Difference between revisions of "Part:BBa K5108006"
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+ | <ol style="color: black; padding: auto -1rem; margin= 0"> <b>Contents</b> | ||
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This RBS was synthesized in an operon with two genes and another RBS and cloned into a plasmid. After transformation in <i>P. fluorescens</i>, our team had successful protein expression with this RBS. Check out composite part BBa_K5108009 for more information. | This RBS was synthesized in an operon with two genes and another RBS and cloned into a plasmid. After transformation in <i>P. fluorescens</i>, our team had successful protein expression with this RBS. Check out composite part BBa_K5108009 for more information. | ||
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+ | <h2 style="color: blue;"><b>References</b></h2> | ||
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Revision as of 09:41, 29 September 2024
aprA RBS from Pseudomonas protegens (CHA0)
aprA RBS from Pseudomonas protegens (CHA0)
- Contents
- Usage and Biology
- References
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]
Usage and Biology
Ribosome Binding Site of gene aprA of P. fluorescens. It was used for protein translation in P. fluorescens from [1]. This RBS was synthesized in an operon with two genes and another RBS and cloned into a plasmid. After transformation in P. fluorescens, our team had successful protein expression with this RBS. Check out composite part BBa_K5108009 for more information.
References
- Blumer, C., Heeb, S., Pessi, G., & Haas, D. (1999). Global GacA-steered control of cyanide and exoprotease production in Pseudomonas fluorescens involves specific ribosome binding sites. Proceedings Of The National Academy Of Sciences, 96(24), 14073‑14078. https://doi.org/10.1073/pnas.96.24.14073