Difference between revisions of "Part:BBa K892009"
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The gene fucO, which codes for glycolaldehyde reductase, is one of the genes required for <i>E. coli</i> to utilize ethylene glycol as a food source. The coding sequence is put behind a strong biofab promoter and RBS. This part should be used with [https://parts.igem.org/wiki/index.php?title=Part:BBa_K892010 aldA] for the desired effect. | The gene fucO, which codes for glycolaldehyde reductase, is one of the genes required for <i>E. coli</i> to utilize ethylene glycol as a food source. The coding sequence is put behind a strong biofab promoter and RBS. This part should be used with [https://parts.igem.org/wiki/index.php?title=Part:BBa_K892010 aldA] for the desired effect. | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
− | This part was characterized by [http://2012.igem.org/Team:Washington Washington 2012] using the turbidostat. MG1655 cells were cotransformed with fucO and aldA, the assay is described on the [http://2012.igem.org/Team:Washington/Protocols/EG_Assay wiki] and | + | This part was characterized by [http://2012.igem.org/Team:Washington Washington 2012] using the turbidostat. MG1655 cells were cotransformed with fucO and aldA, the assay is described on the [http://2012.igem.org/Team:Washington/Protocols/EG_Assay wiki] and the data is also presented on the [http://2012.igem.org/Team:Washington/Plastics#Results wiki]. |
+ | [[Image:Washington_Plastic_Overview.png|border|900px|center|thumb|The fucO aldA protein pathway as part of the plastic degradation project]] | ||
− | + | <!-- Add more about the biology of this part here | |
− | + | ===Usage and Biology=== | |
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Latest revision as of 00:32, 4 October 2012
fucO
The gene fucO, which codes for glycolaldehyde reductase, is one of the genes required for E. coli to utilize ethylene glycol as a food source. The coding sequence is put behind a strong biofab promoter and RBS. This part should be used with aldA for the desired effect.
Usage and Biology
This part was characterized by [http://2012.igem.org/Team:Washington Washington 2012] using the turbidostat. MG1655 cells were cotransformed with fucO and aldA, the assay is described on the [http://2012.igem.org/Team:Washington/Protocols/EG_Assay wiki] and the data is also presented on the [http://2012.igem.org/Team:Washington/Plastics#Results wiki].
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 251
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 251
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 251
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 251
Illegal AgeI site found at 967
Illegal AgeI site found at 1168 - 1000COMPATIBLE WITH RFC[1000]