Difference between revisions of "Part:BBa K3425032"
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</p> | </p> | ||
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− | <b> | + | <b>Aligned Spacing</b> |
<p> | <p> | ||
The distance between an RBS and a start codon is an important factor affecting the strength of an RBS. Whereas BioBrick assembly generates six-nucleotide scar between the RBS and the start codon, | The distance between an RBS and a start codon is an important factor affecting the strength of an RBS. Whereas BioBrick assembly generates six-nucleotide scar between the RBS and the start codon, | ||
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for its use in Type IIS assembly. However, note that the nucleotides of the spacer are different from the BioBrick scar, which might influence the performance of RBS. | for its use in Type IIS assembly. However, note that the nucleotides of the spacer are different from the BioBrick scar, which might influence the performance of RBS. | ||
</p> | </p> | ||
− | <b> | + | <b>Sequence Context Dependence</b> |
− | + | ||
− | + | ||
− | + | ||
− | + | ||
+ | <p> | ||
+ | Generally, the strength of an RBS depends heavily on <i><b>1)</b> the sequence of the RBS <b>2)</b> the aligned spacing and <b>3)</b> the upstream and downstream genetic context.</i> Therefore, the same RBS element performs differently in different sequence context. This means, that identical RBS element results in different expression levels for different genes. An interesting solution to this problem might be implementation of bicistronic architecture [1], for example BCD2 | ||
+ | <a href="https://parts.igem.org/Part:BBa_K1114107">BBa_K1114107</a> or | ||
+ | <a href="https://parts.igem.org/Part:BBa_J364100">BBa_J364100</a>. | ||
+ | </p> | ||
+ | <b>Characterization Issues</b> | ||
+ | <p> | ||
+ | The ancestral RBS of this part, | ||
+ | <a href="https://parts.igem.org/Part:BBa_B0034">BBa_B0034</a> | ||
+ | was characterized as medium strong. However, due to the inherent dependence on the sequence context described above, the results are necessarily affected by the choice of the reporter. | ||
+ | <br> | ||
In line with that, previous characterizations report different relative strengths of <a href="https://parts.igem.org/Part:BBa_B0034">BBa_B0034</a> and other members of <a href="https://parts.igem.org/Ribosome_Binding_Sites/Prokaryotic/Constitutive/Community_Collection"> RBS Community Collection</a>. | In line with that, previous characterizations report different relative strengths of <a href="https://parts.igem.org/Part:BBa_B0034">BBa_B0034</a> and other members of <a href="https://parts.igem.org/Ribosome_Binding_Sites/Prokaryotic/Constitutive/Community_Collection"> RBS Community Collection</a>. | ||
+ | </p> | ||
+ | <p> | ||
Aligned spacing is the distance between the centre of Shine-Dalgarno sequence and ATG start codon (see <a href="https://parts.igem.org/Ribosome_Binding_Sites/Design">iGEM resources</a>or [1]). Aligned spacing gener6lly varies from 5 to 13 bases [1] and optimal distance varies for organisms. Final aligned spacing of BBa_K3425032 is 10 nucleotides when assembled using<a href="https://parts.igem.org/Help:Standards/Assembly/Type_IIS"> Type IIS iGEM Standard assembly</a>. | Aligned spacing is the distance between the centre of Shine-Dalgarno sequence and ATG start codon (see <a href="https://parts.igem.org/Ribosome_Binding_Sites/Design">iGEM resources</a>or [1]). Aligned spacing gener6lly varies from 5 to 13 bases [1] and optimal distance varies for organisms. Final aligned spacing of BBa_K3425032 is 10 nucleotides when assembled using<a href="https://parts.igem.org/Help:Standards/Assembly/Type_IIS"> Type IIS iGEM Standard assembly</a>. | ||
</p> | </p> | ||
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− | <span class='h3bb'>Sequence and Features</span> | + | <span class='h3bb'><b>Sequence and Features</b></span> |
<partinfo>BBa_K3425032 SequenceAndFeatures</partinfo> | <partinfo>BBa_K3425032 SequenceAndFeatures</partinfo> | ||
Revision as of 10:20, 19 October 2020
RBS for Type IIS iGEM Standard Assembly
BBa_K3425032 is an RBS (BBa_B0034) modified for Type IIS iGEM Standard assembly (RFC1000) by adding a five-nucleotide spacer (TAGTA) to the end of the sequence.
Aligned Spacing
The distance between an RBS and a start codon is an important factor affecting the strength of an RBS. Whereas BioBrick assembly generates six-nucleotide scar between the RBS and the start codon, Type IIS iGEM Standard assembly generates only one-nucleotide scar. Therefore, five nucleotides were added to the BBa_B0034 for its use in Type IIS assembly. However, note that the nucleotides of the spacer are different from the BioBrick scar, which might influence the performance of RBS.
Sequence Context DependenceGenerally, the strength of an RBS depends heavily on 1) the sequence of the RBS 2) the aligned spacing and 3) the upstream and downstream genetic context. Therefore, the same RBS element performs differently in different sequence context. This means, that identical RBS element results in different expression levels for different genes. An interesting solution to this problem might be implementation of bicistronic architecture [1], for example BCD2 BBa_K1114107 or BBa_J364100.
Characterization Issues
The ancestral RBS of this part,
BBa_B0034
was characterized as medium strong. However, due to the inherent dependence on the sequence context described above, the results are necessarily affected by the choice of the reporter.
In line with that, previous characterizations report different relative strengths of BBa_B0034 and other members of RBS Community Collection.
Aligned spacing is the distance between the centre of Shine-Dalgarno sequence and ATG start codon (see iGEM resourcesor [1]). Aligned spacing gener6lly varies from 5 to 13 bases [1] and optimal distance varies for organisms. Final aligned spacing of BBa_K3425032 is 10 nucleotides when assembled using Type IIS iGEM Standard assembly.
In conclusion, the performance of BBa_K3425032 can be only approximated by the characterization available for BBa_B0034 and it will always vary when used for expression of different genes.
Refereces
[1] Ma, J., Campbell, A., and Karlin, S. (2002) Correlations between Shine-Dalgarno Sequences and Gene Features Such as Predicted Expression Levels and Operon Structures. J. Bacteriol. 184, 5733–5745
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]