Team:UPO-Sevilla/Notebook/09 29
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<h2>Assay Team</h2> | <h2>Assay Team</h2> | ||
- | <p>We analyzed plates spread in the | + | <p>We have analyzed plates spread in the previous chemotaxis assay. There were no colonies coming from non succinate cubicles in those plates. That could mean that <i>P. Putida</i> KT2442 needs succinate as an energy source to show chemotaxis behaviour. We wanted to observe if the results were reproducible and in this case they were not.Needles are supposed to show a similar number of colonies when having the same content and being in the same cubicle. Yet only in the 10mM Asp + Succ cubicle that would |
- | + | happen. We had to continue working on the design of the chemotaxis assays to achieve reproducible results. Finally we could observe that there was a tendency to increase the number of bacteria in needles when using aspartate (in cubicles with succinate). Nonetheless, owing to the | |
- | non reproducible results, we could not admit that | + | non reproducible results, we could not admit that as a success.</p> |
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Revision as of 23:14, 19 October 2010
September, 29th
Assay Team
We have analyzed plates spread in the previous chemotaxis assay. There were no colonies coming from non succinate cubicles in those plates. That could mean that P. Putida KT2442 needs succinate as an energy source to show chemotaxis behaviour. We wanted to observe if the results were reproducible and in this case they were not.Needles are supposed to show a similar number of colonies when having the same content and being in the same cubicle. Yet only in the 10mM Asp + Succ cubicle that would happen. We had to continue working on the design of the chemotaxis assays to achieve reproducible results. Finally we could observe that there was a tendency to increase the number of bacteria in needles when using aspartate (in cubicles with succinate). Nonetheless, owing to the non reproducible results, we could not admit that as a success.
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