Difference between revisions of "Team:CHINA CD UESTC/Future"

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&nbsp;&nbsp;In order to further improve our project, our work is going on in two aspects: (1) making <i>E.coli</i> produce magnetosomes stably;(2) improving our EBFC. If you have any better ideas, please tell us.
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&nbsp;&nbsp;In order to further improve our project, our work is going on in two aspects: (1) making <i>E.coli</i> produce magnetosomes stably; (2) improving our EBFC. If you have any better ideas, please tell us.
 
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(1)Our project has already realized the fusion expression of red fluorescent protein and laccase, and laccase has great activity. We also successfully constructed the recombinant expression vector of <i>mamW</i>+RFP +laccase, but the expression quantity and activity didn’t up to our expectation. <strong>So next</strong>, to increase the expression quantity of mamW+RFP+laccase fusion protein and realize their respective functions, we are planning to optimize the induction condition.
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(1) Our project has already realized the fusion expression of red fluorescent protein and laccase, and laccase has great activity. We also successfully constructed the recombinant expression vector of <i>mamW</i>+RFP +laccase, but the expression quantity and activity didn’t up to our expectation. <strong>So next</strong>, to increase the expression quantity of mamW+RFP+laccase fusion protein and realize their respective functions, we are planning to optimize the induction condition.
 
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(2)We transformed the four operons related to magnetosome formation into <i>E.coli</i> and found some structures like magnetosome crystals. In order to verify these structures, <strong>we are going on</strong> verifying the native promoters whether they can work in <i>E.coli</i> stably.
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(2) We transformed the four operons related to magnetosome formation into <i>E.coli</i> and found some structures like magnetosome crystals. In order to verify these structures, <strong>we are going on</strong> verifying the native promoters whether they can work in <i>E.coli</i> stably.
 
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(3)We are cloning single gene related to magnetosome formation explore to investigate the function of every gene. After the basic function of each gene was found, we will simplify the expression system of magnetosome formation, to find the essential genes of magnetosome formation and simplify the expression system.
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(3) We are cloning single gene related to magnetosome formation explore to investigate the function of every gene. After the basic function of each gene was found, we will simplify the expression system of magnetosome formation, to find the essential genes of magnetosome formation and simplify the expression system.
 
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Revision as of 05:55, 16 September 2015


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FUTURE

  In order to further improve our project, our work is going on in two aspects: (1) making E.coli produce magnetosomes stably; (2) improving our EBFC. If you have any better ideas, please tell us.

Work going on

  • (1) Our project has already realized the fusion expression of red fluorescent protein and laccase, and laccase has great activity. We also successfully constructed the recombinant expression vector of mamW+RFP +laccase, but the expression quantity and activity didn’t up to our expectation. So next, to increase the expression quantity of mamW+RFP+laccase fusion protein and realize their respective functions, we are planning to optimize the induction condition.

  • (2) We transformed the four operons related to magnetosome formation into E.coli and found some structures like magnetosome crystals. In order to verify these structures, we are going on verifying the native promoters whether they can work in E.coli stably.

  • (3) We are cloning single gene related to magnetosome formation explore to investigate the function of every gene. After the basic function of each gene was found, we will simplify the expression system of magnetosome formation, to find the essential genes of magnetosome formation and simplify the expression system.

    (4) We are improving our EBFC to reduce the internal resistance and lower the cell cost. Meanwhile, we are optimizing the types and contents of the components in the cell to increase the efficiency of electricity generation.

Application Prospect

  • (1) Energy: We made an enzyme biofuel cell ourselves, we used glucose oxidase at the anode, it can provide electrons to the cathode. Laccase was used at the cathode; it can catalyze the oxidation of a variety of aymolytes and at the same time reduce oxygen to water, with copper ion active center as a support group. Our purpose is to express laccase on the membrane of magnetosome, thus increases the concentration of laccase, increase the efficiency of electron transfer. Similarly, we can replace laccase with glucose oxidase and can fix glucose oxidase at the anode to improve electron transfer efficiency of the anode. If more efficient and stable enzymes could be found, the enzyme fuel cell will replace the existing lithium-ion batteries and others.

  • (2) Medical treatment: Laccase of mamW + RFP + laccase expression vector can be replaced to antibody drugs, the expressed magnetosomes can carry antibody drugs. So it can realize target therapy under the action of outside or internal magnetic field.

  • (3) Biosensor : We can refit our enzyme fuel cell into a small biosensor to detect the concentration of sugar and polyphenols in sewage. At the same time, if we can transplant these biosensors to human bodies, we can monitor blood glucose levels in diabetics in real time.

    (4) Environment : Laccase can decompose many kinds of phenol and aromatic amine compounds, etc. Immobilizing laccase can realize the degradation of phenol and aromatic amine compounds and generate electricity at the same time.

    (5) Food industry : Laccase can be used to remove phenol turbidity of fruit juice and beer, realizing the long-term storage of them. At the same time, the device can also generate electricity, realizing the energy recycling. In the papermaking industry, laccase can selectively degrade lignin to produce pulp.

In addition, we believe that our project has a lot of potential application values to be found. We believe that under the impetus of the science and technology, things seems impossible before will become possible.