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| | <h1 class="box-heading">Design</h1> | | <h1 class="box-heading">Design</h1> |
| − | <p>“Human Practices is the study of how your work affects the world, and how the world affects the work.” (Peter Carr, Director of Judging) is the comment which gives a clear definition of all Human Practices activities. Therefore, we tried to answer two questions: how can synthetic biology affect the world? And in which way can the world affect Iron Guardian? To answer the former one, we chose to collaborate with different teams and thought the issues we are working on vary from team to team, we all wish and try to utilize what we learn to solve practical problems and make the world a better one. What’s more, we integrated the social influence into our project to answer the latter question. With communication, economic benefit and responsibility as our important focus, we interviewed professors and employees in related industry, and showcased the great economic benefit of our project. By distributing questionnaire and analyzing the data acquired, we managed to explain and improve our project according to the public concerns and suggestions. The new concept of “3+ net” raised by ECUST will also help all teams to create, to reflect, and to improve.</p> | + | <p>no</p> |
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| | <h1 class="box-heading">Result</h1> | | <h1 class="box-heading">Result</h1> |
| − | <p>In order to test the biofilm removal effect of DSPB, we constructed the vector pET28a-DSPB</p> | + | <p>In order to test the autolysis effect of Lysin, we constructed the vector pET28a-Lysin. </p> |
| − | <p>The plasmid was transformed into E. coli BL21, cultured at 37 °C for 12 h, and the plasmid was extracted and verified by PCR.</p> | + | <p>The plasmid was transformed to E. coli BL21 and cultured at 37 °C for 12 h. positive monoclonal bacteria were cultured and verified by PCR. </p> |
| − | <p>To test the expression of DSPB, we cultured E. coli in LB medium containing 0.1% kan. E. coli was cultured at 37℃ and 220 rpm for all night, then inoculated into fresh medium and cultured until logarithmic phase.Add IPTG to final concentration of 20uM and culture E. coli over night at 25℃. Final OD600=0.437(diluted 16 fold) </p> | + | <p>In order to verify whether the cell expression of Lysin can perforate on the plasma membrane, we test the growth curve of recombinant E.coli and check them under the scanning electron microscope. </p> |
| − | <p>The expression of DSPB was verified by SDS-PAGE(Figure). The cell culture medium was blank control, and the pre-induction cell supernatant was used as a negative control. </p>
| + | <p>Recombinant bacteria is cultured by LB medium adding with 0.1% kanamycin till logarithmic phase and induced by IPTG. Then culture solution is transferred into 96-well microtiter plates and measured the light absorption of 600 nm. </p> |
| − | <p>From figure 11 we can see that there are bands at about 37 kDa, these band of experimental groups are thicker than the negative control. And our target protein is about 40kDa. We think the protein here may be DSPB. </p> | + | |
| − | <p>Then, we tested whether the engineered bacteria expressed active DSPB through enzyme activity experiments. </p>
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| − | <p>4-nitrophenyl-N-acetyl -β-D-glucosaminide(NP-GlcNAc) is hydrolysed by DspB and become 4-nitrophenol with the maximum light absorption at 405 nm. 20 mLbacteria solution is disrupted and acted supernatant as DSPB enzyme solution.
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| − | We washed and shred the bacterial solution after induction, and took the supernatant as the enzyme reaction solution of DSPB while NP-GlcNAc working as a substrate.The enzyme activity experiment was carried out by using 100 uL of enzyme reaction solution and 100 uL of substrate solution (substrate concentration is 5 mM). </p>
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| − | <p>The enzyme activity of the supernatant calculated by the enzyme activity calculation formulais (Activity/(U/mL)=(kOD405-kseldecomposition)*18231.26 *dilution ratio) is 66.363U/mL. </p>
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| − | <p>The experiment proved that the recombinant bacteria expressed active DSPB, and we used the E. coli supernatant with DSPB activity to carry out the biofilm removal experiment.DH5a was cultured overnight in LB at 37 ° C and 220 rpm, and transferred to a 96-well plate at 37 ° C and cultured for 48 h, then discarded the supernatant .The biofilm was washed with PBS, and 200 uL of the reaction solution was added to react for the whole night. Add crystal violet to stain, wash the solution into the new well plate after alcohol washing, and measure the absorbance at 570 nm. The smaller the absorbance value, the better the membrane removal effect. </p>
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| − | <p>From Fig.13, The supernatant of the recombinant E. coli has the highest biofilm removal rate, and the biofilm removal effect is getting better with time. </p>
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| | </div> | | </div> |
