Part:BBa_K2170050:Design
Secretory prokaryotic biotin binding receptor with enhanced monomeric avidin
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 2448
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 889
Keywords:
Abbreviations:
Design Notes
Related BioBrick:
- Related BioBricks:
BBa_K2170052: Secretory prokaryotic biotin binding receptor with single chain avidin
BBa_K2170050: Secretory prokaryotic biotin binding receptor with enhanced monomeric avidin
Cloning details:
- Designed in RFC10
Quality control measures:
- Test digestion using EcoRI & PstI
- Sequencing using primer VF2 & VR
- Part was partly sequenced/Part was totally sequenced
Backbone:
- Backbone name: pSB1C3
- Resistance: Cp
- Copynumber: high
Protein coding:
- Protein: Secretory prokaryotic biotin presenting receptor with biotin acceptor peptide [Nucleotide 1030 to 2652]-->
- Tag: internal A3C5 Tag
Enzymatic activity:
- NanoLuc
Cytotoxicity:
- none
Safety notes:
Known and anticipated sefety issues: none
Known and anticipated security issues: none
Source
Source:
- Preexisting BioBrick BBa_I739001; BBa_B0015; BBa_K1159001
- Parts Synthesized by IDT
- Professor Dr. Arne Skerra (Chair biological chemistry of TUM)
Organism:
Genesequence derived from Escherichia coli
- Designed for the following Chassis: procaryotic cells
References
Literature references:
1. [http://jcb.rupress.org/content/108/2/229.short Kozak, M. (1989). The scanning model for translation: an update. The Journal of cell biology, 108(2), 229-241.]
2. [http://journals.plos.org/plosone/article?id=10.1371/journal.pone.000439 Kredel, S., Oswald, F., Nienhaus, K., Deuschle, K., Röcker, C., Wolff, M., ... & Wiedenmann, J. (2009). mRuby, a bright monomeric red fluorescent protein for labeling of subcellular structures. PloS one, 4(2), e4391.]
3. Bajar, B. T., Wang, E. S., Lam, A. J., Kim, B. B., Jacobs, C. L., Howe, E. S., ... & Chu, J. (2016). Improving brightness and photostability of green and red fluorescent proteins for live cell imaging and FRET reporting. Scientific reports, 6.
4. [http://www.nature.com/nprot/journal/v2/n6/abs/nprot.2007.209.html Schmidt, T. G., & Skerra, A. (2007). The Strep-tag system for one-step purification and high-affinity detection or capturing of proteins. Nature protocols, 2(6), 1528-1535.]
Database references: