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Molecular Identification of UDP-Sugar-Dependent Glycosyltransferase and Acyltransferase Involved in the Phenylethanoid Glycoside Biosynthesis Induced by Methyl Jasmonate in Sesamum indicum L.
Fuji, Yushiro; Uchida, Kai; Akashi, Tomoyoshi; Ohtsuki, Takashi; Matsufuji, Hiroshi; Hirai, Masami Yokota.
Affiliation
  • Fuji Y; RIKEN Center for Sustainable Resource Science, Yokohama, 230-0045 Japan.
  • Uchida K; Department of Food Science and Technology, College of Bioresource Sciences, Nihon University, Fujisawa, Kanagawa, 252-0880 Japan.
  • Akashi T; RIKEN Center for Sustainable Resource Science, Yokohama, 230-0045 Japan.
  • Ohtsuki T; Department of Applied Biological Science, College of Bioresource Sciences, Nihon University, Fujisawa, Kanagawa, 252-0880 Japan.
  • Matsufuji H; Department of Food Science and Technology, College of Bioresource Sciences, Nihon University, Fujisawa, Kanagawa, 252-0880 Japan.
  • Hirai MY; Department of Food Science and Technology, College of Bioresource Sciences, Nihon University, Fujisawa, Kanagawa, 252-0880 Japan.
Plant Cell Physiol ; 64(7): 716-728, 2023 Jul 17.
Article in En | MEDLINE | ID: mdl-37233612
ABSTRACT
Sesame (Sesamum indicum L.) plants contain large amounts of acteoside, a typical phenylethanoid glycoside (PhG) that exhibits various pharmacological activities. Although there is increasing interest in the biosynthesis of PhGs for improved production, the pathway remains to be clarified. In this study, we established sesame-cultured cells and performed transcriptome analysis of methyl jasmonate (MeJA)-treated cultured cells to identify enzyme genes responsible for glucosylation and acylation in acteoside biosynthesis. Among the genes annotated as UDP-sugar-dependent glycosyltransferase (UGT) and acyltransferase (AT), 34 genes and one gene, respectively, were upregulated by MeJA in accordance with acteoside accumulation. Based on a phylogenetic analysis, five UGT genes (SiUGT1-5) and one AT gene (SiAT1) were selected as candidate genes involved in acteoside biosynthesis. Additionally, two AT genes (SiAT2-3) were selected based on sequence identity. Enzyme assays using recombinant SiUGT proteins revealed that SiUGT1, namely, UGT85AF10, had the highest glucosyltransferase activity among the five candidates against hydroxytyrosol to produce hydroxytyrosol 1-O-glucoside. SiUGT1 also exhibited glucosyltransferase activity against tyrosol to produce salidroside (tyrosol 1-O-glucoside). SiUGT2, namely, UGT85AF11, had similar activity against hydroxytyrosol and tyrosol. Enzyme assay using the recombinant SiATs indicated that SiAT1 and SiAT2 had activity transferring the caffeoyl group to hydroxytyrosol 1-O-glucoside and salidroside (tyrosol 1-O-glucoside) but not to decaffeoyl-acteoside. The caffeoyl group was attached mainly at the 4-position of glucose of hydroxytyrosol 1-O-glucoside, followed by attachment at the 6-position and the 3-position of glucose. Based on our results, we propose an acteoside biosynthetic pathway induced by MeJA treatment in sesame.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sesamum Type of study: Diagnostic_studies Language: En Journal: Plant Cell Physiol Journal subject: BOTANICA Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sesamum Type of study: Diagnostic_studies Language: En Journal: Plant Cell Physiol Journal subject: BOTANICA Year: 2023 Document type: Article