Difference between revisions of "Part:BBa K4329004"

m
Line 3: Line 3:
 
<partinfo>BBa_K4329004 short</partinfo>
 
<partinfo>BBa_K4329004 short</partinfo>
  
By using CRISPR i system, we are able to decrease the expression of Bifunctional BirA enzyme which is an enzyme to consume the biotin in the E. coli. In our project, we are aiming at biosynthesizing biotin through the metabolic pathways to generate more biotin in the E. coli.   
+
===What it is?===
 +
 
 +
By using the CRISPRi system, we are able to decrease the expression of the Bifunctional BirA enzyme which is an enzyme to consume the biotin in E. coli. In our project, we are aiming at biosynthesizing biotin through the metabolic pathways to generate more biotin in E. coli.   
  
 
===Usage and Biology===
 
===Usage and Biology===
 +
 +
With the CRISPRi/dCas9 system targeting the bifunctional BirA enzyme after the production of biotin, the dCas9 system will attach to the enzyme, blocking other DNA from combining with the enzyme. Thus, the enzyme would be in a temporary dysfunctional state. 
  
 
===Characterization===  
 
===Characterization===  

Revision as of 13:04, 28 September 2022


Knockdown of Bifunctional BirA enzyme

What it is?

By using the CRISPRi system, we are able to decrease the expression of the Bifunctional BirA enzyme which is an enzyme to consume the biotin in E. coli. In our project, we are aiming at biosynthesizing biotin through the metabolic pathways to generate more biotin in E. coli.

Usage and Biology

With the CRISPRi/dCas9 system targeting the bifunctional BirA enzyme after the production of biotin, the dCas9 system will attach to the enzyme, blocking other DNA from combining with the enzyme. Thus, the enzyme would be in a temporary dysfunctional state.

Characterization

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1202
    Illegal NheI site found at 4217
    Illegal NheI site found at 4240
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 4264
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 49