Difference between revisions of "Part:BBa K4885003:Design"
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===References=== | ===References=== | ||
Revision as of 06:10, 10 October 2023
Pcat1-Cat1
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
In C. tyrobutyricum L319, glucose is converted to pyruvate and subsequently to acetyl-CoA. Then, one part of acetyl-CoA is converted to acetate, , another part is converted to ethanol, and the rest is converted into butyryl-CoA. Butyryl-CoA is respectively converted to butyrate by butyryl-CoA/acetate CoA transferase. The CoA transferase also converts acetate back to acetyl-CoA. So CoA transferase reduces the acetyl-CoA to acetate flux and enhances the acetyl-CoA to butyrate flux. Therefore, the higher the expression of CoA transferase, the higher the butyrate/acetate ratio in the final product. The endogenous Cat1 gene of C. tyrobutyricum L319 codes the butyryl-CoA/acetate CoA transferase. Using the cat1 gene and the native Pcat1 promoter of this gene, we constructed the part of Pcat1-cat1 to overexpress cat1 in C. tyrobutyricum, in order to suppress the acetyl-CoA conversion to acetate and indirectly enhance the metabolic flux of butyrate synthesis.
Source
BBa_K4119011+ BBa_K4119031+BBa_K3585002