Difference between revisions of "Part:BBa K3110021:Design"

(Source)
Line 14: Line 14:
 
===Source===
 
===Source===
  
Strong promoter -Medium RBS-lldR flank and lldD flank-terminator were synthesized by IDT <br>
+
Weak promoter -Weak RBS-lldR flank and lldD flank-terminator were synthesized by IDT <br>
 
lldR+lldD was amplified from the genome
 
lldR+lldD was amplified from the genome
 
 
 
  
 
===References===
 
===References===

Revision as of 15:51, 21 October 2019


Weak Promoter Weak RBS lldR+lldD


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1987
    Illegal AgeI site found at 619
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1424


Design Notes

Source

Weak promoter -Weak RBS-lldR flank and lldD flank-terminator were synthesized by IDT
lldR+lldD was amplified from the genome

References

iGEM ETH zurich 2015
iGEM NUS Singapore 2016
Aguilera, L., Campos, E., Gimenez, R., Badia, J., Aguilar, J., & Baldoma, L. (2008). Dual Role of LldR in Regulation of the lldPRD Operon, Involved in L-Lactate Metabolism in Escherichia coli. Journal of Bacteriology, 190(8), 2997–3005. doi:10.1128/jb.02013-07