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<p>Broad Host Range assemblies encoding a shuttle vector, pAMBI, were assembled using standard Golden Gate assembly protocols. BHR 925 (E2-Crimson + pAMBI Origin + CRB resistance), 920 (E2-Crimson + pAMBI Origin + KAN resistance), and 922 produced darker, bluish colonies under visible light. When viewed under a UV light, the colonies were red, indicating the successful expression of E2-Crimson</p> | <p>Broad Host Range assemblies encoding a shuttle vector, pAMBI, were assembled using standard Golden Gate assembly protocols. BHR 925 (E2-Crimson + pAMBI Origin + CRB resistance), 920 (E2-Crimson + pAMBI Origin + KAN resistance), and 922 produced darker, bluish colonies under visible light. When viewed under a UV light, the colonies were red, indicating the successful expression of E2-Crimson</p> | ||
− | <figure> <img class="squad" src = "https://static.igem.org/mediawiki/2018/0/0e/T--Austin_UTexas--ShuttleVectorAssembly1.jpeg | + | <figure> <img class="squad" src = "https://static.igem.org/mediawiki/2018/0/0e/T--Austin_UTexas--ShuttleVectorAssembly1.jpeg"> |
<figcaption> | <figcaption> | ||
<b>Fig 1. BHR 925 Golden Gate Assembly</b> | <b>Fig 1. BHR 925 Golden Gate Assembly</b> | ||
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− | <figure><img class="squad" src = "https://static.igem.org/mediawiki/2018/c/c6/T--Austin_UTexas--ShuttleVectorAssembly2.png | + | <figure><img class="squad" src = "https://static.igem.org/mediawiki/2018/c/c6/T--Austin_UTexas--ShuttleVectorAssembly2.png"> |
<figcaption> <b>Fig 2.</b> Sequence alignment of BHR 925 | <figcaption> <b>Fig 2.</b> Sequence alignment of BHR 925 | ||
Sequencing confirmed the BHR 4 barcode, BHR 701 (origin of transfer), and forward portion of the pAMBI origin were present in the BHR 925 assembly. Sequencing was inconclusive for BHR 922 but colonies grew on KAN plate and expressed E2- Crimson. | Sequencing confirmed the BHR 4 barcode, BHR 701 (origin of transfer), and forward portion of the pAMBI origin were present in the BHR 925 assembly. Sequencing was inconclusive for BHR 922 but colonies grew on KAN plate and expressed E2- Crimson. |
Revision as of 00:35, 15 October 2018
Assembly Plasmids
Using five single parts and one bridge-type part, full plasmids are assembled in a single BsaI reaction. An assembled plasmid then contains an antibiotic resistance gene, origin of replication, origin of transfer, barcode sequence, and a part 1-5 bridge, which contains a colored reporter protein coding sequence. The same promoters, terminators, and origins of transfer are used within all assemblies. This is not true for the barcode, and reporter protein sequences, as they indicated which origin of replication the plasmid contains. This design eliminates as many variables as possible, allowing the origin of replication to be the single largest factor determining whether or not the bacteria sustain and express the plasmid.
Shuttle Vector Assemblies
Broad Host Range assemblies encoding a shuttle vector, pAMBI, were assembled using standard Golden Gate assembly protocols. BHR 925 (E2-Crimson + pAMBI Origin + CRB resistance), 920 (E2-Crimson + pAMBI Origin + KAN resistance), and 922 produced darker, bluish colonies under visible light. When viewed under a UV light, the colonies were red, indicating the successful expression of E2-Crimson
Minpreps of the BHR 922 assemby, which produced colonies but was shown to be only the E2-Crimson 1 – 5 bridge, was re-transformed into E. coli along with BHR 920 and BHR 925 to better view expression