Difference between revisions of "Team:NCKU Tainan/Integrated Human Practices"

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                                                 the factory is not completely carbon dioxide, but will contain some
 
                                                 the factory is not completely carbon dioxide, but will contain some
 
                                                 impurities like SOx and NOx. So
 
                                                 impurities like SOx and NOx. So
                                                 they asked more about whether E. coli can survive and react in this
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                                                 they asked more about whether <i>E. coli</i> can survive and react in this
 
                                                 environment. In addition, they
 
                                                 environment. In addition, they
 
                                                 also praise our idea of removing carbon and solving the disadvantages
 
                                                 also praise our idea of removing carbon and solving the disadvantages
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                                             <p class="hpcontent">Various useful advice was given by her. She emphasized
 
                                             <p class="hpcontent">Various useful advice was given by her. She emphasized
 
                                                 the
 
                                                 the
                                                 advantage of protein production by E. coli, she also suggested us
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                                                 advantage of protein production by <i>E. coli</i>, she also suggested us
 
                                                 to study more on high cell density fermentation. Without her timely
 
                                                 to study more on high cell density fermentation. Without her timely
 
                                                 advice, our team cannot improve our project.</p>
 
                                                 advice, our team cannot improve our project.</p>
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                                             <p class="hpcontent">The host organism in our project is E. coli. Professor
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                                             <p class="hpcontent">The host organism in our project is <i>E. coli</i>. Professor
 
                                                 Hashimoto is
 
                                                 Hashimoto is
                                                 familiar with the genetic manipulation of E. coli, therefore we
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                                                 familiar with the genetic manipulation of <i>E. coli</i>, therefore we
 
                                                 introduced our idea to him. One of his research is about the effect of
 
                                                 introduced our idea to him. One of his research is about the effect of
                                                 carbonic anhydrase (CA) to the growth of E. coli. Since we wanted to
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                                                 carbonic anhydrase (CA) to the growth of <i>E. coli</i>. Since we wanted to
                                                 introduce heterologous CA into the E. coli, he suggested us to consider
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                                                 introduce heterologous CA into the <i>E. coli</i>, he suggested us to consider
                                                 whether it will compete with the native CA of E.coli, which might
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                                                 whether it will compete with the native CA of <i>E. coli</i>, which might
 
                                                 affect the function of the heterologous CA. Also, Professor Hashimoto
 
                                                 affect the function of the heterologous CA. Also, Professor Hashimoto
 
                                                 introduced the concept of homologous recombination to us as we had the
 
                                                 introduced the concept of homologous recombination to us as we had the
                                                 idea to insert our construction into E.coli chromosome. However, we
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                                                 idea to insert our construction into <i>E. coli</i> chromosome. However, we
 
                                                 were suggested not to do the homologous recombination due to the
 
                                                 were suggested not to do the homologous recombination due to the
 
                                                 limited time we had. </p>
 
                                                 limited time we had. </p>
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                                             <p class="hpcontent">After the discussion, we started to review journals
 
                                             <p class="hpcontent">After the discussion, we started to review journals
 
                                                 and found out the
 
                                                 and found out the
                                                 feasibility of expressing both native and non-native CA in E. coli. We
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                                                 feasibility of expressing both native and non-native CA in <i>E. coli</i>. We
 
                                                 found out that there were research which expressed heterologous CA
 
                                                 found out that there were research which expressed heterologous CA
 
                                                 successfully. Therefore we decided to clone the CA gene into the E
 
                                                 successfully. Therefore we decided to clone the CA gene into the E
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                                                 possible point that is more inefficient. The benefit of the whole
 
                                                 possible point that is more inefficient. The benefit of the whole
 
                                                 project is very great. For example, what kind of way we can use to let
 
                                                 project is very great. For example, what kind of way we can use to let
                                                 every <i>E.coli</i> to eat most CO<sub>2</sub>, the way we replace our cultured <i>E.coli</i>.
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                                                 every <i>E. coli</i> to eat most CO<sub>2</sub>, the way we replace our cultured <i>E. coli</i>.
 
