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Week 9: Monday 6th September - Sunday 12th September



86. Expt: Extract CDABEG from pJS555

  • Using 2 primers
    • prefix start of O
    • suffix end of G
  • Hope that it will glow in its own right without luxR+I
  • Need to put under a new promoter

87. Expt: Gibson transformation (cont. from p.70)

3 colonies on one plate were not pink. These were streaked out on new Chl plated and put into liquid cultures along with 2 of the red colonies.

Next check for the right sized fragment with colony PCR and try to induce with arabinose.

88. Expt: Plate Reader G28

Well Arabinose conc.
A1 0 x1,9
A2 1µM
A3 5µM
A4 10µM
A5 100µM
A6 Blank
A7 pSB1C3
A8 Blank x8,16

Reads every 10 mins

89. Expt: Extracting YFP, CFP, Luc tetR, G28 via miniprep (Paul)

Nanodrop readings (ng/µl)
YFP 33.3, 55.4
CFP 17.9 20.4
Luc tetR 33.7
G28 125.3 96.9
G28? 17.9

90. Expt: Colony PCR to extract the thioesterase gene from E. coli K12 (Paul)

We used TOP10 cells, a substrain of DH10B, which is a substrain of K12.

We did a colony PCR to isolate the gene:

3 replicates with: 1 negative control:
2x Phusion Mastermix 10µl 10µl
Template DNA 1µl 0
Primer 1 1µl 1µl
Primer 2 1µl 1µl
Nuclease-free H20 7µl 8µl

The negative control was to check for primer/dimer and contamination.

PCR protocol:

  • Initial denaturation: 5min @ 98°C
  • Touchdown: 16 cycles
    • Denaturation: 10s @ 98°C
    • Annealing: 20s @ 65°C to 57°C
    • Elongation: 15s @ 72°C