Difference between revisions of "Part:BBa K1682018:Experience"
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===Applications of BBa_K1682018=== | ===Applications of BBa_K1682018=== | ||
| + | This year, Lambert_GA is working on demonstrating that this part can be transformed into competent E.coli cells while retaining functionality. Attempts at ligation both with restriction digest cloning and gibson cloning failed. | ||
===Team Lambert_GA 2020=== | ===Team Lambert_GA 2020=== | ||
Revision as of 18:53, 27 October 2020
This experience page is provided so that any user may enter their experience using this part.
Please enter
how you used this part and how it worked out.
Applications of BBa_K1682018
This year, Lambert_GA is working on demonstrating that this part can be transformed into competent E.coli cells while retaining functionality. Attempts at ligation both with restriction digest cloning and gibson cloning failed.
Team Lambert_GA 2020
To optimize functionality, Lambert_GA altered the original part designed by HKUST-Rice 2015 by replacing the original terminators with rrNB T1 terminator and T7Te terminator after super folder GFP and a rrnBT1 T1 terminator after TetR. Nar Operon Background Native to E. coli, the Nar Operon regulates anaerobic gene expression in response to two electron acceptors: nitrate and nitrite. This system consists of two homologous membrane-bound sensor proteins (NarX and NarQ) as well as two homologous DNA-binding response regulators (NarL and NarP). NarL’s conjugate is the membrane-bound NarX protein while NarP’s conjugate is the membrane-bound NarQ protein. Our team is utilizing this system to test nitrate and nitrite levels, NarL and NarP expression, and downstream GFP expression through mathematical models.
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UNIQd3b9aaf985cb940c-partinfo-00000000-QINU UNIQd3b9aaf985cb940c-partinfo-00000001-QINU