Team:Paris Saclay/Notebook/August/19

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Contents

Tuesday 19th August

Lab work

B and D

Electrophoresis with the PpsI plasmide (obtain on thursday) + the chromoprotein PCR: we obtain results as expected

  1. ladder 10µl
  2. pPSI 1.2µl
  3. pPSI 1.2µl
  4. pPSI 1.2µl
  5. pPSI 1.2µl
  6. pPSI 1.2µl
  7. p cola 1.2µl
  8. PCR chromoprotein 2µl

Paris Saclay 140819.jpg

D - Lemon Scent

Digestion of PCR results

by Sean, Hoang Vu, Eugene

components volumes
PCR purified LS 15 μl
FastDigest green buffer 10X 2 μl
PacI 1 µl
H2O 2 µl
components volumes
PCR purified GS 15 μl
FastDigest green buffer 10X 2 μl
PacI 1 µl
H2O 2 µl
components volumes
PCR purified PS 15 μl
FastDigest green buffer 10X 2 μl
PacI 1 µl
H2O 2 µl
components volumes
Purified pPS1 30 μl
FastDigest green buffer 10X 4 μl
PacI 2 µl
H2O 4 µl

Purification of PCR products of limonen synthase

by Laetitia

We used the PCR products of limonen synthase prepared previously : August 18th

The five samples were pooled in one and then purified using this protocol : protocol

Bacterial transformation

by Laetitia

We used DH5alpha competent bacteria (prepared the 14/08) and they were transformed using the ligation product prepared previously August 18th using this protocol : protocol

We transformed 100µL of competent bacteria and we added the totality of the ligation product (pGEMTeasy containing LS or PS or GS)

Preparation of petri dishes

by Terry

10 dishes with:
Antibiotic Concentration
XGal 80μg/ml
IPTG 2*10-3
Ampicillin 10-3
4 dishes with:
Antibiotic Concentration
Ampicillin 4*10-4

Bacterial culture

by Laetitia

After the bacterial transformation, we spread for each strain (LS or PS or GS):

dish type 100µl 200µl concentrate control
Ampicillin X
Ampicillin+IPTG+XGal X X X X

We leave the dishes overnight at 37°C.

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