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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 | + | 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 | + | 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 | + | <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 | + | 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 | + | 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 | + | 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 | + | 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 | + | 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 | + | 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>. | + | 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 | + | 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> | + | 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 | + | 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 | + | 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 | + | 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 | + | 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 | + | 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