Difference between revisions of "Part:BBa K3292001"
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<partinfo>BBa_K3292001 short</partinfo> | <partinfo>BBa_K3292001 short</partinfo> | ||
− | This device uses Bba_K2406020, | + | This device uses Bba_K2406020, Bba_K2406020 and Bba_B0010 to regulate the expression of a sialidase from M. viridifaciens. The coding sequence for this enzyme comes from Micromonospora viridifaciens and was optimized for its expression in E. coli BL21 cells. |
Encoded by the gen ned A, this enzyme releases sialic acids (N-acetylneuraminic acid) moieties from glycoproteins and glycolipids for use as carbon and energy sources due to its hydrolytic activity. | Encoded by the gen ned A, this enzyme releases sialic acids (N-acetylneuraminic acid) moieties from glycoproteins and glycolipids for use as carbon and energy sources due to its hydrolytic activity. |
Revision as of 01:14, 17 October 2019
T7-LacO Promoter + strong RBS + sialidase + sfGFP + 6x his-tag + double terminator
This device uses Bba_K2406020, Bba_K2406020 and Bba_B0010 to regulate the expression of a sialidase from M. viridifaciens. The coding sequence for this enzyme comes from Micromonospora viridifaciens and was optimized for its expression in E. coli BL21 cells.
Encoded by the gen ned A, this enzyme releases sialic acids (N-acetylneuraminic acid) moieties from glycoproteins and glycolipids for use as carbon and energy sources due to its hydrolytic activity.
Additionally, for the proper characterization of this part, the sequence of the sfGFP was added to the construct and complemented with a His-Tag to facilitate its purification.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 721
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1986
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 646
Illegal BsaI.rc site found at 510
Illegal BsaI.rc site found at 1647
Illegal SapI.rc site found at 2055