Team:Heidelberg/Notebook/Sensing Group/Notebook/4thweek

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Contents

Monday, 08/25/2008

  • sequentiell and simultaneous digestion of pDk48 NcoI/NdeI and NcoI/KpnI

--> not successful

  • preparation of O/N culture of pDK48 transformed cells

Tuesday, 08/26/2008

Cloning

Digestion of pDK48 with xbaI and PstI yield expected results
  • digestion of pDK48 with XbaI and PstI to check wether the vector is the right one
  • digestion of Fusion-1 (from 08/21/2008) with NcoI/NdeI, with subsequent gelextraction
  • Ligation of Fusion-1 and pDk48 and transformation into DH5a competent cells

LuxS Test

Material: 500 mM IPTG-stock (A), 10 mM IPTG-stock (B)

  1. negative control: just 1 ml cell suspension
  2. 10 µM IPTG induced (1 µl stock B + 999 µl cell suspension)
  3. 20 µM IPTG induced (2 µl stock B + 998 µl cell suspension)
  4. 50 µM IPTG induced (5 µl stock B + 995 µl cell suspension)
  5. 100 µM IPTG induced (10 µl stock B + 990 µl cell suspension)
  6. 500 µM IPTG induced (1 µl stock A + 999 µl cell suspension)
  7. 1 mM IPTG induced (2 µl stock A + 998 µl celll suspension)

Measurement was done like described in the Materials & Methods section

Wednesday, 08/27/2008

  • PCR of LuxQ from V. harveyi with Phusion Mastermix

PCR cycle: 98 °C, 5 min |98 °C, 10 sec --- 50 °C, 30 sec --- 72 °C, 1 min|30x --- 72 °C, 5 min --- 4 °C, forever --> NO PCR product

  • preparation of pTrc99a and pDK48 O/N cultures for Maxipreps

Thursday, 08/28/2008

Friday, 08/29/2008

Go to 5th week