Difference between revisions of "Part:BBa K3102038:Design"

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We mutated a Cytosine into Guanine at the 1609bp position (C1609T) because of the Esp3I enzyme that we used for our Golden Gate Assembly (GGA) construct. (e.g. BBa_K3102022)
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We mutated the ACS seqeune with a Cytosine into Guanine at the 1566bp position (C1566G) because of the Esp3I enzyme that we used for our Golden Gate Assembly (GGA) construct. (BBa_K3102022)
  
 
===Source===
 
===Source===

Latest revision as of 10:23, 16 October 2019


T7-RBS-ACS-Ter


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 966
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

We mutated the ACS seqeune with a Cytosine into Guanine at the 1566bp position (C1566G) because of the Esp3I enzyme that we used for our Golden Gate Assembly (GGA) construct. (BBa_K3102022)

Source

This sequence comes from Shewanella Oneidensis and was found through Biocyc: https://biocyc.org/gene?orgid=SONE211586&id=G1GMP-2522#tab=TU

Promoter (BBa_I719005), RBS (BBa_B0034) and Terminator (BBa_B0015) are from the iGEM Registry.

References

Brown TD. et al., The enzymic interconversion of acetate and acetyl-coenzyme A in Escherichia coli, J Gen Microbiol. 1977 Oct;102(2):327-36.

Kumari S. et al., Cloning, characterization, and functional expression of acs, the gene which encodes acetyl coenzyme A synthetase in Escherichia coli, J Bacteriol. 1995 May;177(10):2878-86.