Difference between revisions of "Part:BBa K3993012"
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[[File:T--SHSID--BBa K3993012-Figure2.png|500px|thumb|center|Figure 2. DNA sequence map of plasmid PTDH3-AsADC-TCYC1..]] | [[File:T--SHSID--BBa K3993012-Figure2.png|500px|thumb|center|Figure 2. DNA sequence map of plasmid PTDH3-AsADC-TCYC1..]] | ||
+ | |||
+ | ===The profiles of every basic part are as follows:=== | ||
+ | == BBa_K3993002== | ||
+ | ====Name: AsADC==== | ||
+ | ====Base Pairs: 1821bp==== | ||
+ | ====Origin: Saccharomyces cerevisiae, synthesis==== | ||
+ | ====Properties: codon optimized SPE1==== | ||
+ | |||
+ | === Usage and Biology === | ||
+ | This protein is involved in step 1 of the subpathway that synthesizes agmatine from L-arginine. This subpathway is part of the pathway agmatine biosynthesis, which is itself part of Amine and polyamine biosynthesis. | ||
+ | |||
+ | == BBa_K3993003 == | ||
+ | ====Name: PTDH3==== | ||
+ | ====Base Pairs: 673bp==== | ||
+ | ====Origin: Addgene==== | ||
+ | ====Properties: Yeast centromeric vector with the TDH3 (glyceraldehyde 3-phosphate dehydrogenase) promoter.==== | ||
+ | |||
+ | === Usage and Biology === | ||
+ | Yeast CEN/ARS vector (Leu2) that contains multiple cloning site ( MCS ) and TDH3 promoter. | ||
+ | |||
+ | == BBa_K3993004 == | ||
+ | ====Name: TCYC1==== | ||
+ | ====Base Pairs: 242bp==== | ||
+ | ====Origin: Saccharomyces cerevisiae, genome==== | ||
+ | ====Properties: CYC1 terminator==== | ||
+ | |||
+ | === Usage and Biology === | ||
+ | This is a common transcriptional terminator. Placed after a gene, it completing the transcription process and impacting mRNA half-life. This terminator can be used for in vivo systems, and can be used for modulating gene expression in yeast. | ||
+ | |||
+ | == Experimental approach == | ||
+ | ====1. Fragments PCR products Electrophoresis==== | ||
+ | |||
+ | [[File:T--SHSID--BBa K3993012-Figure3.png|500px|thumb|center|Figure 3. Gel electrophoresis of amplified fragments..]] | ||
+ | |||
+ | Lane 1 is target gene AsADC, Lane 2 is promoter PTDH3. | ||
+ | |||
+ | === proof of function === | ||
+ | ====Modeling for predicting the performance of our engineered bacteria to produce tropine==== | ||
+ | Firstly, we get the polynomial linear regression-2 shown in figure 4. (Data from the published articles, according to references3/4 ) | ||
+ | |||
+ | [[File:T--SHSID--BBa K3993012-Figure3.png|500px|thumb|center|Figure 3. Gel electrophoresis of amplified fragments..]] | ||
+ | |||
+ | |||
Revision as of 01:39, 20 October 2021
PTDH3-AsADC-TCYC1
Profile
Name: PTDH3-AsADC-TCYC1
Base Pairs: 2736bp
Origin: Saccharomyces cerevisiae, E. coli, synthesis
Properties: Arginine metabolism and polyamine biosynthesis chemical reactions
Usage and Biology
Kl tropane alkaloids (TAs) refers to a kind of alkaloids containing the tropane alkyl skeleton formed by the combination of pyrrole ring and piperidine ring in structure. It is a natural product of plant and has a long history and important medicinal value. tropane alkaloids have great market demand and often appear in global shortages. A method that can produce Tas in scale is expected. Using synthetic biology to create a microbial cell factory to produce TAs is a highly potential strategy.
The Tropane alkaloid (TAs) is obtained by a series of chemical reactions through the formation of Putrescine (1, 4-butylenediamine, Putrescine) from Arginine. Putrescine is an essential polyamine for ribosomal biogenesis and mRNA translation, but is regulated by polyamines and remains at low concentrations during normal cell growth. In this study, by overexpressing the natural genes involved in arginine metabolism and polyamine biosynthesis, the regulatory mechanism of polyamine biosynthesis is adjusted, so as to engineer the production of excessive putrescine strains.
Construct design
The Tropine part of Tropane alkaloids (TAs) is obtained from arginine to putrescine (1,4-butanediamine, putrescine), and then through a series of chemical reactions. In this project, natural genes involved in arginine metabolism and polyamine biosynthesis was designed to overexpress in yeast. The engineer strains that produced excess putrescine. (Figure 2).
The profiles of every basic part are as follows:
BBa_K3993002
Name: AsADC
Base Pairs: 1821bp
Origin: Saccharomyces cerevisiae, synthesis
Properties: codon optimized SPE1
Usage and Biology
This protein is involved in step 1 of the subpathway that synthesizes agmatine from L-arginine. This subpathway is part of the pathway agmatine biosynthesis, which is itself part of Amine and polyamine biosynthesis.
BBa_K3993003
Name: PTDH3
Base Pairs: 673bp
Origin: Addgene
Properties: Yeast centromeric vector with the TDH3 (glyceraldehyde 3-phosphate dehydrogenase) promoter.
Usage and Biology
Yeast CEN/ARS vector (Leu2) that contains multiple cloning site ( MCS ) and TDH3 promoter.
BBa_K3993004
Name: TCYC1
Base Pairs: 242bp
Origin: Saccharomyces cerevisiae, genome
Properties: CYC1 terminator
Usage and Biology
This is a common transcriptional terminator. Placed after a gene, it completing the transcription process and impacting mRNA half-life. This terminator can be used for in vivo systems, and can be used for modulating gene expression in yeast.
Experimental approach
1. Fragments PCR products Electrophoresis
Lane 1 is target gene AsADC, Lane 2 is promoter PTDH3.
proof of function
Modeling for predicting the performance of our engineered bacteria to produce tropine
Firstly, we get the polynomial linear regression-2 shown in figure 4. (Data from the published articles, according to references3/4 )
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1362
Illegal BglII site found at 1583 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]