Difference between revisions of "Part:BBa I723019:Design"
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| − | <partinfo> | + | <partinfo>BBa_I723019 short</partinfo> |
| − | <partinfo> | + | <partinfo>BBa_I723019 SequenceAndFeatures</partinfo> |
===Design Notes=== | ===Design Notes=== | ||
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| + | '''''It does not physically exist as a basic part due to time constraints; it was cloned as part of composite part which incorporates all of the components necessary for expression of a reporter gene under the control of DntR.''''' For this reason, the ends of the supplied sequence may not accurately represent the boundaries of the functional unit. | ||
===Source=== | ===Source=== | ||
Latest revision as of 16:26, 25 October 2007
RBS for XylR
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
It does not physically exist as a basic part due to time constraints; it was cloned as part of composite part which incorporates all of the components necessary for expression of a reporter gene under the control of DntR. For this reason, the ends of the supplied sequence may not accurately represent the boundaries of the functional unit.
Source
Cloned from the TOL plasmid from Pseudomonas putida MT2
References
Worsey, M., and Williams, P. 1975. Metabolism of toluene and xylenes by Pseudomonas putida (arvilla) MT-2: evidence for a new function of the TOL plasmid. J Bacteriol 124, 7-13.