Difference between revisions of "Part:BBa K3739052"
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<partinfo>BBa_K3739052 short</partinfo> | <partinfo>BBa_K3739052 short</partinfo> | ||
− | + | We anchor LCI-KR2 protein onto membranes through OmpA to stick the engineered bacteria on the polypropylene. We use <partinfo>BBa_K3739052</partinfo> to construct the expression system and anchor LCI-KR2 on the surface of VnDX. | |
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+ | ===Biology=== | ||
+ | OmpA is an anchor protein from E. coli, also find in Vibrio Species, which can anchor its passenger protein to the cell membrane. It has been widely used in cell-surface display. LCI-KR2, A mutant of a peptide called LCI from ''Bacillus subtilis'', can sticks to polypropylene strongly. LCI-KR2 is fused at C terminal with Lpp-OmpA so that LCI-KR2 can be displayed on the surface of VnDX. | ||
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+ | ===Characterization=== | ||
+ | ====1. Identification==== | ||
+ | After receiving the synthesized DNA, PCR was done to certify that the plasmid was correct, and the experimental results were shown in figure1. | ||
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> |
Revision as of 18:38, 20 October 2021
J23100-B0030-OmpA-LC1KR-2-GFP-B0010
We anchor LCI-KR2 protein onto membranes through OmpA to stick the engineered bacteria on the polypropylene. We use BBa_K3739052 to construct the expression system and anchor LCI-KR2 on the surface of VnDX.
Biology
OmpA is an anchor protein from E. coli, also find in Vibrio Species, which can anchor its passenger protein to the cell membrane. It has been widely used in cell-surface display. LCI-KR2, A mutant of a peptide called LCI from Bacillus subtilis, can sticks to polypropylene strongly. LCI-KR2 is fused at C terminal with Lpp-OmpA so that LCI-KR2 can be displayed on the surface of VnDX.
Characterization
1. Identification
After receiving the synthesized DNA, PCR was done to certify that the plasmid was correct, and the experimental results were shown in figure1. Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 494
Illegal SapI.rc site found at 1109