Difference between revisions of "Part:BBa K5291031"

Line 5: Line 5:
 
A system used to deal with CO<sub>2</sub> released from <i>Pseudomonas aeruginosa</i> during PE degradation.
 
A system used to deal with CO<sub>2</sub> released from <i>Pseudomonas aeruginosa</i> during PE degradation.
  
<!-- Add more about the biology of this part here
 
 
===Usage and Biology===
 
===Usage and Biology===
 +
 +
We have known from papers related to PE degradation that during this process a huge amount of CO<sub>2</sub> will be released, which is hard to solute in the water and exists risks of exceeding the absorption limit of mangroves. Therefore, we introduce this system to address the problem of CO<sub>2</sub>. The gene <i>PAO102</i> is native in <i>Pseudomonas aeruginosa</i> and can speed up the conversion between CO<sub>2</sub> and bicarbonate. And the promoter pS is verified that it is able to come into effect in <i>P. aeruginosa</i>.<br><br>
 +
<html><img width = "550" src="https://static.igem.wiki/teams/5291/images/part-cr/pao102-schema.png" /></html><br>
 +
<b>Fig.1 The schema of pAB1-pS-<i>PAO102</i>.</b><br><br>
 +
We apply the method of <i>PAO102</i> high copies, so that CO<sub>2</sub> produced by engineered <i>P. aeruginosa</i> can be swiftly conversed to bicarbonate, easily transporting in the biofilm.<br>
 +
<html><img width = "260" src="https://static.igem.wiki/teams/5291/images/part-cr/pao102-colonypcr.png" /></html><br>
 +
<b>Fig.2 The AGE figure of <i>PAO102</i> colony PCR.</b><br><br>
  
 
<!-- -->
 
<!-- -->

Revision as of 17:50, 30 September 2024


pAB1-pS-PAO102

A system used to deal with CO2 released from Pseudomonas aeruginosa during PE degradation.

Usage and Biology

We have known from papers related to PE degradation that during this process a huge amount of CO2 will be released, which is hard to solute in the water and exists risks of exceeding the absorption limit of mangroves. Therefore, we introduce this system to address the problem of CO2. The gene PAO102 is native in Pseudomonas aeruginosa and can speed up the conversion between CO2 and bicarbonate. And the promoter pS is verified that it is able to come into effect in P. aeruginosa.


Fig.1 The schema of pAB1-pS-PAO102.

We apply the method of PAO102 high copies, so that CO2 produced by engineered P. aeruginosa can be swiftly conversed to bicarbonate, easily transporting in the biofilm.

Fig.2 The AGE figure of PAO102 colony PCR.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 110
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal PstI site found at 110
    Illegal NotI site found at 291
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 110
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 110
  • 1000
    COMPATIBLE WITH RFC[1000]