Part:BBa_K5327012:Design
S-alkyl-thiohydroximate lyase SUR1
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 369
Illegal XhoI site found at 529 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 526
Illegal BsaI.rc site found at 892
Illegal SapI site found at 165
Design Notes
The design of the S-alkyl-thiohydroximate lyase (SUR1) gene is based on the coding sequence (CDS) from Arabidopsis thaliana and has been codon-optimized for efficient expression in Saccharomyces cerevisiae (S288C). SUR1 plays a crucial role in glucosinolate biosynthesis, catalyzing the conversion of S-(alkylacetohydroximoyl)-L-cysteine to thiohydroximate, and may be involved in glucosinolate activation in response to pathogens.[1]To ensure high-level expression and mRNA stability, the design employs the HXT7 promoter(BBa_K4000003) and HXT7 terminator(BBa_K5327019). The optimized gene will be cloned into a vector, introduced into yeast S288C through homologous recombination, and validated using a knockout strain. This design aims to enhance the production efficiency of glucosinolates in yeast and further optimize yeast as a platform for metabolic engineering.
Plasmid
- Fig 1. The plasmid expression of S-alkyl-thiohydroximate lyase SUR1
Source
Arabidopsis thaliana
References
- ↑ MIKKELSEN M D, NAUR P, HALKIER B A. Arabidopsis mutants in the C-S lyase of glucosinolate biosynthesis establish a critical role for indole-3-acetaldoxime in auxin homeostasis [J]. The Plant journal : for cell and molecular biology, 2004, 37(5): 770-7.