Difference between revisions of "Part:BBa K3866031"

 
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<partinfo>BBa_K3866031 short</partinfo>
 
<partinfo>BBa_K3866031 short</partinfo>
  
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===Usage and Biology===
  
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This composite part consists of the following Transcription Units:
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<p><i>ygfG</i>: <bbpart>BBa_K3866006</bbpart> & <i>ygfH</i>: <bbpart>BBa_K3866019</bbpart>
  
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===Design Notes===
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The coding sequences were domesticated. We removed BsmBI and BsaI sites in order to be compatible with GoldenBraid and MoClo. The sequences are cloned in seva ω2 vector and have overhangs compatible for GoldenBraid cloning.
  
<!-- Add more about the biology of this part here
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[[Image:T--Thessaly--YGH-term.png|600px|thumb|none|<I><b>Figure 1.</b> The ω module of the Propionate Production: ω2:ParaBAD:RBS-ygfG-Double terminator:ParaBAD:RBS-ygfH-Double terminator </i>]]
===Usage and Biology===
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===Verification of Cloning===
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[[File:T--Thessaly--YGHgel.png|800px|thumb|none|<i><b>Figure 2.</b>: (C=Cut, U=Uncut) Restriction digestion of ω2-ygfG-ygfH (C4-C5-C6-C7-C8) with: EcoRI + EcoRV, Expected bands: 6674bp, 2571bp, 2167bp, 309bp Positive result: C7</i>]]
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===Experimental Use and Experience===
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This part showed functionality at part <bbpart>BBa_K3866031</bbpart>
  
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===Sequence and Features===
<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K3866030 SequenceAndFeatures</partinfo>
<partinfo>BBa_K3866031 SequenceAndFeatures</partinfo>
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===References===
===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
<partinfo>BBa_K3866031 parameters</partinfo>
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Revision as of 23:33, 25 September 2021


Propionate Production Construct

Usage and Biology

This composite part consists of the following Transcription Units:

ygfG: BBa_K3866006 & ygfH: BBa_K3866019

Design Notes

The coding sequences were domesticated. We removed BsmBI and BsaI sites in order to be compatible with GoldenBraid and MoClo. The sequences are cloned in seva ω2 vector and have overhangs compatible for GoldenBraid cloning.

Figure 1. The ω module of the Propionate Production: ω2:ParaBAD:RBS-ygfG-Double terminator:ParaBAD:RBS-ygfH-Double terminator

Verification of Cloning

Figure 2.: (C=Cut, U=Uncut) Restriction digestion of ω2-ygfG-ygfH (C4-C5-C6-C7-C8) with: EcoRI + EcoRV, Expected bands: 6674bp, 2571bp, 2167bp, 309bp Positive result: C7

Experimental Use and Experience

This part showed functionality at part BBa_K3866031

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 4655
    Illegal BamHI site found at 1148
    Illegal BamHI site found at 1424
    Illegal BamHI site found at 3343
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 983
    Illegal AgeI site found at 3178
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 965
    Illegal SapI site found at 3160
    Illegal SapI.rc site found at 1883


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