Difference between revisions of "Part:BBa K3332035"
 
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<partinfo>BBa_K3332035 short</partinfo>
 
<partinfo>BBa_K3332035 short</partinfo>
  
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Engineered cyan fluorescent protein tagged with ssrAtag(mf-lon), which can be recognised and degraded by mf-lon .We use it to model the feedback of mf-lon and check the function of mf-lon.
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Engineered cyan fluorescent protein tagged with ssrAtag(mf-lon), which can be recognised and degraded by mf-lon .We use it to model the feedback of mf-lon and check the function of mf-lon. ssAtag（mf-lon）is tag pdt#1，which is recognized by mf-lon hydrolases. It is attached to the 3’ end of the genes of ECFP. If there is mf-lon hydrolases, ECFP will be degraded.
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ssAtag（mf-lon）is tag pdt#1，which is recognized by mf-lon hydrolases. It is attached to the 3’ end of the genes of ECFP. If there is mf-lon hydrolases, ECFP will be degraded.
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===Usage and Biology===
 
===Usage and Biology===
  
 
[[File:2035 fig.1.png|none|500px|caption]]
 
[[File:2035 fig.1.png|none|500px|caption]]
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Fig.1 Circuit
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'''Fig 1.''' pLtetO_B0034_ecfp-ssrAtag(mf-lon)_B0015_pTrc-2 derivative_B0034_mf-lon_B0015
  
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To construct this part, we moved pLtetO-1 (BBa_K3332034) ，E0020-ssrAtag（mf-lon）(BBa_K3332035) ，Terminator(BBa_B0034)，pTrc-2 derivative promoter (BBa_K3332040) and RBS(BBa_B0034) and mf-lon(BBa_K2333011) into the expression vector pUC57 by standard assembly. Then the ligation mixture was transformed into E. coli BL21(DE3) to characterize mf-Lon hydrolase.
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To construct this part, we moved pLtetO-1 (<partinfo>BBa_K3332034</partinfo>) ，E0020-ssrAtag（mf-lon）(<partinfo>BBa_K3332035</partinfo>) ，Terminator(<partinfo>BBa_B0015</partinfo>)，pTrc-2 derivative promoter (<partinfo>BBa_K3332040</partinfo>), RBS(<partinfo>BBa_B0034</partinfo>) and mf-lon (<partinfo>BBa_K2333011</partinfo>) into the expression vector pUC57 by standard assembly. Then the ligation mixture was transformed into ''E. coli'' BL21(DE3) to characterize mf-lon hydrolase.
  
 
===Reference:===
 
===Reference:===

Latest revision as of 23:08, 27 October 2020


E0020-ssrAtag（mf-lon）

Engineered cyan fluorescent protein tagged with ssrAtag(mf-lon), which can be recognised and degraded by mf-lon .We use it to model the feedback of mf-lon and check the function of mf-lon. ssAtag（mf-lon）is tag pdt#1，which is recognized by mf-lon hydrolases. It is attached to the 3’ end of the genes of ECFP. If there is mf-lon hydrolases, ECFP will be degraded.

Usage and Biology

caption

Fig 1. pLtetO_B0034_ecfp-ssrAtag(mf-lon)_B0015_pTrc-2 derivative_B0034_mf-lon_B0015

To construct this part, we moved pLtetO-1 (BBa_K3332034) ，E0020-ssrAtag（mf-lon）(BBa_K3332035) ，Terminator(BBa_B0015)，pTrc-2 derivative promoter (BBa_K3332040), RBS(BBa_B0034) and mf-lon (BBa_K2333011) into the expression vector pUC57 by standard assembly. Then the ligation mixture was transformed into E. coli BL21(DE3) to characterize mf-lon hydrolase.

Reference:

[1] Chan CT, Lee JW, Cameron DE, Bashor CJ, Collins JJ. 'Deadman' and 'Passcode' microbial kill switches for bacterial containment. Nat Chem Biol. 2016;12(2):82-86. doi:10.1038/nchembio.1979


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]