Team:Evry/Notebook/CellCharacterization/Antibiotic test/08-16-2014

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(The last one was the control of the growth of our bacteria without antibiotics)
(The last one was the control of the growth of our bacteria without antibiotics)
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We sowed 10µL of a liquid LB culture of Bl21, and we let them incubate overnight at 37°C.
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We sowed 10µL of a liquid LB culture of Bl21, and we let them incubate overnight at 37°C.<br>
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<u>Survivability tests</u>
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<u>Survivability tests</u><br>
Two plates of MB 1X and M9 1X were made and divised in two parts.
Two plates of MB 1X and M9 1X were made and divised in two parts.
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Each plate was sowed with 5µL of a liquid MB 1X culture of Pseudovibrio denitrificans(dated 12th August) in a part and with 5µL of a liquid M9 1X culture Pseudovibrio denitrificans (dated 12th August) in the other part.
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Each plate was sowed with 5µL of a liquid MB 1X culture of Pseudovibrio denitrificans(dated 12th August) in a part and with 5µL of a liquid M9 1X culture Pseudovibrio denitrificans (dated 12th August) in the other part.<br>
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  <u>Pre-cultures</u>  
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  <u>Pre-cultures</u> <br>
Cultures in MB 1X and M9 1X of Pseudovibrio were passed by a 1/10 dilution and let incubate overnight at 30°C.
Cultures in MB 1X and M9 1X of Pseudovibrio were passed by a 1/10 dilution and let incubate overnight at 30°C.
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New cultures of different E.Coli were also started from glycerol or plate and let incubated overnight at 37°C.
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New cultures of different E.Coli were also started from glycerol or plate and let incubated overnight at 37°C.<br>
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<u>From glycerol stocks:</u>
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<u>From glycerol stocks:</u><br>
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<li>Bl21
<li>Bl21

Revision as of 17:33, 25 August 2014

Picture

Tests of antibiotics' stocks Six plates of LB agar were made. Five of them contained one of those antibiotics in the dilution 1:1000:

  • Chloramphénicol
  • Kanamycin
  • Erythromycin
  • Ampicilin
  • Tetracyclin
(The last one was the control of the growth of our bacteria without antibiotics) We sowed 10µL of a liquid LB culture of Bl21, and we let them incubate overnight at 37°C.
Survivability tests
Two plates of MB 1X and M9 1X were made and divised in two parts. Each plate was sowed with 5µL of a liquid MB 1X culture of Pseudovibrio denitrificans(dated 12th August) in a part and with 5µL of a liquid M9 1X culture Pseudovibrio denitrificans (dated 12th August) in the other part.
Pre-cultures
Cultures in MB 1X and M9 1X of Pseudovibrio were passed by a 1/10 dilution and let incubate overnight at 30°C. New cultures of different E.Coli were also started from glycerol or plate and let incubated overnight at 37°C.
From glycerol stocks:
  • Bl21
  • Top10
  • DH5a
From plates:
  • DH5a tranformed with pCB1C3
  • Top10 transformed with pQexp
  • DH5a pyr tranformed with pMK2
Bacteria tranformed with plasmid were cultivated with the corresponding antibiotic for the selection. For each medium we make a negative contrôle without bacteria.

Aug 16