Paris/July 5

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* Culture of 150 ml of MG1655.
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== Preliminary work on w121 strain ==
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At OD = 0.2 : Centrifugation of 25ml of culture, filtration of the supernatant. ==> S0.2 <br>
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As previously observed, the w121 strain did not grow at all in the S0 medium... We supposed that their might be no nutriments left in the medium because we used a medium in which MG1655 grew ON...
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Same thing at OD= 0.4 , 0.6 and 0.8 , leading to the solutions: S0.2, S0.4, S0.6 and S0.8
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We will redo the experiment but this time, the medium will be recovered from exponential phase culture of MG1655
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* We started a culture 150 ml of MG1655, and we take samples of the culture at different OD during exponential phase :
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** At OD = 0.2 : Centrifugation of 25ml of culture, filtration of the supernatant. ==> S0.2  
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** At OD = 0.4 : Centrifugation of 25ml of culture, filtration of the supernatant. ==> S0.4
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** At OD = 0.6 : Centrifugation of 25ml of culture, filtration of the supernatant. ==> S0.6
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** At OD = 0.8 : Centrifugation of 25ml of culture, filtration of the supernatant. ==> S0.8
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* Transduction of the DapA deletion into MG1655 failed... We will redo the stock
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== Transduction of the DapA deletion into MG1655 failed... ==
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We will redo the stock ''(of phages?? [[User:Nicolas C.|Nicolas C.]])''
[[Paris|<<home]]
[[Paris|<<home]]

Revision as of 22:18, 10 July 2007

Preliminary work on w121 strain

As previously observed, the w121 strain did not grow at all in the S0 medium... We supposed that their might be no nutriments left in the medium because we used a medium in which MG1655 grew ON... We will redo the experiment but this time, the medium will be recovered from exponential phase culture of MG1655

  • We started a culture 150 ml of MG1655, and we take samples of the culture at different OD during exponential phase :
    • At OD = 0.2 : Centrifugation of 25ml of culture, filtration of the supernatant. ==> S0.2
    • At OD = 0.4 : Centrifugation of 25ml of culture, filtration of the supernatant. ==> S0.4
    • At OD = 0.6 : Centrifugation of 25ml of culture, filtration of the supernatant. ==> S0.6
    • At OD = 0.8 : Centrifugation of 25ml of culture, filtration of the supernatant. ==> S0.8


Transduction of the DapA deletion into MG1655 failed...

We will redo the stock (of phages?? Nicolas C.)

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