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Team:Edinburgh/Cell Display
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<partinfo>BBa_K265008</partinfo> is the first 211 and last 97 amino acids of ice nucleation protein (INP, coded by ''[http://www.uniprot.org/uniprot/O30611 inaK]'' gene) from ''Pseudomonas syringae''. It seems promising as a carrier of enzymes. [http://www.sciencedirect.com/science/article/pii/S016777991000199X Van Bloois ''et al'' (2011)] speak highly of INP. Fusions are carried out at the INP C-terminal. | <partinfo>BBa_K265008</partinfo> is the first 211 and last 97 amino acids of ice nucleation protein (INP, coded by ''[http://www.uniprot.org/uniprot/O30611 inaK]'' gene) from ''Pseudomonas syringae''. It seems promising as a carrier of enzymes. [http://www.sciencedirect.com/science/article/pii/S016777991000199X Van Bloois ''et al'' (2011)] speak highly of INP. Fusions are carried out at the INP C-terminal. | ||
| - | [[Team:Edinburgh/Berkeley 2009 Parts|Berkeley 2009 Parts]] may be helpful: they tried several different carrier proteins. They had [https://2009.igem.org/Team:Berkeley_Wetlab/Passenger:_Cellulases some success] getting endoglucanase expressed on several carriers, the best of which was <partinfo>BBa_K197007</partinfo>. | + | [[Team:Edinburgh/Berkeley 2009 Parts|Berkeley 2009 Parts]] may be helpful: they tried several different carrier proteins. They had [https://2009.igem.org/Team:Berkeley_Wetlab/Passenger:_Cellulases some success] getting endoglucanase expressed on several carriers, the best of which was <partinfo>BBa_K197007</partinfo>. This is a natural trimer and I'm not sure how the fusion is supposed to work... |
==References== | ==References== | ||
Revision as of 14:02, 30 June 2011
An obvious type of bioreactor is an E. coli cell that displays the desired proteins on its outer membrane. This type of display is called cell surface display.
This works by fusing the protein of interest to a carrier protein which is naturally found on the outer membrane.
Notes
<partinfo>BBa_K265008</partinfo> is the first 211 and last 97 amino acids of ice nucleation protein (INP, coded by [http://www.uniprot.org/uniprot/O30611 inaK] gene) from Pseudomonas syringae. It seems promising as a carrier of enzymes. [http://www.sciencedirect.com/science/article/pii/S016777991000199X Van Bloois et al (2011)] speak highly of INP. Fusions are carried out at the INP C-terminal.
Berkeley 2009 Parts may be helpful: they tried several different carrier proteins. They had some success getting endoglucanase expressed on several carriers, the best of which was <partinfo>BBa_K197007</partinfo>. This is a natural trimer and I'm not sure how the fusion is supposed to work...
References
- Van Bloois E, Winter RT, Kolmar H, Fraaije MW (2011) [http://www.sciencedirect.com/science/article/pii/S016777991000199X Decorating microbes: surface display of proteins on Escherichia coli]. Trends in Biotechnology 29(2): 79-86 (doi: 10.1016/j.tibtech.2010.11.003).
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