Difference between revisions of "Part:BBa K1045002:Design"
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===Source=== | ===Source=== | ||
− | This composite part consists of parts either derived from PCR amplification of ''B. subtilis'' chromosomal DNA or from the distribution kit 2013. For more information, see "Design Notes" above. | + | This composite part consists of parts either derived from PCR amplification of wild type ''B. subtilis'' chromosomal DNA (strain ''B. subtilis'' 168; Laboratory collection AG Stülke, Department for General Microbiology, University Göttingen) or from the distribution kit 2013. For more information, see "Design Notes" above. |
===References=== | ===References=== | ||
Peter Y Watson & Martha J Fedor (2012) “The ''ydaO'' motif is an ATP-sensing riboswitch in ''Bacillus subtilis''“, Nature Chemical Biology No. 8, pp. 963-965 | Peter Y Watson & Martha J Fedor (2012) “The ''ydaO'' motif is an ATP-sensing riboswitch in ''Bacillus subtilis''“, Nature Chemical Biology No. 8, pp. 963-965 |
Revision as of 18:15, 17 October 2013
CFP Reporter under control of the c-di-AMP-dependent YdaO Riboswitch
- 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 part was amplified from Bacillus subtilis genomic DNA and ligated into the EcoRI and PstI digested pSB1C3 backbone (see BBa_K1045004). It was then further SpeI and EcoRI digested and ligated with the XbaI and EcoRI digested CFP (BBa_E0020). Altogether this composes BBa_K1045002.
Source
This composite part consists of parts either derived from PCR amplification of wild type B. subtilis chromosomal DNA (strain B. subtilis 168; Laboratory collection AG Stülke, Department for General Microbiology, University Göttingen) or from the distribution kit 2013. For more information, see "Design Notes" above.
References
Peter Y Watson & Martha J Fedor (2012) “The ydaO motif is an ATP-sensing riboswitch in Bacillus subtilis“, Nature Chemical Biology No. 8, pp. 963-965