Difference between revisions of "Team:Aachen/InteractiveTour31"
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<p class="headline" style="display:none;">Biological Approach</p> | <p class="headline" style="display:none;">Biological Approach</p> | ||
+ | After it became clear that we wanted to enable ''Escherichia coli'' to convert methanol into glycogen we had to find a suitable pathway for methanol assimilation. We found the Methanol Condensation Cycle (MCC) to be the most promising one. For implementing the MCC in ''E. coli'', four additional genes are required: | ||
+ | * methanol dehydrogenase 2 from ''Bacillus methanolicus'' (Mdh) | ||
+ | * 3-hexulose-6-phosphate synthase from ''Bacillus methanolicus'' (Hps) | ||
+ | * 6-phospho 3-hexuloisomerase from ''Bacillus methanolicus'' (Phi) | ||
+ | * phosphoketolase from ''Bifidobacterium adolescentis'' (Xpk) | ||
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+ | In parallel we developed a strategy for our second module: glycogen accumulation. To enhance glycogen formation, the whole synthesis pathway needs to be upregulated. The three enzymes involved in synthesis are: | ||
+ | * GlgC, ADP-glucose pyrophosphorylase | ||
+ | * GlgA, the glycogen synthase | ||
+ | * GlgB, the branching enzyme | ||
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+ | On top of that accumulation can be considerably increased by knocking out glycogen degradation enzymes. Those are GlgP, the glycogen phosphorylase and GlgX, the debranching enyzme. | ||
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{{Team:Aachen/Footer|color=green}} | {{Team:Aachen/Footer|color=green}} |
Revision as of 22:04, 18 September 2015