Difference between revisions of "Team:HokkaidoU Japan/Proof"

 
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The results are shown the below pictures. The fluorescence of GFPs was not detected any condition.
 
The results are shown the below pictures. The fluorescence of GFPs was not detected any condition.
 
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Latest revision as of 03:10, 20 October 2016

Team:HokkaidoU Japan - 2016.igem.org

 

Team:HokkaidoU Japan

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Proof of concept

We made a functional unit to regulate gene expression. BBa_K2015012 codes constitutive promoter (BBa_J23101), RBS (BBa_B0032), LacI (BBa_C0012), dT (BBa_B0015), PLac (BBa_R0011) and RBS (BBa_B0034). To insert mRFP at the downstream we identified this construct could regulate the expression (Fig. 1).
result1
Fig. 1. Change of expression by IPTG induction
left: not induced, right: induced


And also we induced BBa_K2015012 + BBa_K2015008 / BBa_K2015012 + BBa_K2015009 on pSB1C3 of E. coli (DH5α). BBa_K2015008 consists Self Assembling Regions (SAR, RADA16-I) and GFP. And BBa_K2015009 this part consists Self Assembling Region (SAR, P11-4) and GFP.


The results are shown the below pictures. The fluorescence of GFPs was not detected any condition.
result1
Fig. 2. BBa_K2015012-BBa_K2015008
BBa_K2015012-BBa_K2015008 on pSB1C3 vector were induced by IPTG and incubated at 37°C. (-): not induced, (+): 0.5 mM IPTG and (++): 1.0 mM IPTG

result2 result3
Fig. 3. BBa_K2015012-BBa_K2015009
BBa_K2015012-BBa_K2015009 on pSB1C3 vector were induced by IPTG and incubated at 25°C for 24 h (left)
and at 37°C for 16 h (right). (-): not induced, (+): 0.5 mM IPTG and (++): 1.0 mM IPTG