Team:Evry/Notebook/CellCharacterization/Antibiotic test
From 2014.igem.org
(Difference between revisions)
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</table> | </table> | ||
- | Any liquid culture can be plated and will grow up. Of course, it works better | + | Any liquid culture can be plated and will grow up. Of course, it works better on MB medium, wich is a rich medium than on M9. |
+ | |||
+ | <h6>08-18-2014</h6> | ||
+ | <h4> <u>Tests of antibiotics' stocks - Results(2)</u> </h4> | ||
+ | <table border="1"> | ||
+ | <tr > | ||
+ | <td> <b>Plates </b> </td> | ||
+ | <td>LB Agar only </td> | ||
+ | <td>LB+Kan </td> | ||
+ | <td>LB+Erm (1:100)</td> | ||
+ | </tr> | ||
+ | |||
+ | |||
+ | <tr> | ||
+ | <td> <b>E.coli</b> </td> | ||
+ | <td>X </td> | ||
+ | <td>0 </td> | ||
+ | <td>0 </td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | |||
+ | New stocks are ready for antibiotics' tests on Pseudovribrio | ||
+ | <h4> <u>Plates for antibiotics's tests</u> </h4> | ||
+ | For each tested antibiotic we made the following range of concentrations: | ||
+ | |||
+ | <table border="1"> | ||
+ | <tr > | ||
+ | <td> <b>0 </b> </td> | ||
+ | <td> <b>1:500 </b> </td> | ||
+ | <td> <b>1:1000 </b> </td> | ||
+ | <td> <b>1:50 000 </b> </td> | ||
+ | <td> <b>1:100 000 </b> </td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | We made these range two time to have a replicate and we added a controle plate without antibiotic on which we showed all our tested bacteria. | ||
+ | We made these same ranges of tested antibiotic's concentrations for three media: | ||
+ | <ul> | ||
+ | <li>MB agar 1X | ||
+ | <li>MB agar 0.5X | ||
+ | <li>M9 agar 1X | ||
+ | <ul> | ||
+ | |||
+ | Each plate is made like in the following table: | ||
+ | <table border="1"> | ||
+ | <tr > | ||
+ | <td> <b>/ </b> </td> | ||
+ | <td> <b>0 </b> </td> | ||
+ | <td> <b>1:500 </b> </td> | ||
+ | <td> <b>1:1000 </b> </td> | ||
+ | <td> <b>1:50 000 </b> </td> | ||
+ | <td> <b>1:100 000 </b> </td> | ||
+ | </tr> | ||
+ | |||
+ | <tr > | ||
+ | <td> <b>Medium+agar </b> </td> | ||
+ | <td>20mL </td> | ||
+ | <td>20mL </td> | ||
+ | <td>20mL </td> | ||
+ | <td>20mL </td> | ||
+ | <td>20mL </td> | ||
+ | </tr> | ||
+ | |||
+ | <tr > | ||
+ | <td> <b>Antibiotic </b> </td> | ||
+ | <td>0 </td> | ||
+ | <td>40µL of stock</td> | ||
+ | <td>20µL of stock</td> | ||
+ | <td>40µL of stock diluted 1/100</td> | ||
+ | <td>20µL of stock diluted 1/100</td> | ||
+ | </tr> | ||
+ | |||
+ | </table> | ||
+ | |||
+ | And plates are organised like shown in the following picture: | ||
+ | <img src="https://static.igem.org/mediawiki/2014/7/71/EVRYSch%C3%A9maplates.jpg" alt="GROSSE NAZE T'AS PAS REUSSI A METTRE L'IMAGE" /> | ||
+ | |||
+ | |||
+ | |||
</p> | </p> | ||
<span class="cd-date"></span> | <span class="cd-date"></span> |
Revision as of 10:37, 25 August 2014
Preparation of antibiotic stocks
Antibiotic | Stock concentration | Protocol |
Kanamycin | 25 mg/mL | Weight 0.56g of Kanamycin powder, solubilization into 20mL of miliQ water. Vortex 5min and filtration with a 200nm filter. Stock : -20°C (aliquots of 1mL) |
Streptomycin | 100 mg/mL | Weight 1g of Streptomycin powder, solubilization into 20mL of miliQ water. Vortex 5min and filtration with a 200nm filter. Stock : -20°C (aliquots of 1mL) |
Amplicilin | 50 mg/mL | Weight 1g of Amplicilin powder, solubilization into 40mL of miliQ water. Vortex 5min and filtration with a 200nm filter. Stock : -20°C (aliquots of 1mL) |
Tetracyclin | 15 mg/mL | Weight 0.6g of Tetracyclin powder, solubilization into 20mL of ethanol 50%. Vortex 5min and filtration with a 200nm filter. Stock : -20°C and hiden from light(aliquots of 1mL) |
Chloramphenicol | 34 mg/mL | Weight 0.34g of Chloramphenicol powder, solubilization into 10mL of ethanol 100%. Vortex 5min and filtration with a 200nm filter. Stock : -20°C and hiden from light(aliquots of 1mL) |
08-16-2014
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
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
- DH5a tranformed with pCB1C3
- Top10 transformed with pQexp
- DH5a pyr tranformed with pMK2
08-17-2014
Tests of antibiotics' stocks - Results
Plates | LB Agar only | LB+Cam | LB+Kan | LB+Amp | LB+Erm | LB+Tet |
E.coli | X | 0 | X | 0 | X | 0 |
Survivability tests - Results
liquid cultures/Plates | MB | M9 |
MB | ++++ | ++ |
M9 | ++ | + |
08-18-2014
Tests of antibiotics' stocks - Results(2)
Plates | LB Agar only | LB+Kan | LB+Erm (1:100) |
E.coli | X | 0 | 0 |
Plates for antibiotics's tests
For each tested antibiotic we made the following range of concentrations:0 | 1:500 | 1:1000 | 1:50 000 | 1:100 000 |
- MB agar 1X
- MB agar 0.5X
- M9 agar 1X
-
Each plate is made like in the following table:
/ 0 1:500 1:1000 1:50 000 1:100 000 Medium+agar 20mL 20mL 20mL 20mL 20mL Antibiotic 0 40µL of stock 20µL of stock 40µL of stock diluted 1/100 20µL of stock diluted 1/100