Difference between revisions of "Part:BBa K1493200"
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== Ferric regulator <i>Pfri</i> == | == Ferric regulator <i>Pfri</i> == | ||
<p><i>Pfri</i> was obtained from <i>Pseudomonas putida</i> KT2440, it functions as a transcription regulator that initiates transcription of genes involved in pyoverdine synthesis. Pyoverdine is a flourescent compound that is produced by <i>P.putida</i> that binds to iron (III). This gene was used in order to try to increase pyoverdine production <i>P.putida</i> Read more on our wiki...</p> | <p><i>Pfri</i> was obtained from <i>Pseudomonas putida</i> KT2440, it functions as a transcription regulator that initiates transcription of genes involved in pyoverdine synthesis. Pyoverdine is a flourescent compound that is produced by <i>P.putida</i> that binds to iron (III). This gene was used in order to try to increase pyoverdine production <i>P.putida</i> Read more on our wiki...</p> | ||
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| + | =Characterization= | ||
| + | <p>The biobrick was tested in a shuttle plasmid (SEVA) and was coupled behind an IPTG inducible promoter. Plasmid was transformed in <i>P.putida</i> KT2440. Cultures were inoculated in 10ml M9 minimal medium containing iron and were incubated in 30°C while shaken overnight. The next morning it was noted that transformants were greener than other cultures, those being Wildtype KT2400 and <i>P.putida</i> containing an empty plasmid. | ||
| + | </p> | ||
=Characterization= | =Characterization= | ||
Revision as of 20:24, 10 October 2014
Ferric regulator Pfri
Pfri was obtained from Pseudomonas putida KT2440, it functions as a transcription regulator that initiates transcription of genes involved in pyoverdine synthesis. Pyoverdine is a flourescent compound that is produced by P.putida that binds to iron (III). This gene was used in order to try to increase pyoverdine production P.putida Read more on our wiki...
Characterization
The biobrick was tested in a shuttle plasmid (SEVA) and was coupled behind an IPTG inducible promoter. Plasmid was transformed in P.putida KT2440. Cultures were inoculated in 10ml M9 minimal medium containing iron and were incubated in 30°C while shaken overnight. The next morning it was noted that transformants were greener than other cultures, those being Wildtype KT2400 and P.putida containing an empty plasmid.
Characterization
The biobrick was tested in a shuttle plasmid (SEVA) and was coupled behind an IPTG inducible promoter. Plasmid was transformed in P.putida KT2440. Cultures were inoculated in 10ml M9 minimal medium containing iron and were incubated in 30°C while shaken overnight. The next morning it was noted that transformants were greener than other cultures, those being Wildtype KT2400 and P.putida containing an empty plasmid.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]