                                                 It is true that there are existing ways we can think more about
 
                                                 It is true that there are existing ways we can think more about
 
                                                 how we can improve. Also, professor telled us we must be very
 
                                                 how we can improve. Also, professor telled us we must be very
 
                                                 understandable about our project, it included our advantages,
 
                                                 understandable about our project, it included our advantages,
 
                                                 disadvantages, potential threat, our whole project process, and the
 
                                                 disadvantages, potential threat, our whole project process, and the
                                                 most optimum environment we should provide for our <i>E.coli</i>. The more we
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                                                 most optimum environment we should provide for our <i>E. coli</i>. The more we
 
                                                 realized our project, we could find more possibility of development. After
 
                                                 realized our project, we could find more possibility of development. After
 
                                                 talking with professor, we inspired more ideas and found direction
 
                                                 talking with professor, we inspired more ideas and found direction
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                                     <div id="cardtext">We had an opportunity to speak with Dr. Huang Chieh-Chen from
 
                                     <div id="cardtext">We had an opportunity to speak with Dr. Huang Chieh-Chen from
 
                                         NCHU, whose
 
                                         NCHU, whose
                                         work includes the reverse TCA cycle of engineered carbon capturing E. coli.</div>
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                                         work includes the reverse TCA cycle of engineered carbon capturing <i>E. coli</i>.</div>
 
                                 </div>
 
                                 </div>
 
                                 <h9>31</h9>
 
                                 <h9>31</h9>
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                                                 Chieh-Chen from National Chung Hsing University (NCHU) in the Asia
 
                                                 Chieh-Chen from National Chung Hsing University (NCHU) in the Asia
 
                                                 Pacific Conference, whose work includes the reverse TCA cycle of
 
                                                 Pacific Conference, whose work includes the reverse TCA cycle of
                                                 engineered carbon capturing E. coli. Upon our discussion, Dr. Huang
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                                                 engineered carbon capturing <i>E. coli</i>. Upon our discussion, Dr. Huang
 
                                                 raised the issue of the low efficiency of one of our enzymes, Rubisco
 
                                                 raised the issue of the low efficiency of one of our enzymes, Rubisco
                                                 and suggested that we cultured our engineered E.coli in an anaerobic
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                                                 and suggested that we cultured our engineered <i>E. coli</i> in an anaerobic
 
                                                 condition. Since Rubisco, the ribulose-1,5-biphosphate
 
                                                 condition. Since Rubisco, the ribulose-1,5-biphosphate
 
                                                 carboxylase/oxygenase is an enzyme catalyzing the reaction of either
 
                                                 carboxylase/oxygenase is an enzyme catalyzing the reaction of either
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                                                 the
 
                                                 the
 
                                                 reverse TCA cycle of
 
                                                 reverse TCA cycle of
                                                 engineered carbon capturing E. coli. Upon our discussion, Dr. Huang
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                                                 engineered carbon capturing <i>E. coli</i>. Upon our discussion, Dr. Huang
 
                                                 raised
 
                                                 raised
 
                                                 the issue of the low
 
                                                 the issue of the low
 
                                                 efficiency of one of our enzymes, Rubisco and suggested that we culture
 
                                                 efficiency of one of our enzymes, Rubisco and suggested that we culture
 
                                                 our
 
                                                 our
                                                 engineered <i>E.coli</i> in an
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                                                 engineered <i>E. coli</i> in an
 
                                                 anaerobic condition. Since Rubisco, the ribulose-1,5-biphosphate
 
                                                 anaerobic condition. Since Rubisco, the ribulose-1,5-biphosphate
 
                                                 carboxylase/oxygenase is an enzyme
 
                                                 carboxylase/oxygenase is an enzyme
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                                             <p class="hpcontent">Our project is to reuse the carbon dioxide emitted
 
                                             <p class="hpcontent">Our project is to reuse the carbon dioxide emitted
 
                                                 form the industrial
 
                                                 form the industrial
                                                 with a biological way. Although the pathway of carbon flow in E. coli
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                                                 with a biological way. Although the pathway of carbon flow in <i>E. coli</i>
 
                                                 and in microalge are quite different, it is really important for us to
 
                                                 and in microalge are quite different, it is really important for us to
 
                                                 understand the current method of biological carbon utilization before
 
                                                 understand the current method of biological carbon utilization before

Revision as of 12:34, 15 October 2018

Integrated Human Practices

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