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in: PubMed | Google Scholar 1 Department of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan

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To further explore the substrate scope of arGSTs, additional yeast systems were engineered using a one-plasmid strategy containing genes encoding dihydroflavonol-4-reductase (DFR), LDOX, a range of arGST and non-arGSTs (as negative controls) and anthocyanidin-3- O -glucosyl transferase (A3GT) (Fig