Difference between revisions of "Part:BBa K3866027"

 
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<partinfo>BBa_K3866027 short</partinfo>
 
<partinfo>BBa_K3866027 short</partinfo>
  
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===Usage and Biology===
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This TU includes the <i>ygfG</i> gene placed under the control of the arabinosed-induced promoter. Initially, the level 1 cloning was performed using the trc promoter, though we weren't able to isolate a colony with the desired construct, as there is a possibility that the bacteria's metabolism went out of balance so no colonies survived to be chosen for screening. Instead we used the arabinose-indused promoter, which seemed to be working more than well.
  
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===Design Notes===
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The coding sequence was domesticated. We removed BsmBI and BsaI sites in order to be compatible with GoldenBraid and MoClo. The sequence is cloned in seva α1 vector and has overhangs compatible for GoldenBraid cloning.
  
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[[Image:T--Thessaly--arac-ygfG-term.png|800px|thumb|none|<I><b>Figure 1.</b> The level α module of the Propionate Production: α1:ParaBAD:RBS-ygfG-Double terminator </i>]]
  
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===Verification of Cloning===
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===Usage and Biology===
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[[File:T--Thessaly--arac-ygfGgel.png|500px|thumb|none|<i><b>Figure 2.</b>: (C=Cut, U=Uncut) Restriction digestion of α1-sbm with: EcoRI, Expected bands: 6345bp, 2185bp, Positive result: C2</i>]]
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===Experimental Use and Experience===
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This part showed functionality at the following parts: <bbpart>BBa_K3866030</bbpart>, <bbpart>BBa_K3866031</bbpart>
  
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===Sequence and Features===
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<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K3866026 SequenceAndFeatures</partinfo>
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<partinfo>BBa_K3866027 SequenceAndFeatures</partinfo>
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===References===
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===Functional Parameters===
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Akawi L, Srirangan K, Liu X, Moo-Young M, Perry Chou C. Engineering Escherichia coli for high-level production of propionate. J Ind Microbiol Biotechnol. 2015 Jul;42(7):1057-72. https://doi.org/10.1007/s10295-015-1627-4
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<partinfo>BBa_K3866027 parameters</partinfo>
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Revision as of 22:29, 25 September 2021


ParaBAD:ygfG:Terminator

Usage and Biology

This TU includes the ygfG gene placed under the control of the arabinosed-induced promoter. Initially, the level 1 cloning was performed using the trc promoter, though we weren't able to isolate a colony with the desired construct, as there is a possibility that the bacteria's metabolism went out of balance so no colonies survived to be chosen for screening. Instead we used the arabinose-indused promoter, which seemed to be working more than well.

Design Notes

The coding sequence was domesticated. We removed BsmBI and BsaI sites in order to be compatible with GoldenBraid and MoClo. The sequence is cloned in seva α1 vector and has overhangs compatible for GoldenBraid cloning.

Figure 1. The level α module of the Propionate Production: α1:ParaBAD:RBS-ygfG-Double terminator

Verification of Cloning

Figure 2.: (C=Cut, U=Uncut) Restriction digestion of α1-sbm with: EcoRI, Expected bands: 6345bp, 2185bp, Positive result: C2

Experimental Use and Experience

This part showed functionality at the following parts: BBa_K3866030, BBa_K3866031

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 2948
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 2948
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 2948
    Illegal BamHI site found at 1148
    Illegal BamHI site found at 2236
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 2948
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 2948
    Illegal NgoMIV site found at 3263
    Illegal AgeI site found at 983
    Illegal AgeI site found at 1400
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 965


References

Akawi L, Srirangan K, Liu X, Moo-Young M, Perry Chou C. Engineering Escherichia coli for high-level production of propionate. J Ind Microbiol Biotechnol. 2015 Jul;42(7):1057-72. https://doi.org/10.1007/s10295-015-1627-4