Difference between revisions of "Part:BBa K5108006"
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<partinfo>BBa_K5108006 short</partinfo>
 
<partinfo>BBa_K5108006 short</partinfo>
  
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<i>aprA</i> RBS from <i>Pseudomonas protegens</i> (CHA0)
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Ribosome Binding Site of gene <i>aprA</i> of <i>P. protogens</i>
  
 
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===Usage and Biology===
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<div style="background-color: #f8f6f5; width: 40%; border: 2px solid #000;">
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<ol style="color: black; padding: auto -1rem; margin= 0"> <b>Contents</b>
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    <li style="color: blue;">Usage and Biology</li>
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    <li style="color: blue;">References</li>
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<h2 style="color: blue;"> <b>Usage and Biology</b></h2>
 
<h2 style="color: blue;"> <b>Usage and Biology</b></h2>
  
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<p>Ribosome Binding Site of gene <i>aprA</i> of <i>P. fluorescens</i>. It was used for protein translation in <i>P. fluorescens</i> from [1].  
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<p>Ribosome Binding Site of gene <i>aprA</i> from <i>P. protogens</i>. It was used for protein translation in <i>P. fluorescens</i> [1].  
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This RBS was synthesized in an operon with two genes and another RBS and cloned into a plasmid. After transformation in <i>P. fluorescens</i>, our team had successful protein expression with this RBS. Check out composite part BBa_K5108009 for more information.  
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This RBS was synthesized in an operon with two genes and another RBS, and cloned into a plasmid. After transformation in <i>P. fluorescens</i>, our team had successful protein expression with this RBS. Check out composite part <a href="https://parts.igem.org/Part:BBa_K5108009" target="blank">BBa_K5108009</a>for more information.  
 
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<h2 style="color: blue;"><b>References</b></h2>
  
 
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Revision as of 13:38, 29 September 2024

aprA RBS from Pseudomonas protegens (CHA0)

Ribosome Binding Site of gene aprA of P. protogens


    Contents
  1. Usage and Biology
  2. References



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]

Usage and Biology

Ribosome Binding Site of gene aprA from P. protogens. It was used for protein translation in P. fluorescens [1]. This RBS was synthesized in an operon with two genes and another RBS, and cloned into a plasmid. After transformation in P. fluorescens, our team had successful protein expression with this RBS. Check out composite part BBa_K5108009for more information.


References

  1. Blumer, C., Heeb, S., Pessi, G., & Haas, D. (1999). Global GacA-steered control of cyanide and exoprotease production in Pseudomonas fluorescens involves specific ribosome binding sites. Proceedings Of The National Academy Of Sciences, 96(24), 14073‑14078. https://doi.org/10.1073/pnas.96.24.14073
    2.