Difference between revisions of "Part:BBa K255002"

Revision as of 18:46, 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 number

is 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. After this the expression profile of YFP between 0 and 100 μM was measured. Once can observe that the variability is decreasing as compared to that seen in the open loop(BBa_K255004).

Expression of BBa_K255002 in lacI deleted E.coli strain

Following figure 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.

Variation of YFP expression at various IPTG concentrations in Strain BBa_K255002.

Safety

Because this part is from commonly used elements in bacteria. No safety problem can be arised by this part.

Sequence and Features

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
COMPATIBLE WITH RFC[12]
21
INCOMPATIBLE WITH RFC[21]
Illegal XhoI site found at 1161
23
COMPATIBLE WITH RFC[23]
25
COMPATIBLE WITH RFC[25]
1000
COMPATIBLE WITH RFC[1000]

@@ Line 1: / Line 1: @@
 __NOTOC__
 <partinfo>BBa_K255002 short</partinfo>
-network with a positive feedforward and a negative feedback loop, present in pSB2K3 vector.
+ It has got single negative feedback loop on the plasmid(pSB2K3) copy number.Plasmid copy number
+is 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.
+After this the expression profile of YFP between 0 and 100 μM was measured. Once can observe that the variability is decreasing as compared to that seen in the open loop(BBa_K255004).
+[[Image:p2.png|thumb|600px|center|alt=A |Expression of BBa_K255002 in lacI deleted E.coli strain]]
+Following figure 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 |Variation of YFP expression at various IPTG concentrations in Strain BBa_K255002.]]
+===Safety===
+Because this part is from commonly used elements in bacteria. No safety problem can be arised by this part.
 <!-- Add more about the biology of this part here