Difference between revisions of "Part:BBa K1139150:Experinece"
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Fig. 2-2 is the extracted data which shows the comparison of N99 (IPTG+, with constitutive CI) and JM2.300 (IPTG+, without CI).<br> | Fig. 2-2 is the extracted data which shows the comparison of N99 (IPTG+, with constitutive CI) and JM2.300 (IPTG+, without CI).<br> | ||
| − | [[Image: | + | [[Image:Titech2013_parts_K1139150_Fig1B.jpg|thumb|center|500px|'''Fig. 2-1.''' Fluorescence intensity detected by flow cytometer]] |
| − | [[Image: | + | [[Image:Titech2013_parts_K1139150_Fig1C.jpg|thumb|center|500px|'''Fig. 2-2.''' Comparison of N99 and JM2.300]] |
'''3. Discussion''' | '''3. Discussion''' | ||
N99 cells (CI+) showed higher fluorescence intensity than JM2.300 cells (CI-). From this experiment, we assume that our ''rm/lac'' hybrid promoter is actually activated by CI.<br> | N99 cells (CI+) showed higher fluorescence intensity than JM2.300 cells (CI-). From this experiment, we assume that our ''rm/lac'' hybrid promoter is actually activated by CI.<br> | ||
We are now confirming that our ''rm/lac'' hybrid promoter is not only activated by CI but also repressed by LacI. | We are now confirming that our ''rm/lac'' hybrid promoter is not only activated by CI but also repressed by LacI. | ||
Revision as of 02:38, 26 September 2013
1. Materials and Methods
- 1-1. Construction
-pSB6A1-Ptet-GFP (N99)…positive control
-pSB6A1-promoterless-GFP (N99)…negative control
-pSB6A1-Prm/lac-GFP (N99)…sample with CI*
-pSB6A1--Prm/lac-GFP (JM2.300)…sample without CI
This N99 expresses CI from its genome constitutively.
- 1-2. Assay protocol
1. Prepare overnight culture of each cell at 37°C for 12 hours.
2. Take 30 microL of the overnight cultures into LB (3 mL) containing antibiotics (Amp 50 µg/mL) and 1 mM of IPTG* (→fresh culture)
We added IPTG in order to make sure to repress the expression of LacI derived from E. coli genome.
3. After 4 hours of induction, flow cytometer measurements for GFP expression.
2. Results
Fig. 2-1 shows the fluorescence intensity detected by flow cytometer.
Fig. 2-2 is the extracted data which shows the comparison of N99 (IPTG+, with constitutive CI) and JM2.300 (IPTG+, without CI).
3. Discussion
N99 cells (CI+) showed higher fluorescence intensity than JM2.300 cells (CI-). From this experiment, we assume that our rm/lac hybrid promoter is actually activated by CI.
We are now confirming that our rm/lac hybrid promoter is not only activated by CI but also repressed by LacI.