Difference between revisions of "Part:BBa K2762010"
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| − | We did two experiment to confirm the expression of this part. First we inserted the part on pSB1C3 and cloned the plasmid into DH5 alpha. We extracted the plasmid after the colony formed and did the enzyme digestion to confirm the insertion was successful. Second, we cloned the plasmid into W3110. We than did the SDS-PAGE to confirm the present of the | + | We did two experiment to confirm the expression of this part. First we inserted the part on pSB1C3 and cloned the plasmid into DH5 alpha. We extracted the plasmid after the colony formed and did the enzyme digestion to confirm the insertion was successful. Second, we cloned the plasmid into W3110. We than did the SDS-PAGE to confirm the present of the rbcX and rbcS protein. |
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[[File:T--NCKU Tainan--part BBa K2762010.png|200px|centre]] | [[File:T--NCKU Tainan--part BBa K2762010.png|200px|centre]] | ||
| + | [[File:T--NCKU Tainan--part BBa K2762010 sds.png|200px|centre]] | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
Revision as of 08:15, 6 October 2018
PlacI-B0034-rbcX-B0034-rbcS-B0015
Usage
The rbcXS part encode the RbcS subunit of RubisCO and the chaperon RbcX. The RbcS affect the activity of RubisCO and RbcX contribute to the correct folding of the whole RubisCO enzyme.
Biology
The rbcX and rbcS gene are from cynobacteria Synechococcus elongatus PCC 7002. We designed the PlacI (BBa_R0010) promoter for the gene and cloned gene in DH5 alpha in order to test the function while consecutive expression.It has reported that the expression of RubisCO could not be detectable while only add single promoter of the rbcL-rbcX-rbcS gene fragment. Therefore we added another PlacI promoter on the upstream of rbcX-rbcS gene and named the part as rbcXS. We also did the coden optimization for the gene to ensure successful expression. The activation of RubisCo will be maximize after the binding of the RbcS subunit. To get more information, see our composite part: BBa_K2762012.
Characterization
We did two experiment to confirm the expression of this part. First we inserted the part on pSB1C3 and cloned the plasmid into DH5 alpha. We extracted the plasmid after the colony formed and did the enzyme digestion to confirm the insertion was successful. Second, we cloned the plasmid into W3110. We than did the SDS-PAGE to confirm the present of the rbcX and rbcS protein.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]