Part:BBa_K5327035
pRS424-ADH1p-GGP1-PYK1t-GPDp-GSTF9-ADH1t-HXT7p-SUR1-HXT7t-ADH1t-UGT-PGK1p
Function:
This product utilizes GGP1, GSTF9, SUR1, and UGT genes to construct a catalytic element, further optimizing the biosynthetic pathway of sulforaphane. The GGP1 enzyme hydrolyzes the γ-glutamyl peptide bond of glutathione (GSH) conjugates, producing Cys-Gly conjugates related to thiohydroximates, specifically S-Alkyl thiohydroxime. SUR1, acting as a CS lyase, participates in the biosynthesis of thiohydroximates by converting S-Alkyl thiohydroxime to Thiohydroxime. UGT is involved in glycosylation reactions, synthesizing Desulfo-glucosinolate. This process represents a critical step in the sulforaphane biosynthesis pathway. The gene fragments are integrated into the genome of the yeast strain S288C through genomic homologous recombination. The transformed yeast cells are then subjected to expression validation to screen for positive clones.
Usage and Biology
Expression diagram:
- Fig 1. The expression diagram of pRS424-ADH1p-GGP1-PYK1t-GPDp-GSTF9-ADH1t-HXT7p-SUR1-HXT7t-ADH1t-UGT-PGK1p
PCR result:
- Fig 2. The PCR result of pRS424-ADH1p-GGP1-PYK1t-GPDp-GSTF9-ADH1t-HXT7p-SUR1-HXT7t-ADH1t-UGT-PGK1p
Design Notes
Using CDS sequences from Arabidopsis thaliana (Ath), codon-optimized for S288C, this design employs fundamental molecular biology techniques. The GGP1, GSTF9, SUR1, and UGT genes, which play critical roles in the metabolic pathway, are used as core elements. These genes are combined with ADH1p, PYK1t, GPDp, ADH1t, HXT7p, HXT7t, ADH1t, and PGK1p to create a composite fragment. This combination facilitates the synthesis of the target intermediate, Desulfo-glucosinolate. Subsequent genomic homologous recombination in Saccharomyces cerevisiae S288C ensures the stable expression of this gene fragment, ultimately validating the effective synthesis of sulforaphane intermediates.
Plasmid
- Fig 3. The plasmid expression of pRS424-ADH1p-GGP1-PYK1t-GPDp-GSTF9-ADH1t-HXT7p-SUR1-HXT7t-ADH1t-UGT-PGK1p
Source
Arabidopsis thaliana
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 1626
Illegal SpeI site found at 2022
Illegal PstI site found at 4763
Illegal PstI site found at 5081 - 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 1626
Illegal SpeI site found at 2022
Illegal PstI site found at 4763
Illegal PstI site found at 5081 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2662
Illegal BglII site found at 4895
Illegal BglII site found at 6449
Illegal BglII site found at 8935
Illegal BamHI site found at 1752
Illegal BamHI site found at 3969
Illegal BamHI site found at 8830
Illegal XhoI site found at 6609 - 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 1626
Illegal SpeI site found at 2022
Illegal PstI site found at 4763
Illegal PstI site found at 5081 - 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 1626
Illegal SpeI site found at 2022
Illegal PstI site found at 4763
Illegal PstI site found at 5081
Illegal NgoMIV site found at 180
Illegal AgeI site found at 1494 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 830
Illegal BsaI site found at 3770
Illegal BsaI site found at 6606
Illegal BsaI.rc site found at 6972
Illegal SapI site found at 1600
Illegal SapI site found at 6245
None |