Difference between revisions of "Team:CHINA CD UESTC/Future"
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− | 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. | + | 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. | + | (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. | + | (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. | + | (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.