Difference between revisions of "Part:BBa K622005:Experience"
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[[Image:Kyoto-sigma54-1.png|400px|thumb|center|Fig.1: The σ<sup>54</sup> promoter activity in the different glutamine concentration. The activity in 0.0 % glutamine was measured as a standard and the activities in 0.2 and 2.0 % glutamine were the relative values.]] | [[Image:Kyoto-sigma54-1.png|400px|thumb|center|Fig.1: The σ<sup>54</sup> promoter activity in the different glutamine concentration. The activity in 0.0 % glutamine was measured as a standard and the activities in 0.2 and 2.0 % glutamine were the relative values.]] | ||
− | After the overnight cultivation in M9 medium with glucose and casamino acids, the medium was replaced with fresh M9 medium with glutamine not containing glucose or casamino acids. | + | After the overnight cultivation in M9 medium with glucose and casamino acids, the medium was replaced with fresh M9 medium with glutamine not containing glucose or casamino acids and the incubation at 37 degrees was started. |
===User Reviews=== | ===User Reviews=== |
Revision as of 17:19, 14 October 2011
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Characterization of σ54 promoter activity
We performed the function check of σ54 promoter in the genome of E. coli.
By measuring the amount of mRNA of glnG, the promoter activities in the different glutamine concentration were measured (Fig.1). The activity in 0.0 % glutamine was measured as a standard and those in 0.2 and 2.0 % glutamine were compared to the standard. Figure 1 shows that the activities in 0.2 and 2.0 % glutamine are repressed to less than one-fifth of that in 0.0 % glutamine.
After the overnight cultivation in M9 medium with glucose and casamino acids, the medium was replaced with fresh M9 medium with glutamine not containing glucose or casamino acids and the incubation at 37 degrees was started.
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