Difference between revisions of "Part:BBa K4368000"
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<partinfo>BBa_K4368000 short</partinfo>
 
<partinfo>BBa_K4368000 short</partinfo>
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''CenA'' encodes for the endoglucanase gene of ''Celullomonas fimi'' (<partinfo>BBa_K118023</partinfo>). This enzyme is responsible of the degradation of celullose working coordinated with th genes cex and bglX. In addition, this part includes the composition used by the team, which includes a strong rbs (<partinfo>BBa_B0030</partinfo>), a double terminator (<partinfo>BBa_B0015</partinfo>) as well as a promoter inducible by the glucose concentration (<partinfo>BBA_K118011</partinfo>). Furthermore, we improve this composite adding a gen encoding a motor protein named YebF (<partinfo>BBa_K1610300</partinfo>) that secrete the enzyme out of the ''E. coli'' membrane.
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The gene has been placed under the control of this promoter to build the glucose concentration-based gene regulatory circuit that integrates all our parts.
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 08:03, 6 October 2022

pcstA + rbs + yebF + cenA + terminator CenA encodes for the endoglucanase gene of Celullomonas fimi (BBa_K118023). This enzyme is responsible of the degradation of celullose working coordinated with th genes cex and bglX. In addition, this part includes the composition used by the team, which includes a strong rbs (BBa_B0030), a double terminator (BBa_B0015) as well as a promoter inducible by the glucose concentration (BBa_K118011). Furthermore, we improve this composite adding a gen encoding a motor protein named YebF (BBa_K1610300) that secrete the enzyme out of the E. coli membrane. The gene has been placed under the control of this promoter to build the glucose concentration-based gene regulatory circuit that integrates all our parts.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NotI site found at 554
    Illegal NotI site found at 1698
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 268
    Illegal BglII site found at 1611
    Illegal BamHI site found at 747
    Illegal XhoI site found at 1109
    Illegal XhoI site found at 1358
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 889
    Illegal NgoMIV site found at 1814
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 793