Difference between revisions of "Part:BBa K255002"
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− | + | It has got single negative feedback loop on the plasmid(pSB2K3) copy number.Plasmid copy numberis dependent on IPTG concentration (inducer). Here there is no control on the lacI expression.The copy number is | |
− | + | ||
characterized by YFP while LacI is characterized by LacI-CFP fusion | characterized by YFP while LacI is characterized by LacI-CFP fusion | ||
protein. YFP was measured using FACS and the distribution obtained was | protein. YFP was measured using FACS and the distribution obtained was | ||
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===Result=== | ===Result=== | ||
− | The YFP Expression increased around 10 folds from 0 to 100 μM of IPTG Conc and thereafter its value was almost constant to 200 and 500 μM of IPTG conc. | + | The YFP Expression increased around 10 folds from 0 to 100 μM of IPTG Conc and thereafter its value was almost constant to 200 and 500 μM of IPTG conc(fig.1). |
− | After this the expression profile of YFP between 0 and 100 μM was measured. | + | |
− | + | [[Image:p2.png|thumb|600px|center|alt=A |Figure 1. Expression of BBa_K255002 in lacI deleted E.coli strain]] | |
− | + | After this the expression profile of YFP between 0 and 100 μM was measured. One can observe that the variability is decreasing as compared to that seen in the open loop(BBa_K255004). | |
− | [[Image:p2_2.png|thumb|200px|center|alt=A |Variation of YFP expression at various IPTG concentrations in Strain BBa_K255002.]] | + | Fig.2 shows variation of YFP expression at various IPTG concentrations in Strain BBa_K255002, where the copy number is regulated. YFP indicates the status of copy number |
+ | [[Image:p2_2.png|thumb|200px|center|alt=A |Figure 2.Variation of YFP expression at various IPTG concentrations in Strain BBa_K255002.]] | ||
===Safety=== | ===Safety=== | ||
Because this part is from commonly used elements in bacteria. No safety problem can be arised by this part. | Because this part is from commonly used elements in bacteria. No safety problem can be arised by this part. |
Revision as of 18:54, 31 October 2009
pTet.lacI-cfp(fusion).terminator.pTet.yfp.terminator
It has got single negative feedback loop on the plasmid(pSB2K3) copy number.Plasmid copy numberis dependent on IPTG concentration (inducer). Here there is no control on the lacI expression.The copy number is
characterized by YFP while LacI is characterized by LacI-CFP fusion
protein. YFP was measured using FACS and the distribution obtained was
independent of IPTG. Beta-galactosidase was also measured at various
lactose concentration to characterize the expression of gene in the host
genome. Further the growth of the transformant was also characterized at
different lactose concentrations.
Characterization
Steady state concentration of YFP was measured using FACS. Illustrative FACS results are given below: The mean, variance and standard error were noted for difference strains and at different IPTG concentration. The FACS results are shown for varying IPTG concentrations varying from 0um to 500um.
Result
The YFP Expression increased around 10 folds from 0 to 100 μM of IPTG Conc and thereafter its value was almost constant to 200 and 500 μM of IPTG conc(fig.1).
After this the expression profile of YFP between 0 and 100 μM was measured. One can observe that the variability is decreasing as compared to that seen in the open loop(BBa_K255004). Fig.2 shows variation of YFP expression at various IPTG concentrations in Strain BBa_K255002, where the copy number is regulated. YFP indicates the status of copy number
Safety
Because this part is from commonly used elements in bacteria. No safety problem can be arised by this part.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 1161
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]