Team:EPF-Lausanne/Notebook/Wet Lab

From 2009.igem.org

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===10.07.09===
===10.07.09===

Revision as of 14:11, 9 July 2009

Contents

Wet Lab

July

06.07.09

LOVTAP plasmid AND TrpR plasmid were transformed in competent E. Coli following received protocol, and grown overnight (see Lab book for more details).
One problem: we actually don't know TrpR plasmid resistance, so we tried with three resistances available in the lab: Amp., Kana. and Chl. LOVTAP is in a plasmid called pCal-n (see picture below):

pCal-n plasmid


Some comments on the plasmid:
-CBP is a small peptide with which we could purify LOVTAP protein
-Thrombin target is a nucleotidic sequence that can be recognized by thrombin a peptidase. This peptidase will cut CBP once LOVTAP is purified

07.07.09

We have to grow the 3 strains generously sent by Tom Beatty

The three strains are :

  • R.Palustris CEA001 (wild type) ; should be grown on LB medium only
  • R.Palustris BPHP1+ ; should be grown on LB with gentamycin (100 micrograms/ml)
  • E.Coli DH10B (pBPH/hmu0) ; should be grown on LB with gentamycin (20 micorgrams/ml)


The transformed LOVTAP and TrpR worked well (N.B. the plasmid of TrpR is pUC19 so the antibiotic resistance is Amp -> see below)


pUC19 plasmid


We did the glycerol stock, located in the -80 fridge, first floor of the iGEM compartement.

Then, a miniprep was done with both cultures. A LOVTAP plasmid aliquot was done, a TrpR plasmid aliquot was done, located in the -20 fridge, 2nd floor.

08.07.09

1. R. Palustris culture grew. A glycerol stock has been done. A pellet is on the fridge level 2, waiting for a miniprep.

2. iGEM parts have been transformed:

Parts&Characteristics
Part Resistance Well (Kit Plate)

BBa_B0010 (terminator)

A

13D (1)

BBa_R0010 (promoter LacI)

A

1D (1)

BBa_B0030 (RBS)

A

1H (1)

BBa_E0240 (RBS-GFP-TER)

A

12M (1)

BBa_I13507(RBS-mRFP-TER)

A

22O (1)

BBa_J13002(pTetR-RBS)

A

13B (1)

BBa_I6007 (inverter TetR)

A

1C (2)

09.07.09

1. Miniprep and isolations of the yesterdey transformed plasmids. (cf. 08.09.09 subpart) Concentrations of the plasmids: cf. lab notebook pp. 8-9

2. PCR of pCal-n to PCR up LOVTAP with the different primers designed the 06.09.09, the products are: - Prom_T7-RBS-CBP-LOVTAP - RBS-CBP-LOVTAP - CBP-LOVTAP - LOVTAP

3. A gel was runned to check PCR products

4. PCR products were digested and BBa_B0010 was digested, the digestion products were treated with phosphatase. Then, PCR products were purified. Finally, LOVTAP (PCR products) were ligated on BBa_B0010 (a plasmid containing a terminator).

Two more iGEM parts have been transformed:

Parts&Characteristics
Part Resistance Well (Kit Plate)

BBa_I6007

A

1C (2)

BBa_P1010 (death gene)

C

5E (1)

10.07.09

August