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Team:ETH Zurich/Mutant
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<p align="justify">In order to use the orthogonal hydrolases as our reporter system in the sender-receiver set-up, we needed to use a strain of E.coli that was knocked out of expression of native hydrolase genes to prevent background hydrolysis. Hence, three hydrolase genes were knocked out of E.coli strain MG1655. The hydrolase genes are namely gusA, aes and nagZ. The gusA hydrolase was knocked out by a scarless deletion scheme that left no scar sequences after the deletion method. The subsequent deletions of aes and nagZ was carried out by the P1 phage transduction by using deletion strain from the Keio collection. Thus we were able to use this strain MG1655deltagusAdeltaaesdeltanagZknocked out of expression of the three hydrolase genes in our project.<br> </p> | <p align="justify">In order to use the orthogonal hydrolases as our reporter system in the sender-receiver set-up, we needed to use a strain of E.coli that was knocked out of expression of native hydrolase genes to prevent background hydrolysis. Hence, three hydrolase genes were knocked out of E.coli strain MG1655. The hydrolase genes are namely gusA, aes and nagZ. The gusA hydrolase was knocked out by a scarless deletion scheme that left no scar sequences after the deletion method. The subsequent deletions of aes and nagZ was carried out by the P1 phage transduction by using deletion strain from the Keio collection. Thus we were able to use this strain MG1655deltagusAdeltaaesdeltanagZknocked out of expression of the three hydrolase genes in our project.<br> </p> | ||
Revision as of 22:33, 30 September 2013
Triple knockout strain
In order to use the orthogonal hydrolases as our reporter system in the sender-receiver set-up, we needed to use a strain of E.coli that was knocked out of expression of native hydrolase genes to prevent background hydrolysis. Hence, three hydrolase genes were knocked out of E.coli strain MG1655. The hydrolase genes are namely gusA, aes and nagZ. The gusA hydrolase was knocked out by a scarless deletion scheme that left no scar sequences after the deletion method. The subsequent deletions of aes and nagZ was carried out by the P1 phage transduction by using deletion strain from the Keio collection. Thus we were able to use this strain MG1655deltagusAdeltaaesdeltanagZknocked out of expression of the three hydrolase genes in our project.
The triple mutant is used for the sender cells which are made to constitutively express nagZ. In the receiver cells, the hydrolases aes and gusA are expressed under the control of OHHL induced pluxR promoters.
