Difference between revisions of "Part:BBa K3496006"
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Eriodictyol producing composite part | Eriodictyol producing composite part | ||
+ | This is a composite part,a collection of BBa_K1033001 (4CL), BBa_K1497001 (CHS), | ||
+ | BBa_K1497000 (CHI), BBa_K3496005 (F3‘H), aiming to biosynthesis Eriodictyol in Saccharomyces cerevisiae and improve the existing part BBa_K1497017. | ||
+ | BBa_K1497017 is another composite part Naringenin producing operon under the T7 promoter. | ||
+ | Firstly, in terms of final product, compared with Naringenin, Eriodictyol has one more hydroxyl group on the B ring and higher anti-oxidation activity and higher Medicinal Value for health care. | ||
+ | Secondly, since in the last step of eriodictyol metabolic pathway when P450 enzyme F3‘H hydroxylated naringenin to obtain the final product eriodictyol, it is supposed to happen in eukaryotic organisms instead of a prokaryotic cell which is unable to provide the membrane structure required for post-modification of the enzyme. As the biological chassis, Saccharomyces cerevisiae meets the need. | ||
+ | Thirdly, when we look at the entire pathway throughout,this improved part is coordinating with enzyme TAL in E. coli which addresses the separation of metabolic pathways. The sharing of the burden of gene expression as well as the cross-feeding of metabolites, together improve metabolic efficiency and robustness to achieve high‐efficiency bioproduction of the final product. | ||
+ | ‘ | ||
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Revision as of 16:26, 26 October 2020
Eriodictyol producing composite part
Eriodictyol producing composite part This is a composite part,a collection of BBa_K1033001 (4CL), BBa_K1497001 (CHS), BBa_K1497000 (CHI), BBa_K3496005 (F3‘H), aiming to biosynthesis Eriodictyol in Saccharomyces cerevisiae and improve the existing part BBa_K1497017. BBa_K1497017 is another composite part Naringenin producing operon under the T7 promoter. Firstly, in terms of final product, compared with Naringenin, Eriodictyol has one more hydroxyl group on the B ring and higher anti-oxidation activity and higher Medicinal Value for health care. Secondly, since in the last step of eriodictyol metabolic pathway when P450 enzyme F3‘H hydroxylated naringenin to obtain the final product eriodictyol, it is supposed to happen in eukaryotic organisms instead of a prokaryotic cell which is unable to provide the membrane structure required for post-modification of the enzyme. As the biological chassis, Saccharomyces cerevisiae meets the need. Thirdly, when we look at the entire pathway throughout,this improved part is coordinating with enzyme TAL in E. coli which addresses the separation of metabolic pathways. The sharing of the burden of gene expression as well as the cross-feeding of metabolites, together improve metabolic efficiency and robustness to achieve high‐efficiency bioproduction of the final product. ‘
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1108
Illegal NheI site found at 2239
Illegal NheI site found at 4621 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1675
Illegal BglII site found at 2248
Illegal XhoI site found at 3201
Illegal XhoI site found at 4848
Illegal XhoI site found at 4877 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 2219
Illegal NgoMIV site found at 2795 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 2168
Illegal BsaI.rc site found at 1307
Illegal BsaI.rc site found at 3605
Illegal BsaI.rc site found at 4851