Difference between revisions of "Part:BBa K1217008"
(→Usage and Biology) |
(→Usage and Biology) |
||
Line 6: | Line 6: | ||
==Usage and Biology== | ==Usage and Biology== | ||
− | Efficiency of this construct is compared with Two other designs [https://parts.igem.org/Part: | + | Efficiency of this construct is compared with Two other designs [https://parts.igem.org/Part:BBa_K1217003 BBa_K1217003] and [https://parts.igem.org/Part:BBa_K1217010 BBa_K1217010]. |
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. | ||
<gallery> | <gallery> |
Revision as of 06:37, 5 October 2013
Localizing polyphosphate kinase (ppk1) into native Eut microcompartment (BBa_K311004)
Under construction
Usage and Biology
Efficiency of this construct is compared with Two other designs BBa_K1217003 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
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NotI site found at 2631
Illegal NotI site found at 3541 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2289
Illegal BglII site found at 2844
Illegal BglII site found at 3754
Illegal XhoI site found at 2639
Illegal XhoI site found at 3549 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 3468
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 3056
Illegal SapI.rc site found at 366