Difference between revisions of "Part:BBa K1216004"
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− | A form of this protein without TEV and poly-HIS tags can be found [[Part: | + | A form of this protein without TEV and poly-HIS tags can be found [[Part:BBa_K1216000| here]]. |
===Usage and Biology=== | ===Usage and Biology=== |
Revision as of 13:12, 6 September 2013
β-Glucuronidase (gusA) from Bacillis Subtilis with TEV and poly-HIS tags
gusA (also called uidA[1]) encodes β-Glucuronidase, an intracellular enzyme that catalyzes the hydrolysis of β-D-glucuronides. The poly-HIS tag can be used for protein purification (IMAC)[2]. The TEV tag can then be used to have the TEV protease specifically cleave off the poly-HIS tag from the purified protein [3].
A form of this protein without TEV and poly-HIS tags can be found here.
Usage and Biology
β-Glucuronidase is used as a fusion protein marker in higher plants, due to them lacking intrinsic β-Glucuronidase activity[4]. Generally it can be used as reporter enzyme with detection by biochemical activity assays, immunological assays or by histochemical staining of tissue sections or cells[5].
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 538
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
References
- [http://ecoliwiki.net/colipedia/index.php/uidA:Gene ecoliwiki]
- Loghran ST, "Purification of poly-histidine-tagged proteins.",Methods Mol Biol. 2011;681:311-35. doi: 10.1007/978-1-60761-913-0_17.[http://www.ncbi.nlm.nih.gov/pubmed/20978973]
- [http://homepage.univie.ac.at/nikos.pinotsis/tev_protease.html University of Vienna TEV Protease info]
- Jefferson A R, "GUS fusions: beta-glucuronidase as a sensitive and versatile gene fusion marker in higher plants.", EMBO J. 1987 December 20; 6(13): 3901–3907 [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC553867/]
- [http://www.sigmaaldrich.com/etc/medialib/docs/Sigma/Bulletin/gusabul.Par.0001.File.tmp/gusabul.pdf Sigma Aldrich]