Difference between revisions of "Part:BBa K4047019"

Latest revision as of 20:05, 20 October 2021

Kanamycin Resistance for Synechococcus

Confers resistance to the antibiotic kanamycin. This sequence was used within the plasmid BBa_K4047039. This plasmid, which deletes the target gene glpX by insertion of kanamycin, simultaneously using this resistance-coding gene (KanR) as a selective marker for successful transformation.

Colonies were grown on BG11 media containing kanamycin. PCR was used to verify the change in genomic content, with an increasing band width indicating successful integration of the kanamycin resistance gene into the target site. See the Experience tab for more details on the successful operation of this part in the MiamiU_OH project.

This part is only the coding region for kanamycin resistance, with the promoter BBa_K4047020 and terminator BBa_K4047021 being vital accessory components to its functional operation.

This part is an improvement to the documented part BBa_K1424003, which was optimized for Synechocystis sp. PCC 6803. This has been optimized here for use in the organism Synechococcus elongatus PCC 7942, and as such has a different DNA sequence.

Sequence and Features

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
COMPATIBLE WITH RFC[12]
21
INCOMPATIBLE WITH RFC[21]
Illegal XhoI site found at 782
23
COMPATIBLE WITH RFC[23]
25
COMPATIBLE WITH RFC[25]
1000
COMPATIBLE WITH RFC[1000]

@@ Line 3: / Line 3: @@
 <partinfo>BBa_K4047019 short</partinfo>
-Sequence used within the plasmid BBa_K4047039. This plasmid, which causes deletes a target gene by insertion of kanamycin, uses this resistance-coding gene (KanR) as a selective marker for successful transformation. Colonies were grown on BG11 media containing kanamycin. PCR was used to verify the change in genomic content, with an increasing band width indicating successful integration of the kanamycin resistance gene. See the Experience tab for more details on the successful operation of this part in the MiamiU_OH project.
+Confers resistance to the antibiotic kanamycin. This sequence was used within the plasmid <partinfo>BBa_K4047039</partinfo>. This plasmid, which deletes the target gene glpX by insertion of kanamycin, simultaneously using this resistance-coding gene (KanR) as a selective marker for successful transformation.
-This part is only the coding region for kanamycin resistance, with the promoter BBa_K4047020 and terminator BBa_K4047021 being vital accessory components to its functional operation.
+Colonies were grown on BG11 media containing kanamycin. PCR was used to verify the change in genomic content, with an increasing band width indicating successful integration of the kanamycin resistance gene into the target site. See the Experience tab for more details on the successful operation of this part in the MiamiU_OH project.
-This part is an improvement to the documented part K1424003, which is optimized for Synechocystis sp. PCC 6803. It has been optimized for use in the organism Synechococcus elongatus PCC 7942 here, and as such has a different part sequence.
+This part is only the coding region for kanamycin resistance, with the promoter <partinfo>BBa_K4047020</partinfo> and terminator <partinfo>BBa_K4047021</partinfo> being vital accessory components to its functional operation.
+This part is an improvement to the documented part  <partinfo>K1424003</partinfo>, which was optimized for Synechocystis sp. PCC 6803. This has been optimized here for use in the organism Synechococcus elongatus PCC 7942, and as such has a different DNA sequence.