Difference between revisions of "Part:BBa K4229066:Design"
NikitaEdel (Talk | contribs) |
NikitaEdel (Talk | contribs) |
||
Line 13: | Line 13: | ||
===Source=== | ===Source=== | ||
− | + | The plasmid containing this protein was kindly sent to us by the Kerfeld group. | |
===References=== | ===References=== |
Latest revision as of 07:16, 12 October 2022
mVenus with N-terminal spyCatcher regulated by tetA/B promotor
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 59
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 59
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 59
Illegal BglII site found at 68
Illegal XhoI site found at 1075 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 59
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 59
Illegal AgeI site found at 508 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
none
Source
The plasmid containing this protein was kindly sent to us by the Kerfeld group.
References
H. Kirst and C. A. Kerfeld, “Bacterial microcompartments: Catalysis-enhancing metabolic modules for next generation metabolic and biomedical engineering,” BMC Biol., vol. 17, no. 1, pp. 1–11, 2019, DOI: 10.1186/s12915-019-0691-z.
H. Kirst, B. H. Ferlez, S. N. Lindner, C. A. R. Cotton, A. Bar-Even, and C. A. Kerfeld, “Toward a glycyl radical enzyme containing synthetic bacterial microcompartment to produce pyruvate from formate and acetate,” Proc. Natl. Acad. Sci. U. S. A., vol. 119, no. 8, pp. 1–10, 2022, doi: 10.1073/pnas.2116871119.