Difference between revisions of "Part:BBa K1217003"
(→Usage and Biology) |
(→Usage and Biology) |
||
Line 30: | Line 30: | ||
'''Phosphate level in the medium''' | '''Phosphate level in the medium''' | ||
[[File:Malachiteassay.png|400px|thumb|left|Supernatant medium collected at each time point is quantified using Malachite green colorimetric assay. Phosphate standard curve is shown.]] | [[File:Malachiteassay.png|400px|thumb|left|Supernatant medium collected at each time point is quantified using Malachite green colorimetric assay. Phosphate standard curve is shown.]] | ||
+ | [[File:Pimedium.png|400px|thumb|none|Phosphate level in medium. Blue: Wild type indicate the basal phosphate removal from the medium by wild type cell. Red: BBa_K1217003. Green: BBa_K1217008. The two constructs have higher phosphate removal from the medium.]] | ||
+ | |||
Testing | Testing |
Latest revision as of 06:35, 5 October 2013
pT7-ppk1(K.oralis)
Polyphosphate kinase (ppk1) (E.C. 2.7.4.1) catalyzes the formation of polyphosphate from ATP. In BBa_K1217003, ppk1 was under the control of T7 promotor. Under iptg induction, over-expression of ppk1 can reduce the phosphate level in the medium by its incorporation into polyphosphate synthesis inside the bacteria.
Usage and Biology
Efficiency of this construct is compared with Two other designs BBa_K1217008 and BBa_K1217010. We test the constructs' efficiency from 2 parameters: poly-P synthesis efficiency and phosphate removal efficiency from the medium.
Expression of BBa_K1217003
We confirm the expression of PPK1 enzyme in e.coli.
Efficiency of poly-P synthesis and phosphate removal from environment
Intracellular poly-P quantification
Phosphate level in the medium
Testing
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 309