Difference between revisions of "Part:BBa K346030"
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<partinfo>BBa_K346030 short</partinfo> | <partinfo>BBa_K346030 short</partinfo> | ||
This part is composed of a T7promoter, a rbs and the periplasm display protein Dsba-MBP, which binding the lead of the enviroment. | This part is composed of a T7promoter, a rbs and the periplasm display protein Dsba-MBP, which binding the lead of the enviroment. | ||
+ | DsbA, a protein that can export its C-terminal fusion protein into periplasm more efficiently and faster than maltose binding protein, was used as the key component to express our Metal Binding Peptide periplasmically . | ||
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+ | [[Image:pb dsab.jpg]] | ||
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+ | Figure 1: The expression of DsbA+MBP. This MBP is engineered to bind lead more efficiently. We use this part to capture lead in the periplasm. | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 07:57, 26 October 2010
T7p(BBa_I719005)+RBS(B0034)+DsbA+MBP(periplasm display of lead binding peptide)
This part is composed of a T7promoter, a rbs and the periplasm display protein Dsba-MBP, which binding the lead of the enviroment. DsbA, a protein that can export its C-terminal fusion protein into periplasm more efficiently and faster than maltose binding protein, was used as the key component to express our Metal Binding Peptide periplasmically .
Figure 1: The expression of DsbA+MBP. This MBP is engineered to bind lead more efficiently. We use this part to capture lead in the periplasm.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 520
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 520
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 308
Illegal XhoI site found at 1005 - 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 520
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 520
Illegal AgeI site found at 140 - 1000COMPATIBLE WITH RFC[1000]