Difference between revisions of "Part:BBa K5226029"

 
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<partinfo>BBa_K5226029 short</partinfo>
 
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===Introduction===
 
Li et al. [1] analyzed the proteomic characteristics of Halomonas TD01 using SDS-PAGE. They identified a strongly expressed endogenous gene encoding a porin and preliminarily determined its promoter region. Furthermore, they identified the core region and constructed a constitutive promoter library by randomizing the sequences between the -35 and -10 regions. Shen et al. [2] performed 3-nucleotide saturation mutagenesis upstream of the -10 box and 4-nucleotide saturation mutagenesis within the -10 box to further expand the promoter library.
 
Li et al. [1] analyzed the proteomic characteristics of Halomonas TD01 using SDS-PAGE. They identified a strongly expressed endogenous gene encoding a porin and preliminarily determined its promoter region. Furthermore, they identified the core region and constructed a constitutive promoter library by randomizing the sequences between the -35 and -10 regions. Shen et al. [2] performed 3-nucleotide saturation mutagenesis upstream of the -10 box and 4-nucleotide saturation mutagenesis within the -10 box to further expand the promoter library.
 
We have only included the porin constitutive promoters that are relevant to our team.
 
We have only included the porin constitutive promoters that are relevant to our team.
  
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===Sequence and Features===
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===Usage and Biology===
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<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K5226029 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K5226029 SequenceAndFeatures</partinfo>
  
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===References===
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[1]Li T, Li T, Ji W, et al. Engineering of core promoter regions enables the construction of constitutive and inducible promoters in Halomonas sp[J]. Biotechnology Journal, 2016, 11(2): 219-227.
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[2]Shen R, Yin J, Ye JW, Xiang RJ, Ning ZY, Huang WZ, Chen GQ. Promoter Engineering for Enhanced P(3HB- co-4HB) Production by Halomonas bluephagenesis. ACS Synth Biol. 2018 Aug 17;7(8):1897-1906. doi: 10.1021/acssynbio.8b00102. Epub 2018 Jul 31. PMID: 30024739.
  
 
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Revision as of 01:03, 20 August 2024


porin281

Introduction

Li et al. [1] analyzed the proteomic characteristics of Halomonas TD01 using SDS-PAGE. They identified a strongly expressed endogenous gene encoding a porin and preliminarily determined its promoter region. Furthermore, they identified the core region and constructed a constitutive promoter library by randomizing the sequences between the -35 and -10 regions. Shen et al. [2] performed 3-nucleotide saturation mutagenesis upstream of the -10 box and 4-nucleotide saturation mutagenesis within the -10 box to further expand the promoter library. We have only included the porin constitutive promoters that are relevant to our team.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]

References

[1]Li T, Li T, Ji W, et al. Engineering of core promoter regions enables the construction of constitutive and inducible promoters in Halomonas sp[J]. Biotechnology Journal, 2016, 11(2): 219-227.

[2]Shen R, Yin J, Ye JW, Xiang RJ, Ning ZY, Huang WZ, Chen GQ. Promoter Engineering for Enhanced P(3HB- co-4HB) Production by Halomonas bluephagenesis. ACS Synth Biol. 2018 Aug 17;7(8):1897-1906. doi: 10.1021/acssynbio.8b00102. Epub 2018 Jul 31. PMID: 30024739.