Difference between revisions of "Part:BBa K4463003"
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<img src="https://static.igem.wiki/teams/4463/wiki/figures-for-engineering-and-parts/mbp3.png | <img src="https://static.igem.wiki/teams/4463/wiki/figures-for-engineering-and-parts/mbp3.png | ||
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Figure1. In different concentrations of AgNO3 solution, modified <i>E.coli</i> that express MBP3 adsorbed more Ag(I) than Mg1655 pGEX-4T-1, which is the control group. | Figure1. In different concentrations of AgNO3 solution, modified <i>E.coli</i> that express MBP3 adsorbed more Ag(I) than Mg1655 pGEX-4T-1, which is the control group. | ||
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− | We used ICP-MS to measure the unbinding Ag(I) in the supernatant, for detailed information about our measurement method, please visit our | + | We used ICP-MS to measure the unbinding Ag(I) in the supernatant, for detailed information about our measurement method and result analysis, please visit our <a href="https://2022.igem.wiki/xjtlu-china/experiments">Experiments</a>and <a href="https://2022.igem.wiki/xjtlu-china/results">Results</a>on wiki. |
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Latest revision as of 01:23, 12 October 2022
csgA-MBP3
This is a composite part that consist of CsgA and MBP3. CsgA is the major curli subunit protein of E.coli. Therefor, the surface display of MBP3, which can bind Ag(I) and produce nano Ag, achieved by linking to csgA. MBP3 is identified from a combinatorial phage display peptide library, for more information about MBP3, please visit the page of MBP3 that created by iGEM XJTLU_China 2022.
We have tested the function of CsgA-MBP3 part and compared with Mg1655 as control.
We used ICP-MS to measure the unbinding Ag(I) in the supernatant, for detailed information about our measurement method and result analysis, please visit our Experimentsand Resultson wiki.
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]
- 1000COMPATIBLE WITH RFC[1000]