Results:
  The corresponding gel showed bands of the expected size.