Difference between revisions of "Part:BBa K2276010"
 
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===Functional Parameters===
 
===Functional Parameters===
 
<partinfo>BBa_K2276010 parameters</partinfo>
 
<partinfo>BBa_K2276010 parameters</partinfo>
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<partinfo>BBa_K2276007 short</partinfo>
 
  
 
The part was designed based on the Part: BBa_I13521, while the RBS binding site is modified. The RBS is special designed for strainS whose last 9 nucleotides of the 16S rRNA are ACCTCCTTA. And it can be regard as a improvement for it has a high translation rate compared with Part: BBa_I13521.The promoter is TetR repressible promoter which is also used in the repressilator system. And the mRFP served as the reporter to help us measure the translation rate of the designed RBS.
 
The part was designed based on the Part: BBa_I13521, while the RBS binding site is modified. The RBS is special designed for strainS whose last 9 nucleotides of the 16S rRNA are ACCTCCTTA. And it can be regard as a improvement for it has a high translation rate compared with Part: BBa_I13521.The promoter is TetR repressible promoter which is also used in the repressilator system. And the mRFP served as the reporter to help us measure the translation rate of the designed RBS.
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===Usage and Biology===
 
===Usage and Biology===
  
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<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K2276007 SequenceAndFeatures</partinfo>
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===Measurement===
 
===Measurement===
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We constructed strains that contain Part:BBa K2276007 and measure the fluorescence intensity and OD600 changes of it. Due to the limit of the experiment condition, we measure the change at the first 8hours and 10~16 hours after inoculated separately. As what Fig 1 and Fig 2 show,Part: BBa_K2276007 has a much strong expression than Part: BBa_I13521.
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In order to improve the expression of the original part:BBa_I13521, we predicted a synthetic RBS sequence, named P3, with much higher translation initiation rate via the RBS Calculator designed by H.M. Salis, and constructed this part BBa_K2276010 containing RBS P3.
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And then, we measured the fluorescence intensity and OD600 changes of it. As Fig 1 and Fig 2 showed,Part: the expression of BBa_K2276010 was much stronger than the original part: BBa_I13521.
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In addition, we calculated the relative RBS strength via dividing the ratio of fluorescence intensity and OD 600 by fluorescence intensity of B0034. And this result further illustrated that this part contained a obviously stronger RBS than BBa_B0034. Thus, the function of the original part BBa_I13521 was indeed improved by us.  
  
 
[[File:FT3.png|500px|thumb|left|'''fig.1'''The fluorescence intensity changes over time (0h~16h). P1 represent the strain containing part: BBa_K2276007. P2 represent the strain containing part: BBa_K2276008. P3 represent the strain containing part: BBa_K2276010. TetR represent the strain that only has tetR repressible promoter without RBS and protein coding sequence. B0034 represent the strain that containing Part: BBa_I13521.
 
[[File:FT3.png|500px|thumb|left|'''fig.1'''The fluorescence intensity changes over time (0h~16h). P1 represent the strain containing part: BBa_K2276007. P2 represent the strain containing part: BBa_K2276008. P3 represent the strain containing part: BBa_K2276010. TetR represent the strain that only has tetR repressible promoter without RBS and protein coding sequence. B0034 represent the strain that containing Part: BBa_I13521.

Latest revision as of 23:22, 1 November 2017


a composite of TetR repressible promoter、special designed RBS and the coding sequence of mRFP

The part was designed based on the Part:BBa_I13521,while the RBS binding site is modified. The RBS is special designed for strainS whose last 9 nucleotides of the 16S rRNA is ACCTCCTTA.And it can be regard as a improvement for it has a high translation rate compared with Part:BBa_I13521.The promoter is TetR repressible promoter which is also used in the repressilator system. And the mRFP served as the reporter to help us measure the translation rate of the designed RBS.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 635
    Illegal AgeI site found at 747
  • 1000
    COMPATIBLE WITH RFC[1000]


Measurement

In order to improve the expression of the original part:BBa_I13521, we predicted a synthetic RBS sequence, named P3, with much higher translation initiation rate via the RBS Calculator designed by H.M. Salis, and constructed this part BBa_K2276010 containing RBS P3. And then, we measured the fluorescence intensity and OD600 changes of it. As Fig 1 and Fig 2 showed,Part: the expression of BBa_K2276010 was much stronger than the original part: BBa_I13521. In addition, we calculated the relative RBS strength via dividing the ratio of fluorescence intensity and OD 600 by fluorescence intensity of B0034. And this result further illustrated that this part contained a obviously stronger RBS than BBa_B0034. Thus, the function of the original part BBa_I13521 was indeed improved by us.

fig.1The fluorescence intensity changes over time (0h~16h). P1 represent the strain containing part: BBa_K2276007. P2 represent the strain containing part: BBa_K2276008. P3 represent the strain containing part: BBa_K2276010. TetR represent the strain that only has tetR repressible promoter without RBS and protein coding sequence. B0034 represent the strain that containing Part: BBa_I13521.
fig.2 The OD600 changes over time(0~16 h).P1 represent the strain containing part: BBa_K2276007. P2 represent the strain containing part: BBa_K2276008. P3 represent the strain containing part: BBa_K2276010. TetR represent the strain that only has tetR repressible promoter without RBS and protein coding sequence. B0034 represent the strain that containing Part: BBa_I13521.

Source

BBa_I13521

References

[1] Borujeni A E, Salis H M. Translation Initiation is Controlled by RNA Folding Kinetics via a Ribosome Drafting Mechanism[J]. Journal of the American Chemical Society, 2016, 138(22):7016.