Difference between revisions of "Part:BBa K3332035"
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[[File:2035 fig.1.png|none|500px|caption]] | [[File:2035 fig.1.png|none|500px|caption]] | ||
− | Fig | + | '''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( | + | 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:=== | ===Reference:=== |
Revision as of 16:21, 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
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
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]