Difference between revisions of "Team:JiangnanU China/Improve"
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<b>Improvement</b> | <b>Improvement</b> | ||
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<img src="https://static.igem.org/mediawiki/2019/9/95/T--JiangnanU_China--improvement_0.png" | <img src="https://static.igem.org/mediawiki/2019/9/95/T--JiangnanU_China--improvement_0.png" | ||
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| − | This year, we improved the sequence of the RBS BBa_B0033, and got the RBS BBa_K3137001. | + | This year, we improved the sequence of the RBS <a href="http://parts.igem.org/wiki/index.php/Part:BBa_B0033" style="color:blue;"alt="">BBa_B0033</a>, |
| + | and got the RBS <a href="http://parts.igem.org/Part:BBa_K3137001" style="color:blue;"alt="">BBa_K3137001</a> . | ||
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| − | <img src="https://static.igem.org/mediawiki/2019/2/22/T--JiangnanU_China-- | + | <img src="https://static.igem.org/mediawiki/2019/2/22/T--JiangnanU_China--imp.png" |
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| − | Then we ligated the two RBS with promotor rsmH (BBa_K3137000) and gene gfp (BBa_K3137011 ) and transform | + | Then we ligated the two RBS with promotor P<I>rsmH</i> (BBa_K3137000) and gene <I>gfp</i> (BBa_K3137011 ) and transform |
| − | into E. coli BL21 to compare their green fluorescence brightness. | + | into <i>E. coli</i> BL21 to compare their green fluorescence brightness. |
The figure below shows that BBa_K3137001 has the stronger fluorescently protein expression than | The figure below shows that BBa_K3137001 has the stronger fluorescently protein expression than | ||
BBa_B0033, that means it’s efficient to increase the protein expression by increasing the number of | BBa_B0033, that means it’s efficient to increase the protein expression by increasing the number of | ||
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| − | + | <img src="https://static.igem.org/mediawiki/2019/1/1b/T--JiangnanU_China--improvement_2.png" | |
| + | style="width: 42%;height: 420px;margin: 4%"> | ||
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| + | <img src="https://static.igem.org/mediawiki/2019/2/21/T--JiangnanU_China--improved2.png" | ||
| + | style="width: 50%;height: 480px;margin: 4%"> | ||
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Latest revision as of 20:08, 21 October 2019
Improvement
This year, we improved the sequence of the RBS BBa_B0033,
and got the RBS BBa_K3137001 .
As we all know, RBS refers to a sputum-rich untranslated region upstream of the initiation codon AUG.
BBa_B0033 is a weaker RBS based on Ron Weiss thesis. Compared with BBa_B0030, BBa_B0031, BBa_B0032,
BBa_B0034, B0033 is weakest, and whose RBS strength is 0.35% of B0034. By analyzing their sequence, we
found that B0033 has fewer purines and no not have AAA sequence. SO we designed the RBS by adjusting the
proportion of bases.
Then we ligated the two RBS with promotor PrsmH (BBa_K3137000) and gene gfp (BBa_K3137011 ) and transform
into E. coli BL21 to compare their green fluorescence brightness.
The figure below shows that BBa_K3137001 has the stronger fluorescently protein expression than
BBa_B0033, that means it’s efficient to increase the protein expression by increasing the number of
purines in the RBS sequence, which is beneficial to the binding of ribosomes.
