Team:Paris Saclay/Notebook/August/1

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(Friday 1st August)
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{{Team:Paris_Saclay/notebook_header}}
=Friday 1st August=
=Friday 1st August=
==Lab work==
==Lab work==
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===A - The frame coli Odor free===
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===The frame coli Odor free===
====Stria on LB dishes====
====Stria on LB dishes====
''by Romain''
''by Romain''
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Strains used: MG1655 and MG1655Z1, striated on 4 LB dishes per strain.
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Strains used: MG1655 and MG1655Z1, transformed the [https://2014.igem.org/Team:Paris_Saclay/Notebook/July/30 30th July], striated on 4 LB dishes per strain.
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===C - Salicylate Inducible Suppressing System===
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===Salicylate Inducible Suppressing System===
====Liquid Culture====
====Liquid Culture====
''by Fabio''
''by Fabio''
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8 liquid cultures with 3ml of LB and 3µl of amp (at 10am - 8°C), all from the colonies made the [https://2014.igem.org/Team:Paris_Saclay/Notebook/July/31#Bacterial_Culture 31st July]. The colonies will be put at 37°C on sunday 3rd in order to have grown colonies on monday.
8 liquid cultures with 3ml of LB and 3µl of amp (at 10am - 8°C), all from the colonies made the [https://2014.igem.org/Team:Paris_Saclay/Notebook/July/31#Bacterial_Culture 31st July]. The colonies will be put at 37°C on sunday 3rd in order to have grown colonies on monday.
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===D - Lemon scent===
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===Lemon scent===
====Results of the Transformation of electrocompetent cells====
====Results of the Transformation of electrocompetent cells====
''by Arnaud & Terry''
''by Arnaud & Terry''
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*Failure, nothing has grown on the dishes which contain DY330 with pJBE1
*Failure, nothing has grown on the dishes which contain DY330 with pJBE1
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====New Transformation of electrocompetent cells====
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''by Terry''
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Strain used: DY330. Plasmid used: pJBEI-6409 (code for enzymes to produce limonene from glucose in E. coli)
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Make 3 électroporations in cold electroporation cuvettes:
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*A control cuvette(without DNA): 50µl of DY330.
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*A second cuvette: 50µl of DY330 culture + 2µl of pJBEI-6409 plasmid.
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*A third cuvette: 50µl of DY330 culture + 0.5µl of pJBEI-6409 plasmid.
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Electroporation : 2500V, 132W, 40µF.
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After that, add 1ml of cold LB in each cuvette and transfer in tubes to incubate during 1 to 2h at 30°C.
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Spread on 7 dishes LB + Cm:
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*100µl of control (without plasmid)
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*50µl of transformed DY330 with 0.5µl of pJBEI-6409
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*100µl of transformed DY330 with 0.5µl of pJBEI-6409
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*The rest of transformed DY330 with 0.5µl pJBEI-6409
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*50µl of transformed DY330 with 2µl of pJBEI-6409
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*100µl of transformed DY330 with 2µl of pJBEI-6409
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*The rest of transformed DY330 with 2µl pJBEI-6409
 +
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Incubate for 2 days at 30°C.
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==Photo of the Day==
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[[File:Paris Saclay 1_august.jpg|600px|center]]
'''Members there''':
'''Members there''':
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* Students: Arnaud, Fabio, Romain, Sean and Terry.
* Students: Arnaud, Fabio, Romain, Sean and Terry.
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[https://2014.igem.org/Team:Paris_Saclay/Notebook Back to the calendar]
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{{Team:Paris_Saclay/notebook_footer}}

Latest revision as of 14:23, 14 October 2014

Contents

Friday 1st August

Lab work

The frame coli Odor free

Stria on LB dishes

by Romain

Strains used: MG1655 and MG1655Z1, transformed the 30th July, striated on 4 LB dishes per strain.

Salicylate Inducible Suppressing System

Liquid Culture

by Fabio

8 liquid cultures with 3ml of LB and 3µl of amp (at 10am - 8°C), all from the colonies made the 31st July. The colonies will be put at 37°C on sunday 3rd in order to have grown colonies on monday.

Lemon scent

Results of the Transformation of electrocompetent cells

by Arnaud & Terry

Transformation of electrocompetent cells made the July 29th. Strains used: DY330. Plasmid used: pJBEI-6409 (code for enzymes to produce limonene from glucose in E. coli)

Results:

  • Nothing has grown on the control dishes.
  • Failure, nothing has grown on the dishes which contain DY330 with pJBE1

New Transformation of electrocompetent cells

by Terry

Strain used: DY330. Plasmid used: pJBEI-6409 (code for enzymes to produce limonene from glucose in E. coli)

Make 3 électroporations in cold electroporation cuvettes:

  • A control cuvette(without DNA): 50µl of DY330.
  • A second cuvette: 50µl of DY330 culture + 2µl of pJBEI-6409 plasmid.
  • A third cuvette: 50µl of DY330 culture + 0.5µl of pJBEI-6409 plasmid.

Electroporation : 2500V, 132W, 40µF.

After that, add 1ml of cold LB in each cuvette and transfer in tubes to incubate during 1 to 2h at 30°C.

Spread on 7 dishes LB + Cm:

  • 100µl of control (without plasmid)
  • 50µl of transformed DY330 with 0.5µl of pJBEI-6409
  • 100µl of transformed DY330 with 0.5µl of pJBEI-6409
  • The rest of transformed DY330 with 0.5µl pJBEI-6409
  • 50µl of transformed DY330 with 2µl of pJBEI-6409
  • 100µl of transformed DY330 with 2µl of pJBEI-6409
  • The rest of transformed DY330 with 2µl pJBEI-6409

Incubate for 2 days at 30°C.


Photo of the Day

Paris Saclay 1 august.jpg

Members there:

  • Instructors and advisors: Alice, Solenne and Sylvie.
  • Students: Arnaud, Fabio, Romain, Sean and Terry.

Back to the calendar