Difference between revisions of "Part:BBa K2455008:Design"

 
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===References===
 
===References===
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Gu, P. <i>et al.</i> (2012). One-step of tryptophan attenuator inactivation and promoter swapping to improve the production of L-tryptophan in Escherichia coli. <i>Microbial Cell Factories</i>, <b>11(1)</b>, p.30.
 +
 +
Wang, J. <i>et al.</i> (2013). Genetic engineering of <i>Escherichia coli</i> to enhance production of l-tryptophan. <i>Applied Microbiology and Biotechnology</i>, <b>97(17)</b>, pp.7587-7596.

Revision as of 16:39, 28 October 2017


YddG-AroG construct with an E. coli RBS between (BBa_K2455004 & BBa_K2455000)


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal XhoI site found at 1847
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 577
    Illegal AgeI site found at 639
    Illegal AgeI site found at 756
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 1154


Design Notes

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Source

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References

Gu, P. et al. (2012). One-step of tryptophan attenuator inactivation and promoter swapping to improve the production of L-tryptophan in Escherichia coli. Microbial Cell Factories, 11(1), p.30.

Wang, J. et al. (2013). Genetic engineering of Escherichia coli to enhance production of l-tryptophan. Applied Microbiology and Biotechnology, 97(17), pp.7587-7596.