Difference between revisions of "Part:BBa K3739027"

 
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<partinfo>BBa_K3739027 short</partinfo>
 
<partinfo>BBa_K3739027 short</partinfo>
  
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sandwich
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We anchor LCI-KR2 protein onto membranes through LamB to stick the engineered bacteria on the polypropylene with an improved solution. We use <partinfo>BBa_K3739057</partinfo> to construct the expression system and anchor LCI-KR2 on the surface of VnDX.
  
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===Biology===
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===Usage and Biology===
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LamB is an anchor protein from 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 with LamB used as a sandwich-anchoring motif so that LCI-KR2 can be displayed on the surface of VnDX.
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===Characterization===
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====1. Identification====
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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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Revision as of 05:35, 21 October 2021


LamB1-LC1KR2-LamB2-his

We anchor LCI-KR2 protein onto membranes through LamB to stick the engineered bacteria on the polypropylene with an improved solution. We use BBa_K3739057 to construct the expression system and anchor LCI-KR2 on the surface of VnDX.

Biology

LamB is an anchor protein from 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 with LamB used as a sandwich-anchoring motif 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


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 612
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 760