Difference between revisions of "Part:BBa K3102000:Design"

 
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===References===
 
===References===
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Foor F. et al., "Purification and properties of guanosine triphosphate cyclohydrolase II from Escherichia coli.". Biol. Chem. 250:3545-3551(1975)
 +
 +
Lin Z, et al., "Metabolic engineering of Escherichia coli for the production of riboflavin". Microb Cell Fact. 2014;13(1):1–12.
 +
 +
Zhenquan Lin et al., “Metabolic engineering of Escherichia coli for the production of riboflavin," Microbial Cell Factories, 2014, 13:104.

Latest revision as of 16:47, 12 October 2019


RibA (coding for GTP cyclohydrolase-2)


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 319
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal PstI site found at 319
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 319
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 319
    Illegal AgeI site found at 166
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

none


Source

E.coli, sequence found through Biocyc https://biocyc.org/gene?orgid=ECOLI&id=EG11331


References

Foor F. et al., "Purification and properties of guanosine triphosphate cyclohydrolase II from Escherichia coli.". Biol. Chem. 250:3545-3551(1975)

Lin Z, et al., "Metabolic engineering of Escherichia coli for the production of riboflavin". Microb Cell Fact. 2014;13(1):1–12.

Zhenquan Lin et al., “Metabolic engineering of Escherichia coli for the production of riboflavin," Microbial Cell Factories, 2014, 13:104.