Difference between revisions of "Part:BBa K3183000:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | This promoter was specifically selected as it conformed to the RF10, RF25, and | + | This promoter was specifically selected as an ideal promoter for <i> L. reuteri </i> because it conformed to the RF10, RF12, RF21, RF23, RF25, and RF1000 standards. |
===Source=== | ===Source=== |
Revision as of 17:36, 14 October 2019
Erythromycin Constitutive Promoter
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This promoter was specifically selected as an ideal promoter for L. reuteri because it conformed to the RF10, RF12, RF21, RF23, RF25, and RF1000 standards.
Source
It is the erythromycin ribosomal methylase (ermB) promoter from the broad-host range plasmid pAMβ1 isolated from Enterococcus faecalis. We ordered the sequence as a gBlock from IDT.