"
Team:BCCS-Bristol/Calendar-Notebook/14 July 2008
From 2008.igem.org
Rodgerread (Talk | contribs) |
Tgorochowski (Talk | contribs) |
||
| (2 intermediate revisions not shown) | |||
| Line 1: | Line 1: | ||
| - | <html><link rel="stylesheet" href="http:// | + | <html><link rel="stylesheet" href="http://homepage.mac.com/tgorochowski/iGEM/bccs-igem.css" type="text/css"></html> |
__NOTOC__ | __NOTOC__ | ||
<div class="bccsNavBar"> | <div class="bccsNavBar"> | ||
| Line 15: | Line 15: | ||
</div> | </div> | ||
| - | + | ==Swimming agar assay with L-aspartic acid== | |
| - | + | This time, only 0.3 % agar plates were used. Two wells were made using the thick end of a 1000 µl pipette tip. In the left hole some aspartate solution was put and on the right some water (control). To half of the plates the solutions were added in the morning to allow chemotactic gradient to set up, to the second half the solutions were added immediately before the inoculation in the afternoon (arond 5 hours later). The ''E. coli'' MG1655 strain was inoculated three times on a line in the centre between the two holes and incubated overnight at the different temperatures: 25<sup>o</sup>C, 30<sup>o</sup>C and 37<sup>o</sup>C. | |
| + | |||
| + | Today, the plates were photographed and measured. There was some significant movement more towards the aspartate (chemoattractant), but the difference should be more visible. Thus, various conditions should be tested during the next experiments. | ||
| + | |||
| + | ==Comparision of motility between ''E. coli'' MG1655 and MC1000== | ||
| + | |||
| + | The agar plates were inoculated. Details on [[Team:BCCS-Bristol/Calendar-Notebook/15 July 2008 | 15 July 2008]]. | ||
Latest revision as of 09:52, 14 September 2008
Swimming agar assay with L-aspartic acid
This time, only 0.3 % agar plates were used. Two wells were made using the thick end of a 1000 µl pipette tip. In the left hole some aspartate solution was put and on the right some water (control). To half of the plates the solutions were added in the morning to allow chemotactic gradient to set up, to the second half the solutions were added immediately before the inoculation in the afternoon (arond 5 hours later). The E. coli MG1655 strain was inoculated three times on a line in the centre between the two holes and incubated overnight at the different temperatures: 25oC, 30oC and 37oC.
Today, the plates were photographed and measured. There was some significant movement more towards the aspartate (chemoattractant), but the difference should be more visible. Thus, various conditions should be tested during the next experiments.
Comparision of motility between E. coli MG1655 and MC1000
The agar plates were inoculated. Details on 15 July 2008.
