Difference between revisions of "Part:BBa K1217003"
(→Efficiency of poly-P synthesis and phosphate removal from environment) |
(→Efficiency of poly-P synthesis and phosphate removal from environment) |
||
Line 19: | Line 19: | ||
==='''Efficiency of poly-P synthesis and phosphate removal from environment'''=== | ==='''Efficiency of poly-P synthesis and phosphate removal from environment'''=== | ||
− | [[File: | + | [[File:HkuProcedure.png|350px|thumb|left|Experiment procedure. Wide type and blank act as a control to indicate the normal phosphate uptake of wide type e.coli and the phosphate level change along with time. Upon iptg induction, cultural samples are collected in every three hours. The cell pellet harvested is used to measure the intracellular poly-P level and the supernatant is used for phosphate quantification]] |
'''Intracellular poly-P quantification''' | '''Intracellular poly-P quantification''' | ||
'''Phosphate level in the medium''' | '''Phosphate level in the medium''' |
Revision as of 06:00, 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