Team:BNU-China/Results
Results
Microtubule
Plasmid construction
We have accomplished the construction of 6 main parts whose functions are described respectively in previous design page. (Microtubule module)
Figure 1 The electrophoresis image of these 6 plasmids.
Protein expression
These are images recorded by the Fluorescence microscope.The engineered yeasts were induced at 30°C for 20 hours. And from the image, we can notice that our engineered yeasts have successfully expressed our recombinant proteins mCherry-αand mCherry. Moreover, the expression rate of mCherry is almost up to 100%.
Figure 2 Induced 20h in SG-Ura medium；
A,B recipient strain with empty plasmid; C a bright-field micrograph of S. cerevisiae
INVSc1 cells harbouring pYCα–mCherry-α; D fluorescence micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–mCherry-α;
E a bright-field micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–mCherry; F fluorescence micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–mCherry;
The image shows the results of a Western blot analysis carried out with an anti-V5 antibody. The target proteins are expressed by the engineered yeasts which contain pYCα-alpha, pYCα-beta, pYCα-mCherry and pYCα-mCherry-αtubulin, respectively.
Figure 3 The results of a Western blot analysis carried out with an anti-V5 antibody.
Our engineered yeasts, containing pYD1-β tubulin vector, have been proved successfully expressing exogenous βtubulin by Western blot analysis.
Figure 4 The partly results of a Western blot analysis carried out with an anti-V5 antibody.
Flagellar Filament
Plasmid construction
We have successfully constructed the following 11 parts that have been described in detail in previous design page. (Filagellar filament module)The parts are named: , , , ,
The electrophoresis image of our parts.
Protein expression
The below image shows the expression of the S. cerevisiae INVSc1 cells harbouring pYCα-FilC-eGFP. The strong fluorescence signal validates the expression of recombinant protein: FilC fused with eGFP.
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