Difference between revisions of "Part:BBa K1689012"
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<partinfo>BBa_K1689012 short</partinfo>
 
<partinfo>BBa_K1689012 short</partinfo>
  
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Nterminal of β-lactamase fused with dCas9<br/>
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N-terminal fragment of β-lactamase fused with dCas9<br/>
  
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β-Lactamase(Amp) is produced by some bacteria, providing resistance against penicilins and so on. Theβ-Lactamase hydrolyzes β-lactam's conservative ring region, deactivating the antibiotic, and it can be use for the treatment of bacterial infection. <br/>
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β-Lactamase (AmpR) is produced by some bacteria, providing resistance against penicilins and so on. The β-Lactamase hydrolyzes β-lactam's conservative ring region, deactivating the antibiotic, and it can be used for the treatment of bacterial infection. <br/>
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In our project, β-Lactamase is used to catalyze the hydrolysis of penicillin to penicillinoic acid, leading to current changes to be detected using A3 electrode system. We can dissect β-Lactamase between Gly196 and Leu198, for this is opposite to the active site; meanwhile we can acquire a more active and metabolically stable pattern by introducing a mutation M182T, which disrupts an inactive molten-globule intermediate of β-Lactamase.<br/>
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In our project, β-Lactamase is used to catalyze the hydrolysis of penicillin to penicillinoic acid. This redox reaction leads to current changes, which can be detected using A3 electrode system [1]. We dissected β-Lactamase between Gly196 and Leu198 [2], for they are on the opposite side of the active site. Moreover, we can enhance the activity and metabolically stability of β-Lactamase by introducing M182T mutation [2], which disrupts an inactive molten-globule intermediate of β-Lactamase.<br/><br/>
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[https://static.igem.org/mediawiki/parts/4/4a/Peking-speculation-Amp.png  ]<br/><br/><br/>
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[[File:Peking-speculation-Amp.png|400px| ]]
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<br/><br/><br/>
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Reference:<br/>
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1. Prado, T. M., Foguel, M. V., Gonçalves, L. M., & Maria del Pilar, T. S. (2015). β-Lactamase-based biosensor for the electrochemical determination of benzylpenicillin in milk. Sensors and Actuators B: Chemical, 210, 254-258.<br/>
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2. Galarneau, A., Primeau, M., Trudeau, L. E., & Michnick, S. W. (2002). β-Lactamase protein fragment complementation assays as in vivo and in vitro sensors of protein–protein interactions. Nature biotechnology, 20(6), 619-622.<br/><br/>
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===Part Improvement===
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Group: HK_SSC, 2019 <br>
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Author: LEE Hong Kiu, CHOI Justin Yuet Hei <br>
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Please see https://parts.igem.org/Part:BBa_K3219000 for more information. <br>
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here
 
===Usage and Biology===
 
===Usage and Biology===

Latest revision as of 11:04, 13 October 2019

dCas9-Nlact

N-terminal fragment of β-lactamase fused with dCas9

β-Lactamase (AmpR) is produced by some bacteria, providing resistance against penicilins and so on. The β-Lactamase hydrolyzes β-lactam's conservative ring region, deactivating the antibiotic, and it can be used for the treatment of bacterial infection.
In our project, β-Lactamase is used to catalyze the hydrolysis of penicillin to penicillinoic acid. This redox reaction leads to current changes, which can be detected using A3 electrode system [1]. We dissected β-Lactamase between Gly196 and Leu198 [2], for they are on the opposite side of the active site. Moreover, we can enhance the activity and metabolically stability of β-Lactamase by introducing M182T mutation [2], which disrupts an inactive molten-globule intermediate of β-Lactamase.

Peking-speculation-Amp.png


Reference:
1. Prado, T. M., Foguel, M. V., Gonçalves, L. M., & Maria del Pilar, T. S. (2015). β-Lactamase-based biosensor for the electrochemical determination of benzylpenicillin in milk. Sensors and Actuators B: Chemical, 210, 254-258.
2. Galarneau, A., Primeau, M., Trudeau, L. E., & Michnick, S. W. (2002). β-Lactamase protein fragment complementation assays as in vivo and in vitro sensors of protein–protein interactions. Nature biotechnology, 20(6), 619-622.

Part Improvement

Group: HK_SSC, 2019
Author: LEE Hong Kiu, CHOI Justin Yuet Hei
Please see https://parts.igem.org/Part:BBa_K3219000 for more information.
Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1150
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 4
    Illegal BamHI site found at 3429
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]