Difference between revisions of "Part:BBa K1217003"
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We test the constructs' efficiency from 2 parameters: poly-P synthesis efficiency and phosphate removal efficiency from the medium. | We test the constructs' efficiency from 2 parameters: poly-P synthesis efficiency and phosphate removal efficiency from the medium. | ||
[[File:Ppkonly.png|150px|thumb|none|Expected model of BBa_K1217003 ]] | [[File:Ppkonly.png|150px|thumb|none|Expected model of BBa_K1217003 ]] | ||
− | + | [[File:PpkEutK.png|150px|thumb|none|Expected model of BBa_K1217008 ]] | |
+ | [[File:PpkEutS.png|150px|thumb|none|Expected model of BBa_K1217010 ]] | ||
==='''Expression of ppk1 enzyme'''=== | ==='''Expression of ppk1 enzyme'''=== | ||
We confirm the expression of PPK1 enzyme in e.coli. | We confirm the expression of PPK1 enzyme in e.coli. |
Revision as of 05:35, 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 ppk1 enzyme
We confirm the expression of PPK1 enzyme in e.coli.
Efficiency in Poly-P synthesis
Efficiency in phosphate removal from the environment
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