Difference between revisions of "Team:Peking"

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out design is a CRISPR based DNA replication control system
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Through a series of demonstration experiments, we have proved that our system can increase the expression of some products, and our strain has good adhesion.
 
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</p>
 
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</center>
 
</center>
 
<p>
 
<p>
out design is a CRISPR based DNA replication control system
+
The function of our system is to slow down bacterial replication by combining dcas9 with oriC. On this basis, we also designed many different gene circuits to expand the function of our system.
 
</p>
 
</p>
 
</div>
 
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</center>
 
</center>
 
<p>
 
<p>
out design is a CRISPR based DNA replication control system
+
We set up a series of models to quantitatively describe and analyze our experimental phenomena. Ode, stochastic simulation and other methods are used to solve the model. Our model can explain all kinds of phenomena observed in our experiment very well. They explain the working principle of our system very well.
 
</p>
 
</p>
 
</div>
 
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</center>
 
</center>
 
<p>
 
<p>
out design is a CRISPR based DNA replication control system
+
We have carefully characterized the engineered bacteria we designed, found that they can work in the way we expected, and explored their potential functions.
 
</p>
 
</p>
 
</div>
 
</div>

Revision as of 01:48, 20 October 2019

Abstract

How did we think about

Scientists in the field of synthetic biology have always been making analogies between elements in a cell and electronic components. They want to make a rigid and immutable framework. However, even E. coli, the most ordinary host cell in a lab, can exhibit remarkable variance in its general physiology, and can be characterized from different aspects. These parameters can affect the 'desired' function of synthetic bio-parts directly or indirectly, which makes it difficult to build an absolutely rigid system. Previously, scientists using antibiotic or killer switch to kill the cell completely in order to control cell growth. But we thought that a reversible and tunable tool can be a better way to control cell growth. Curious about solving this problem, we took months of work to build our system, the dCas9 based DNA replication control system, a growth control toolbox directly targeting genome replication.

Demonstrate

Through a series of demonstration experiments, we have proved that our system can increase the expression of some products, and our strain has good adhesion.

Design

The function of our system is to slow down bacterial replication by combining dcas9 with oriC. On this basis, we also designed many different gene circuits to expand the function of our system.

Model

We set up a series of models to quantitatively describe and analyze our experimental phenomena. Ode, stochastic simulation and other methods are used to solve the model. Our model can explain all kinds of phenomena observed in our experiment very well. They explain the working principle of our system very well.

Results

We have carefully characterized the engineered bacteria we designed, found that they can work in the way we expected, and explored their potential functions.