Difference between revisions of "Part:BBa K4432013"
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<partinfo>BBa_K4432013 short</partinfo> | <partinfo>BBa_K4432013 short</partinfo> | ||
− | This part is a synthetic RBS specifically designed for the ''Escherichia coli'' | + | This part is a synthetic RBS specifically designed for the ''Escherichia coli'' 1-deoxyxylulose-5-phosphate synthase (dxs) ([[Part:BBa_K3166061|BBa_K3166061]]) using the [https://www.denovodna.com/ Salis Lab RBS Calculator v2.0] [1, 2]. |
===Usage and Biology=== | ===Usage and Biology=== | ||
− | This RBS was used to drive the expression of | + | This RBS was used to drive the expression of dxs ([[Part:BBa_K3166068|BBa_K3166068]]) under the control of the T5 promoter ([[Part:BBa_K4432000|BBa_K4432000]]) in the composite parts [[Part:BBa_K4432122|BBa_K4432122]], [[Part:BBa_K4432320|BBa_K4432320]] and [[Part:BBa_K4432321|BBa_K4432321]]. |
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: |
Latest revision as of 21:48, 1 October 2022
Synthetic RBS designed for dxs
This part is a synthetic RBS specifically designed for the Escherichia coli 1-deoxyxylulose-5-phosphate synthase (dxs) (BBa_K3166061) using the Salis Lab RBS Calculator v2.0 [1, 2].
Usage and Biology
This RBS was used to drive the expression of dxs (BBa_K3166068) under the control of the T5 promoter (BBa_K4432000) in the composite parts BBa_K4432122, BBa_K4432320 and BBa_K4432321.
Using the Salis Lab RBS Calculator v2.0 [1,2], the predicted features of this RBS are:
Translation Initiation Rate (au) : 1125127.53 dG_total (kcal/mol) : -13.58 dG_mRNA_rRNA (kcal/mol) : -18.48 dG_spacing (kcal/mol) : 0.0 dG_standby (kcal/mol) : 0.0 dG_start (kcal/mol) : -1.19 dG_mRNA (kcal/mol) : -6.1 Accuracy (warnings) : OK
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
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1
Illegal BamHI site found at 8 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]