Difference between revisions of "Part:BBa K4012017"
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[[Image:yeast PCR.jpg|thumbnail|750px|center|'''Figure 3:''' | [[Image:yeast PCR.jpg|thumbnail|750px|center|'''Figure 3:''' | ||
[https://parts.igem.org/Part:BBa_K4012017] A: The results of colony PCR of upstream transformant; B: The results of colony PCR of downstream transformant; C: Construction of catechin metabolic pathway; D:Construction of naringenin metabolic pathway]] | [https://parts.igem.org/Part:BBa_K4012017] A: The results of colony PCR of upstream transformant; B: The results of colony PCR of downstream transformant; C: Construction of catechin metabolic pathway; D:Construction of naringenin metabolic pathway]] | ||
− | + | Pc4CL is successfully inserted into the vector type9 C-mTurquoise-Ura. |
Revision as of 13:11, 21 October 2021
Pc4CL
Produces CoA thioesters of a variety of hydroxy- and methoxy-substituted cinnamic acids, which are used to synthesize several phenylpropanoid-derived compounds, including anthocyanins, flavonoids, isoflavonoids, coumarins, lignin, suberin and wall-bound phenolics.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Pc4CL in Level1 plasmid assembly
The construction schematic of GbCHS sequence demonstrated as Fig .2. The initiation of the GbCHS sequence is done by promoter pTEF1, with termination done by tADH1. The sequence ConL2 and ConR3 are connector sequences within the Level 1 plasmid assembly. Furthermore, typr9-KVF and type9-VR are imposed to enact selection through colonies PCR, results shown in Fig.2 The band length 2500bp match with expectations. The sequence analysis results show no significant mutations or deletions, representing the success of the assembly.
Pc4CL in Level2 plasmid assembly
Pc4CL is successfully inserted into the vector type9 C-mTurquoise-Ura.