Difference between revisions of "Part:BBa K302012:Experience"
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|'''Graph1''': | |'''Graph1''': | ||
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− | |Distribution of cell lengths is not normal, so mean is misleading; | + | |Distribution of cell lengths is not normal, so the mean is misleading; we are reporting the median instead. |
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|[[Image:Teamnewcastle_yneA168.png|800px]] | |[[Image:Teamnewcastle_yneA168.png|800px]] |
Revision as of 11:43, 27 October 2010
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Applications of BBa_K302012
Characterisation by Team Newcastle 2010
We integrated our part into the Bacillus subtilis 168 chromosome at amyE (using the integration vector pGFP-rrnB) and selected for integration by testing for the ability to hydrolyse starch. Homologous recombination at amyE destroys endogenous expression of amylase. Colonies that are not able to break down starch on agar plate do not have a white halo when exposed to iodine.
The part was co-transcribed with gfp fluorescent marker by transcriptional fusion after the yneA coding sequence.
We characterised the part first without, and then with, LacI repression (using the integration vector pMutin4 to integrate lacI into the Bacillus subtilis 168 chromosome).
Graphs 2,3 and 4 show a greater proportion of cells at a higher concentration of IPTG(1mM IPTG), compared with Bacillus subtilis 168 our control population.
User Reviews
UNIQdd3bb0fa819fcb5c-partinfo-00000000-QINU UNIQdd3bb0fa819fcb5c-partinfo-00000001-QINU