Difference between revisions of "Part:BBa K539712:Design"
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===Source=== | ===Source=== | ||
| − | The gene is cloned by Zeng lab | + | The gene is cloned by Zeng lab, NCTU-Formosa. |
It comes from Escherichia coli str. K-12 substr. MG1655 | It comes from Escherichia coli str. K-12 substr. MG1655 | ||
===References=== | ===References=== | ||
Latest revision as of 10:45, 8 October 2011
ilvD (dihydroxyacid dehydratase)
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 1721
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1507
Illegal BsaI site found at 1764
Design Notes
Because of the four RE site, EcoR1, Xba1, Spe1 and Pst1, before and after the coding sequence, those RE site should not exist in coding sequence. There is one Pst1 in original sequence of ilvD. However, the RE site in ilvD has been modified by point mutation.
Source
The gene is cloned by Zeng lab, NCTU-Formosa. It comes from Escherichia coli str. K-12 substr. MG1655