Difference between revisions of "Part:BBa K4722009"

 
 
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<partinfo>BBa_K4722009 short</partinfo>
 
<partinfo>BBa_K4722009 short</partinfo>
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===Usage and Biology===
 
  
 
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<partinfo>BBa_K4722009 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K4722009 SequenceAndFeatures</partinfo>
  
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===Usage and Biology===
  
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It is the E. coli autotransporter AIDA-I, diffusing adhesion adhesin, membrane entity.
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===Functional Parameters===
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<partinfo>BBa_K4722009 parameters</partinfo>
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===Design Consideration===
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The genetic construct was ligated into a pET28a plasmid vector and subsequently introduced into Escherichia coli strain BL21 (DE3).
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NicX was genetically connected with AIDAI to enable its direct translation onto the surface of BL21. This innovation eliminated the need for protein purification steps, allowing for the direct utilization of E. coli as a host for enzymes in various applications.

Latest revision as of 17:36, 8 October 2023

AIDA-I

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1280
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]

Usage and Biology

It is the E. coli autotransporter AIDA-I, diffusing adhesion adhesin, membrane entity.

Design Consideration

The genetic construct was ligated into a pET28a plasmid vector and subsequently introduced into Escherichia coli strain BL21 (DE3). NicX was genetically connected with AIDAI to enable its direct translation onto the surface of BL21. This innovation eliminated the need for protein purification steps, allowing for the direct utilization of E. coli as a host for enzymes in various applications.