Difference between revisions of "Part:BBa K2789032"
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Latest revision as of 08:48, 17 October 2018
Contents
PPX+RBS+PPN
This part can catalyze the degradation of PolyP(heterochromatic granules). It adds PPX(exopolyphosphotase) that this protein can cut the PolyP from the internal site while PPX can only cut the Polyp from the ends of Poly P, this two protein together can dramatically release the phosphorus from the bacteria. This two proteins play the opposite effect from PPK(Polyphosphokinase).
Fragment size
At first, we directly synthesize the ppx+rbs+ppn on the pET28a(+) vector and use the lac promoter on the vector. The plasmids extracted from the bacteria are used as templates to perform PCR and the results show the fragment is right about 4000bps.
Function proof
We add 100μL WT and the transformed BL21 separately into 100ml LB culture and incubate the bacteria at 37°C with 200rpm in about 8 hours. At the same time,we arbitrarily extract the culture to measure the OD600 and no distinct difference occurs(OD600WT:0.8 OD600test group:0.9). The IPTG is added after the sampling to 0.5mM and incubation continues.
We use the kit manufactured by HANGZHOU LOHAND BIOLOGICAL Co. Ltd. to measure the phosphorus concentration in the media after 16h. Before that, the culture is measured at 600nm to test the concentration of bacteria and centrifuged at 10,000×g for 3 minutes to clear the most bacteria. The supernatant is diluted with 49times water to make the phosphorus suitable to measure. The reaction result shows below:
Conclusion
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 2094
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 3744
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 872