Difference between revisions of "Part:BBa K5226024"

 
 
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<partinfo>BBa_K5226024 short</partinfo>
 
<partinfo>BBa_K5226024 short</partinfo>
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===Sequence and Features===
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<partinfo>BBa_K5226024 SequenceAndFeatures</partinfo>
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<br>
  
One of the goals of iGEM24-SCUT-China-A is to use synthetic biology tools to obtain Halomonas TD strains that can metabolize formate. We chose to introduce the formate assimilation pathway to enable it to utilize formate, a difficult-to-recover product in CDE. As a second approach, based on the homology between Vibrio natriegens and Halomonas TD, we chose to import the C1, C2, and C3 modules from Vibrio natriegens (parts:).
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===Introduction===
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One of the goals of iGEM24-SCUT-China-A is to use synthetic biology tools to obtain <i>Halomonas</i> TD strains that can <b>metabolize formate</b>. We chose to <b>introduce the formate assimilation pathway</b> to enable it to utilize formate, a difficult-to-recover product in CDE. As a second approach, <b>based on the homology between <i>Vibrio natriegens</i> and <i>Halomonas</i> TD</b>, we chose to <b>import the C1, C2, and C3 modules from <i>Vibrio natriegens</i></b>.
  
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===Usage and Biology===
 
===Usage and Biology===
 
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This part is a <b>native ribosomal binding site of Vib-gcvT</b>, which has not yet been characterized. We assessed the ease of plasmid construction and ultimately chose to utilize this part in the composite parts to <b>facilitate the expression of aminomethyltransferase.</b>
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<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K5226024 SequenceAndFeatures</partinfo>
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Latest revision as of 02:37, 14 September 2024

RBS for Vib-gcvT

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]


Introduction

One of the goals of iGEM24-SCUT-China-A is to use synthetic biology tools to obtain Halomonas TD strains that can metabolize formate. We chose to introduce the formate assimilation pathway to enable it to utilize formate, a difficult-to-recover product in CDE. As a second approach, based on the homology between Vibrio natriegens and Halomonas TD, we chose to import the C1, C2, and C3 modules from Vibrio natriegens.

Usage and Biology

This part is a native ribosomal binding site of Vib-gcvT, which has not yet been characterized. We assessed the ease of plasmid construction and ultimately chose to utilize this part in the composite parts to facilitate the expression of aminomethyltransferase.