Difference between revisions of "Part:BBa K2675013"
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===Usage and Biology=== | ===Usage and Biology=== | ||
− | This RBS was used to drive the expression of PelB-SAIRGA ([[Part:BBa_K2675003|BBa_K2675003]]) under the control of the | + | This RBS was used to drive the expression of PelB-SAIRGA ([[Part:BBa_K2675003|BBa_K2675003]]) under the control of the [[Part:BBa_J23100|BBa_J23100]] promoter in the composite part [[Part:BBa_K2675043|BBa_K2675043]]. |
Using the Salis Lab RBS calculator v2.0 [1, 2], the predicted features of this RBS are: | Using the Salis Lab RBS calculator v2.0 [1, 2], the predicted features of this RBS are: | ||
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Accuracy (warnings) : NoEQ | Accuracy (warnings) : NoEQ | ||
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+ | <h2 style="font-weight:800;">REFERENCES</h2> | ||
+ | <p style="font-size:15px;" class="bibliographie">[1] Espah Borujeni A, Channarasappa AS, Salis HM. Translation rate is controlled by coupled trade-offs between site accessibility, selective RNA unfolding and sliding at upstream standby sites. Nucleic Acids Res (2014) 42, 2646-2659.</p> | ||
+ | <p style="font-size:15px;" class="bibliographie">[2] Salis HM, Mirsky EA, Voigt CA. Automated design of synthetic ribosome binding sites to control protein expression. Nat Biotechnol (2009) 27, 946-50.</p> | ||
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> |
Latest revision as of 21:04, 15 October 2018
Synthetic RBS designed for PelB-SAIRGA
This part is a synthetic RBS designed for PelB-SAIRGA (BBa_K2675003) using the Salis Lab RBS calculator v2.0 [1, 2].
Usage and Biology
This RBS was used to drive the expression of PelB-SAIRGA (BBa_K2675003) under the control of the BBa_J23100 promoter in the composite part BBa_K2675043.
Using the Salis Lab RBS calculator v2.0 [1, 2], the predicted features of this RBS are: Translation Initiation Rate (au) : 413347,83 dG_total (kcal/mol) : -12,92 dG_mRNA_rRNA (kcal/mol) : -22,03 dG_spacing (kcal/mol) : 0 dG_standby (kcal/mol) : 0 dG_start (kcal/mol) : -2,76 dG_mRNA (kcal/mol) : -12,44 Accuracy (warnings) : NoEQ
REFERENCES
[1] Espah Borujeni A, Channarasappa AS, Salis HM. Translation rate is controlled by coupled trade-offs between site accessibility, selective RNA unfolding and sliding at upstream standby sites. Nucleic Acids Res (2014) 42, 2646-2659.
[2] Salis HM, Mirsky EA, Voigt CA. Automated design of synthetic ribosome binding sites to control protein expression. Nat Biotechnol (2009) 27, 946-50.
Sequence and Features
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]