Difference between revisions of "Part:BBa K4348005"

 
 
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A plasmid backbone we developed that is intended for use with the hag promoter. It integrates into the flgM site of the B. subtilis genome. flgM binds the SigD transcription factor and inactivates it, thus blocking the P hag promoter, one of the strongest promoters discovered.  
 
A plasmid backbone we developed that is intended for use with the hag promoter. It integrates into the flgM site of the B. subtilis genome. flgM binds the SigD transcription factor and inactivates it, thus blocking the P hag promoter, one of the strongest promoters discovered.  
  
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=Introduction=
===Usage and Biology===
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The Bacillus BioBrick Box designed by LMU-Munich iGEM 2012 was used extensively in the McGill 2022 project. The box contains three B. subtilis integrative vectors targeted to the amyE, thrC, and lacA sites, as well as constitutive and inducible promoters with varying strengths. We decided to design a fourth integrative vector and an accompanying promoter as our parts contribution.
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==Biology==
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[[File:PBSChag.png|300px|thumb|left]]
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pBSChag is a modification of pBS1C of the BioBrick Box to integrate into the flgM site. Like pBS1C, pBSChag will have an ampicillin selection marker for E. coli and chloramphenicol for B. subtilis. The “hag” in the vector name indicates that it is designed to be used with Phag as the promoter, but others also work fine. The flgM gene is an inhibitor of Phag; pBSChag eliminates this inhibition by integrating and disrupting flgM.
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
 
<partinfo>BBa_K4348005 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K4348005 SequenceAndFeatures</partinfo>

Latest revision as of 21:39, 13 October 2022


pBSChag

A plasmid backbone we developed that is intended for use with the hag promoter. It integrates into the flgM site of the B. subtilis genome. flgM binds the SigD transcription factor and inactivates it, thus blocking the P hag promoter, one of the strongest promoters discovered.

Introduction

The Bacillus BioBrick Box designed by LMU-Munich iGEM 2012 was used extensively in the McGill 2022 project. The box contains three B. subtilis integrative vectors targeted to the amyE, thrC, and lacA sites, as well as constitutive and inducible promoters with varying strengths. We decided to design a fourth integrative vector and an accompanying promoter as our parts contribution.

Biology

PBSChag.png

pBSChag is a modification of pBS1C of the BioBrick Box to integrate into the flgM site. Like pBS1C, pBSChag will have an ampicillin selection marker for E. coli and chloramphenicol for B. subtilis. The “hag” in the vector name indicates that it is designed to be used with Phag as the promoter, but others also work fine. The flgM gene is an inhibitor of Phag; pBSChag eliminates this inhibition by integrating and disrupting flgM.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Plasmid lacks a prefix.
    Plasmid lacks a suffix.
    Illegal EcoRI site found at 5854
    Illegal SpeI site found at 2
    Illegal PstI site found at 16
    Illegal NotI site found at 9
    Illegal NotI site found at 5860
  • 21
    INCOMPATIBLE WITH RFC[21]
    Plasmid lacks a prefix.
    Plasmid lacks a suffix.
    Illegal EcoRI site found at 5854
    Illegal XhoI site found at 3181
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal prefix found at 5854
    Illegal suffix found at 2
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal prefix found at 5854
    Plasmid lacks a suffix.
    Illegal XbaI site found at 5869
    Illegal SpeI site found at 2
    Illegal PstI site found at 16
    Illegal NgoMIV site found at 1128
    Illegal NgoMIV site found at 1507
    Illegal NgoMIV site found at 3145
    Illegal NgoMIV site found at 4284
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Plasmid lacks a prefix.
    Plasmid lacks a suffix.
    Illegal BsaI site found at 2034
    Illegal BsaI.rc site found at 4108
    Illegal SapI.rc site found at 1675
    Illegal SapI.rc site found at 5505