Difference between revisions of "Team:Dalhousie/Improve"
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<li><a href="https://2017.igem.org/Team:Dalhousie/Human_Practices">Summary</a></li> | <li><a href="https://2017.igem.org/Team:Dalhousie/Human_Practices">Summary</a></li> | ||
<li><a href="https://2017.igem.org/Team:Dalhousie/HP/Silver">Science Communication</a></li> | <li><a href="https://2017.igem.org/Team:Dalhousie/HP/Silver">Science Communication</a></li> | ||
| − | <li><a href="https://2017.igem.org/Team:Dalhousie/HP/Gold_Integrated"> | + | <li><a href="https://2017.igem.org/Team:Dalhousie/HP/Gold_Integrated">Integrated and Gold</a></li> |
<li><a href="https://2017.igem.org/Team:Dalhousie/Engagement">Public Engagement</a></li> | <li><a href="https://2017.igem.org/Team:Dalhousie/Engagement">Public Engagement</a></li> | ||
<li><a href="https://2017.igem.org/Team:Dalhousie/SocialMedia">Social Media</a></li> | <li><a href="https://2017.igem.org/Team:Dalhousie/SocialMedia">Social Media</a></li> | ||
Revision as of 03:33, 27 October 2017
Improve
Part Improvement
Background This part is the coding region for an endoglucanse from Ruminiclostridium thermocellum that was previously created by the iGEM16_Dalhousie_NS_Halifax (BBa_K2160000). Its function is to cleave internal Beta-1,4-D-glycosidic bonds in the cellulose crystal to release the disaccharide cellobiose. Improvement We improved the endoglucanase part by adding a C-terminal His-tag and a N-terminal PelB sequence. The C-terminal His-tag allows identification via western blot or immuno-fluorescence, and protein purification. The PelB sequence is a localization sequence that traffics the protein to the periplasm (Sockolosky & Szoka, 2013). This is especially important for our project because we need to get all the enzymes out of the E. coli to digest cellulose. Using a western blot to probe for the HIS-Tag, we were able to show expression of our optimized endoglucanase. The main species traveled at 46 kDa, which was the predicted migration of endoglucanase with a HIS-tag and PelB sequence. A secondary, smaller species was seen at ~30 kDa. The 30 kDa species can be explained due to a second methionine codon with an imperfect ribosomal binding sequence 5-10 bp upstream from the Met codon.
Sockolosky, J. and Szoka, F. (2013). Periplasmic production via the pET expression system of soluble, bioactive human growth hormone. Protein Expression and Purification, 87(2), pp.129-135.
