Difference between revisions of "Team:Dalhousie/Improve"
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<center><img src="https://static.igem.org/mediawiki/2017/2/2d/Endoglucoptimized.png"></center> | <center><img src="https://static.igem.org/mediawiki/2017/2/2d/Endoglucoptimized.png"></center> | ||
| − | <center><font color= "#ffffff"> Figure 1. Western blot probing for 6xHis Tag</Center></font> | + | <center><font color= "#ffffff"> Figure 1. Western blot probing for 6xHis Tag</Center></font></br></br> |
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| + | <font color= "#C1D35D">Part Number</font></br> | ||
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| + | <font color= "#ffffff">Our part can be found here: | ||
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Revision as of 00:58, 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.
Learn more... hopefully have links to next pages here
