Difference between revisions of "Part:BBa K4837000:Design"
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===Design Notes=== | ===Design Notes=== | ||
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+ | <a href='https://static.igem.wiki/teams/4837/wiki/engineering-plasmid.png' target="_blank"><img src="https://static.igem.wiki/teams/4837/wiki/engineering-plasmid.png" width="100%"/> | ||
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+ | pSBIK3 vector was adopted in this plasmid.The promoter used in these two basic parts was arabinose promoter. Purification tag and fluorescent tag were also included for better detection of the optimized enzyme synthesized. | ||
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+ | Other biobricks such as BBa_K4837001 are required to perform its function. | ||
===Source=== | ===Source=== |
Revision as of 00:15, 12 October 2023
Lignin peroxidase
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 126
Illegal NheI site found at 1694 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 66
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 260
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 2352
Design Notes
pSBIK3 vector was adopted in this plasmid.The promoter used in these two basic parts was arabinose promoter. Purification tag and fluorescent tag were also included for better detection of the optimized enzyme synthesized.
Other biobricks such as BBa_K4837001 are required to perform its function.
Source
It is designed based on part of Phanerochaete chrysosporium.