Difference between revisions of "Part:BBa K1217008"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K1217008 short</partinfo> | <partinfo>BBa_K1217008 short</partinfo> | ||
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Under construction | Under construction | ||
− | < | + | ==Usage and Biology== |
− | === | + | |
+ | 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. | ||
+ | <gallery> | ||
+ | File:Ppkonly.png|Expected model of BBa_K1217003 | ||
+ | File:PpkEutK.png|Expected model of BBa_K1217008 | ||
+ | File:PpkEutS.png|Expected model of BBa_K1217010 | ||
+ | </gallery> | ||
+ | ==='''Efficiency of poly-P synthesis and phosphate removal from environment'''=== | ||
+ | |||
+ | [[File:HkuProcedure.png|400px|thumb|none|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]] | ||
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+ | '''Intracellular poly-P quantification''' | ||
+ | [[File:Dapi measure.png|400px|thumb|left|Intracellular poly-P is extracted from the cells and quantified using DAPI fluorescence measurement. DAPI is a fluorescent probe that binds DNA and poly-P. Since DNA in the sample has been removed during poly-p extraction step, it reduce nonspecific fluorescent signal due to DNA-DAPI binding. Poly-P standard curve is shown.]] | ||
+ | [[File:Polyp dapi.png|400px|thumb|none|Intracellular Poly-P level of all samples. Blue: Wild type indicate the basal poly-P level inside wild type cell. Red: BBa_K1217003. Black: BBa_K1217010. Green:BBa_K1217008. All 3 constructs have higher poly-P amount accumulated.]] | ||
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+ | '''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: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.]] | ||
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+ | |||
+ | Testing | ||
+ | |||
+ | <!-- --> | ||
+ | <span class='h3bb'>Sequence and Features</span> | ||
+ | <partinfo>BBa_K1217003 SequenceAndFeatures</partinfo> | ||
+ | |||
+ | |||
+ | <!-- Uncomment this to enable Functional Parameter display | ||
+ | ===Functional Parameters=== | ||
+ | <partinfo>BBa_K1217003 parameters</partinfo> | ||
+ | <!-- --> | ||
+ | |||
<!-- --> | <!-- --> |
Latest revision as of 06:38, 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.
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