Team:Cambridge/Lab book/Week 8

Monday (13/08/12)

Tuesday (14/08/12)

Gibson assembly of positive control

• Fragments used:

• Protocol changed slightly: 0.5 μl of each DNA fragment solution mixed in with master mix to make up 4 μl total volume (1μl DNA and 3μl master mix).

Transformation of e.coli with positive control DNA

• Chemically competent e.coli cells transformed with plasmid DNA produced by Gibson assembly step.

• Transformants plated out on 50 μg/ml kanomycin plates. Incubated overnight at 37 °C.

Wednesday (15/08/12)

PCR of positive control fragments

• Standard PCR settings used

Extraction of positive control DNA

• Positive control DNA from gel excised and purified.

• Additional elution steps used to concentrate resultant solution.

• Verified with nanodropper - final DNA concentrations:

Gibson assembly of positive control DNA

Transformation of positive control DNA into e.coli

• Chemically competent e.coli transformed with positive control Gibson products made previously.

• Transformants plated out onto 50 μg/ml kanomycin plates and incubated at 37 °C overnight.

Characterization of fluoride riboswitch construct

• Strain of bacillus lacking fluoride transporter system tested. Concentrations used:

• 0mM - 0.5mM - 1mM - 2.5mM - 5mM - 10mM - 20mM - 30mM

Thursday (16/08/12)

Characterization of fluoride riboswitch construct

The results of our fluoride assay.

• Eppindorfs containing the bacillus with the fluoride riboswitch removed from incubator and imaged.

• Now this definitely works, we will try quantifying this riboswitch with an ONPG assay and the plate reader.

PCR ran by paul - insert photos/discuss

• Only positive control and two sets of triplicates worked
• YFP and CFP extracted successfully

Friday (17/08/12)

• Team meet up today! No lab work was done.

Saturday (18/08/12)

PCR of Fluoride biobrick format

Gels from PCR of Fluoride BB and PJS130 fragments. Top: Lanes 2-4: Gibson compatable Fluoride biobrick fragment. Lanes 5-7: Ligation compatable Fluoride biobrick fragment. Lane 8: PJS130 fragment A. Bottom: Lanes 1-2: PJS130 fragment A. Lanes 3-5: PJS 130 fragment B. Lane 6: Positive control. Lane 7: Negative control.

• Two sets of primers used: one to allow insertion into backbone by ligation, and one to allow insertion by Gibson assembly.

• Cycle settings:

• Melting - 98 &degC - 10 seconds

• Annealing - 58 &degC - 30 seconds

• Elongation - 72 &degC - 100 seconds

• Products run on gel. Fragments produced of correct size, however they overlapped with the primer dimer band due to the small size of the fragments.

• DNA extracted and purified.

PCR of Mg2+ riboswitch construct vector

• Separate reactions for

• Cycle settings:

• Melting - 98 &degC - 10 seconds

• Annealing - 58 &degC - 30 seconds

• Elongation - 72 &degC - 100 seconds

• Productos