Team:TCU Taiwan/Modeling
From 2014.igem.org
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<p><font size="3" face="Verdana" color="#333">We chose two variables to find the best release amount of phage after helper phage infecting. The first variable is the time after we input helper phages M13KO7 into <em>E.Coli </em>(JM101) with phagemid pBluescript II SK(-)(We have put<a href="http://parts.igem.org/Part:BBa_I13521"> BBa_I13521</a> inside as an reporter gene.). This is the time for helper phages to infect bacterium.<br><br> | <p><font size="3" face="Verdana" color="#333">We chose two variables to find the best release amount of phage after helper phage infecting. The first variable is the time after we input helper phages M13KO7 into <em>E.Coli </em>(JM101) with phagemid pBluescript II SK(-)(We have put<a href="http://parts.igem.org/Part:BBa_I13521"> BBa_I13521</a> inside as an reporter gene.). This is the time for helper phages to infect bacterium.<br><br> | ||
After the infection, we added kanamycin into these JM101 for selection becauseJM101 can get kanamycin resistance only when they are infected by M13KO7. Then we incubated these JM101 so they can have time to release phagemid-carrying phage, and the incubating time is the second variable in our test.<br><br> | After the infection, we added kanamycin into these JM101 for selection becauseJM101 can get kanamycin resistance only when they are infected by M13KO7. Then we incubated these JM101 so they can have time to release phagemid-carrying phage, and the incubating time is the second variable in our test.<br><br> | ||
- | As we can see in this figure, the most amount of phage being released is at the time when we add kanamycin after 30 minutes of infection and then incubate them for 14 hours. Under this condition, the best releasing amount of phage is 4×10^10 pfu/ml.</font></p | + | As we can see in this figure, the most amount of phage being released is at the time when we add kanamycin after 30 minutes of infection and then incubate them for 14 hours. Under this condition, the best releasing amount of phage is 4×10^10 pfu/ml.</font></p><br><br> |
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<font size="3" face="Verdana" color="#333"><p>Then we came up with another question: Under which condition will we get the best infection rate of our phagemid-carrying phage? We believe this is influenced by the MOI between phages and bacterium. MOI means multiplicity of infection, it is the ratio of agents (phage-carrying phage) to infection targets (<em>E.coli</em> JM101). So we choose MOI as the variable, and incubate bacterium for 1 hour after infecting.<br> | <font size="3" face="Verdana" color="#333"><p>Then we came up with another question: Under which condition will we get the best infection rate of our phagemid-carrying phage? We believe this is influenced by the MOI between phages and bacterium. MOI means multiplicity of infection, it is the ratio of agents (phage-carrying phage) to infection targets (<em>E.coli</em> JM101). So we choose MOI as the variable, and incubate bacterium for 1 hour after infecting.<br> | ||
- | In our test, we found that as long as the MOI is higher than 6 pfu/cfu, the infection rate can access 100%. This is an exciting result!!</p></font | + | In our test, we found that as long as the MOI is higher than 6 pfu/cfu, the infection rate can access 100%. This is an exciting result!!</p></font><br><br> |
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Revision as of 19:01, 15 October 2014
Modeling |
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