Difference between revisions of "Part:BBa K2273116:Design"
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===References=== | ===References=== | ||
+ | [http://www.subtiwiki.uni-goettingen.de/v3/gene/view/713BAB7190E1F86C55103049B29072F00E0DFFB3] | ||
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+ | [http://www.uniprot.org/uniprot/P39824] | ||
+ | |||
+ | Marta Toth <i>et al.</i> (2015) Class D Beta-Lactamases Do Exist in Gram-Positive Bacteria. <i>Nature Chemical Biology</i> <b>(12)</b>: 9-14. |
Revision as of 13:16, 3 October 2017
Long version of the Promoter PpenP found in B. subtilis
- 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 designed to be cloned in front of the luxABCDE operon serving a a reporter gene in the pBS3C vector backbone. Therefore, the RFC10 Standard Restriction sites have been added as prefix and suffix via PCR.
RFC10 prefix and suffix sequences:
Prefix with | EcoRI, NotI, XbaI | GAATTCGCGGCCGCTTCTAGA |
Suffix with | SpeI, NotI and PstI | ACTAGTAGCGGCCGCTGCAGA |
Sites of restriction enzymes generating compatible overhangs are indicated by sharing one color. (EcoRI and PstI are marked in blue, NotI in green, XbaI and SpeI in red
As the overall promoter sequence was amplified from the B.subtilis W168 genome using primers featuring the RFC10 standard restriction sites:
Forward Primer Sequence containing RFC10 prefix: 5`-gatcGGAATTCGCGGCCGCTTCTAGATCTGGTTTTATGCTTAATCCTC-3`
Revers Primer Sequence containing RFC10 suffix: 5`-gatcCTGCAGCGGCCGCTACTAGTTCAAATGATTTTGTATTACCTTTG-3`
Source
This part sequence was derived from the Bacillus subtilis W168 genome sequence.
References
[http://www.subtiwiki.uni-goettingen.de/v3/gene/view/713BAB7190E1F86C55103049B29072F00E0DFFB3]
[http://www.uniprot.org/uniprot/P39824]
Marta Toth et al. (2015) Class D Beta-Lactamases Do Exist in Gram-Positive Bacteria. Nature Chemical Biology (12): 9-14.