Difference between revisions of "Part:BBa K4376003"
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Construction of the bpsA gene and tac inducible promoter to control the production of the blue-pigment indigoidine synthetase. The composite part is inserted into C.glutamicum in plasmid, resulting in the successful biosynthesis of indigodine pigment. | Construction of the bpsA gene and tac inducible promoter to control the production of the blue-pigment indigoidine synthetase. The composite part is inserted into C.glutamicum in plasmid, resulting in the successful biosynthesis of indigodine pigment. | ||
− | We amplified two bpsA fragments then transformed recombinant vector into | + | We amplified two bpsA fragments then transformed recombinant vector into DH5α E.coli strain and Corynebacterium glutamicum. |
[[File:engineering-1.png|600px||centre]] | [[File:engineering-1.png|600px||centre]] | ||
Revision as of 13:35, 11 October 2022
the composite part is used to express the bpsA gene.
Construction of the bpsA gene and tac inducible promoter to control the production of the blue-pigment indigoidine synthetase. The composite part is inserted into C.glutamicum in plasmid, resulting in the successful biosynthesis of indigodine pigment.
We amplified two bpsA fragments then transformed recombinant vector into DH5α E.coli strain and Corynebacterium glutamicum.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 3893
Illegal XhoI site found at 3046
Illegal XhoI site found at 3745 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 292
Illegal NgoMIV site found at 699
Illegal AgeI site found at 1957
Illegal AgeI site found at 2010 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 235
Illegal BsaI site found at 1546
Illegal BsaI site found at 2260
Illegal BsaI.rc site found at 364
Illegal BsaI.rc site found at 3550
Illegal SapI.rc site found at 1798