Difference between revisions of "Part:BBa K2455000:Design"
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===Design Notes=== | ===Design Notes=== | ||
In addition to having a P150L mutation the AroG sequence contains a his-tag in order to allow for detection of expression through the use of Western Blotting. | In addition to having a P150L mutation the AroG sequence contains a his-tag in order to allow for detection of expression through the use of Western Blotting. | ||
− | |||
− | |||
===Source=== | ===Source=== | ||
− | The sequence originated from the MG1655 E. coli strain but carries a Pro150Leu point mutation in order to avoid negative feedback inhibition by L-phenylalanine ( | + | The sequence originated from the MG1655 E. coli strain but carries a Pro150Leu point mutation in order to avoid negative feedback inhibition by L-phenylalanine ([https://microbialcellfactories.biomedcentral.com/articles/10.1186/1475-2859-11-30 Gu <i>et al.</i>, 2012]), in addition a hexa his-tag has been added. |
===References=== | ===References=== | ||
+ | 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. |
Latest revision as of 14:04, 28 October 2017
His-tagged AroG gene from E. coli MG1655
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 934
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 241
Design Notes
In addition to having a P150L mutation the AroG sequence contains a his-tag in order to allow for detection of expression through the use of Western Blotting.
Source
The sequence originated from the MG1655 E. coli strain but carries a Pro150Leu point mutation in order to avoid negative feedback inhibition by L-phenylalanine (Gu et al., 2012), in addition a hexa his-tag has been added.
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.