Difference between revisions of "Part:BBa K5226052"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K5226052 short</partinfo> | <partinfo>BBa_K5226052 short</partinfo> | ||
+ | ===Sequence and Features=== | ||
+ | <partinfo>BBa_K5226052 SequenceAndFeatures</partinfo> | ||
+ | <br> | ||
+ | ===Introduction=== | ||
+ | One of the goals of iGEM SCUT-China-A is to use synthetic biology tools to obtain ,<i>Halomonas</i> strains that can produce tyrian purple. We chose to introduce four enzymes that is either necessary or beneficial to the production of tyrian purple. | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
+ | This part is a <b>native ribosomal binding site of stth</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 facilitate the expression of Stth. | ||
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Revision as of 07:13, 30 September 2024
321(C+cysNC) backbone
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Plasmid lacks a prefix.
Plasmid lacks a suffix. - 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix. - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal BamHI site found at 2528 - 23INCOMPATIBLE WITH RFC[23]Plasmid lacks a prefix.
Plasmid lacks a suffix. - 25INCOMPATIBLE WITH RFC[25]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal NgoMIV site found at 2981
Illegal NgoMIV site found at 3866
Illegal NgoMIV site found at 4977
Illegal NgoMIV site found at 5101
Illegal AgeI site found at 2037 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal SapI site found at 2103
Illegal SapI.rc site found at 2171
Introduction
One of the goals of iGEM SCUT-China-A is to use synthetic biology tools to obtain ,Halomonas strains that can produce tyrian purple. We chose to introduce four enzymes that is either necessary or beneficial to the production of tyrian purple.
Usage and Biology
This part is a native ribosomal binding site of stth, 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 Stth.