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Gene Synthesis> | The haploid R. toruloides strain IFO0880 served as parental strain for this study. BpsA and sfp sequences were codon-optimized for expression in R. toruloides. Gene synthesis and plasmid construction of pgen335.sfp.bpsA were performed by Genscript (Piscataway NJ). Pgen335.sfp.bpsA contains a Nourseothricin selection marker. All genes were expressed from native promoters: BpsA was expressed using Tef1p, while Sfp expression was driven by Acp1p. All strains and plasmids used in this study have been deposited in the public instance of the JBEI Registry27 along with their corresponding information and are available upon request through the Joint BioEnergy Institute Strain Registry (https://public-registry.jbei.org/folders/419). Pgen335.sfp.bpsA was introduced into R. toruloides recipient strain by Agrobacterium tumefaciens-mediated transformation (ATMT) as previously described.21 | Get A Quote |
Non-ribosomal peptides (NRPs) constitute a diverse class of valuable secondary metabolites, with potential industrial applications including use as pharmaceuticals, polymers and dyes. Current industrial production of dyes is predominantly achieved via chemical synthesis, which can involve toxic precursors and generate hazardous byproducts. Thus, alternative routes of dye production are highly desirable to enhance both workplace safety and environmental sustainability. Correspondingly, biological synthesis of dyes from renewable carbon would serve an ideal green chemistry paradigm. Therefore, we engineered the fungal host Rhodosporidium toruloides to produce the blue pigment indigoidine, an NRP with potentia... More